Cib2 binds integrin alpha7Bbeta1D and is reduced in laminin alpha2 chain-deficient muscular dystrophy

Cib2 binds integrin alpha7Bbeta1D and is reduced in laminin alpha2 chain-deficient muscular dystrophy

Item
http://www.wikidata.org/entity/Q28585233
Skeletal muscle laminin and MDC1A: pathogenesis and treatment strategies.Biophysical and structural studies of the human calcium- and integrin-binding protein family: understanding their functional similarities and differencesAlterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.Identification of novel integrin binding partners for calcium and integrin binding protein 1 (CIB1): structural and thermodynamic basis of CIB1 promiscuityCIB1 is a regulator of pathological cardiac hypertrophyA Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic FamilyCIB1 synergizes with EphrinA2 to regulate Kaposi's sarcoma-associated herpesvirus macropinocytic entry in human microvascular dermal endothelial cells.Quantitative proteomic analysis reveals metabolic alterations, calcium dysregulation, and increased expression of extracellular matrix proteins in laminin α2 chain-deficient muscle.Mitochondrial co-chaperone protein Tid1 is required for energy homeostasis during skeletal myogenesis.Advances in genetic hearing loss: CIB2 gene.CIB1 and CIB2 are HIV-1 helper factors involved in viral entry.Molecular analysis of CIB4 gene and protein in Kermani sheep.CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival.Loss of CIB2 Causes Profound Hearing Loss and Abolishes Mechanoelectrical Transduction in Mice.A comprehensive transcriptome analysis of skeletal muscles in two Polish pig breeds differing in fat and meat quality traits.Effects of metformin on congenital muscular dystrophy type 1A disease progression in mice: a gender impact studyPreferential Binding of Mg Over Ca to CIB2 Triggers an Allosteric Switch Impaired in Usher Syndrome Type 1J
P2860

Cib2 binds integrin alpha7Bbeta1D and is reduced in laminin alpha2 chain-deficient muscular dystrophy

Item
http://www.wikidata.org/entity/Q28585233
description
2008 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Journal of Biological Chemistry
@fr
artículu científicu espublizáu en 2008
@ast
im September 2008 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2008/09/05)
@sk
vědecký článek publikovaný v roce 2008
@cs
wetenschappelijk artikel (gepubliceerd op 2008/09/05)
@nl
наукова стаття, опублікована у вересні 2008
@uk
name
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@ast
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@en
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@nl
type
label
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@ast
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@en
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@nl
prefLabel
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@ast
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@en
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@nl
P1433
P1476
P2093
P2860
P304
P31
P3181
P356
P407
P433
P478
P50
P577
P698
P921
P932
P3181
P356
P1433
P1476
Cib2 binds integrin alpha7Bbet ...... n-deficient muscular dystrophy
@en
P2093
P2860
P304
P31
P3181
P356
P407
P433
P478
P50
P577
P698
P921
P932