Search Results - "Mirza, Mahmooda"

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  1. 1
    Dilated Cardiomyopathy Mutations in Three Thin Filament Regulatory Proteins Result in a Common Functional Phenotype

    Dilated Cardiomyopathy Mutations in Three Thin Filament Regulatory Proteins Result in a Common Functional Phenotype by Mirza, Mahmooda, Marston, Steven, Willott, Ruth, Ashley, Christopher, Mogensen, Jens, McKenna, William, Robinson, Paul, Redwood, Charles, Watkins, Hugh

    Published in The Journal of biological chemistry (05-08-2005)
    “…Dilated cardiomyopathy (DCM), characterized by cardiac dilatation and contractile dysfunction, is a major cause of heart failure. Inherited DCM can result from…”
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  2. 2
    Alterations in Thin Filament Regulation Induced by a Human Cardiac Troponin T Mutant That Causes Dilated Cardiomyopathy Are Distinct from Those Induced by Troponin T Mutants That Cause Hypertrophic Cardiomyopathy

    Alterations in Thin Filament Regulation Induced by a Human Cardiac Troponin T Mutant That Causes Dilated Cardiomyopathy Are Distinct from Those Induced by Troponin T Mutants That Cause Hypertrophic Cardiomyopathy by Robinson, Paul, Mirza, Mahmooda, Knott, Adam, Abdulrazzak, Hassan, Willott, Ruth, Marston, Steven, Watkins, Hugh, Redwood, Charles

    Published in The Journal of biological chemistry (25-10-2002)
    “…We have compared the in vitro regulatory properties of recombinant human cardiac troponin reconstituted using wild type troponin T with troponin containing the…”
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  3. 3
    The Effect of Mutations in α-Tropomyosin (E40K and E54K) That Cause Familial Dilated Cardiomyopathy on the Regulatory Mechanism of Cardiac Muscle Thin Filaments

    The Effect of Mutations in α-Tropomyosin (E40K and E54K) That Cause Familial Dilated Cardiomyopathy on the Regulatory Mechanism of Cardiac Muscle Thin Filaments by Mirza, Mahmooda, Robinson, Paul, Kremneva, Elena, Copeland, O'neal, Nikolaeva, Olga, Watkins, Hugh, Levitsky, Dimitry, Redwood, Charles, EL-Mezgueldi, Mohammed, Marston, Steven

    Published in The Journal of biological chemistry (04-05-2007)
    “…E40K and E54K mutations in α-tropomyosin cause inherited dilated cardiomyopathy. Previously we showed, using Ala-Ser α-tropomyosin (AS-α-Tm) expressed in…”
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  4. 4
    Functional characterisation of a mutant actin (Met132Val) from a patient with nemaline myopathy

    Functional characterisation of a mutant actin (Met132Val) from a patient with nemaline myopathy by Marston, Steven, Mirza, Mahmooda, Abdulrazzak, Hassan, Sewry, Caroline

    Published in Neuromuscular disorders : NMD (01-02-2004)
    “…The mutation Met132Val in the ACTA1 gene was identified in a patient with mild nemaline myopathy (NM). We examined actin mRNA and protein from biopsy samples…”
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  5. 5
    The Effect of Mutations in α-Tropomyosin (E40K and E54K) That Cause Familial Dilated Cardiomyopathy on the Regulatory Mechanism of Cardiac Muscle Thin Filaments

    The Effect of Mutations in α-Tropomyosin (E40K and E54K) That Cause Familial Dilated Cardiomyopathy on the Regulatory Mechanism of Cardiac Muscle Thin Filaments by Mahmooda Mirza, Paul Robinson, Elena Kremneva, O'neal Copeland, Olga Nikolaeva, Hugh Watkins, Dimitry Levitsky, Charles Redwood, Mohammed EL-Mezgueldi, Steven Marston

    Published in The Journal of biological chemistry (04-05-2007)
    “…E40K and E54K mutations in α-tropomyosin cause inherited dilated cardiomyopathy. Previously we showed, using Ala-Ser α-tropomyosin (AS-α-Tm) expressed in…”
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