Results 201 to 210 of about 9,233 (239)

Long-QT Trafficking Map. [PDF]

Circulation
London B.
europepmc   +1 more source

Table 1_Pathogenic KCNH2-G53S variant in the PAS domain influences the electrophysiological phenotype in long QT syndrome type 2.docx

Dasom Mun (7022756), Ji-Young Kang (7022753), Malgeum Park (21024236), Gyeongseo Yoo (21024239), Nuri Yun (7022759), YouMi Hwang (15183260), Boyoung Joung (832076)   +6 more
openalex   +1 more source

Enhancing schizophrenia treatment efficacy: The combined impact of Yueju pill and olanzapine through quercetin target modulation. [PDF]

World J Psychiatry
Zhu DM, Lu Y, Xiao XD, Sun Y, Tao G, Long B, Zhao J.   +6 more
europepmc   +1 more source

Induced Pluripotent Stem Cells in Congenital Long QT Syndrome: Research Progress and Clinical Applications. [PDF]

Rev Cardiovasc Med
Li Q, Wang YF, Wang B, Lv TT, Zhang P.
europepmc   +1 more source

Evaluation of the Potential Targets of Shenxian-Shengmai Oral Liquid in Treating Sick Sinus Syndrome Based on Network Pharmacology and Molecular Docking. [PDF]

Food Sci Nutr
Hou P, Zhang H, Min DY, Wu J, Chen C, Wang J, Lu YP, Yao YJ, Li LK, Liu Y.   +9 more
europepmc   +1 more source

Current Perspective for Atrial Fibrillation in Patients with Brugada Syndrome: A Comprehensive Review. [PDF]

Rev Cardiovasc Med
Iqbal M, Bunawan R, Karim K, Karwiky G, Achmad C.   +4 more
europepmc   +1 more source

The Uncommon Phenomenon of Short QT Syndrome: A Scoping Review of the Literature. [PDF]

J Pers Med
Boulmpou A, Giannopoulos A, Papadopoulos C, Giannopoulos G, Papagiannis I, Zormpas G, Keivanidou A, Fidani L, Vassilikos V.   +8 more
europepmc   +1 more source

Mutational effect prediction of two missense mutations 2350C > T (R784W) and 2690A > C (K897T) on the KCNH2 protein structure.

Muhammad Irfan Abdul Jalal (12696668), Muhammad-Redha Abdullah-Zawawi (14067930), Nurfadhlina Musa (5378888), Basyirah Ghazali (21246757), Zalina Zahari (5378891), Nasir Mohamad (5378885)   +5 more
openalex   +1 more source

The Diagnostic Value of Copy Number Variants in Genetic Cardiomyopathies and Channelopathies. [PDF]

J Cardiovasc Dev Dis
Caputo V, Visconti VV, Marchionni E, Ferradini V, Balsano C, De Vico P, Calò L, Mango R, Novelli G, Sangiuolo F.   +9 more
europepmc   +1 more source

In silico development of HASDI-G2 as a novel agent for selective recognition of the DNA sequence. [PDF]

Sci Rep
Zaremba A, Zaremba P, Zahorodnia S.
europepmc   +1 more source