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Longer titles found: Xenopus allofraseri (view), Xenopus boumbaensis (view), Xenopus calcaratus (view), Xenopus egg extract (view), Xenopus eysoole (view), Xenopus fischbergi (view), Xenopus itombwensis (view), Xenopus kobeli (view), Xenopus lenduensis (view), Xenopus mellotropicalis (view), Xenopus parafraseri (view), Xenopus poweri (view), Xenopus victorianus (view), Scopus xenopus (view)

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prenylation for association with plasma and intracellular membranes. In Xenopus embryos, RhoV is encoded by a canonical Wnt response gene and is induced

circuit formation. Expression of mct8 has been characterised in Xenopus laevis and Xenopus tropicalis. Solute carrier family GRCh38: Ensembl release 89:

1016/S1937-6448(08)00807-1. PMID 18703408. Zhang J, King ML (December 1996). "Xenopus VegT RNA is localized to the vegetal cortex during oogenesis and encodes

kinetochore microtubules (Maiato 2003). CLASP homologues in Drosophila, Xenopus, and yeast are required for proper spindle assembly; in mammals, CLASP1

1186/1471-2164-12-554. PMC 3248570. PMID 22077994. "Xenbase - A Xenopus laevis and Xenopus tropicalis resource". "ZFIN Zebrafish Nomenclature". Iverson C

RNA genes have been identified in human, mouse, rat and the amphibian Xenopus laevis. Peculis BA (1997). "The sequence of the 5' end of the U8 small

that belongs to the C/D family of snoRNAs. It is the human orthologue of Xenopus laevis U86 and has no identified RNA target. The snoRNAs U86, U56, U57

including rats and mice, birds such as chickens, and frogs such as Xenopus laevis and Xenopus tropicalis. The SLC39A12 gene is present in some fish such as

They are both encoded in the introns of the ribosomal protein S3. In Xenopus laevis it is located within the introns of ribosomal protein S1 snoR75

directing site-specific 2'-O-methylation of substrate RNAs. In humans and Xenopus laevis there are three closely related copies of U18 (called U18A, U18B

cyclin B just above the activation threshold. Sha et al. did experiments in Xenopus laevis egg extracts in 2003 to demonstrate this hysteretic nature. Using

zoologist and medical statistician. He developed the African clawed frog (Xenopus laevis) as a model organism for biological research in his early career

within intron 12 of the nucleolin gene in human, mouse, rat chicken, and Xenopus laevis. Kiss T (April 2002). "Small nucleolar RNAs: an abundant group of

reported by Schwabacher in 1959, having been isolated in lesions found on a Xenopus laevis, but the possibility of human infection was not confirmed until

Siba, M.; Sidi, S.; Levin, M.; Gillespie, P. G.; Gründer, S. (2005). "Xenopus TRPN1 (NOMPC) localizes to microtubule-based cilia in epithelial cells

effects range from frogs (Xenopus laevis) to humans, with innumerous effects in phenotype and also in development. In Xenopus laevis, REST/NRSF malfunction

U22 host gene) in mammals. U22 has also been identified in the amphibian Xenopus laevis U22 is predicted to guide the 2'-O-ribose methylation guide for

C-terminal half of this protein has been shown to bind DNA. Studies with the Xenopus homolog suggests an essential role in metaphase chromosome alignment and

nervous system through studying frogs. The African clawed frog or platanna, Xenopus laevis, was first widely used in laboratories in pregnancy assays in the

shows significant homology to glycosaminoglycan synthetase (DG42) from Xenopus laevis, and human and murine hyaluronan synthase 1. GRCh38: Ensembl release

receptor tyrosine kinase. NT-4 was first discovered and isolated from xenopus and viper in the year 1991 by Finn Hallbook et.al Tropomyosin receptor

entry will eventually form the dorsal portion of the body. In the frog Xenopus laevis, the animal pole is heavily pigmented while the vegetal pole remains

high affinity transport of L-cystine shared with dibasic amino acids in Xenopus oocytes". J. Biol. Chem. 268 (20): 14842–9. doi:10.1016/S0021-9258(18)82410-3

BMP and activin membrane-bound inhibitor homolog (Xenopus laevis), also known as BAMBI, is a protein which in humans is encoded by the BAMBI gene. This

from behind. Areas of the Xenopus brain responding to surface waves have been identified. It has been speculated that both Xenopus and the European grassfrog

CHRD gene. Chordin was originally identified in the African clawed frog (Xenopus laevis) in the laboratory of Edward M. De Robertis as a key developmental

Falguni Guharay and Frederick Sachs. They were also observed (pub. 1986) in Xenopus oocytes, and frequently studied since that time. Since then, MSCs have

lymphocytes. At around the same time, the Xenopus NO38 was discovered and was found to be homologous to Xenopus Nucleoplasmin and rat B23. The NPM1 protein

and has several species named after him, such as Peracca's clawed frog (Xenopus clivii), Mantidactylus peraccae, Anolis peraccae, and Lepidoblepharis peraccae

have many Plk family members including Plk1 (Xenopus Plx1), Plk2/Snk (Xenopus Plx2), Plk3/Prk/FnK (Xenopus Plx3), Plk4/Sak and Plk5. Of the vertebrate

formerly known as IPF1. The gene was originally identified in the clawed frog Xenopus laevis and is present widely across the evolutionary diversity of bilaterian

are a class of antimicrobial peptides found in the African clawed frog (Xenopus laevis). The peptides are cationic, generally lack a stable conformation

of nucleoli by John Gurdon and Donald Brown in the African clawed frog Xenopus laevis generated increasing interest in the function and detailed structure

The Drosophila homolog is SAK, the C. elegans homolog is zyg-1, and the Xenopus homolog is Plx4. PLK4 encodes a member of the polo family of serine/threonine

the tiger salamander (Ambystoma tigrinum), and the African clawed frog (Xenopus laevi). The discovery of lep in puffer fish (Takifugu rubripes) demonstrates

orientation of body and wing hairs. There are vertebrate homologs in zebrafish, Xenopus (Xdsh), mice (Dvl1, -2, -3) and humans (DVL-1, -2, -3). Dsh relays complex

gene. Anterior gradient homolog 2 was originally discovered in Xenopus laevis. In Xenopus AGR2 plays a role in cement gland differentiation, but in human

beta 4, h alpha 4 beta 2, h alpha 4 beta 4 and h alpha 7 expressed in Xenopus oocytes". J. Pharmacol. Exp. Ther. 280 (1): 346–56. PMID 8996215. Groot

In Xenopus laevis, the specification of the three germ layers (endoderm, mesoderm and ectoderm) occurs at the blastula stage. Great efforts have been

The crocodile-faced dtella (Gehyra xenopus) is a species of gecko endemic to Western Australia. It was first described in 1978 by Glen Milton Storr. Oliver

In Xenopus laevis, the specification of the three germ layers (endoderm, mesoderm and ectoderm) occurs at the blastula stage. Great efforts have been

Harry Zwarenstein, with whom he was later to co-operate in developing the Xenopus laevis pregnancy test. But his initial research was into amphibian metabolism

in insulin physiology as well. The first intelectin was discovered in Xenopus laevis oocyte and is named XL35 or XCGL-1. X. laevis oocyte also contains

creation of Siamese twins. De Robertis identified the genes expressed in Xenopus embryos in this area, beginning with the goosecoid homeobox gene. Together

small nuclear ribonucleoprotein particle and histone RNA 3' processing in Xenopus egg extracts". J Biol Chem. 275 (32): 24284–24293. doi:10.1074/jbc.M003253200

effects of tramadol on 5-hydroxytryptamine type 2C receptors expressed in Xenopus oocytes". Anesthesia and Analgesia. 98 (5): 1401–6, table of contents.

