UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Elevated expression of artemis in human fibroblast cells is associated with cellular radiosensitivity and increased apoptosis

British journal of cancer, 2012-10, Vol.107 (9), p.1506-1513

2012

Volltextzugriff (PDF)

Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient

Current biology, 1999-07, Vol.9 (13), p.699,S1-702,S2

1999

Volltextzugriff (PDF)

Hypersensitivity of ataxia telangiectasia fibroblasts to ionizing radiation is associated with a repair deficiency of DNA double-strand breaks

International journal of radiation biology, 1997-09, Vol.72 (3), p.271-283

FORAY, A. PRIESTLEY, G. ALSBEIH, C. BADIE, E. P. CAPULAS, C. F. ARLETT and E. P. MALAISE, N.

1997

Volltextzugriff (PDF)

Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia

British journal of cancer, 1999-03, Vol.79 (7-8), p.1304-1307

1999

Volltextzugriff (PDF)

Short Tandem Repeat Profiling Provides an International Reference Standard for Human Cell Lines

Proceedings of the National Academy of Sciences - PNAS, 2001-07, Vol.98 (14), p.8012-8017

2001

Volltextzugriff (PDF)

Induction of Interleukin-6 Production by Ultraviolet Radiation in Normal Human Epidermal Keratinocytes and in a Human Keratinocyte Cell Line is Mediated by DNA Damage

Journal of investigative dermatology, 1998-09, Vol.111 (3), p.354-359

1998

Volltextzugriff (PDF)

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3

American journal of human genetics, 1994-02, Vol.54 (2), p.191-200

1994

Volltextzugriff (PDF)

V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder

The Journal of biological chemistry, 1993-09, Vol.268 (27), p.20105-20109

1993

Volltextzugriff (PDF)

Underestimation of the small residual damage when measuring DNA double-strand breaks (DSB): is the repair of radiation-induced DSB complete?

International journal of radiation biology, 1999, Vol.75 (12), p.1589-1595

Foray, C. F. Arlett, E. P. Malaise, N.

1999

Volltextzugriff (PDF)

A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy

American journal of human genetics, 1993-10, Vol.53 (4), p.817-821

1993

Volltextzugriff (PDF)

Radiation-induced DNA double-strand breaks and the radiosensitivity of human cells: A closer look

Biochimie, 1997-10, Vol.79 (9), p.567-575

1997

Volltextzugriff (PDF)

The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect

Cancer research (Chicago, Ill.), 2000-01, Vol.60 (2), p.431-438

2000

Volltextzugriff (PDF)

A DNA double-strand break defective fibroblast cell line (180BR) derived from a radiosensitive patient represents a new mutant phenotype

Cancer research (Chicago, Ill.), 1997-10, Vol.57 (20), p.4600-4607

1997

Volltextzugriff (PDF)

Defective repair of DNA double-strand breaks and chromosome damage in fibroblasts from a radiosensitive leukemia patient

Cancer research (Chicago, Ill.), 1995-03, Vol.55 (6), p.1232-1234

1995

Volltextzugriff (PDF)

Xeroderma Pigmentosum and Trichothiodystrophy are Associated with Different Mutations in the XPD (ERCC2) Repair/Transcription Gene

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (16), p.8658-8663

1997

Volltextzugriff (PDF)

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and cockayne syndrome

American journal of human genetics, 1995, Vol.56 (1), p.167-174

1995

Volltextzugriff (PDF)

Repair of radiation-induced DNA double-strand breaks in human fibroblasts is consistent with a continuous spectrum of repair probability

International journal of radiation biology, 1998, Vol.74 (5), p.551-560

FORAY, N.

1998

Volltextzugriff (PDF)

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

Cancer research (Chicago, Ill.), 1993-02, Vol.53 (3), p.609-614

1993

Volltextzugriff (PDF)

Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line

Journal of molecular biology, 1991-01, Vol.217 (2), p.217-222

1991

Volltextzugriff (PDF)

The use of dubious cell lines in research: is trust enough?

