Search Results - "Arrington, Cammon B."

The history and geographic distribution of a KCNQ1 atrial fibrillation risk allele 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., Lemmon, Gordon, Boyden, Steven, Scott Watkins, W., Karren, Mary Anne, Knight, Stacey, Brent Muhlestein, J., Carlquist, John F., Anderson, Jeffrey L., Chahine, Kenneth G., Shah, Khushi U., Ball, Catherine A., Benjamin, Ivor J., Yandell, Mark, Tristani-Firouzi, Martin

“…The genetic architecture of atrial fibrillation (AF) encompasses low impact, common genetic variants and high impact, rare variants. Here, we characterize a…”
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Extra-embryonic syndecan 2 regulates organ primordia migration and fibrillogenesis throughout the zebrafish embryo by Arrington, Cammon B, Yost, H Joseph

“…One of the first steps in zebrafish heart and gut organogenesis is the migration of bilateral primordia to the midline to form cardiac and gut tubes. The…”
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Shared Segment Analysis and Next-Generation Sequencing Implicates the Retinoic Acid Signaling Pathway in Total Anomalous Pulmonary Venous Return (TAPVR) 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

“…Most isolated congenital heart defects are thought to be sporadic and are often ascribed to multifactorial mechanisms with poorly understood genetics. Total…”
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Validation of association of the apolipoprotein E ε2 allele with neurodevelopmental dysfunction after cardiac surgery in neonates and infants by Gaynor, J. William, MD, Kim, Daniel Seung, BS, Arrington, Cammon B., MD, PhD, Atz, Andrew M., MD, Bellinger, David C., PhD, Burt, Amber A., MSPH, Ghanayem, Nancy S., MD, Jacobs, Jeffery P., MD, Lee, Teresa M., MD, Lewis, Alan B., MD, Mahle, William T., MD, Marino, Bradley S., MD, Miller, Stephen G., MD, Newburger, Jane W., MD, MPH, Pizarro, Christian, MD, Ravishankar, Chitra, MD, Santani, Avni B., PhD, Wilder, Nicole S., MD, Jarvik, Gail P., MD, PhD, Mital, Seema, MD, Russell, Mark W., MD

“…Objective Apolipoprotein E ( APOE ) genotype is a determinant of neurologic recovery after brain ischemia and traumatic brain injury. The APOE ε2 allele has…”
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A Functional Assay for Sick Sinus Syndrome Genetic Variants 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

“…Background/Aims: Congenital Sick Sinus Syndrome (SSS) is a disorder associated with sudden cardiac death due to severe bradycardia and prolonged pauses…”
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Sdc2 and Tbx16 regulate Fgf2-dependent epithelial cell morphogenesis in the ciliated organ of asymmetry by Arrington, Cammon B, Peterson, Annita G, Yost, H Joseph

“…Heparan sulfate proteoglycans (HSPGs) control many cellular processes and have been implicated in the regulation of left-right (LR) development by as yet…”
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Neonatal Flail Tricuspid Valve: Diagnosis and Management by Loftus, Patrick D., HBS, Arrington, Cammon B., MD, PhD, Kaza, Aditya K., MD

“…Flail tricuspid valve in the neonate is a rare and often fatal condition requiring early diagnosis and intervention. We report 3 infants born without antenatal…”
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White Matter Lesions in Children and Adolescents With Migraine by Candee, Meghan S., MD MS, McCandless, Rachel T., MD, Moore, Kevin R., MD, Arrington, Cammon B., MD PhD, Minich, L. LuAnn, MD, Bale, James F., MD

“…Abstract Background The etiology and clinical importance of white matter lesions in migraine remain poorly understood. To understand these issues more fully,…”
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Somatic mosaicism contributes to phenotypic variation in Timothy syndrome 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

“…Timothy syndrome type 1 (TS‐1) is a rare disorder that affects multiple organ systems and has a high incidence of sudden death due to profound QT prolongation…”
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Patent Foramen Ovale in Children with Migraine Headaches by McCandless, Rachel T., MD, Arrington, Cammon B., MD, Nielsen, Douglas C, Bale, James F., MD, Minich, L. LuAnn, MD

“…Objective To determine the prevalence of patent foramen ovale (PFO) in children with migraine. Study design Children aged 6.0 to 18.0 years with migraine…”
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Absence of TGFBR1 and TGFBR2 Mutations in Patients With Bicuspid Aortic Valve and Aortic Dilation by Arrington, Cammon B., MD, PhD, Sower, C. Todd, BS, Chuckwuk, Naomi, BS, Stevens, Jeff, BS, Leppert, Mark F., PhD, Yetman, Anji T., MD, Bowles, Neil E., PhD

