UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 53

Sortiert nach

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

Cell, 1996-11, Vol.87 (3), p.543-552

1996

Volltextzugriff (PDF)

An integrated metric physical map of human chromosome 19

Nature genetics, 1995-12, Vol.11 (4), p.422-427

1995

Volltextzugriff (PDF)

Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1

Nucleic acids research, 1998-08, Vol.26 (16), p.3762

1998

Volltextzugriff (PDF)

XRCC2 and XRCC3, New Human Rad51-Family Members, Promote Chromosome Stability and Protect against DNA Cross-Links and Other Damages

Molecular cell, 1998-05, Vol.1 (6), p.783-793

1998

Volltextzugriff (PDF)

ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs

Molecular and Cellular Biology, 1996-11, Vol.16 (11), p.6553-6562

1996

Volltextzugriff (PDF)

Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions

Genomics (San Diego, Calif.), 1995-01, Vol.25 (2), p.547-554

1995

Volltextzugriff (PDF)

Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes

Genomics (San Diego, Calif.), 1996-06, Vol.34 (3), p.399-409

1996

Volltextzugriff (PDF)

Restoration of Nucleotide Excision Repair in a Helicase-Deficient XPD Mutant from Intragenic Suppression by a Trichothiodystrophy Mutation

Molecular and cellular biology, 2001-11, Vol.21 (21), p.7355-7365

2001

Volltextzugriff (PDF)

Characterization of the Mouse Xpf DNA Repair Gene and Differential Expression during Spermatogenesis

Genomics (San Diego, Calif.), 1999-12, Vol.62 (3), p.427-435

1999

Volltextzugriff (PDF)

Alu fossil relics--distribution and insertion polymorphism

Genome research, 1996-11, Vol.6 (11), p.1084

1996

Volltextzugriff (PDF)

Comparative Analysis of a Conserved Zinc Finger Gene Cluster on Human Chromosome 19q and Mouse Chromosome 7

Genomics (San Diego, Calif.), 1996-04, Vol.33 (1), p.112-120

1996

Volltextzugriff (PDF)

Automated fluorescence-based restriction fragment analysis

BioTechniques, 1993-08, Vol.15 (2), p.294

1993

Volltextzugriff (PDF)

The Human XRCC9 Gene Corrects Chromosomal Instability and Mutagen Sensitivities in CHO UV40 Cells

Proceedings of the National Academy of Sciences - PNAS, 1997-08, Vol.94 (17), p.9232-9237

1997

Volltextzugriff (PDF)

Cloning and Molecular Characterization of the Chinese Hamster ERCC2 Nucleotide Excision Repair Gene

Genomics (San Diego, Calif.), 1994-10, Vol.23 (3), p.592-599

1994

Volltextzugriff (PDF)

Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12

Genome research, 1998-08, Vol.8 (8), p.791

1998

Volltextzugriff (PDF)

The atherogenic lipoprotein phenotype is not caused by a mutation in the coding region of the low density lipoprotein receptor gene

Clinical genetics, 1997-04, Vol.51 (4), p.236-240

1997

Volltextzugriff (PDF)

Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints

Genome research, 2000-09, Vol.10 (9), p.1369

2000

Volltextzugriff (PDF)

Isolation and Characterization of Mouse Xrcc-1, a DNA Repair Gene Affecting Ligation

Genomics (San Diego, Calif.), 1994-07, Vol.22 (1), p.180-188

1994

Volltextzugriff (PDF)

Acetaldehyde stimulates FANCD2 monoubiquitination, H2AX phosphorylation, and BRCA1 phosphorylation in human cells in vitro: Implications for alcohol-related carcinogenesis

Mutation research, 2009-05, Vol.664 (1), p.77-83

2009

Volltextzugriff (PDF)

Fanconi Anemia FANCG Protein in Mitigating Radiation- and Enzyme-Induced DNA Double-Strand Breaks by Homologous Recombination in Vertebrate Cells

Molecular and Cellular Biology, 2003-08, Vol.23 (15), p.5421-5430

2003

Volltextzugriff (PDF)

High-resolution cartography of recently integrated human chromosome 19-specific Alu fossils

Journal of molecular biology, 1998-09, Vol.281 (5), p.843-856

1998

Volltextzugriff (PDF)

Characterization of the hamster FancG/Xrcc9 gene and mutations in CHO UV40 and NM3

Mutagenesis, 2004-05, Vol.19 (3), p.237-244

2004

Volltextzugriff (PDF)

Chromosomal localization and expressed sequence tag generation of clones from a normalized human adult thymus cDNA library

Genome research, 1995-11, Vol.5 (4), p.359

1995

Volltextzugriff (PDF)

Identification and characterization of two polymorphic Ya5 Alu repeats

Mutation research, 1997-09, Vol.382 (1-2), p.5-11

1997

Volltextzugriff (PDF)

Construction of a functional cDNA clone of the hamster ERCC2 DNA repair and transcription gene

Somatic cell and molecular genetics, 1996-11, Vol.22 (6), p.453-460

1996

Volltextzugriff (PDF)

1 – 25 von 53

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(52)
Mit Volltextzugriff
(46)

Publikationsform

Artikel
(53)

Sprache

Englisch
(53)
Japanisch
(11)

Erscheinungsjahr

n.n

Thema

Science & Technology
(45)
Life Sciences & Biomedicine
(39)
Humans
(34)
Molecular Sequence Data
(31)
Genetics & Heredity
(23)
Base Sequence
(21)
Biochemistry & Molecular Biology
(21)
Animals
(20)
Biological And Medical Sciences
(20)
Biotechnology & Applied Microbiology
(18)
Fundamental And Applied Biological Sciences. Psychology
(16)
Amino Acid Sequence
(14)
Chromosome Mapping
(14)
Chromosomes, Human, Pair 19
(11)
Cloning, Molecular
(11)
Cricetinae
(11)
Cosmids
(10)
Genes
(10)
Cell Biology
(9)
Dna-Binding Proteins - Genetics
(9)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

An integrated metric physical map of human chromosome 19

Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1

XRCC2 and XRCC3, New Human Rad51-Family Members, Promote Chromosome Stability and Protect against DNA Cross-Links and Other Damages

ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs

Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions

Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes

Restoration of Nucleotide Excision Repair in a Helicase-Deficient XPD Mutant from Intragenic Suppression by a Trichothiodystrophy Mutation

Characterization of the Mouse Xpf DNA Repair Gene and Differential Expression during Spermatogenesis

Alu fossil relics--distribution and insertion polymorphism

Comparative Analysis of a Conserved Zinc Finger Gene Cluster on Human Chromosome 19q and Mouse Chromosome 7

Automated fluorescence-based restriction fragment analysis

The Human XRCC9 Gene Corrects Chromosomal Instability and Mutagen Sensitivities in CHO UV40 Cells

Cloning and Molecular Characterization of the Chinese Hamster ERCC2 Nucleotide Excision Repair Gene

Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12

The atherogenic lipoprotein phenotype is not caused by a mutation in the coding region of the low density lipoprotein receptor gene

Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints

Isolation and Characterization of Mouse Xrcc-1, a DNA Repair Gene Affecting Ligation

Acetaldehyde stimulates FANCD2 monoubiquitination, H2AX phosphorylation, and BRCA1 phosphorylation in human cells in vitro: Implications for alcohol-related carcinogenesis

Fanconi Anemia FANCG Protein in Mitigating Radiation- and Enzyme-Induced DNA Double-Strand Breaks by Homologous Recombination in Vertebrate Cells

High-resolution cartography of recently integrated human chromosome 19-specific Alu fossils

Characterization of the hamster FancG/Xrcc9 gene and mutations in CHO UV40 and NM3

Chromosomal localization and expressed sequence tag generation of clones from a normalized human adult thymus cDNA library

Identification and characterization of two polymorphic Ya5 Alu repeats

Construction of a functional cDNA clone of the hamster ERCC2 DNA repair and transcription gene

Suchergebnisse filtern