Authors:
WALLACE RH
WANG DW
SINGH R
SCHEFFER IE
GEORGE AL
PHILLIPS HA
SAAR K
REIS A
JOHNSON EW
SUTHERLAND GR
BERKOVIC SF
MULLEY JC
Citation: Rh. Wallace et al., FEBRILE SEIZURES AND GENERALIZED EPILEPSY ASSOCIATED WITH A MUTATION IN THE NA-CHANNEL BETA-1 SUBUNIT GENE SCN1B(), Nature genetics, 19(4), 1998, pp. 366-370
Citation: N. Mitrovic et al., INDEPENDENT VERSUS COUPLED INACTIVATION - ROLE OF THE D2 S4 SEGMENT IN SODIUM-CHANNELS/, Naunyn-Schmiedeberg's archives of pharmacology, 358(1), 1998, pp. 2810-2810
Citation: Al. George, CHLORIDE CHANNELS AND ENDOCYTOSIS - CLC-5 MAKES A DENT, Proceedings of the National Academy of Sciences of the United Statesof America, 95(14), 1998, pp. 7843-7845
Citation: Ds. Green et al., HUMAN SODIUM-CHANNEL GATING DEFECTS CAUSED BY MISSENSE MUTATIONS IN S6 SEGMENTS ASSOCIATED WITH MYOTONIA - S804F AND V1293I, Journal of physiology, 510(3), 1998, pp. 685-694
Authors:
PLASSARTSCHIESS E
LHUILLIER L
GEORGE AL
FONTAINE B
TABTI N
Citation: E. Plassartschiess et al., FUNCTIONAL EXPRESSION OF THE ILE693THR NA-CONGENITA IN A HUMAN CELL-LINE( CHANNEL MUTATION ASSOCIATED WITH PARAMYOTONIA), Journal of physiology, 507(3), 1998, pp. 721-727
Citation: N. Mitrovic et al., INDEPENDENT VERSUS COUPLED INACTIVATION IN SODIUM-CHANNELS - ROLE OF THE DOMAIN-2 S4 SEGMENT, The Journal of general physiology, 111(3), 1998, pp. 451-462
Authors:
WANG DW
WEI J
ALINGS M
RODEN DM
GEORGE AL
Citation: Dw. Wang et al., A MUTATION (E1784K) IN THE CARBOXYL-TERMINUS OF THE CARDIAC NA-DOMINANT CONGENITAL LONG QT SYNDROME( CHANNEL CAUSES AUTOSOMAL), Circulation, 98(17), 1998, pp. 278-278
Citation: P. Bennett et al., FUNCTIONAL CONSEQUENCES OF A D1 S6 SODIUM-CHANNEL MUTATION ASSOCIATEDWITH MYOTONIA/, Biophysical journal, 74(2), 1998, pp. 26-26
Citation: N. Mitrovic et al., SLUGGISH MOVEMENT OF A SODIUM-CHANNEL S4 SEGMENT INDUCED BY CYSTEINE MODIFICATION, Biophysical journal, 74(2), 1998, pp. 31-31
Authors:
PIERNO S
DELUCA A
BECK CL
GEORGE AL
CONTECAMERINO D
Citation: S. Pierno et al., REDUCED EXPRESSION OF CLC-1 PARALLELS THE DECREASE IN SARCOLEMMAL CHLORIDE CONDUCTANCE IN AGED RAT MUSCLE, Biophysical journal, 74(2), 1998, pp. 360-360
Citation: Ht. Yu et al., IDENTIFICATION OF PORE-FORMING SEGMENTS IN CLC CHLORIDE CHANNELS USING A CHIMERIC APPROACH, Journal of the American Society of Nephrology, 8, 1997, pp. 231-231
Citation: J. Rosenfeld et al., A NOVEL MUSCLE SODIUM-CHANNEL MUTATION CAUSES PAINFUL CONGENITAL MYOTONIA, Annals of neurology, 42(5), 1997, pp. 811-814
Citation: Ds. Green et al., A PROPOSED MUTATION, VAL781ILE, ASSOCIATED WITH HYPERKALEMIC PERIODICPARALYSIS AND CARDIAC DYSRHYTHMIA IS A BENIGN POLYMORPHISM, Annals of neurology, 42(2), 1997, pp. 253-256
Citation: Dm. Roden et Al. George, STRUCTURE AND FUNCTION OF CARDIAC SODIUM AND POTASSIUM CHANNELS, American journal of physiology. Heart and circulatory physiology, 42(2), 1997, pp. 511-525
Authors:
ENDSLEY JK
PHILLIPS JA
HRUSKA KA
DENNEBERG T
CARLSON J
GEORGE AL
Citation: Jk. Endsley et al., GENOMIC ORGANIZATION OF A HUMAN CYSTINE TRANSPORTER GENE (SLC3A1) ANDIDENTIFICATION OF NOVEL MUTATIONS CAUSING CYSTINURIA, Kidney international, 51(6), 1997, pp. 1893-1899
Citation: C. Fahlke et al., A MUTATION IN THE HUMAN MUSCLE CHLORIDE CHANNEL THAT CAUSES PROFOUND EFFECTS ON PORE PROPERTIES, Pflugers Archiv, 433(6), 1997, pp. 64-64
Citation: Ll. Kurz et al., PROBING THE MAJOR SKELETAL-MUSCLE CHLORIDE CHANNEL WITH ZN2-REACTIVE COMPOUNDS( AND OTHER SULFHYDRYL), Pflugers Archiv, 433(3), 1997, pp. 357-363
Authors:
WAGNER S
LERCHE H
MITROVIC N
HEINE R
GEORGE AL
LEHMANNHORN F
Citation: S. Wagner et al., A NOVEL SODIUM-CHANNEL MUTATION CAUSING A HYPERKALEMIC PARALYTIC AND PARAMYOTONIC SYNDROME WITH VARIABLE CLINICAL EXPRESSIVITY, Neurology, 49(4), 1997, pp. 1018-1025
Citation: K. Sloanbrown et Al. George, INHERITANCE OF 3 DISTINCT MUSCLE CHLORIDE CHANNEL GENE (CLCN1) MUTATIONS IN A SINGLE RECESSIVE MYOTONIA-CONGENITA FAMILY, Neurology, 48(2), 1997, pp. 542-543