Premature centromere division in patients with multiple endocrine neoplasia type 1 (Q74626471)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Premature centromere division in patients with multiple endocrine neoplasia type 1 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

multiple endocrine neoplasia

12 November 2019

main subject

1 reference

multiple endocrine neoplasia type 1

inferred from title

1 reference

A Sakurai

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

M Katai

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Y Itakura

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Y Ikeo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

K Hashizume

5

1 reference

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12 November 2019

publication date

1 March 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

Cancer Genetics and Cytogenetics

12 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

volume

109

1 reference

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12 November 2019

issue

2

1 reference

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12 November 2019

page(s)

138-140

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Non-Random Centromere Division: a Mechanism of Non-Disjunction Causing Aneuploidy?

12 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Sequence of centromere separation: Occurrence, possible significance, and control

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Parental centromere separation sequence and aneuploidy in the offspring

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

"Premature anaphase" in a couple with recurrent miscarriages

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Premature centromere division: a possible manifestation of chromosome instability

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Chromosomal breakage in multiple endocrine adenomatosis (types I and II)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type 1

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Chromosomal instability in multiple endocrine neoplasia type 1. Cytogenetic evaluation with DEB test

1 reference

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7 January 2021

Genetic screening in hereditary multiple endocrine neoplasia type 1: absence of a founder effect among Japanese families.

1 reference

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7 January 2021

Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1

1 reference

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7 January 2021

Cytogenetics of multiple endocrine neoplasia syndromes. III. Analysis of an insulinoma from a subject with MEN 1 by chromosome painting

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Chromosome analysis of nine endocrine neoplasms of the pancreas

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Genetic abnormalities in sporadic parathyroid adenomas: loss of heterozygosity for chromosome 3q markers flanking the calcium receptor locus

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

Somatic mutation of the MEN1 gene in parathyroid tumours.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-4608%2898%2900156-3

7 January 2021

10.1016/S0165-4608(98)00156-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10087948%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference