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Search results 1 to 100 out of 412 for Dst

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0.054s
Type Details Score
Gene
Type: gene
Organism: human
Gene
Type: gene
Organism: chimpanzee
Gene
Type: gene
Organism: dog, domestic
Gene
Type: gene
Organism: cattle
Gene
Type: gene
Organism: chicken
Gene
Type: gene
Organism: zebrafish
Gene
Type: gene
Organism: macaque, rhesus
Gene
Type: gene
Organism: frog, western clawed
Gene
Type: gene
Organism: rat
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Gene
Type: gene
Organism: human
Publication      
First Author: Harris B
Year: 2006
Journal: MGI Direct Data Submission
Title: Dst35J, a remutation of Dst
GXD Expression    
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1689419
Pattern: Not Specified
Stage: TS19
Assay Id: MGI:6190154
Age: embryonic day 11.5
Specimen Label: Table S2 - E11.5 - Dst
Detected: true
Specimen Num: 1
GXD Expression    
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689424
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:6190154
Age: embryonic day 15.5
Specimen Label: Table S2 - E15.5 - Dst
Detected: true
Specimen Num: 3
GXD Expression    
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689426
Pattern: Not Specified
Stage: TS26
Assay Id: MGI:6190154
Age: embryonic day 18.5
Specimen Label: Table S2 - E18.5 - Dst
Detected: true
Specimen Num: 4
GXD Expression    
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689428
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6190154
Age: postnatal day 14
Specimen Label: Table S2 - P14 - Dst
Detected: true
Specimen Num: 6
GXD Expression    
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689428
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6190154
Age: postnatal day 28
Specimen Label: Table S2 - P28 - Dst
Detected: true
Specimen Num: 7
GXD Expression    
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1689421
Pattern: Not Specified
Stage: TS21
Assay Id: MGI:6190154
Age: embryonic day 13.5
Specimen Label: Table S2 - E13.5 - Dst
Detected: true
Specimen Num: 2
GXD Expression    
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689428
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6190154
Age: postnatal day 4
Specimen Label: Table S2 - P4 - Dst
Detected: true
Specimen Num: 5
Publication  
First Author: Yoshioka N
Year: 2020
Journal: Dis Model Mech
Title: Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum mice.
Volume: 13
Issue: 5
Publication      
First Author: Dionne L
Year: 2010
Journal: Personal Communication
Title: Dystonia musculorum 39 Jackson
Publication      
First Author: Harris BS
Year: 1998
Journal: Personal Communication, The Jackson Laboratory
Title: Documentation of phenotype for allele Dstdt-31J
Publication      
First Author: Harris BS
Year: 1998
Journal: Personal Communication, The Jackson Laboratory
Title: Documentation of information for allele Dstdt-30J
Publication
First Author: Horie M
Year: 2014
Journal: Eur J Neurosci
Title: Disruption of actin-binding domain-containing Dystonin protein causes dystonia musculorum in mice.
Volume: 40
Issue: 10
Pages: 3458-71
Publication
First Author: Hossain MI
Year: 2018
Journal: Neurochem Res
Title: Reduced Proliferation of Oligodendrocyte Progenitor Cells in the Postnatal Brain of Dystonia Musculorum Mice.
Volume: 43
Issue: 1
Pages: 92-100
Publication  
First Author: Horie M
Year: 2016
Journal: Neurobiol Dis
Title: Characterization of novel dystonia musculorum mutant mice: Implications for central nervous system abnormality.
Volume: 96
Pages: 271-283
Publication
First Author: Horie M
Year: 2020
Journal: Glia
Title: Disruption of dystonin in Schwann cells results in late-onset neuropathy and sensory ataxia.
Volume: 68
Issue: 11
Pages: 2330-2344
Protein
Organism: Mus musculus/domesticus
Length: 232  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 267  
Fragment?: true
Publication    
First Author: Yoshioka N
Year: 2022
Journal: Elife
Title: Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy.
Volume: 11
Publication      
First Author: SoRelle J
Year: 2015
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for tinsel
Publication      
First Author: Hossain MI
Year: 2017
Journal: Neurochem Int
Title: Motoneuron degeneration in the trigeminal motor nucleus innervating the masseter muscle in Dystonia musculorum mice.
Publication      
First Author: The Jackson Laboratory Office of Genetic Resources
Year: 2000
Journal: MGI Direct Data Submission
Title: Registry of Remutation at The Jackson Laboratory
Publication
First Author: Bernier G
Year: 1998
Journal: Dev Genet
Title: Prenatal onset of axonopathy in Dystonia musculorum mice.
Volume: 22
Issue: 2
Pages: 160-8
Publication
First Author: Ferrier A
Year: 2014
Journal: Hum Mol Genet
Title: Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI.
Volume: 23
Issue: 10
Pages: 2694-710
Publication
First Author: Bernier G
Year: 1996
Journal: Genomics
Title: Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins.
