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...

816 K-Ras Mutation Detection in Colorectal Cancer – a Combined Approach Using TaqMan® Mutation Detection Assays (TMDA) and Digital PCR

European journal of cancer (1990), 2012-07, Vol.48, p.S195-S195

2012

Volltextzugriff (PDF)

PrP genotype in Sarda breed sheep and its relevance to scrapie

Archives of virology, 2001-10, Vol.146 (10), p.2029-2037

2001

Volltextzugriff (PDF)

Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients

American journal of human genetics, 1996-04, Vol.58 (4), p.888-889

1996

Volltextzugriff (PDF)

Primer extension assay for prion protein genotype determination in sheep

Molecular and cellular probes, 2004-02, Vol.18 (1), p.33-37

2004

Volltextzugriff (PDF)

181 Accuracy of castPCR-based KRAS testing on paraffin embedded tissues

European journal of cancer supplements, 2010, Vol.8 (5), p.47-48

2010

Volltextzugriff (PDF)

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)

Neurology, 1996-09, Vol.47 (3), p.734-741

1996

Volltextzugriff (PDF)

Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients

Brain research bulletin, 1999-08, Vol.49 (6), p.429-433

1999

Volltextzugriff (PDF)

Fatal familial insomnia in a new Italian kindred

Neurology, 1998-11, Vol.51 (5), p.1491-1494

1998

Volltextzugriff (PDF)

Mortality trend from sporadic Creutzfeldt-Jakob disease (CJD) in Italy, 1993–2000

Journal of clinical epidemiology, 2003-05, Vol.56 (5), p.494-499

2003

Volltextzugriff (PDF)

High incidence of Creutzfeldt-Jakob disease in rural Calabria, Italy

The Lancet (British edition), 1998-12, Vol.352 (9145), p.1989-1990

1998

Volltextzugriff (PDF)

Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease

Journal of neurology, neurosurgery and psychiatry, 1996-07, Vol.61 (1), p.111-112

1996

Volltextzugriff (PDF)

A rapid and efficient method for the detection of point mutations of the human prion protein gene (PRNP) by direct sequencing

Journal of neuroscience methods, 2000-06, Vol.99 (1), p.59-63

2000

Volltextzugriff (PDF)

Polymorphisms of the Prion Protein gene in Italian patients with Creutzfeldt-Jakob disease

Human genetics, 1994-10, Vol.94 (4), p.375-379

1994

Volltextzugriff (PDF)

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease

Annals of neurology, 1993-12, Vol.34 (6), p.802-807

1993

Volltextzugriff (PDF)

Genomic allelotyping for distinction of recurrent and de novo hepatocellular carcinoma after orthotopic liver transplantation

Diagnostic molecular pathology, 2005-03, Vol.14 (1), p.34-38

2005

Volltextzugriff (PDF)

Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family

Canadian journal of neurological sciences, 2003-08, Vol.30 (3), p.233-236

2003

Volltextzugriff (PDF)

Recent Italian FFI Cases

Brain pathology (Zurich, Switzerland), 1998-07, Vol.8 (3), p.564-566

1998

Volltextzugriff (PDF)

Assignment 1 of the mouse Vegfb gene to mouse chromosome 19 B by in situ hybridization

Cytogenetic and genome research, 2001-12, Vol.95 (3-4), p.242-243

2001

Volltextzugriff (PDF)

Apolipoprotein E in sporadic and familial Creutzfeldt-Jakob disease

Neuroscience letters, 1995-10, Vol.199 (2), p.95-98

1995

Volltextzugriff (PDF)

PrP genotype in Sarda breed sheep and its relevance to scrapie. Brief report

Archives of virology, 2001-10, Vol.146 (10), p.2029-2037

2001

Volltextzugriff (PDF)

Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease

American journal of medical genetics, 2001-10, Vol.103 (2), p.133-137

2001

Volltextzugriff (PDF)

Therapeutical approaches to transmissible spongiform encephalopathies (TSE): the case of amphotericin-B

Journal of biological regulators and homeostatic agents, 1996-10, Vol.10 (4), p.69

1996

Volltextzugriff (PDF)

Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt–Jakob disease

Neuroscience letters, 1997-05, Vol.227 (2), p.140-142

1997

Volltextzugriff (PDF)

Codon 200 mutation in a new family of chilean origin with Creutzfeld-Jakob disease

Journal of neurology, neurosurgery and psychiatry, 1996, Vol.61 (1), p.111-112

1996

Volltextzugriff (PDF)

1 – 25 von 60

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(55)
Mit Volltextzugriff
(49)

Publikationsform

Artikel
(58)
Berichte
(2)

Sprache

Englisch
(59)
Italienisch
(1)

Erscheinungsjahr

n.n

Thema

Science & Technology
(43)
Life Sciences & Biomedicine
(38)
Humans
(33)
Female
(25)
Male
(24)
Biological And Medical Sciences
(19)
Medical Sciences
(17)
Middle Aged
(15)
Adult
(14)
Aged
(13)
Creutzfeldt-Jakob Syndrome - Genetics
(11)
Neurosciences & Neurology
(11)
Neurology
(10)
Prions - Genetics
(10)
Creutzfeldt-Jakob Disease
(7)
Italy
(7)
Mutation
(7)
Clinical Neurology
(6)
Endocrinology & Metabolism
(6)
Genotype
(6)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

816 K-Ras Mutation Detection in Colorectal Cancer – a Combined Approach Using TaqMan® Mutation Detection Assays (TMDA) and Digital PCR

Simultaneous detection of lung fusions using a multiplex RT-PCR next generation sequencing-based approach: a multi-institutional research study

PrP genotype in Sarda breed sheep and its relevance to scrapie

Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients

Primer extension assay for prion protein genotype determination in sheep

181 Accuracy of castPCR-based KRAS testing on paraffin embedded tissues

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)

Prion protein glycotype analysis in familial and sporadic Creutzfeldt-Jakob disease patients

Fatal familial insomnia in a new Italian kindred

Mortality trend from sporadic Creutzfeldt-Jakob disease (CJD) in Italy, 1993–2000

High incidence of Creutzfeldt-Jakob disease in rural Calabria, Italy

Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease

A rapid and efficient method for the detection of point mutations of the human prion protein gene (PRNP) by direct sequencing

Polymorphisms of the Prion Protein gene in Italian patients with Creutzfeldt-Jakob disease

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease

Genomic allelotyping for distinction of recurrent and de novo hepatocellular carcinoma after orthotopic liver transplantation

Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family

Recent Italian FFI Cases

Assignment 1 of the mouse Vegfb gene to mouse chromosome 19 B by in situ hybridization

Apolipoprotein E in sporadic and familial Creutzfeldt-Jakob disease

PrP genotype in Sarda breed sheep and its relevance to scrapie. Brief report

Mutation of the PRNP gene at codon 211 in familial Creutzfeldt-Jakob disease

Therapeutical approaches to transmissible spongiform encephalopathies (TSE): the case of amphotericin-B

Alpha1 antichymotrypsin signal peptide polymorphism in sporadic Creutzfeldt–Jakob disease

Codon 200 mutation in a new family of chilean origin with Creutzfeld-Jakob disease

Suchergebnisse filtern