Xenobots, named after the African clawed frog (Xenopus laevis), are synthetic lifeforms that are designed by computers to perform some desired function

PMC 324341. PMID 7008030. Salim M, Maden EH (1981). "Nucleotide sequence of Xenopus laevis 18S ribosomal RNA inferred from gene sequence". Nature. 291 (5812):

easily be kept in the laboratory. Xenopus laevis is increasingly being displaced by its smaller relative, Xenopus tropicalis, which reaches its reproductive

certain nuclear transport proteins of Xenopus and human. The predicted amino acid sequence shows similarity to Xenopus importin, yeast SRP1, and human RCH1

lead to carcinogenesis. Additionally, in the amphibian model organism Xenopus laevis, it has been shown that Gli2 plays a key role in the induction,

the intestine. KCNE3 also interacts with hERG, and when co-expressed in Xenopus laevis oocytes KCNE3 inhibits hERG activity by an unknown mechanism. It

identified in humans. The Xenopus Mix gene and human Mix genese are homologues. Mixl1 is functionally similar to the Xenopus Mix.1. Mixl1 is transiently

Rattus norvegicus, Canis lupus familiaris, Bos taurus, Gallus gallus, Xenopus tropicalis, Danio rerio" "Drosophila melanogaster, Anopheles gambiae, Caenorhabditis

similar principles. Widespread export and traffic in African clawed frogs (Xenopus laevis) used for these tests is believed to have been the primary cause

described the internal movements in more detail using pregastrular explants of Xenopus laevis. Gastrulation in amphibians is initiated by formation of bottle

cited as the first to purify single genes, the ribosomal RNA genes from Xenopus laevis, three years before the successful isolation of the lac operon.

isolation of a fraction of RNA from rat kidney that, when injected into Xenopus oocytes, produced an unusually slow-activating, voltage-dependent, potassium-selective

70 kDa family contain only one kinase domain. Rsk was first identified in Xenopus laevis eggs by Erikson and Maller in 1985. Frödin, M; Gammeltoft, S (May

knockout mice have no eyes and abnormal forebrain formation. In the frog Xenopus tropicalis, Rax mutants are eyeless; the future retinal tissue instead

and Pleurodeles watl. Genetically modified frogs, in particular Xenopus laevis and Xenopus tropicalis, are used in development biology. GM frogs can also

human condensin complex containing hCAP-C-hCAP-E and CNAP1, a homolog of Xenopus XCAP-D2, colocalizes with phosphorylated histone H3 during the early stage

Xenopus laevis. Carvalho KM, Joudiou C, Boussetta H, Leseney AM, Cohen P (January 1992). "A peptide-hormone-inactivating endopeptidase in Xenopus laevis

in the Japanese toad (Bufo japonicus) and in the African clawed frog (Xenopus laevis). Ovulated coelomic egg cells are not fertilisable in these species

synthetic Xhox-1A homeobox mRNA disrupts somite formation in developing Xenopus embryos". Cell. 53 (5): 687–97. doi:10.1016/0092-8674(88)90087-6. ISSN 0092-8674

1999). "Isolation and characterization of a human cDNA homologous to the Xenopus laevis XCAP-C gene belonging to the structural maintenance of chromosomes

(1972). The cytology and biochemistry of DNA amplification in the ovary of Xenopus laevis (Thesis). University of Edinburgh. hdl:1842/11977. EThOS uk.bl.ethos

complete feminization and chemical castration in male African clawed frogs (Xenopus laevis)". Proc. Natl. Acad. Sci. U.S.A. 107 (10): 4612–7. Bibcode:2010PNAS

including cartilage. Human FGF20 was identified based on its homology to Xenopus FGF-20 (XFGF-20). FGF15 through FGF23 were described later and functions

zoologist and ornithologist who specialised in allometry. He described Xenopus laevis, the African clawed frog, for the first time in his doctoral thesis

L.; Solomon, Keith R. (July 2005). "Gonadal Development of Larval Male Xenopus laevis Exposed to Atrazine in Outdoor Microcosms". Environmental Science

response to the microtubule poison nocodazole. Subsequent cloning of the Xenopus laevis orthologue, facilitated by the sharing of the human sequence, allowed

missing the region homologous to the human exon 5 have been detected in both Xenopus laevis and Mus musculus. GRCh38: Ensembl release 89: ENSG00000180879 –

(January 1998). "Drosophila Shaking-B protein forms gap junctions in paired Xenopus oocytes". Nature. 391 (6663): 181–4. Bibcode:1998Natur.391..181P. doi:10

BS, Tata JR, Xu Q (1993). "Developmental and hormonal regulation of the Xenopus liver-type arginase gene". Eur. J. Biochem. 211 (3): 891–898. doi:10.1111/j

for example, into a new area of the embryo. Grafting experiments done in Xenopus and chicken embryos show the neural plate's capability to induce other

Caenorhabditis elegans and Caenorhabditis briggsae, and Xenbase for Xenopus tropicalis and Xenopus laevis frogs. Numerous databases attempt to document the diversity

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proceedings of the National Academy of Sciences of the United States

desynchronization of the segmentation oscillations. Many studies with Xenopus and zebrafish have analyzed the factors of this development and how they

family of karyopherins such as importin subunit alpha-1. These include the Xenopus protein importin and its yeast homolog, SRP1 (a suppressor of certain

PS4), a serum and growth factor induced protein. Mammalian spermadhesins. Xenopus laevis embryonic protein UVS.2, which is expressed during dorsoanterior

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proceedings of the National Academy of Sciences of the United States

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proceedings of the National Academy of Sciences of the United States

that katanin is responsible for severing microtubules during M-phase in Xenopus laevis. The disassembly of microtubules from their interphase structures

starfish), the tardigrade water bear (Hypsibius dujardini), and the tadpole of Xenopus laevis. Searches of publicly available databases of genetic sequences have

P (2007). "The human histamine H3 receptor couples to GIRK channels in Xenopus oocytes". European Journal of Pharmacology. 567 (3): 206–210. doi:10.1016/j

suppresses the activation of MAP kinase by oncogenic ras in extracts of Xenopus oocytes. Thus, DUSP1 may play an important role in the human cellular response

Wohlschlegel JA, Dhar SK, Prokhorova TA, Dutta A, Walter JC (2002). "Xenopus Mcm10 binds to origins of DNA replication after Mcm2-7 and stimulates origin

Speedy homolog E1 (Xenopus laevis) is a protein that in humans is encoded by the SPDYE1 gene. This gene is located at chromosome 7p13 which is close to

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proceedings of the National Academy of Sciences of the United States

secretion; intestinal trefoil factor (ITF) (TFF3); Xenopus laevis stomach proteins xP1 and xP4; xenopus integumentary mucins A.1 (preprospasmolysin) and

of G. Steven Martin at UC Berkeley.[citation needed] Through studies of Xenopus laevis oocyte maturation, Ferrell showed how graded changes in the inductive

to vertebrae, ribs, skeletal muscle, cartilage, tendons, and skin. In Xenopus laevis, the transition from the gastrula to the neurula involves morphological

synthetic Xhox-1A homeobox mRNA disrupts somite formation in developing Xenopus embryos". Cell. 53 (5): 687–697. doi:10.1016/0092-8674(88)90087-6. PMID 2897242

