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...

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

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

2008

Volltextzugriff (PDF)

Expression Pattern of G Protein-Coupled Receptor 30 in LacZ Reporter Mice

Endocrinology (Philadelphia), 2009-04, Vol.150 (4), p.1722-1730

2009

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Effects of G-protein mutations on skin color

Nature genetics, 2004-09, Vol.36 (9), p.961-968

2004

Volltextzugriff (PDF)

Modeling hepatic osteodystrophy in Abcb4 deficient mice

Bone (New York, N.Y.), 2013-08, Vol.55 (2), p.501-511

2013

Volltextzugriff (PDF)

The transcription factor Smad-interacting protein 1 controls pain sensitivity via modulation of DRG neuron excitability

Pain (Amsterdam), 2011-10, Vol.152 (10), p.2384-2398

2011

Volltextzugriff (PDF)

Sex-Dependent Susceptibility to Listeria monocytogenes Infection Is Mediated by Differential Interleukin-10 Production

Infection and Immunity, 2005-09, Vol.73 (9), p.5952-5960

2005

Volltextzugriff (PDF)

Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice

Investigative ophthalmology & visual science, 2004-02, Vol.45 (2), p.601-609

2004

Volltextzugriff (PDF)

Clinical Chemistry of Congenic Mice with Quantitative Trait Loci for Predicted Responses to Trypanosoma congolense Infection

Infection and Immunity, 2009-09, Vol.77 (9), p.3948-3957

2009

Volltextzugriff (PDF)

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

Nature genetics, 2009-05, Vol.41 (5), p.614-618

2009

Volltextzugriff (PDF)

Characterization of a Mutation in the Lens-specific MP70 Encoding Gene of the Mouse Leading to a Dominant Cataract

Experimental eye research, 2001-12, Vol.73 (6), p.867-876

2001

Volltextzugriff (PDF)

Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport

Science (American Association for the Advancement of Science), 2003-05, Vol.300 (5620), p.808-812

2003

Volltextzugriff (PDF)

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36

Nature genetics, 2002-03, Vol.30 (3), p.257-258

2002

Volltextzugriff (PDF)

A New Fgf10 Mutation in the Mouse Leads to Atrophy of the Harderian Gland and Slit-Eye Phenotype in Heterozygotes: A Novel Model for Dry-Eye Disease?

Investigative ophthalmology & visual science, 2009-09, Vol.50 (9), p.4311-4318

2009

Volltextzugriff (PDF)

Genomewide Linkage Analysis Identifies Novel Genetic Loci for Lung Function in Mice

American journal of respiratory and critical care medicine, 2005-04, Vol.171 (8), p.880-888

2005

Volltextzugriff (PDF)

Mutation in a Novel Connexin-like Gene (Gjf1) in the Mouse Affects Early Lens Development and Causes a Variable Small-Eye Phenotype

Investigative ophthalmology & visual science, 2008-04, Vol.49 (4), p.1525-1532

2008

Volltextzugriff (PDF)

A Novel Missense Mutation in the Mouse Growth Hormone Gene Causes Semidominant Dwarfism, Hyperghrelinemia, and Obesity

Endocrinology (Philadelphia), 2004-05, Vol.145 (5), p.2531-2541

2004

Volltextzugriff (PDF)

Three Novel Pax6 Alleles in the Mouse Leading to the Same Small-Eye Phenotype Caused by Different Consequences at Target Promoters

Investigative ophthalmology & visual science, 2005-12, Vol.46 (12), p.4671-4683

2005

Volltextzugriff (PDF)

A Mouse Keratin 1 Mutation Causes Dark Skin and Epidermolytic Hyperkeratosis

Journal of investigative dermatology, 2006-05, Vol.126 (5), p.1013-1016

2006

Volltextzugriff (PDF)

Systematic gene expression profiling of mouse model series reveals coexpressed genes: Human Brain Proteomics

Proteomics (Weinheim), 2008, Vol.8 (6), p.1248-1256

2008

Volltextzugriff (PDF)

