(Q48100816)

8 February 2018

title

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

1 reference

8 February 2018

multiple endocrine neoplasia

main subject

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multiple endocrine neoplasia type 1

inferred from title

1 reference

5

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8 February 2018

author name string

Larsson C

1

1 reference

8 February 2018

Skogseid B

2

1 reference

8 February 2018

Oberg K

3

1 reference

8 February 2018

Nakamura Y

4

1 reference

8 February 2018

language of work or name

English

0 references

publication date

1 March 1988

1 reference

8 February 2018

published in

Nature

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8 February 2018

volume

332

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8 February 2018

page(s)

85-87

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8 February 2018

issue

6159

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8 February 2018

https://scigraph.springernature.com/pub.10.1038/332085a0

exact match

0 references

cites work

Mutation and cancer: statistical study of retinoblastoma

1 reference

7 January 2021

Genetic origin of mutations predisposing to retinoblastoma

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Localization of the gene for familial adenomatous polyposis on chromosome 5.

1 reference

7 January 2021

Chromosome 5 allele loss in human colorectal carcinomas.

1 reference

7 January 2021

A standardized meal stimulation test of the endocrine pancreas for early detection of pancreatic endocrine tumors in multiple endocrine neoplasia type 1 syndrome: five years experience

1 reference

7 January 2021

Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping

1 reference

7 January 2021

High-resolution chromosome sorting and DNA spot-blot analysis assign McArdle's syndrome to chromosome 11.

1 reference

7 January 2021

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

1 reference

7 January 2021

Identifiers

DOI

10.1038/332085A0

1 reference

8 February 2018

Dimensions Publication ID

1042110245

0 references

Fatcat ID

release_h53xmgy5erfp7e5h3y63llimw4

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/h53xmgy5erfp7e5h3y63llimw4

24 November 2022

mapped directly with Wikidata item

PubMed ID

2894610

1 reference

8 February 2018