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Publications by Lauren Tal
Pathophysiologic Changes Induced by Mutations in the TNT1 Domain of cTnT That Cause FHC
Biophysical Journal
Biophysics
D230N Mutation in Tropomyosin and R92L Mutation in Cardiac Troponin T Have Strikingly Different Impact on Calcium-Regulated Activation of Cardiac Myofilaments
Biophysical Journal
Biophysics
Related publications
Differential CaMK-II Activation in the Progression of HCM in cTnT Mutations
Biophysical Journal
Biophysics
Barth Syndrome Mutations That Cause Tafazzin Complex Lability
Journal of Cell Biology
Medicine
Cell Biology
Mutations in the First MyTH4 Domain ofMYO15Aare a Common Cause of DFNB3 Hearing Loss
Laryngoscope
Otorhinolaryngology
Mutations in KCNK4 That Affect Gating Cause a Recognizable Neurodevelopmental Syndrome
American Journal of Human Genetics
Genetics
Carrier Frequency of the GJB2 Mutations That Cause Hereditary Hearing Loss in the Japanese Population
Journal of Human Genetics
Genetics
Clinical Implications of Pathophysiologic Changes in the Midlife Hypertensive Patient
American Heart Journal
Cardiovascular Medicine
Cardiology
Altered Regulation of Cardiac Muscle Contraction by Troponin T Mutations That Cause Familial Hypertrophic Cardiomyopathy
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome That Expands the Phenotypic Spectrum of Condensinopathies
American Journal of Human Genetics
Genetics
Mutations That Bypass tRNA Binding Activate the Intrinsically Defective Kinase Domain in GCN2
Genes and Development
Genetics
Developmental Biology
