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RET ligand-induced internalization and its consequences for downstream signaling

Oncogene, 2006-05, Vol.25 (22), p.3206-3211

2006

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Immunohistochemical Evidence of Loss of PTEN Expression in Primary Ductal Adenocarcinomas of the Breast

The American journal of pathology, 1999-10, Vol.155 (4), p.1253-1260

1999

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Multiple endocrine neoplasia type 2 and RET : from neoplasia to neurogenesis

Journal of medical genetics, 2000-11, Vol.37 (11), p.817-827

2000

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Genetic basis of endocrine disease : multiple endocrine neoplasia type 2

The journal of clinical endocrinology and metabolism, 1995-07, Vol.80 (7), p.1989-1995

1995

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Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma

British journal of cancer, 1999-02, Vol.79 (5-6), p.718-723

1999

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

Journal of internal medicine, 1995-10, Vol.238 (4), p.343-346

1995

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Analysis of PTEN and the 10q23 region in primary prostate carcinomas

Oncogene, 1998-04, Vol.16 (13), p.1743-1748

1998

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Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system

Journal of neurology, neurosurgery and psychiatry, 2001-05, Vol.70 (5), p.644-648

2001

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Mechanisms of p53 Loss in Human Sarcomas

Proceedings of the National Academy of Sciences - PNAS, 1990-08, Vol.87 (15), p.5863-5867

1990

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Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation

The journal of clinical endocrinology and metabolism, 1997-11, Vol.82 (11), p.3902-3904

1997

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Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma

Cancer research (Chicago, Ill.), 1996-05, Vol.56 (9), p.2167-2170

1996

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Reduction in membranous immunohistochemical staining for the intracellular domain of epithelial cell adhesion molecule correlates with poor patient outcome in primary colorectal adenocarcinoma

Current oncology (Toronto), 2016-06, Vol.23 (3), p.e171-178

2016

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

Nature (London), 1993-06, Vol.363 (6428), p.458-460

1993

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Low frequency of germline mutations in the RET protooncogene in patients with apparently sporadic medullary thyroid carcinoma

Clinical endocrinology (Oxford), 1995-07, Vol.43 (1), p.123-127

1995

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

Nature (London), 1994-01, Vol.367 (6461), p.378-380

1994

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

Nature genetics, 1994-01, Vol.6 (1), p.70-74

1994

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Investigation of germline GFRα-1 mutations in Hirschsprung disease

Journal of medical genetics, 1999-03, Vol.36 (3), p.217-220

1999

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

Human molecular genetics, 1995-08, Vol.4 (8), p.1381-1386

1995

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Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

Human molecular genetics, 1994-02, Vol.3 (2), p.237-241

1994

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Conservation of RET proto-oncogene splicing variants and implications for RET isoform function

Cytogenetic and genome research, 2001-01, Vol.95 (3-4), p.169-176

2001

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Germline and somatic mutations in an oncogene : RET mutations in inherited medullary thyroid carcinoma

Cancer research (Chicago, Ill.), 1996-03, Vol.56 (6), p.1241-1243

1996

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Expression of RET 3' splicing variants during human kidney development

Oncogene, 1998-02, Vol.16 (8), p.991-996

1998

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Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II

JAMA : the journal of the American Medical Association, 1995-10, Vol.274 (14), p.1149

1995

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Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung disease

Human genetics, 2001-05, Vol.108 (5), p.409-415

2001

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Localisation of the gene for multiple endocrine neoplasia type 2A to a 480 kb region in chromosome band 10q11.2

Human molecular genetics, 1993-03, Vol.2 (3), p.247-252

1993

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RET ligand-induced internalization and its consequences for downstream signaling

Immunohistochemical Evidence of Loss of PTEN Expression in Primary Ductal Adenocarcinomas of the Breast

Multiple endocrine neoplasia type 2 and RET : from neoplasia to neurogenesis

Genetic basis of endocrine disease : multiple endocrine neoplasia type 2

Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma

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

Analysis of PTEN and the 10q23 region in primary prostate carcinomas

Reconsideration of biallelic inactivation of the VHL tumour suppressor gene in hemangioblastomas of the central nervous system

Mechanisms of p53 Loss in Human Sarcomas

Germline dinucleotide mutation in codon 883 of the RET proto-oncogene in multiple endocrine neoplasia type 2B without codon 918 mutation

Heterogeneous mutation of the RET proto-oncogene in subpopulations of medullary thyroid carcinoma

Reduction in membranous immunohistochemical staining for the intracellular domain of epithelial cell adhesion molecule correlates with poor patient outcome in primary colorectal adenocarcinoma

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

Low frequency of germline mutations in the RET protooncogene in patients with apparently sporadic medullary thyroid carcinoma

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

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

Investigation of germline GFRα-1 mutations in Hirschsprung disease

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

Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

Conservation of RET proto-oncogene splicing variants and implications for RET isoform function

Germline and somatic mutations in an oncogene : RET mutations in inherited medullary thyroid carcinoma

Expression of RET 3' splicing variants during human kidney development

Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type II

Cloning and characterization of the human GFRA2 locus and investigation of the gene in Hirschsprung disease

Localisation of the gene for multiple endocrine neoplasia type 2A to a 480 kb region in chromosome band 10q11.2

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