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...

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

Molecular psychiatry, 2005-04, Vol.10 (4), p.329-332

2005

Volltextzugriff (PDF)

MECP2 structural and 3′-UTR variants in schizophrenia, autism and other psychiatric diseases: A possible association with autism

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-07, Vol.128B (1), p.50-53

2004

Volltextzugriff (PDF)

Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers

Human mutation, 2005-10, Vol.26 (4), p.303-307

2005

Volltextzugriff (PDF)

The incidence of venous thromboembolism among Factor V Leiden carriers: a community‐based cohort study

Journal of thrombosis and haemostasis, 2005-02, Vol.3 (2), p.305-311

2005

Volltextzugriff (PDF)

Single-Tube Polymerase Chain Reaction for Rapid Diagnosis of the Inversion Hotspot of Mutation in Hemophilia A

Blood, 1998-08, Vol.92 (4), p.1458-1459

1998

Volltextzugriff (PDF)

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

Genomics (San Diego, Calif.), 1998-08, Vol.52 (1), p.44-49

1998

Volltextzugriff (PDF)

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer

JAMA : the journal of the American Medical Association, 2005-02, Vol.293 (7), p.799

2005

Volltextzugriff (PDF)

The "megaprimer" method of site-directed mutagenesis

BioTechniques, 1990-04, Vol.8 (4), p.404

1990

Volltextzugriff (PDF)

PAP: Detection of ultra rare mutations depends on P oligonucleotides: "Sleeping Beauties" awakened by the kiss of pyrophosphorolysis

Human mutation, 2004-05, Vol.23 (5), p.426-436

2004

Volltextzugriff (PDF)

Diagnosis of Duchenne dystrophy by enhanced detection of small mutations

Neurology, 2001-08, Vol.57 (4), p.645-650

2001

Volltextzugriff (PDF)

Identification of novel variants of the flavin-containing monooxygenase gene family in African Americans

Drug metabolism and disposition, 2003-02, Vol.31 (2), p.187-193

2003

Volltextzugriff (PDF)

Pyrophosphorolysis-Activated Polymerization (PAP): Application to Allele-Specific Amplification

BioTechniques, 2000-11, Vol.29 (5), p.1072-1083

2000

Volltextzugriff (PDF)

Detection of extremely rare alleles by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification (Bi-PAP-A): measurement of mutation load in mammalian tissues

BioTechniques, 2004-01, Vol.36 (1), p.156-166

2004

Volltextzugriff (PDF)

Comparison of statistics for candidate-gene association studies using cases and parents

American journal of human genetics, 1994-08, Vol.55 (2), p.402-409

1994

Volltextzugriff (PDF)

Genotype relative risks : methods for design and analysis of candidate-gene association studies

American journal of human genetics, 1993-11, Vol.53 (5), p.1114-1126

1993

Volltextzugriff (PDF)

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy

Molecular genetics and metabolism, 2002-09, Vol.77 (1), p.119-126

2002

Volltextzugriff (PDF)

Overlapping PCR for bidirectional PCR amplification of specific alleles: a rapid one-tube method for simultaneously differentiating homozygotes and heterozygotes

Genome research, 1997-04, Vol.7 (4), p.389-398

1997

Volltextzugriff (PDF)

Spontaneous mutation in Big Blue® mice from fetus to old age: Tissue-specific time courses of mutation frequency but similar mutation types

Environmental and molecular mutagenesis, 2004, Vol.43 (2), p.110-120

2004

Volltextzugriff (PDF)

Shedding light on PCR contamination

Nature (London), 1990-01, Vol.343 (6253), p.27-27

1990

Volltextzugriff (PDF)

The molecular epidemiology of P53 gene mutations in human breast cancer

Trends in Genetics, 1997, Vol.13 (1), p.27-33

1997

Volltextzugriff (PDF)

