Tenascin-X deficiency is associated with Ehlers-Danlos syndrome (Q43500561)

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scientific article published in September 1997

Language	Label	Description	Also known as
English	Tenascin-X deficiency is associated with Ehlers-Danlos syndrome	scientific article published in September 1997

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

Tenascin-X deficiency is associated with Ehlers-Danlos syndrome (English)

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Europe PubMed Central

PubMed publication ID

24 November 2017

Ehlers-Danlos syndrome

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author name string

Burch GH

1

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24 November 2017

Gong Y

2

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24 November 2017

Liu W

3

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24 November 2017

Dettman RW

4

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24 November 2017

Curry CJ

5

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24 November 2017

Smith L

6

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24 November 2017

Miller WL

7

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24 November 2017

Bristow J

8

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24 November 2017

language of work or name

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publication date

1 September 1997

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24 November 2017

Nature Genetics

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24 November 2017

17

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1

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24 November 2017

104-108

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24 November 2017

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

Tenascin: an extracellular matrix protein involved in tissue interactions during fetal development and oncogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

The chicken neural extracellular matrix molecule restrictin: similarity with EGF-, fibronectin type III-, and fibrinogen-like motifs

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

Molecular characterization and in situ mRNA localization of the neural recognition molecule J1-160/180: a modular structure similar to tenascin

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

Mechanism and consequences of the duplication of the human C4/P450c21/gene X locus

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

Skin wounds and severed nerves heal normally in mice lacking tenascin-C

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Cluster of fibronectin type III repeats found in the human major histocompatibility complex class III region shows the highest homology with the repeats in an extracellular matrix protein, tenascin

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

A six-armed oligomer isolated from cell surface fibronectin preparations

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

A cDNA clone for cytotactin contains sequences similar to epidermal growth factor-like repeats and segments of fibronectin and fibrinogen

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Tenascin-C, tenascin-R and tenascin-X: a family of talented proteins in search of functions

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Distinct tissue distribution in pigs of tenascin-X and tenascin-C transcripts

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Extracellular matrix protein tenascin-like gene found in human MHC class III region

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI 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://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Rearrangements and point mutations of P450c21 genes are distinguished by five restriction endonuclease haplotypes identified by a new probing strategy in 57 families with congenital adrenal hyperplasia

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Mice develop normally without tenascin

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

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

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI 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://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

A Heritable Disorder of Connective Tissue

1 reference

https://api.crossref.org/works/10.1038%2FNG0997-104

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/NG0997-104

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

ResearchGate publication ID

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