about
Characterization and expression of the laminin gamma3 chain: a novel, non-basement membrane-associated, laminin chainDiseased muscles that lack dystrophin or laminin-alpha2 have altered compositions and proliferation of mononuclear cell populationsA splice site mutation in laminin-α2 results in a severe muscular dystrophy and growth abnormalities in zebrafishTissue-specific expression of the human laminin alpha5-chain, and mapping of the gene to human chromosome 20q13.2-13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutationIntegrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophyCostameric proteins in human skeletal muscle during muscular inactivityPCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophyAmelioration of laminin-alpha2-deficient congenital muscular dystrophy by somatic gene transfer of miniagrin.Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.Extrasynaptic location of laminin beta 2 chain in developing and adult human skeletal muscle.A new in vitro mouse oligodendrocyte precursor cell migration assay reveals a role for integrin-linked kinase in cell motilityThe roles of integrin-linked kinase in the regulation of myogenic differentiation.Extracellular cues influencing oligodendrocyte differentiation and (re)myelinationAdhesion G-protein coupled receptors and extracellular matrix proteins: Roles in myelination and glial cell development.Merosin-integrin promotion of skeletal myofiber cell survival: Differentiation state-distinct involvement of p60Fyn tyrosine kinase and p38alpha stress-activated MAP kinase.Overexpression of laminin-8 in human dermal microvascular endothelial cells promotes angiogenesis-related functions.A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield.Merosin (laminin-2/4)-driven survival signaling: complex modulations of Bcl-2 homologs.A Homozygous LAMA2 Mutation of c.818G>A Caused Partial Merosin Deficiency in a Japanese patient.Muscle MRI in pediatrics: clinical, pathological and genetic correlation.
P2860
Q22009477-B92C4D1E-31A7-4ACE-B2DF-4074F153A9C9Q24791491-80675CEC-E081-49A4-BDDC-01BCFEFFBEDCQ27322025-D2C85266-BF1F-41D2-9B45-D4C0FAAD6520Q28247223-48C3FB9F-8269-41BC-BB47-78552BB0BA12Q28249995-C06C7359-4882-4F32-ABF0-ECC1B9F27687Q28283040-59F923CE-BC5F-487D-88AD-51CA655E2D47Q33680352-D339BCE1-7A50-4940-8B55-8093A6701BB2Q33922811-09BEA580-C942-4048-B9F6-22DF69285727Q35249710-6F4F1012-B2D4-4999-B61F-BA32B7A9DF11Q35763916-BE453FD5-EF96-420D-8BC0-38FD5E565A20Q35910607-45DB1066-1188-475B-9165-EDC39C95F701Q36328735-BE895275-9B6E-48D6-908F-77BCD3FB7442Q38789322-C355327C-A0CA-4C0E-A02F-CBB87DCAB026Q39012388-5A455AEA-E150-4C97-A152-03086EE18D89Q40741641-2B9B6318-CD9E-45BB-B387-D80F803F80C6Q42528537-69C7C75A-85FB-4BAE-B983-9DFF2FE0CD2EQ43754788-86A60AE3-D25E-4C14-B8F5-EF6F3632332AQ44536761-9282B744-710C-460B-BCEA-00EB1BFD6F09Q49963380-E54C9FB4-D6A9-4B69-9214-3723C9FB06BAQ52924614-48A8C999-B141-4318-93FD-80B8CFD836B8
P2860
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh
1996年學術文章
@zh-hant
name
Merosin/laminin-2 and muscular dystrophy.
@en
type
label
Merosin/laminin-2 and muscular dystrophy.
@en
prefLabel
Merosin/laminin-2 and muscular dystrophy.
@en
P1476
Merosin/laminin-2 and muscular dystrophy.
@en
P2093
P304
P356
10.1016/S0960-8966(96)00384-7
P577
1996-12-01T00:00:00Z