Tenascin-X, collagen, elastin, and the Ehlers-Danlos syndrome (Q24294425)

Europe PubMed Central

title

Tenascin-X, collagen, elastin, and the Ehlers-Danlos syndrome (English)

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main subject

Ehlers-Danlos syndrome

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Tenascin XB

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GOA release 2020-03-11

collagen fibril binding

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GOA release 2020-03-11

author name string

James Bristow

1

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William Carey

2

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David Egging

3

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Joost Schalkwijk

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

4

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language of work or name

English

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publication date

15 November 2005

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published in

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volume

139C

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issue

1

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page(s)

24-30

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cites work

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

1 reference

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

21 January 2018

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Tenascin-X deficiency in autosomal recessive Ehlers-Danlos syndrome

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Matrix loading: assembly of extracellular matrix collagen fibrils during embryogenesis

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Sex, MHC and complement C4 in autoimmune diseases

1 reference

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Deficiency of tenascin-X causes a decrease in the level of expression of type VI collagen

1 reference

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7 January 2021

Modulation of collagen fibrillogenesis by tenascin-X and type VI collagen

1 reference

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7 January 2021

Binding of tenascin-X to decorin

1 reference

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Flexilin: a new extracellular matrix glycoprotein localized on collagen fibrils

1 reference

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7 January 2021

Tenascin-N: characterization of a novel member of the tenascin family that mediates neurite repulsion from hippocampal explants

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7 January 2021

A six-armed oligomer isolated from cell surface fibronectin preparations

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Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

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A tenascin knockout with a phenotype

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

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7 January 2021

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

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

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Congenital adrenal hyperplasia.

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Cytotactin, an extracellular matrix protein of neural and non-neural tissues that mediates glia-neuron interaction

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

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

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Identification and characterization of a conformational heparin-binding site involving two fibronectin type III modules of bovine tenascin-X.

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

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7 January 2021

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

1 reference

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7 January 2021

Coalignment of plasma membrane channels and protrusions (fibripositors) specifies the parallelism of tendon

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Genetic sophistication of human complement components C4A and C4B and RP-C4-CYP21-TNX (RCCX) modules in the major histocompatibility complex

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7 January 2021

Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome

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7 January 2021

Carriership of a defective tenascin-X gene in steroid 21-hydroxylase deficiency patients: TNXB -TNXA hybrids in apparent large-scale gene conversions

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7 January 2021

Mice develop normally without tenascin

1 reference

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7 January 2021

Deficiency of tenascin-X causes abnormalities in dermal elastic fiber morphology

1 reference

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7 January 2021

The Ehlers-Danlos syndrome: on beyond collagens

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7 January 2021

Murine tenascin-W: a novel mammalian tenascin expressed in kidney and at sites of bone and smooth muscle development

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7 January 2021