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Search results 1 to 100 out of 678 for Mpz

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0.045s
Type Details Score
Gene
Type: gene
Organism: Not Specified
Gene
Type: gene
Organism: human
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: cattle
Gene
Type: gene
Organism: rat
Gene
Type: gene
Organism: dog, domestic
Gene
Type: gene
Organism: chimpanzee
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
GXD Expression
Probe: MGI:7423877
Assay Type: RNA in situ
Annotation Date: 2023-01-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1757624
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:7424994
Age: embryonic day 16.5
Image: 6 - Mpz
Note: The Schwann cells show expression.
Specimen Label: 6 - Mpz
Detected: true
Specimen Num: 1
GXD Expression  
Probe: MGI:7423877
Assay Type: RNA in situ
Annotation Date: 2023-01-11
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:3561424
Stage: TS24
Assay Id: MGI:7424994
Age: embryonic day 16.5
Image: 6 - Mpz
Note: The ONL-OECs lack expression.
Specimen Label: 6 - Mpz
Detected: false
Specimen Num: 1
GXD Expression
Probe: MGI:7423877
Assay Type: RNA in situ
Annotation Date: 2023-01-11
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1779724
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:7424994
Age: embryonic day 16.5
Image: 6 - Mpz
Note: The mucosal OECs show expression.
Specimen Label: 6 - Mpz
Detected: true
Specimen Num: 1
Publication      
First Author: Karst SY
Year: 2009
Journal: MGI Direct Data Submission
Title: Totterer: a new mutation in the myelin protein Mpz gene
Publication
First Author: Wrabetz L
Year: 2006
Journal: J Neurosci
Title: Different intracellular pathomechanisms produce diverse Myelin Protein Zero neuropathies in transgenic mice.
Volume: 26
Issue: 8
Pages: 2358-68
Publication
First Author: Wrabetz L
Year: 2000
Journal: J Cell Biol
Title: P(0) glycoprotein overexpression causes congenital hypomyelination of peripheral nerves.
Volume: 148
Issue: 5
Pages: 1021-34
Publication
First Author: Previtali SC
Year: 2000
Journal: J Cell Biol
Title: Epitope-tagged P(0) glycoprotein causes Charcot-Marie-Tooth-like neuropathy in transgenic mice.
Volume: 151
Issue: 5
Pages: 1035-46
Publication
First Author: Fratta P
Year: 2019
Journal: Hum Mol Genet
Title: A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function.
Volume: 28
Issue: 1
Pages: 124-132
Publication
First Author: Dacci P
Year: 2010
Journal: Glia
Title: Foot pad skin biopsy in mouse models of hereditary neuropathy.
Volume: 58
Issue: 16
Pages: 2005-16
Publication
First Author: Hayasaka K
Year: 1993
Journal: Genomics
Title: Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ).
Volume: 17
Issue: 3
Pages: 755-8
Publication  
First Author: Quattrini A
Year: 1999
Journal: Ann N Y Acad Sci
Title: Peripheral nerve dysmyelination due to P0 glycoprotein overexpression is dose-dependent.
Volume: 883
Pages: 294-301
Publication      
First Author: Prince L
Year: 2018
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for taz.
Publication
First Author: Shackleford G
Year: 2022
Journal: PLoS Genet
Title: A new mouse model of Charcot-Marie-Tooth 2J neuropathy replicates human axonopathy and suggest alteration in axo-glia communication.
Volume: 18
Issue: 11
Pages: e1010477
Publication
First Author: Bai Y
Year: 2022
Journal: Mol Neurobiol
Title: Treatment with IFB-088 Improves Neuropathy in CMT1A and CMT1B Mice.
Volume: 59
Issue: 7
Pages: 4159-4178
Publication
First Author: Saporta MA
Year: 2012
Journal: Brain
Title: MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
Volume: 135
Issue: Pt 7
Pages: 2032-47
Publication
First Author: LeBlanc SE
Year: 2006
Journal: J Biol Chem
Title: Direct regulation of myelin protein zero expression by the Egr2 transactivator.
Volume: 281
Issue: 9
Pages: 5453-60
Publication
First Author: Fratta P
Year: 2011
Journal: Hum Mol Genet
Title: P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice.
