Barchi RL - Search Results

1

Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis.

Ptacek LJ, Gouw L, Kwieciński H, McManis P, Mendell JR, Barohn RJ, George AL Jr, Barchi RL, Robertson M, Leppert MF. Ptacek LJ, et al. Among authors: barchi rl. Ann Neurol. 1993 Mar;33(3):300-7. doi: 10.1002/ana.410330312. Ann Neurol. 1993. PMID: 8388676

2

Paramyotonia congenita mutations reveal different roles for segments S3 and S4 of domain D4 in hSkM1 sodium channel gating.

Ji S, George AL Jr, Horn R, Barchi RL. Ji S, et al. Among authors: barchi rl. J Gen Physiol. 1996 Feb;107(2):183-94. doi: 10.1085/jgp.107.2.183. J Gen Physiol. 1996. PMID: 8833340 Free PMC article.

3

Primary structure of the adult human skeletal muscle voltage-dependent sodium channel.

George AL Jr, Komisarof J, Kallen RG, Barchi RL. George AL Jr, et al. Among authors: barchi rl. Ann Neurol. 1992 Feb;31(2):131-7. doi: 10.1002/ana.410310203. Ann Neurol. 1992. PMID: 1315496

4

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita.

Ptácek LJ, George AL Jr, Barchi RL, Griggs RC, Riggs JE, Robertson M, Leppert MF. Ptácek LJ, et al. Among authors: barchi rl. Neuron. 1992 May;8(5):891-7. doi: 10.1016/0896-6273(92)90203-p. Neuron. 1992. PMID: 1316765

5

Identification of a mutation in the gene causing hyperkalemic periodic paralysis.

Ptácek LJ, George AL Jr, Griggs RC, Tawil R, Kallen RG, Barchi RL, Robertson M, Leppert MF. Ptácek LJ, et al. Among authors: barchi rl. Cell. 1991 Nov 29;67(5):1021-7. doi: 10.1016/0092-8674(91)90374-8. Cell. 1991. PMID: 1659948

6

Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene.

Ebers GC, George AL, Barchi RL, Ting-Passador SS, Kallen RG, Lathrop GM, Beckmann JS, Hahn AF, Brown WF, Campbell RD, et al. Ebers GC, et al. Among authors: barchi rl. Ann Neurol. 1991 Dec;30(6):810-6. doi: 10.1002/ana.410300610. Ann Neurol. 1991. PMID: 1686388

7

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation.

Chahine M, George AL Jr, Zhou M, Ji S, Sun W, Barchi RL, Horn R. Chahine M, et al. Among authors: barchi rl. Neuron. 1994 Feb;12(2):281-94. doi: 10.1016/0896-6273(94)90271-2. Neuron. 1994. PMID: 8110459 Free article.

8

Genomic organization of the human skeletal muscle sodium channel gene.

George AL Jr, Iyer GS, Kleinfield R, Kallen RG, Barchi RL. George AL Jr, et al. Among authors: barchi rl. Genomics. 1993 Mar;15(3):598-606. doi: 10.1006/geno.1993.1113. Genomics. 1993. PMID: 8385647 Free article.

9

Sodium channel mutations and disorders of excitation in human skeletal muscle.

Ji S, George AL, Horn R, Barchi RL. Ji S, et al. Among authors: barchi rl. Soc Gen Physiol Ser. 1995;50:61-76. Soc Gen Physiol Ser. 1995. PMID: 7676325 Review. No abstract available.

10

Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro.

Yang N, Ji S, Zhou M, Ptácek LJ, Barchi RL, Horn R, George AL Jr. Yang N, et al. Among authors: barchi rl. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12785-9. doi: 10.1073/pnas.91.26.12785. Proc Natl Acad Sci U S A. 1994. PMID: 7809121 Free PMC article.

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