(Q21144869)

English

Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfecta

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Abnormal type I collagen post-translational modification and crosslinking in a cyclophilin B KO mouse model of recessive osteogenesis imperfecta (English)

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osteogenesis imperfecta

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object named as

Sergey Leikin

10

author given names

Sergey

author last names

Leikin

1 reference

17 August 2022

author name string

Wayne A Cabral

1

author given names

Wayne A

author last names

Cabral

1 reference

17 August 2022

Irina Perdivara

2

author given names

Irina

author last names

Perdivara

1 reference

17 August 2022

MaryAnn Weis

3

author given names

MaryAnn

author last names

Weis

1 reference

17 August 2022

Masahiko Terajima

4

author given names

Masahiko

author last names

Terajima

1 reference

17 August 2022

Angela R Blissett

5

author given names

Angela R

author last names

Blissett

1 reference

17 August 2022

Weizhong Chang

6

author given names

Weizhong

author last names

Chang

1 reference

17 August 2022

Joseph E Perosky

7

author given names

Joseph E

author last names

Perosky

1 reference

17 August 2022

Elena N Makareeva

8

author given names

Elena N

author last names

Makareeva

1 reference

17 August 2022

Edward L Mertz

9

author given names

Edward L

author last names

Mertz

1 reference

17 August 2022

Kenneth B Tomer

11

author given names

Kenneth B

author last names

Tomer

1 reference

17 August 2022

Kenneth M Kozloff

12

author given names

Kenneth M

author last names

Kozloff

1 reference

17 August 2022

David R Eyre

13

author given names

David R

author last names

Eyre

1 reference

17 August 2022

Mitsuo Yamauchi

14

author given names

Mitsuo

author last names

Yamauchi

1 reference

17 August 2022

Joan C Marini

15

author given names

Joan C

author last names

Marini

1 reference

17 August 2022

language of work or name

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publication date

June 2014

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10

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6

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e1004465

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copyright license

Creative Commons CC0 License

26 June 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

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An interaction map of endoplasmic reticulum chaperones and foldases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Prolyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Lack of cyclophilin B in osteogenesis imperfecta with normal collagen folding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Prolyl 3-hydroxylase 1, enzyme characterization and identification of a novel family of enzymes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

A subset of chaperones and folding enzymes form multiprotein complexes in endoplasmic reticulum to bind nascent proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Cloning and characterization of a third human lysyl hydroxylase isoform

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Bone collagen: new clues to its mineralization mechanism from recessive osteogenesis imperfecta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Core glycosylation of collagen is initiated by two beta(1-O)galactosyltransferases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

The third activity for lysyl hydroxylase 3: galactosylation of hydroxylysyl residues in collagens in vitro.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Lysyl hydroxylase 3 is a multifunctional protein possessing collagen glucosyltransferase activity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Severe osteogenesis imperfecta in cyclophilin B-deficient mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

19 March 2017

Posttranslational modifications in type I collagen from different tissues extracted from wild type and prolyl 3-hydroxylase 1 null mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Kuskokwim syndrome, a recessive congenital contracture disorder, extends the phenotype of FKBP10 mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Lysyl hydroxylase 3-mediated glucosylation in type I collagen: molecular loci and biological significance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Peptidyl 3-hydroxyproline binding properties of type I collagen suggest a function in fibril supramolecular assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

New perspectives on osteogenesis imperfecta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Lysyl hydroxylase 3 glucosylates galactosylhydroxylysine residues in type I collagen in osteoblast culture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Generalized connective tissue disease in Crtap-/- mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

PPIB mutations cause severe osteogenesis imperfecta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

A connective tissue disorder caused by mutations of the lysyl hydroxylase 3 gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Components of the collagen prolyl 3-hydroxylation complex are crucial for normal bone development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Expanding the lysyl hydroxylase toolbox: new insights into the localization and activities of lysyl hydroxylase 3 (LH3).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Collagens, modifying enzymes and their mutations in humans, flies and worms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Identification of PLOD2 as telopeptide lysyl hydroxylase, an important enzyme in fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Peptidylprolyl cis/trans isomerases (immunophilins): biological diversity--targets--functions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Peptidyl-prolyl cis-trans isomerases, a superfamily of ubiquitous folding catalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Collagen structural microheterogeneity and a possible role for glycosylated hydroxylysine in type I collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Reducible Crosslinks in Hydroxylysine-Deficient Collagens of a Heritable Disorder of Connective Tissue