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proceedings of the National Academy of Sciences of the United States

(1995). "Identification of the yeast MCM3-related protein as a component of Xenopus DNA replication licensing factor". Cell. 81 (4): 601–9. doi:10.1016/0092-8674(95)90081-0

RanGTP-induced microtubule nucleation. This has been demonstrated both in vitro in Xenopus laevis egg extracts, and with the human homologue in vivo in HeLa cells

a simple anterior organ, the mucus-secreting cement gland of the frog Xenopus, to define the genetic network required for anterior position. The EAD

gremlin 1, cysteine knot superfamily, homolog (Xenopus laevis) Identifiers Symbol GREM1 Alt. symbols CKTSF1B1 NCBI gene 26585 HGNC 2001 OMIM 603054 RefSeq

larger populations of the dorsal mesoderm and neural ectoderm of frogs (Xenopus) and fish. Many characteristics of convergent extension are conserved in

development, expression is localised to the node and notochord. In Xenopus laevis, Xbra (the Xenopus T homologue, also recently renamed t) is expressed in the

(CDC10-dependent transcript 1) Drosophila melanogaster – 'double parked' or Dup Xenopus laevis - CDT1 DNA replication factor CDT1 has been shown to interact with

58 106-115 2016 Regulation of growth rate and developmental timing by Xenopus thyroid hormone receptor α. 2016 Kwok Yeung Tsang, Danny Chan and Kathryn

bullfrog (Lithobates catesbeiana) — successfully bred African clawed toad (Xenopus laevis) — two populations survived in the UK for 50 years, now extinct

1101/gr.9.2.121. PMID 10022976. Chang C, Hemmati-Brivanlou A (1999). "Xenopus GDF6, a new antagonist of noggin and a partner of BMPs". Development. 126

xenopodis (Monogenea: Polystomatidae) infecting the African clawed frog Xenopus laevis". Parasite. 21: 20. doi:10.1051/parasite/2014020. ISSN 1776-1042

is also a body of work concerning epiboly in the African clawed frog, Xenopus laevis. Comparisons of epiboly in amniotes, teleosts and X. laevis show

"Brain-specific expression of novel G-protein-coupled receptors, with homologies to Xenopus PSP24 and human GPR45". Biochem. Biophys. Res. Commun. 276 (3): 952–6.

chemoattractant receptor is encoded by a 2 kilobase messenger RNA. Expression in Xenopus oocytes". FEBS Letters. 261 (2): 353–7. doi:10.1016/0014-5793(90)80590-f

the development of the wing disc, survival and cell growth. Finally in Xenopus, it has been demonstrated that the homolog of TEAD regulates muscle differentiation

(Frogs and Toads) African clawed frog (Xenopus laevis)  (505 genes, 118 families) Tropical clawed frog (Xenopus tropicalis)  (355 genes, 106 families)

"Brain-specific expression of novel G-protein-coupled receptors, with homologies to Xenopus PSP24 and human GPR45". Biochem. Biophys. Res. Commun. 276 (3): 952–6.

J. & North, R.A. Expression of a cloned rat brain potassium channel in Xenopus oocytes. Science 244: 221–224, 1989 Christie, M.J., North, R.A., Osborne

tadpole into the terrestrial, carnivorous frog. In fact, amphibian frog Xenopus laevis serves as an ideal model system for the study of the mechanisms

barbiturate-, and benzodiazepine-insensitive gamma-aminobutyric acid responses in Xenopus oocytes". Mol. Pharmacol. 41 (4): 683–687. PMID 1314944. Kusama T, Spivak

indicating multiple functions during early development. Experiments in Xenopus also support the idea that Zic5 can regulate formation of neural crest

PMID 9335334. Losada A, Hirano M, Hirano T (1998). "Identification of Xenopus SMC protein complexes required for sister chromatid cohesion". Genes Dev

PMC 24960. PMID 9405610. Sato N, Arai K, Masai H (Sep 1997). "Human and Xenopus cDNAs encoding budding yeast Cdc7-related kinases: in vitro phosphorylation

BW284c51 is a potent blocker of Torpedo nicotinic AchRs incorporated into the Xenopus oocyte membrane". British Journal of Pharmacology. 144 (1): 88–97. doi:10

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proc. Natl. Acad. Sci. U.S.A. 93 (25): 14480–5. Bibcode:1996PNAS...9314480T

properties of native receptors and functional alpha 7 homomers expressed in Xenopus oocytes". Mol. Pharmacol. 45 (3): 546–554. PMID 8145738. Hillier LD, Lennon

doctoral work at Harvard University studying germ layer formation using Xenopus as a model. As a National Science Foundation pre-doctoral Fellow working

Michalak P (December 2011). "Misexpression of testicular microRNA in sterile Xenopus hybrids points to tetrapod-specific microRNAs associated with male fertility"

family Hylidae found in Canada and the United States Western clawed frog (Xenopus tropicalis), a frog in the family Pipidae found in Africa Western marsh

of Streptococcus pyogenes, a glycosaminoglycan synthetase (DG42) from Xenopus laevis, and a recently described murine hyaluronan synthase. GRCh38: Ensembl

especially well recognized for studies of the development of the model organism Xenopus laevis (African clawed frog). With Metta Riebesell, he coauthored a widely

(April 2015). "A New Nomenclature of Xenopus laevis Chromosomes Based on the Phylogenetic Relationship to Silurana/Xenopus tropicalis". Cytogenetic and Genome

"Xenbase Gene: Summary for pax8, species: Xenopus tropicalis". Xenbase. xenbase.org. Retrieved 2009-07-17. A Xenopus laevis and tropicalis resource This article

of Streptococcus pyogenes, a glycosaminoglycan synthetase (DG42) from Xenopus laevis, and a recently described murine hyaluronan synthase. GRCh38: Ensembl

little grass frog Sphaenorhynchus lacteus, rana fantasma (tree frog) Xenopus laevis, African clawed frog Genus Spiroglyptus, wormsnails, family Vermetidae

"Rhynchophylline and Isorhynchophylline Inhibit NMDA Receptors Expressed in Xenopus Oocytes". European Journal of Pharmacology. 455 (1): 27–34. doi:10

T (Feb 2001). "Chromosome condensation by a human condensin complex in Xenopus egg extracts". The Journal of Biological Chemistry. 276 (8): 5417–20. doi:10

dickkopf homolog 1 (Xenopus laevis)". Schneider VA, Mercola M (1999). "Spatially distinct head and heart inducers within the Xenopus organizer region".

