The MEN1 gene and associated diseases: an update (Q28210134)

Germline MEN1 mutations in sixteen Japanese families with multiple endocrine neoplasia type 1 (MEN1).

Europe PubMed Central

title

The MEN1 gene and associated diseases: an update (English)

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author name string

T Tsukada

series ordinal

1

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K Yamaguchi

series ordinal

2

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T Kameya

series ordinal

3

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language of work or name

English

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publication date

2001

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published in

Endocrine Pathology

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volume

12

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issue

3

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page(s)

259-73

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cites work

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DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory

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Multiple facial angiofibromas and collagenomas in patients with multiple endocrine neoplasia type 1

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Proliferation-associated expression of the MEN1 gene as revealed by in situ hybridization: possible role of the menin as a negative regulator of cell proliferation under DNA damage

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Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms

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Haplotype analysis defines a minimal interval for the multiple endocrine neoplasia type 1 (MEN1) gene

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Pituitary macroadenoma in a 5-year-old: an early expression of multiple endocrine neoplasia type 1.

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Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland.

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Premature centromere division in patients with multiple endocrine neoplasia type 1

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11q13 allelotype analysis in 27 northern American MEN1 kindreds identifies two distinct founder chromosomes

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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

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Positional cloning of the gene for multiple endocrine neoplasia-type 1

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Molecular diagnosis of familial adenomatous polyposis.

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Multiple endocrine neoplasia type 1 (MEN1): clinical heterogeneity in a large family with a nonsense mutation in the MEN1 gene (Trp471Stop)

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Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families.

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An intronic splicing mutation of the MEN1 gene

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The variable penetrance and spectrum of manifestations of multiple endocrine neoplasia type 1

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Surgical versus medical management of multiple endocrine neoplasia (MEN) type I.

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Germline mutations in the MEN1 gene: creation of a new splice acceptor site and insertion of 7 intron nucleotides into the mRNA.

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Identification and characterization of JunD missense mutants that lack menin binding

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Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription

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Stable overexpression of MEN1 suppresses tumorigenicity of RAS.

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Determination of Gene Dosage by a Quantitative Adaptation of the Polymerase Chain Reaction (gd-PCR): Rapid Detection of Deletions and Duplications of Gene Sequences

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Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1.

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Menin mutations in MEN1 patients

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

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Loss of heterozygosity on chromosome 11q13 in two families with acromegaly/gigantism is independent of mutations of the multiple endocrine neoplasia type I gene.

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Heterogeneity at the 5'-end of MEN1 transcripts

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Comparative genomics of the eukaryotes

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Clinical features of multiple endocrine neoplasia type 1 (MEN1) phenocopy without germline MEN1 gene mutations: analysis of 20 Japanese sporadic cases with MEN1.

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Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma.

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Recent advances in multiple endocrine neoplasia syndromes

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Expression analysis of endogenous menin, the product of the multiple endocrine neoplasia type 1 gene, in cell lines and human tissues

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

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A large germline deletion of the MEN1 gene in a family with multiple endocrine neoplasia type 1.

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Menin represses JunD-activated transcription by a histone deacetylase-dependent mechanism

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Somatic mutations of the MEN1 tumor suppressor gene in sporadic gastrinomas and insulinomas

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Mutation of the multiple endocrine neoplasia type 1 gene in nonfamilial, malignant tumors of the endocrine pancreas

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Germline mutation of the multiple endocrine neoplasia type 1 (MEN1) gene in a family with primary hyperparathyroidism

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Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism

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A newly recognized germline mutation of MEN1 gene identified in a patient with parathyroid adenoma and carcinoma

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Constitutional von Hippel-Lindau (VHL) gene deletions detected in VHL families by fluorescence in situ hybridization

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Studies of the murine homolog of the multiple endocrine neoplasia type 1 (MEN1) gene, men1.

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Novel V184E MEN1 germline mutation in a Japanese kindred with familial hyperparathyroidism

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Menin, the product of the MEN1 gene, is a nuclear protein

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Germline mutations in the multiple endocrine neoplasia type 1 gene: evidence for frequent splicing defects

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12 December 2020

Prolactinomas in familial multiple endocrine neoplasia syndrome type I. Relationship to HLA and carcinoid tumors

1 reference

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Identification of five novel germline mutations of the MEN1 gene in Japanese multiple endocrine neoplasia type 1 (MEN1) families

1 reference

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Menin mutations in patients with multiple endocrine neoplasia type 1

1 reference

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MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1

1 reference

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Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1)

1 reference

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Variant multiple endocrine neoplasia I (MEN IBurin): further studies and non-linkage to HLA

1 reference

12 December 2020

Identification of MEN1 gene mutations in families with MEN 1 and related disorders

1 reference

12 December 2020

Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1

1 reference

12 December 2020

A 5178-9g--> A splice donor site mutation in intron 4 of the MEN1 gene causing multiple endocrine neoplasia type 1

1 reference

12 December 2020

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

1 reference

12 December 2020

Perivascular cells harboring multiple endocrine neoplasia type 1 alterations are neoplastic cells in angiofibromas.

1 reference

12 December 2020

Primary structure, gene expression and chromosomal mapping of rodent homologs of the MEN1 tumor suppressor gene

1 reference

12 December 2020

Characterization of mutations in patients with multiple endocrine neoplasia type 1.

1 reference

12 December 2020

Dimensions Publication ID

Identifiers

DOI

10.1385/EP:12:3:259

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1011569010

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Fatcat ID

release_lkepbzyp4rajraafurjer7c5qu

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lkepbzyp4rajraafurjer7c5qu

24 November 2022