|
| Entrez Id: |
4359 |
| Gene Symbol: |
MPZ |
MPZ
|
0.200 |
Biomarker
|
disease |
MGD |
Mouse P0 gene disruption leads to hypomyelination, abnormal expression of recognition molecules, and degeneration of myelin and axons.
|
1384988 |
1992 |
|
| Entrez Id: |
4359 |
| Gene Symbol: |
MPZ |
MPZ
|
0.200 |
Biomarker
|
disease |
MGD |
MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B.
|
22689911 |
2012 |
|
| Entrez Id: |
81846 |
| Gene Symbol: |
SBF2 |
SBF2
|
0.200 |
Biomarker
|
disease |
MGD |
Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2.
|
17855448 |
2007 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.200 |
Biomarker
|
disease |
MGD |
Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J.
|
17572665 |
2007 |
|
| Entrez Id: |
121512 |
| Gene Symbol: |
FGD4 |
FGD4
|
0.200 |
Biomarker
|
disease |
MGD |
Myelin is dependent on the Charcot-Marie-Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells.
|
23171661 |
2012 |
|
| Entrez Id: |
1959 |
| Gene Symbol: |
EGR2 |
EGR2
|
0.200 |
Biomarker
|
disease |
MGD |
Nab proteins are essential for peripheral nervous system myelination.
|
16136673 |
2005 |
|
| Entrez Id: |
10397 |
| Gene Symbol: |
NDRG1 |
NDRG1
|
0.200 |
Biomarker
|
disease |
MGD |
Ndrg1 in development and maintenance of the myelin sheath.
|
21303696 |
2011 |
|
| Entrez Id: |
10397 |
| Gene Symbol: |
NDRG1 |
NDRG1
|
0.200 |
Biomarker
|
disease |
MGD |
Ndrg1-deficient mice exhibit a progressive demyelinating disorder of peripheral nerves.
|
15082788 |
2004 |
|
| Entrez Id: |
5376 |
| Gene Symbol: |
PMP22 |
PMP22
|
0.200 |
Biomarker
|
disease |
MGD |
Nerve conduction abnormalities in the trembler-j mouse: a model for Charcot-Marie-Tooth disease type 1A?
|
15363066 |
2004 |
|
| Entrez Id: |
4747 |
| Gene Symbol: |
NEFL |
NEFL
|
0.200 |
Biomarker
|
disease |
MGD |
Neurofilament light polypeptide gene N98S mutation in mice leads to neurofilament network abnormalities and a Charcot-Marie-Tooth Type 2E phenotype.
|
25552649 |
2015 |
|
| Entrez Id: |
9896 |
| Gene Symbol: |
FIG4 |
FIG4
|
0.200 |
Biomarker
|
disease |
MGD |
Neuronal expression of Fig4 is both necessary and sufficient to prevent spongiform neurodegeneration.
|
22581779 |
2012 |
|
| Entrez Id: |
5376 |
| Gene Symbol: |
PMP22 |
PMP22
|
0.200 |
Biomarker
|
disease |
MGD |
Oral curcumin mitigates the clinical and neuropathologic phenotype of the Trembler-J mouse: a potential therapy for inherited neuropathy.
|
17701891 |
2007 |
|
| Entrez Id: |
4359 |
| Gene Symbol: |
MPZ |
MPZ
|
0.200 |
Biomarker
|
disease |
MGD |
Protein zero (P0)-deficient mice show myelin degeneration in peripheral nerves characteristic of inherited human neuropathies.
|
7581451 |
1995 |
|
| Entrez Id: |
79628 |
| Gene Symbol: |
SH3TC2 |
SH3TC2
|
0.200 |
Biomarker
|
disease |
MGD |
SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system.
|
19805030 |
2009 |
|
| Entrez Id: |
2705 |
| Gene Symbol: |
GJB1 |
GJB1
|
0.200 |
Biomarker
|
disease |
MGD |
Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32.
|
9169515 |
1997 |
|
| Entrez Id: |
5376 |
| Gene Symbol: |
PMP22 |
PMP22
|
0.200 |
Biomarker
|
disease |
MGD |
The formation of peripheral myelin protein 22 aggregates is hindered by the enhancement of autophagy and expression of cytoplasmic chaperones.
|
17174099 |
2007 |
|
| Entrez Id: |
9990 |
| Gene Symbol: |
SLC12A6 |
SLC12A6
|
0.200 |
Biomarker
|
disease |
MGD |
The K-Cl cotransporter KCC3 is mutant in a severe peripheral neuropathy associated with agenesis of the corpus callosum.
|
12368912 |
2002 |