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Results: 1 to 20 of 29

Related Articles by Review for PubMed (Select 16790356)

1.

The effects of a dominant connexin32 mutant in myelinating Schwann cells.

Jeng LJ, Balice-Gordon RJ, Messing A, Fischbeck KH, Scherer SS.

Mol Cell Neurosci. 2006 Jul;32(3):283-98. Epub 2006 Jun 21.

PMID:
16790356
2.

The role of the gap junction protein connexin32 in the pathogenesis of X-linked Charcot-Marie-Tooth disease.

Scherer SS, Bone LJ, Deschênes SM, Abel A, Balice-Gordon RJ, Fischbeck KH.

Novartis Found Symp. 1999;219:175-85; discussion 185-7. Review.

PMID:
10207904
3.

Connexin32 and X-linked Charcot-Marie-Tooth disease.

Bone LJ, Deschênes SM, Balice-Gordon RJ, Fischbeck KH, Scherer SS.

Neurobiol Dis. 1997;4(3-4):221-30. Review.

PMID:
9361298
4.

Molecular genetics of X-linked Charcot-Marie-Tooth disease.

Kleopa KA, Scherer SS.

Neuromolecular Med. 2006;8(1-2):107-22. Review.

PMID:
16775370
5.

X-linked Charcot-Marie-Tooth disease and connexin32.

Fischbeck KH, Abel A, Lin GS, Scherer SS.

Ann N Y Acad Sci. 1999 Sep 14;883:36-41. Review.

PMID:
10586227
6.

Gap junction disorders of myelinating cells.

Kleopa KA, Orthmann-Murphy J, Sargiannidou I.

Rev Neurosci. 2010;21(5):397-419. Review.

PMID:
21280457
7.

How do mutations in GJB1 cause X-linked Charcot-Marie-Tooth disease?

Kleopa KA, Abrams CK, Scherer SS.

Brain Res. 2012 Dec 3;1487:198-205. doi: 10.1016/j.brainres.2012.03.068. Epub 2012 Jul 6. Review.

8.

Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease.

Ressot C, Bruzzone R.

Brain Res Brain Res Rev. 2000 Apr;32(1):192-202. Review.

PMID:
10751670
9.

Molecular mechanisms of gap junction mutations in myelinating cells.

Sargiannidou I, Markoullis K, Kleopa KA.

Histol Histopathol. 2010 Sep;25(9):1191-206. Review.

PMID:
20607661
10.

Mutations in connexin 32: the molecular and biophysical bases for the X-linked form of Charcot-Marie-Tooth disease.

Abrams CK, Oh S, Ri Y, Bargiello TA.

Brain Res Brain Res Rev. 2000 Apr;32(1):203-14. Review.

PMID:
10751671
11.
12.

Role of immune cells in animal models for inherited peripheral neuropathies.

Wang Ip C, Kroner A, Fischer S, Berghoff M, Kobsar I, Mäurer M, Martini R.

Neuromolecular Med. 2006;8(1-2):175-90. Review.

PMID:
16775375
13.

The biology and pathobiology of Schwann cells.

Scherer SS.

Curr Opin Neurol. 1997 Oct;10(5):386-97. Review.

PMID:
9330884
14.

The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22.

Niemann S, Sereda MW, Rossner M, Stewart H, Suter U, Meinck HM, Griffiths IR, Nave KA.

Ann N Y Acad Sci. 1999 Sep 14;883:254-61. Review.

PMID:
10586250
15.

Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy.

Kamholz J, Menichella D, Jani A, Garbern J, Lewis RA, Krajewski KM, Lilien J, Scherer SS, Shy ME.

Brain. 2000 Feb;123 ( Pt 2):222-33. Review.

16.

Gap junction communication in myelinating glia.

Nualart-Marti A, Solsona C, Fields RD.

Biochim Biophys Acta. 2013 Jan;1828(1):69-78. doi: 10.1016/j.bbamem.2012.01.024. Epub 2012 Feb 3. Review.

17.

Connexins, gap junctions and peripheral neuropathy.

Kleopa KA, Sargiannidou I.

Neurosci Lett. 2015 Jun 2;596:27-32. doi: 10.1016/j.neulet.2014.10.033. Epub 2014 Oct 24. Review.

PMID:
25449862
18.

Biological functions of connexin genes revealed by human genetic defects, dominant negative approaches and targeted deletions in the mouse.

Willecke K, Kirchhoff S, Plum A, Temme A, Thönnissen E, Ott T.

Novartis Found Symp. 1999;219:76-88; discussion 88-96. Review.

PMID:
10207899
19.

Myelin mutants: model systems for the study of normal and abnormal myelination.

Griffiths IR.

Bioessays. 1996 Oct;18(10):789-97. Review.

PMID:
8885716
20.

The function of the Periaxin gene during nerve repair in a model of CMT4F.

Williams AC, Brophy PJ.

J Anat. 2002 Apr;200(4):323-30. Review.

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