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

12 September 2017

Lysine hydroxylation and cross-linking of collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

27 September 2017

BayGenomics: a resource of insertional mutations in mouse embryonic stem cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

27 September 2017

Thermal stability and folding of the collagen triple helix and the effects of mutations in osteogenesis imperfecta on the triple helix of type I collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Biochemical characterization of the prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B complex.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Characterization of collagenous peptides bound to lysyl hydroxylase isoforms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Collagen cross-links in mineralizing tissues: a review of their chemistry, function, and clinical relevance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Chicken FK506-binding protein, FKBP65, a member of the FKBP family of peptidylprolyl cis-trans isomerases, is only partially inhibited by FK506.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Abnormal formation of collagen cross-links in skin fibroblasts cultured from patients with Ehlers-Danlos syndrome type VI.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Cyclosporin A slows collagen triple-helix formation in vivo: indirect evidence for a physiologic role of peptidyl-prolyl cis-trans-isomerase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

30 May 2018

Delayed triple helix formation of mutant collagen from patients with osteogenesis imperfecta.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

The kyphoscoliotic type of Ehlers-Danlos syndrome (type VI): differential effects on the hydroxylation of lysine in collagens I and II revealed by analysis of cross-linked telopeptides from urine

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

Lysine hydroxylation of collagen in a fibroblast cell culture system

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

A Heritable Disorder of Connective Tissue

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

Lower bone cellular activities in male and female mature C3H/HeJ mice are associated with higher bone mass and different pyridinium crosslink profiles compared to C57BL/6J mice.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

Cross-link profile of bone collagen correlates with structural organization of trabeculae

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

Mechanical properties of adult vertebral cancellous bone: correlation with collagen intermolecular cross-links

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

Type I collagen triplet duplication mutation in lethal osteogenesis imperfecta shifts register of alpha chains throughout the helix and disrupts incorporation of mutant helices into fibrils and extracellular matrix

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1004465

21 January 2018

Urinary pyridinoline cross-links in Ehlers-Danlos syndrome type VI.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4072593

29 November 2018

Pyridinium cross-links in bone of patients with osteogenesis imperfecta: evidence of a normal intrafibrillar collagen packing

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of a crosslinked peptide from calf bone collagen: evidence that hydroxylysyl glycoside participates in the crosslink

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteogenesis imperfecta: biochemical studies of bone collagen

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Folding mechanism of the triple helix in type-III collagen and type-III pN-collagen. Role of disulfide bridges and peptide bond isomerization

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Altered triple helical structure of type I procollagen in lethal perinatal osteogenesis imperfecta

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collagen cross-linking amino acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The post-translational chemistry and molecular packing of mineralizing tendon collagens

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deposition and selective degradation of structurally-abnormal type I collagen in a collagen matrix produced by osteogenesis imperfecta fibroblasts in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic Comparison of an Osteogenesis Imperfecta Type IV Proband with ade Novoα2(I) Gly922 → Ser Substitution in Type I Collagen and an Unrelated Patient with an Identical Mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential expression of human lysyl hydroxylase genes, lysine hydroxylation, and cross-linking of type I collagen during osteoblastic differentiation in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations Near Amino End of α1(I) Collagen Cause Combined Osteogenesis Imperfecta/Ehlers-Danlos Syndrome by Interference with N-propeptide Processing

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tissue-specific changes in the hydroxylysine content and cross-links of collagens and alterations in fibril morphology in lysyl hydroxylase 1 knock-out mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Secretion and assembly of type IV and VI collagens depend on glycosylation of hydroxylysines

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Osteoblast isolation from murine calvaria and long bones

1 reference

https://pubmed.ncbi.nlm.nih.gov/24968150

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PGEN.1004465

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

ResearchGate publication ID

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