Mutation of the Na+-K+-2Cl- cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia

American journal of physiology. Renal physiology, 2010, Vol.67 (6)

2010

Volltextzugriff (PDF)

Identification of a Keratin 4 Mutation in a Chemically Induced Mouse Mutant that Models White Sponge Nevus

Journal of investigative dermatology, 2007-01, Vol.127 (1), p.60-64

2007

Volltextzugriff (PDF)

Hush Puppy: A New Mouse Mutant With Pinna, Ossicle, and Inner Ear Defects

The Laryngoscope, 2005-01, Vol.115 (1), p.116-124

2005

Volltextzugriff (PDF)

1 – 25 von 184

Suche als RSS-Feed

Aktive Filter

ThemaBiological And Medical Sciences

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(173)
Mit Volltextzugriff
(153)

Publikationsform

Artikel
(184)

Sprache

Englisch
(184)
Japanisch
(31)

Erscheinungsjahr

n.n

Thema

Science & Technology
(166)
Life Sciences & Biomedicine
(162)
Humans
(141)
Medical Sciences
(136)
Male
(103)
Female
(98)
Neopterin
(65)
Biopterins - Analogs & Derivatives
(64)
Fundamental And Applied Biological Sciences. Psychology
(59)
Adult
(52)
Middle Aged
(49)
Aged
(43)
Animals
(43)
Mice
(34)
Immunology
(33)
Immunopathology
(29)
Biopterins - Urine
(26)
Immunodeficiencies. Immunoglobulinopathies
(25)
Immunodeficiencies
(24)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects

Expression Pattern of G Protein-Coupled Receptor 30 in LacZ Reporter Mice

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

Effects of G-protein mutations on skin color

Modeling hepatic osteodystrophy in Abcb4 deficient mice

The transcription factor Smad-interacting protein 1 controls pain sensitivity via modulation of DRG neuron excitability

Immune modulation by Fas ligand reverse signaling: lymphocyte proliferation is attenuated by the intracellular Fas ligand domain

Sex-Dependent Susceptibility to Listeria monocytogenes Infection Is Mediated by Differential Interleukin-10 Production

Electroretinography as a Screening Method for Mutations Causing Retinal Dysfunction in Mice

Clinical Chemistry of Congenic Mice with Quantitative Trait Loci for Predicted Responses to Trypanosoma congolense Infection

An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice

Characterization of a Mutation in the Lens-specific MP70 Encoding Gene of the Mouse Leading to a Dominant Cataract

Genome-wide, large-scale production of mutant mice by ENU mutagenesis

Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36

A New Fgf10 Mutation in the Mouse Leads to Atrophy of the Harderian Gland and Slit-Eye Phenotype in Heterozygotes: A Novel Model for Dry-Eye Disease?

Genomewide Linkage Analysis Identifies Novel Genetic Loci for Lung Function in Mice

Mutation in a Novel Connexin-like Gene (Gjf1) in the Mouse Affects Early Lens Development and Causes a Variable Small-Eye Phenotype

A Novel Missense Mutation in the Mouse Growth Hormone Gene Causes Semidominant Dwarfism, Hyperghrelinemia, and Obesity

Three Novel Pax6 Alleles in the Mouse Leading to the Same Small-Eye Phenotype Caused by Different Consequences at Target Promoters

A Mouse Keratin 1 Mutation Causes Dark Skin and Epidermolytic Hyperkeratosis

Systematic gene expression profiling of mouse model series reveals coexpressed genes: Human Brain Proteomics

Mutation of the Na+-K+-2Cl- cotransporter NKCC2 in mice is associated with severe polyuria and a urea-selective concentrating defect without hyperreninemia

Identification of a Keratin 4 Mutation in a Chemically Induced Mouse Mutant that Models White Sponge Nevus

Hush Puppy: A New Mouse Mutant With Pinna, Ossicle, and Inner Ear Defects

Aktive Filter

Suchergebnisse filtern