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...

The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome

Neurology, 2009-04, Vol.72 (14), p.1242-1247

2009

Volltextzugriff (PDF)

Novel FOXG1 mutations associated with the congenital variant of Rett syndrome

Journal of medical genetics, 2010-01, Vol.47 (1), p.49-53

2010

Volltextzugriff (PDF)

Common Genetic Variants of Microsomal Epoxide Hydrolase Affect Warfarin Dose Requirements Beyond the Effect of Cytochrome P450 2C9

Clinical pharmacology and therapeutics, 2005-05, Vol.77 (5), p.365-372

2005

Volltextzugriff (PDF)

Thoracic Aortic Dissection Associated with Marijuana Use

The Journal of emergency medicine, 2019-08, Vol.57 (2), p.235-237

2019

Volltextzugriff (PDF)

Brief Motivational Interviewing for Substance Use by Medical Students Is Effective in the Emergency Department

The Journal of emergency medicine, 2019-07, Vol.57 (1), p.114-117

2019

Volltextzugriff (PDF)

Combined genetic profiles of components and regulators of the vitamin K-dependent gamma-carboxylation system affect individual sensitivity to warfarin

Thrombosis and haemostasis, 2006-02, Vol.95 (2), p.205-211

2006

Volltextzugriff (PDF)

Comprehensive diagnosis of Rett’s syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients

Journal of medical genetics, 2006-12, Vol.43 (12), p.e56-e56

2006

Volltextzugriff (PDF)

Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients

Journal of medical genetics, 2007-02, Vol.44 (2), p.e56-e56

2007

Volltextzugriff (PDF)

Association between anorexia nervosa and the hsKCa3 gene: a family-based and case control study

Molecular psychiatry, 2002, Vol.7 (1), p.82-85

2002

Volltextzugriff (PDF)

The economic pattern of the settlement Rykan-3 (The Middle Don Catacomb culture)

Rossiiskaia arkheologiia, 2019-06 (2), p.19-34

2019

Volltextzugriff (PDF)

The Dating and Historical Context around the Logboat Exhibited at the State Historical Museum, Based on the Integrated Studies

Stratum, 2021-05 (2), p.235-252

2021

Volltextzugriff (PDF)

Magnetic Treatment of Irrigation Water: Experimental Results and Application Conditions

Environmental science & technology, 1999-04, Vol.33 (8), p.1280-1285

1999

Volltextzugriff (PDF)

The effect of genetic polymorphisms on warfarin pharmacodynamics

Clinical pharmacology and therapeutics, 2005-02, Vol.77 (2), p.P96-P96

2005

Volltextzugriff (PDF)

VKORC1 Asp36Tyr warfarin resistance marker is common in Ethiopian individuals

Blood, 2008-04, Vol.111 (7), p.3903-3904

2008

Volltextzugriff (PDF)

Effect of the VKORC1 D36Y variant on warfarin dose requirement and pharmacogenetic dose prediction

Thrombosis and haemostasis, 2012-10, Vol.108 (4), p.781-788

2012

Volltextzugriff (PDF)

Cloning, sequencing, and mutation of a gene for azurin in Methylobacillus flagellatum KT

Journal of Bacteriology, 1995-08, Vol.177 (15), p.4575-4578

1995

Volltextzugriff (PDF)

Organization of methylamine utilization genes (mau) in 'Methylobacillus flagellatum ' KT and analysis of mau mutants

Microbiology (Society for General Microbiology), 1997-06, Vol.143 ( Pt 6) (6), p.1827-1835

1997

Volltextzugriff (PDF)

VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations

Journal of applied genetics, 2014-05, Vol.55 (2), p.163-171

2014

Volltextzugriff (PDF)

A role of information-education programs in the treatment of patients with chronic headache

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 2013, Vol.113 (11), p.59

2013

Volltextzugriff (PDF)

Application of MHD effects in electrolytes for modeling vortex processes in natural phenomena and in solving engineering-physical problems

