OpenURL Connection Search

Select item for more details and to access through your institution.

Myocardial Fas Ligand Expression Increases Susceptibility to AZT-Induced Cardiomyopathy.
Published in:
Cardiovascular Toxicology, 2007, v. 7, n. 4, p. 255, doi. 10.1007/s12012-007-9004-9
By:
- Purevjav, Enkhsaikhan;
- Nelson, David P.;
- Varela, Jacquelin J.;
- Jimenez, Shinawe;
- Kearney, Debra L.;
- Sanchez, Ximena V.;
- Defreitas, Gilberto;
- Carabello, Blasé;
- Taylor, Michael D.;
- Vatta, Matteo;
- Shearer, William T.;
- Towbin, Jeffrey A.;
- Bowles, Neil E.
Publication type:
Article
A Functional Assay for Sick Sinus Syndrome Genetic Variants.
Published in:
Cellular Physiology & Biochemistry (Karger AG), 2017, v. 42, n. 5, p. 2021, doi. 10.1159/000479897
By:
- Jou, Chuanchau J.;
- Arrington, Cammon B.;
- Barnett, Spencer;
- Shen, Jiaxiang;
- Cho, Scott;
- Sheng, Xiaoming;
- McCullagh, Patrick C.;
- Bowles, Neil E.;
- Pribble, Chase M.;
- Saarel, Elizabeth V.;
- Pilcher, Thomas A.;
- Etheridge, Susan P.;
- Tristani-Firouzi, Martin
Publication type:
Article
Etiologies of cardiomyopathy and heart failure.
Published in:
Nature Medicine, 1999, v. 5, n. 3, p. 266, doi. 10.1038/6474
By:
- Towbin, Jeffrey A.;
- Bowles, Karla R.;
- Bowles, Neil E.
Publication type:
Article
The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele.
Published in:
Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26741-7
By:
- Hateley, Shannon;
- Lopez-Izquierdo, Angelica;
- Jou, Chuanchau J.;
- Cho, Scott;
- Schraiber, Joshua G.;
- Song, Shiya;
- Maguire, Colin T.;
- Torres, Natalia;
- Riedel, Michael;
- Bowles, Neil E.;
- Arrington, Cammon B.;
- Kennedy, Brett J.;
- Etheridge, Susan P.;
- Lai, Shuping;
- Pribble, Chase;
- Meyers, Lindsay;
- Lundahl, Derek;
- Byrnes, Jake;
- Granka, Julie M.;
- Kauffman, Christopher A.
Publication type:
Article
Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events.
Published in:
American Journal of Medical Genetics. Part A, 2017, v. 173, n. 8, p. 2176, doi. 10.1002/ajmg.a.38309
By:
- Hanchard, Neil A.;
- Umana, Luis A.;
- D'Alessandro, Lisa;
- Azamian, Mahshid;
- Poopola, Mojisola;
- Morris, Shaine A.;
- Fernbach, Susan;
- Lalani, Seema R.;
- Towbin, Jeffrey A.;
- Zender, Gloria A.;
- Fitzgerald‐Butt, Sara;
- Garg, Vidu;
- Bowman, Jessica;
- Zapata, Gladys;
- Hernandez, Patricia;
- Arrington, Cammon B.;
- Furthner, Dieter;
- Prakash, Siddharth K.;
- Bowles, Neil E.;
- McBride, Kim L.
Publication type:
Article
Exome Analysis of a Family with Wolff-Parkinson-White Syndrome Identifies a Novel Disease Locus.
Published in:
American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 12, p. 2975, doi. 10.1002/ajmg.a.37297
By:
- Bowles, Neil E.;
- Jou, Chuanchau J.;
- Arrington, Cammon B.;
- Kennedy, Brett J.;
- Earl, Aubree;
- Matsunami, Norisada;
- Meyers, Lindsay L.;
- Etheridge, Susan P.;
- Saarel, Elizabeth V.;
- Bleyl, Steven B.;
- Yost, H. Joseph;
- Yandell, Mark;
- Leppert, Mark F.;
- Tristani‐Firouzi, Martin;
- Gruber, Peter J.
Publication type:
Article
A family-based paradigm to identify candidate chromosomal regions for isolated congenital diaphragmatic hernia.
