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...

Cell‐Free DNA: An Upcoming Biomarker in Transplantation

American journal of transplantation, 2015-10, Vol.15 (10), p.2541-2551

2015

Volltextzugriff (PDF)

Progranulin locus deletion in frontotemporal dementia

Human mutation, 2008, Vol.29 (1), p.53-58

2008

Volltextzugriff (PDF)

Meta-analyses of genetic studies on major depressive disorder

Molecular psychiatry, 2008-08, Vol.13 (8), p.772-785

2008

Volltextzugriff (PDF)

MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets

Molecular psychiatry, 2015-04, Vol.20 (4), p.472-481

2015

Volltextzugriff (PDF)

Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

Molecular psychiatry, 2001-09, Vol.6 (5), p.579-585

2001

Volltextzugriff (PDF)

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

Neurology, 2010-09, Vol.75 (13), p.1159-1165

2010

Volltextzugriff (PDF)

A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression

Molecular psychiatry, 2004-03, Vol.9 (3), p.287-292

2004

Volltextzugriff (PDF)

Mutations in SACS cause atypical and late-onset forms of ARSACS

Neurology, 2010-09, Vol.75 (13), p.1181-1188

2010

Volltextzugriff (PDF)

Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila

Psychopharmacology, 2016-05, Vol.233 (9), p.1751-1762

2016

Volltextzugriff (PDF)

HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study

Molecular psychiatry, 2007-09, Vol.12 (9), p.797-798

2007

Volltextzugriff (PDF)

Caspase deficiency alters the murine gut microbiome

Cell death & disease, 2011-10, Vol.2 (10), p.e220-e220

2011

Volltextzugriff (PDF)

Gene expression analysis of estrogenic compounds in the liver of common carp (Cyprinus carpio) using a custom cDNA microarray

Journal of biochemical and molecular toxicology, 2007-01, Vol.21 (5), p.299-311

2007

Volltextzugriff (PDF)

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families

Molecular psychiatry, 2008-04, Vol.13 (4), p.442-450

2008

Volltextzugriff (PDF)

Association between COMT (Val Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study

Molecular psychiatry, 2005-06, Vol.10 (6), p.598-605

2005

Volltextzugriff (PDF)

Comprehensive Profiling of the Androgen Receptor in Liquid Biopsies from Castration-resistant Prostate Cancer Reveals Novel Intra-AR Structural Variation and Splice Variant Expression Patterns

European urology, 2017-08, Vol.72 (2), p.192-200

2017

Volltextzugriff (PDF)

Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q

Neurology, 2007-06, Vol.68 (23), p.1995-2002

2007

Volltextzugriff (PDF)

Evaluation of a multiplex-PCR detection in combination with an isolation method for STEC O26, O103, O111, O145 and sorbitol fermenting O157 in food

Food microbiology, 2012-02, Vol.29 (1), p.49-55

2012

Volltextzugriff (PDF)

The serotonin transporter promoter repeat length polymorphism, seasonal affective disorder and seasonality

Psychological medicine, 2003-07, Vol.33 (5), p.785-792

2003

Volltextzugriff (PDF)

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.2977-2983

2006

Volltextzugriff (PDF)

Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

Journal of medical genetics, 2004-09, Vol.41 (9), p.710-714

2004

Volltextzugriff (PDF)

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

American journal of human genetics, 2001-06, Vol.68 (6), p.1327-1332

2001

Volltextzugriff (PDF)

De novo KCNQ2 mutations in patients with benign neonatal seizures

Neurology, 2004-12, Vol.63 (11), p.2155-2158

2004

Volltextzugriff (PDF)

novoSNP, a novel computational tool for sequence variation discovery

Genome research, 2005-03, Vol.15 (3), p.436-442

2005

Volltextzugriff (PDF)

A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus

Journal of medical genetics, 2005-12, Vol.42 (12), p.947-952

2005

Volltextzugriff (PDF)

P.1.a.004 Associations between AVPR1b and NR3C1 gene variants and HPA axis responses to psychosocial stress

European neuropsychopharmacology, 2010, Vol.20, p.S214-S215

2010

Volltextzugriff (PDF)

1 – 25 von 255

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(218)
Mit Volltextzugriff
(206)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(162)
Life Sciences & Biomedicine
(151)
Humans
(135)
Male
(78)
Biological And Medical Sciences
(77)
Female
(76)
Medical Sciences
(63)
Adult
(56)
Middle Aged
(49)
Genetics & Heredity
(43)
Psychiatry
(37)
Neurosciences & Neurology
(36)
Neurosciences
(35)
Biochemistry & Molecular Biology
(33)
Aged
(27)
Animals
(26)
Bipolar Disorder - Genetics
(25)
Genotype
(25)
Fundamental And Applied Biological Sciences. Psychology
(23)
Bipolar Disorder
(20)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Cell‐Free DNA: An Upcoming Biomarker in Transplantation

Progranulin locus deletion in frontotemporal dementia

Meta-analyses of genetic studies on major depressive disorder

MIR137 variants identified in psychiatric patients affect synaptogenesis and neuronal transmission gene sets

Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder

Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression

Mutations in SACS cause atypical and late-onset forms of ARSACS

Mood stabilizing drugs regulate transcription of immune, neuronal and metabolic pathway genes in Drosophila

HTR2C (cys23ser) polymorphism influences early onset in bipolar patients in a large European multicenter association study

Caspase deficiency alters the murine gut microbiome

Gene expression analysis of estrogenic compounds in the liver of common carp (Cyprinus carpio) using a custom cDNA microarray

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families

Association between COMT (Val Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study

Comprehensive Profiling of the Androgen Receptor in Liquid Biopsies from Castration-resistant Prostate Cancer Reveals Novel Intra-AR Structural Variation and Splice Variant Expression Patterns

Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q

Evaluation of a multiplex-PCR detection in combination with an isolation method for STEC O26, O103, O111, O145 and sorbitol fermenting O157 in food

The serotonin transporter promoter repeat length polymorphism, seasonal affective disorder and seasonality

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

Novel locus on chromosome 12q22–q23.3 responsible for familial temporal lobe epilepsy associated with febrile seizures

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

De novo KCNQ2 mutations in patients with benign neonatal seizures

novoSNP, a novel computational tool for sequence variation discovery

A novel susceptibility locus at 2p24 for generalised epilepsy with febrile seizures plus

P.1.a.004 Associations between AVPR1b and NR3C1 gene variants and HPA axis responses to psychosocial stress

Suchergebnisse filtern