Works matching DE "HEART disease genetics"

Results: 211

SNPing Away at Genome-Wide Disease Association Studies.

Published in:

Bio-IT World, 2007, v. 6, n. 6, p. 28

By:

Glaser, Vicki

Publication type:

Article

NitroMed Ties Gene Biomarkers to BiDil Benefit.

Published in:

Bio-IT World, 2006, v. 5, n. 3, p. 21

By:

Davies, Kevin

Publication type:

Article

Influence of genetic modifiers on sudden cardiac death cases.

Published in:

International Journal of Legal Medicine, 2018, v. 132, n. 2, p. 379, doi. 10.1007/s00414-017-1739-7

By:

Jenewein, Tina;
Verhoff, Marcel A.;
Kauferstein, Silke;
Neumann, Thomas;
Kuniss, Malte;
Erkapic, Damir;
Thiel, Gerhard

Publication type:

Article

Chronic creatine kinase deficiency eventually leads to congestive heart failure, but severity is dependent on genetic background, gender and age.

Published in:

Basic Research in Cardiology, 2012, v. 107, n. 5, p. 1, doi. 10.1007/s00395-012-0276-2

By:

Lygate, Craig;
Medway, Debra;
Ostrowski, Philip;
Aksentijevic, Dunja;
Sebag-Montefiore, Liam;
Hunyor, Imre;
Zervou, Sevasti;
Schneider, Jurgen;
Neubauer, Stefan

Publication type:

Article

Myocardial Fibrosis in the Pathogenesis, Diagnosis, and Treatment of Hypertrophic Cardiomyopathy.

Published in:

Cardiovascular Innovations & Applications (CVIA), 2021, v. 5, n. 4, p. 267, doi. 10.15212/CVIA.2021.0008

By:

Zeyi Cheng;
Miaomiao Qi;
Chengyuan Zhang;
Yanxia Mao

Publication type:

Article

ACE Gene Polymorphism in Coronary Artery Disease in West Bank, Palestine.

Published in:

Hebron University Research Journal (Natural Sciences), 2020, v. 9, p. 1

By:

Saghir, Sabri;
Darwish, Alaa;
Rajabi, Raghad;
Huiseen, Ayman

Publication type:

Article

Muscle-Specific Mis-Splicing and Heart Disease Exemplified by RBM20.

Published in:

Genes, 2018, v. 9, n. 1, p. 18, doi. 10.3390/genes9010018

By:

Rexiati, Maimaiti;
Sun, Mingming;
Guo, Wei

Publication type:

Article

The Ratio of Second to Fourth Digit Length (2D:4D) and Heart Disease.

Published in:

Bangladesh Journal of Medical Science, 2016, v. 15, n. 4, p. 529, doi. 10.3329/bjms.v15i4.23958

By:

Kumar, N.;
Sallehuddin, M. A. B.;
Syed, S. M. F. B.;
Idris, M. H. B.;
Jamba, T. A.;
Ravindra, S.;
patil, J.;
Aithal, A.

Publication type:

Article

The Eisenmenger malformation: a morphologic study.

Published in:

2016

By:

Restivo, Angelo;
di Gioia, Cira R. T.;
Anderson, Robert H.;
Carletti, Raffaella;
Gallo, Pietro

Publication type:

journal article

Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood.

Published in:

2007

By:

Kaski, Juan Pablo;
Burch, Michael;
Elliott, Perry M.

Publication type:

Case Study

Variants of the CFC1 gene in patients with laterality defects associated with congenital cardiac disease.

Published in:

Cardiology in the Young, 2007, v. 17, n. 3, p. 268, doi. 10.1017/S1047951107000455

By:

Tierney, Elif Seda Selamet;
Marans, Zvi;
Rutkin, Melissa B.;
Chung, Wendy K.

Publication type:

Article

Clinical investigations over 13 years to establish the nature of the cardiac defects in patients having abnormalities of lateralization.

Published in:

2007

By:

Yildirim, Selman Vefa;
Tokel, Kürsad;
Varan, Birgül;
Aslamaci, Sait;
Ekici, Enver;
Tokel, Kürsad;
Varan, Birgül

Publication type:

journal article

Searching for order among disorders of laterality.

