Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 386

1.

Transgenic expression of human connexin32 in myelinating Schwann cells prevents demyelination in connexin32-null mice.

Scherer SS, Xu YT, Messing A, Willecke K, Fischbeck KH, Jeng LJ.

J Neurosci. 2005 Feb 9;25(6):1550-9.

2.
3.

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
4.

Connexin32-null mice develop demyelinating peripheral neuropathy.

Scherer SS, Xu YT, Nelles E, Fischbeck K, Willecke K, Bone LJ.

Glia. 1998 Sep;24(1):8-20.

PMID:
9700485
5.

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
6.

Intraneural GJB1 gene delivery improves nerve pathology in a model of X-linked Charcot-Marie-Tooth disease.

Sargiannidou I, Kagiava A, Bashiardes S, Richter J, Christodoulou C, Scherer SS, Kleopa KA.

Ann Neurol. 2015 Aug;78(2):303-16. doi: 10.1002/ana.24441. Epub 2015 Jun 30.

PMID:
26010264
7.

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
8.

Studies in transgenic mice indicate a loss of connexin32 function in X-linked Charcot-Marie-Tooth disease.

Abel A, Bone LJ, Messing A, Scherer SS, Fischbeck KH.

J Neuropathol Exp Neurol. 1999 Jul;58(7):702-10.

PMID:
10411340
9.

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
10.

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
11.

Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients.

Hattori N, Yamamoto M, Yoshihara T, Koike H, Nakagawa M, Yoshikawa H, Ohnishi A, Hayasaka K, Onodera O, Baba M, Yasuda H, Saito T, Nakashima K, Kira J, Kaji R, Oka N, Sobue G; Study Group for Hereditary Neuropathy in Japan.

Brain. 2003 Jan;126(Pt 1):134-51. Review.

PMID:
12477701
12.

Gap junction disorders of myelinating cells.

Kleopa KA, Orthmann-Murphy J, Sargiannidou I.

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

PMID:
21280457
13.

Connexin32 is a myelin-related protein in the PNS and CNS.

Scherer SS, Deschênes SM, Xu YT, Grinspan JB, Fischbeck KH, Paul DL.

J Neurosci. 1995 Dec;15(12):8281-94.

14.

Phenotypic and cellular expression of two novel connexin32 mutations causing CMT1X.

Kleopa KA, Zamba-Papanicolaou E, Alevra X, Nicolaou P, Georgiou DM, Hadjisavvas A, Kyriakides T, Christodoulou K.

Neurology. 2006 Feb 14;66(3):396-402.

PMID:
16476939
15.

Attenuation of MCP-1/CCL2 expression ameliorates neuropathy in a mouse model for Charcot-Marie-Tooth 1X.

Groh J, Heinl K, Kohl B, Wessig C, Greeske J, Fischer S, Martini R.

Hum Mol Genet. 2010 Sep 15;19(18):3530-43. doi: 10.1093/hmg/ddq269. Epub 2010 Jun 30.

PMID:
20591826
16.

Regulation of myelin-specific gene expression. Relevance to CMT1.

Kamholz J, Awatramani R, Menichella D, Jiang H, Xu W, Shy M.

Ann N Y Acad Sci. 1999 Sep 14;883:91-108. Review.

PMID:
10586235
17.

Functional analysis of connexin-32 mutants associated with X-linked dominant Charcot-Marie-Tooth disease.

Wang HL, Chang WT, Yeh TH, Wu T, Chen MS, Wu CY.

Neurobiol Dis. 2004 Mar;15(2):361-70.

PMID:
15006706
18.

A second alternative transcript of the gap junction gene connexin32 is expressed in murine Schwann cells and modulated in injured sciatic nerve.

Söhl G, Gillen C, Bosse F, Gleichmann M, Müller HW, Willecke K.

Eur J Cell Biol. 1996 Mar;69(3):267-75.

PMID:
8900491
19.

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.

20.

Cellular mechanisms of connexin32 mutations associated with CNS manifestations.

Kleopa KA, Yum SW, Scherer SS.

J Neurosci Res. 2002 Jun 1;68(5):522-34.

PMID:
12111842

Supplemental Content

Support Center