(Q34306976)

1 August 2017

title

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). (English)

1 reference

1 August 2017

1 reference

6

Sabine Tejpar

0 references

Gabriela M Repetto

object named as

Gabriela M Repetto

2

0 references

Douglas A Marchuk

object named as

Douglas A Marchuk

10

1 reference

ORCID Public Data File 2021

author name string

Carol J Gallione

1

1 reference

1 August 2017

Eric Legius

3

1 reference

1 August 2017

Anil K Rustgi

4

1 reference

1 August 2017

Susan L Schelley

5

1 reference

1 August 2017

Grant Mitchell

7

1 reference

1 August 2017

Eric Drouin

8

1 reference

1 August 2017

Cornelius J J Westermann

9

1 reference

1 August 2017

language of work or name

English

0 references

publication date

1 March 2004

1 reference

1 August 2017

1 reference

1 August 2017

volume

363

1 reference

1 August 2017

issue

9412

1 reference

1 August 2017

page(s)

852-859

1 reference

Mutations in the SMAD4/DPC4 gene in juvenile polyposis

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Endoglin, a TGF-beta binding protein of endothelial cells, is the gene for hereditary haemorrhagic telangiectasia type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Mutations in the activin receptor-like kinase 1 gene in hereditary haemorrhagic telangiectasia type 2.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Generalized juvenile polyposis with pulmonary arteriovenous malformations and hypertrophic osteoarthropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Association of juvenile and adenomatous polyposis with pulmonary arteriovenous malformation and hypertrophic osteoarthropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Hereditary generalized juvenile polyposis: association with arteriovenous malformations and risk of malignancy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

A survey of phenotypic features in juvenile polyposis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Juvenile polyposis occurring in hereditary hemorrhagic telangiectasia.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

SMAD genes in juvenile polyposis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Novel de novo mutation of MADH4/SMAD4 in a patient with juvenile polyposis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Diagnostic criteria for hereditary hemorrhagic telangiectasia (Rendu-Osler-Weber syndrome).

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Hereditary haemorrhagic telangiectasia (Osler-Weber-Rendu syndrome): a view from the 21st century.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Association of hypertrophic osteoarthropathy with gastrointestinal polyposis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Colonic hamartomatous polyposis associated with hypertrophic osteoarthropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Hereditary haemorrhagic telangiectasia: a questionnaire based study to delineate the different phenotypes caused by endoglin and ALK1 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Balancing the activation state of the endothelium via two distinct TGF-beta type I receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Vascular morphogenesis: tales of two syndromes.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

From developmental disorder to heritable cancer: it's all in the BMP/TGF-beta family

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

How cells read TGF-beta signals

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

TGF-beta induces fibronectin synthesis through a c-Jun N-terminal kinase-dependent, Smad4-independent pathway

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

ATF-2 is a common nuclear target of Smad and TAK1 pathways in transforming growth factor-beta signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

Involvement of the p38 mitogen-activated protein kinase pathway in transforming growth factor-beta-induced gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

The tumor suppressor gene Smad4/Dpc4 is required for gastrulation and later for anterior development of the mouse embryo

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

A structural basis for mutational inactivation of the tumour suppressor Smad4

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2804%2915732-2

7 January 2021

10.1016/S0140-6736(04)15732-2

Identifiers

DOI

1 reference

1 August 2017

1 reference