Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Cammon B. Arrington"'
Autor:
Shannon Hateley, Angelica Lopez-Izquierdo, Chuanchau J. Jou, Scott Cho, Joshua G. Schraiber, Shiya Song, Colin T. Maguire, Natalia Torres, Michael Riedel, Neil E. Bowles, Cammon B. Arrington, Brett J. Kennedy, Susan P. Etheridge, Shuping Lai, Chase Pribble, Lindsay Meyers, Derek Lundahl, Jake Byrnes, Julie M. Granka, Christopher A. Kauffman, Gordon Lemmon, Steven Boyden, W. Scott Watkins, Mary Anne Karren, Stacey Knight, J. Brent Muhlestein, John F. Carlquist, Jeffrey L. Anderson, Kenneth G. Chahine, Khushi U. Shah, Catherine A. Ball, Ivor J. Benjamin, Mark Yandell, Martin Tristani-Firouzi
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Many rare high-impact variants have been associated with disease, but the origins and functional impact are not always explored. Here, the authors trace the ancestry of a rare high impact atrial fibrillation allele in KCNQ1, and use iPSC-derived card
Externí odkaz:
https://doaj.org/article/fc7dba9c47974f5aa229e04e2b3a9d14
Autor:
Chuanchau J. Jou, Cammon B. Arrington, Spencer Barnett, Jiaxiang Shen, Scott Cho, Xiaoming Sheng, Patrick C. McCullagh, Neil E. Bowles, Chase M. Pribble, Elizabeth V. Saarel, Thomas A. Pilcher, Susan P. Etheridge, Martin Tristani-Firouzi
Publikováno v:
Cellular Physiology and Biochemistry, Vol 42, Iss 5, Pp 2021-2029 (2017)
Background/Aims: Congenital Sick Sinus Syndrome (SSS) is a disorder associated with sudden cardiac death due to severe bradycardia and prolonged pauses. Mutations in HCN4, the gene encoding inward Na+/K+ current (If), have been described as a cause o
Externí odkaz:
https://doaj.org/article/7737dfc076d945d09d15b2a1c15f6913
Autor:
Neil E. Bowles, Cammon B. Arrington, Keiichi Hirono, Tsuneyuki Nakamura, Long Ngo, Yin Shen Wee, Fukiko Ichida, John H. Weis
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 4, Pp 356-361 (2014)
Externí odkaz:
https://doaj.org/article/295ed0ecfa2046649289f892c1a3c0ab
Autor:
W. Scott Watkins, Derek Lundahl, Steven E. Boyden, Shiya Song, Mary Anne Karren, J. Brent Muhlestein, Shannon Hateley, Chuanchau J. Jou, Colin T. Maguire, Jeffrey L. Anderson, Khushi U Shah, Susan P. Etheridge, Kenneth G. Chahine, Brett Kennedy, Martin Tristani-Firouzi, Gordon Lemmon, Lindsay Meyers, Ivor J. Benjamin, Stacey Knight, Chase Pribble, Catherine A. Ball, Shuping Lai, Christopher A. Kauffman, Scott Cho, Cammon B. Arrington, Natalia S. Torres, Michael Riedel, Joshua G. Schraiber, John F. Carlquist, Jake K. Byrnes, Julie M. Granka, Neil E. Bowles, Mark Yandell, Angelica Lopez-Izquierdo
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Nature Communications
Nature Communications
The genetic architecture of atrial fibrillation (AF) encompasses low impact, common genetic variants and high impact, rare variants. Here, we characterize a high impact AF-susceptibility allele, KCNQ1 R231H, and describe its transcontinental geograph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::337f8a6f32b99a4e0658f6fc97ff031f
https://doaj.org/article/fc7dba9c47974f5aa229e04e2b3a9d14
https://doaj.org/article/fc7dba9c47974f5aa229e04e2b3a9d14
Publikováno v:
Energy & Fuels. 35:17490-17498
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::299149de13da3be83c252cc6b9119da8
https://doi.org/10.1021/acs.energyfuels.1c02452
https://doi.org/10.1021/acs.energyfuels.1c02452
Autor:
