(Q40735434)

23 September 2017

Genetic analysis of RET, GFR alpha 1 and GDNF genes in Spanish families with multiple endocrine neoplasia type 2A. (English)

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multiple endocrine neoplasia

23 September 2017

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Laura Gil

1

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23 September 2017

Marta Azañedo

2

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23 September 2017

Marina Pollán

3

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23 September 2017

Eva Cristobal

4

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23 September 2017

Begoña Arribas

5

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23 September 2017

Luis García-Albert

6

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23 September 2017

Alfredo García-Sáiz

7

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23 September 2017

María Luisa Maestro

8

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23 September 2017

Antonio Torres

9

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23 September 2017

Javier Menárguez

10

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23 September 2017

José M Rojas

11

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23 September 2017

language of work or name

English

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publication date

1 May 2002

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International Journal of Cancer

23 September 2017

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23 September 2017

99

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23 September 2017

2

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23 September 2017

299-304

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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.

23 September 2017

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Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.

21 January 2018

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GDNF signalling through the Ret receptor tyrosine kinase

21 January 2018

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Characterization of a multicomponent receptor for GDNF.

21 January 2018

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GDNF-induced activation of the ret protein tyrosine kinase is mediated by GDNFR-alpha, a novel receptor for GDNF

21 January 2018

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Neurturin, a relative of glial-cell-line-derived neurotrophic factor

21 January 2018

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Persephin, a novel neurotrophic factor related to GDNF and neurturin

21 January 2018

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Artemin, a novel member of the GDNF ligand family, supports peripheral and central neurons and signals through the GFRalpha3-RET receptor complex

21 January 2018

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TrnR2, a novel receptor that mediates neurturin and GDNF signaling through Ret.

21 January 2018

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Neurturin responsiveness requires a GPI-linked receptor and the Ret receptor tyrosine kinase.

21 January 2018

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A GPI-linked protein that interacts with Ret to form a candidate neurturin receptor

21 January 2018

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GFR alpha-4 and the tyrosine kinase Ret form a functional receptor complex for persephin

21 January 2018

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The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

21 January 2018

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Analysis of RET protooncogene point mutations distinguishes heritable from nonheritable medullary thyroid carcinomas

21 January 2018

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Mutations of the RET proto-oncogene in Hirschsprung's disease

21 January 2018

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Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease

21 January 2018

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Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease

21 January 2018

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Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

21 January 2018

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Glial cell line-derived neurotrophic factor (GDNF) and its receptor (GFR-alpha 1) are strongly expressed in human gliomas

21 January 2018

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Human GFRA1: cloning, mapping, genomic structure, and evaluation as a candidate gene for Hirschsprung disease susceptibility

21 January 2018

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Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease

21 January 2018

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Analysis of the human GDNF gene reveals an inducible promoter, three exons, a triplet repeat within the 3'-UTR and alternative splice products

21 January 2018

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Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

21 January 2018

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Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

21 January 2018

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Mutational analysis of the GDNF/RET-GDNFR alpha signaling complex in a kindred with vesicoureteral reflux

21 January 2018

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Glial cell line-derived neurotrophic factor differentially stimulates ret mutants associated with the multiple endocrine neoplasia type 2 syndromes and Hirschsprung's disease.

21 January 2018

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Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease

21 January 2018

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Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression

21 January 2018

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Genetic Linkage of Lung Cancer-Associated MspI Polymorphisms with Amino Acid Replacement in the Heme Binding Region of the Human Cytochrome P450IA1 Gene1

21 January 2018

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A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

21 January 2018

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Deletion of genes on chromosome 1 in endocrine neoplasia

21 January 2018

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Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease

21 January 2018

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Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC

21 January 2018

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Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

21 January 2018

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Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTC

21 January 2018

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Identification of a polymorphism in exon 11 of the RET protooncogene

21 January 2018

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Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutation

21 January 2018

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Mutation analysis of glial cell line-derived neurotrophic factor, a ligand for an RET/coreceptor complex, in multiple endocrine neoplasia type 2 and sporadic neuroendocrine tumors

21 January 2018

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Two alleles of the human paraoxonase gene produce different amounts of mRNA. An explanation for differences in serum concentrations of paraoxonase associated with the (Leu-Met54) polymorphism

21 January 2018

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21 January 2018

Identifiers

DOI

10.1002/IJC.10298

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23 September 2017

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