Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome. (Q55460687)

12 July 2018

title

Multiple skin hamartomata: a possible novel clinical presentation of SUFU neoplasia syndrome. (English)

1 reference

12 July 2018

author

Ingrid Winship

7

1 reference

12 July 2018

Brigitte Bressac-de Paillerets

5

object named as

Brigitte Bressac-de Paillerets

1 reference

12 July 2018

author name string

Kirsty Mann

1

1 reference

12 July 2018

Jill Magee

2

1 reference

12 July 2018

Marine Guillaud-Bataille

3

1 reference

12 July 2018

Christophe Blondel

4

1 reference

12 July 2018

Josie Yeatman

6

1 reference

12 July 2018

publication date

1 March 2015

1 reference

12 July 2018

published in

Familial Cancer

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12 July 2018

volume

14

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12 July 2018

issue

1

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12 July 2018

page(s)

151-155

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12 July 2018

The 2007 WHO classification of tumours of the central nervous system

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Retrospective family study of childhood medulloblastoma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Heterogeneity of familial medulloblastoma and contribution of germline PTCH1 and SUFU mutations to sporadic medulloblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Mutations in SUFU predispose to medulloblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Kif7 regulates Gli2 through Sufu-dependent and -independent functions during skin development and tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Loss of suppressor-of-fused function promotes tumorigenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Loss of Trp53 promotes medulloblastoma development but not skin tumorigenesis in Sufu heterozygous mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Identification of a SUFU germline mutation in a family with Gorlin syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Loss of SUFU function in familial multiple meningioma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Lessons from the skin--cutaneous features of familial cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10689-014-9752-1

Birt-Hogg-Dubé syndrome: a novel marker of kidney neoplasia.

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25287320

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Incomplete penetrance of the predisposition to medulloblastoma associated with germ-line SUFU mutations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25287320

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10689-014-9752-1

1 reference

12 July 2018

Dimensions Publication ID

1005940820

0 references

Fatcat ID

release_pyqq4sltcrg2jidbvlukbhurmi

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/pyqq4sltcrg2jidbvlukbhurmi

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

12 July 2018