UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 134

Sortiert nach

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

Science (American Association for the Advancement of Science), 1995-06, Vol.268 (5218), p.1749-1753

1995

Link zum Volltext

Verfügbarkeit prüfen

Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum

British journal of radiology, 2006-06, Vol.79 (942), p.510

2006

Link zum Volltext

Verfügbarkeit prüfen

Neurological symptoms and natural course of xeroderma pigmentosum

Brain (London, England : 1878), 2008-08, Vol.131 (8), p.1979-1989

2008

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts

British journal of radiology, 2008-01, Vol.81 (961), p.51

2008

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

The 0.8% ultraviolet B content of an ultraviolet A sunlamp induces 75% of cyclobutane pyrimidine dimers in human keratinocytes in vitro

British journal of dermatology (1951), 1999-06, Vol.140 (6), p.1023-1030

1999

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Characterization of photosensitivity in the Smith-Lemli-Opitz syndrome: a new congenital photosensitivity syndrome

British journal of dermatology (1951), 1999-09, Vol.141 (3), p.406-414

1999

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Contrasting effects of an ultraviolet B and an ultraviolet A tanning lamp on interleukin-6, tumour necrosis factor-α and intercellular adhesion molecule-1 expression

British journal of dermatology (1951), 2001-07, Vol.145 (1), p.54-62

2001

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Photosensitivity associated with the Smith-Lemli-Opitz syndrome

British journal of dermatology (1951), 1998-05, Vol.138 (5), p.885-888

1998

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Frequencies of hprt– mutations and bcl-2 translocations in circulating human lymphocytes are correlated with United Kingdom sunlight records

Mutagenesis, 1999-11, Vol.14 (6), p.527-532

1999

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene

Human molecular genetics, 2001-10, Vol.10 (22), p.2539-2547

2001

Link zum Volltext

Verfügbarkeit prüfen

Possible association between mutant frequency in peripheral lymphocytes and domestic radon concentrations

The Lancet (British edition), 1991-05, Vol.337 (8751), p.1187-1189

1991

Link zum Volltext

Verfügbarkeit prüfen

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

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

1993

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 134

Suche als RSS-Feed

Aktive Filter

KollektionTaylor & Francis Current Content Access

Zeitschrift / SerieMutation Research

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(121)
Mit Volltextzugriff
(114)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

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

A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase

Clinical and cellular ionizing radiation sensitivity in a patient with xeroderma pigmentosum

Neurological symptoms and natural course of xeroderma pigmentosum

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

Minimal ionizing radiation sensitivity in a large cohort of xeroderma pigmentosum fibroblasts

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

The 0.8% ultraviolet B content of an ultraviolet A sunlamp induces 75% of cyclobutane pyrimidine dimers in human keratinocytes in vitro

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

Characterization of photosensitivity in the Smith-Lemli-Opitz syndrome: a new congenital photosensitivity syndrome

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

Contrasting effects of an ultraviolet B and an ultraviolet A tanning lamp on interleukin-6, tumour necrosis factor-α and intercellular adhesion molecule-1 expression

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

Photosensitivity associated with the Smith-Lemli-Opitz syndrome

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

Frequencies of hprt– mutations and bcl-2 translocations in circulating human lymphocytes are correlated with United Kingdom sunlight records

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

Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene

Possible association between mutant frequency in peripheral lymphocytes and domestic radon concentrations

Hypersensitivity of human lymphocytes to UV-B and solar irradiation

Aktive Filter

Suchergebnisse filtern