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1دورية أكاديمية
المؤلفون: Reddy, Rohin K, Howard, James P, Ahmad, Yousif, Shun-Shin, Matthew J, Simader, Florentina A, Miyazawa, Alejandra A, Saleh, Keenan, Naraen, Akriti, Samways, Jack W, Katritsis, George, Mohal, Jagdeep S, Kaza, Nandita, Porter, Bradley, Keene, Daniel, Linton, Nicholas WF, Francis, Darrel P, Whinnett, Zachary I, Luther, Vishal, Kanagaratnam, Prapa, Arnold, Ahran D
المصدر: Arrhythmia & Electrophysiology Review ; volume 12 ; ISSN 2050-3377 2050-3369
مصطلحات موضوعية: Physiology (medical), Cardiology and Cardiovascular Medicine
الإتاحة: https://doi.org/10.15420/aer.2023.07Test
https://www.aerjournal.com/articleindex/aer.2023.07Test -
2دورية أكاديمية
المؤلفون: Arnold, Ahran, Cheng, Timothy, Chow, Ji-Jian, Shun-Shin, Matthew J., Samways, Jack W., Naraen, Akriti, Mohal, Jagdeep S., Tanner, Mark A., Muthumala, Amal G., Ng, Fu Siong, Linton, Nick F., Kanagaratnam, Prapa, Peters, Nicholas S., Francis, Darrel P., Whinnett, Zachary I.
المصدر: Heart Rhythm ; volume 20, issue 5, page S106-S107 ; ISSN 1547-5271
مصطلحات موضوعية: Physiology (medical), Cardiology and Cardiovascular Medicine
الإتاحة: https://doi.org/10.1016/j.hrthm.2023.03.418Test
https://api.elsevier.com/content/article/PII:S1547527123007233?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1547527123007233?httpAccept=text/plainTest -
3دورية أكاديمية
المؤلفون: Harmer, Stephen C, Mohal, Jagdeep S, Royal, Alice A, McKenna, William J, Lambiase, Pier D, Tinker, Andrew
المصدر: Harmer , S C , Mohal , J S , Royal , A A , McKenna , W J , Lambiase , P D & Tinker , A 2014 , ' Cellular mechanisms underlying the increased disease severity seen for patients with long QT syndrome caused by compound mutations in KCNQ1 ' , Biochemical Journal , vol. 462 , no. 1 , pp. 133-42 . https://doi.org/10.1042/BJ20140425Test
مصطلحات موضوعية: Animals, Arrhythmias, Cardiac/etiology, CHO Cells, Cricetulus, Genetic Predisposition to Disease, Heterozygote, Humans, KCNQ1 Potassium Channel/genetics, Long QT Syndrome/complications, Mutation, Patch-Clamp Techniques, Potassium Channels, Voltage-Gated/genetics
الإتاحة: https://doi.org/10.1042/BJ20140425Test
https://hdl.handle.net/1983/5e7f21f6-3b3f-41c7-a867-fa0e19e6accfTest
https://research-information.bris.ac.uk/en/publications/5e7f21f6-3b3f-41c7-a867-fa0e19e6accfTest -
4دورية أكاديمية
المؤلفون: Harmer, Stephen C, Mohal, Jagdeep S, Kemp, Duncan, Tinker, Andrew
المصدر: Harmer , S C , Mohal , J S , Kemp , D & Tinker , A 2012 , ' Readthrough of long-QT syndrome type 1 nonsense mutations rescues function but alters the biophysical properties of the channel ' , Biochemical Journal , vol. 443 , no. 3 , pp. 635-42 . https://doi.org/10.1042/BJ20111912Test
مصطلحات موضوعية: Biophysics, Blotting, Western, Cell Line, Codon, Nonsense, Electrophoresis, Polyacrylamide Gel, Humans, KCNQ1 Potassium Channel/genetics, Long QT Syndrome/genetics
العلاقة: https://research-information.bris.ac.uk/en/publications/7a0b88fa-b035-4fd4-a749-e0f9a19185d3Test
الإتاحة: https://doi.org/10.1042/BJ20111912Test
https://hdl.handle.net/1983/7a0b88fa-b035-4fd4-a749-e0f9a19185d3Test
https://research-information.bris.ac.uk/en/publications/7a0b88fa-b035-4fd4-a749-e0f9a19185d3Test -
5دورية أكاديمية
المؤلفون: HARMER, Stephen C., MOHAL, Jagdeep S., ROYAL, Alice A., MCKENNA, William J., LAMBIASE, Pier D., TINKER, Andrew
المصدر: Biochemical Journal; 8/15/2014, Vol. 462 Issue 1, following p133-142, 14p
مصطلحات موضوعية: GENETIC mutation, LONG QT syndrome, VOLTAGE-gated ion channels, ARRHYTHMIA, ENDOPLASMIC reticulum
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6دورية أكاديمية
المؤلفون: HARMER, Stephen C., MOHAL, Jagdeep S., KEMP, Duncan, TINKER, Andrew
المصدر: Biochemical Journal; 5/ 1/2012, Vol. 443 Issue 3, following p635-642, 9p
مصطلحات موضوعية: SYNDROMES, GENETIC mutation, GENTAMICIN, AMINO acids, THERAPEUTICS