(Q35201291)

7 August 2017

title

Enhanced G2 chromatid radiosensitivity in dyskeratosis congenita fibroblasts (English)

1 reference

7 August 2017

main subject

dyskeratosis congenita

1 reference

DeBauche DM

1

1 reference

7 August 2017

Pai GS

series ordinal

2

1 reference

7 August 2017

Stanley WS

series ordinal

3

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 February 1990

1 reference

American Journal of Human Genetics

7 August 2017

published in

1 reference

7 August 2017

volume

46

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7 August 2017

issue

2

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7 August 2017

page(s)

350-357

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Chromatid damage after G2 phase x-irradiation of cells from cancer-prone individuals implicates deficiency in DNA repair

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Defective Repair Replication of DNA in Xeroderma Pigmentosum

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Mechanisms of chromosomal aberration production. 3. Chemicals and ionizing radiation

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Zinsser-Cole-Engman syndrome. Apropos of 2 cases of dominant autosomic transmission

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Biochemical evidence for deficient DNA repair leading to enhanced G2 chromatid radiosensitivity and susceptibility to cancer

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Selective removal of transcription-blocking DNA damage from the transcribed strand of the mammalian DHFR gene

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Chromosomal fragile sites and cancer-specific rearrangements

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Chromosomal abnormalities in leukemia and lymphoma: clinical and biological significance

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Abnormality of platelet size and T-lymphocyte proliferation in an autosomal recessive form of dyskeratosis congenita.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Preferential DNA repair of an active gene in human cells

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Etiologic heterogeneity in dyskeratosis congenita

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Sister chromatid exchange in dyskeratosis congenita lymphocytes

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

X-linked Dyskeratosis Congenita With Pancytopenia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

G2 chromosomal radiosensitivity in Fanconi's anemia

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Psoralen-DNA Cross-linking Photoadducts in Dyskeratosis Congenita: Delay in Excision and Promotion of Sister Chromatid Exchange

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Active and Suppressor T Cells: Diminution in a Patient with Dyskeratosis Congenita and in First-Degree Relatives

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Molecular mechanisms involved in the production of chromosomal aberrations. I. Utilization of Neurospora endonuclease for the study of aberration production in G2 stage of the cell cycle

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Dyskeratosis congenita: two examples of this multisystem disorder.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Chromosomal radiosensitivity of human tumor cells during the G2 cell cycle period.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684970

Clastogen-induced fragility may differentiate pancytopenia of congenital dyskeratosis from Fanconi anaemia

26 September 2018

1 reference

12 December 2020

DYSKERATOSIS CONGENITA. A CASE WITH NEW FEATURES

1 reference

12 December 2020

THE ASSOCIATION OF DYSKERATOSIS CONGENITA AND FANCONI'S ANAEMIA

1 reference

12 December 2020

Zinsser-Cole-Engman syndrome (dyskeratosis congenita) with cataract--a rare association

1 reference

12 December 2020

The effect of cytosine arabinoside on the frequency of X-ray-induced chromosome aberrations in normal human leukocytes

1 reference

12 December 2020

Dyskeratosis congenita: survival, sister-chromatid exchange and repair following treatments with crosslinking agents

1 reference

12 December 2020

Chromatin structure, DNA structure

1 reference

12 December 2020

G2 chromosomal radiosensitivity of ataxia-telangiectasia heterozygotes

1 reference

12 December 2020

Assignment of the gene for dyskeratosis congenita to Xq28

1 reference

12 December 2020

Congenital dyskeratosis. Zinsser-Engman-Cole syndrome with thymic dysplasia and aplastic anemia

1 reference

12 December 2020

A simple G-banding technique

1 reference

12 December 2020

Dyskeratosis congenita: two extremes

1 reference

12 December 2020

Dyskeratosis congenita Zinsser-Cole-Engmann Form with Abnormal Karyotype

1 reference

12 December 2020

Identifiers

PMC publication ID

1684970

1 reference

7 August 2017

1 reference