P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA

Collagen structure: new tricks from a very old dog

(2016) J. Bella   BIOCHEMICAL JOURNAL

Cyclophilin-B Modulates Collagen Cross-linking by Differentially Affecting Lysine Hydroxylation in the Helical and Telopeptidyl Domains of Tendon Type I Collagen

(2016) Masahiko Terajima et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Fibromodulin Interacts with Collagen Cross-linking Sites and Activates Lysyl Oxidase

(2016) Sebastian Kalamajski et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2

(2016) Rutger A. F. Gjaltema et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl Hydroxylation

(2016) Melissa E. Heard et al.   PLoS Genetics

Post-translationally Abnormal Collagens of Prolyl 3-Hydroxylase-2 Null Mice Offer a Pathobiological Mechanism for the High Myopia Linked to HumanLEPREL1Mutations

(2015) David M. Hudson et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Comprehensive Characterization of Glycosylation and Hydroxylation of Basement Membrane Collagen IV by High-Resolution Mass Spectrometry

(2015) Trayambak Basak et al.   JOURNAL OF PROTEOME RESEARCH

Osteogenesis imperfecta due to mutations in non-collagenous genes

(2014) Joan C. Marini et al.   CURRENT OPINION IN PEDIATRICS

Lysine post-translational modifications of collagen

(2014) Mitsuo Yamauchi et al.   Essays in Biochemistry

Connective tissue alterations in Fkbp10−/− mice

(2014) Caressa D. Lietman et al.   HUMAN MOLECULAR GENETICS

Increased C-telopeptide Cross-linking of Tendon Type I Collagen in Fibromodulin-deficient Mice

(2014) Sebastian Kalamajski et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Recessive Mutations inLEPREL1Underlie a Recognizable Lens Subluxation Phenotype

(2014) Arif O. Khan et al.   OPHTHALMIC GENETICS

Evolutionary Origins of C-Terminal (GPP)n 3-Hydroxyproline Formation in Vertebrate Tendon Collagen

(2014) David M. Hudson et al.   PLoS One

Differential Effects of Collagen Prolyl 3-Hydroxylation on Skeletal Tissues

(2014) Erica P. Homan et al.   PLoS Genetics

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

(2014) Wayne A. Cabral et al.   PLoS Genetics

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

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

Homozygous loss-of-function mutation of theLEPREL1gene causes severe non-syndromic high myopia with early-onset cataract

(2013) H. Guo et al.   CLINICAL GENETICS

Collagen prolyl 3-hydroxylation: a major role for a minor post-translational modification?

(2013) David M. Hudson et al.   CONNECTIVE TISSUE RESEARCH

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

Sc65 Is a Novel Endoplasmic Reticulum Protein That Regulates Bone Mass Homeostasis

(2013) Katrin Gruenwald et al.   JOURNAL OF BONE AND MINERAL RESEARCH

Biological role of prolyl 3-hydroxylation in type IV collagen

(2013) E. Pokidysheva et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

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

Comprehensive Mass Spectrometric Mapping of the Hydroxylated Amino Acid residues of the α1(V) Collagen Chain

(2012) Chenxi Yang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Identification and Characterization of a New Autoimmune Protein in Membranous Nephropathy by Immunoscreening of a Renal cDNA Library

(2012) Fabrizio Cavazzini et al.   PLoS One

High Myopia Caused by a Mutation in LEPREL1, Encoding Prolyl 3-Hydroxylase 2

(2011) Shikma Mordechai et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Lack of Cyclophilin B in Osteogenesis Imperfecta with Normal Collagen Folding

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

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

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

Location of 3-Hydroxyproline Residues in Collagen Types I, II, III, and V/XI Implies a Role in Fibril Supramolecular Assembly

(2009) Mary Ann Weis et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

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