Published in:

2007

By:

McElhinney, Doff B.

Publication type:

commentary

Psychological symptoms in patients after surgery for congenital cardiac disease.

Published in:

Cardiology in the Young, 2006, v. 16, n. 6, p. 540, doi. 10.1017/S1047951106001442

By:

Geyer, Siegfried;
Norozi, Kambiz;
Zoege, Monika;
Kempa, Almut;
Buchhorn, Reiner;
Wessel, Armin

Publication type:

Article

Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth.

Published in:

PLoS ONE, 2019, v. 14, n. 01, p. 1, doi. 10.1371/journal.pone.0210017

By:

Sahlin, Ellika;
Gréen, Anna;
Gustavsson, Peter;
Liedén, Agne;
Nordenskjöld, Magnus;
Papadogiannakis, Nikos;
Pettersson, Karin;
Nilsson, Daniel;
Jonasson, Jon;
Iwarsson, Erik

Publication type:

Article

The Genetics of Cardiac Arrhythmias.

Published in:

Pacing & Clinical Electrophysiology, 2000, v. 23, n. 1, p. 106, doi. 10.1111/j.1540-8159.2000.tb00655.x

By:

Towbin, Jeffrey A.;
Vatta, Matteo

Publication type:

Article

PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases.

Published in:

2018

By:

Adler, Angela;
Kirchmeier, Pia;
Reinhard, Julian;
Brauner, Barbara;
Dunger, Irmtraud;
Fobo, Gisela;
Frishman, Goar;
Montrone, Corinna;
Mewes, H.-Werner;
Arnold, Matthias;
Ruepp, Andreas

Publication type:

journal article

Mitochondrial deficiency and cardiac sudden death in mice lacking the MEF2A transcription factor.

Published in:

Nature Medicine, 2002, v. 8, n. 11, p. 1303, doi. 10.1038/nm789

By:

Naya, Francisco J.;
Black, Brian L.;
Wu, Hai;
Bassel-Duby, Rhonda;
Richardson, James A.;
Hill, Joseph A.;
Olson, Eric N.

Publication type:

Article

microRNA-29a inhibits cardiac fibrosis in Sprague-Dawley rats by downregulating the expression of DNMT3A.

Published in:

Anatolian Journal of Cardiology / Anadolu Kardiyoloji Dergisi, 2018, v. 20, n. 4, p. 198, doi. 10.14744/AnatolJCardiol.2018.98511

By:

Run-He Qin;
Hui Tao;
Shi-Hao Ni;
Peng Shi;
Chen Dai;
Kai-Hu Shi

Publication type:

Article

Large-scale discovery of enhancers from human heart tissue.

Published in:

Nature Genetics, 2012, v. 44, n. 1, p. 89, doi. 10.1038/ng.1006

By:

May, Dalit;
Blow, Matthew J;
Kaplan, Tommy;
McCulley, David J;
Jensen, Brian C;
Akiyama, Jennifer A;
Holt, Amy;
Plajzer-Frick, Ingrid;
Shoukry, Malak;
Wright, Crystal;
Afzal, Veena;
Simpson, Paul C;
Rubin, Edward M;
Black, Brian L;
Bristow, James;
Pennacchio, Len A;
Visel, Axel

Publication type:

Article

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.

Published in:

Nature Genetics, 2011, v. 43, n. 6, p. 531, doi. 10.1038/ng.834

By:

Kato, Norihiro;
Takeuchi, Fumihiko;
Tabara, Yasuharu;
Kelly, Tanika N.;
Min Jin Go;
Xueling Sim;
Wan Ting Tay;
Chien-Hsiun Chen;
Yi Zhang;
Yamamoto, Ken;
Katsuya, Tomohiro;
Yokota, Mitsuhiro;
Young Jin Kim;
Ong, Rick Twee Hee;
Nabika, Toru;
Dongfeng Gu;
Li-ching Chang;
Kokubo, Yoshihiro;
Wei Huang;
Ohnaka, Keizo

Publication type:

Article

Research highlights.

