(Q41920923)

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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B.

scientific article published on 10 October 2004

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Europe PubMed Central

PubMed publication ID

14 October 2017

Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B. (English)

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Europe PubMed Central

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14 October 2017

David FitzPatrick

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14 October 2017

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14 October 2017

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Helen Firth

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14 October 2017

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Sandra Hanks

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14 October 2017

Kim Coleman

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14 October 2017

Sarah Reid

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14 October 2017

Alberto Plaja

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14 October 2017

Alexa Kidd

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14 October 2017

Károly Méhes

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14 October 2017

Richard Nash

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14 October 2017

Nathanial Robin

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14 October 2017

Nora Shannon

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14 October 2017

John Tolmie

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14 October 2017

John Swansbury

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14 October 2017

Alexandre Irrthum

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14 October 2017

Jenny Douglas

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14 October 2017

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publication date

10 October 2004

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14 October 2017

Nature Genetics

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14 October 2017

36

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14 October 2017

11

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14 October 2017

1159-1161

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14 October 2017

The spindle checkpoint, aneuploidy, and cancer

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https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Chromosome segregation and genomic stability

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https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic instabilities in human cancers

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https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Siblings with chromosome mosaicism, microcephaly, and growth retardation: the phenotypic expression of a human mitotic mutant?

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Child with mosaic variegated aneuploidy and embryonal rhabdomyosarcoma

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https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Variegated aneuploidy related to premature centromere division (PCD) is expressed in vivo and is a cancer-prone disease.

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Cancer-prone syndrome of mosaic variegated aneuploidy and total premature chromatid separation: report of five infants

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https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

High risk of malignancy in mosaic variegated aneuploidy syndrome

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https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Mad2-Independent inhibition of APCCdc20 by the mitotic checkpoint protein BubR1.

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Activating and silencing the mitotic checkpoint through CENP-E-dependent activation/inactivation of BubR1.

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Dual roles of human BubR1, a mitotic checkpoint kinase, in the monitoring of chromosomal instability

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Slippage of mitotic arrest and enhanced tumor development in mice with BubR1 haploinsufficiency

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

BubR1 insufficiency causes early onset of aging-associated phenotypes and infertility in mice

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of mitotic checkpoint genes in human cancers

1 reference

https://api.crossref.org/works/10.1038/NG1449

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

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Europe PubMed Central

PubMed publication ID

14 October 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 October 2017

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