UB Paderborn / Katalog / Suche / in CDI

1 – 24 von 24

Sortiert nach

Whole exome sequencing identifies a novel variant causing cockayne syndrome type I in a consanguineous Pakistani family

International journal of neuroscience, 2024-06, Vol.ahead-of-print (ahead-of-print), p.1-6

2024

Volltextzugriff (PDF)

Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth

Cell cycle (Georgetown, Tex.), 2014-07, Vol.13 (13), p.2029-2037

2014

Volltextzugriff (PDF)

CSA and CSB proteins interact with p53 and regulate its Mdm2-dependent ubiquitination

Cell cycle (Georgetown, Tex.), 2011-11, Vol.10 (21), p.3719-3730

2011

Volltextzugriff (PDF)

Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome

Molecular and cellular biology, 2015-09, Vol.35 (18), p.3178-3188

2015

Volltextzugriff (PDF)

Ocular findings in a patient with Cockayne syndrome with two mutations in the ERCC6 gene

Ophthalmic genetics, 2017-03, Vol.38 (2), p.175-177

2017

Volltextzugriff (PDF)

Nucleotide Excision Repair Disorders and the Balance Between Cancer and Aging

Cell cycle (Georgetown, Tex.), 2006-12, Vol.5 (24), p.2886-2888

2006

Volltextzugriff (PDF)

ATP-Dependent Chromatin Remodeling by the Cockayne Syndrome B DNA Repair-Transcription-Coupling Factor

Molecular and Cellular Biology, 2000-10, Vol.20 (20), p.7643-7653

2000

Volltextzugriff (PDF)

Different Effects of CSA and CSB Deficiency on Sensitivity to Oxidative DNA Damage

Molecular and Cellular Biology, 2004-09, Vol.24 (18), p.7941-7948

2004

Volltextzugriff (PDF)

Computational image analysis of nuclear morphology associated with various nuclear-specific aging disorders

Nucleus (Austin, Tex.), 2011-11, Vol.2 (6), p.570-579

2011

Volltextzugriff (PDF)

Transcription-Associated Breaks in Xeroderma Pigmentosum Group D Cells from Patients with Combined Features of Xeroderma Pigmentosum and Cockayne Syndrome

Molecular and Cellular Biology, 2005-09, Vol.25 (18), p.8368-8378

2005

Volltextzugriff (PDF)

Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes

Molecular and Cellular Biology, 1997-12, Vol.17 (12), p.6803-6814

1997

Volltextzugriff (PDF)

Cockayne syndrome, underlying molecular defects and p53

Cell cycle (Georgetown, Tex.), 2011-12, Vol.10 (23), p.3999-3998

2011

Volltextzugriff (PDF)

Identification of the XPG Region That Causes the Onset of Cockayne Syndrome by Using Xpg Mutant Mice Generated by the cDNA-Mediated Knock-In Method

Molecular and Cellular Biology, 2004-05, Vol.24 (9), p.3712-3719

2004

Volltextzugriff (PDF)

Regulation of active genome integrity and expression by Rad26p

Nucleus (Austin, Tex.), 2014-11, Vol.5 (6), p.520-526

2014

Volltextzugriff (PDF)

Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase II

Molecular and cellular biology, 2001-12, Vol.21 (24), p.8651-8656

2001

Volltextzugriff (PDF)

Unraveling DNA Repair in Human: Molecular Mechanisms and Consequences of Repair Defect

Critical reviews in biochemistry and molecular biology, 2001, Vol.36 (3), p.261-290

2001

Volltextzugriff (PDF)

The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes

Molecular and Cellular Biology, 1996-08, Vol.16 (8), p.4436-4444

1996

Volltextzugriff (PDF)

Disruption of the Cockayne Syndrome B Gene Impairs Spontaneous Tumorigenesis in Cancer-Predisposed Ink4a/ARF Knockout Mice

Molecular and Cellular Biology, 2001-03, Vol.21 (5), p.1810-1818

2001

Volltextzugriff (PDF)

Cataract in early onset and classic Cockayne syndrome

Ophthalmic genetics, 1997, Vol.18 (4), p.193-197

1997

Volltextzugriff (PDF)

An Xpb Mouse Model for Combined Xeroderma Pigmentosum and Cockayne Syndrome Reveals Progeroid Features upon Further Attenuation of DNA Repair

Molecular and Cellular Biology, 2009-03, Vol.29 (5), p.1276-1290

2009

Volltextzugriff (PDF)

Coupling between nucleotide excision repair and gene expression

RNA biology, 2018-07, Vol.15 (7), p.845-848

2018

Volltextzugriff (PDF)

Cooperation of the Cockayne Syndrome Group B Protein and Poly(ADP-Ribose) Polymerase 1 in the Response to Oxidative Stress

Molecular and Cellular Biology, 2005-09, Vol.25 (17), p.7625-7636

2005

Volltextzugriff (PDF)

Retinal Degeneration and Ionizing Radiation Hypersensitivity in a Mouse Model for Cockayne Syndrome

Molecular and Cellular Biology, 2007-02, Vol.27 (4), p.1433-1441

2007

Volltextzugriff (PDF)

Replication fork breakage and re-start: New insights into Rad3/XPD-associated deficiencies

Cell cycle (Georgetown, Tex.), 2010-08, Vol.9 (15), p.3030-3034

2010

Volltextzugriff (PDF)

1 – 24 von 24

Suche als RSS-Feed

Aktive Filter

KollektionTaylor & Francis Current Content Access

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(24)
Mit Volltextzugriff
(24)

Publikationsform

Artikel
(24)

Sprache

Englisch
(24)
Japanisch
(3)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Molecular And Cellular Biology
(12)
Cell Cycle
(5)
Nucleus
(2)
Ophthalmic Genetics
(2)
Critical Reviews In Biochemistry And Molecular Biology
(1)
International Journal Of Neuroscience
(1)
Ophthalmic Paediatrics And Genetics
(1)
Rna Biology
(1)

3 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Whole exome sequencing identifies a novel variant causing cockayne syndrome type I in a consanguineous Pakistani family

Cockayne syndrome protein A is a transcription factor of RNA polymerase I and stimulates ribosomal biogenesis and growth

CSA and CSB proteins interact with p53 and regulate its Mdm2-dependent ubiquitination

Regulation of Transcription Elongation by the XPG-TFIIH Complex Is Implicated in Cockayne Syndrome

Ocular findings in a patient with Cockayne syndrome with two mutations in the ERCC6 gene

Nucleotide Excision Repair Disorders and the Balance Between Cancer and Aging

ATP-Dependent Chromatin Remodeling by the Cockayne Syndrome B DNA Repair-Transcription-Coupling Factor

Different Effects of CSA and CSB Deficiency on Sensitivity to Oxidative DNA Damage

Computational image analysis of nuclear morphology associated with various nuclear-specific aging disorders

Transcription-Associated Breaks in Xeroderma Pigmentosum Group D Cells from Patients with Combined Features of Xeroderma Pigmentosum and Cockayne Syndrome

Recruitment of the putative transcription-repair coupling factor CSB/ERCC6 to RNA polymerase II elongation complexes

Cockayne syndrome, underlying molecular defects and p53

Identification of the XPG Region That Causes the Onset of Cockayne Syndrome by Using Xpg Mutant Mice Generated by the cDNA-Mediated Knock-In Method

Regulation of active genome integrity and expression by Rad26p

Requirement for yeast RAD26, a homolog of the human CSB gene, in elongation by RNA polymerase II

Unraveling DNA Repair in Human: Molecular Mechanisms and Consequences of Repair Defect

The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes

Disruption of the Cockayne Syndrome B Gene Impairs Spontaneous Tumorigenesis in Cancer-Predisposed Ink4a/ARF Knockout Mice

Cataract in early onset and classic Cockayne syndrome

An Xpb Mouse Model for Combined Xeroderma Pigmentosum and Cockayne Syndrome Reveals Progeroid Features upon Further Attenuation of DNA Repair

Coupling between nucleotide excision repair and gene expression

Cooperation of the Cockayne Syndrome Group B Protein and Poly(ADP-Ribose) Polymerase 1 in the Response to Oxidative Stress

Retinal Degeneration and Ionizing Radiation Hypersensitivity in a Mouse Model for Cockayne Syndrome

Replication fork breakage and re-start: New insights into Rad3/XPD-associated deficiencies

Aktive Filter

Suchergebnisse filtern