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searching for HNRNPA1 18 found (29 total)

alternate case: hNRNPA1

Pyruvate kinase (4,042 words) [view diff] case mismatch in snippet view article find links to article

PKM gene is regulated through heterogenous ribonucleotide proteins like hnRNPA1 and hnRNPA2. Human PKM2 monomer has 531 amino acids and is a single chain

IκBα (1,526 words) [view diff] case mismatch in snippet view article find links to article

Hay DC, Kemp GD, Dargemont C, Hay RT (May 2001). "Interaction between hnRNPA1 and IkappaBalpha is required for maximal activation of NF-kappaB-dependent

BAT2 (1,020 words) [view diff] exact match in snippet view article find links to article

described for this gene. BAT2 has been shown to interact with: C1QBP, EIF3S6, HNRNPA1, IFT88, IMMT, and UBAP2L. ENSG00000206427, ENSG00000231825, ENSG00000231370

Paraspeckle (1,862 words) [view diff] exact match in snippet view article find links to article

FAM98A Important Yes FIGN Important Yes FUS Essential Yes Yes Yes Core HNRNPA1 Important Yes Yes Yes HNRNPA1L2 n.d. Yes HNRNPF n.d. No HNRNPH1 n.d. Yes

Flap structure-specific endonuclease 1 (2,642 words) [view diff] exact match in snippet view article find links to article

endonuclease 1 has been shown to interact with: APEX1, BLM CDK2, CCNA2, EP300, HNRNPA1, PCNA, and WRN. FEN1 is over-expressed in the majority of cancers of the

NFKB1 (2,363 words) [view diff] case mismatch in snippet view article find links to article

Hay DC, Kemp GD, Dargemont C, Hay RT (May 2001). "Interaction between hnRNPA1 and IkappaBalpha is required for maximal activation of NF-kappaB-dependent

Prion (10,988 words) [view diff] case mismatch in snippet view article find links to article

prion-like domains of heterogeneous nuclear riboproteins hnRNPA2B1 and hnRNPA1 in familial cases of muscle, brain, bone and motor neuron degeneration

Gideon Dreyfuss (1,130 words) [view diff] case mismatch in snippet view article find links to article

Gemin2 (Previously known as SIP1) Gemin3/DDX20 Gemin4 Gemin5 Gemin6 Gemin7 hnRNPA1 RA33 hnRNPC PTBP1 hnRNPK hnRNPM hnRNPR hnRNPU hnRNPQ Y14 Magoh SMN1 SMN2

HNRNPAB (1,081 words) [view diff] case mismatch in snippet view article find links to article

Hay DC, Kemp GD, Dargemont C, Hay RT (May 2001). "Interaction between hnRNPA1 and IkappaBalpha is required for maximal activation of NF-kappaB-dependent

RNA splicing (4,660 words) [view diff] case mismatch in snippet view article find links to article

structure of Intronic splicing silencer and its interaction to host protein hnRNPA1 give insight into specific recognition. However, adding to the complexity

Alternative splicing (7,813 words) [view diff] case mismatch in snippet view article find links to article

repressors are heterogeneous nuclear ribonucleoproteins (hnRNPs) such as hnRNPA1 and polypyrimidine tract binding protein (PTB). Splicing enhancers are

RELA (6,507 words) [view diff] case mismatch in snippet view article find links to article

Hay DC, Kemp GD, Dargemont C, Hay RT (May 2001). "Interaction between hnRNPA1 and IkappaBalpha is required for maximal activation of NF-kappaB-dependent

KHDRBS1 (2,812 words) [view diff] case mismatch in snippet view article find links to article

prostate cancer cells proliferation. In addition, Sam68 in conjunction with hnRNPA1 influences the choice of the alternative 5' splice sites of Bcl-x regulating

J. Paul Taylor (physician) (844 words) [view diff] case mismatch in snippet view article

J, Taylor JP (2013). "Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS". Nature. 495 (7442): 467–73. Bibcode:2013Natur

TAR DNA-binding protein 43 (4,646 words) [view diff] case mismatch in snippet view article find links to article

et al. (March 2013). "Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS". Nature. 495 (7442): 467–473.

Stress granule (12,460 words) [view diff] exact match in snippet view article find links to article

Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation". Neurobiology of Aging. 61: 255.e9–255.e16. doi:10.1016/j.neurobiolaging

N6-Methyladenosine (5,629 words) [view diff] case mismatch in snippet view article find links to article

et al. (March 2013). "Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS". Nature. 495 (7442): 467–473.

Valosin-containing protein (5,868 words) [view diff] case mismatch in snippet view article find links to article

Kabashi E, Jornea L, Hannequin D, Brice A (April 2014). "hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal