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Arthur M. Brown

Affiliations: 
ChanTest, Garfield Heights, OH, United States 
Area:
Ion Channels
Website:
http://www.chantest.com/
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"Arthur Brown"
Mean distance: 17.83 (cluster 11)
 
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Parents

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Eric 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

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Paola 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

Collaborators

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BETA: Related publications

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
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