The lancet oncology, 2001-08, Vol.2 (8), p.467-467

Arlett, Colin F

2001

Volltextzugriff (PDF)

Effect of diet and vitamin C on DNA strand breakage in freshly-isolated human white blood cells

Mutation research, 1994-08, Vol.316 (2), p.91-102

1994

Volltextzugriff (PDF)

Use of Fluorescence in Situ Hybridization to Determine the Relationship between Chromosome Aberrations and Cell Survival in Eight Human Fibroblast Strains

International journal of radiation biology, 1995, Vol.68 (2), p.185-196

1995

Volltextzugriff (PDF)

Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity

Human genetics, 1986-10, Vol.74 (2), p.107-112

1986

Volltextzugriff (PDF)

Four radiation hypersensitivity cases and their implications for clinical radiotherapy

Radiotherapy and oncology, 2000-11, Vol.57 (2), p.143-154

2000

Volltextzugriff (PDF)

Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects

Cancer research (Chicago, Ill.), 2000-09, Vol.60 (17), p.4881-4888

2000

Volltextzugriff (PDF)

1 – 25 von 158

Suche als RSS-Feed

Aktive Filter

KollektionJournals@Ovid Complete

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(94)
Mit Volltextzugriff
(106)

Publikationsform

Sprache

Englisch
(156)
Französisch
(2)

Erscheinungsjahr

n.n

Thema

Humans
(86)
Science & Technology
(84)
Life Sciences & Biomedicine
(78)
Biological And Medical Sciences
(47)
Cell Line
(38)
Dna Repair
(38)
Ultraviolet Rays
(37)
Fibroblasts - Radiation Effects
(34)
Mutation
(34)
Animals
(31)
Genetics & Heredity
(30)
Cells, Cultured
(27)
Cell Survival - Radiation Effects
(26)
Male
(25)
Medical Sciences
(24)
Toxicology
(24)
Fundamental And Applied Biological Sciences. Psychology
(23)
Female
(22)
Dose-Response Relationship, Radiation
(19)
Oncology
(18)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Elevated expression of artemis in human fibroblast cells is associated with cellular radiosensitivity and increased apoptosis

Identification of a defect in DNA ligase IV in a radiosensitive leukaemia patient

Hypersensitivity of ataxia telangiectasia fibroblasts to ionizing radiation is associated with a repair deficiency of DNA double-strand breaks

Risk of breast cancer and other cancers in heterozygotes for ataxia-telangiectasia

Short Tandem Repeat Profiling Provides an International Reference Standard for Human Cell Lines

Induction of Interleukin-6 Production by Ultraviolet Radiation in Normal Human Epidermal Keratinocytes and in a Human Keratinocyte Cell Line is Mediated by DNA Damage

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3

V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder

Underestimation of the small residual damage when measuring DNA double-strand breaks (DSB): is the repair of radiation-induced DSB complete?

A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophy

Radiation-induced DNA double-strand breaks and the radiosensitivity of human cells: A closer look

The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect

A DNA double-strand break defective fibroblast cell line (180BR) derived from a radiosensitive patient represents a new mutant phenotype

Defective repair of DNA double-strand breaks and chromosome damage in fibroblasts from a radiosensitive leukemia patient

Xeroderma Pigmentosum and Trichothiodystrophy are Associated with Different Mutations in the XPD (ERCC2) Repair/Transcription Gene

Molecular and cellular analysis of the DNA repair defect in a patient in xeroderma pigmentosum complementation group D who has the clinical features of xeroderma pigmentosum and cockayne syndrome

Repair of radiation-induced DNA double-strand breaks in human fibroblasts is consistent with a continuous spectrum of repair probability

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell line

The use of dubious cell lines in research: is trust enough?

Effect of diet and vitamin C on DNA strand breakage in freshly-isolated human white blood cells

Use of Fluorescence in Situ Hybridization to Determine the Relationship between Chromosome Aberrations and Cell Survival in Eight Human Fibroblast Strains

Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity

Four radiation hypersensitivity cases and their implications for clinical radiotherapy

Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects

Aktive Filter

Suchergebnisse filtern