Proofreading genotyping assays mediated by high fidelity exo + DNA polymerases

Trends in biotechnology (Regular ed.), 2005-02, Vol.23 (2), p.92-96

2005

Volltextzugriff (PDF)

Restriction endonuclease fingerprinting (REF): a sensitive method for screening mutations in long, contiguous segments of DNA

BioTechniques, 1995-03, Vol.18 (3), p.470

1995

Volltextzugriff (PDF)

Pyrophosphorolysis-activatable oligonucleotides may facilitate detection of rare alleles, mutation scanning and analysis of chromatin structures

Nucleic acids research, 2002-01, Vol.30 (2), p.598-604

2002

Volltextzugriff (PDF)

Subcycling-PCR for Multiplex Long-Distance Amplification of Regions with High and Low GC Content: Application to the Inversion Hotspot in the Factor VIII Gene

BioTechniques, 1998-12, Vol.25 (6), p.1022-1028

1998

Volltextzugriff (PDF)

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy

Journal of the American College of Cardiology, 2002-09, Vol.40 (6), p.1120-1124

2002

Volltextzugriff (PDF)

1 – 25 von 209

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(187)
Mit Volltextzugriff
(179)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(204)
Life Sciences & Biomedicine
(191)
Humans
(145)
Biological And Medical Sciences
(116)
Genetics & Heredity
(97)
Mutation
(86)
Base Sequence
(69)
Male
(65)
Biochemistry & Molecular Biology
(63)
Female
(63)
Medical Sciences
(63)
Fundamental And Applied Biological Sciences. Psychology
(60)
Molecular Sequence Data
(59)
Factor Ix - Genetics
(57)
Animals
(39)
Molecular And Cellular Biology
(39)
Hemophilia B - Genetics
(36)
Genes
(34)
Biochemical Research Methods
(31)
Polymerase Chain Reaction
(29)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients

MECP2 structural and 3′-UTR variants in schizophrenia, autism and other psychiatric diseases: A possible association with autism

Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers

The incidence of venous thromboembolism among Factor V Leiden carriers: a community‐based cohort study

Single-Tube Polymerase Chain Reaction for Rapid Diagnosis of the Inversion Hotspot of Mutation in Hemophilia A

Blind Analysis of Denaturing High-Performance Liquid Chromatography as a Tool for Mutation Detection

Conversion analysis for mutation detection in MLH1 and MSH2 in patients with colorectal cancer

The "megaprimer" method of site-directed mutagenesis

PAP: Detection of ultra rare mutations depends on P oligonucleotides: "Sleeping Beauties" awakened by the kiss of pyrophosphorolysis

Diagnosis of Duchenne dystrophy by enhanced detection of small mutations

Identification of novel variants of the flavin-containing monooxygenase gene family in African Americans

Pyrophosphorolysis-Activated Polymerization (PAP): Application to Allele-Specific Amplification

Detection of extremely rare alleles by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification (Bi-PAP-A): measurement of mutation load in mammalian tissues

Comparison of statistics for candidate-gene association studies using cases and parents

Genotype relative risks : methods for design and analysis of candidate-gene association studies

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy

Overlapping PCR for bidirectional PCR amplification of specific alleles: a rapid one-tube method for simultaneously differentiating homozygotes and heterozygotes

Spontaneous mutation in Big Blue® mice from fetus to old age: Tissue-specific time courses of mutation frequency but similar mutation types

Shedding light on PCR contamination

The molecular epidemiology of P53 gene mutations in human breast cancer

Proofreading genotyping assays mediated by high fidelity exo + DNA polymerases

Restriction endonuclease fingerprinting (REF): a sensitive method for screening mutations in long, contiguous segments of DNA

Pyrophosphorolysis-activatable oligonucleotides may facilitate detection of rare alleles, mutation scanning and analysis of chromatin structures

Subcycling-PCR for Multiplex Long-Distance Amplification of Regions with High and Low GC Content: Application to the Inversion Hotspot in the Factor VIII Gene

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathy

Suchergebnisse filtern