Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors (Q24558744)

23 June 2017

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

1 reference

23 June 2017

9

Nordenskjöld M

1 reference

23 June 2017

Byström C

1

1 reference

23 June 2017

Larsson C

2

1 reference

23 June 2017

Blomberg C

3

1 reference

23 June 2017

Sandelin K

4

1 reference

23 June 2017

Falkmer U

5

1 reference

23 June 2017

Skogseid B

6

1 reference

23 June 2017

Oberg K

7

1 reference

23 June 2017

Werner S

8

1 reference

23 June 2017

language of work or name

English

0 references

publication date

1 March 1990

1 reference

Proceedings of the National Academy of Sciences of the United States of America

23 June 2017

1 reference

23 June 2017

87

1 reference

23 June 2017

1968-1972

1 reference

23 June 2017

5

1 reference

Mutation and cancer: statistical study of retinoblastoma

23 June 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Clonality of parathyroid tumors in familial 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=53606

A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Identification of the cystic fibrosis gene: genetic analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Identification of the cystic fibrosis gene: chromosome walking and jumping

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

26 May 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Familial multiple endocrine neoplasia type I: a new look at pathophysiology

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Genetic linkage of Beckwith-Wiedemann syndrome to 11p15.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Genetic origin of mutations predisposing to 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=53606

Suppression of the neoplastic phenotype by replacement of the RB gene in human cancer cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Structural evidence for the authenticity of the human retinoblastoma 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=53606

Human retinoblastoma susceptibility gene: cloning, identification, and sequence.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Deletion mapping in human renal cell carcinoma

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=53606

Monoclonality and abnormal parathyroid hormone genes in parathyroid adenomas

28 November 2018

1 reference

12 December 2020

Multiple endocrine neoplasia type 1

1 reference

12 December 2020

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

12 December 2020

Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

1 reference

12 December 2020

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

12 December 2020

Prediction of the Risk of Hereditary Retinoblastoma, Using DNA Polymorphisms within the Retinoblastoma Gene

1 reference

12 December 2020

Gene losses in human tumours

1 reference

12 December 2020

Report of the committee on human gene mapping by recombinant DNA techniques

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.87.5.1968

1 reference

release_ryloc75qvbhmfdup5n72jgq7u4

23 June 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ryloc75qvbhmfdup5n72jgq7u4

24 November 2022

mapped directly with Wikidata item

0 references

1 reference