(Q35630667)

English

Collagen V is a dominant regulator of collagen fibrillogenesis: dysfunctional regulation of structure and function in a corneal-stroma-specific Col5a1-null mouse model

scientific article published on 8 December 2011

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Collagen V is a dominant regulator of collagen fibrillogenesis: dysfunctional regulation of structure and function in a corneal-stroma-specific Col5a1-null mouse model (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

author name string

Mei Sun

1

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Shoujun Chen

2

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Sheila M Adams

3

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Jane B Florer

4

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Hongshan Liu

5

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Winston W-Y Kao

6

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Richard J Wenstrup

7

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

David E Birk

8

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

language of work or name

0 references

publication date

8 December 2011

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Journal of Cell Science

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

124

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Pt 23

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

4096-4105

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

describes a project that uses

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3244988/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Regulation of collagen fibril nucleation and initial fibril assembly involves coordinate interactions with collagens V and XI in developing tendon

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Clinical and genetic aspects of Ehlers-Danlos syndrome, classic type

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Cell therapy of congenital corneal diseases with umbilical mesenchymal stem cells: lumican null mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Fibromodulin regulates collagen fibrillogenesis during peripheral corneal development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Second harmonic generation imaging of collagen fibrils in cornea and sclera

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Type XIV Collagen Regulates Fibrillogenesis: PREMATURE COLLAGEN FIBRIL GROWTH AND TISSUE DYSFUNCTION IN NULL MICE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Genetic evidence for the coordinated regulation of collagen fibrillogenesis in the cornea by decorin and biglycan

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Differential gene expression associated with postnatal equine articular cartilage maturation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Quantitative real-time RT-PCR data analysis: current concepts and the novel "gene expression's CT difference" formula

1 reference

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27 July 2018

Murine model of the Ehlers-Danlos syndrome. col5a1 haploinsufficiency disrupts collagen fibril assembly at multiple stages

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Structural abnormalities of the cornea and lid resulting from collagen V mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Tenascin-X, collagen, elastin, and the Ehlers-Danlos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Congenital stromal dystrophy of the cornea caused by a mutation in the decorin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Inducible gene trapping with drug-selectable markers and Cre/loxP to identify developmentally regulated genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Type V collagen controls the initiation of collagen fibril assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Novel types of mutation responsible for the dermatosparactic type of Ehlers-Danlos syndrome (Type VIIC) and common polymorphisms in the ADAMTS2 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Reduced type I collagen utilization: a pathogenic mechanism in COL5A1 haplo-insufficient Ehlers-Danlos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Differential expression of lumican and fibromodulin regulate collagen fibrillogenesis in developing mouse tendons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Null alleles of the COL5A1 gene of type V collagen are a cause of the classical forms of Ehlers-Danlos syndrome (types I and II).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Lumican regulates collagen fibril assembly: skin fragility and corneal opacity in the absence of lumican

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Ehlers-Danlos syndromes: revised nosology, Villefranche, 1997. Ehlers-Danlos National Foundation (USA) and Ehlers-Danlos Support Group (UK).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Mutations in the COL5A1 gene are causal in the Ehlers-Danlos syndromes I and II

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

An exon skipping mutation of a type V collagen gene (COL5A1) in Ehlers-Danlos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Reduction of type V collagen using a dominant-negative strategy alters the regulation of fibrillogenesis and results in the loss of corneal-specific fibril morphology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

A translocation interrupts the COL5A1 gene in a patient with Ehlers-Danlos syndrome and hypomelanosis of Ito.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Type V collagen: molecular structure and fibrillar organization of the chicken alpha 1(V) NH2-terminal domain, a putative regulator of corneal fibrillogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Extracellular compartments in matrix morphogenesis: collagen fibril, bundle, and lamellar formation by corneal fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Collagen type I and type V are present in the same fibril in the avian corneal stroma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Pleomorphism in type I collagen fibrils produced by persistence of the procollagen N-propeptide

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Abnormal collagen fibril structure in the gravis form (type I) of Ehlers-Danlos syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

27 July 2018

Identification of binding partners interacting with the α1-N-propeptide of type V collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

25 September 2018

The molecular basis of corneal transparency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

25 September 2018

Promiscuous recombination of LoxP alleles during gametogenesis in cornea Cre driver mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

25 September 2018

A global double-fluorescent Cre reporter mouse

1 reference

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25 September 2018

Noninvasive corneal stromal collagen imaging using two-photon-generated second-harmonic signals.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

25 September 2018

Type V collagen: heterotypic type I/V collagen interactions in the regulation of fibril assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3244988

25 September 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene encoding collagen alpha1(V)(COL5A1) is linked to mixed Ehlers-Danlos syndrome type I/II

1 reference

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A syndrome of joint laxity and impaired tendon integrity in lumican- and fibromodulin-deficient mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Keratocan-deficient mice display alterations in corneal structure

1 reference

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Collagen Made of Extended alpha-Chains, Procollagen, in Genetically-Defective Dermatosparaxic Calves

1 reference

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage to the collagen alpha 1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential ultrastructural aberrations of collagen fibrils in Ehlers-Danlos syndrome types I-IV as a means of diagnostics and classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/22159420

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1242/JCS.091363

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

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