(Q55003069)

15 June 2018

title

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

1 reference

15 June 2018

multiple endocrine neoplasia

main subject

1 reference

multiple endocrine neoplasia type 1

inferred from title

1 reference

1 reference

A Sakurai

1

1 reference

15 June 2018

M Katai

2

1 reference

15 June 2018

Y Itakura

3

1 reference

15 June 2018

K Nakajima

4

1 reference

15 June 2018

K Baba

5

1 reference

15 June 2018

K Hashizume

6

1 reference

15 June 2018

publication date

1 September 1996

1 reference

15 June 2018

number of pages

10

1 reference

Japanese Journal of Cancer Research

inferred from page(s)

published in

1 reference

15 June 2018

volume

87

1 reference

15 June 2018

issue

9

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15 June 2018

page(s)

985-994

1 reference

15 June 2018

A comprehensive genetic map of the human genome based on 5,264 microsatellites

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Biology of polycystic kidney disease

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

The molecular genetics of the multiple endocrine neoplasia syndromes

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Isolation and characterization of a novel gene encoding nuclear protein at a locus (D11S636) tightly linked to multiple endocrine neoplasia type 1 (MEN1)

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Mapping the gene for hereditary hyperparathyroidism and prolactinoma (MEN1Burin) to chromosome 11q: evidence for a founder effect in patients from Newfoundland

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Multiple disease genes cause hypertrophic cardiomyopathy

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

The 1993-94 Généthon human genetic linkage map

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Mutation and cancer: statistical study of retinoblastoma

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Clonality of parathyroid tumors in familial multiple endocrine neoplasia type 1

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Should we test children for "adult" genetic diseases?

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Dinucleotide repeat polymorphism at the D11S534 locus

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Allele loss on chromosome 11 in a pituitary tumor from a patient with multiple endocrine neoplasia type 1.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Prospective screening in multiple endocrine neoplasia type 1.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

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

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921204

Multiple endocrine neoplasia type 1 (MEN1) in two Asian families

13 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1996.TB02130.X

Cause of death in multiple endocrine neoplasia type 1

21 January 2018

1 reference

12 December 2020

The natural history of multiple endocrine neoplasia type 1. Highly uncommon or highly unrecognized?

1 reference

12 December 2020

The influence of genetic counselling in the era of DNA testing on knowledge, reproductive intentions and psychological wellbeing

1 reference

12 December 2020

Genetic screening to identify the gene carrier in Italian and German kindreds affected by multiple endocrine neoplasia type 1 (MEN 1) syndrome

1 reference

12 December 2020

The importance of screening for the MEN 1 syndrome: diagnostic results and clinical management

1 reference

12 December 2020

Improved carrier testing for multiple endocrine neoplasia, type 1, using new microsatellite-type DNA markers

1 reference

12 December 2020

Mapping eight new polymorphisms in 11q13 in the vicinity of multiple endocrine neoplasia type 1: identification of a new distal recombinant

1 reference

12 December 2020

Loss of the same alleles of HRAS1 and D11S151 in two independent pancreatic cancers from a patient with multiple endocrine neoplasia type 1

1 reference

12 December 2020

Candidate genes for multiple endocrine neoplasia type 1

1 reference

12 December 2020

10.1111/J.1349-7006.1996.TB02130.X

Identifiers

DOI

1 reference

15 June 2018

PMCID

5921204

1 reference

15 June 2018

PubMed ID

8878463

1 reference

15 June 2018