Keith Henry Stockman (1988). Aspects of cell cycle regulation in yeast and Xenopus (PhD thesis). University of Sussex. OCLC 757094117. "Lecture editorial

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proc. Natl. Acad. Sci. U.S.A. 93 (25): 14480–5. Bibcode:1996PNAS...9314480T

1999). "Characterization of a novel member of the FGF family, XFGF-20, in Xenopus laevis". Biochemical and Biophysical Research Communications. 261 (3):

(DAN) is involved in poly(A) tail removal during the meiotic maturation of Xenopus oocytes". The EMBO Journal. 17 (18): 5427–37. doi:10.1093/emboj/17.18.5427

resulting effects. Using the 8-cell-embryos of the African clawed frog, Xenopus, she used antibody injections to block the channels in the connections

TATA-binding protein (TBP). Orthologs have been identified in mouse, frog (Xenopus tropicalis) and fish (Danio rerio). Whereas the TBP gene is found in all

Baum LG, Moremen KW, Pierce M (January 2001). "Human homologs of the Xenopus oocyte cortical granule lectin XL35". Glycobiology. 11 (1): 65–73. doi:10

1002/jez.1400920303. Gaze, R. M. (1959). "REGENERATION OF THE OPTIC NERVE IN XENOPUS LÆVIS". Quarterly Journal of Experimental Physiology and Cognate Medical

perinatal heart development. ssTnI is not expressed in the embryonic hearts of Xenopus and zebrafish, while it is expressed in the somites and skeletal muscles

brain Na channel is sufficient for expression of functional channels in Xenopus oocytes". Proceedings of the National Academy of Sciences of the United

nucleolar RNA requirement for site-specific ribose methylation of rRNA in Xenopus". Proceedings of the National Academy of Sciences of the United States

Tran U, Wessely O (December 2009). "The miR-30 miRNA family regulates Xenopus pronephros development and targets the transcription factor Xlim1/Lhx1"

gamma-aminobutyric acid actions on gamma-aminobutyric acidA receptors expressed by Xenopus oocytes: lack of involvement of intracellular calcium". The Journal of

chromosome condensation protein complexes containing XCAP-C, XCAP-E and a Xenopus homolog of the Drosophila Barren protein". Cell. 89 (4): 511–521. doi:10

in the retinal photoreceptors of Xenopus laevis, where Noc mRNA displayed rhythmic expression in an isolated Xenopus eye in light/dark and constant conditions

species such as Xenopus laevis, urocortin is expressed in tissues such as brain, pituitary, kidney, heart, and skin. Urocortin in Xenopus has been shown

structures relative to the mouse, while eggs and embryos from Xenopus tropicalis and Xenopus laevis (African clawed frog) are used in developmental biology

effects of toxins of several species of tarantulas on Kv2-channels of Xenopus laevis (the African clawed frog) (Escoubas et al. 2002). Bioassay guided

; James, B. (2013). "Plasticity of lung development in the amphibian, Xenopus laevis". Biology Open. 2 (12): 1324–1335. doi:10.1242/bio.20133772. PMC 3863417

glycoprotein); A5 antigen (a developmentally-regulated cell surface protein; Xenopus nrp1; P28824); and receptor-like tyrosine protein phosphatase. The MAM

She uses egg cytoplasmic extracts from the frog Xenopus laevis and the related, smaller frog Xenopus tropicalis to study the behavior and size scaling

S2CID 2996948. "Entrez Gene: CDK7 cyclin-dependent kinase 7 (MO15 homolog, Xenopus laevis, cdk-activating kinase)". Patel H, Abduljabbar R, Lai CF, Periyasamy

frogs, regeneration does not occur (Xenopus can grow a cartilaginous spike after amputation). The adult Xenopus laevis is used as a model organism for

Sciences in 2004. Her dissertation was titled, The induction and function of xenopus six 1 in cranial placode development. In 2010, Brugmann then finished her

similarity of its chromodomain. It contains a region of homology shared by Xenopus and Drosophila in the fifth exon. Polycomb genes in Drosophila mediate

of ovarian cells in Xenopus. Through her work, she was able to conclude that the localization of binding in the oocytes of Xenopus is specific. Pardue

barbiturate-, and benzodiazepine-insensitive gamma-aminobutyric acid responses in Xenopus oocytes". Mol. Pharmacol. 41 (4): 683–7. PMID 1314944. Kusama T, Spivak

irreversible transition into mitosis driven by hysteresis. Through experiments in Xenopus laevis cell-free egg extracts, such model was confirmed as the basis for

organisms. Zebrafish MBT occurs at cycle 10, but it occurs at cycle 13 in both Xenopus and Drosophila. Cells are thought to time the MBT by measuring the nucleocytoplasmic

members of the histone deacetylase family. This gene is orthologous to the Xenopus and mouse MITR genes. The MITR protein lacks the histone deacetylase catalytic

chromatin. Within a Xenopus nucleus-free system, it has been demonstrated that Cdc45 is required for the unwinding of plasmid DNA. The Xenopus nucleus-free system

organisms including the Saccharomyces cerevisiae, Dictyostelium discoideum and Xenopus laevis. REMI has been used for large-scale transgenesis in X. laevis embryos

members of the histone deacetylase family. This gene is orthologous to the Xenopus and mouse MITR genes. The MITR protein lacks the histone deacetylase catalytic

Xenopus_laevis/latest_assembly_versions/GCF_001663975.1_Xenopus_laevis_v2". ftp.ncbi.nih.gov. Retrieved 2020-11-30. "Xenopus laevis (ID 81)

chromatin. Within a Xenopus nucleus-free system, it has been demonstrated that Cdc45 is required for the unwinding of plasmid DNA. The Xenopus nucleus-free system

"Poly(A)-binding protein and eRF3 are associated in vivo in human and Xenopus cells". Biology of the Cell. 94 (4–5): 205–16. doi:10.1016/S0248-4900(02)01194-2

AP; Ghannadan, M (2009). "The anatomy and development of the claws of Xenopus laevis (Lissamphibia: Anura) reveal alternate pathways of structural evolution

(Dec 1992). "Sequence and localization of human NASP: conservation of a Xenopus histone-binding protein". Dev Biol. 154 (1): 37–44. doi:10.1016/0012-1606(92)90045-I

Tyrosinase sequences from ten vertebrates species( Genus: Ambystoma, Xenopus, Homo, Elaphe, Thamnophis, Bufo, Rugosa, and Rana) were analyzed. The multiple

dissertation dealt with the role of the egg-jelly on the fertilization of Xenopus laevis. Upon returning to Ecuador in 1972 she became professor of Biology

studied regulation of the embryonic cell cycle in (the African clawed frog Xenopus laevis) in 1994. During her doctorate she particularly enjoyed meeting

channel Kv 4.3 by serum- and glucocorticoid-inducible kinase isoforms in Xenopus oocytes". Pflügers Arch. 450 (1): 26–33. doi:10.1007/s00424-004-1369-z

model systems like Drosophila melanogaster, C. elegans, zebrafish and Xenopus laevis. However, since 1980, a wealth of information on plant morphology

Transcriptional Effects of Thyroid-Disrupting Agents in Premetamorphic Xenopus Tadpoles". Environmental Health Perspectives. 113 (11): 1588–1593. doi:10

blockade of diverse types of voltage-gated Ca2+ channels expressed in Xenopus oocytes by the Ca2+ channel antagonist mibefradil (Ro 40-5967)". Molecular

yellow-billed amazon, zebu, zebra finch Lissamphibia Leisan spiny toad, Xenopus tropicalis Teleosts Amazon molly, asian arowana, atlantic cod, atlantic

is the pentamer. By way of comparison, the structure of IgM from frogs (Xenopus) is predominantly hexameric, IgM from bony fish is predominantly tetrameric

expressed in subsets of mesodermal cells and is closely related to the Xenopus X-twi and the Drosophila twist genes". Developmental Biology. 143 (2):