“…Mutations in the genes encoding transforming growth factor–β receptor types I and II (TGFBR1 and TGFBR2, respectively) are commonly identified in patients with…”
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Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development by BHOJ, Elizabeth J, RAMOS, Purita, VANHOUTTEGHEM, Amandine, DJIAN, Philippe, ZINN, Andrew R, BAKER, Linda A, COST, Nicholas, NORDENSKJÖLD, Agneta, ELDER, Frederick F, BLEYL, Steven B, BOWLES, Neil E, ARRINGTON, Cammon B, DELHOMME, Brigitte

“…We studied a man with distal hypospadias, partial anomalous pulmonary venous return, mild limb-length inequality and a balanced translocation involving…”
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Effects of High-Temperature Burnout Level and Devolatilization/Oxidation Conditions on Char Properties for Low Rank Coal Chars: Correlation of CaO Surface Area with Intrinsic Char Oxidation Rates by Cope, Richard F, McDonald, Kent M, Arrington, Cammon B, Hecker, William C, Wu, Ruochen

“…This work investigates the influence of burnout level on CaO surface areas and intrinsic oxidation rates of partially burned-out coal chars, and then attempts…”
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Kawasaki disease patients homozygous for the rs12252‐C variant of interferon‐induced transmembrane protein‐3 are significantly more likely to develop coronary artery lesions by Bowles, Neil E., Arrington, Cammon B., Hirono, Keiichi, Nakamura, Tsuneyuki, Ngo, Long, Wee, Yin Shen, Ichida, Fukiko, Weis, John H.

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An assessment of the electrocardiogram as a screening test for large atrial septal defects in children by Arrington, Cammon B., MD, PhD, Tani, Lloyd Y., MD, Minich, L. LuAnn, MD, Bradley, David J., MD

“…Abstract Background and Purpose The electrocardiogram (ECG) is commonly used as a screening tool for diagnosis of the ostium secundum atrial septal defect…”
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Novel Mutation in the α-Myosin Heavy Chain Gene Is Associated With Sick Sinus Syndrome by Ishikawa, Taisuke, Jou, Chuanchau J, Nogami, Akihiko, Kowase, Shinya, Arrington, Cammon B, Barnett, Spencer M, Harrell, Daniel T, Arimura, Takuro, Tsuji, Yukiomi, Kimura, Akinori, Makita, Naomasa

“…BACKGROUND—Recent genome-wide association studies have demonstrated an association between MYH6, the gene encoding α-myosin heavy chain (α-MHC), and sinus node…”
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Renin-Angiotensin-Aldosterone Genotype Influences Ventricular Remodeling in Infants With Single Ventricle by MITAL, Seema, CHUNG, Wendy K, LI, Jennifer S, LEVINE, Jami C, LEE, Teresa M, MARGOSSIAN, Renee, HSU, Daphne T, COLAN, Steven D, SLEEPER, Lynn A, MANLHIOT, Cedric, ARRINGTON, Cammon B, CNOTA, James F, GRAHAM, Eric M, MITCHELL, Michael E, GOLDMUNTZ, Elizabeth

“…We investigated the effect of polymorphisms in the renin-angiotensin-aldosterone system (RAAS) genes on ventricular remodeling, growth, renal function, and…”
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Rer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levels by Jurisch-Yaksi, Nathalie, Rose, Applonia J, Lu, Huiqi, Raemaekers, Tim, Munck, Sebastian, Baatsen, Pieter, Baert, Veerle, Vermeire, Wendy, Scales, Suzie J, Verleyen, Daphne, Vandepoel, Roel, Tylzanowski, Przemko, Yaksi, Emre, de Ravel, Thomy, Yost, H Joseph, Froyen, Guy, Arrington, Cammon B, Annaert, Wim

“…Cilia project from the surface of most vertebrate cells and are important for several physiological and developmental processes. Ciliary defects are linked to…”
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Microsecond Protein Folding Kinetics from Native-State Hydrogen Exchange by Arrington, Cammon B, Robertson, Andrew D

“…Native-state amide proton (NH) exchange in turkey ovomucoid third domain (OMTKY3) has been used to determine rates of unfolding and folding at the 13 most…”
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Exome Analysis of a Family With Pleiotropic Congenital Heart Disease by Arrington, Cammon B, Bleyl, Steven B, Matsunami, Norisada, Bonnell, Gabriel D, Otterud, Brith E.M, Nielsen, Douglas C, Stevens, Jeffrey, Levy, Shawn, Leppert, Mark F, Bowles, Neil E

“…BACKGROUND—A number of single gene defects have been identified in patients with isolated or nonsyndromic congenital heart defects (CHDs). However, due to…”
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