Volume: 20
Issue: 11
Pages: 2081-90
Publication
First Author: Rünker AE
Year: 2004
Journal: J Cell Biol
Title: Pathology of a mouse mutation in peripheral myelin protein P0 is characteristic of a severe and early onset form of human Charcot-Marie-Tooth type 1B disorder.
Volume: 165
Issue: 4
Pages: 565-73
Publication
First Author: Volpi VG
Year: 2019
Journal: PLoS Genet
Title: Schwann cells ER-associated degradation contributes to myelin maintenance in adult nerves and limits demyelination in CMT1B mice.
Volume: 15
Issue: 4
Pages: e1008069
Publication  
First Author: Liu X
Year: 2011
Journal: J Biomed Biotechnol
Title: ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant mice.
Volume: 2011
Pages: 130947
Publication
First Author: Louvet C
Year: 2009
Journal: J Exp Med
Title: A novel myelin P0-specific T cell receptor transgenic mouse develops a fulminant autoimmune peripheral neuropathy.
Volume: 206
Issue: 3
Pages: 507-14
Publication
First Author: Nagoshi N
Year: 2011
Journal: Glia
Title: Schwann cell plasticity after spinal cord injury shown by neural crest lineage tracing.
Volume: 59
Issue: 5
Pages: 771-84
Publication
First Author: Scapin C
Year: 2020
Journal: J Neurosci
Title: Phosphorylation of eIF2α Promotes Schwann Cell Differentiation and Myelination in CMT1B Mice with Activated UPR.
Volume: 40
Issue: 42
Pages: 8174-8187
Publication
First Author: Pennuto M
Year: 2008
Journal: Neuron
Title: Ablation of the UPR-mediator CHOP restores motor function and reduces demyelination in Charcot-Marie-Tooth 1B mice.
Volume: 57
Issue: 3
Pages: 393-405
Publication
First Author: VerPlank JJS
Year: 2018
Journal: Glia
Title: Impairment of protein degradation and proteasome function in hereditary neuropathies.
Volume: 66
Issue: 2
Pages: 379-395
Publication
First Author: D'Antonio M
Year: 2013
Journal: J Exp Med
Title: Resetting translational homeostasis restores myelination in Charcot-Marie-Tooth disease type 1B mice.
Volume: 210
Issue: 4
Pages: 821-38
Publication
First Author: Belin S
Year: 2019
Journal: Hum Mol Genet
Title: Neuregulin 1 type III improves peripheral nerve myelination in a mouse model of congenital hypomyelinating neuropathy.
Volume: 28
Issue: 8
Pages: 1260-1273
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: Hayasaka K
Year: 1993
Journal: Biochem Biophys Res Commun
Title: Mutation of the myelin P0 gene in Charcot-Marie-tooth neuropathy type 1.
Volume: 194
Issue: 3
Pages: 1317-22
Publication
First Author: Hayasaka K
Year: 1993
Journal: Nat Genet
Title: De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
Volume: 5
Issue: 3
Pages: 266-8
Publication
First Author: Veneri FA
Year: 2022
Journal: Hum Mol Genet
Title: A novel mouse model of CMT1B identifies hyperglycosylation as a new pathogenetic mechanism.
Volume: 31
Issue: 24
Pages: 4255-4274
Publication
First Author: Avila RL
Year: 2010
Journal: J Biol Chem
Title: P0 (protein zero) mutation S34C underlies instability of internodal myelin in S63C mice.
Volume: 285
Issue: 53
Pages: 42001-12
Publication
First Author: Giese KP
Year: 1992
Journal: Cell
Title: Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
Volume: 71
Issue: 4
Pages: 565-76
Publication
First Author: Frei R
Year: 1999
Journal: J Neurosci
Title: Loss of distal axons and sensory Merkel cells and features indicative of muscle denervation in hindlimbs of P0-deficient mice.
Volume: 19
Issue: 14
Pages: 6058-67
Publication
First Author: Ey B
Year: 2007
Journal: Mol Cell Neurosci
Title: Visualization of degenerating axons in a dysmyelinating mouse mutant with axonal loss.
