(Q43890772)

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title

The role of TNXB single-nucleotide polymorphisms in recurrent shoulder dislocation (English)

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single-nucleotide polymorphism

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main subject

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Emanuel V Geiger

1

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Dirk Henrich

2

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Sebastian Wutzler

3

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Dorien Schneidmüller

4

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Heike Jakob

5

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Johannes M Frank

6

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Ingo Marzi

7

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publication date

18 September 2012

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Journal of Orthopaedic Research

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published in

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volume

31

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issue

2

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page(s)

295-299

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

27 November 2017

cites work

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Tenascin-C in development and disease: gene regulation and cell function

21 January 2018

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

21 January 2018

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Tenascin-X deficiency is associated with Ehlers-Danlos syndrome

21 January 2018

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

21 January 2018

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Functional outcomes of early arthroscopic bankart repair in adolescents aged 11 to 18 years

21 January 2018

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Recurrent transient subluxation of the shoulder

21 January 2018

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Development of an upper extremity outcome measure: the DASH (disabilities of the arm, shoulder and hand) [corrected]. The Upper Extremity Collaborative Group (UECG)

21 January 2018

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A standard method of shoulder strength measurement for the Constant score with a spring balance.

21 January 2018

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Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population

21 January 2018

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Mendelian proportions in a mixed population

21 January 2018

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Synthesis of genetic association studies for pertinent gene-disease associations requires appropriate methodological and statistical approaches

21 January 2018

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Haploview: analysis and visualization of LD and haplotype maps

21 January 2018

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The lowdown on linkage disequilibrium.

21 January 2018

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Association of the PTPN22 R620W polymorphism with anti-topoisomerase I- and anticentromere antibody-positive systemic sclerosis

21 January 2018

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TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/JOR.22231

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27 November 2017

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