Published in:

Nature Genetics, 2007, v. 39, n. 6, p. 713, doi. 10.1038/ng0607-713

By:

Niemitz, Emily;
Packer, Alan;
Vogan, Kyle

Publication type:

Article

PATHOGENIC MECHANISMS OF CONGENITAL HEART DISEASE.

Published in:

Fetal & Pediatric Pathology, 2010, v. 29, n. 5, p. 359, doi. 10.3109/15513811003789628

By:

Huang, Jing-Bin;
Liu, Ying-Long;
Lv, Xiao-Dong

Publication type:

Article

Tetra primer ARMS-PCR relates folate/homocysteine pathway genes and ACE gene polymorphism with coronary artery disease.

Published in:

Molecular & Cellular Biochemistry, 2011, v. 355, n. 1/2, p. 289, doi. 10.1007/s11010-011-0866-6

By:

Masud, Rizwan;
Qureshi, Irfan

Publication type:

Article

Cell type-specific expression of endogenous cardiac Troponin I antisense RNA in the neonatal rat heart.

Published in:

Molecular & Cellular Biochemistry, 2009, v. 324, n. 1/2, p. 1

By:

Stefanie Voigtsberger;
Holger Bartsch;
Gert Baumann;
Hans Luther

Publication type:

Article

A novel variant in plakophilin-2 gene detected in a family with arrhythmogenic right ventricular cardiomyopathy.

Published in:

Journal of Interventional Cardiac Electrophysiology, 2012, v. 34, n. 1, p. 11, doi. 10.1007/s10840-011-9643-4

By:

Ostrowska Dahlgren, Bozena;
Allen, Marie;
Lindström, Anne-Cristine;
Bjerke, Mia;
Blomström-Lundqvist, Carina

Publication type:

Article

The Classification Concept of the ESC Working Group on Myocardial and Pericardial Diseases for Dilated Cardiomyopathy.

Published in:

Herz (0340-9937), 2007, v. 32, n. 6, p. 446, doi. 10.1007/s00059-007-3045-5

By:

Kaski, Juan Pablo;
Elliott, Perry

Publication type:

Article

Phenotypic Variation of Familial Hypertrophic Cardiomyopathy Caused by the Phe[sup 110] →Ile Mutation in Cardiac Troponin T.

Published in:

Cardiology, 2000, v. 93, n. 3, p. 155, doi. 10.1159/000007020

By:

Tong-Lang Lin, Boris;
Ichihara, Sahoko;
Yamada, Yoshiji;
Nagasaka, Tetsuo;
Ishihara, Hitoshi;
Nakashima, Nobuo;
Yokota, Mitsuhiro

Publication type:

Article

Variants in structural cardiac genes in patients with cancer therapy-related cardiac dysfunction after anthracycline chemotherapy: a case control study.

Published in:

Cardio-Oncology, 2024, v. 10, n. 1, p. 1, doi. 10.1186/s40959-024-00231-3

By:

Boen, Hanne M.;
Alaerts, Maaike;
Goovaerts, Inge;
Saenen, Johan B.;
Franssen, Constantijn;
Vorlat, Anne;
Vermeulen, Tom;
Heidbuchel, Hein;
Van Laer, Lut;
Loeys, Bart;
Van Craenenbroeck, Emeline M.

Publication type:

Article

What Is QT Interval Prolongation?

Published in:

Journal of Family Practice, 2005, v. 54, p. S4

By:

Vorchheimer, David A.

Publication type:

Article

Implementation of reimbursement for genomic testing in Australia: early successes and the pathway ahead.

Published in:

2024

By:

Mallett, Andrew J.;
Ingles, Jodie;
Goranitis, Ilias;
Stark, Zornitza

Publication type:

Editorial

Pulmonary artery dilatation due to pressure or volume overload in congenital heart disease.

