UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 58

Sortiert nach

The social value of genomic sequencing for disadvantaged families facing rare disease

Social science & medicine (1982), 2022-12, Vol.314, p.115465-115465, Article 115465

2022

Volltextzugriff (PDF)

Oxidative stress, cell cycle, and neurodegeneration

The Journal of clinical investigation, 2003-03, Vol.111 (6), p.785-793

2003

Volltextzugriff (PDF)

Divide and die: cell cycle events as triggers of nerve cell death

The Journal of neuroscience, 2004-10, Vol.24 (42), p.9232-9239

2004

Volltextzugriff (PDF)

Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP

Nature genetics, 2005-09, Vol.37 (9), p.974-979

2005

Volltextzugriff (PDF)

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition

Human molecular genetics, 2001-03, Vol.10 (5), p.433-443

2001

Volltextzugriff (PDF)

The Netrin 1 Receptors Unc5h3 and Dcc Are Necessary at Multiple Choice Points for the Guidance of Corticospinal Tract Axons

The Journal of neuroscience, 2002-12, Vol.22 (23), p.10346-10356

2002

Volltextzugriff (PDF)

Vertebrate homologues of C. elegans UNC-5 are candidate netrin receptors

Nature (London), 1997-04, Vol.386 (6627), p.833-838

1997

Volltextzugriff (PDF)

Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells

The Journal of neuroscience, 2001-08, Vol.21 (16), p.6095-6104

2001

Volltextzugriff (PDF)

Dorsally derived netrin 1 provides an inhibitory cue and elaborates the `waiting period' for primary sensory axons in the developing spinal cord

Development (Cambridge), 2006-04, Vol.133 (7), p.1379-1387

2006

Volltextzugriff (PDF)

Downregulation of Apoptosis-Inducing Factor in Harlequin Mutant Mice Sensitizes the Myocardium to Oxidative Stress–Related Cell Death and Pressure Overload–Induced Decompensation

Circulation research, 2005-06, Vol.96 (12), p.e92-e101

2005

Volltextzugriff (PDF)

Phosphatidylinositol transfer protein-α in netrin-1-induced PLC signalling and neurite outgrowth

Nature cell biology, 2005-11, Vol.7 (11), p.1124-1132

2005

Volltextzugriff (PDF)

In Vivo Magnetic Resonance Imaging and Semiautomated Image Analysis Extend the Brain Phenotype for cdf/cdf Mice

The Journal of neuroscience, 2006-04, Vol.26 (17), p.4455-4459

2006

Volltextzugriff (PDF)

Netrin 1-mediated chemoattraction regulates the migratory pathway of LHRH neurons

The European journal of neuroscience, 2004-01, Vol.19 (1), p.11-20

2004

Volltextzugriff (PDF)

Deletion in Catna2 , encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Nature genetics, 2002-07, Vol.31 (3), p.279-284

2002

Volltextzugriff (PDF)

The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein

Nature (London), 1997-04, Vol.386 (6627), p.838-842

1997

Volltextzugriff (PDF)

Effect of alcaftadine 0.25% on ocular itch associated with seasonal or perennial allergic conjunctivitis: a pooled analysis of two multicenter randomized clinical trials

Clinical ophthalmology (Auckland, N.Z.), 2015-01, Vol.9 (default), p.765-772

2015

Volltextzugriff (PDF)

Embryonic phenotype of Unc5h3 mutant mice suggests chemorepulsion during the formation of the rostral cerebellar boundary

Development (Cambridge), 1998-01, Vol.125 (1), p.41-50

1998

Volltextzugriff (PDF)

Abnormal dispersion of a purkinje cell subset in the mouse mutant cerebellar deficient folia (cdf)

Journal of comparative neurology (1911), 2001-07, Vol.436 (1), p.42-51

2001

Volltextzugriff (PDF)

New member of the Snf1/AMPK kinase family, Melk, is expressed in the mouse egg and preimplantation embryo

Molecular reproduction and development, 1997-06, Vol.47 (2), p.148-156

1997

Volltextzugriff (PDF)

Genomewide two-generation screens for recessive mutations by ES cell mutagenesis

Mammalian genome, 2004-12, Vol.15 (12), p.960-965

2004

Volltextzugriff (PDF)

Mouse models for the Wolf-Hirschhorn deletion syndrome

Human molecular genetics, 2001-01, Vol.10 (2), p.91-98

2001

Volltextzugriff (PDF)