Journal of engineering physics and thermophysics, 2002-09, Vol.75 (5), p.1234-1247

2002

Volltextzugriff (PDF)

No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome

Human genetics, 1997-12, Vol.101 (2), p.186-189

1997

Volltextzugriff (PDF)

Screening for fragile X syndrome in women of reproductive age

Prenatal diagnosis, 2000-08, Vol.20 (8), p.611-614

2000

Volltextzugriff (PDF)

The experience of identifying and systematization of the infrastructure characteristics of the settlement of the catacomb culture Rykan-3 in the forest steppe Don region

Rossiiskaia arkheologiia, 2014 (4), p.19-28

2014

Volltextzugriff (PDF)

Screening for fragile X syndrome in women of reproductive age

Prenatal diagnosis, 2000-08, Vol.20 (8), p.611-614

2000

Volltextzugriff (PDF)

Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosa

Journal of psychiatric research, 2007-01, Vol.41 (1-2), p.160-167

2007

Volltextzugriff (PDF)

1 – 25 von 177

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(134)
Mit Volltextzugriff
(140)

Publikationsform

Sprache

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(109)
Life Sciences & Biomedicine
(76)
Humans
(58)
Biological And Medical Sciences
(39)
Male
(39)
Female
(33)
Medical Sciences
(31)
Middle Aged
(23)
Adult
(22)
Physical Sciences
(21)
Technology
(21)
Economic Growth
(20)
Aged
(19)
Political Economy
(19)
Genetics & Heredity
(13)
Fundamental And Applied Biological Sciences. Psychology
(12)
Animals
(11)
Mutation
(11)
Radiology, Nuclear Medicine & Medical Imaging
(11)
Radionuclide Imaging
(11)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome

Novel FOXG1 mutations associated with the congenital variant of Rett syndrome

Common Genetic Variants of Microsomal Epoxide Hydrolase Affect Warfarin Dose Requirements Beyond the Effect of Cytochrome P450 2C9

Thoracic Aortic Dissection Associated with Marijuana Use

Brief Motivational Interviewing for Substance Use by Medical Students Is Effective in the Emergency Department

Combined genetic profiles of components and regulators of the vitamin K-dependent gamma-carboxylation system affect individual sensitivity to warfarin

Comprehensive diagnosis of Rett’s syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients

Comprehensive diagnosis of Rett's syndrome relying on genetic, epigenetic and expression evidence of deficiency of the methyl-CpG-binding protein 2 gene: study of a cohort of Israeli patients

Association between anorexia nervosa and the hsKCa3 gene: a family-based and case control study

The economic pattern of the settlement Rykan-3 (The Middle Don Catacomb culture)

The Dating and Historical Context around the Logboat Exhibited at the State Historical Museum, Based on the Integrated Studies

Magnetic Treatment of Irrigation Water: Experimental Results and Application Conditions

The effect of genetic polymorphisms on warfarin pharmacodynamics

VKORC1 Asp36Tyr warfarin resistance marker is common in Ethiopian individuals

Effect of the VKORC1 D36Y variant on warfarin dose requirement and pharmacogenetic dose prediction

Cloning, sequencing, and mutation of a gene for azurin in Methylobacillus flagellatum KT

Organization of methylamine utilization genes (mau) in 'Methylobacillus flagellatum ' KT and analysis of mau mutants

VKORC1 Asp36Tyr variant and VKORC1 haplotype diversity in Ashkenazi and Ethiopian populations

A role of information-education programs in the treatment of patients with chronic headache

Application of MHD effects in electrolytes for modeling vortex processes in natural phenomena and in solving engineering-physical problems

No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome

Screening for fragile X syndrome in women of reproductive age

The experience of identifying and systematization of the infrastructure characteristics of the settlement of the catacomb culture Rykan-3 in the forest steppe Don region

Screening for fragile X syndrome in women of reproductive age

Dual contribution of NR2B subunit of NMDA receptor and SK3 Ca(2+)-activated K+ channel to genetic predisposition to anorexia nervosa

Suchergebnisse filtern