Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition (Q28590272)

31 January 2017

title

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

1 reference

31 January 2017

main subject

Ehlers-Danlos syndrome

0 references

4

Diane R. Wagner

1 reference

31 January 2017

7

Edward M. Rubin

1 reference

31 January 2017

Jau Ren Mao

1

1 reference

31 January 2017

Glen Taylor

2

1 reference

31 January 2017

Willow B. Dean

3

1 reference

31 January 2017

Veena Afzal

5

1 reference

31 January 2017

Jeffrey C. Lotz

6

1 reference

31 January 2017

James Bristow

8

1 reference

31 January 2017

language of work or name

English

0 references

publication date

1 April 2002

1 reference

31 January 2017

1 reference

31 January 2017

volume

30

1 reference

31 January 2017

issue

4

1 reference

31 January 2017

page(s)

421–425

1 reference

Tenascin-X: a novel extracellular matrix protein encoded by the human XB gene overlapping P450c21B

31 January 2017

cites work

1 reference

7 January 2021

Flexilin: a new extracellular matrix glycoprotein localized on collagen fibrils

1 reference

7 January 2021

The distribution of tenascin-X is distinct and often reciprocal to that of tenascin-C

1 reference

7 January 2021

Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

1 reference

7 January 2021

A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency

1 reference

7 January 2021

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

1 reference

7 January 2021

A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VI

1 reference

7 January 2021

Mutations in the COL3A1 gene result in the Ehlers-Danlos syndrome type IV and alterations in the size and distribution of the major collagen fibrils of the dermis

1 reference

7 January 2021

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

1 reference

7 January 2021

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

7 January 2021

The Ehlers-Danlos syndrome: on beyond collagens

1 reference

7 January 2021

Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus

1 reference

7 January 2021

Biomechanical properties of dermis

1 reference

7 January 2021

Embryonic expression of tenascin-X suggests a role in limb, muscle, and heart development

1 reference

7 January 2021

Transgenic mouse model of the mild dominant form of osteogenesis imperfecta

1 reference

7 January 2021

Tumour invasion and metastasis are promoted in mice deficient in tenascin-X.

1 reference

7 January 2021

Altered surfactant homeostasis and alveolar type II cell morphology in mice lacking surfactant protein D

1 reference

7 January 2021

An improved method for the determination of hydroxyproline in rat skin

1 reference

7 January 2021

Balloon angioplasty significantly increases collagen content but does not alter collagen subtype I/III ratios in the atherosclerotic rabbit iliac model.

1 reference

7 January 2021

Collagen defects in lethal perinatal osteogenesis imperfecta

1 reference

7 January 2021

Type I osteogenesis imperfecta: a nonfunctional allele for pro alpha 1 (I) chains of type I procollagen

1 reference

7 January 2021

Mice develop normally without tenascin

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG850

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017