Arthur M. Brown
Affiliations: | ChanTest, Garfield Heights, OH, United States |
Area:
Ion ChannelsWebsite:
http://www.chantest.com/Google:
"Arthur Brown"Mean distance: 17.83 (cluster 11)
Parents
Sign in to add mentorEric Neil | grad student | 1961-1964 | Middlesex Hospital Medical School (Physiology Academic Tree) | |
(https://www.physiology.org/doi/pdf/10.1152/physiologyonline.1991.6.4.194) |
Children
Sign in to add traineePaola Perin | research assistant | 1993-1994 | Baylor |
Michael C. Andresen | grad student | 1975-1978 | UTMB |
Laura Bianchi | grad student | 1994-1998 | |
Mariella De Biasi | post-doc | Baylor | |
Michael C. Andresen | post-doc | 1977-1979 | UTMB |
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Publications
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Ficker E, Kuryshev YA, Dennis AT, et al. (2004) Mechanisms of arsenic-induced prolongation of cardiac repolarization. Molecular Pharmacology. 66: 33-44 |
Ficker E, Dennis AT, Wang L, et al. (2003) Role of the cytosolic chaperones Hsp70 and Hsp90 in maturation of the cardiac potassium channel HERG. Circulation Research. 92: e87-100 |
Bianchi L, Priori SG, Napolitano C, et al. (2000) Mechanisms of I(Ks) suppression in LQT1 mutants. American Journal of Physiology. Heart and Circulatory Physiology. 279: H3003-11 |
Napolitano C, Schwartz PJ, Brown AM, et al. (2000) Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias. Journal of Cardiovascular Electrophysiology. 11: 691-6 |
Bianchi L, Shen Z, Dennis AT, et al. (1999) Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome. Human Molecular Genetics. 8: 1499-507 |
Bianchi L, Priori SG, Shen Z, et al. (1999) Corrigendum: Cellular dysfunction of LQT5-minK mutants: Abnormalities of IKs, IKr and trafficking in long QT syndrome (Human Molecular Genetics (1999) 8 (1499-1507)) Human Molecular Genetics. 8: 2335 |
Kramer JW, Post MA, Brown AM, et al. (1998) Modulation of potassium channel gating by coexpression of Kv2.1 with regulatory Kv5.1 or Kv6.1 alpha-subunits. The American Journal of Physiology. 274: C1501-10 |
Priori SG, Schwartz PJ, Napolitano C, et al. (1998) A recessive variant of the Romano-Ward long-QT syndrome? Circulation. 97: 2420-5 |
Schwalbe RA, Bianchi L, Accili EA, et al. (1998) Functional consequences of ROMK mutants linked to antenatal Bartter's syndrome and implications for treatment. Human Molecular Genetics. 7: 975-80 |
Schwalbe RA, Bianchi L, Brown AM. (1997) Mapping the kidney potassium channel ROMK1. Glycosylation of the pore signature sequence and the COOH terminus. The Journal of Biological Chemistry. 272: 25217-23 |