Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors (original) (raw)

Alterations of the MEN1 Gene in Sporadic Parathyroid Tumors 1

K. Sandelin

The Journal of Clinical Endocrinology & Metabolism, 1998

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A Family with Isolated Hyperparathyroidism Segregating a Missense MEN1 Mutation and Showing Loss of the Wild-Type Alleles in the Parathyroid Tumors

Bin Teh

The American Journal of Human Genetics, 1998

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Somatic mutations of the multiple endocrine neoplasia type 1 (MEN1) gene in patients with sporadic, nonfamilial primary hyperparathyroidism

Takahiro Okamoto

Surgery, 2000

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Allelic Loss in Parathyroid Tumors from Individuals Homozygous for Multiple Endocrine Neoplasia Type 1 1

Sergio Ortolani

The Journal of Clinical Endocrinology & Metabolism, 1997

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Carcinoma of Two Parathyroid Glands Caused by a Novel MEN1 Gene Mutation – a Rare Feature of the MEN 1 Syndrome

Aurelija Krasauskienė

Medicina, 2011

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Novel association of MEN1 gene mutations with parathyroid carcinoma

Massimiliano Chetta

Oncology letters, 2017

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Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states

Stephen Marx

Human Molecular Genetics, 1997

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Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism 1

Magnus Nordenskjöld

The Journal of Clinical Endocrinology & Metabolism, 1998

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Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type …

Lance Liotta

Human Molecular …, 1997

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Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated Hyperparathyroidism

JT Stewart

2010

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Homozygous inactivation of the MEN1 gene as a specific somatic event in a case of secondary hyperparathyroidism

Svetlana Lagercrantz

European Journal of Endocrinology, 2001

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Identification of somatic mutations of the MEN1 gene in sporadic endocrine tumours

Jane Palmer

British journal of …, 2000

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Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1)

Jennifer N . IGWELA

American journal of human genetics, 1992

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Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1

Michel Pugeat

Human Molecular Genetics, 1997

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Novel 14 Base-Pair Deletion of the MEN1 Gene in a Patient with Recurrent Primary Hyperparathyroidism

Shinya Uchino

Japanese Journal of Clinical Oncology, 2006

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Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysis

Lance Liotta

Cancer research, 1997

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Absence of Germ-Line Mutations of the Multiple Endocrine Neoplasia Type 1 ( MEN1 ) Gene in Familial Pituitary Adenoma in Contrast to MEN1 in Japanese 1

Hiroshi Nishioka

The Journal of Clinical Endocrinology & Metabolism, 1998

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Allelic Loss from Chromosome 11 in Parathyroid Tumors

Stephen Marx

1992

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Coincidence of Multiple Endocrine Neoplasia Types 1 and 2: Mutations in theRETProtooncogene andMEN1Tumor Suppressor Gene in a Family Presenting with Recurrent Primary Hyperparathyroidism

Friedhelm Raue

The Journal of Clinical Endocrinology and Metabolism, 2005

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A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1

Filomena Cetani

European Journal of Endocrinology, 1999

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MEN1 intragenic deletions may represent the most prevalent somatic event in sporadic primary hyperparathyroidism

Paula Soares

European Journal of Endocrinology, 2012

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Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism

Frances A Flinter

Clinical Endocrinology, 2003

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MEN1 gene mutations in Hungarian patients with multiple endocrine neoplasia type 1

Miklós Tóth, Attila Patócs

Clinical Endocrinology, 2007

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Clonal Analysis by Chromosome 11 Microsatellite-PCR of Microdissected Parathyroid Tumors from MEN 1 Patients

Annamaria Morelli

Biochemical and Biophysical Research Communications, 1996

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Localisation of a gene causing endocrine neoplasia to a 4 cM region on chromosome 1p35-p36

John Monson

Journal of Medical Genetics, 1997

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