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Items: 1 to 50 of 110

1.

Genetic disorders of neuromuscular ion channels.

Kleopa KA, Barchi RL.

Muscle Nerve. 2002 Sep;26(3):299-325. Review.

PMID:
12210360
2.

Nomenclature of voltage-gated sodium channels.

Goldin AL, Barchi RL, Caldwell JH, Hofmann F, Howe JR, Hunter JC, Kallen RG, Mandel G, Meisler MH, Netter YB, Noda M, Tamkun MM, Waxman SG, Wood JN, Catterall WA.

Neuron. 2000 Nov;28(2):365-8. No abstract available.

3.
4.

Altered gene expression in steroid-treated denervated muscle.

Rich MM, Kraner SD, Barchi RL.

Neurobiol Dis. 1999 Dec;6(6):515-22.

PMID:
10600407
6.

Interaction between the skeletal muscle type 1 Na+ channel promoter E-box and an upstream repressor element. Release of repression by myogenin.

Kraner SD, Rich MM, Sholl MA, Zhou H, Zorc CS, Kallen RG, Barchi RL.

J Biol Chem. 1999 Mar 19;274(12):8129-36.

7.

Ion channel mutations affecting muscle and brain.

Barchi RL.

Curr Opin Neurol. 1998 Oct;11(5):461-8. Review.

PMID:
9847995
8.

Phenotype and genotype in the myotonic disorders.

Barchi RL.

Muscle Nerve. 1998 Sep;21(9):1119-21. No abstract available.

PMID:
9703436
9.

Inactivation and secondary structure in the D4/S4-5 region of the SkM1 sodium channel.

Filatov GN, Nguyen TP, Kraner SD, Barchi RL.

J Gen Physiol. 1998 Jun;111(6):703-15.

10.

Two E-boxes are the focal point of muscle-specific skeletal muscle type 1 Na+ channel gene expression.

Kraner SD, Rich MM, Kallen RG, Barchi RL.

J Biol Chem. 1998 May 1;273(18):11327-34.

11.

Analysis of local structure in the D2/S1-S2 region of the rat skeletal muscle type 1 sodium channel using insertional mutagenesis.

Kraner SD, Filatov GN, Sun W, Bannerman P, Lindstrom J, Barchi RL.

J Neurochem. 1998 Apr;70(4):1628-35.

12.

Loss of electrical excitability in an animal model of acute quadriplegic myopathy.

Rich MM, Pinter MJ, Kraner SD, Barchi RL.

Ann Neurol. 1998 Feb;43(2):171-9.

PMID:
9485058
13.

Quality of care in academic neurology departments.

Barchi RL.

Arch Neurol. 1997 Nov;54(11):1336-40. Review.

PMID:
9362978
14.

Ion channel mutations and diseases of skeletal muscle.

Barchi RL.

Neurobiol Dis. 1997;4(3-4):254-64. Review.

PMID:
9361302
15.
16.
18.

Molecular pathology of the skeletal muscle sodium channel.

Barchi RL.

Annu Rev Physiol. 1995;57:355-85. Review. No abstract available.

PMID:
7778872
19.

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

Ji S, George AL, Horn R, Barchi RL.

Soc Gen Physiol Ser. 1995;50:61-76. Review. No abstract available.

PMID:
7676325
20.

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.

Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12785-9.

21.

Voltage-dependent regulation of modal gating in the rat SkM1 sodium channel expressed in Xenopus oocytes.

Ji S, Sun W, George AL Jr, Horn R, Barchi RL.

J Gen Physiol. 1994 Oct;104(4):625-43.

22.

Pharmacological modulation of human cardiac Na+ channels.

Krafte DS, Davison K, Dugrenier N, Estep K, Josef K, Barchi RL, Kallen RG, Silver PJ, Ezrin AM.

Eur J Pharmacol. 1994 Feb 15;266(3):245-54.

PMID:
8174607
23.

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.

Neuron. 1994 Feb;12(2):281-94.

PMID:
8110459
25.
26.

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.

Ann Neurol. 1993 Mar;33(3):300-7.

PMID:
8388676
27.

Genomic organization of the human skeletal muscle sodium channel gene.

George AL Jr, Iyer GS, Kleinfield R, Kallen RG, Barchi RL.

