(Q40038376)

16 September 2017

title

SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients (English)

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16 September 2017

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Heidi Greulich

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16 September 2017

Marcelo Reis

3

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Matthew Meyerson

19

object named as

Matthew Meyerson

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16 September 2017

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Ralph H Hruban

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16 September 2017

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Michael A Caligiuri

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16 September 2017

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Charles J Yeo

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16 September 2017

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Jordan M Winter

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16 September 2017

Kenneth D Swanson

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16 September 2017

Mohamed Bentires-Alj

4

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16 September 2017

Rupinder Grewal

6

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16 September 2017

Yosuf Yassin

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16 September 2017

Oleg Iartchouk

10

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16 September 2017

Kate Montgomery

11

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16 September 2017

Susan P Whitman

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Mignon L Loh

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16 September 2017

D Gary Gilliland

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16 September 2017

A Thomas Look

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16 September 2017

Raju Kucherlapati

17

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16 September 2017

Scott E Kern

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16 September 2017

Benjamin G Neel

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16 September 2017

language of work or name

English

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publication date

1 March 2008

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Genes, Chromosomes and Cancer

16 September 2017

published in

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16 September 2017

volume

47

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16 September 2017

issue

3

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16 September 2017

page(s)

253-259

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Regulation of Sos activity by intramolecular interactions

16 September 2017

cites work

1 reference

Consed: a graphical tool for sequence finishing

21 January 2018

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Germline mutations in HRAS proto-oncogene cause Costello syndrome

21 January 2018

1 reference

7 January 2021

Stops along the RAS pathway in human genetic disease

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7 January 2021

NF1 tumor suppressor gene function: narrowing the GAP

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7 January 2021

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

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7 January 2021

Sprouty 2, an inhibitor of mitogen-activated protein kinase signaling, is down-regulated in hepatocellular carcinoma.

1 reference

7 January 2021

Mutation analysis of the BRAF, ARAF and RAF-1 genes in human colorectal adenocarcinomas

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7 January 2021

Proliferation of human malignant astrocytomas is dependent on Ras activation

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7 January 2021

Loss of neurofibromatosis 1 (NF1) gene expression in NF1-associated pilocytic astrocytomas.

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7 January 2021

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

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7 January 2021

Essential role for Ras signaling in glioblastoma maintenance

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7 January 2021

Detection of high incidence of H-RAS oncogene point mutations in acute myelogenous leukemia

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7 January 2021

BRAF and K-ras gene mutations in human pancreatic cancers.

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7 January 2021

Germ line gain of function with SOS1 mutation in hereditary gingival fibromatosis.

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7 January 2021

RAS gene mutations in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders, and myelodysplastic syndromes

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7 January 2021

Distinct requirements for the Sprouty domain for functional activity of Spred proteins

1 reference

7 January 2021

Mutation analysis of Son of Sevenless in juvenile myelomonocytic leukemia

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7 January 2021

The ras/mitogen-activated protein kinase pathway inhibitor and likely tumor suppressor proteins, sprouty 1 and sprouty 2 are deregulated in breast cancer.

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7 January 2021

Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis

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7 January 2021

Noonan syndrome associated with neuroblastoma: a case report.

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7 January 2021

Leukemia in Cardio-facio-cutaneous (CFC) syndrome: a patient with a germline mutation in BRAF proto-oncogene.

1 reference

7 January 2021

Epigenetic inactivation of the human sprouty2 (hSPRY2) homologue in prostate cancer.

1 reference

7 January 2021

Association between high levels of expression of the TRK gene and favorable outcome in human neuroblastoma

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7 January 2021

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

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7 January 2021

Efficient suppression of FGF-2-induced ERK activation by the cooperative interaction among mammalian Sprouty isoforms

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7 January 2021

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

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7 January 2021

EGF receptor gene mutations are common in lung cancers from "never smokers" and are associated with sensitivity of tumors to gefitinib and erlotinib

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7 January 2021

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

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7 January 2021

Sequence survey of receptor tyrosine kinases reveals mutations in glioblastomas

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7 January 2021

Germline gain-of-function mutations in RAF1 cause Noonan syndrome

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7 January 2021

RasGRP4 is a novel Ras activator isolated from acute myeloid leukemia

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7 January 2021

Germline gain-of-function mutations in SOS1 cause Noonan syndrome

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7 January 2021

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

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7 January 2021

Germline KRAS mutations cause Noonan syndrome

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7 January 2021

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

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7 January 2021

New class of Son-of-sevenless (Sos) alleles highlights the complexities of Sos function

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7 January 2021

The consensus coding sequences of human breast and colorectal cancers

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7 January 2021

Studies of the HER-2/neu proto-oncogene in human breast and ovarian cancer

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7 January 2021

Structural analysis of autoinhibition in the Ras activator Son of sevenless

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7 January 2021

Congenital ulcerating hemangioma in a baby with KRAS mutation and cardio-facio-cutaneous syndrome

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Acute myelomonocytic leukemia in a boy with LEOPARD syndrome (PTPN11 gene mutation positive)

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7 January 2021

Sprouty4, a suppressor of tumor cell motility, is down regulated by DNA methylation in human prostate cancer

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7 January 2021

The Grb2 binding domain of mSos1 is not required for downstream signal transduction

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7 January 2021

Overexpression of the EGF receptor and p53 mutations are mutually exclusive in the evolution of primary and secondary glioblastomas

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7 January 2021

Structural alterations of the epidermal growth factor receptor gene in human gliomas

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7 January 2021

Identifiers

DOI

10.1002/GCC.20527

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16 September 2017

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