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。Structure of human peptidyl-prolyl cis-trans isomerase FKBP22 containing two EF-hand motifs
Sergei P. Boudko et al.
PROTEIN SCIENCE (2014)
A molecular ensemble in the rER for procollagen maturation
Yoshihiro Ishikawa et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2013)
Bone Collagen: New Clues to Its Mineralization Mechanism from Recessive Osteogenesis Imperfecta
David R. Eyre et al.
CALCIFIED TISSUE INTERNATIONAL (2013)
Fragility of Reconstituted Type V Collagen Fibrils with the Chain Composition of α1(V)α2(V)α3(V) Respective of the D-Periodic Banding Pattern
Kazunori Mizuno et al.
CONNECTIVE TISSUE RESEARCH (2013)
FKBP14 is an essential gene that regulates Presenilin protein levels and Notch signaling in Drosophila
Diana L. van de Hoef et al.
DEVELOPMENT (2013)
Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen
Ulrike Schwarze et al.
HUMAN MOLECULAR GENETICS (2013)
Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype of FKBP10 Mutations
Aileen M. Barnes et al.
HUMAN MUTATION (2013)
Vascular Ehlers-Danlos Syndrome Mutations in Type III Collagen Differently Stall the Triple Helical Folding
Kazunori Mizuno et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
An Additional Function of the Rough Endoplasmic Reticulum Protein Complex Prolyl 3-Hydroxylase 1.Cartilage-associated Protein.Cyclophilin B THE CXXXC MOTIF REVEALS DISULFIDE ISOMERASE ACTIVITY IN VITRO
Yoshihiro Ishikawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Posttranslational Modifications in Type I Collagen from Different Tissues Extracted from Wild Type and Prolyl 3-Hydroxylase 1 Null Mice
Elena Pokidysheva et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2013)
Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss
Matthias Baumann et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
The Helix Located between the Two Domains of a Mip-like Peptidyl-Prolyl cis-trans Isomerase Is Crucial for Its Structure, Stability, and Protein Folding Ability
Biswanath Jana et al.
BIOCHEMISTRY (2012)
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect
Giacomo Venturi et al.
BONE (2012)
A novel homozygous 5 bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient
E. D. Setijowati et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2012)
Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix
Aileen M. Barnes et al.
HUMAN MUTATION (2012)
Mutation in Cyclophilin B That Causes Hyperelastosis Cutis in American Quarter Horse Does Not Affect Peptidylprolyl cis-trans Isomerase Activity but Shows Altered Cyclophilin B-Protein Interactions and Affects Collagen Folding
Yoshihiro Ishikawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2012)
Mutations in FKBP10 Cause Both Bruck Syndrome and Isolated Osteogenesis Imperfecta in Humans
Ranad Shaheen et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2011)
Mouse FKBP23 mediates conformer-specific functions of BiP by catalyzing Pro117 cis/trans isomerization
Miao Feng et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2011)
Insights into modulation of calcium signaling by magnesium in calmodulin, troponin C and related EF-hand proteins
Zenon Grabarek
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
Ortrud K. Steinlein et al.
BMC MEDICAL GENETICS (2011)
Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes
Shawna M. Pyott et al.
HUMAN MOLECULAR GENETICS (2011)
FK506-Binding Protein 22 from a Psychrophilic Bacterium, a Cold Shock-Inducible Peptidyl Prolyl Isomerase with the Ability to Assist in Protein Folding
Cahyo Budiman et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2011)
Mutations in FKBP10 Cause Recessive Osteogenesis Imperfecta and Bruck Syndrome
Brian P. Kelley et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2011)
Crystal structure of N-domain of FKBP22 from Shewanella sp SIB1: Dimer dissociation by disruption of Val-Leu knot
Cahyo Budiman et al.
PROTEIN SCIENCE (2011)
Chaperoning osteogenesis: new protein-folding disease paradigms
Elena Makareeva et al.
TRENDS IN CELL BIOLOGY (2011)
FKBP10 and Bruck Syndrome: Phenotypic Heterogeneity or Call for Reclassification?
Ranad Shaheen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
Yasemin Alanay et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2010)
Structural Basis of Cyclophilin B Binding by the Calnexin/Calreticulin P-domain
Guennadi Kozlov et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding
Aileen M. Barnes et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
PPIB Mutations Cause Severe Osteogenesis Imperfecta
Fleur S. van Dijk et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Biochemical Characterization of the Prolyl 3-Hydroxylase 1.Cartilage-associated Protein.Cyclophilin B Complex
Yoshihiro Ishikawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2009)
Genetic diseases of connective tissues: cellular and extracellular effects of ECM mutations
John F. Bateman et al.
NATURE REVIEWS GENETICS (2009)
Severe Osteogenesis Imperfecta in Cyclophilin B-Deficient Mice
Jae Won Choi et al.
PLOS GENETICS (2009)
The Rough Endoplasmic Reticulum-resident FK506-binding Protein FKBP65 Is a Molecular Chaperone That Interacts with Collagens
Yoshihiro Ishikawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2008)
Crystal-Structure and Biochemical Characterization of Recombinant Human Calcyphosine Delineates a Novel EF-Hand-Containing Protein Family
Hui Dong et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
Neurospora crassa FKBP22 is a novel ER chaperone and functionally cooperates with BiP
Dirk Tremmel et al.
JOURNAL OF MOLECULAR BIOLOGY (2007)
FKBP22 is part of chaperone/folding catalyst complexes in the endoplasmic reticulum of Neurospora crassa
Dirk Tremmel et al.
FEBS LETTERS (2007)
The human FK506-binding proteins: characterization of human FKBP19
SL Rulten et al.
MAMMALIAN GENOME (2006)
Roles of cyclophilins in cancers and other organ systems
QZ Yao et al.
WORLD JOURNAL OF SURGERY (2005)
Nevo syndrome is allelic to the kyphoscoliotic type of the Ehlers-Danlos syndrome (EDS VIA)
C Giunta et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Prolyl 3-hydroxylase 1, enzyme characterization and identification of a novel family of enzymes
JA Vranka et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
The chaperone activity of protein disulfide isomerase is affected by cyclophilin B and cyclosporin A in vitro
T Horibe et al.
JOURNAL OF BIOCHEMISTRY (2002)
The Ehlers-Danlos syndrome: on beyond collagens
JR Mao et al.
JOURNAL OF CLINICAL INVESTIGATION (2001)
Coexpression of α and β subunits of prolyl 4-hydroxylase stabilizes the triple helix of recombinant human type X collagen
K Wagner et al.
BIOCHEMICAL JOURNAL (2000)
Developmental regulation of FKBP65 -: An ER-localized extracellular matrix binding-protein
CE Patterson et al.
MOLECULAR BIOLOGY OF THE CELL (2000)
Structure-function studies on Hsp47:: pH-dependent inhibition of collagen fibril formation in vitro
CA Thomson et al.
BIOCHEMICAL JOURNAL (2000)
DsbG, a protein disulfide isomerase with chaperone activity
F Shao et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Mutations in the lysyl hydroxylase 1 gene that result in enzyme deficiency and the clinical phenotype of Ehlers-Danlos syndrome type VI
HN Yeowell et al.
MOLECULAR GENETICS AND METABOLISM (2000)
分享论文