The cerebellar deficient folia (cdf) gene acts intrinsically in Purkinje cell migrations

Genesis (New York, N.Y. : 2000), 2002-01, Vol.32 (1), p.32-41

2002

Volltextzugriff (PDF)

Cloning and mapping of the UNC5C gene to human chromosome 4q21-q23

Genomics (San Diego, Calif.), 1998-09, Vol.52 (2), p.205-208

1998

Volltextzugriff (PDF)

Functional Significance of an Overlapping Consensus Binding Motif for Sp1 and Zif268 in the Murine Adenosine Deaminase Gene Promoter

Proceedings of the National Academy of Sciences - PNAS, 1991-09, Vol.88 (17), p.7523-7527

1991

Volltextzugriff (PDF)

Genetic and Physical Mapping of the Cerebellar Deficient Folia (cdf) Locus on Mouse Chromosome 6

Genomics (San Diego, Calif.), 2000-10, Vol.69 (1), p.135-138

2000

Volltextzugriff (PDF)

1 – 25 von 58

Suche als RSS-Feed

Aktive Filter

ThemaGenetics

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(53)
Mit Volltextzugriff
(52)

Publikationsform

Artikel
(56)
Tagungsberichte
(2)

Sprache

Englisch
(58)
Japanisch
(16)

Erscheinungsjahr

n.n

Thema

Science & Technology
(57)
Life Sciences & Biomedicine
(48)
Animals
(29)
Humans
(29)
Biological And Medical Sciences
(24)
Mice
(21)
Female
(18)
Male
(17)
Medical Sciences
(15)
Mutation
(15)
Adult
(11)
Genetics & Heredity
(11)
Fundamental And Applied Biological Sciences. Psychology
(10)
Cardiomyopathy, Hypertrophic - Genetics
(9)
Molecular Sequence Data
(9)
Phenotype
(9)
Child
(8)
Homozygote
(8)
Middle Aged
(8)
Cardiac & Cardiovascular Systems
(7)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The social value of genomic sequencing for disadvantaged families facing rare disease

Oxidative stress, cell cycle, and neurodegeneration

Divide and die: cell cycle events as triggers of nerve cell death

Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition

The Netrin 1 Receptors Unc5h3 and Dcc Are Necessary at Multiple Choice Points for the Guidance of Corticospinal Tract Axons

Vertebrate homologues of C. elegans UNC-5 are candidate netrin receptors

Ducky Mouse Phenotype of Epilepsy and Ataxia Is Associated with Mutations in the Cacna2d2 Gene and Decreased Calcium Channel Current in Cerebellar Purkinje Cells

Dorsally derived netrin 1 provides an inhibitory cue and elaborates the `waiting period' for primary sensory axons in the developing spinal cord

Downregulation of Apoptosis-Inducing Factor in Harlequin Mutant Mice Sensitizes the Myocardium to Oxidative Stress–Related Cell Death and Pressure Overload–Induced Decompensation

Phosphatidylinositol transfer protein-α in netrin-1-induced PLC signalling and neurite outgrowth

In Vivo Magnetic Resonance Imaging and Semiautomated Image Analysis Extend the Brain Phenotype for cdf/cdf Mice

Netrin 1-mediated chemoattraction regulates the migratory pathway of LHRH neurons

Deletion in Catna2 , encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

The mouse rostral cerebellar malformation gene encodes an UNC-5-like protein

Effect of alcaftadine 0.25% on ocular itch associated with seasonal or perennial allergic conjunctivitis: a pooled analysis of two multicenter randomized clinical trials

Embryonic phenotype of Unc5h3 mutant mice suggests chemorepulsion during the formation of the rostral cerebellar boundary

Abnormal dispersion of a purkinje cell subset in the mouse mutant cerebellar deficient folia (cdf)

New member of the Snf1/AMPK kinase family, Melk, is expressed in the mouse egg and preimplantation embryo

Genomewide two-generation screens for recessive mutations by ES cell mutagenesis

Mouse models for the Wolf-Hirschhorn deletion syndrome

The cerebellar deficient folia (cdf) gene acts intrinsically in Purkinje cell migrations

Cloning and mapping of the UNC5C gene to human chromosome 4q21-q23

Functional Significance of an Overlapping Consensus Binding Motif for Sp1 and Zif268 in the Murine Adenosine Deaminase Gene Promoter

Genetic and Physical Mapping of the Cerebellar Deficient Folia (cdf) Locus on Mouse Chromosome 6

Aktive Filter

Suchergebnisse filtern