(Q53583249)

15 May 2018

title

Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome. (English)

1 reference

15 May 2018

embryonal rhabdomyosarcoma

main subject

1 reference

7

Martin Zenker

1 reference

15 May 2018

author name string

Christian P Kratz

1

1 reference

15 May 2018

Doris Steinemann

2

1 reference

15 May 2018

Charlotte M Niemeyer

3

1 reference

15 May 2018

Brigitte Schlegelberger

4

1 reference

15 May 2018

Ewa Koscielniak

5

1 reference

15 May 2018

Udo Kontny

6

1 reference

15 May 2018

publication date

12 December 2006

1 reference

15 May 2018

published in

Human Molecular Genetics

1 reference

15 May 2018

volume

16

1 reference

15 May 2018

issue

4

1 reference

15 May 2018

page(s)

374-379

1 reference

15 May 2018

The guanine nucleotide-binding switch in three dimensions

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Germline mutations in components of the Ras signaling pathway in Noonan syndrome and related disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Germline mutations in HRAS proto-oncogene cause Costello syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Germline KRAS mutations cause Noonan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Stops along the RAS pathway in human genetic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Noonan syndrome and related disorders: genetics and pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Tumor predisposition in Costello syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

The cardiofaciocutaneous syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Allelotype of pediatric rhabdomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Rhabdomyosarcoma--working out the pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Is the locus for Costello syndrome on 11p?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

HRAS mutations in Costello syndrome: detection of constitutional activating mutations in codon 12 and 13 and loss of wild-type allele in malignancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Costello syndrome: two cases with embryonal rhabdomyosarcoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

JAKing up hematopoietic proliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Normalization of cDNA microarray data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL458

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL458

1 reference

15 May 2018

1 reference

15 May 2018