S2CID 2647092. Ma P, Zhao S, Zeng W, Yang Q, Li C, Lv X, et al. (August 2011). "Xenopus Dbx2 is involved in primary neurogenesis and early neural plate patterning"

a secreted activator of Wnt/beta-catenin signaling and is required for Xenopus myogenesis". Developmental Cell. 7 (4): 525–34. doi:10.1016/j.devcel.2004

Typell DNA topoisomerase. Much of his work was characterized using various Xenopus laevis cell types, including oocytes, unfertilized eggs, and kidney cells;

their influence on CaV2.1 voltage-dependent calcium channels expressed in Xenopus oocytes". BMC Neuroscience. 4: 23. doi:10.1186/1471-2202-4-23. PMC 270087

S2CID 44743817. Harland, R; Weintraub, H (1985). "Translation of mRNA injected into Xenopus oocytes is specifically inhibited by antisense RNA". J Cell Biol. 101 (3):

lupus familiaris] - Protein - NCBI". "WD repeat-containing protein 75 [Xenopus laevis] - Protein - NCBI". "PREDICTED: WD repeat-containing protein 75

subunits on pharmacological properties of α3β1 GABAA receptors expressed in Xenopus oocytes". BMC Pharmacol. 6: 1. doi:10.1186/1471-2210-6-1. PMC 1363348.

v t e PDB gallery 1l6o: XENOPUS DISHEVELLED PDZ DOMAIN 2f0a: Crystal Structure of Monomeric Uncomplexed form of Xenopus dishevelled PDZ domain

Associated with Pigmentary Effector Activity and Pituitary Removal in Xenopus Laevis.—I. Respiratory Exchange", Proceedings of the Royal Society B: Biological

of two large subdomains in TFIIE-alpha on the basis of homology between Xenopus and human sequences". Nucleic Acids Res. 20 (21): 5838. doi:10.1093/nar/20

They play a crucial role in activating CDKs. Originally identified in Xenopus, these proteins primarily bind to and activate CDK1 and CDK2, despite lacking

Family: Pipidae Genus: Hymenochirus Species: H. boettgeri Binomial name Hymenochirus boettgeri (Tornier, 1896) Synonyms Xenopus boettgeri Tornier, 1896

et al. (2003). "Glucose transporter GLUT12-functional characterization in Xenopus laevis oocytes". Biochem. Biophys. Res. Commun. 308 (3): 422–6. doi:10

growth of new synapses The role of the CPE was first characterized in Xenopus oocytes and embryos but recent research has identified roles for the CPE

determinant of high-affinity dofetilide binding to HERG1 expressed in Xenopus oocytes: involvement of S6 sites". Molecular Pharmacology. 57 (2): 367–74

Fortriede JD, Dahdul WM, et al. (October 2013). "Enhanced XAO: the ontology of Xenopus anatomy and development underpins more accurate annotation of gene expression

growth of new synapses The role of the CPE was first characterized in Xenopus oocytes and embryos but recent research has identified roles for the CPE

mimic the cytoplasmic tails of AMPA receptors are expressed in individual Xenopus neurons, trafficking of AMPA receptors to nascent synapses is minimized

PMC 108837. PMID 9488439. Roose J, Molenaar M, Peterson J, et al. (1998). "The Xenopus Wnt effector XTcf-3 interacts with Groucho-related transcriptional repressors"

(Ornithorhynchus anatinus), Japanese medaka (Oryzias latipes), African clawed frog (Xenopus laevis), Tasmanian devil (Sarcophilus harrisii), pig (Sus scrofa) and zebra

R, Hunt T, Stillman B (Dec 1998). "The Orc4p and Orc5p subunits of the Xenopus and human origin recognition complex are related to Orc1p and Cdc6p". The

discovered mycobacterial pathogen isolated from laboratory colonies of Xenopus species with lethal infections produces a novel form of mycolactone, the

Fortriede JD, Dahdul WM, et al. (October 2013). "Enhanced XAO: the ontology of Xenopus anatomy and development underpins more accurate annotation of gene expression

P, Pieler T, Gurdon JB, Papalopulu N (January 1998). "Xiro3 encodes a Xenopus homolog of the Drosophila Iroquois genes and functions in neural specification"

hamster. This gene is mapped in close proximity to APXL (Apical protein Xenopus laevis-like) and OA1 (Ocular albinism type I), which are both located on

periods to be studied. Firing frequencies have shown in in vitro studies of Xenopus laevis egg extract to increase as S phase progresses. In another study

their influence on CaV2.1 voltage-dependent calcium channels expressed in Xenopus oocytes". BMC Neuroscience. 4: 23. doi:10.1186/1471-2202-4-23. PMC 270087

recombinant neuronal nicotinic receptors containing the β3 subunit expressed in Xenopus oocytes". J. Physiol. 529 Pt 3 (Pt 3): 565–77. doi:10.1111/j.1469-7793

development of embryos, found in zebrafish oocyte by Bruce et al 2003 and Xenopus laevis oocyte by Xanthos et al 2001. They are also expressed in later stages

Vulcu SD, Liewald JF, et al. (2005). "Monovalent cation conductance in Xenopus laevis oocytes expressing hCAT-3". Biochim. Biophys. Acta. 1668 (2): 234–9

tadpole into that of the terrestrial, carnivorous adult. The frog species Xenopus laevis has proven to be an ideal model organism for experimental study

T (Feb 2001). "Chromosome condensation by a human condensin complex in Xenopus egg extracts". J. Biol. Chem. 276 (8): 5417–20. doi:10.1074/jbc.C000873200

Grg4 physically interact to repress transcription and induce mesoderm in Xenopus". The Journal of Biological Chemistry. 282 (4): 2548–2557. doi:10.1074/jbc

1856) Hypopachus variolosus (Cope, 1866) Order: Anura. Family: Pipidae Xenopus laevis (Daudin, 1802) Order: Anura. Family: Ranidae Glandirana rugosa (Temminck

effectiveness of analgesia. Early studies showed that African clawed frogs (Xenopus laevis) learn to avoid electric shocks in an aquatic shuttle-box test and

PMID 2876518. Reverte CG, Ahearn MD, Hake LE (2001). "CPEB degradation during Xenopus oocyte maturation requires a PEST domain and the 26S proteasome". Dev.

phenomena. The Kinesin-related protein XKCM1 stimulates catastrophes in Xenopus microtubules. The Kinesin-Related Protein 13 MCAK increases the frequency

human gene can induce neurogenic differentiation in non-neuronal cells in Xenopus embryos, and is thought to play a role in the determination and maintenance

Gerhart, John C. (April 1996). "Confocal microscopy analysis of living Xenopus eggs and the mechanism of cortical rotation" (PDF). Development. 122 (4):

beta 4, h alpha 4 beta 2, h alpha 4 beta 4 and h alpha 7 expressed in Xenopus oocytes". J. Pharmacol. Exp. Ther. 280 (1): 346–56. PMID 8996215. Navaneetham

"Elongation factor EF-1 delta, a new target for maturation-promoting factor in Xenopus oocytes". The Journal of Biological Chemistry. 269 (31): 20201–7. doi:10

Fukuda M, Onuma Y, Asashima M (December 2006). "Expression of Sox1 during Xenopus early embryogenesis". Biochemical and Biophysical Research Communications

outwardly rectifying Cl- channels and volume regulation in HeLa cells and Xenopus laevis oocytes". J. Biol. Chem. 277 (42): 40066–74. doi:10.1074/jbc.M205132200

