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Search results 1 to 100 out of 390 for Mpz

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Type Details Score
Publication
- | J:149880
     
First Author: Karst SY
Year: 2009
Journal: MGI Direct Data Submission
Title: Totterer: a new mutation in the myelin protein Mpz gene
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Publication
10704451 | J:78758
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
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Publication
16495463 | J:105751
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
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Publication
11086005 | J:77658
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
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Publication
30239779 | J:267903
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
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Publication
20878767 | J:167389
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
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Publication
7503936 | J:14536
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
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Publication
10586254 | J:59845
 
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
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Publication
- | J:265100
     
First Author: Prince L
Year: 2018
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for taz.
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Publication
36350884 | J:334486
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
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Publication
35501630 | J:338996
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
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Publication
22689911 | J:241742
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
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Publication
16373334 | J:109227
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
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Publication
21363884 | J:171510
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
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Publication
15148307 | J:91162
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
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Publication
30995221 | J:275856
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
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Publication
22219655 | J:196547
 
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
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Publication
19221395 | J:146797
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
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Publication
21351159 | J:169749
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
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32973043 | J:296601
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
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18255032 | J:135317
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
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Publication
29076578 | J:256284
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
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Publication
23547100 | J:198199
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
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Publication
30535360 | J:274585
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
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Publication
7688964 | J:14581
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
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7506095 | J:42837
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
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35908287 | J:335549
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
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Publication
1384988 | J:3234
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
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Publication
10586252 | J:59847
 
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
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Publication
10861783 | J:113170
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
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9210878 | J:42650
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
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11749037 | J:73865
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
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12616486 | J:82432
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
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14962742 | J:109704
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
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20937820 | J:167380
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
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23439028 | J:203581
 
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 P₀ gene.
Volume: 247
Pages: 552-61
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10407042 | J:56296
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
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17383197 | J:123228
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
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7581451 | J:42838
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
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Publication
10586253 | J:59846
 
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
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19028581 | J:144742
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
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11782960 | J:104917
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
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8756159 | J:35081
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
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18383340 | J:156268
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
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15607947 | J:97751
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
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23250879 | J:241833
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
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Publication
1688933 | J:10270
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
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2483091 | J:20088
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
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7693129 | J:42836
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
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10086618 | J:54142
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
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Publication
32170207 | J:289572
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
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Publication
26406915 | J:226388
First Author: Brügger V
Year: 2015
Journal: PLoS Biol
Title: HDAC1/2-Dependent P0 Expression Maintains Paranodal and Nodal Integrity Independently of Myelin Stability through Interactions with Neurofascins.
Volume: 13
Issue: 9
Pages: e1002258
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Publication
33879538 | J:307142
First Author: Sidoli M
Year: 2021
Journal: J Neurosci
Title: Calcineurin Activity Is Increased in Charcot-Marie-Tooth 1B Demyelinating Neuropathy.
Volume: 41
Issue: 20
Pages: 4536-4548
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21536740 | J:177298
First Author: Kubota Y
Year: 2011
Journal: J Exp Med
Title: Isolation and function of mouse tissue resident vascular precursors marked by myelin protein zero.
Volume: 208
Issue: 5
Pages: 949-60
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7540676 | J:26097
First Author: Martini R
Year: 1995
Journal: J Neurosci
Title: Mice doubly deficient in the genes for P0 and myelin basic protein show that both proteins contribute to the formation of the major dense line in peripheral nerve myelin.
Volume: 15
Issue: 6
Pages: 4488-95
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2483096 | J:10329
First Author: Popko B
Year: 1988
Journal: Neuron
Title: A novel mutation in myelin-deficient mice results in unstable myelin basic protein gene transcripts.
Volume: 1
Issue: 3
Pages: 221-5
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26393339 | J:226848
First Author: Patzig J
Year: 2016
Journal: Glia
Title: Proteolipid protein modulates preservation of peripheral axons and premature death when myelin protein zero is lacking.
Volume: 64
Issue: 1
Pages: 155-74
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11266447 | J:67581
First Author: Carenini S
Year: 2001
Journal: J Cell Biol
Title: The role of macrophages in demyelinating peripheral nervous system of mice heterozygously deficient in p0.
Volume: 152
Issue: 2
Pages: 301-8
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24526449 | J:209146
First Author: Klein D
Year: 2014
Journal: Glia
Title: Nonuniform molecular features of myelinating Schwann cells in models for CMT1: distinct disease patterns are associated with NCAM and c-Jun upregulation.
Volume: 62
Issue: 5
Pages: 736-50
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27215377 | J:240846
 
First Author: Rosberg MR
Year: 2016
Journal: Neurobiol Dis
Title: Progression of motor axon dysfunction and ectopic Nav1.8 expression in a mouse model of Charcot-Marie-Tooth disease 1B.
Volume: 93
Pages: 201-14
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25066805 | J:216220
First Author: Yin X
Year: 2015
Journal: Glia
Title: Proteolipid protein cannot replace P0 protein as the major structural protein of peripheral nervous system myelin.
Volume: 63
Issue: 1
Pages: 66-77
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9726425 | J:49754
First Author: Neuberg DH
Year: 1998
Journal: J Neurosci Res
Title: Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero.
Volume: 53
Issue: 5
Pages: 542-50
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16458537 | J:108620
First Author: Kobsar I
Year: 2006
Journal: Mol Cell Neurosci
Title: Attenuated demyelination in the absence of the macrophage-restricted adhesion molecule sialoadhesin (Siglec-1) in mice heterozygously deficient in P0.
Volume: 31
Issue: 4
Pages: 685-91
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10856243 | J:88339
First Author: Mandemakers W
Year: 2000
Journal: EMBO J
Title: A distal Schwann cell-specific enhancer mediates axonal regulation of the Oct-6 transcription factor during peripheral nerve development and regeneration.
Volume: 19
Issue: 12
Pages: 2992-3003
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16962581 | J:141511
First Author: Müller M
Year: 2007
Journal: Exp Neurol
Title: Macrophage colony stimulating factor is a crucial factor for the intrinsic macrophage response in mice heterozygously deficient for the myelin protein P0.
Volume: 203
Issue: 1
Pages: 55-62
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8663988 | J:33762
First Author: Yoshida M
Year: 1996
Journal: Neuron
Title: Parallel evolution and coexpression of the proteolipid proteins and protein zero in vertebrate myelin.
Volume: 16
Issue: 6
Pages: 1115-26
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21911936 | J:178222
First Author: Asada N
Year: 2011
Journal: J Clin Invest
Title: Dysfunction of fibroblasts of extrarenal origin underlies renal fibrosis and renal anemia in mice.
Volume: 121
Issue: 10
Pages: 3981-90
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28880149 | J:248325
   
First Author: Figlia G
Year: 2017
Journal: Elife
Title: Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system.
Volume: 6
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10797391 | J:113066
First Author: Zielasek J
Year: 2000
Journal: Muscle Nerve
Title: Neuromyotonia in mice with hereditary myelinopathies.
Volume: 23
Issue: 5
Pages: 696-701
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Publication
30481294 | J:330107
First Author: Scapin C
Year: 2019
Journal: Hum Mol Genet
Title: Enhanced axonal neuregulin-1 type-III signaling ameliorates neurophysiology and hypomyelination in a Charcot-Marie-Tooth type 1B mouse model.
Volume: 28
Issue: 6
Pages: 992-1006
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1384766 | J:2357
First Author: Garbay B
Year: 1992
Journal: Neuroreport
Title: P0 protein in normal, trembler heterozygous/homozygous mice during active PNS myelination.
Volume: 3
Issue: 7
Pages: 594-6
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10559784 | J:59665
First Author: Carenini S
Year: 1999
Journal: Glia
Title: Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice.
Volume: 28
Issue: 3
Pages: 256-64
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10632602 | J:59319
First Author: Schmid CD
Year: 2000
Journal: J Neurosci
Title: Immune deficiency in mouse models for inherited peripheral neuropathies leads to improved myelin maintenance.
Volume: 20
Issue: 2
Pages: 729-35
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Publication
23143399 | J:195251
First Author: Rinkevich Y
Year: 2012
Journal: Nat Cell Biol
Title: Identification and prospective isolation of a mesothelial precursor lineage giving rise to smooth muscle cells and fibroblasts for mammalian internal organs, and their vasculature.
Volume: 14
Issue: 12
Pages: 1251-60
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Publication
18326085 | J:133028
First Author: Fischer S
Year: 2008
Journal: Mol Cell Neurosci
Title: Monocyte chemoattractant protein-1 is a pathogenic component in a model for a hereditary peripheral neuropathy.
Volume: 37
Issue: 2
Pages: 359-66
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Publication
20553884 | J:171328
First Author: Oberländer M
Year: 2010
Journal: Mol Cell Neurosci
Title: Effects of the CC chemokine receptor 2 in mice deficient for the myelin protein zero (P0).
Volume: 45
Issue: 1
Pages: 59-65
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Publication
19050296 | J:142046
First Author: Kim HJ
Year: 2008
Journal: J Immunol
Title: Targeting of myelin protein zero in a spontaneous autoimmune polyneuropathy.
Volume: 181
Issue: 12
Pages: 8753-60
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Publication
24709684 | J:329107
First Author: Brunn A
Year: 2014
Journal: J Neuropathol Exp Neurol
Title: Costimulatory molecule CD40 is essential for myelin protein 0 peptide 106-125-induced experimental autoimmune neuritis in mice.
Volume: 73
Issue: 5
Pages: 454-66
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Publication
25859045 | J:221856
First Author: Das I
Year: 2015
Journal: Science
Title: Preventing proteostasis diseases by selective inhibition of a phosphatase regulatory subunit.
Volume: 348
Issue: 6231
Pages: 239-42
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Publication
10586256 | J:59844
 
First Author: Zielasek J
Year: 1999
Journal: Ann N Y Acad Sci
Title: Nerve conduction abnormalities and neuromyotonia in genetically engineered mouse models of human hereditary neuropathies.
Volume: 883
Pages: 310-20
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Publication
30931926 | J:273263
First Author: Fledrich R
Year: 2019
Journal: Nat Commun
Title: NRG1 type I dependent autoparacrine stimulation of Schwann cells in onion bulbs of peripheral neuropathies.
Volume: 10
Issue: 1
Pages: 1467
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Publication
20071523 | J:157710
First Author: Bai Y
Year: 2010
Journal: J Neurosci
Title: Conduction block in PMP22 deficiency.
Volume: 30
Issue: 2
Pages: 600-8
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Publication
10457367 | J:113080
First Author: Carenini S
Year: 1999
Journal: Glia
Title: Subtle roles of neural cell adhesion molecule and myelin-associated glycoprotein during Schwann cell spiralling in P0-deficient mice.
Volume: 27
Issue: 3
Pages: 203-12
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Publication
19439587 | J:155650
First Author: Saher G
Year: 2009
Journal: J Neurosci
Title: Cholesterol regulates the endoplasmic reticulum exit of the major membrane protein P0 required for peripheral myelin compaction.
Volume: 29
Issue: 19
Pages: 6094-104
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Publication
18996482 | J:145018
First Author: Kroner A
Year: 2009
Journal: Neurobiol Dis
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