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...

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways

PLoS genetics, 2017-08, Vol.13 (8), p.e1006969

2017

Volltextzugriff (PDF)

Quiet as a mouse: dissecting the molecular and genetic basis of hearing

Nature reviews. Genetics, 2008-04, Vol.9 (4), p.277-290

2008

Volltextzugriff (PDF)

Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness

PloS one, 2013-02, Vol.8 (2), p.e56274

2013

Volltextzugriff (PDF)

A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse

Human molecular genetics, 2006-11, Vol.15 (22), p.3273-3279

2006

Volltextzugriff (PDF)

Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media

PLoS genetics, 2006-10, Vol.2 (10), p.e149-e149

2006

Volltextzugriff (PDF)

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

Nature genetics, 2003-08, Vol.34 (4), p.421-428

2003

Volltextzugriff (PDF)

The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media

Journal of the Association for Research in Otolaryngology, 2003-06, Vol.4 (2), p.130-138

2003

Volltextzugriff (PDF)

A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment

Nature protocols, 2010-01, Vol.5 (1), p.177-190

2010

Volltextzugriff (PDF)

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti

Human molecular genetics, 2001-03, Vol.10 (5), p.507-512

2001

Volltextzugriff (PDF)

Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells

The Journal of neuroscience, 2013-03, Vol.33 (10), p.4395-4404

2013

Volltextzugriff (PDF)

Mutagenesis strategies for identifying novel loci associated with disease phenotypes

Seminars in cell & developmental biology, 2003-02, Vol.14 (1), p.19-24

2003

Volltextzugriff (PDF)

Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice

Mammalian genome, 2010-12, Vol.21 (11-12), p.565-576

2010

Volltextzugriff (PDF)

A mutation in Nischarin causes otitis media via LIMK1 and NF-KB pathways

PLoS genetics, 2017-08, Vol.13 (8)

2017

Volltextzugriff (PDF)

The molecular genetics of inherited deafness – current knowledge and recent advances

Journal of laryngology and otology, 1998-05, Vol.112 (5), p.432-437

1998

Volltextzugriff (PDF)

Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B)

Biochemical journal, 2001-03, Vol.354 (Pt 2), p.267-274

2001

Volltextzugriff (PDF)

Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B)

Biochemical journal, 2001-03, Vol.354 (2), p.267-274

2001

Volltextzugriff (PDF)

Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study

Archives of otolaryngology--head & neck surgery, 2006-07, Vol.132 (7), p.729

2006

Volltextzugriff (PDF)

Regulation of TGF-beta signalling by Fbxo11, the gene mutated in the Jeff otitis media mouse mutant

PathoGenetics, 2009-07, Vol.2 (1), p.5-5, Article 5

2009

Volltextzugriff (PDF)

Models of congenital deafness: Mouse and zebrafish

Drug discovery today. Disease models, 2005, Vol.2 (2), p.85-92

2005

Volltextzugriff (PDF)

Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss

The Journal of neuroscience, 2016-01, Vol.36 (1), p.222-234

2016

Volltextzugriff (PDF)

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

Nature genetics, 2000-08, Vol.25 (4), p.440-443

2000

Volltextzugriff (PDF)

A radiation hybrid map of mouse genes

Nature genetics, 2001-10, Vol.29 (2), p.201-205

2001

Volltextzugriff (PDF)

1 – 23 von 23

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(22)
Mit Volltextzugriff
(21)

Publikationsform

Artikel
(23)

Sprache

Englisch
(23)

Erscheinungsjahr

n.n

Thema

Animals
(19)
Mice
(19)
Science & Technology
(18)
Life Sciences & Biomedicine
(17)
Genetics & Heredity
(10)
Phenotype
(10)
Chromosome Mapping
(9)
Disease Models, Animal
(9)
Biological And Medical Sciences
(8)
Mutagenesis
(8)
Mutation
(8)
Genetics
(7)
Humans
(7)
Fundamental And Applied Biological Sciences. Psychology
(6)
Genes
(6)
Genetic Aspects
(6)
Hearing Loss
(6)
Amino Acid Sequence
(5)
Biochemistry & Molecular Biology
(5)
Deafness - Genetics
(5)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways

Quiet as a mouse: dissecting the molecular and genetic basis of hearing

Headbobber: a combined morphogenetic and cochleosaccular mouse model to study 10qter deletions in human deafness

A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse

Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media

Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31

The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media

A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti

Noddy, a mouse harboring a missense mutation in protocadherin-15, reveals the impact of disrupting a critical interaction site between tip-link cadherins in inner ear hair cells

Mutagenesis strategies for identifying novel loci associated with disease phenotypes

Melody, an ENU mutation in Caspase 3, alters the catalytic cysteine residue and causes sensorineural hearing loss in mice

A mutation in Nischarin causes otitis media via LIMK1 and NF-KB pathways

The molecular genetics of inherited deafness – current knowledge and recent advances

Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B)

Myosin VIIA is specifically associated with calmodulin and microtubule-associated protein-2B (MAP-2B)

Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study

Regulation of TGF-beta signalling by Fbxo11, the gene mutated in the Jeff otitis media mouse mutant

Models of congenital deafness: Mouse and zebrafish

Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

A radiation hybrid map of mouse genes

Towards a mutant map of the mouse--new models of neurological, behavioural, deafness, bone, renal and blood disorders

Suchergebnisse filtern