Volume: 38
Issue: 1
Pages: 19-29
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
Publication
First Author: Dalpé G
Year: 1999
Journal: Dev Biol
Title: Dystonin-deficient mice exhibit an intrinsic muscle weakness and an instability of skeletal muscle cytoarchitecture.
Volume: 210
Issue: 2
Pages: 367-80
Publication
First Author: Leung CL
Year: 2001
Journal: J Cell Biol
Title: The BPAG1 locus: Alternative splicing produces multiple isoforms with distinct cytoskeletal linker domains, including predominant isoforms in neurons and muscles.
Volume: 154
Issue: 4
Pages: 691-7
Publication
First Author: Young KG
Year: 2006
Journal: Exp Cell Res
Title: A Bpag1 isoform involved in cytoskeletal organization surrounding the nucleus.
Volume: 312
Issue: 2
Pages: 121-34
Publication
First Author: Guo L
Year: 1995
Journal: Cell
Title: Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration.
Volume: 81
Issue: 2
Pages: 233-43
Publication
First Author: Yang Y
Year: 1996
Journal: Cell
Title: An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.
Volume: 86
Issue: 4
Pages: 655-65
Publication
First Author: Boyer JG
Year: 2010
Journal: PLoS One
Title: Hearts of dystonia musculorum mice display normal morphological and histological features but show signs of cardiac stress.
Volume: 5
Issue: 3
Pages: e9465
Publication      
First Author: Harris BS
Year: 2000
Journal: MGI Direct Data Submission
Title: The Jackson Laboratory Mouse Mutant Resource 2000 Mutation Reports
Publication
First Author: Eyer J
Year: 1998
Journal: Nature
Title: Pathogenesis of two axonopathies does not require axonal neurofilaments.
Volume: 391
Issue: 6667
Pages: 584-7
Publication
First Author: Pool M
Year: 2005
Journal: Mamm Genome
Title: Genetic alterations at the Bpag1 locus in dt mice and their impact on transcript expression.
Volume: 16
Issue: 12
Pages: 909-17
Publication
First Author: Messer A
Year: 1979
Journal: Life Sci
Title: Changes in whole tissue biosynthesis of gamma-amino butyric acid (GABA) in basal ganglia of the dystonia (dtAlb) mouse.
Volume: 25
Issue: 26
Pages: 2217-21
Publication  
First Author: Messer A
Year: 1978
Journal: Mouse News Lett
Title: Dstdt-alb - dystonia musculorum-Albany
Volume: 59
Pages: 39
Publication
First Author: Riker DK
Year: 1981
Journal: J Neurochem
Title: Increased noradrenergic metabolism in the cerebellum of the mouse mutant dystonia musculorum.
Volume: 37
Issue: 3
Pages: 649-54
Publication
First Author: Messer A
Year: 1980
Journal: Neuroscience
Title: An allele of the mouse mutant dystonia musculorum exhibits lesions in red nucleus and striatum.
Volume: 5
Issue: 3
Pages: 543-9
Publication
First Author: Dalpé G
Year: 1998
Journal: Mol Cell Neurosci
Title: Dystonin Is Essential for Maintaining Neuronal Cytoskeleton Organization.
Volume: 10
Issue: 5/6
Pages: 243-57
Publication  
First Author: Goryunov D
Year: 2007
Journal: Brain Res
Title: Molecular characterization of the genetic lesion in Dystonia musculorum (dt-Alb) mice.
Volume: 1140
Pages: 179-87
Publication
First Author: Bernier G
Year: 1995
Journal: Mol Cell Neurosci
Title: Dystonin expression in the developing nervous system predominates in the neurons that degenerate in dystonia musculorum mutant mice.
Volume: 6
Issue: 6
Pages: 509-20
Publication
First Author: Ryan SD
Year: 2012
Journal: Mol Biol Cell
Title: Neuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and function.
Volume: 23
Issue: 4
Pages: 553-66
Publication
First Author: De Repentigny Y
Year: 2003
Journal: J Neurochem
Title: Impaired fast axonal transport in neurons of the sciatic nerves from dystonia musculorum mice.
Volume: 86
Issue: 3
Pages: 564-71
Publication
First Author: De Repentigny Y
Year: 2011
Journal: PLoS One
Title: Motor unit abnormalities in Dystonia musculorum mice.
Volume: 6
Issue: 6
Pages: e21093
Publication  
First Author: Sweet HO
Year: 1994
Journal: Mouse Genome
Title: Remutation - dt27J
Volume: 92
Pages: 672
Publication
First Author: Kornfeld SF
Year: 2016
Journal: PLoS One
Title: Cytoskeletal Linker Protein Dystonin Is Not Critical to Terminal Oligodendrocyte Differentiation or CNS Myelination.
Volume: 11
Issue: 2
Pages: e0149201
Publication
First Author: Lynch-Godrei A
Year: 2018
Journal: Hum Mol Genet
Title: Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI.
Volume: 27
Issue: 20
Pages: 3598-3611
Publication
First Author: Bernier G
Year: 1998
Journal: Development
Title: Dystonin is an essential component of the Schwann cell cytoskeleton at the time of myelination.
