ORA - Oxford University Research Archive

1 - 9 of 9

1

Journal article

Molecular mechanism of the E99K mutation in cardiac actin (ACTC Gene) that causes apical hypertrophy in man and mouse.

Song, W, Dyer, E, Stuckey, DJ, et al.
2011-08-05

2

Conference

Two DCM mutations in cardiac tropomyosin alter thin filament function by different mechanisms

Marston, S, Mirza, M, Copeland, O, et al.
2007-01-05

3

Conference

Direct evidence in man for haploinsufficiency as the mechanism of action of myosin-binding protein C mutations that cause hypertrophic cardiomyopathy

Carballo, S, Copeland, O, Livesey, K, et al.
2008-07-05

4

Journal article

Myofibrillar Ca(2+) sensitivity is uncoupled from troponin I phosphorylation in hypertrophic obstructive cardiomyopathy due to abnormal troponin T.

Bayliss, CR, Jacques, AM, Leung, MC, et al.
2013-03-05

5

Journal article

The effect of mutations in alpha-tropomyosin (E40K and E54K) that cause familial dilated cardiomyopathy on the regulatory mechanism of cardiac muscle thin filaments.

Mirza, M, Robinson, P, Kremneva, E, et al.
2007-05-05

6

Journal article

Erratum: How do MYBPC3 mutations cause hypertrophic cardiomyopathy? (Journal of Muscle Research and Cell Motility DOI 10.1007/s10974-011-9268-3)

Marston, S, Copeland, O, Gehmlich, K, et al.
2012-05-05

7

Journal article

How do MYBPC3 mutations cause hypertrophic cardiomyopathy?

Marston, S, Copeland, O, Gehmlich, K, et al.
2012-05-05

8

Conference

Evidence for haploinsufficiency as the mechanism of action of MyBP-C mutations that cause HCM

Carballo, S, Copeland, O, Jacques, A, et al.
2008-04-05

9

Journal article

Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency.

Marston, S, Copeland, O, Jacques, A, et al.
2009-07-05

TO TOP