(Q43531454)

24 November 2017

Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey (English)

1 reference

24 November 2017

1 reference

1 reference

Minoru Takemoto

1

1 reference

24 November 2017

Seijiro Mori

2

1 reference

24 November 2017

Masafumi Kuzuya

3

1 reference

24 November 2017

Shinya Yoshimoto

4

1 reference

24 November 2017

Akira Shimamoto

5

1 reference

24 November 2017

Masahiko Igarashi

6

1 reference

24 November 2017

Yasuhito Tanaka

7

1 reference

24 November 2017

Tetsuro Miki

8

1 reference

24 November 2017

Koutaro Yokote

9

1 reference

24 November 2017

23 July 2012

1 reference

Geriatrics and Gerontology International

24 November 2017

1 reference

24 November 2017

13

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24 November 2017

2

1 reference

24 November 2017

475-481

1 reference

A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

24 November 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Positional cloning of the Werner's syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Elevation of serum hyaluronan level in Werner's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Immunological diagnosis of Werner syndrome by down-regulated and truncated gene products

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

A case of Werner syndrome without metabolic abnormality: implications for the early pathophysiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

LMNA mutations in atypical Werner's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

The Bloom's syndrome gene product is homologous to RecQ helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Extension of the life span in patients with Werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Dysadipocytokinemia in werner syndrome and its recovery by treatment with pioglitazone

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Biguanide, but not thiazolidinedione, improved insulin resistance in Werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

Primary lung cancer associated with Werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1447-0594.2012.00913.X

10.1111/J.1447-0594.2012.00913.X

21 January 2018

Identifiers

DOI

1 reference

24 November 2017

1 reference