Literature DB >> 3097418

Human DNA repair defects.

C F Arlett.   

Abstract

A number of human genetic diseases have come to be described as being defective in DNA repair. The minimum criterion on which this assignment is based is hypersensitivity to the clastogenic or lethal action of specific DNA damaging agents. In one disease, xeroderma pigmentosum, the molecular evidence for a defect in DNA repair is unequivocal. This condition then acts as a model for dissecting others. For the other diseases the formal evidence for defects in repair is less secure or even lacking. The evidence for repair in each disease is assembled together with any methods that have been used to support the differential diagnosis or for prenatal diagnosis. Attempts to clone human DNA repair genes are in hand and may provide the necessary evidence to decide if all the putative DNA repair defective diseases are genuine. Neoplastic disease and neurological degeneration together with immune defects are frequent clinical features linking this set of diseases, suggesting that effective DNA repair may be important in many aspects of human health.

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Year:  1986        PMID: 3097418     DOI: 10.1007/bf01800860

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  66 in total

1.  The relationship between chromosome damage and cell killing in UV-irradiated normal and xeroderma pigmentosum cells.

Authors:  R R Marshall; D Scott
Journal:  Mutat Res       Date:  1976-09       Impact factor: 2.433

2.  Bloom's syndrome. V. Surveillance for cancer in affected families.

Authors:  J German; D Bloom; E Passarge
Journal:  Clin Genet       Date:  1977-09       Impact factor: 4.438

3.  Ataxia-telangiectasia: genetics, neuropathology, and immunology of a degenerative disease of childhood. Proceedings of a conference. Solvang, California, January 16-20, 1984.

Authors: 
Journal:  Kroc Found Ser       Date:  1985

4.  Xeroderma pigmentosum fibroblasts including cells from XP variants are abnormally sensitive to the mutagenic and cytotoxic action of broad spectrum simulated sunlight.

Authors:  J D Patton; L A Rowan; A L Mendrala; J N Howell; V M Maher; J J McCormick
Journal:  Photochem Photobiol       Date:  1984-01       Impact factor: 3.421

5.  Ataxia-telangiectasis: a multisystem hereditary disease with immunodeficiency, impaired organ maturation, x-ray hypersensitivity, and a high incidence of neoplasia.

Authors:  T A Waldmann; J Misiti; D L Nelson; K H Kraemer
Journal:  Ann Intern Med       Date:  1983-09       Impact factor: 25.391

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

Authors:  A B Krepinsky; A J Rainbow; J A Heddle
Journal:  Mutat Res       Date:  1980-02       Impact factor: 2.433

7.  Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method.

Authors:  A D Auerbach; B Adler; R S Chaganti
Journal:  Pediatrics       Date:  1981-01       Impact factor: 7.124

8.  Xeroderma pigmentosum patients from the Federal Republic of Germany: decrease in post-UV colony-forming ability in 30 xeroderma pigmentosum fibroblast strains is quantitatively correlated with a decrease in DNA-incising capacity.

Authors:  H W Thielmann; L Edler; O Popanda; S Friemel
Journal:  J Cancer Res Clin Oncol       Date:  1985       Impact factor: 4.553

Review 9.  Chromosome-breakage syndromes: different genes, different treatments, different cancers.

Authors:  J German
Journal:  Basic Life Sci       Date:  1980

10.  Xeroderma pigmentosum cells with normal levels of excision repair have a defect in DNA synthesis after UV-irradiation.

Authors:  A R Lehmann; S Kirk-Bell; C F Arlett; M C Paterson; P H Lohman; E A de Weerd-Kastelein; D Bootsma
Journal:  Proc Natl Acad Sci U S A       Date:  1975-01       Impact factor: 11.205

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  4 in total

Review 1.  Medical genetics.

Authors:  M Super
Journal:  Postgrad Med J       Date:  1991-07       Impact factor: 2.401

2.  Spontaneous and induced chromosome breakage in chorionic villus samples: a cytogenetic approach to first trimester prenatal diagnosis of ataxia telangiectasia syndrome.

Authors:  J Llerena; M Murer-Orlando; M McGuire; L Zahed; R J Sheridan; A C Berry; M Bobrow
Journal:  J Med Genet       Date:  1989-03       Impact factor: 6.318

3.  G2 chromosomal radiosensitivity in families with ataxia-telangiectasia.

Authors:  Y Shiloh; R Parshad; M Frydman; K K Sanford; S Portnoi; Y Ziv; G M Jones
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

4.  Alterations of NAD and adenylyl dinucleotide metabolism in Chediak-Higashi syndrome fibroblasts.

Authors:  J C Baker; B N Ames
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

  4 in total

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