Disease-causing mutations in proteins: structural analysis of the CYP1B1 mutations causing primary congenital glaucoma in humans.
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Effects of single nucleotide polymorphisms on human N-acetyltransferase 2 structure and dynamics by molecular dynamics simulationIn silico analysis of five missense mutations in CYP1B1 gene in Pakistani families affected with primary congenital glaucoma.Overexpression of myocilin in the Drosophila eye activates the unfolded protein response: implications for glaucoma.Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.Role of E542 and E545 missense mutations of PIK3CA in breast cancer: a comparative computational approach.Screening of CYP1B1 and LTBP2 genes in Saudi families with primary congenital glaucoma: genotype-phenotype correlation.Cytochrome P450 1B1 and Primary Congenital GlaucomaFunctional and Structural Analyses of CYP1B1 Variants Linked to Congenital and Adult-Onset Glaucoma to Investigate the Molecular Basis of These Diseases.Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma.A novel 9-bp insertion detected in steroid 21-hydroxylase gene (CYP21A2): prediction of its structural and functional implications by computational methods.Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patientsCyp1b1 Regulates Ocular Fissure Closure Through a Retinoic Acid-Independent Pathway.Primary Congenital Glaucoma and the Involvement of CYP1B1.Functional characterization of eight rare missense CYP1B1 variants involved in congenital glaucoma and their association with null genotypes.Interaction of polycyclic aromatic hydrocarbons with human cytochrome P450 1B1 in inhibiting catalytic activity.Effects of disease causing mutations on the essential motions in proteins.Mutation spectrum of CYP1B1 in Chinese patients with primary open-angle glaucoma.
P2860
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P2860
Disease-causing mutations in proteins: structural analysis of the CYP1B1 mutations causing primary congenital glaucoma in humans.
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
Disease-causing mutations in p ...... congenital glaucoma in humans.
@ast
Disease-causing mutations in p ...... congenital glaucoma in humans.
@en
type
label
Disease-causing mutations in p ...... congenital glaucoma in humans.
@ast
Disease-causing mutations in p ...... congenital glaucoma in humans.
@en
prefLabel
Disease-causing mutations in p ...... congenital glaucoma in humans.
@ast
Disease-causing mutations in p ...... congenital glaucoma in humans.
@en
P2093
P2860
P1433
P1476
Disease-causing mutations in p ...... congenital glaucoma in humans.
@en
P2093
Aramati B M Reddy
Dorairajan Balasubramanian
Hampapathalu A Nagarajaram
Malkaram S Achary
Niyaz Ahmed
Seyed E Hasnain
Shirly G Panicker
Subhabrata Chakrabarti
P2860
P304
P356
10.1529/BIOPHYSJ.106.085498
P407
P577
2006-09-08T00:00:00Z