(Q30982897)

21 September 2017

Generalized connective tissue disease in Crtap-/- mouse (English)

1 reference

connective tissue disease

21 September 2017

1 reference

1 reference

10

Peter H Byers

1 reference

21 September 2017

Dustin Baldridge

1

1 reference

21 September 2017

Jennifer Lennington

2

1 reference

21 September 2017

MaryAnn Weis

3

1 reference

21 September 2017

Erica P Homan

4

1 reference

21 September 2017

Ming-Ming Jiang

5

1 reference

21 September 2017

Elda Munivez

6

1 reference

21 September 2017

Douglas R Keene

7

1 reference

21 September 2017

William R Hogue

8

1 reference

21 September 2017

Shawna Pyott

9

1 reference

21 September 2017

Deborah Krakow

11

1 reference

21 September 2017

Daniel H Cohn

12

1 reference

21 September 2017

David R Eyre

13

1 reference

21 September 2017

Brendan Lee

14

1 reference

21 September 2017

Roy Morello

15

1 reference

21 September 2017

language of work or name

English

0 references

publication date

11 May 2010

1 reference

21 September 2017

1 reference

21 September 2017

5

1 reference

21 September 2017

5

1 reference

21 September 2017

e10560

1 reference

Creative Commons Attribution 4.0 International

21 September 2017

start time

11 May 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2868021/fullTextXML

inferred from PubMed Central ID database lookup

cites work

The extracellular matrix: not just pretty fibrils

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

PPIB mutations cause severe osteogenesis imperfecta

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

CRTAP mutations in lethal and severe osteogenesis imperfecta: the importance of combining biochemical and molecular genetic analysis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Osteogenesis imperfecta: diagnosis and treatment.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Characterization of recombinant human prolyl 3-hydroxylase isoenzyme 2, an enzyme modifying the basement membrane collagen IV

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Brachy-syndactyly caused by loss of Sfrp2 function

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Osteogenesis Imperfecta: update on presentation and management

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Type V collagen controls the initiation of collagen fibril assembly

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

cDNA cloning, characterization and chromosome mapping of Crtap encoding the mouse cartilage associated protein.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British families

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Osteogenesis imperfecta Type IIA and pulmonary hypoplasia with normal alveolar development

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Causes of death in osteogenesis imperfecta

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Structural abnormalities in the dermal collagen and elastic matrix from the skin of patients with inherited connective tissue disorders

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Transgenic mouse model of the mild dominant form of osteogenesis imperfecta

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

Abnormal collagen metabolism in cultured cells in osteogenesis imperfecta

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2868021

CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta

28 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010560

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010560

Type V collagen regulates the assembly of collagen fibrils in cultures of bovine vascular smooth muscle cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010560

Joint hypermobility and skin elasticity: the hereditary disorders of connective tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010560

Hypercalciuria in osteogenesis imperfecta: a follow-up study to assess renal effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010560

Severe osteogenesis imperfecta in cyclophilin B-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010560

CX3CL1 up-regulation is associated with recruitment of CX3CR1+ mononuclear phagocytes and T lymphocytes in the lungs during cigarette smoke-induced emphysema

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0010560

Novel collagen glomerulopathy in a homotrimeric type I collagen mouse (oim)

21 January 2018

1 reference

12 December 2020

Osteogenesis imperfecta: a histometric analysis

1 reference

12 December 2020

Covalent structure of mouse type-IV collagen. Isolation, order and partial amino-acid sequence of cyanogen-bromide and tryptic peptides of pepsin fragment P1 from the alpha 1(IV) chain

1 reference

12 December 2020

Pulmonary hypoplasia and osteogenesis imperfecta type II with defective synthesis of alpha I(1) procollagen

1 reference

12 December 2020

Osteogenesis imperfecta in childhood: cardiac and renal manifestations

1 reference

12 December 2020

Collagen fibrillogenesis in vitro: interaction of types I and V collagen regulates fibril diameter

1 reference

12 December 2020

The mechanical properties of skin in osteogenesis imperfecta

1 reference

12 December 2020

A splice-junction mutation in the region of COL5A1 that codes for the carboxyl propeptide of pro alpha 1(V) chains results in the gravis form of the Ehlers-Danlos syndrome (type I)

1 reference

12 December 2020

Spinal deformity, pulmonary compromise, and quality of life in osteogenesis imperfecta

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0010560

Identifiers

DOI

1 reference

21 September 2017

0 references

1 reference

21 September 2017

1 reference