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...

Human Mendelian pain disorders: a key to discovery and validation of novel analgesics

Clinical genetics, 2012-10, Vol.82 (4), p.367-373

2012

Volltextzugriff (PDF)

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

Clinical genetics, 2007-04, Vol.71 (4), p.311-319

2007

Volltextzugriff (PDF)

Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23

American journal of human genetics, 2001-03, Vol.68 (3), p.661-673

2001

Volltextzugriff (PDF)

A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12

Molecular psychiatry, 2005-06, Vol.10 (6), p.545-552

2005

Volltextzugriff (PDF)

Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Human molecular genetics, 1998-01, Vol.7 (1), p.43-51

1998

Volltextzugriff (PDF)

P39 Nutritional assessments in COPD: the respiratory nurse perspective on current practice across the UK

Thorax, 2011-12, Vol.66 (Suppl 4), p.A83-A84

2011

Volltextzugriff (PDF)

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Nature (London), 1995-06, Vol.375 (6534), p.754-760

1995

Volltextzugriff (PDF)

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

Nature (London), 1995-08, Vol.376 (6543), p.775-778

1995

Volltextzugriff (PDF)

C.1 The molecular diagnostic landscape of children with seizure onset in the first three years of life

Canadian journal of neurological sciences, 2023-06, Vol.50 (s2), p.S51-S51

2023

Volltextzugriff (PDF)

Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant

Human molecular genetics, 1996-07, Vol.5 (7), p.985-988

1996

Volltextzugriff (PDF)

Analysis of the 5' sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease

Genomics (San Diego, Calif.), 1997-03, Vol.40 (3), p.415-424

1997

Volltextzugriff (PDF)

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease

Human molecular genetics, 1995-07, Vol.4 (7), p.1137-1146

1995

Volltextzugriff (PDF)

Standardised ("plain") packaging of cigarettes regulations must be passed before the general election

BMJ (Online), 2014-12, Vol.349 (dec29 1), p.g7751-g7751

2014

Volltextzugriff (PDF)

Identification of a Novel Gene ( HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates

American journal of human genetics, 2004-05, Vol.74 (5), p.1064-1073

2004

Volltextzugriff (PDF)

No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins

Human genetics, 1998-07, Vol.103 (1), p.41-47

1998

Volltextzugriff (PDF)

A Genome-Wide Scan for Linkage to Chromosomal Regions in 382 Sibling Pairs With Schizophrenia or Schizoaffective Disorder

The American journal of psychiatry, 2002-05, Vol.159 (5), p.803-812

2002

Volltextzugriff (PDF)

Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid β-protein in both transfected cells and transgenic mice

Nature medicine, 1997-01, Vol.3 (1), p.67-72

1997

Volltextzugriff (PDF)

A Schizophrenia-Susceptibility Locus at 6q25, in One of the World's Largest Reported Pedigrees

American journal of human genetics, 2001-07, Vol.69 (1), p.96-105

2001

Volltextzugriff (PDF)

Conservation of Synteny between the Genome of the Pufferfish (Fugu rubripes) and the Region on Human Chromosome 14 (14q24.3) Associated with Familial Alzheimer Disease (AD3 Locus)

Proceedings of the National Academy of Sciences - PNAS, 1996-02, Vol.93 (4), p.1366-1369

1996

Volltextzugriff (PDF)

Reponses of human V6 to random motion, egomotion_incompatible and egomotion-compatible optic flow

Journal of vision (Charlottesville, Va.), 2011-09, Vol.11 (11), p.711-711

2011

Volltextzugriff (PDF)

Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder

American journal of medical genetics, 2000-06, Vol.96 (3), p.335-341

2000

Volltextzugriff (PDF)

Intergenerational Instability of the CAG Repeat of the Gene for Machado-Joseph Disease (MJD1) is Affected by the Genotype of the Normal Chromosome: Implications for the Molecular Mechanisms of the Instability of the CAG Repeat

Human molecular genetics, 1996-07, Vol.5 (7), p.923-932

1996

Volltextzugriff (PDF)

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Nature (London), 1995-06, Vol.375 (6534), p.754-760

1995

Volltextzugriff (PDF)

Demonstration of cerebral perfusion abnormalities in moyamoya disease using susceptibility perfusion- and diffusion-weighted MRI

Neuroradiology, 1999-02, Vol.41 (2), p.86-92

1999

Volltextzugriff (PDF)

A genome-wide search for schizophrenia susceptibility genes

American journal of medical genetics, 1998-09, Vol.81 (5), p.364-376

1998

Volltextzugriff (PDF)

1 – 25 von 550

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(459)
Mit Volltextzugriff
(473)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(345)
Life Sciences & Biomedicine
(226)
Humans
(208)
Physical Sciences
(109)
Aged
(103)
Female
(100)
Male
(99)
Biological And Medical Sciences
(85)
Medical Sciences
(72)
Exact Sciences And Technology
(71)
Older People
(64)
Aged, 80 And Over
(60)
Chemistry
(60)
Falls
(59)
Accidental Falls - Prevention & Control
(52)
Rehabilitation
(51)
Middle Aged
(50)
Exercise
(47)
Accidental Falls
(42)
Applied Sciences
(39)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Human Mendelian pain disorders: a key to discovery and validation of novel analgesics

Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populations

Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23

A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12

Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

P39 Nutritional assessments in COPD: the respiratory nurse perspective on current practice across the UK

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene

C.1 The molecular diagnostic landscape of children with seizure onset in the first three years of life

Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant

Analysis of the 5' sequence, genomic structure, and alternative splicing of the presenilin-1 gene (PSEN1) associated with early onset Alzheimer disease

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease

Standardised ("plain") packaging of cigarettes regulations must be passed before the general election

Identification of a Novel Gene ( HSN2) Causing Hereditary Sensory and Autonomic Neuropathy Type II through the Study of Canadian Genetic Isolates

No evidence of expansion of CAG or GAA repeats in schizophrenia families and monozygotic twins

A Genome-Wide Scan for Linkage to Chromosomal Regions in 382 Sibling Pairs With Schizophrenia or Schizoaffective Disorder

Mutant presenilins of Alzheimer's disease increase production of 42-residue amyloid β-protein in both transfected cells and transgenic mice

A Schizophrenia-Susceptibility Locus at 6q25, in One of the World's Largest Reported Pedigrees

Conservation of Synteny between the Genome of the Pufferfish (Fugu rubripes) and the Region on Human Chromosome 14 (14q24.3) Associated with Familial Alzheimer Disease (AD3 Locus)

Reponses of human V6 to random motion, egomotion_incompatible and egomotion-compatible optic flow

Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder

Intergenerational Instability of the CAG Repeat of the Gene for Machado-Joseph Disease (MJD1) is Affected by the Genotype of the Normal Chromosome: Implications for the Molecular Mechanisms of the Instability of the CAG Repeat

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Demonstration of cerebral perfusion abnormalities in moyamoya disease using susceptibility perfusion- and diffusion-weighted MRI

A genome-wide search for schizophrenia susceptibility genes

Suchergebnisse filtern