Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.

Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид:	Blair, E, Redwood, C, Watkins, H
Формат:	Journal article
Хэл сонгох:	English
Хэвлэсэн:	2003

Ижил төстэй зүйлс

Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy.
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Double mutations in CIS can confound genotype-phenotype correlations in hypertrophic cardiomyopathy
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Linked genetic modifiers in hypertrophic cardiomyopathy
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-н: Abdulrazzak, H, зэрэг
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Effects of hypertrophic cardiomyopathy mutations in troponin I on contractility of skinned cardiac muscle fibres
-н: Burton, D, зэрэг
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Early onset malignant hypertrophic cardiomyopathy caused by mutations in MYBPC3
-н: Carballo, S, зэрэг
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Sudden death in hypertrophic cardiomyopathy.
-н: Watkins, H
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Correlates of myocardial fibrosis in hypertrophic cardiomyopathy
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Altered inhibitory and troponin C-binding activities in cardiac troponin I mutants known to cause hypertrophic cardiomyopathy
-н: Elliott, K, зэрэг
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Novel mutations in cardiac MYBPC3 and early onset malignant hypertrophic cardiomyopathy
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Myocardial dysfunction in hypertrophic cardiomyopathy.
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Delineating the role of adenosine monophosphate (AMP)-activated protein kinase (AMP) gamma 2 subunit in hypertrophic cardiomyopathy (HCM)
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Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
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Hypertrophic cardiomyopathy mutations in the gamma 2 subunit of AMP-activated kinase suggest a central role of energy compromise in disease pathogenesis
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Is DNA testing for hypertrophic cardiomyopathy cost-effective?
-н: Wordsworth, S, зэрэг
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Comparison of the functional effects of mutations in troponin T which cause dilated and hypertrophic cardiomyopathies
-н: Robinson, P, зэрэг
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Novel mutations in cardiac MYBPC3 causing early onset malignant hypertrophic cardiomyopathy
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Metabolic perturbations in the pathogenesis of hypertrophic cardiomyopathy
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Novel mutations in cardiac MYPBC3 cause early onset malignant hypertrophic cardiomyopathy (HCM)
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Spectrum and genotype–phenotype relationship of ALPK3 variants in Chinese patients with hypertrophic cardiomyopathy
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Late gadolinium enhancement cardiovascular magnetic resonance in genotyped hypertrophic cardiomyopathy with normal phenotype
-н: Jassal Davinder S, зэрэг
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Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
-н: Robinson, P, зэрэг
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The genetics of hypertrophic cardiomyopathy: Teare redux.
-н: Watkins, H, зэрэг
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Hypertrophic cardiomyopathy in Noonan Syndrome closely mimics familial hypertrophic cardiomyopathy due to sarcomeric mutations.
-н: Hudsmith, L, зэрэг
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Genetic determinants of clinical phenotype in hypertrophic cardiomyopathy
-н: Lazar Velicki, зэрэг
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Hypertrophic Cardiomyopathy: From Phenotype and Pathogenesis to Treatment
-н: Zeyi Cheng, зэрэг
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A troponin I mutant known to cause hypertrophic cardiomyopathy shows reduced inhibition of Ca2+ independent tension
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DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model.
-н: Wordsworth, S, зэрэг
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DNA testing for hypertrophic cardiomyopathy: a cost-effectiveness model
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Genetic clues to disease pathways in hypertrophic and dilated cardiomyopathies.
-н: Watkins, H
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[Abnormal tropomyosin function in ATPase cycle in hypertrophic and dilated cardiomyopathies].
-н: Borovikov, I, зэрэг
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Hypertrophic cardiomyopathy mutations in MYBPC3 dysregulate myosin
-н: Toepfer, C, зэрэг
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Two mutations in human cardiac troponin I known to cause hypertrophic cardiomyopathy have different effects on cardiac muscle contraction
-н: Burton, D, зэрэг
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A protocol to ascertain whether sepsis-induced cardiomyopathy constitutes a phenotype of Takotsubo syndrome
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