Volume: 35
Issue: 1
Pages: 153-60
Publication
First Author: Ulzheimer JC
Year: 2004
Journal: Mol Cell Neurosci
Title: Altered expression of ion channel isoforms at the node of Ranvier in P0-deficient myelin mutants.
Volume: 25
Issue: 1
Pages: 83-94
Publication
First Author: Xu W
Year: 2000
Journal: J Neurosci Res
Title: Absence of P0 leads to the dysregulation of myelin gene expression and myelin morphogenesis.
Volume: 60
Issue: 6
Pages: 714-24
Publication
First Author: Zielasek J
Year: 1996
Journal: Muscle Nerve
Title: Functional abnormalities in P0-deficient mice resemble human hereditary neuropathies linked to P0 gene mutations.
Volume: 19
Issue: 8
Pages: 946-52
Publication
First Author: Berghoff M
Year: 2005
Journal: Mol Cell Neurosci
Title: Neuroprotective effect of the immune system in a mouse model of severe dysmyelinating hereditary neuropathy: enhanced axonal degeneration following disruption of the RAG-1 gene.
Volume: 28
Issue: 1
Pages: 118-27
Publication
First Author: Martini R
Year: 1995
Journal: Nat Genet
Title: Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
Volume: 11
Issue: 3
Pages: 281-6
Publication  
First Author: Menichella DM
Year: 1999
Journal: Ann N Y Acad Sci
Title: The absence of myelin P0 protein produces a novel molecular phenotype in Schwann cells.
Volume: 883
Pages: 281-93
Publication  
First Author: Martini R
Year: 1999
Journal: Ann N Y Acad Sci
Title: P0-deficient knockout mice as tools to understand pathomechanisms in Charcot-Marie-Tooth 1B and P0-related Déjérine-Sottas syndrome.
Volume: 883
Pages: 273-80
Publication  
First Author: Alvarez S
Year: 2013
Journal: Exp Neurol
Title: Prolonged high frequency electrical stimulation is lethal to motor axons of mice heterozygously deficient for the myelin protein Pâ‚€ gene.
Volume: 247
Pages: 552-61
Publication
First Author: Shy ME
Year: 1997
Journal: J Neuropathol Exp Neurol
Title: Heterozygous P0 knockout mice develop a peripheral neuropathy that resembles chronic inflammatory demyelinating polyneuropathy (CIDP).
Volume: 56
Issue: 7
Pages: 811-21
Publication
First Author: Samsam M
Year: 2002
Journal: J Neurosci Res
Title: Impaired sensory function in heterozygous P0 knockout mice is associated with nodal changes in sensory nerves.
Volume: 67
Issue: 2
Pages: 167-73
Publication
First Author: Miyamoto K
Year: 2003
Journal: Eur J Immunol
Title: Heterozygous null mutation of myelin P0 protein enhances susceptibility to autoimmune neuritis targeting P0 peptide.
Volume: 33
Issue: 3
Pages: 656-65
Publication
First Author: Menichella DM
Year: 2001
Journal: Mol Cell Neurosci
Title: Protein zero is necessary for E-cadherin-mediated adherens junction formation in Schwann cells.
Volume: 18
Issue: 6
Pages: 606-18
Publication
First Author: Fischer S
Year: 2008
Journal: Glia
Title: Increase of MCP-1 (CCL2) in myelin mutant Schwann cells is mediated by MEK-ERK signaling pathway.
Volume: 56
Issue: 8
Pages: 836-43
Publication
First Author: Ip CW
Year: 2009
Journal: Neurobiol Dis
Title: Tacrolimus (FK506) causes disease aggravation in models for inherited peripheral myelinopathies.
Volume: 33
Issue: 2
Pages: 207-12
Publication
First Author: Patzkó A
Year: 2012
Journal: Brain
Title: Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice.
Volume: 135
Issue: Pt 12
Pages: 3551-66
Publication
First Author: Kuhn R
Year: 1990
Journal: J Neurosci
Title: The gene encoding peripheral myelin protein zero is located on mouse chromosome 1.
Volume: 10
Issue: 1
Pages: 205-9
Publication
First Author: Lemke G
Year: 1988
Journal: Neuron
Title: Isolation and analysis of the gene encoding peripheral myelin protein zero.
