(Q85883397)

English

Association of the formiminotransferase N-terminal sub-domain containing gene and thrombospondin, type 1, domain-containing 7A gene with the prevalence of vertebral fracture in 2427 consecutive autopsy cases

scientific article published on 10 January 2013

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21 February 2020

Association of the formiminotransferase N-terminal sub-domain containing gene and thrombospondin, type 1, domain-containing 7A gene with the prevalence of vertebral fracture in 2427 consecutive autopsy cases (English)

1 reference

Europe PubMed Central

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21 February 2020

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21 February 2020

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Heying Zhou

1

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21 February 2020

Seijiro Mori

2

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21 February 2020

Ikuyo Kou

3

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21 February 2020

Makiko Naka Mieno

5

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21 February 2020

Naoko Honma

6

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21 February 2020

Tomio Arai

7

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21 February 2020

Motoji Sawabe

8

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21 February 2020

Masashi Tanaka

9

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21 February 2020

Shiro Ikegawa

10

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21 February 2020

Hideki Ito

11

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21 February 2020

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10 January 2013

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21 February 2020

Journal of Human Genetics

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21 February 2020

58

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21 February 2020

2

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21 February 2020

109-112

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21 February 2020

Osteoporosis: a still increasing prevalence

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnostic criteria for primary osteoporosis: year 2000 revision

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic determinants of susceptibility to osteoporosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetics of osteoporosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

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Bona fide genetic associations with bone mineral density

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic regulation of bone mass and susceptibility to osteoporosis

1 reference

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7 January 2021

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Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

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Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

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Cumulative incidence and changes in the prevalence of vertebral fractures in a rural Japanese community: a 10-year follow-up of the Miyama cohort.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

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The Two Monofunctional Domains of Octameric Formiminotransferase-Cyclodeaminase Exist as Dimers

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

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Secretion of L-glutamate from osteoclasts through transcytosis.

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

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The tryptophan-rich motifs of the thrombospondin type 1 repeats bind VLAL motifs in the latent transforming growth factor-beta complex

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

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inferred from DOI database lookup

TGF beta/Smad signaling system and its pathologic correlates

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2012.145

7 January 2021

based on heuristic

inferred from DOI database lookup

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