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...

Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations

Nature neuroscience, 2002-01, Vol.5 (1), p.41-47

2002

Volltextzugriff (PDF)

Pitpnm1 is expressed in hair cells during development but is not required for hearing

Neuroscience, 2013-09, Vol.248, p.620-625

2013

Volltextzugriff (PDF)

A type VII myosin encoded by the mouse deafness gene shaker-1

Nature (London), 1995-03, Vol.374 (6517), p.62-64

1995

Volltextzugriff (PDF)

Mutation of the Na-K-Cl Co-Transporter Gene Slc12a2 Results in Deafness in Mice

Human molecular genetics, 1999-08, Vol.8 (8), p.1579-1584

1999

Volltextzugriff (PDF)

Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip Link formation

Neuroscience, 2009-01, Vol.158 (2), p.365-368

2009

Volltextzugriff (PDF)

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

Nature genetics, 1997-06, Vol.16 (2), p.188-190

1997

Volltextzugriff (PDF)

Myosin VIIA Is Required for Aminoglycoside Accumulation in Cochlear Hair Cells

The Journal of neuroscience, 1997-12, Vol.17 (24), p.9506-9519

1997

Volltextzugriff (PDF)

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

Human molecular genetics, 2000, Vol.9 (1), p.63-67

2000

Volltextzugriff (PDF)

Electroretinographic Anomalies in Mice with Mutations in Myo7a, the Gene Involved in Human Usher Syndrome Type 1B

Investigative ophthalmology & visual science, 2001-03, Vol.42 (3), p.770-778

2001

Volltextzugriff (PDF)

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Current biology, 2003-07, Vol.13 (13), p.1129-1133

2003

Volltextzugriff (PDF)

TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor

Development (Cambridge), 1992-08, Vol.115 (4), p.1111-1119

1992

Volltextzugriff (PDF)

A New Era in the Genetics of Deafness

The New England journal of medicine, 1998-11, Vol.339 (21), p.1545-1547

Steel, Karen P

1998

Volltextzugriff (PDF)

Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear

Development (Cambridge), 1989-11, Vol.107 (3), p.453-463

1989

Volltextzugriff (PDF)

A genetic approach to understanding auditory function

Nature genetics, 2001-02, Vol.27 (2), p.143-149

2001

Volltextzugriff (PDF)

Mutations in Cdh23 , encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

Nature genetics, 2001-01, Vol.27 (1), p.103-107

2001

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)

Analysis of the Pax-3 Gene in the Mouse Mutant Splotch

Genomics (San Diego, Calif.), 1993-08, Vol.17 (2), p.355-363

1993

Volltextzugriff (PDF)

Genes and deafness

Trends in Genetics, 1994-12, Vol.10 (12), p.428-435

1994

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 Mutation (2314delG) in the Usher Syndrome Type IIA Gene: High Prevalence and Phenotypic Variation

American journal of human genetics, 1999-04, Vol.64 (4), p.1221-1225

1999

Volltextzugriff (PDF)

Combined cochleo-saccular and neuroepithelial abnormalities in the Varitint-waddler-J ( Va J) mouse

Hearing research, 1998-09, Vol.123 (1), p.125-136

1998

Volltextzugriff (PDF)

Myosin VIIa Participates in Opsin Transport through The Photoreceptor Cilium

The Journal of neuroscience, 1999-08, Vol.19 (15), p.6267-6274

1999

Volltextzugriff (PDF)

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

Developmental biology, 1999-10, Vol.214 (2), p.331-341

1999

Volltextzugriff (PDF)

Genetic deafness: a step closer

Pediatrics (Evanston), 1999-03, Vol.103 (3), p.674-674

Steel, K P

1999

Volltextzugriff (PDF)

1 – 25 von 534

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(459)
Mit Volltextzugriff
(448)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(392)
Life Sciences & Biomedicine
(305)
Humans
(190)
Animals
(167)
Mice
(139)
Biological And Medical Sciences
(122)
Female
(102)
Male
(89)
Medical Sciences
(87)
Mutation
(86)
Physical Sciences
(63)
Genetics & Heredity
(62)
Deafness - Genetics
(61)
Adult
(44)
Mice, Mutant Strains
(43)
Middle Aged
(43)
Neurosciences & Neurology
(43)
Fundamental And Applied Biological Sciences. Psychology
(42)
Biochemistry & Molecular Biology
(41)
Aged
(38)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations

Pitpnm1 is expressed in hair cells during development but is not required for hearing

A type VII myosin encoded by the mouse deafness gene shaker-1

Mutation of the Na-K-Cl Co-Transporter Gene Slc12a2 Results in Deafness in Mice

Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip Link formation

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

Myosin VIIA Is Required for Aminoglycoside Accumulation in Cochlear Hair Cells

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

Electroretinographic Anomalies in Mice with Mutations in Myo7a, the Gene Involved in Human Usher Syndrome Type 1B

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

TRP-2/DT, a new early melanoblast marker, shows that steel growth factor (c-kit ligand) is a survival factor

A New Era in the Genetics of Deafness

Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear

A genetic approach to understanding auditory function

Mutations in Cdh23 , encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

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

Analysis of the Pax-3 Gene in the Mouse Mutant Splotch

Genes and deafness

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

A Mutation (2314delG) in the Usher Syndrome Type IIA Gene: High Prevalence and Phenotypic Variation

Combined cochleo-saccular and neuroepithelial abnormalities in the Varitint-waddler-J ( Va J) mouse

Myosin VIIa Participates in Opsin Transport through The Photoreceptor Cilium

Role of Myosin VI in the Differentiation of Cochlear Hair Cells

Genetic deafness: a step closer

Suchergebnisse filtern