Bloom syndrome: a single complementation group defines patients of diverse ethnic origin. (Q35245638)

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19 September 2019

title

Bloom syndrome: a single complementation group defines patients of diverse ethnic origin (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3163468%20AND%20SRC:MED&resulttype=core&format=json

19 September 2019

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Weksberg R

1

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19 September 2019

Smith C

series ordinal

2

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19 September 2019

Anson-Cartwright L

series ordinal

3

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19 September 2019

Maloney K

series ordinal

4

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19 September 2019

language of work or name

English

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publication date

1 June 1988

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American Journal of Human Genetics

19 September 2019

published in

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19 September 2019

volume

42

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19 September 2019

issue

6

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19 September 2019

page(s)

816-824

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Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts.

19 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Elevated spontaneous mutation rate in Bloom syndrome fibroblasts

27 July 2018

1 reference

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Susceptibility of Fanconi's anemia lymphoblasts to DNA-cross-linking and alkylating agents

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Interallelic complementation in an inborn error of metabolism: genetic heterogeneity in argininosuccinate lyase deficiency

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Identification of two complementation groups in Fanconi anemia

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Complementation analysis of ataxia-telangiectasia.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Altered DNA ligase I activity in Bloom's syndrome cells

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

DNA ligase I deficiency in Bloom's syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Bloom syndrome in a Mexican mestizo girl

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Structural alterations of DNA ligase I in Bloom syndrome

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Bloom's syndrome. IV. Sister-chromatid exchanges in lymphocytes

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Ultraviolet light sensitivity and delayed DNA-chain maturation in Bloom's syndrome fibroblasts

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Normalisation of sister chromatid exchange frequencies in Bloom's syndrome by euploid cell hybridisation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Bloom's syndrome: evidence for an increased mutation frequency in vivo.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Cytogenetic study in a mentally retarded child with Bloom syndrome and acute lymphoblastic leukemia.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

Different Properties in Lymphoblastoid Cell Lines from Patients with Bloom Syndrome

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1715193

CHROMOSOMAL BREAKAGE IN A RARE AND PROBABLY GENETICALLY DETERMINED SYNDROME OF MAN

26 September 2018

1 reference

12 December 2020

Bloom's syndrome XI. Progress report for 1983

1 reference

12 December 2020

Bloom's syndrome. Possible pitfalls in clinical diagnosis

1 reference

12 December 2020

Analysis of Sister Chromatid Exchanges in Bloom Syndrome by Use of Endomitotic and Three-Way Differentiation Procedures

1 reference

12 December 2020

Suppression of the frequencies of sister chromatid exchanges in Bloom's syndrome fibroblasts by co-cultivation with Chinese hamster cells

1 reference

12 December 2020

Studies on the ultraviolet light sensitivity of Bloom's syndrome fibroblasts

1 reference

12 December 2020

Bloom's syndrome in a Japanese girl

1 reference

12 December 2020

A ninth complementation group in xeroderma pigmentosum, XP I

1 reference

12 December 2020

High rate of sister chromatid exchanges of Bloom's syndrome chromosomes is corrected in rodent human somatic cell hybrids

1 reference

12 December 2020

Bloom's syndrome in a Japanese boy with lymphoma

1 reference

12 December 2020

DNA repair in Bloom's syndrome fibroblasts after UV irradiation or treatment with mitomycin C

1 reference

12 December 2020

Formation of DNA single-strand breaks by near-ultraviolet and gamma-rays in normal and Bloom's syndrome skin fibroblasts

1 reference

12 December 2020

Three complementation groups in Cockayne syndrome

1 reference

12 December 2020

Wilms tumor in three patients with Bloom syndrome

1 reference

12 December 2020

Complementation analysis in Gaucher disease using single cell microassay techniques. Evidence for a single "Gaucher gene"

1 reference

12 December 2020

Identifiers

1 reference

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19 September 2019

PubMed publication ID

3163468

1 reference