(Q42273863)

19 October 2017

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

1 reference

19 October 2017

Williamson C

1

1 reference

19 October 2017

Pannett AA

2

1 reference

19 October 2017

Pang JT

3

1 reference

19 October 2017

Wooding C

4

1 reference

19 October 2017

McCarthy M

5

1 reference

19 October 2017

Sheppard MN

6

1 reference

19 October 2017

Monson J

7

1 reference

19 October 2017

Clayton RN

8

1 reference

19 October 2017

Thakker RV

9

1 reference

19 October 2017

language of work or name

English

0 references

publication date

1 August 1997

1 reference

Journal of Medical Genetics

19 October 2017

1 reference

19 October 2017

34

1 reference

19 October 2017

8

1 reference

19 October 2017

617-619

1 reference

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

19 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

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

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

The retinoblastoma protein binds to a family of E2F transcription factors

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

The human paired domain gene PAX7 (Hup1) maps to chromosome 1p35-1p36.2

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

The molecular genetics of the multiple endocrine neoplasia syndromes

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Identification of human DAN gene, mapping to the putative neuroblastoma tumor suppressor locus

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

The gene for PAX7, a member of the paired-box-containing genes, is localized on human chromosome arm 1p36

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Frequent loss of chromosome arm 1p DNA in parathyroid adenomas

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

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

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Localization of the expressed human p58 protein kinase chromosomal gene to chromosome 1p36 and a highly related sequence to chromosome 15

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Mutually exclusive expression of a helix-loop-helix gene and N-myc in human neuroblastomas and in normal development

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Clustering of C2-H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomes

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Loss of heterozygosity studies at the retinoblastoma and breast cancer susceptibility (BRCA2) loci in pituitary, parathyroid, pancreatic and carcinoid tumours.

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

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

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Report and abstracts of the First International Workshop on Human Chromosome 1 Mapping 1994. Bethesda, Maryland, March 25-27, 1994.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

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

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051020

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

17 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9279750

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular genetic studies of sporadic pituitary tumors

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/9279750

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JMG.34.8.617

1 reference

19 October 2017

1 reference

19 October 2017

PubMed publication ID

9279750

1 reference