"Effects of temperature on human L-type cardiac Ca2+ channels expressed in Xenopus oocytes". Pflügers Arch. 436 (2): 238–47. doi:10.1007/s004240050628. PMID 9594024

receptors but not ionotropic glutamate receptors in striatal neurons and Xenopus oocytes". Mol. Pharmacol. 38 (1): 1–6. PMID 2164627. McDonald JW, Fix AS

Gehyra wongchan Pauwels, Meesook, Kunya, Donbundit, & Sumontha, 2022 Gehyra xenopus Storr, 1978 – crocodile-faced dtella Nota bene: A binomial authority in

metalloproteinase (MMP), CMMP, from chicken embryo fibroblasts. CMMP, Xenopus XMMP, and human MMP19 have a conserved unique cysteine in the catalytic

quantification reveals tight regulation of protein expression in single Xenopus eggs". Nucleic Acids Research. 42 (15): 9880–9891. doi:10.1093/nar/gku661

crustaceans and insects. But is also found in the African clawed frog (Xenopus laevis). Wagner et al., suggest that chitin might have a microscopic function

"Rhynchophylline and Isorhynchophylline Inhibit NMDA Receptors Expressed in Xenopus Oocytes". European Journal of Pharmacology. 455 (1): 27–34. doi:10

Pyxicephalus edulis Edible Frog Pouandi bouali Poondré Tomopterna cryptotis Cryptic sand frog Louand boani Louang boudi Xenopus muelleri Savanna Clawed Frog

pathway that is mediated by AIF (apoptosis-inducing factor). The frog Xenopus laevis serves as an ideal model system for the study of the mechanisms

crustaceans and insects. But is also found in the African clawed frog (Xenopus laevis). Wagner et al., suggest that chitin might have a microscopic function

quantification reveals tight regulation of protein expression in single Xenopus eggs". Nucleic Acids Research. 42 (15): 9880–9891. doi:10.1093/nar/gku661

pathway that is mediated by AIF (apoptosis-inducing factor). The frog Xenopus laevis serves as an ideal model system for the study of the mechanisms

adder, Bitis atropos – venomous African clawed frog, Xenopus laevis Müller's platanna, Xenopus muelleri Inyanga toad, Vandijkophrynus inyangae Flat-backed

"Rhynchophylline and Isorhynchophylline Inhibit NMDA Receptors Expressed in Xenopus Oocytes". European Journal of Pharmacology. 455 (1): 27–34. doi:10

Pyxicephalus edulis Edible Frog Pouandi bouali Poondré Tomopterna cryptotis Cryptic sand frog Louand boani Louang boudi Xenopus muelleri Savanna Clawed Frog

blockade of diverse types of voltage-gated Ca2+ channels expressed in Xenopus oocytes by the Ca2+ channel antagonist mibefradil (Ro 40-5967)". Mol. Pharmacol

the development of the wing disc, survival and cell growth. Finally in Xenopus it has been demonstrated that the ortholog of TEAD1 regulates muscle differentiation

chemoattractant receptor is encoded by a 2 kilobase messenger RNA. Expression in Xenopus oocytes". FEBS Letters. 261 (2): 353–7. doi:10.1016/0014-5793(90)80590-f

tilapia, painted turtle, stickleback, Tetraodon, Nanorana parkeri, turkey, Xenopus tropicalis, zebra finch, zebrafish invertebrates Anopheles gambiae, Apis

activity of various subtypes of recombinant GABA(A) receptors expressed in Xenopus laevis oocytes". European Journal of Pharmacology. 558 (1–3): 37–42. doi:10

functional inward rectifier potassium channel in both mammalian cells and Xenopus oocytes". FEBS Letters. 531 (2): 250–4. Bibcode:2002FEBSL.531..250K. doi:10

African clawed frog, a species of South African aquatic frog of the genus Xenopus Algebraically closed field, an algebraic structure Meade Advanced Coma-Free

characterization of mouse urea transporters UT-A2 and UT-A3 expressed in purified Xenopus laevis oocyte plasma membranes". Am. J. Physiol. Renal Physiol. 294 (4):

therapeutics. 1989 John Gurdon  United Kingdom for his introduction of the xenopus oocyte into molecular biology and his demonstration that the nucleus of

Richardson P (December 2002). "Genetic and genomic tools for Xenopus research: The NIH Xenopus initiative". Developmental Dynamics. 225 (4): 384–91. doi:10

recombinant neuronal nicotinic receptors containing the b3 subunit expressed in Xenopus oocytes". J. Physiol. 529 (3): 565–77. doi:10.1111/j.1469-7793.2000.00565

Levi G (December 2010). "Irreversible effects of retinoic acid pulse on Xenopus jaw morphogenesis: new insight into cranial neural crest specification"

divalent cations of GABA rho 1 receptor from human retina expressed in Xenopus oocytes". Biomed. Environ. Sci. 14 (4): 269–277. PMID 11862606. Sedelnikova

RNA based techniques) Model organisms (includes Drosophila, C. elegans, Xenopus, zebrafish, mouse, Arabidopsis, Aspergillus, Dictyostelium and others )

R, Hunt T, Stillman B (Dec 1998). "The Orc4p and Orc5p subunits of the Xenopus and human origin recognition complex are related to Orc1p and Cdc6p". The

decision. Studies have shown that numerous biological systems, such as Xenopus oocyte maturation, mammalian calcium signal transduction, and polarity

Sasai, Y; Lu, B; De Robertis, E. M. (1996). "Dorsoventral patterning in Xenopus: Inhibition of ventral signals by direct binding of chordin to BMP-4".

et al. (2012). "Xenopus laevis RIC-3 enhances the functional expression of the C. elegans homomeric nicotinic receptor, ACR-16, in Xenopus oocytes". J. Neurochem

(November 2010). "Programming pluripotent precursor cells derived from Xenopus embryos to generate specific tissues and organs". Genes. 1 (3): 413–426

Noradrenergic cell group A6 Subfamily A6, a subfamily of Rhodopsin-like receptors Xenopus A6 kidney epithelial cells in cell culture A6, the IATA code for Air Alps

human PRDX5 in other organisms or tissues such as yeast, mouse brain, and Xenopus embryos also leads to protection against oxidative stress. PRDX5 in Drosophila

R, Hunt T, Stillman B (Dec 1998). "The Orc4p and Orc5p subunits of the Xenopus and human origin recognition complex are related to Orc1p and Cdc6p". The

could abolish sensitivity to artemisinin compounds. Evidence came from a Xenopus oocyte system describing specific interactions between artemisinins and

S2CID 24586216. Ames RS, Nuthulaganti P, Kumar C (October 1996). "In Xenopus oocytes the human C3a and C5a receptors elicit a promiscuous response to

"Visual deprivation and the maturation of the retinotectal projection in Xenopus laevis". Journal of Embryology and Experimental Morphology. 91: 101–115

Protein Kinase Activity in Fibroblasts, and Promotes Meiotic Maturation of Xenopus Oocytes in a Grb2- and Ras-Dependent Manner". Mol Cell Biol. 19 (6): 4379–89

