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Functional analysis of a unique troponin c mutation, GLY159ASP, that causes familial dilated cardiomyopathy, studied in explanted heart muscle. [electronic resource] by
- Dyer, Emma C
- Jacques, Adam M
- Hoskins, Anita C
- Ward, Douglas G
- Gallon, Clare E
- Messer, Andrew E
- Kaski, Juan Pablo
- Burch, Michael
- Kentish, Jonathan C
- Marston, Steven B
Producer: 20091027
In:
Circulation. Heart failure vol. 2
Availability: No items available.
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11.
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Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T. [electronic resource] by
- Bayliss, Christopher R
- Jacques, Adam M
- Leung, Man-Ching
- Ward, Douglas G
- Redwood, Charles S
- Gallon, Clare E
- Copeland, O'Neal
- McKenna, William J
- Dos Remedios, Cristobal
- Marston, Steven B
- Messer, Andrew E
Producer: 20130906
In:
Cardiovascular research vol. 97
Availability: No items available.
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The molecular phenotype of human cardiac myosin associated with hypertrophic obstructive cardiomyopathy. [electronic resource] by
- Jacques, Adam M
- Briceno, Natalia
- Messer, Andrew E
- Gallon, Clare E
- Jalilzadeh, Shapour
- Garcia, Edwin
- Kikonda-Kanda, Gaelle
- Goddard, Jennifer
- Harding, Sian E
- Watkins, Hugh
- Esteban, M Tomé
- Tsang, Victor T
- McKenna, William J
- Marston, Steven B
Producer: 20081202
In:
Cardiovascular research vol. 79
Availability: No items available.
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