Published in:
American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 12, p. 3137, doi. 10.1002/ajmg.a.35664
By:
- Arrington, Cammon B.;
- Bleyl, Steven B.;
- Matsunami, Nori;
- Bowles, Neil E.;
- Leppert, Tami I.;
- Demarest, Bradley L.;
- Osborne, Karen;
- Yoder, Bradley A.;
- Byrne, Janice L.;
- Schiffman, Joshua D.;
- Null, Donald M.;
- DiGeronimo, Robert;
- Rollins, Michael;
- Faix, Roger;
- Comstock, Jessica;
- Camp, Nicola J.;
- Leppert, Mark F.;
- Yost, H. Joseph;
- Brunelli, Luca
Publication type:
Article
The Red Edge Problem in asteroid band parameter analysis.
Published in:
Meteoritics & Planetary Science, 2016, v. 51, n. 4, p. 806, doi. 10.1111/maps.12611
By:
- Lindsay, Sean S.;
- Dunn, Tasha L.;
- Emery, Joshua P.;
- Bowles, Neil E.
Publication type:
Article
Shared Segment Analysis and Next-Generation Sequencing Implicates the Retinoic Acid Signaling Pathway in Total Anomalous Pulmonary Venous Return (TAPVR).
Published in:
PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0131514
By:
- Nash, Dustin;
- Arrington, Cammon B.;
- Kennedy, Brett J.;
- Yandell, Mark;
- Wu, Wilfred;
- Zhang, Wenying;
- Ware, Stephanie;
- Jorde, Lynn B.;
- Gruber, Peter J.;
- Yost, H. Joseph;
- Bowles, Neil E.;
- Bleyl, Steven B.
Publication type:
Article
Assessment of the CTNNA3 gene encoding human αT-catenin regarding its involvement in dilated cardiomyopathy.
Published in:
Human Genetics, 2003, v. 112, n. 3, p. 227, doi. 10.1007/s00439-002-0857-5
By:
- Janssens, Barbara;
- Mohapatra, Bhagyalaxmi;
- Vatta, Matteo;
- Goossens, Steven;
- Vanpoucke, Griet;
- Kools, Patrick;
- Montoye, Tony;
- van Hengel, Jolanda;
- Bowles, Neil E.;
- van Roy, Frans;
- Towbin, Jeffrey A.
Publication type:
Article
Dilated Cardiomyopathy: A Tale of Cytoskeletal Proteins and Beyond.
Published in:
Journal of Cardiovascular Electrophysiology, 2006, v. 17, n. 8, p. 919, doi. 10.1111/j.1540-8167.2006.00530.x
By:
- TOWBIN, JEFFREY A.;
- BOWLES, NEIL E.
Publication type:
Article
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.
Published in:
2012
By:
- Bhoj, Elizabeth J;
- Ramos, Purita;
- Baker, Linda A;
- Garg, Vidu;
- Cost, Nicholas;
- Nordenskjöld, Agneta;
- Elder, Frederick F;
- Bleyl, Steven B;
- Bowles, Neil E;
- Arrington, Cammon B;
- Delhomme, Brigitte;
- Vanhoutteghem, Amandine;
- Djian, Philippe;
- Zinn, Andrew R
Publication type:
Correction Notice
Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development.
Published in:
European Journal of Human Genetics, 2011, v. 19, n. 5, p. 540, doi. 10.1038/ejhg.2010.245
By:
- Bhoj, Elizabeth J.;
- Ramos, Purita;
- Baker, Linda A.;
- Cost, Nicholas;
- Nordenskjöld, Agneta;
- Elder, Frederick F.;
- Bleyl, Steven B.;
- Bowles, Neil E.;
- Arrington, Cammon B.;
- Delhomme, Brigitte;
- Vanhoutteghem, Amandine;
- Djian, Philippe;
- Zinn, Andrew R.
Publication type:
Article
Prospects for adenovirus-mediated gene therapy of inherited diseases of the myocardium.
Published in:
Cardiovascular Research, 1997, v. 35, n. 3, p. 422, doi. 10.1016/S0008-6363(97)00162-4
By:
- Bowles, Neil E.;
- Wang, Qing;
- Towbin, Jeffrey A.
Publication type:
Article
Kawasaki disease patients homozygous for the rs12252-C variant of interferon-induced transmembrane protein-3 are significantly more likely to develop coronary artery lesions.
