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Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24. (Q41107570)

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scientific article published on June 1997

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English	Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24.	scientific article published on June 1997

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4 November 2019

Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24 (English)

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4 November 2019

Nijmegen breakage syndrome

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inferred from title

10

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4 November 2019

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Matsuura S

1

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4 November 2019

Weemaes C

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4 November 2019

Smeets D

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4 November 2019

Takami H

4

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4 November 2019

Kondo N

5

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4 November 2019

Sakamoto S

6

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4 November 2019

Yano N

7

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4 November 2019

Nakamura A

8

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4 November 2019

Tauchi H

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4 November 2019

Oshimura M

11

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4 November 2019

Komatsu K

12

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4 November 2019

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1 June 1997

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4 November 2019

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American Journal of Human Genetics

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4 November 2019

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4 November 2019

6

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4 November 2019

1487-1494

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4 November 2019

Nijmegen breakage syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Mutations associated with variant phenotypes in ataxia-telangiectasia

1 reference

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26 September 2017

cDNA cloning and gene mapping of a candidate human cell cycle checkpoint protein

1 reference

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26 September 2017

Positional cloning of the Werner's syndrome gene

1 reference

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26 September 2017

Severe microcephaly with normal intellectual development: the Nijmegen breakage syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Relationship of the ataxia-telangiectasia protein ATM to phosphoinositide 3-kinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Functional complementation in mouse-human radiation hybrids assigns the putative murine scid gene to the pericentric region of human chromosome 8.

1 reference

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26 September 2017

Assignment of xeroderma pigmentosum group C (XPC) gene to chromosome 3p25

1 reference

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26 September 2017

Defective DNA-dependent protein kinase activity is linked to V(D)J recombination and DNA repair defects associated with the murine scid mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

ATM-related genes: What do they tell us about functions of the human gene?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

PIK-related kinases: DNA repair, recombination, and cell cycle checkpoints

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Expression cloning of multiple human cDNAs that complement the phenotypic defects of ataxia-telangiectasia group D fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

A new chromosomal instability disorder: the Nijmegen breakage syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Genetic heterogeneity in ataxia-telangiectasia studied by cell fusion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Monoclonal antibodies against human factor VIII molecular neutralize antihemophilic factor and ristocetin cofactor activities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Chromosome sublocalization of a cDNA for human DNA polymerase-beta to 8p11----p12.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

Correction of radiation sensitivity in ataxia telangiectasia cells by a truncated I kappa B-alpha

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

26 September 2017

The gene for Nijmegen breakage syndrome (V2) is not located on chromosome 11

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

14 June 2018

The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

14 June 2018

Irradiation microcell-mediated chromosome transfer (XMMCT): the generation of specific chromosomal arm deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

14 June 2018

Restoration of radiation resistance in ataxia telangiectasia cells by the introduction of normal human chromosome 11.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

14 June 2018

Studies on phenotypic complementation of ataxia-telangiectasia cells by chromosome transfer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

19 August 2018

Physical mapping of human chromosome 17 using fragment-containing microcell hybrids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1716114

19 August 2018

A chromosomal breakage syndrome with profound immunodeficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/9199571

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of correlation between radiosensitivity and inhibition of DNA synthesis in hybrids (A-T x HeLa)

1 reference

https://pubmed.ncbi.nlm.nih.gov/9199571

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional complementation studies with X-ray-sensitive mutants of Chinese hamster cells closely resembling ataxia-telangiectasia cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/9199571

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional Complementation Studies with X-ray-sensitive Mutants of Chinese Hamster Cells Closely Resembling Ataxia-telangiectasia Cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/9199571

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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4 November 2019

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4 November 2019

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4 November 2019

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