G8: a novel domain associated with polycystic kidney disease and non-syndromic hearing loss
about
Murine homologue of the human KIAA1199 is implicated in hyaluronan binding and depolymerizationKIAA1199, a deafness gene of unknown function, is a new hyaluronan binding protein involved in hyaluronan depolymerizationA genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21A mammalian homolog of the zebrafish transmembrane protein 2 (TMEM2) is the long-sought-after cell-surface hyaluronidaseDomainRBF: a Bayesian regression approach to the prioritization of candidate domains for complex diseases.Transcriptional and epigenetic regulation of KIAA1199 gene expression in human breast cancerNF-κB-induced KIAA1199 promotes survival through EGFR signalling.The novel transmembrane protein Tmem2 is essential for coordination of myocardial and endocardial morphogenesis.KIAA1199 as a potential diagnostic biomarker of rheumatoid arthritis related to angiogenesis.Messenger RNA profile analysis deciphers new Esrrb responsive genes in prostate cancer cells.Induction of KIAA1199/CEMIP is associated with colon cancer phenotype and poor patient survival.TMEM2 Is a SOX4-Regulated Gene That Mediates Metastatic Migration and Invasion in Breast CancerIdentification of KIAA1199 as a Biomarker for Pancreatic Intraepithelial NeoplasiaTMEM2 inhibits hepatitis B virus infection in HepG2 and HepG2.2.15 cells by activating the JAK-STAT signaling pathway.N-Terminal signal sequence is required for cellular trafficking and hyaluronan-depolymerization of KIAA1199.Central Role of CEMIP in Tumorigenesis and Its Potential as Therapeutic Target.Expansion of divergent SEA domains in cell surface proteins and nucleoporin 54.Novel genetic risk markers for ulcerative colitis in the IL2/IL21 region are in epistasis with IL23R and suggest a common genetic background for ulcerative colitis and celiac disease.Inhibition of mTOR with sirolimus does not attenuate progression of liver and kidney disease in PCK rats.Expanding the mutation spectrum in 130 probands with ARPKD: identification of 62 novel PKHD1 mutations by sanger sequencing and MLPA analysis.
P2860
Q24307877-615E396B-50B6-46CC-AD0E-FEF896406D64Q24336831-6E69E0F0-ECD7-4554-AEBF-AF0F990A7574Q24649802-EE2517CF-4ED3-4D13-B31E-1B1D3A5FA594Q29871434-8A468256-EBC5-4386-8A0B-CD5473D9FAADQ33876948-41731AC6-C0C9-45F0-B440-704612A40229Q34412672-66FBF238-A50E-40F5-BDB1-DF23D8CE66ABQ34563758-F11C687F-0157-42F1-B52F-9EF8B03AFB3EQ35208712-964DCF8E-1139-4D69-82DB-2B28CDF45A83Q35663729-CBE95500-6078-469F-9E59-671B0B4ED6A0Q35857930-565CE0BF-50CD-4DA3-9313-E5EC9C335FC4Q36544364-3D30BC15-F7B2-4CB7-B291-395A0E5F6146Q37415841-C4243501-42FD-4C87-8445-EEA868EDBAE0Q37476029-606C72F5-804B-484D-B63B-F57334FB8702Q37482744-2C954CF0-58E6-436B-A6C4-6FFDDC5C3E91Q39057042-496AC288-5233-4BE0-A9BD-4F55296F97A9Q41441007-7030B179-D6FA-4F80-8E2B-7E6CADA156A4Q47249307-EFEB4164-7943-4826-BF54-FBF15486BA0CQ47764326-546BFC13-1F30-4765-865F-32DB76215704Q51554260-9CA0168C-9366-4660-B4DF-0CED10643775Q53091941-C4365104-05C0-430F-AFBF-02970EA658D1
P2860
G8: a novel domain associated with polycystic kidney disease and non-syndromic hearing loss
description
2006 nî lūn-bûn
@nan
2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
G8: a novel domain associated ...... and non-syndromic hearing loss
@ast
G8: a novel domain associated ...... and non-syndromic hearing loss
@en
G8: a novel domain associated ...... and non-syndromic hearing loss
@en-gb
G8: a novel domain associated ...... and non-syndromic hearing loss
@nl
type
label
G8: a novel domain associated ...... and non-syndromic hearing loss
@ast
G8: a novel domain associated ...... and non-syndromic hearing loss
@en
G8: a novel domain associated ...... and non-syndromic hearing loss
@en-gb
G8: a novel domain associated ...... and non-syndromic hearing loss
@nl
prefLabel
G8: a novel domain associated ...... and non-syndromic hearing loss
@ast
G8: a novel domain associated ...... and non-syndromic hearing loss
@en
G8: a novel domain associated ...... and non-syndromic hearing loss
@en-gb
G8: a novel domain associated ...... and non-syndromic hearing loss
@nl
P2093
P3181
P356
P1433
P1476
G8: a novel domain associated ...... and non-syndromic hearing loss
@en
P2093
Quan-yuan He
Song-ping Liang
Xiang-hua Liu
Xuan-wen Li
P304
P3181
P356
10.1093/BIOINFORMATICS/BTL123
P407
P577
2006-09-15T00:00:00Z