Characterization of mutations in patients with multiple endocrine neoplasia type 1. (Q24538768)

6 July 2017

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

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multiple endocrine neoplasia

6 July 2017

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multiple endocrine neoplasia type 1

inferred from title

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14

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6 July 2017

8

Besser GM

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6 July 2017

Bassett JH

1

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6 July 2017

Forbes SA

2

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6 July 2017

Pannett AA

3

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6 July 2017

Lloyd SE

4

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6 July 2017

Christie PT

5

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6 July 2017

Wooding C

6

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6 July 2017

Harding B

7

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6 July 2017

Edwards CR

9

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6 July 2017

Monson JP

10

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6 July 2017

Sampson J

11

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6 July 2017

Wass JA

12

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6 July 2017

Wheeler MH

13

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6 July 2017

language of work or name

English

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publication date

1 February 1998

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American Journal of Human Genetics

6 July 2017

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6 July 2017

62

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6 July 2017

232-244

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6 July 2017

2

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Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5)

6 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

A common molecular basis for three inherited kidney stone diseases

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Genetic aspects of adenomatosis of endocrine glands

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Studies on inherited cancers: outcomes and challenges of 25 years

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

The spectrum of RB1 germ-line mutations in hereditary retinoblastoma

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

The rapid detection of unknown mutations in nucleic acids.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

The molecular genetics of the multiple endocrine neoplasia syndromes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Multiple endocrine neoplasia type 1 (MEN1).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

The molecular genetics of cellular oncogenes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Predictive testing for multiple endocrine neoplasia type 1 using DNA polymorphisms

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

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

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1376903

A kindred with a variant of multiple endocrine neoplasia type 1 demonstrating frequent expression of pituitary tumors but not linked to the multiple endocrine neoplasia type 1 locus at chromosome region 11q13

29 November 2018

1 reference

12 December 2020

Mechanisms of insertional mutagenesis in human genes causing genetic disease

1 reference

12 December 2020

Spectrum of spontaneous frameshift mutations. Sequences of bacteriophage T4 rII gene frameshifts

1 reference

12 December 2020

Molecular tools for presymptomatic testing in multiple endocrine neoplasia type 1

1 reference

12 December 2020

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

1 reference

12 December 2020

Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

1 reference

12 December 2020

Definition of the MinimalMEN1Candidate Area Based on a 5-Mb Integrated Map of Proximal 11q13

1 reference

7 January 2021

Construction of a 1.2-Mb sequence-ready contig of chromosome 11q13 encompassing the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.

1 reference

7 January 2021

Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)

1 reference

7 January 2021

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

1 reference

7 January 2021

Identifiers

DOI

10.1086/301729

1 reference

OpenCitations bibliographic resource ID

6 July 2017

3991062

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

6 July 2017

1 reference