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Identification and functional characterization of cardiac troponin I as a novel disease gene in autosomal dominant dilated cardiomyopathy. [electronic resource] by
- Carballo, Sebastian
- Robinson, Paul
- Otway, Robyn
- Fatkin, Diane
- Jongbloed, Jan D H
- de Jonge, Nicolaas
- Blair, Edward
- van Tintelen, J Peter
- Redwood, Charles
- Watkins, Hugh
Producer: 20090922
In:
Circulation research vol. 105
Availability: No items available.
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Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation? [electronic resource] by
- Otway, Robyn
- Vandenberg, Jamie I
- Guo, Guanglan
- Varghese, Anthony
- Castro, M Leticia
- Liu, Jian
- Zhao, JingTing
- Bursill, Jane A
- Wyse, Ken R
- Crotty, Haley
- Baddeley, Olivia
- Walker, Bruce
- Kuchar, Dennis
- Thorburn, Charles
- Fatkin, Diane
Producer: 20070403
In:
Journal of the American College of Cardiology vol. 49
Availability: No items available.
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Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice. [electronic resource] by
- Nikolova, Vesna
- Leimena, Christiana
- McMahon, Aisling C
- Tan, Ju Chiat
- Chandar, Suchitra
- Jogia, Dilesh
- Kesteven, Scott H
- Michalicek, Jan
- Otway, Robyn
- Verheyen, Fons
- Rainer, Stephen
- Stewart, Colin L
- Martin, David
- Feneley, Michael P
- Fatkin, Diane
Producer: 20040316
In:
The Journal of clinical investigation vol. 113
Availability: No items available.
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9.
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Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk. [electronic resource] by
- Mann, Stefan A
- Otway, Robyn
- Guo, Guanglan
- Soka, Magdalena
- Karlsdotter, Lina
- Trivedi, Gunjan
- Ohanian, Monique
- Zodgekar, Poonam
- Smith, Robert A
- Wouters, Merridee A
- Subbiah, Rajesh
- Walker, Bruce
- Kuchar, Dennis
- Sanders, Prashanthan
- Griffiths, Lyn
- Vandenberg, Jamie I
- Fatkin, Diane
Producer: 20120423
In:
Journal of the American College of Cardiology vol. 59
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Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC). [electronic resource] by
- van der Klift, Heleen
- Wijnen, Juul
- Wagner, Anja
- Verkuilen, Paul
- Tops, Carli
- Otway, Robyn
- Kohonen-Corish, Maija
- Vasen, Hans
- Oliani, Cristina
- Barana, Daniela
- Moller, Pal
- Delozier-Blanchet, Celia
- Hutter, Pierre
- Foulkes, William
- Lynch, Henry
- Burn, John
- Möslein, Gabriela
- Fodde, Riccardo
Producer: 20050926
In:
Genes, chromosomes & cancer vol. 44
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11.
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Investigation of association between PFO complicated by cryptogenic stroke and a common variant of the cardiac transcription factor GATA4. [electronic resource] by
- Moradi Marjaneh, Mahdi
- Kirk, Edwin P
- Posch, Maximilian G
- Ozcelik, Cemil
- Berger, Felix
- Hetzer, Roland
- Otway, Robyn
- Butler, Tanya L
- Blue, Gillian M
- Griffiths, Lyn R
- Fatkin, Diane
- Martinson, Jeremy J
- Winlaw, David S
- Feneley, Michael P
- Harvey, Richard P
Producer: 20110930
In:
PloS one vol. 6
Availability: No items available.
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Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy. [electronic resource] by
- Costa, Mauro W
- Guo, Guanglan
- Wolstein, Orit
- Vale, Molly
- Castro, Maria L
- Wang, Libin
- Otway, Robyn
- Riek, Peter
- Cochrane, Natalie
- Furtado, Milena
- Semsarian, Christopher
- Weintraub, Robert G
- Yeoh, Thomas
- Hayward, Christopher
- Keogh, Anne
- Macdonald, Peter
- Feneley, Michael
- Graham, Robert M
- Seidman, Jonathan G
- Seidman, Christine E
- Rosenthal, Nadia
- Fatkin, Diane
- Harvey, Richard P
Producer: 20131018
In:
Circulation. Cardiovascular genetics vol. 6
Availability: No items available.
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13.
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Tinman/Nkx2-5 acts via miR-1 and upstream of Cdc42 to regulate heart function across species. [electronic resource] by
- Qian, Li
- Wythe, Joshua D
- Liu, Jiandong
- Cartry, Jerome
- Vogler, Georg
- Mohapatra, Bhagyalaxmi
- Otway, Robyn T
- Huang, Yu
- King, Isabelle N
- Maillet, Marjorie
- Zheng, Yi
- Crawley, Timothy
- Taghli-Lamallem, Ouarda
- Semsarian, Christopher
- Dunwoodie, Sally
- Winlaw, David
- Harvey, Richard P
- Fatkin, Diane
- Towbin, Jeffrey A
- Molkentin, Jeffery D
- Srivastava, Deepak
- Ocorr, Karen
- Bruneau, Benoit G
- Bodmer, Rolf
Producer: 20110902
In:
The Journal of cell biology vol. 193
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Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy. [electronic resource] by
- Kirk, Edwin P
- Sunde, Margaret
- Costa, Mauro W
- Rankin, Scott A
- Wolstein, Orit
- Castro, M Leticia
- Butler, Tanya L
- Hyun, Changbaig
- Guo, Guanglan
- Otway, Robyn
- Mackay, Joel P
- Waddell, Leigh B
- Cole, Andrew D
- Hayward, Christopher
- Keogh, Anne
- Macdonald, Peter
- Griffiths, Lyn
- Fatkin, Diane
- Sholler, Gary F
- Zorn, Aaron M
- Feneley, Michael P
- Winlaw, David S
- Harvey, Richard P
Producer: 20070921
In:
American journal of human genetics vol. 81
Availability: No items available.
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