Differential Effects of Collagen Prolyl 3-Hydroxylation on Skeletal Tissues

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

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

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

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

(2012) David M. Hudson et al.   BIOCHEMISTRY

A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta

(2012) Masaki Takagi et al.   PLoS One

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

PyETV: a PyMOL evolutionary trace viewer to analyze functional site predictions in protein complexes

(2010) Rhonald C. Lua et al.   BIOINFORMATICS

Molecular and structural mapping of collagen fibril interactions

(2010) J. P. R. O. Orgel et al.   CONNECTIVE TISSUE RESEARCH

Molecular determinants of extracellular matrix mineralization in bone and blood vessels

(2010) Monzur Murshed et al.   CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION

Evolution: a guide to perturb protein function and networks

(2010) Olivier Lichtarge et al.   CURRENT OPINION IN STRUCTURAL BIOLOGY

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

Bone histomorphometry: Standardization of nomenclature, symbols, and units: Report of the asbmr histomorphometry nomenclature committee

(2010) A. Michael Parfitt et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Mineralization of the metre-long biosilica structures of glass sponges is templated on hydroxylated collagen

(2010) Hermann Ehrlich et al.   Nature Chemistry

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

Null mutations in LEPRE1 and CRTAP cause severe recessive osteogenesis imperfecta

(2009) Joan C. Marini et al.   CELL AND TISSUE RESEARCH

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

Production, concentration and titration of pseudotyped HIV-1-based lentiviral vectors

(2009) Robert H Kutner et al.   Nature Protocols

Severe Osteogenesis Imperfecta in Cyclophilin B–Deficient Mice

(2009) Jae Won Choi et al.   PLoS Genetics

Effect of the -Gly-3(S)-hydroxyprolyl-4(R)-hydroxyprolyl- tripeptide unit on the stability of collagen model peptides

(2008) Kazunori Mizuno et al.   FEBS Journal

CRTAPandLEPRE1mutations in recessive osteogenesis imperfecta

(2008) Dustin Baldridge et al.   HUMAN MUTATION

Characterization of Recombinant Human Prolyl 3-Hydroxylase Isoenzyme 2, an Enzyme Modifying the Basement Membrane Collagen IV

(2008) Päivi Tiainen et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Bone Morphometry Strongly Predicts Cortical Bone Stiffness and Strength, but Not Toughness, in Inbred Mouse Models of High and Low Bone Mass

(2008) Romain Voide et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Brachy-syndactyly caused by loss ofSfrp2function

(2008) Roy Morello et al.   JOURNAL OF CELLULAR PHYSIOLOGY

Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation

(2008) A Willaert et al.   JOURNAL OF MEDICAL GENETICS