about
Life cycle of connexins in health and diseaseHuman connexin26 and connexin30 form functional heteromeric and heterotypic channelsHereditary non-syndromic sensorineural hearing loss: transforming silence to soundProperties of human connexin 31, which is implicated in hereditary dermatological disease and deafness.Erythrokeratodermas: a classification in a state of flux?Connexin36 and pancreatic beta-cell functions.Novel mutations in GJA1 cause oculodentodigital syndromeClosing the gap on autosomal dominant connexin-26 and connexin-43 mutants linked to human disease.Inherited hearing loss: molecular genetics and diagnostic testing.Rat epidermal keratinocytes as an organotypic model for examining the role of Cx43 and Cx26 in skin differentiation.Differential potency of dominant negative connexin43 mutants in oculodentodigital dysplasia.
P2860
Q24541428-E3ECC79D-C78C-4402-A6D4-7C93F8456234Q28235511-274860D7-7336-4553-9111-3AD13800E2E1Q30543886-E36AD962-E0E8-45D1-B521-054790248F39Q34597107-8E04928B-9BCB-4904-A090-72325902D603Q36189346-CC4BEB2C-EAD9-4871-B93E-0D1DE7BB2723Q36576528-1B3C0112-3A60-499F-8304-F1CC9AFB8FB3Q36987153-D81A0EA0-D5AA-48C7-997D-19B833BE2CF6Q37035773-66D97E72-9D83-4F73-9216-932590A106DEQ38089731-91A595DC-EC63-49A8-87E0-3AACEF3310C2Q40306110-18BBE54B-D990-4683-977F-955E6CF60E27Q50689999-6FF3A7B2-E86D-42EF-B93F-6674284D865F
P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
name
Connexin gene pathology.
@ast
Connexin gene pathology.
@en
type
label
Connexin gene pathology.
@ast
Connexin gene pathology.
@en
prefLabel
Connexin gene pathology.
@ast
Connexin gene pathology.
@en
P2860
P1476
Connexin gene pathology.
@en
P2093
P2860
P304
P356
10.1046/J.1365-2230.2003.01312.X
P577
2003-07-01T00:00:00Z