相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Three-dimensional Structure of Steroid 21-Hydroxylase (Cytochrome P450 21A2) with Two Substrates Reveals Locations of Disease-associated Variants
Bin Zhao et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Uncovering the Role of Hydrophobic Residues in Cytochrome P450-Cytochrome P450 Reductase Interactions
Cesar Kenaan et al.
BIOCHEMISTRY (2011)
From Coarse Grained to Atomistic: A Serial Multiscale Approach to Membrane Protein Simulations
Phillip J. Stansfeld et al.
JOURNAL OF CHEMICAL THEORY AND COMPUTATION (2011)
Structure-Based Analysis of Five Novel Disease-Causing Mutations in 21-Hydroxylase-Deficient Patients
Carolina Minutolo et al.
PLOS ONE (2011)
Structure and Dynamics of the Membrane-Bound Cytochrome P450 2C9
Vlad Cojocaru et al.
PLOS COMPUTATIONAL BIOLOGY (2011)
Transmembrane Helix Dynamics of Bacterial Chemoreceptors Supports a Piston Model of Signalling
Benjamin A. Hall et al.
PLOS COMPUTATIONAL BIOLOGY (2011)
Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier
V. Tardy et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2010)
Molecular Modeling on Inhibitor Complexes and Active-Site Dynamics of Cytochrome P450 C17, a Target for Prostate Cancer Therapy
Shozeb M. Haider et al.
JOURNAL OF MOLECULAR BIOLOGY (2010)
Functional Characterization of Three CYP21A2 Sequence Variants (p.A265V, p.W302S, p.D322G) Employing a Yeast Co-Expression System
Caroline Bleicken et al.
HUMAN MUTATION (2009)
Multiple copies of cytochrome oxidase 1 in species of the fungal genus Fusarium
Scott R. Gilmore et al.
MOLECULAR ECOLOGY RESOURCES (2009)
Redox-coupled proton pumping in cytochrome c oxidase:: Further insights from computer simulation
Jiancong Xu et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2008)
Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia:: Potential relevance of helix C for p450 oxidoreductase-21-hydroxylase interaction
Felix G. Riepe et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)
Three novel CYP21A2 mutations and their protein modelling in patients with classical 21-hydroxylase deficiency from northeastern Iran
Alireza Baradaran-Heravi et al.
CLINICAL ENDOCRINOLOGY (2007)
Ethnic-specific distribution of mutations in 716 patients with congenital adrenal hyperplasia owing to 21-hydroxylase deficiency
Robert C. Wilson et al.
MOLECULAR GENETICS AND METABOLISM (2007)
Four novel missense mutations in the CYP21A2 gene detected in Russian patients suffering from the classical form of congenital adrenal hyperplasia:: Identification, functional characterization, and structural analysis
Yulia Grischuk et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Molecular model of human CYP21 based on mammalian CYP2C5: Structural features correlate with clinical severity of mutations causing congenital adrenal hyperplasia
Tiina Robins et al.
MOLECULAR ENDOCRINOLOGY (2006)
Extensive clinical experience - Nonclassical 21-hydroxylase deficiency
Maria I. New
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Structural and functional analysis of a novel mutation of CYP21B in a heterozygote carrier of 21-hydroxylase deficiency
J Bojunga et al.
HUMAN GENETICS (2005)
Crystallographic study on the dioxygen complex of wild-type and mutant cytochrome P450cam - Implications for the dioxygen activation mechanism
S Nagano et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2005)
Not all amino acid substitutions of the common cluster E6 mutation in CYP21 cause congenital adrenal hyperplasia
T Robins et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2005)
Functional characterization of two novel point mutations in the CYP21 gene causing simple virilizing forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
N Krone et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2005)
Structural basis for the role in protein folding of conserved proline-rich regions in cytochromes P450
B Kemper
TOXICOLOGY AND APPLIED PHARMACOLOGY (2004)
Novel mutations in CYP21 detected in individuals with hyperandrogenism
S Lajic et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2002)
The PSIPRED protein structure prediction server
LJ McGuffin et al.
BIOINFORMATICS (2000)
The role of amino-acid residues in the hydrophobic patch surrounding the haem group of cytochrome f in the interaction with plastocyanin
XS Gong et al.
EUROPEAN JOURNAL OF BIOCHEMISTRY (2000)
A 3D model of human P450c21: study of the putative effects of steroid 21-hydroxylase gene mutations
E Mornet et al.
HUMAN GENETICS (2000)
分享论文
