Find link

language:

Find link is a tool written by Edward Betts.

Fibrillin 1 is a redirect to Fibrillin-1

searching for Fibrillin 1 23 found (34 total)

Fibrillin (779 words) [view diff] no match in snippet view article find links to article

are also sometimes associated with adolescent idiopathic scoliosis. Fibrillin-1 is a major component of the microfibrils that form a sheath surrounding

MASS syndrome (417 words) [view diff] no match in snippet view article find links to article

which encodes fibrillin-1. Fibrillin-1 is an extracellular matrix protein that is found in microfibrils; defects in the fibrillin-1 protein cause the

Acromicric dysplasia (232 words) [view diff] exact match in snippet view article find links to article

Myhre syndrome. This condition has been associated with mutations in the Fibrillin 1 (FBN1) gene. Mutations in this gene have also been associated with stiff

Stiff skin syndrome (184 words) [view diff] exact match in snippet view article find links to article

Denver. 19 February 2016. Retrieved 2016-02-23. "FBN1 fibrillin 1". Entrez Gene. Online Mendelian Inheritance in Man (OMIM): FIBRILLIN 1; FBN1 - 134797

Chromosome 15 (3,031 words) [view diff] no match in snippet view article find links to article

is found on chromosome 15, as well as the FBN1 gene, coding for both fibrillin-1 (a protein critical to the proper functioning of connective tissue),

EGF-like domain (3,071 words) [view diff] no match in snippet view article find links to article

appears to be more prevalent than Hya and has been shown to occur in fibrillin-1, an extracellular matrix protein. Both modifications are catalyzed by

Musladin-Lueke syndrome (233 words) [view diff] no match in snippet view article find links to article

Ada Leuke. It is caused by a number of recessive mutations affecting fibrillin-1, a major component of microfibrils. It affects several organ systems

FBLN2 (1,268 words) [view diff] no match in snippet view article find links to article

PMC 2119879. PMID 8245130. Reinhardt DP, Sasaki T, Dzamba BJ, et al. (1996). "Fibrillin-1 and fibulin-2 interact and are colocalized in some tissues". J. Biol

Nonsense-mediated decay (2,066 words) [view diff] exact match in snippet view article find links to article

mutations in the fibrillin 1 (FBN1) gene and is resulted from a dominant negative interaction between mutant and wild-type fibrillin-1 gene. This pathway

EFEMP2 (814 words) [view diff] no match in snippet view article find links to article

PMID 16685658. El-Hallous E, Sasaki T, Hubmacher D, et al. (2007). "Fibrillin-1 interactions with fibulins depend on the first hybrid domain and provide

Elastin (2,438 words) [view diff] no match in snippet view article find links to article

"Functional consequences of homocysteinylation of the elastic fiber proteins fibrillin-1 and tropoelastin". The Journal of Biological Chemistry. 285 (2): 1188–1198

MFAP5 (500 words) [view diff] no match in snippet view article find links to article

Shipley JM (2002). "Microfibril-associated glycoprotein-2 interacts with fibrillin-1 and fibrillin-2 suggesting a role for MAGP-2 in elastic fiber assembly"

MFAP2 (822 words) [view diff] no match in snippet view article find links to article

(2001). "Protein interaction studies of MAGP-1 with tropoelastin and fibrillin-1". J. Biol. Chem. 276 (43): 39661–6. doi:10.1074/jbc.M104533200. PMID 11481325

LTBP2 (831 words) [view diff] no match in snippet view article find links to article

(2007). "LTBP-2 specifically interacts with the amino-terminal region of fibrillin-1 and competes with LTBP-1 for binding to this microfibrillar protein"

Natural skin care (2,765 words) [view diff] no match in snippet view article find links to article

Cho, Hee Chul Eun, and Jin Ho Chung, Heat Modulation of Tropoelastin, Fibrillin-1, and MatrixMetalloproteinase-12 in Human Skin In VivoJ Invest Dermatol

Sudden cardiac death of athletes (2,658 words) [view diff] no match in snippet view article find links to article

the FBN1 gene on chromosome 15, which encodes the connective protein fibrillin-1, inherited as a dominant trait. This protein is essential for synthesis

Pleiotropy (4,796 words) [view diff] no match in snippet view article find links to article

from a mutation in the FBN1 gene, which encodes for the glycoprotein fibrillin-1, a major constituent of extracellular microfibrils which form connective

Vertebral artery dissection (4,362 words) [view diff] no match in snippet view article find links to article

from mutations in the FBN1 gene, defective production of the protein fibrillin-1, and a number of physical abnormalities including aneurysm of the aortic

Boots (company) (4,500 words) [view diff] no match in snippet view article

formerly, No. 7 Refine & Rewind Beauty Serum stimulated the production of fibrillin-1 and appeared to smooth out wrinkles, (published in the British Journal

Mutation (13,965 words) [view diff] no match in snippet view article find links to article

mutations in the FBN1 gene, located on chromosome 15, which encodes fibrillin-1, a glycoprotein component of the extracellular matrix. Marfan syndrome

Mafoprazine (343 words) [view diff] no match in snippet view article find links to article

Hiroshi; Matsumoto, Morio (14 April 2016). "Generation of heterozygous fibrillin-1 mutant cloned pigs from genome-edited foetal fibroblasts". Scientific

Adolescent idiopathic scoliosis (4,807 words) [view diff] exact match in snippet view article find links to article

Fibrillin 1, protein encoded by the FBN1 gene

Steve Wilton (1,837 words) [view diff] no match in snippet view article find links to article

2021). "Proof-of-Concept: Antisense Oligonucleotide Mediated Skipping of Fibrillin-1 Exon 52". International Journal of Molecular Sciences. 22 (7): 3479.