UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 112

Sortiert nach

Efficient Conditional Mutation of the Vertebrate CENP-C Gene

Human molecular genetics, 1997-12, Vol.6 (13), p.2301-2308

1997

Volltextzugriff (PDF)

Human mini-chromosomes with minimal centromeres

Human molecular genetics, 2000-07, Vol.9 (12), p.1891-1902

2000

Volltextzugriff (PDF)

Dissecting the centromere of the human Y chromosome with cloned telomeric DNA

Human molecular genetics, 1994-08, Vol.3 (8), p.1227-1237

1994

Volltextzugriff (PDF)

The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes

Human molecular genetics, 1994-05, Vol.3 (5), p.771-778

1994

Volltextzugriff (PDF)

Early and progressive circadian abnormalities in Huntington's disease sheep are unmasked by social environment

Human molecular genetics, 2014-07, Vol.23 (13), p.3375-3383

2014

Volltextzugriff (PDF)

Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

Human molecular genetics, 2015-04, Vol.24 (8), p.2318-2329

2015

Volltextzugriff (PDF)

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

Human molecular genetics, 2013-02, Vol.22 (4), p.832-841

2013

Volltextzugriff (PDF)

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

Human molecular genetics, 2012-06, Vol.21 (12), p.2768-2778

2012

Volltextzugriff (PDF)

Genetic landscape of auditory dysfunction

Human molecular genetics, 2018-08, Vol.27 (R2), p.R130-R135

2018

Volltextzugriff (PDF)

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

Human molecular genetics, 2001-08, Vol.10 (17), p.1761-1766

2001

Volltextzugriff (PDF)

Reduced striatal dopamine underlies the attention system dysfunction in neurofibromatosis-1 mutant mice

Human molecular genetics, 2010-11, Vol.19 (22), p.4515-4528

2010

Volltextzugriff (PDF)

Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1

Human molecular genetics, 2013-10, Vol.22 (19), p.3947-3959

2013

Volltextzugriff (PDF)

Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth

Human molecular genetics, 2015-09, Vol.24 (17), p.4775-4779

2015

Volltextzugriff (PDF)

A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability

Human molecular genetics, 2017-10, Vol.26 (20), p.3869-3882

2017

Volltextzugriff (PDF)

Genetic control of the alternative pathway of complement in humans and age-related macular degeneration

Human molecular genetics, 2010-01, Vol.19 (1), p.209-215

2010

Volltextzugriff (PDF)

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

Human molecular genetics, 2014-12, Vol.23 (23), p.6139-6146

2014

Volltextzugriff (PDF)

Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study

Human molecular genetics, 2017-09, Vol.26 (17), p.3442-3450

2017

Volltextzugriff (PDF)

Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency

Human molecular genetics, 2004-09, Vol.13 (18), p.1999-2010

2004

Volltextzugriff (PDF)

A genetic modifier suggests that endurance exercise exacerbates Huntington's disease

Human molecular genetics, 2018-05, Vol.27 (10), p.1723-1731

2018

Volltextzugriff (PDF)

The transgenic expression of LARGE exacerbates the muscle phenotype of dystroglycanopathy mice

Human molecular genetics, 2014-04, Vol.23 (7), p.1842-1855

2014

Volltextzugriff (PDF)

Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation

Human molecular genetics, 2017-07, Vol.26 (14), p.2791-2802

2017

Volltextzugriff (PDF)

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia

Human molecular genetics, 2009-02, Vol.18 (3), p.497-516

2009

Volltextzugriff (PDF)

Validation of genome-wide association study (GWAS)-identified disease risk alleles with patient-specific stem cell lines

Human molecular genetics, 2014-07, Vol.23 (13), p.3445-3455

2014

Volltextzugriff (PDF)

1 – 25 von 112

Suche als RSS-Feed

Aktive Filter

KollektionMEDLINE

Zeitschrift / SerieHuman Molecular Genetics

ThemaBiochemistry & Molecular Biology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(112)
Mit Volltextzugriff
(112)

Publikationsform

Artikel
(112)

Sprache

Englisch
(112)
Japanisch
(38)

Erscheinungsjahr

n.n

Thema

Genetics & Heredity
(112)
Life Sciences & Biomedicine
(112)
Science & Technology
(112)
Humans
(98)
Biological And Medical Sciences
(67)
Fundamental And Applied Biological Sciences. Psychology
(50)
Female
(45)
Male
(45)
Molecular And Cellular Biology
(40)
Animals
(38)
Genetics Of Eukaryotes. Biological And Molecular Evolution
(38)
Mice
(29)
Mutation
(29)
Medical Sciences
(27)
Adult
(24)
Association Studies
(22)
Middle Aged
(22)
Genetic Predisposition To Disease
(21)
Molecular Sequence Data
(21)

14 weitere anzeigen...

Weniger anzeigen...

Kollektion

2 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Menü

Weitere Dienste

Einstellungen

Efficient Conditional Mutation of the Vertebrate CENP-C Gene

Human mini-chromosomes with minimal centromeres

Dissecting the centromere of the human Y chromosome with cloned telomeric DNA

The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes

Early and progressive circadian abnormalities in Huntington's disease sheep are unmasked by social environment

Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis

Identification of 70 calcium-sensing receptor mutations in hyper- and hypo-calcaemic patients: evidence for clustering of extracellular domain mutations at calcium-binding sites

Genetic landscape of auditory dysfunction

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle

Reduced striatal dopamine underlies the attention system dysfunction in neurofibromatosis-1 mutant mice

Mitochondrial damage revealed by immunoselection for ALS-linked misfolded SOD1

Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth

A point mutation in the ion conduction pore of AMPA receptor GRIA3 causes dramatically perturbed sleep patterns as well as intellectual disability

Genetic control of the alternative pathway of complement in humans and age-related macular degeneration

Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies

Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis

Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency

A genetic modifier suggests that endurance exercise exacerbates Huntington's disease

The transgenic expression of LARGE exacerbates the muscle phenotype of dystroglycanopathy mice

Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation

Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia

Validation of genome-wide association study (GWAS)-identified disease risk alleles with patient-specific stem cell lines

Aktive Filter

Suchergebnisse filtern