Published in:

Cardiology Letters, 2024, v. 33, n. 3, p. 191, doi. 10.4149/Cardiol_2024_3_7

By:

Kaldararova, Monika;
Bobocka, Katarina;
Kantorova, Andrea;
Drangova, Erika;
Polakova Mistinova, Jana;
Klauco, Filip;
Hlavata, Tereza;
Reptova, Adriana;
Valkovicova, Tatiana;
Simkova, Iveta

Publication type:

Article

Early identification of hERG liability in drug discovery programs by automated patch clamp.

Published in:

Frontiers in Pharmacology, 2014, v. 5, p. 1, doi. 10.3389/fphar.2014.00203

By:

Danker, Timm;
Möller, Clemens

Publication type:

Article

Congenital Aortic Stenosis.

Published in:

Annals of Internal Medicine, 1963, v. 58, n. 3, p. 486, doi. 10.7326/0003-4819-58-3-486

By:

Jones, Robert C.;
Walker, Weldon J.;
Jahnke, Edward J.;
Winn Jr., Dean F.

Publication type:

Article

Kv4.3-Encoded Fast Transient Outward Current Is Presented in Kv4.2 Knockout Mouse Cardiomyocytes.

Published in:

PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0133274

By:

Liu, Jie;
Kim, Kyoung-Han;
Morales, Michael J.;
Heximer, Scott P.;
Hui, Chi-chung;
Backx, Peter H.

Publication type:

Article

Liganded Peroxisome Proliferator-Activated Receptors (PPARs) Preserve Nuclear Histone Deacetylase 5 Levels in Endothelin-Treated Sprague-Dawley Rat Cardiac Myocytes.

Published in:

PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0115258

By:

Zhang, Haining;
Shao, Zongjun;
Alibin, Caroline P.;
Acosta, Crystal;
Anderson, Hope D.

Publication type:

Article

Correction: Ultra High-Resolution Gene Centric Genomic Structural Analysis of a Non-Syndromic Congenital Heart Defect, Tetralogy of Fallot.

Published in:: PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0099148
Publication type:: Article

Opposite Effects of Gene Deficiency and Pharmacological Inhibition of Soluble Epoxide Hydrolase on Cardiac Fibrosis.

Published in:

PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0094092

By:

Li, Lijuan;
Li, Nan;
Pang, Wei;
Zhang, Xu;
Hammock, Bruce D.;
Ai, Ding;
Zhu, Yi

Publication type:

Article

Disruption of Sarcoendoplasmic Reticulum Calcium ATPase Function in <i>Drosophila</i> Leads to Cardiac Dysfunction.

Published in:

PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0077785

By:

Abraham, Dennis M.;
Wolf, Matthew J.

Publication type:

Article

Meta-Analysis of the Association between Transforming Growth Factor-Beta Polymorphisms and Complications of Coronary Heart Disease.

Published in:

PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037878

By:

Morris, Dylan R.;
Moxon, Joseph V.;
Biros, Erik;
Krishna, Smriti M.;
Golledge, Jonathan

Publication type:

Article

A Locus on Chromosome 5 Is Associated with Dilated Cardiomyopathy in Doberman Pinschers.

Published in:

PLoS ONE, 2011, v. 6, n. 5, p. 1, doi. 10.1371/journal.pone.0020042

By:

Mausberg, Theresa-Bernadette;
Wess, Gerhard;
Simak, Julia;
Keller, Lisa;
Drögemüller, Michaela;
Drögemüller1, Cord;
Webster, Matthew T.;
Stephenson^4, Hannah;
Dukes-McEwan, Joanna;
Leeb, Tosso

Publication type:

Article

Scroll-Wave Dynamics in Human Cardiac Tissue: Lessons from a Mathematical Model with Inhomogeneities and Fiber Architecture.

Published in:

PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018052

By:

Majumder, Rupamanjari;
Nayak, Alok Ranjan;
Pandit, Rahul

Publication type:

Article

Genome-Wide Association Study Identifies GPC5 as a Novel Genetic Locus Protective against Sudden Cardiac Arrest.

