Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
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G. Landes | A. Moss | P. Schwartz | J. Towbin | J. Millholland | M. Curran | M. Keating | I. Splawski | K. Timothy | D. Atkinson | G. Vincent | Q. Wang | T. Burn | T. VanRaay | J. Shen | T. D. Jager | T. Connors | Qing Wang | Vincent Gm
[1] S. Priori,et al. Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy. , 1995, Circulation.
[2] F. Charpentier,et al. Mapping of a gene for long QT syndrome to chromosome 4q25-27. , 1995, American journal of human genetics.
[3] S. Priori,et al. Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia. , 1995, Human molecular genetics.
[4] K. Klinger,et al. Increased exon-trapping efficiency through modifications to the pSPL3 splicing vector. , 1995, Gene.
[5] F. Collins,et al. Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349. , 1995, American journal of human genetics.
[6] G. Robertson,et al. HERG, a human inward rectifier in the voltage-gated potassium channel family. , 1995, Science.
[7] M. Sanguinetti,et al. A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel , 1995, Cell.
[8] Arthur J Moss,et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome , 1995, Cell.
[9] E. Green,et al. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome , 1995, Cell.
[10] M. Keating,et al. Isolation of P1 insert ends by direct sequencing. , 1994, BioTechniques.
[11] Cécile Fizames,et al. The 1993–94 Généthon human genetic linkage map , 1994, Nature Genetics.
[12] X. Chen,et al. Genomic organization, nucleotide sequence, biophysical properties, and localization of the voltage-gated K+ channel gene KCNA4/Kv1.4 to mouse chromosome 2/human 11p14 and mapping of KCNC1/Kv3.1 to mouse 7/human 11p14.3-p15.2 and KCNA1/Kv1.1 to human 12p13. , 1994, Genomics.
[13] D. Church,et al. Isolation of genes from complex sources of mammalian genomic DNA using exon amplification , 1994, Nature Genetics.
[14] A. Moss,et al. Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity , 1994, Nature Genetics.
[15] R. MacKinnon,et al. Functional stoichiometry of Shaker potassium channel inactivation. , 1993, Science.
[16] A. Tanigami,et al. Mapping of 262 DNA markers into 24 intervals on human chromosome 11. , 1992, American journal of human genetics.
[17] Robert Lemery,et al. Effect of the antiarrhythmic agent moricizine on survival after myocardial infarction. , 1992, The New England journal of medicine.
[18] M. Leppert,et al. Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11. , 1991, American journal of human genetics.
[19] Lawrence Salkoff,et al. Shaker, Shal, Shab, and Shaw express independent K+ current systems , 1991, Neuron.
[20] M. Leppert,et al. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. , 1991, Science.
[21] P. Sharp,et al. Exon amplification: a strategy to isolate mammalian genes based on RNA splicing. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[22] R. MacKinnon. Determination of the subunit stoichiometry of a voltage-activated potassium channel , 1991, Nature.
[23] F. Collins,et al. Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. , 1991, Nucleic acids research.
[24] A. Tanigami,et al. Isolation and mapping of 62 new RFLP markers on human chromosome 11. , 1991, American journal of human genetics.
[25] M V Olson,et al. Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[26] A. C. Chinault,et al. Rapid identification of yeast artificial chromosome clones by matrix pooling and crude lysate PCR. , 1990, Nucleic acids research.
[27] N. Sternberg,et al. Bacteriophage P1 cloning system for the isolation, amplification, and recovery of DNA fragments as large as 100 kilobase pairs. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[28] D. Hartl,et al. Genetic applications of an inverse polymerase chain reaction. , 1988, Genetics.
[29] O. Pongs,et al. Shaker encodes a family of putative potassium channel proteins in the nervous system of Drosophila. , 1988, The EMBO journal.
[30] D. Levy,et al. Circadian variation in the incidence of sudden cardiac death in the Framingham Heart Study population. , 1987, The American journal of cardiology.
[31] D. Zipes. Proarrhythmic effects of antiarrhythmic drugs. , 1987, The American journal of cardiology.
[32] R. D'Agostino,et al. Sudden death risk in overt coronary heart disease: the Framingham Study. , 1987, American heart journal.
[33] J. Ott,et al. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. , 1985, American journal of human genetics.
[34] A. Malliani,et al. The long Q-T syndrome. , 1975, American heart journal.
[35] A. Moss,et al. Unilateral cervicothoracic sympathetic ganglionectomy for the treatment of long QT interval syndrome. , 1971, The New England journal of medicine.
[36] C. Romano. CONGENITAL CARDIAC ARRHYTHMIA. , 1965, Lancet.
[37] Ward Oc. A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN. , 1964 .
[38] A. Jervell,et al. Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death , 1957 .