(Q39814377)

14 September 2017

0 references

Analysis of aneuploidy frequencies in sperm from patients with hereditary nonpolyposis colon cancer and an hMSH2 mutation (English)

1 reference

14 September 2017

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1 reference

Martin RH

1

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14 September 2017

Green J

2

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14 September 2017

Ko E

3

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14 September 2017

Barclay L

4

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14 September 2017

Rademaker AW

5

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14 September 2017

language of work or name

English

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publication date

1 March 2000

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American Journal of Human Genetics

14 September 2017

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14 September 2017

66

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14 September 2017

3

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14 September 2017

1149-1152

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Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

Mutation of a mutL homolog in hereditary colon cancer

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

Double or nothing: a Drosophila mutation affecting meiotic chromosome segregation in both females and males.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

Sex and the single cell: meiosis in yeast

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288150

A human compound heterozygote for two MLH1 missense mutations

22 September 2017

1 reference

12 December 2020

Single sperm typing demonstrates that reduced recombination is associated with the production of aneuploid 24,XY human sperm

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12 December 2020

Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions

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12 December 2020

Prevalence of chromosome abnormalities during human gestation and implications for studies of environmental mutagens

1 reference

12 December 2020

MSH5, a novel MutS homolog, facilitates meiotic reciprocal recombination between homologs in Saccharomyces cerevisiae but not mismatch repair

1 reference

12 December 2020

Donor age and the frequency of disomy for chromosomes 1, 13, 21 and structural abnormalities in human spermatozoa using multicolour fluorescence in-situ hybridization

1 reference

12 December 2020

Identifiers

DOI

10.1086/302805

1 reference

14 September 2017

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14 September 2017

PubMed publication ID

10712226

1 reference