Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. (Q52000174)

From Wikidata

Jump to navigation Jump to search

The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

scientific article published on 13 December 2006

Language	Label	Description	Also known as
English	Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.	scientific article published on 13 December 2006

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Noonan syndrome

1 reference

based on heuristic

inferred from title

corrigendum / erratum

Erratum: Corrigendum: Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome

1 reference

10.1038/NG0207-276A

12 July 2019

http://api.crossref.org/works?select=update-to&filter=doi:10.1038/NG0207-276A

Marco Tartaglia

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

14

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Francesca Lepri

15

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Bruno Dallapiccola

23

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

24

object named as

Dafna Bar-Sagi

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

Len A. Pennacchio

2

object named as

Len A Pennacchio

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Valentina Fodale

5

object named as

Valentina Fodale

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Juan Pedro López Siguero

20

object named as

Juan Pedro López Siguero

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Wendy Schackwitz

10

object named as

Wendy Schackwitz

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Anna Ustaszewska

11

object named as

Anna Ustaszewska

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Bhaswati Pandit

7

object named as

Bhaswati Pandit

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

17

object named as

Isabella Vasta

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

16

object named as

Cinzia Neri

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

author name string

Chen Zhao

3

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Kamlesh K Yadav

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Anna Sarkozy

6

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Kimihiko Oishi

8

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Simone Martinelli

9

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Joel Martin

12

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

James Bristow

13

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Kate Gibson

18

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Cynthia J Curry

19

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Maria Cristina Digilio

21

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Giuseppe Zampino

22

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

language of work or name

0 references

publication date

13 December 2006

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Nature Genetics

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

39

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

75-79

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Hypertelorism With Turner Phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activation

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Germline KRAS mutations cause Noonan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Diverse biochemical properties of Shp2 mutants. Implications for disease phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

PTPN11 mutations in LEOPARD syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Germline mutations in HRAS proto-oncogene cause Costello syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Regulation of Sos activity by intramolecular interactions

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Computational docking and solution x-ray scattering predict a membrane-interacting role for the histone domain of the Ras activator son of sevenless

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Structural analysis of autoinhibition in the Ras activator Son of sevenless

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Structural evidence for feedback activation by Ras.GTP of the Ras-specific nucleotide exchange factor SOS

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

The Sos1 and Sos2 Ras-specific exchange factors: differences in placental expression and signaling properties

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Mutation in Sos1 dominantly enhances a weak allele of the EGFR, demonstrating a requirement for Sos1 in EGFR signaling and development

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

The EGF receptor provides an essential survival signal for SOS-dependent skin tumor development

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Increasing complexity of the Ras signaling pathway

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Coupling of Ras and Rac guanosine triphosphatases through the Ras exchanger Sos.

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Identification of murine homologues of the Drosophila son of sevenless gene: potential activators of ras

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Differential interactions of human Sos1 and Sos2 with Grb2

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Detecting polymorphisms and mutations in candidate genes

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

A clinical study of Noonan syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1939

21 January 2018

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17143282

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q52000174&oldid=2211394573"