(Q53914105)

English

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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Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

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

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

multiple endocrine neoplasia

1 reference

based on heuristic

inferred from title

multiple endocrine neoplasia type 1

1 reference

based on heuristic

inferred from title

author name string

Hai N

1

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

Aoki N

2

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

Shimatsu A

3

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

Mori T

4

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

Kosugi S

5

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

publication date

1 April 2000

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

Clinical Endocrinology

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

52

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

4

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

509-518

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

A suggested nomenclature for designating mutations.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Somatotrophinomas in multiple endocrine neoplasia type 1: a review of clinical phenotype and insulin-like growth factor-1 levels in a large multiple endocrine neoplasia type 1 kindred

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Identification of MEN1 gene mutations in sporadic carcinoid tumors of the lung

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

A 2.8-Mb clone contig of the multiple endocrine neoplasia type 1 (MEN1) region at 11q13.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

A minisatellite and a microsatellite polymorphism within 1.5 kb at the human muscle glycogen phosphorylase (PYGM) locus can be amplified by PCR and have combined informativeness of PIC 0.95

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

A long-sought needle in the haystack: the multiple endocrine neoplasia type 1 gene

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Genetic screening in hereditary multiple endocrine neoplasia type 1: absence of a founder effect among Japanese families.

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Multiple endocrine syndrome type I. Clinical, laboratory findings, and management in five families

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Multiple Endocrine Neoplasia Type 1: A 10-Year Prospective Screening Study in Four Kindreds*

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2265.2000.00966.X

21 January 2018

Identifiers

10.1046/J.1365-2265.2000.00966.X

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 May 2018

http://europepmc.org/abstract/MED/10762295

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