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Platypnea-Orthodeoxia Syndrome: Diagnostic Challenge and the Importance of Heightened Clinical Suspicion.
Published in:
2015
By:
- Henkin, Stanislav;
- Negrotto, Sara;
- Pollak, Peter M.;
- Cullen, Michael W.;
- O'Cochlain, D. Fearghas;
- Wright, R. Scott
Publication type:
Case Study
Ergotamine-Associated Valvulopathy.
Published in:
2012
By:
- Bois, John P.;
- Ponnada, Vara Venkata;
- O'Cochlain, D. Fearghas;
- Brady, Peter A.;
- Edwards, William D.;
- Klarich, Kyle W.
Publication type:
Case Study
ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating.
Published in:
Nature Genetics, 2004, v. 36, n. 4, p. 382, doi. 10.1038/ng1329
By:
- Bienengraeber, Martin;
- Olson, Timothy M.;
- Selivanov, Vitaliy A.;
- Kathmann, Eva C.;
- O'Cochlain, Fearghas;
- Gao, Fan;
- Karger, Amy B.;
- Ballew, Jeffrey D.;
- Hodgson, Denice M.;
- Zingman, Leonid V.;
- Pang, Yuan-Ping;
- Alekseev, Alexey E.;
- Terzic, Andre
Publication type:
Article
Gene knockout of the KCNJ8-encoded Kir6.1 KATP channel imparts fatal susceptibility to endotoxemia.
Published in:
FASEB Journal, 2006, v. 20, n. 13, p. 2271, doi. 10.1096/fj.06-6349com
By:
- Kane, Garvan C.;
- Chen-Fuh Lam;
- O'Cochlain, Fearghas;
- Hodgson, Denice M.;
- Reyes, Santiago;
- Xiao-Ke Liu;
- Miki, Takashi;
- Seino, Susumu;
- Katusic, Zvonimir S.;
- Terzic, Andre
Publication type:
Article
ABCD-GENE Score and Clinical Outcomes Following Percutaneous Coronary Intervention: Insights from the TAILOR-PCI Trial.
Published in:
2022
By:
- Capodanno, Davide;
- Angiolillo, Dominick J.;
- Lennon, Ryan J.;
- Goodman, Shaun G.;
- Kim, Sang-Wook;
- O'Cochlain, Fearghas;
- So, Derek Y.;
- Sweeney, John;
- Rihal, Charanjit S.;
- Farkouh, Michael;
- Pereira, Naveen L.
Publication type:
journal article
Genetic Disruption of Kir6.2, the Pore-Forming Subunit ofATP-Sensitive K[sup+] Channel, Predisposes toCatecholamine-Induced Ventricular Dysrhythmia.
Published in:
Diabetes, 2004, v. 53, p. S165, doi. 10.2337/diabetes.53.suppl_3.S165
By:
- Liu, Xiao-Ke;
- Yamada, Satsuki;
- Kane, Garvan C.;
- Alekseev, Alexey E.;
- Hodgson, Denice M.;
- O'Cochlain, Fearghas;
- Jahangir, Arshad;
- Miki, Takashi;
- Seino, Susumu;
- Terzic, Andre
Publication type:
Article
ATP-Sensitive K[sup+] Channel Knockout Compromises theMetabolic Benefit of Exercise Training, Resulting inCardiac Deficits.
Published in:
Diabetes, 2004, v. 53, p. S169, doi. 10.2337/diabetes.53.suppl_3.S169
By:
- Kane, Garvan C.;
- Behfar, Atta;
- Yamada, Satsuki;
- Perez-Terzic, Carmen;
- O'Cochlain, Fearghas;
- Reyes, Santiago;
- Dzeja, Petras P.;
- Miki, Takashi;
- Seino, Susumu;
- Terzic, Andre
Publication type:
Article
Safety and Efficacy of CYP2C19 Genotype-Guided Escalation of P2Y12 Inhibitor Therapy After Percutaneous Coronary Intervention in Chronic Kidney Disease: a Post Hoc Analysis of the TAILOR-PCI Study.
Published in:
Cardiovascular Drugs & Therapy, 2024, v. 38, n. 3, p. 447, doi. 10.1007/s10557-022-07392-2
By:
- Mathew, Roy O.;
- Sidhu, Mandeep S.;
- Rihal, Charanjit S.;
- Lennon, Ryan;
- El-Hajjar, Mohammed;
- Yager, Neil;
- Lyubarova, Radmila;
- Abdul-Nour, Khaled;
- Weitz, Steven;
- O'Cochlain, D. Fearghas;
- Murthy, Vishakantha;
- Levisay, Justin;
- Marzo, Kevin;
- Graham, John;
- Dzavik, Vlad;
- So, Derek;
- Goodman, Shaun;
- Rosenberg, Yves D.;
- Pereira, Naveen;
- Farkouh, Michael E.
Publication type:
Article
KCNJ11 gene knockout of the Kir6.2 KATP channel causes maladaptive remodeling and heart failure in hypertension.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 15, p. 2285, doi. 10.1093/hmg/ddl154
By:
- Kane, Garvan C.;
- Behfar, Atta;
- Dyer, Roy B.;
- O'Cochlain, D. Fearghas;
- Liu, Xiao-Ke;
- Hodgson, Denice M.;
- Reyes, Santiago;
- Miki, Takashi;
- Seino, Susumu;
- Terzic, Andre
Publication type:
Article
Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy.
Published in:
Human Molecular Genetics, 2004, v. 13, n. 20, p. 2505, doi. 10.1093/hmg/ddh266
By:
- O'Cochlain, D. Fearghas;
- Perez-Terzic, Carmen;
- Reyes, Santiago;
- Kane, Garvan C.;
- Behfar, Atta;
- Hodgson, Denice M.;
- Strommen, Jeffrey A.;
- Liu, Xiao-Ke;
- van den Broek, Walther;
- Wansink, Derick G.;
- Wieringa, Bé;
- Terzic, Andre
Publication type:
Article

Found: 10

Platypnea-Orthodeoxia Syndrome: Diagnostic Challenge and the Importance of Heightened Clinical Suspicion.

Ergotamine-Associated Valvulopathy.

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic K<sub>ATP</sub> channel gating.

Gene knockout of the KCNJ8-encoded Kir6.1 K<sub>ATP</sub> channel imparts fatal susceptibility to endotoxemia.

ABCD-GENE Score and Clinical Outcomes Following Percutaneous Coronary Intervention: Insights from the TAILOR-PCI Trial.

Genetic Disruption of Kir6.2, the Pore-Forming Subunit ofATP-Sensitive K[sup+] Channel, Predisposes toCatecholamine-Induced Ventricular Dysrhythmia.

ATP-Sensitive K[sup+] Channel Knockout Compromises theMetabolic Benefit of Exercise Training, Resulting inCardiac Deficits.

Safety and Efficacy of CYP2C19 Genotype-Guided Escalation of P2Y<sub>12</sub> Inhibitor Therapy After Percutaneous Coronary Intervention in Chronic Kidney Disease: a Post Hoc Analysis of the TAILOR-PCI Study.

KCNJ11 gene knockout of the Kir6.2 KATP channel causes maladaptive remodeling and heart failure in hypertension.

Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy.