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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2003 | 3 |
2004 | 1 |
2005 | 1 |
2024 | 0 |
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Page 1
Loss of Mtmr2 phosphatase in Schwann cells but not in motor neurons causes Charcot-Marie-Tooth type 4B1 neuropathy with myelin outfoldings.
J Neurosci. 2005 Sep 14;25(37):8567-77. doi: 10.1523/JNEUROSCI.2493-05.2005.
J Neurosci. 2005.
PMID: 16162938
Free PMC article.
Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis.
Bolino A, Bolis A, Previtali SC, Dina G, Bussini S, Dati G, Amadio S, Del Carro U, Mruk DD, Feltri ML, Cheng CY, Quattrini A, Wrabetz L.
Bolino A, et al.
J Cell Biol. 2004 Nov 22;167(4):711-21. doi: 10.1083/jcb.200407010.
J Cell Biol. 2004.
PMID: 15557122
Free PMC article.
Item in Clipboard
Myotubularins, a large disease-associated family of cooperating catalytically active and inactive phosphoinositides phosphatases.
Laporte J, Bedez F, Bolino A, Mandel JL.
Laporte J, et al.
Hum Mol Genet. 2003 Oct 15;12 Spec No 2:R285-92. doi: 10.1093/hmg/ddg273. Epub 2003 Aug 12.
Hum Mol Genet. 2003.
PMID: 12925573
Review.
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Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve.
Previtali SC, Zerega B, Sherman DL, Brophy PJ, Dina G, King RH, Salih MM, Feltri L, Quattrini A, Ravazzolo R, Wrabetz L, Monaco AP, Bolino A.
Previtali SC, et al.
Hum Mol Genet. 2003 Jul 15;12(14):1713-23. doi: 10.1093/hmg/ddg179.
Hum Mol Genet. 2003.
PMID: 12837694
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Mutations in MTMR13, a new pseudophosphatase homologue of MTMR2 and Sbf1, in two families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease associated with early-onset glaucoma.
Azzedine H, Bolino A, Taïeb T, Birouk N, Di Duca M, Bouhouche A, Benamou S, Mrabet A, Hammadouche T, Chkili T, Gouider R, Ravazzolo R, Brice A, Laporte J, LeGuern E.
Azzedine H, et al.
Am J Hum Genet. 2003 May;72(5):1141-53. doi: 10.1086/375034. Epub 2003 Apr 8.
Am J Hum Genet. 2003.
PMID: 12687498
Free PMC article.
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