Genomics. 1993 Mar;15(3):598-606.

PMID:
8385647
28.

Ion channels and disorders of excitation in skeletal muscle.

Barchi RL.

Curr Opin Neurol Neurosurg. 1993 Feb;6(1):40-7. Review.

PMID:
7679017
29.

Voltage-dependent sodium channels.

Cohen SA, Barchi RL.

Int Rev Cytol. 1993;137C:55-103. Review. No abstract available.

PMID:
8387472
30.

Structure, function and expression of voltage-dependent sodium channels.

Kallen RG, Cohen SA, Barchi RL.

Mol Neurobiol. 1993 Fall-Winter;7(3-4):383-428. Review.

PMID:
8179845
31.

Lidocaine block of human heart sodium channels expressed in Xenopus oocytes.

Chahine M, Chen LQ, Barchi RL, Kallen RG, Horn R.

J Mol Cell Cardiol. 1992 Nov;24(11):1231-6.

PMID:
1336062
32.

Sodium channel gene defects in the periodic paralyses.

Barchi RL.

Curr Opin Neurobiol. 1992 Oct;2(5):631-7. Review. Erratum in: Curr Opin Neurobiol 1992 Dec;2(6):852.

PMID:
1330128
33.

Chimeric study of sodium channels from rat skeletal and cardiac muscle.

Chen LQ, Chahine M, Kallen RG, Barchi RL, Horn R.

FEBS Lett. 1992 Sep 14;309(3):253-7.

34.

Cardiac sodium channel structure and function.

Cohen SA, Barchi RL.

Trends Cardiovasc Med. 1992 Jul-Aug;2(4):133-40. doi: 10.1016/1050-1738(92)90020-S.

PMID:
21239259
36.

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.

Neuron. 1992 May;8(5):891-7.

PMID:
1316765
37.

Expressed Na channel clones differ in their sensitivity to external calcium concentration.

Chahine M, Chen LQ, Kallen RG, Barchi RL, Horn R.

Biophys J. 1992 Apr;62(1):37-40. No abstract available.

38.

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

George AL Jr, Komisarof J, Kallen RG, Barchi RL.

Ann Neurol. 1992 Feb;31(2):131-7.

PMID:
1315496
39.

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel.

Gellens ME, George AL Jr, Chen LQ, Chahine M, Horn R, Barchi RL, Kallen RG.

Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):554-8.

40.

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.

Cell. 1991 Nov 29;67(5):1021-7.

PMID:
1659948
41.

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.

Ann Neurol. 1991 Dec;30(6):810-6.

PMID:
1686388
42.
43.

Bad channel genes and weak muscles.

Barchi RL.

Curr Biol. 1991 Jun;1(3):150-2. No abstract available.

PMID:
15336151
44.

SkM2, a Na+ channel cDNA clone from denervated skeletal muscle, encodes a tetrodotoxin-insensitive Na+ channel.

White MM, Chen LQ, Kleinfield R, Kallen RG, Barchi RL.

Mol Pharmacol. 1991 May;39(5):604-8.

PMID:
1851958
45.

Assignment of a human skeletal muscle sodium channel alpha-subunit gene (SCN4A) to 17q23.1-25.3.

George AL Jr, Ledbetter DH, Kallen RG, Barchi RL.

Genomics. 1991 Mar;9(3):555-6. No abstract available.

PMID:
1851726
46.

RFLP for BglII at the human skeletal muscle sodium channel locus.

Ebers GC, Hudson AJ, George AL, Barchi RL, Kallen RG.

Nucleic Acids Res. 1991 Mar 11;19(5):1166. No abstract available.

47.
48.

Expression of sodium channel subtypes during development in rat skeletal muscle.

Schotland DL, Fieles W, Barchi RL.

Muscle Nerve. 1991 Feb;14(2):142-51.

PMID:
1847990
49.

Molecular aspects of voltage-dependent ion channels.

Barchi RL.

Adv Exp Med Biol. 1991;308:107-17. Review.

PMID:
1724871
50.

Primary structure and expression of a sodium channel characteristic of denervated and immature rat skeletal muscle.

Kallen RG, Sheng ZH, Yang J, Chen LQ, Rogart RB, Barchi RL.

Neuron. 1990 Feb;4(2):233-42.

PMID:
2155010

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