Molecular basis for Glanzmann's thrombasthenia (GT) in a compound heterozygote with glycoprotein IIb gene: a proposal for the classification of GT based on the biosynthetic pathway of glycoprotein IIb-IIIa complex.
about
Demystified...adhesion molecule deficiencies.Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia.Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selection.Truncation of the cytoplasmic domain of beta3 in a variant form of Glanzmann thrombasthenia abrogates signaling through the integrin alpha(IIb)beta3 complex.Do cell junction protein mutations cause an airway phenotype in mice or humans?
P2860
Molecular basis for Glanzmann's thrombasthenia (GT) in a compound heterozygote with glycoprotein IIb gene: a proposal for the classification of GT based on the biosynthetic pathway of glycoprotein IIb-IIIa complex.
description
1992 nî lūn-bûn
@nan
1992 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հունիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Molecular basis for Glanzmann' ...... glycoprotein IIb-IIIa complex.
@ast
Molecular basis for Glanzmann' ...... glycoprotein IIb-IIIa complex.
@en
type
label
Molecular basis for Glanzmann' ...... glycoprotein IIb-IIIa complex.
@ast
Molecular basis for Glanzmann' ...... glycoprotein IIb-IIIa complex.
@en
prefLabel
Molecular basis for Glanzmann' ...... glycoprotein IIb-IIIa complex.
@ast
Molecular basis for Glanzmann' ...... glycoprotein IIb-IIIa complex.
@en
P2093
P1433
P1476
Molecular basis for Glanzmann' ...... glycoprotein IIb-IIIa complex.
@en
P2093
P304
P407
P577
1992-06-01T00:00:00Z