Search Results - "Bone, Linda J"

Functional Gap Junctions in the Schwann Cell Myelin Sheath by Balice-Gordon, Rita J., Bone, Linda J., Scherer, Steven S.

“…The Schwann cell myelin sheath is a multilamellar structure with distinct structural domains in which different proteins are localized. Intracellular dye…”
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Studies in Transgenic Mice Indicate a Loss of Connexin32 Function in X-Linked Charcot-Marie-Tooth Disease by Abel, Annette, Bone, Linda J, Messing, Albee, Scherer, Steven S, Fischbeck, Kenneth H

“…X-linked Charcot-Marie-Tooth disease (CMTX) is an inherited demyelinating neuropathy caused by mutations in the gene encoding the gap junction protein…”
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Connexin32-null mice develop demyelinating peripheral neuropathy by Scherer, Steven S., Xu, Yi-Tian, Nelles, Eric, Fischbeck, Kenneth, Willecke, Klaus, Bone, Linda J.

“…Mutations in the gene encoding the gap junction protein connexin32 (Cx32) cause X‐linked Charcot‐Marie‐Tooth disease (CMTX), a common form of inherited…”
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Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome by MUENKE, M, BONE, L. J, TESSIER-LAVIGNE, M, PATTERSON, D, MITCHELL, H. F, HART, I, WALTON, K, HALL-JOHNSON, K, IPPEL, E. F, DIETZ-BAND, J, KVALØY, K, CHEN-MING FAN

“…We set out to define the holoprosencephaly (HPE) critical region on chromosome 21 and also to determine whether there were human homologues of the Drosophila…”
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Functional gap jinctions in the Schwann cell myelin sheath by Balice-Gordon, Rita J, Bone, Linda J, Scherer, Steven S

“…The Schwann cell myelin sheath is a multilamellar structure with distinct structural domains in which different proteins are localized. Intracellular dye…”
Get full text