Its channel varies from 5.2 nanometers in humans to 10.7 nm in the frog Xenopus laevis, with a depth of roughly 45 nm. Additionally, mRNA, being single-stranded

humans is encoded by the FOXH1 gene. FOXH1 encodes a human homolog of Xenopus forkhead activin signal transducer-1. FOXH1 protein binds SMAD2 and activates

produced by Riese und Müller In genetics, "the frog" generally refers to Xenopus laevis The act of ripping out stitches in knitting All pages with titles

snake XP_013914711.1 55.9 69.5 2.75E-69 Xenopus laevis African clawed frog NP_001088778.1 55.4 71.2 1.98E-68 Xenopus tropicalis Western clawed frog NP_001090717

by cystic fibrosis transmembrane conductance regulator co-expression in Xenopus oocytes". J. Biol. Chem. 277 (10): 8395–405. doi:10.1074/jbc.M109465200

molecules. Both types serve as homologous structures in fish and tetrapods. In Xenopus laevis, an amphibia, both class receptors are present, unlike fish or mammals

channel Kv 4.3 by serum- and glucocorticoid-inducible kinase isoforms in Xenopus oocytes". Pflügers Arch. 450 (1): 26–33. doi:10.1007/s00424-004-1369-z

role as a scaffolding protein in a G-coupled protein receptor complex in Xenopus tropicalis. It has been shown to form a cluster with the xtGPR54-2 gene

in a Dot Plot of the Human gene with distantly related species, such as Xenopus tropicalis. A multiple sequence alignment conducted using the SDSC Biology

"Visual deprivation and the maturation of the retinotectal projection in Xenopus laevis". Journal of Embryology and Experimental Morphology. 91: 101–115

proteomics: quantifying translational cell heterogeneity in the 16-cell frog (Xenopus) embryo, Angew. Chem. Int. Ed. 2016, 55, 2454, https://doi.org/10.1002/anie

(Taeniopygia guttata), tetraodon (Tetraodon nigroviridis), western clawed frog (Xenopus tropicalis), human (Homo sapiens). miR-181 may have a regulatory role with

Wade PA, Cheng X (June 2007). "Structure of the SANT domain from the Xenopus chromatin remodeling factor ISWI". Proteins. 67 (4): 1198–202. doi:10.1002/prot

"Cyclic AMP-dependent modulation of N- and Q-type Ca2+ channels expressed in Xenopus oocytes". Neuroscience Letters. 217 (1): 13–16. doi:10.1016/0304-3940(96)13055-X

grayii grayii (clicking stream frog) Tomopterna delalandii (Cape sand frog) Xenopus laevis (common platanna) List of reptiles in the reserve Updated from South

"Effects of ginsenoside Rg2 on the 5-HT3A receptor-mediated ion current in Xenopus oocytes". Mol. Cells. 15 (1): 108–113. doi:10.1016/S1016-8478(23)13715-0

PMID 3313277. Bogenhagen DF, Brown DD (1981). "Nucleotide sequences in Xenopus 5S DNA required for transcription termination". Cell. 24 (1): 261–70. doi:10

by cystic fibrosis transmembrane conductance regulator co-expression in Xenopus oocytes". J. Biol. Chem. 277 (10): 8395–405. doi:10.1074/jbc.M109465200

05006. PMC 1948073. PMID 17710122. Zhang J, King ML (December 1996). "Xenopus VegT RNA is localized to the vegetal cortex during oogenesis and encodes

microtubules can be generated without the aid of the γ-TuRC. Studies using Xenopus egg extracts have identified a novel form of microtubule nucleation that

et al., "Kaitocephalin Antagonism of Glutamate Receptors Expressed in Xenopus Oocytes", ACS Chem. Neurosci. 1 (2010): 175-181 Rishi G. Vaswani et al

Roeder RG (January 1977). "Selective and accurate transcription of the Xenopus laevis 5S RNA genes in isolated chromatin by purified RNA polymerase III"

PMID 10199971. S2CID 21942870. Chang C, Hemmati-Brivanlou A (1999). "Xenopus GDF6, a new antagonist of noggin and a partner of BMPs". Development. 126

of H+ buffering mediated by sodium bicarbonate cotransport expressed in Xenopus oocytes". J. Biol. Chem. 279 (27): 28057–62. doi:10.1074/jbc.M402401200

SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytes". The Journal of Physiology. 549 (Pt 1): 3–19. doi:10.1113/jphysiol

Nelson DJ, Steiner DF (Jan 1991). "Sequence and functional expression in Xenopus oocytes of a human insulinoma and islet potassium channel". Proceedings

instance of a Bd-infected amphibian was a specimen of an African clawed frog (Xenopus laevis) collected in 1938, and this species also appears to be essentially

Ghannadan M (April 2009). "The anatomy and development of the claws of Xenopus laevis (Lissamphibia: Anura) reveal alternate pathways of structural evolution

several cerebroprotective drugs on NMDA channel function: evaluation using Xenopus oocytes and [3H]MK-801 binding". European Journal of Pharmacology. 207

recombinant Escherichia coli nucleoside-H(+) cotransporter (NupC) produced in Xenopus laevis oocytes". Mol. Membr. Biol. 21 (1): 1–10. doi:10.1080/0968768031000140836

1104/pp.47.4.562 Berridge MV, Lane CD.  Translation of Xenopus liver messenger RNA in Xenopus oocytes:  Vitellogenin synthesis and conversion to yolk

dextrorotatory morphinans on α3β4 nicotinic acetylcholine receptors expressed in Xenopus oocytes". European Journal of Pharmacology. 536 (1–2): 85–92. doi:10.1016/j

contributes to sexual arousal. In some animals (such as the claw-toed frog Xenopus laevis) production of MSH is increased when the animal is in a dark location

tailless amphibians is presented below using the African clawed frog (Xenopus laevis) and the northern leopard frog (Lithobates pipiens) as examples

activity of various subtypes of recombinant GABA(A) receptors expressed in Xenopus laevis oocytes". European Journal of Pharmacology. 558 (1–3): 37–42. doi:10

Image Species Common name Xenopus laevis [i] African clawed frog

Broek, O; Destrée, O; Hoppler, S (December 2005). "Distinct roles for Xenopus Tcf/Lef genes in mediating specific responses to Wnt/beta-catenin signalling

"The Pharmacology of Efferent Synapses in the Lateral-Line System of Xenopus Laevis". Journal of Experimental Biology. 54 (3): 643–659. doi:10.1242/jeb

v t e PDB gallery 1l6o: XENOPUS DISHEVELLED PDZ DOMAIN 2f0a: Crystal Structure of Monomeric Uncomplexed form of Xenopus dishevelled PDZ domain

by trade in African clawed frogs (Xenopus laevis). In this study, 697 archived specimens of three species of Xenopus, previously collected from 1879 to

electrophysiological responses mediated by rat kainate and NMDA receptors expressed in Xenopus oocytes". European Journal of Pharmacology. 235 (2–3): 283–289. doi:10

TP, Guggino WB, Agre P (April 1992). "Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein". Science. 256 (5055): 385–7

S2CID 11565940. Guimond, A.; Moss, T. (1999). "A ribosomal orphon sequence from Xenopus laevis flanked by novel low copy number repetitive elements". Biological

ISBN 0-7216-1518-X. Heasman, Janet (2006-04-01). "Patterning the early Xenopus embryo". Development. 133 (7): 1205–1217. doi:10.1242/dev.02304. ISSN 0950-1991

"Requirement for glycine in activation of NMDA-receptors expressed in Xenopus oocytes". Science. 241 (4867): 835–7. Bibcode:1988Sci...241..835K. doi:10

the alkaloids from yew (Taxus baccata) on the action potential in the Xenopus medullated axon". Experientia. 31 (3): 337–338. doi:10.1007/bf01922572

specific for single-stranded DNA. Members include Vibrio cholerae, X1Cry from Xenopus laevis, and AtCry3 from Arabidopsis thaliana. DASH was initially named