Published in:

PLoS ONE, 2010, v. 5, n. 3, p. 1, doi. 10.1371/journal.pone.0009879

By:

Arking, Dan E.;
Reinier, Kyndaron;
Post, Wendy;
Jui, Jonathan;
Hilton, Gina;
O'Connor, Ashley;
Prineas, Ronald J.;
Boerwinkle, Eric;
Psaty, Bruce M.;
Tomaselli, Gordon F.;
Rea, Thomas;
Sotoodehnia, Nona;
Siscovick, David S.;
Burke, Gregory L.;
Marban, Eduardo;
Spooner, Peter M.;
Chakravarti, Aravinda;
Chugh, Sumeet S.

Publication type:

Article

Spiral-Wave Turbulence and Its Control in the Presence of Inhomogeneities in Four Mathematical Models of Cardiac Tissue.

Published in:

PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004738

By:

Shajahan, K.;
Nayak, Alok Ranjan;
Pandit, Rahul

Publication type:

Article

SH2B1 is critical for the regulation of cardiac remodelling in response to pressure overload.

Published in:

Cardiovascular Research, 2015, v. 107, n. 2, p. 203, doi. 10.1093/cvr/cvv170

By:

Gang Wu;
Yu Liu;
He Huang;
Yanhong Tang;
Wanli Liu;
Yang Mei;
Nian Wan;
Xiaoxiong Liu;
Congxin Huang

Publication type:

Article

Arrhythmogenic right ventricular cardiomyopathy mutations alter shear response without changes in cell–cell adhesion.

Published in:

Cardiovascular Research, 2014, v. 104, n. 2, p. 280, doi. 10.1093/cvr/cvu212

By:

Hariharan, Venkatesh;
Asimaki, Angeliki;
Michaelson, Jarett E.;
Plovie, Eva;
MacRae, Calum A.;
Saffitz, Jeffrey E.;
Huang, Hayden

Publication type:

Article

Intercalated disc abnormalities, reduced Na+ current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes.

Published in:

Cardiovascular Research, 2012, v. 95, n. 4, p. 409, doi. 10.1093/cvr/cvs219

By:

Rizzo, Stefania;
Lodder, Elisabeth M.;
Verkerk, Arie O.;
Wolswinkel, Rianne;
Beekman, Leander;
Pilichou, Kalliopi;
Basso, Cristina;
Remme, Carol Ann;
Thiene, Gaetano;
Bezzina, Connie R.

Publication type:

Article

Disease characterization using LQTS-specific induced pluripotent stem cells.

Published in:

Cardiovascular Research, 2012, v. 95, n. 4, p. 419, doi. 10.1093/cvr/cvs206

By:

Egashira, Toru;
Yuasa, Shinsuke;
Suzuki, Tomoyuki;
Aizawa, Yoshiyasu;
Yamakawa, Hiroyuki;
Matsuhashi, Tomohiro;
Ohno, Yohei;
Tohyama, Shugo;
Okata, Shinichiro;
Seki, Tomohisa;
Kuroda, Yusuke;
Yae, Kojiro;
Hashimoto, Hisayuki;
Tanaka, Tomofumi;
Hattori, Fumiyuki;
Sato, Toshiaki;
Miyoshi, Shunichiro;
Takatsuki, Seiji;
Murata, Mitsushige;
Kurokawa, Junko

Publication type:

Article

A novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents.

Published in:

Cardiovascular Research, 2012, v. 93, n. 4, p. 666, doi. 10.1093/cvr/cvr329

By:

Hattori, Tetsuhisa;
Makiyama, Takeru;
Akao, Masaharu;
Ehara, Eiji;
Ohno, Seiko;
Iguchi, Moritake;
Nishio, Yukiko;
Sasaki, Kenichi;
Itoh, Hideki;
Yokode, Masayuki;
Kita, Toru;
Horie, Minoru;
Kimura, Takeshi

Publication type:

Article

Decreased inward rectification of Kir2.1 channels is a novel mechanism underlying the short QT syndrome.

Published in:

Cardiovascular Research, 2012, v. 93, n. 4, p. 535, doi. 10.1093/cvr/cvs084

By:

Casini, Simona;
Postma, Alex V.

Publication type:

Article