Volume: 1
Issue: 1
Pages: 73-83
Publication
First Author: Hayasaka K
Year: 1993
Journal: Nat Genet
Title: Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene.
Volume: 5
Issue: 1
Pages: 31-4
Publication
First Author: Matsuoka H
Year: 1999
Journal: Ann Otol Rhinol Laryngol
Title: Murine model of autoimmune hearing loss induced by myelin protein P0.
Volume: 108
Issue: 3
Pages: 255-64
Publication
First Author: Otani Y
Year: 2020
Journal: Commun Biol
Title: Upregulation of large myelin protein zero leads to Charcot-Marie-Tooth disease-like neuropathy in mice.
Volume: 3
Issue: 1
Pages: 121
GXD Expression        
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Not Specified
Sex: Not Specified
Emaps: EMAPS:1857724
Stage: TS24
Assay Id: MGI:6160803
Age: embryonic day 16.0
Specimen Label: E16
Specimen Num: 1
GXD Expression        
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Not Specified
Sex: Not Specified
Emaps: EMAPS:1857727
Stage: TS27
Assay Id: MGI:6160803
Age: postnatal day 1
Specimen Label: P1
Specimen Num: 2
GXD Expression        
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Not Specified
Sex: Not Specified
Emaps: EMAPS:1857727
Stage: TS27
Assay Id: MGI:6160803
Age: postnatal day 2
Specimen Label: P2
Specimen Num: 3
GXD Expression        
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Not Specified
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6160803
Age: postnatal day 4
Specimen Label: P4
Specimen Num: 4
GXD Expression        
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Not Specified
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6160803
Age: postnatal day 6
Specimen Label: P6
Specimen Num: 5
GXD Expression      
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6160803
Age: postnatal day 8
Specimen Label: P8
Detected: true
Specimen Num: 6
GXD Expression      
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6160803
Age: postnatal day 10
Specimen Label: P10
Detected: true
Specimen Num: 7
GXD Expression      
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6160803
Age: postnatal day 14
Specimen Label: P14
Detected: true
Specimen Num: 8
GXD Expression      
Probe: MGI:6160788
Assay Type: Western blot
Annotation Date: 2018-06-13
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6160803
Age: postnatal adult
Specimen Label: Adult
Detected: true
Specimen Num: 9
GXD Expression      
Probe: MGI:6460031
Assay Type: Western blot
Annotation Date: 2020-10-07
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857727
Stage: TS27
Assay Id: MGI:6460032
Age: postnatal day 1
Specimen Label: P1 +/-
Detected: true
Specimen Num: 1
GXD Expression      
Probe: MGI:6460031
Assay Type: Western blot
Annotation Date: 2020-10-07
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857727
Stage: TS27
Assay Id: MGI:6460032
Age: postnatal day 1
Specimen Label: P1 -/-
Detected: true
Specimen Num: 2
GXD Expression      
Probe: MGI:6460031
Assay Type: Western blot
Annotation Date: 2020-10-07
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6460032
Age: postnatal day 8
Specimen Label: P8 +/-
Detected: true
Specimen Num: 3
GXD Expression      
Probe: MGI:6460031
Assay Type: Western blot
Annotation Date: 2020-10-07
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6460032
Age: postnatal day 8
Specimen Label: P8 -/-
Detected: true
Specimen Num: 4
GXD Expression      
Probe: MGI:6460031
Assay Type: Western blot
Annotation Date: 2020-10-07
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6460032
Age: postnatal day 11
Specimen Label: P11 +/-
Detected: true
Specimen Num: 5
GXD Expression      
Probe: MGI:6460031
Assay Type: Western blot
Annotation Date: 2020-10-07
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6460032
Age: postnatal day 11
Specimen Label: P11 -/-
Detected: true
Specimen Num: 6
GXD Expression      
Probe: MGI:6460031
Assay Type: Western blot
Annotation Date: 2020-10-07
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1857728
Stage: TS28
Assay Id: MGI:6460032
Age: postnatal day 14
Specimen Label: P14 +/-
Detected: true
Specimen Num: 7