Authors describe a protein present in the nuclear fraction, obtained from Xenopus laevis oocytes, which shows the same features as skeletal muscle actin

"Endoderm patterning by the notochord: Development of the hypochord in Xenopus" (PDF). Development. 127 (4): 869–979. doi:10.1242/dev.127.4.869. PMID 10648245

as part of a group of genes involved in FGF signaling in zebrafish and Xenopus laevis embryo. Injection of 1-cell stage embryo with sef mRNA lead to ventralization

This research is focused on development of a multiplexed, microfluidic, Xenopus embryo culture system that will enable discovery of new drug targets and

DJ, Steiner DF (January 1991). "Sequence and functional expression in Xenopus oocytes of a human insulinoma and islet potassium channel". Proceedings

(November 2010). "Programming pluripotent precursor cells derived from Xenopus embryos to generate specific tissues and organs". Genes. 1 (3): 413–426

thesis on endocrinology and behaviour of the South African clawed frog, Xenopus laevis. As part of his thesis study he developed, together with Richard

PER1 (Bos taurus) per1b (Danio rerio) PER (Drosophila melanogaster) PER1 (Xenopus tropicalis) PER1 (Equus caballus) PER1 (Macaca mulatta) PER1 (Sus scrofa)

reinhardtii] - Protein - NCBI". "Radial spoke head component 1 L homeolog [Xenopus laevis] - Protein - NCBI". "Membrane occupation and recognition nexus protein

of genes in animals, particularly the genes specifying ribosomal RNA in Xenopus and silk fibroin in Bombix. 1974 David Baltimore for his distinguished

ten Dijke P (1998). "Physical and functional interaction of murine and Xenopus Smad7 with bone morphogenetic protein receptors and transforming growth

PMID 12921737. Tada, M.; Smith, J. C. (1 May 2000). "Xwnt11 is a target of Xenopus Brachyury: regulation of gastrulation movements via Dishevelled, but not

Moriyama, K.; Sakai, H.; Akiyama, T.; Gotoh, Y.; Nishida, E. (1 March 1992). "Xenopus MAP kinase activator: identification and function as a key intermediate

(Zebrasoma flavescens) Axolotl (Ambystoma mexicanum) African clawed frog (Xenopus laevis) Indian python (Python molurus) Rock monitor (Varanus albigularis)

F (2006). "Functional coassembly of KCNQ4 with KCNE-beta- subunits in Xenopus oocytes". Cellular Physiology and Biochemistry. 18 (1–3): 57–66. doi:10

medium and preliminary validation of the Frog Embryo Teratogenesis Assay Xenopus (FETAX)', Volume 7, Issue 4, Aug 1987, Pages: 237–244, Dawson DA and Bantle

pattern of MID1 transcript at different times of gestation: mouse, chicken, xenopus and also human embryos. At the very early stage of embryonic development

Sharp P.A.; Constantine-Paton M. (April 15, 2006). "RNA Interference of Xenopus NMDAR NR1 in vitro and in vivo". J Neurosci Methods. 152 (1–2): 65–73.

Invasive European Buckthorn Metabolite on Embryo Survival and Development in Xenopus laevis and Pseudacris triseriata" (PDF). Journal of Herpetology. 48 (1):

(November 2010). "Programming pluripotent precursor cells derived from Xenopus embryos to generate specific tissues and organs". Genes. 1 (3): 413–426

screening. Fam183b has been characterized as essential for motile cilia in Xenopus but Fam183b loss-of-function studies have yielded no defects (in cilia

(1999). "Biosynthesis of the vacuolar H+-ATPase accessory subunit Ac45 in Xenopus pituitary". Eur. J. Biochem. 262 (2): 484–91. doi:10.1046/j.1432-1327.1999

encodes a protein showing 99% and 91% amino acid identity to the mouse and Xenopus Wnt7A proteins, respectively. Among members of the human WNT family, this

difference also occurred in comparisons with other species, with 92% and 39% of Xenopus laevis L1a and L1b. The protein can interact with the beta subunit of protein

Tomopterna delalandii (Cape sand frog) Vandijkophrynus angusticeps (sand toad) Xenopus laevis (common platanna) Insects present in Cape Town, as of 2011[update]

Students Council, see Macquarie University Campus Experience#Hogben Toad Xenopus laevis, a toad used by Hogben for pregnancy testing, after which the newsletter

pombe pre-RC because it is required for Cdc18 binding. The pre-RC of Xenopus laevis (X. laevis) also has an additional protein, MCM9, which helps load

beta-arrestin 2-mediated desensitization of the mu-opioid receptor in Xenopus oocytes". The Journal of Biological Chemistry. 276 (7): 4894–900. doi:10

Krebs EG (Mar 1977). "Progesterone-stimulated meiotic cell division in Xenopus oocytes. Induction by regulatory subunit and inhibition by catalytic subunit

4% 22.2% 22.2% 11.1% - Mus musculis Mouse 39.1% 4.3% 17.4% 8.7% 21.7% Xenopus laevis Frog 55.6% - 22.2% 11.1% - Danio rerio Zebra fish 33.3% 11.1% 11

ten Dijke P (1998). "Physical and functional interaction of murine and Xenopus Smad7 with bone morphogenetic protein receptors and transforming growth

Blockade of Diverse Types of Voltage-Gated Ca2+ Channels Expressed in Xenopus Oocytes by the Ca2+ Channel Antagonist Mibefradil (Ro 40-5967)". Molecular

the Mg2+-block site in NR1-1a/NR2A NMDA receptor channels expressed in Xenopus oocytes". Life Sciences. 68 (16): 1817–1826. doi:10.1016/S0024-3205(01)00975-4

M210184200. PMID 12477722. "Entrez Gene: AGR3 anterior gradient homolog 3 (Xenopus laevis)". Human AGR3 genome location and AGR3 gene details page in the

receptor functionally expressed in human embryonic kidney 293 cells and Xenopus laevis oocytes". Journal of Neuroscience. 19 (1): 7426–7433. doi:10.1093/chemse/bji002

"Myelin protein zero exists as dimers and tetramers in native membranes of Xenopus laevis peripheral nerve". Journal of Neuroscience Research. 67 (6): 766–71

important cellular events, including exiting G2 cell cycle arrests in Xenopus laevis oocytes, a stage to which the cell or organism would not want to

480 IRX-1 Gallus gallus Red Junglefowl 296 NP_001025509 72.9% 467 IRX-1 Xenopus tropicalis Western clawed frog 371.2 NP_001188351 68% 467 IRX-1 Latimeria

Ferroportin-mediated iron efflux is calcium-activated; studies of human Fpn expressed in Xenopus laevis oocytes demonstrated that calcium is a required cofactor for Fpn

Lang F, Busch AE (April 1996). "Blockade of HERG channels expressed in Xenopus oocytes by the histamine receptor antagonists terfenadine and astemizole"

species, Grammostola rosea and Haplopelma lividum, using frog embryos from Xenopus laevis". BIOS. 84 (3): 127–135. doi:10.1893/0005-3155-84.3.127. ISSN 0005-3155

chromosome condensation protein complexes containing XCAP-C, XCAP-E and a Xenopus homolog of the Drosophila Barren protein". Cell. 89 (4): 511–521. doi:10