Nani Maharani, M.Si.Med, Ph.D

Biography

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Ab081. variable major phenotypes in familial marfan syndrome in indonesia: a case report

ANNALS OF TRANSLATIONAL MEDICINE 5 (SUPPL 2), 2017

Authors: N Maharani, AN Setyawati, S Rifqi, MA Sungkar, G Pals, SMH Faradz

2017

0 cited

Sociocultural aspects of disorders of sex development

BIRTH DEFECTS RESEARCH PART C: EMBRYO TODAY: REVIEWS 108 (4), 380-383, 2016

Authors: A Ediati, N Maharani, A Utari

2016

15 cited

Hyperuricemia and atrial fibrillation

INTERNATIONAL HEART JOURNAL 57 (4), 395-399, 2016

Authors: N Maharani, M Kuwabara, I Hisatome

2016

60 cited

Effects of uric acid on the no production of huvecs and its restoration by urate lowering agents

DRUG RESEARCH, 2016

Authors: M Mishima, T Hamada, N Maharani, N Ikeda, T Onohara, T Notsu, ...

2016

49 cited

M3 muscarinic receptor signaling stabilizes a novel mutant human ether-a-go-go-related gene channel protein via phosphorylation of heat shock factor 1 in tr...

CIRCULATION JOURNAL 80 (12), 2443-2452

Authors: E Mahati, P Li, Y Kurata, N Maharani, N Ikeda, S Sakata, K Ogura, J Miake, ...

2016

1 cited

M3 muscarinic receptor signaling stabilizes a novel mutant human ether-a-go-go-related gene channel protein via phosphorylation of heat shock factor 1 in transfected cells

CIRCULATION JOURNAL 80 (12), 2443-2452, 2016

Authors: E Mahati, P Li, Y Kurata, N Maharani, N Ikeda, S Sakata, K Ogura, J Miake, ...

2016

6 cited

Hyperuricemia-induced stabilization of kv1. 5 protein

GOUT AND NUCLEIC ACID METABOLISM 40 (1), 74, 2016

Authors: N Maharani, P Li, J Cheng, M Kuwabara, K Yamamoto, I Hisatome

2016

0 cited

Apoptosis induced by an uromodulin mutant c112y and its suppression by topiroxostat

CLINICAL AND EXPERIMENTAL NEPHROLOGY 19 (4), 576-584, 2015

Authors: SB Utami, E Mahati, P Li, N Maharani, N Ikeda, U Bahrudin, C Munemura, ...

2015

12 cited

Fbn1 mutation screening in a marfan syndrome patient

MEDICA HOSPITALIA: JOURNAL OF CLINICAL MEDICINE 3 (1), 2015

Authors: A Setyawati, N Maharani, S Faradz, G Pals, S Rifqi, M Sungkar

2015

0 cited

Depletion of uric acid due to slc22a12 (urat1) loss-of-function mutation causes endothelial dysfunction in hypouricemia

CIRCULATION JOURNAL 79 (5), 1125-1132, 2015

Authors: S Sugihara, I Hisatome, M Kuwabara, K Niwa, N Maharani, M Kato, ...

2015

91 cited