Volume: 125
Issue: 11
Pages: 2135-48
Publication  
First Author: DUCHEN LW
Year: 1964
Journal: Brain
Title: CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM).
Volume: 87
Pages: 367-78
Publication
First Author: Moss TH
Year: 1981
Journal: J Neurol Sci
Title: Schwann cell involvement in the neurological lesion of the dystonic mutant mouse. A nerve grafting study.
Volume: 49
Issue: 2
Pages: 207-22
Publication  
First Author: Duchen LW
Year: 1976
Journal: Adv Neurol
Title: Dystonia musculorum--an inherited disease of the nervous system in the mouse.
Volume: 14
Pages: 353-65
Publication
First Author: Campbell RM
Year: 1992
Journal: Neuron
Title: An intrinsic neuronal defect operates in dystonia musculorum: a study of dt/dt<==>+/+ chimeras.
Volume: 9
Issue: 4
Pages: 693-703
Publication  
First Author: Falconer DS
Year: 1961
Journal: Mouse News Lett
Title: Mutation Dstdt dystonia musculorum
Volume: 25
Pages: 30
Publication
First Author: Hartmann N
Year: 1999
Journal: J Cell Biochem
Title: Dystonia musculorum mutation and myosin heavy chain expression in skeletal and cardiac muscles.
Volume: 74
Issue: 1
Pages: 90-8
Publication
First Author: Janota I
Year: 1972
Journal: Brain
Title: Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum).
Volume: 95
Issue: 3
Pages: 529-36
Publication  
First Author: Hanker JS
Year: 1976
Journal: Neuropathol Appl Neurobiol
Title: Histochemical and ultrastructural studies on primary sensory neurons in mice with dystonia musculorum. I. Acetylcholinesterase and lysosomal hydrolases.
Volume: 2
Pages: 79-97
Publication  
First Author: Lane PW
Year: 1958
Journal: Mouse News Lett
Title: Athetoid - ah
Volume: 19
Pages: 25
Publication
First Author: Lalonde R
Year: 2005
Journal: Physiol Behav
Title: Primary neurologic screening and motor coordination of Dstdt-J mutant mice (dystonia musculorum) with spinocerebellar atrophy.
Volume: 86
Issue: 1-2
Pages: 46-51
Publication
First Author: Lalonde R
Year: 1994
Journal: Physiol Behav
Title: Exploration and motor coordination in dystonia musculorum mutant mice.
Volume: 56
Issue: 2
Pages: 277-80
Publication
First Author: Lalonde R
Year: 1993
Journal: Physiol Behav
Title: Swimming activity in dystonia musculorum mutant mice.
Volume: 54
Issue: 1
Pages: 119-20
Publication
First Author: Kothary R
Year: 1988
Journal: Nature
Title: A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube.
Volume: 335
Issue: 6189
Pages: 435-7
Publication  
First Author: Falconer DS
Year: 1964
Journal: Mouse News Lett
Title: Allelism of athetoid (ah) and dystonia (dt)
Volume: 31
Pages: 21
Publication
First Author: Ongali B
Year: 2000
Journal: Synapse
Title: Dopamine D(1) and D(2) receptors in the forebrain of dystonia musculorum mutant mice: an autoradiographic survey in relation to dopamine contents.
Volume: 37
Issue: 1
Pages: 1-15
Publication
First Author: Strazielle C
Year: 2002
Journal: J Chem Neuroanat
Title: Biochemical and autoradiographic studies of the central noradrenergic system in dystonia musculorum mutant mice.
Volume: 23
Issue: 2
Pages: 143-55
Publication  
First Author: Ichikawa H
Year: 2008
Journal: Brain Res
Title: The number of nociceptors in the trigeminal ganglion but not proprioceptors in the mesencephalic trigeminal tract nucleus is reduced in dystonin deficient dystonia musculorum mice.
Volume: 1226
Pages: 33-8
Publication
First Author: Ichikawa H
Year: 2006
Journal: Neuroscience
Title: The survival of vagal and glossopharyngeal sensory neurons is dependent upon dystonin.
Volume: 137
Issue: 2
Pages: 531-6
Publication
First Author: Carlsten JA
Year: 2001
Journal: J Comp Neurol
Title: Glial cell line-derived neurotrophic factor-responsive and neurotrophin-3-responsive neurons require the cytoskeletal linker protein dystonin for postnatal survival.
Volume: 432
Issue: 2
Pages: 155-68
Publication
First Author: Brown A
Year: 1994
Journal: Genomics
Title: The genomic structure of an insertional mutation in the dystonia musculorum locus.
Volume: 20
Issue: 3
Pages: 371-6
Publication
First Author: Bernier G
Year: 1995
Journal: Biochem Cell Biol
Title: Dystonin transcripts are altered and their levels are reduced in the mouse neurological mutant dt24J.
Volume: 73
Issue: 9-10
Pages: 605-9
Publication      
First Author: Reyna C
Year: 2015
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for phelps