UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 78

Sortiert nach

Epigenetic germline inheritance of diet-induced obesity and insulin resistance

Nature genetics, 2016-05, Vol.48 (5), p.497-499

2016

Link zum Volltext

Verfügbarkeit prüfen

AMPK Subunits Harbor Largely Nonoverlapping Genetic Determinants for Body Fat Mass, Glucose Metabolism, and Cholesterol Metabolism

The journal of clinical endocrinology and metabolism, 2020-01, Vol.105 (1), p.14-25

2020

Link zum Volltext

Verfügbarkeit prüfen

New mutation in the mouse Xpd/Ercc2 gene leads to recessive cataracts

PloS one, 2015-05, Vol.10 (5), p.e0125304

2015

Link zum Volltext

Verfügbarkeit prüfen

Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice

Human molecular genetics, 2013-10, Vol.22 (20), p.4148-4163

2013

Link zum Volltext

Verfügbarkeit prüfen

Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in mice

Journal of inherited metabolic disease, 2016-03, Vol.39 (2), p.309-319

2016

Link zum Volltext

Verfügbarkeit prüfen

Maintenance of somite borders in mice requires the Delta homologue Dll1

Nature (London), 1997-04, Vol.386 (6626), p.717-721

1997

Link zum Volltext

Verfügbarkeit prüfen

Uromodulin retention in thick ascending limb of Henle's loop affects SCD1 in neighboring proximal tubule: renal transcriptome studies in mouse models of uromodulin-associated kidney disease

PloS one, 2014-11, Vol.9 (11), p.e113125

2014

Link zum Volltext

Verfügbarkeit prüfen

Common genetic variation in the human FNDC5 locus, encoding the novel muscle-derived 'browning' factor irisin, determines insulin sensitivity

PloS one, 2013-04, Vol.8 (4), p.e61903-e61903

2013

Link zum Volltext

Verfügbarkeit prüfen

Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum

PLoS genetics, 2008-11, Vol.4 (11), p.e1000282-e1000282

2008

Link zum Volltext

Verfügbarkeit prüfen

Metabolic footprint of diabetes: a multiplatform metabolomics study in an epidemiological setting

PloS one, 2010-11, Vol.5 (11), p.e13953

2010

Link zum Volltext

Verfügbarkeit prüfen

Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors

Human molecular genetics, 2013-12, Vol.22 (24), p.4871-4887

2013

Link zum Volltext

Verfügbarkeit prüfen

Mitochondrial glutathione peroxidase 4 disruption causes male infertility

The FASEB journal, 2009-09, Vol.23 (9), p.3233-3242

2009

Link zum Volltext

Verfügbarkeit prüfen

INFRAFRONTIER quality principles in systemic phenotyping

Mammalian genome, 2022-03, Vol.33 (1), p.120-122

2022

Link zum Volltext

Verfügbarkeit prüfen

Unbiased analysis of obesity related, fat depot specific changes of adipocyte volumes and numbers using light sheet fluorescence microscopy

PloS one, 2021-03, Vol.16 (3), p.e0248594-e0248594

2021

Link zum Volltext

Verfügbarkeit prüfen

Impact of temporal variation on design and analysis of mouse knockout phenotyping studies

PloS one, 2014-10, Vol.9 (10), p.e111239-e111239

2014

Link zum Volltext

Verfügbarkeit prüfen

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

Nature genetics, 2008-08, Vol.40 (8), p.963-970

2008

Link zum Volltext

Verfügbarkeit prüfen

Clinical chemistry of human FcRn transgenic mice

Mammalian genome, 2012-04, Vol.23 (3-4), p.259-269

2012

Link zum Volltext

Verfügbarkeit prüfen

From dynamic expression patterns to boundary formation in the presomitic mesoderm

PLoS computational biology, 2012-06, Vol.8 (6), p.e1002586

2012

Link zum Volltext

Verfügbarkeit prüfen

Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms

Human molecular genetics, 2012-08, Vol.21 (16), p.3535-3545

2012

Link zum Volltext

Verfügbarkeit prüfen

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis

Mammalian genome, 2012-08, Vol.23 (7-8), p.416-430

2012

Link zum Volltext

Verfügbarkeit prüfen

Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation

The Journal of biological chemistry, 2010-07, Vol.285 (28), p.21724-21735

2010

Link zum Volltext

Verfügbarkeit prüfen

ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta

PLoS genetics, 2008-02, Vol.4 (2), p.e7

2008

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 78

Suche als RSS-Feed

Aktive Filter

ThemaGenetics

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(73)
Mit Volltextzugriff
(72)

Publikationsform

Sprache

Englisch
(78)
Japanisch
(45)

Erscheinungsjahr

n.n

Thema

Science & Technology
(64)
Animals
(58)
Mice
(53)
Life Sciences & Biomedicine
(49)
Genetics & Heredity
(37)
Male
(32)
Mutation
(29)
Female
(26)
Humans
(24)
Biochemistry & Molecular Biology
(23)
Genomes
(22)
Phenotype
(22)
Life Sciences
(19)
Biotechnology & Applied Microbiology
(17)
Disease Models, Animal
(17)
Mutagenesis
(17)
Proteins
(17)
Rodents
(16)
Genes
(15)

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Mammalian Genome
(15)
Plos One
(14)
Nature Genetics
(7)
Plos Genetics
(5)
Genetics
(3)
Human Molecular Genetics
(3)
Nature
(3)
Mutation Research
(2)
The Faseb Journal
(2)
American Journal Of Respiratory And Critical Care Medicine
(1)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Epigenetic germline inheritance of diet-induced obesity and insulin resistance

AMPK Subunits Harbor Largely Nonoverlapping Genetic Determinants for Body Fat Mass, Glucose Metabolism, and Cholesterol Metabolism

New mutation in the mouse Xpd/Ercc2 gene leads to recessive cataracts

Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice

Mildly compromised tetrahydrobiopterin cofactor biosynthesis due to Pts variants leads to unusual body fat distribution and abdominal obesity in mice

Maintenance of somite borders in mice requires the Delta homologue Dll1

Uromodulin retention in thick ascending limb of Henle's loop affects SCD1 in neighboring proximal tubule: renal transcriptome studies in mouse models of uromodulin-associated kidney disease

Common genetic variation in the human FNDC5 locus, encoding the novel muscle-derived 'browning' factor irisin, determines insulin sensitivity

Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum

Metabolic footprint of diabetes: a multiplatform metabolomics study in an epidemiological setting

Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors

Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project

Mitochondrial glutathione peroxidase 4 disruption causes male infertility

INFRAFRONTIER quality principles in systemic phenotyping

Laboratory mouse housing conditions can be improved using common environmental enrichment without compromising data

Unbiased analysis of obesity related, fat depot specific changes of adipocyte volumes and numbers using light sheet fluorescence microscopy

Impact of temporal variation on design and analysis of mouse knockout phenotyping studies

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

Clinical chemistry of human FcRn transgenic mice

From dynamic expression patterns to boundary formation in the presomitic mesoderm

Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms

New mouse models for metabolic bone diseases generated by genome-wide ENU mutagenesis

Calcium Oxalate Stone Formation in the Inner Ear as a Result of an Slc26a4 Mutation

ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta

Cox4i2, Ifit2, and Prdm11 Mutant Mice: Effective Selection of Genes Predisposing to an Altered Airway Inflammatory Response from a Large Compendium of Mutant Mouse Lines

Aktive Filter

Suchergebnisse filtern