Dustin Nash, Cammon B Arrington, Brett J Kennedy, Mark Yandell, Wilfred Wu, Wenying Zhang, Stephanie Ware, Lynn B Jorde, Peter J Gruber, H Joseph Yost, Neil E Bowles, Steven B Bleyl
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0131514 (2015)
Most isolated congenital heart defects are thought to be sporadic and are often ascribed to multifactorial mechanisms with poorly understood genetics. Total Anomalous Pulmonary Venous Return (TAPVR) occurs in 1 in 15,000 live-born infants and occurs
Externí odkaz:
https://doaj.org/article/5d296e46b76342a9aa6f37b0d2e1d6c3
Autor:
Patrick C McCullagh, Susan P. Etheridge, Chase Pribble, Xiaoming Sheng, Spencer M. Barnett, Martin Tristani-Firouzi, Elizabeth V. Saarel, Cammon B. Arrington, Neil E. Bowles, Jiaxiang Shen, Chuanchau J. Jou, Thomas A. Pilcher, Scott Cho
Publikováno v:
Cellular Physiology and Biochemistry, Vol 42, Iss 5, Pp 2021-2029 (2017)
Background/Aims: Congenital Sick Sinus Syndrome (SSS) is a disorder associated with sudden cardiac death due to severe bradycardia and prolonged pauses. Mutations in HCN4, the gene encoding inward Na+/K+ current (If), have been described as a cause o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19dda2af977b01203729c8b4ac892617
https://doi.org/10.1159/000479897
https://doi.org/10.1159/000479897
Autor:
Susan P. Etheridge, Mark Leppert, Elizabeth V. Saarel, Aubree M. Earl, Brett Kennedy, Steven B. Bleyl, Neil E. Bowles, Cammon B. Arrington, Chuanchau J. Jou, Mark Yandell, Martin Tristani-Firouzi, Norisada Matsunami, Lindsay Meyers, H. Joseph Yost, Peter J. Gruber
Publikováno v:
American Journal of Medical Genetics Part A. 167:2975-2984
Wolff–Parkinson–White (WPW) syndrome is a common cause of supraventricular tachycardia that carries a risk of sudden cardiac death. To date, mutations in only one gene, PRKAG2, which encodes the 5’ -AMP-activated protein kinase subunit γ-2, ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d79f195ab3f8f6fa58c52b6ed34f041c
https://doi.org/10.1002/ajmg.a.37297
https://doi.org/10.1002/ajmg.a.37297
Autor:
Shinya Kowase, Akinori Kimura, Cammon B. Arrington, Akihiko Nogami, Taisuke Ishikawa, Naomasa Makita, Takuro Arimura, Daniel Toshio Harrell, Chuanchau J. Jou, Spencer M. Barnett, Yukiomi Tsuji
Publikováno v:
Circulation: Arrhythmia and Electrophysiology. 8(2):400-408
Background— Recent genome-wide association studies have demonstrated an association between MYH6 , the gene encoding α-myosin heavy chain (α-MHC), and sinus node function in the general population. Moreover, a rare MYH6 variant, R721W, predisposi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9b81ec942183f48b40a160e4493619f
http://hdl.handle.net/10069/36003
http://hdl.handle.net/10069/36003
Autor:
Stephen G. Miller, J. William Gaynor, Jeffery P. Jacobs, Andrew M. Atz, Gail P. Jarvik, Bradley S. Marino, Christian Pizarro, Seema Mital, William T. Mahle, Nicole S. Wilder, Cammon B. Arrington, Avni Santani, David C. Bellinger, Jane W. Newburger, Amber A. Burt, Alan B. Lewis, Teresa M. Lee, Nancy S. Ghanayem, Mark W. Russell, Daniel Seung Kim, Chitra Ravishankar
Publikováno v:
The Journal of Thoracic and Cardiovascular Surgery. 148(6):2560-2568
Objective Apolipoprotein E ( APOE ) genotype is a determinant of neurologic recovery after brain ischemia and traumatic brain injury. The APOE e2 allele has been associated with worse neurodevelopmental (ND) outcome after repair of congenital heart d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1281bfd3aaa34d9396bdec776d89fcab