Published in:
Molecular Genetics & Genomic Medicine, 2014, v. 2, n. 4, p. 356, doi. 10.1002/mgg3.79
By:
- Bowles, Neil E.;
- Arrington, Cammon B.;
- Hirono, Keiichi;
- Nakamura, Tsuneyuki;
- Ngo, Long;
- Wee, Yin Shen;
- Ichida, Fukiko;
- Weis, John H.
Publication type:
Article
A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.
Published in:
2017
By:
- Wang, Ce;
- Hata, Yukiko;
- Hirono, Keiichi;
- Takasaki, Asami;
- Ozawa, Sayaka Watanabe;
- Nakaoka, Hideyuki;
- Saito, Kazuyoshi;
- Miyao, Nariaki;
- Okabe, Mako;
- Ibuki, Keijiro;
- Nishida, Naoki;
- Origasa, Hideki;
- Yu, Xianyi;
- Bowles, Neil E.;
- Ichida, Fukiko
Publication type:
journal article
Thermal infrared emissivity measurements under a simulated lunar environment: Application to the Diviner Lunar Radiometer Experiment.
Published in:
Journal of Geophysical Research. Planets, 2012, v. 117, n. E1, p. n/a, doi. 10.1029/2011JE003862
By:
- Donaldson Hanna, Kerri L.;
- Wyatt, Michael B.;
- Thomas, Ian R.;
- Bowles, Neil E.;
- Greenhagen, Benjamin T.;
- Maturilli, Alessandro;
- Helbert, Joern;
- Paige, David A.
Publication type:
Article
Somatic mosaicism contributes to phenotypic variation in Timothy syndrome.
Published in:
American Journal of Medical Genetics. Part A, 2011, v. 155A, n. 10, p. 2578, doi. 10.1002/ajmg.a.34223
By:
- Etheridge, Susan P.;
- Bowles, Neil E.;
- Arrington, Cammon B.;
- Pilcher, Thomas;
- Rope, Alan;
- Wilde, Arthur A.M.;
- Alders, Marielle;
- Saarel, Elizabeth V.;
- Tavernier, Rene;
- Timothy, Katherine W.;
- Tristani-Firouzi, Martin
Publication type:
Article
A cardiac myosin binding protein C mutation in the Maine Coon cat with familial hypertrophic cardiomyopathy.
Published in:
Human Molecular Genetics, 2005, v. 14, n. 23, p. 3587, doi. 10.1093/hmg/ddi386
By:
- Meurs, Kathryn M.;
- Sanchez, Ximena;
- David, Ryan M.;
- Bowles, Neil E.;
- Towbin, Jeffrey A.;
- Reiser, Peter J.;
- Kittleson, Judith A.;
- Munro, Marcia J.;
- Dryburgh, Keith;
- MacDonald, Kristin A.;
- Kittleson, Mark D.
Publication type:
Article
Genetic and biophysical basisof sudden unexplained nocturnal death syndrome (SUNDS), a diseaseallelic to Brugada syndrome.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 3, p. 337, doi. 10.1093/hmg/11.3.337
By:
- Vatta, Matteo;
- Dumaine, Robert;
- Varghese, George;
- Richard, Todd A.;
- Shimizu, Wataru;
- Aihara, Naohiko;
- Nademanee, Koonlawee;
- Brugada, Ramon;
- Brugada, Josep;
- Veerakul, Gumpanart;
- Li, Hua;
- Bowles, Neil E.;
- Brugada, Pedro;
- Antzelevitch, Charles;
- Towbin, Jeffrey A.
Publication type:
Article
Conditional transgenic expression of TIR-domain-containing adaptor-inducing interferon-β (TRIF) in the adult mouse heart is protective in acute viral myocarditis.
Published in:
Basic Research in Cardiology, 2011, v. 106, n. 6, p. 1159, doi. 10.1007/s00395-011-0226-4
By:
- Zhaohui Xu;
- Desai, Moreshwar;
- Philip, Joseph;
- Sivsubramanian, Natarajan;
- Bowles, Neil E.;
- Vallejo, Jesus G.
Publication type:
Article
Depletion of the 26S Proteasome Adaptor Ecm29 Increases Toll-Like Receptor 3 Signaling.
Published in:
Science Signaling, 2013, v. 6, n. 295, p. 1, doi. 10.1126/scisignal.2004301
By:
- Gorbea, Carlos;
- Rechsteiner, Martin;
- Vallejo, Jesús G.;
- Bowles, Neil E.
Publication type:
Article

Found: 22