Literature DB >> 23591039

IKs in heart and hearing, the ear can do with less than the heart.

Zahurul A Bhuiyan, Arthur A M Wilde.   

Abstract

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Year:  2013        PMID： 23591039     DOI： 10.1161/CIRCGENETICS.113.000143

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN： 1942-3268


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  7 in total

1.  The residue I257 at S4-S5 linker in KCNQ1 determines KCNQ1/KCNE1 channel sensitivity to 1-alkanols.

Authors:  Chang Xie; Hao-wen Liu; Na Pan; Jiu-ping Ding; Jing Yao
Journal:  Acta Pharmacol Sin       Date:  2016-01       Impact factor: 6.150

2.  Recessive cardiac phenotypes in induced pluripotent stem cell models of Jervell and Lange-Nielsen syndrome: disease mechanisms and pharmacological rescue.

Authors:  Miao Zhang; Cristina D'Aniello; Arie O Verkerk; Eva Wrobel; Stefan Frank; Dorien Ward-van Oostwaard; Ilaria Piccini; Christian Freund; Jyoti Rao; Guiscard Seebohm; Douwe E Atsma; Eric Schulze-Bahr; Christine L Mummery; Boris Greber; Milena Bellin
Journal:  Proc Natl Acad Sci U S A       Date:  2014-12-01       Impact factor: 11.205

Review 3.  Congenital Long QT Syndrome: An Update and Present Perspective in Saudi Arabia.

Authors:  Zahurul A Bhuiyan; Safar Al-Shahrani; Jumana Al-Aama; Arthur A M Wilde; Tarek S Momenah
Journal:  Front Pediatr       Date:  2013-11-20       Impact factor: 3.418

4.  Autosomal recessive long QT syndrome, type 1 in eight families from Saudi Arabia.

Authors:  Amnah Y Bdier; Saleh Al-Ghamdi; Prashant K Verma; Khalid Dagriri; Bandar Alshehri; Omamah A Jiman; Sherif E Ahmed; Arthur A M Wilde; Zahurul A Bhuiyan; Jumana Y Al-Aama
Journal:  Mol Genet Genomic Med       Date:  2017-06-21       Impact factor: 2.183

5.  Atypical long QT syndrome phenotype in heterozygous/homozygous KCNQ1 Ala590Thr.

Authors:  Justin D Smith; Jeffrey M Vinocur
Journal:  HeartRhythm Case Rep       Date:  2017-01-27

6.  Molecular Mechanism of Autosomal Recessive Long QT-Syndrome 1 without Deafness.

Authors:  Annemarie Oertli; Susanne Rinné; Robin Moss; Stefan Kääb; Gunnar Seemann; Britt-Maria Beckmann; Niels Decher
Journal:  Int J Mol Sci       Date:  2021-01-23       Impact factor: 5.923

7.  Novel frameshift mutation in the KCNQ1 gene responsible for Jervell and Lange-Nielsen syndrome.

Authors:  Azam Amirian; Seyed Mohammad Dalili; Zahra Zafari; Siamak Saber; Morteza Karimipoor; Vahid Akbari; Amir Farjam Fazelifar; Sirous Zeinali
Journal:  Iran J Basic Med Sci       Date:  2018-01       Impact factor: 2.699
  7 in total

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