A L George - JoVE Visualize

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Genomics|October 1, 1994

Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B)N Makita, K Sloan-Brown, D O Weghuis, et al.

FEBS Letters|May 4, 1999

Aging-associated down-regulation of ClC-1 expression in skeletal muscle: phenotypic-independent relation to the decrease of chloride conductanceS Pierno, A De Luca, C L Beck, et al.

Human Mutation|March 29, 2000

Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518XJ Wei, F A Fish, R J Myerburg, et al.

Genomics|March 1, 1993

Genomic organization of the human skeletal muscle sodium channel geneA L George, G S Iyer, R Kleinfield, et al.

Neuron|November 1, 1993

Expression of the sodium channel beta 1 subunit in rat skeletal muscle is selectively associated with the tetrodotoxin-sensitive alpha subunit isoformJ S Yang, P B Bennett, N Makita, et al.

Human Molecular Genetics|July 1, 1994

Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletionR Heine, A L George, U Pika, et al.

Neurology|October 27, 1997

A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivityS Wagner, H Lerche, N Mitrovic, et al.

FEBS Letters|April 28, 1999

Functional consequences of a domain 1/S6 segment sodium channel mutation associated with painful congenital myotoniaD W Wang, D VanDeCarr, P C Ruben, et al.

Nature Genetics|April 1, 1993

Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)A L George, M A Crackower, J A Abdalla, et al.

Kidney International|June 1, 1997

Genomic organization of a human cystine transporter gene (SLC3A1) and identification of novel mutations causing cystinuriaJ K Endsley, J A Phillips, K A Hruska, et al.

Pageof 12

Showing results (61-70 of 114) with videos related to

Sort By:

Pageof 12

Genomics|October 1, 1994

Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B)N Makita, K Sloan-Brown, D O Weghuis, et al.

FEBS Letters|May 4, 1999

Aging-associated down-regulation of ClC-1 expression in skeletal muscle: phenotypic-independent relation to the decrease of chloride conductanceS Pierno, A De Luca, C L Beck, et al.

Human Mutation|March 29, 2000

Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518XJ Wei, F A Fish, R J Myerburg, et al.

Genomics|March 1, 1993

Genomic organization of the human skeletal muscle sodium channel geneA L George, G S Iyer, R Kleinfield, et al.

Neuron|November 1, 1993

Expression of the sodium channel beta 1 subunit in rat skeletal muscle is selectively associated with the tetrodotoxin-sensitive alpha subunit isoformJ S Yang, P B Bennett, N Makita, et al.

Human Molecular Genetics|July 1, 1994

Proof of a non-functional muscle chloride channel in recessive myotonia congenita (Becker) by detection of a 4 base pair deletionR Heine, A L George, U Pika, et al.

Neurology|October 27, 1997

A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivityS Wagner, H Lerche, N Mitrovic, et al.

FEBS Letters|April 28, 1999

Functional consequences of a domain 1/S6 segment sodium channel mutation associated with painful congenital myotoniaD W Wang, D VanDeCarr, P C Ruben, et al.

Nature Genetics|April 1, 1993

Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)A L George, M A Crackower, J A Abdalla, et al.

Kidney International|June 1, 1997

Genomic organization of a human cystine transporter gene (SLC3A1) and identification of novel mutations causing cystinuriaJ K Endsley, J A Phillips, K A Hruska, et al.

Pageof 12