Abnormal Type I Collagen Post-translational Modification and Crosslinking in a Cyclophilin B KO Mouse Model of Recessive Osteogenesis Imperfecta

Bone Collagen: New Clues to Its Mineralization Mechanism from Recessive Osteogenesis Imperfecta

(2013) David R. Eyre et al.   CALCIFIED TISSUE INTERNATIONAL

Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype ofFKBP10  Mutations

(2013) Aileen M. Barnes et al.   HUMAN MUTATION

Posttranslational Modifications in Type I Collagen from Different Tissues Extracted from Wild Type and Prolyl 3-Hydroxylase 1 Null Mice

(2013) Elena Pokidysheva et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

(2012) Matthias Baumann et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Peptidyl 3-Hydroxyproline Binding Properties of Type I Collagen Suggest a Function in Fibril Supramolecular Assembly

(2012) David M. Hudson et al.   BIOCHEMISTRY

Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

(2012) U. Schwarze et al.   HUMAN MOLECULAR GENETICS

Absence ofFKBP10in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix

(2012) Aileen M. Barnes et al.   HUMAN MUTATION

Mutation in Cyclophilin B That Causes Hyperelastosis Cutis in American Quarter Horse Does Not Affect Peptidylprolylcis-transIsomerase Activity but Shows Altered Cyclophilin B-Protein Interactions and Affects Collagen Folding

(2012) Yoshihiro Ishikawa et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Lysyl Hydroxylase 3-mediated Glucosylation in Type I Collagen

(2012) Marnisa Sricholpech et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Sclerostin antibody improves skeletal parameters in a Brtl/+ mouse model of osteogenesis imperfecta

(2012) Benjamin P Sinder et al.   JOURNAL OF BONE AND MINERAL RESEARCH

An Interaction Map of Endoplasmic Reticulum Chaperones and Foldases

(2012) Gregor Jansen et al.   MOLECULAR & CELLULAR PROTEOMICS

Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes

(2011) Shawna M. Pyott et al.   HUMAN MOLECULAR GENETICS

Lysyl Hydroxylase 3 Glucosylates Galactosylhydroxylysine Residues in Type I Collagen in Osteoblast Culture

(2011) Marnisa Sricholpech et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

New perspectives on osteogenesis imperfecta

(2011) Antonella Forlino et al.   Nature Reviews Endocrinology

Prolyl 3-Hydroxylase 1 Null Mice Display Abnormalities in Fibrillar Collagen-rich Tissues Such as Tendons, Skin, and Bones

(2010) Janice A. Vranka et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Collagen crosslinks and mineral crystallinity in bone of patients with osteogenesis imperfecta

(2010) Ulrich Vetter et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding

(2010) Aileen M. Barnes et al.   NEW ENGLAND JOURNAL OF MEDICINE

Generalized Connective Tissue Disease in Crtap-/- Mouse

(2010) Dustin Baldridge et al.   PLoS One

PPIB Mutations Cause Severe Osteogenesis Imperfecta

(2009) Fleur S. van Dijk et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Prolyl 3-hydroxylase 1 and CRTAP are mutually stabilizing in the endoplasmic reticulum collagen prolyl 3-hydroxylation complex

(2009) Weizhong Chang et al.   HUMAN MOLECULAR GENETICS

Biochemical Characterization of the Prolyl 3-Hydroxylase 1·Cartilage-associated Protein·Cyclophilin B Complex

(2009) Yoshihiro Ishikawa et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Severe Osteogenesis Imperfecta in Cyclophilin B–Deficient Mice

(2009) Jae Won Choi et al.   PLoS Genetics

A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene

(2008) Antti M. Salo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Core Glycosylation of Collagen Is Initiated by Two  (1-O)Galactosyltransferases

(2008) B. Schegg et al.   MOLECULAR AND CELLULAR BIOLOGY