1,526 results on '"MacRae, Calum"'
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102. Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest
103. Efficacy and Safety of ARRY-371797 in LMNA -Related Dilated Cardiomyopathy: A Phase 2 Study
104. The cerebral cavernous malformation proteins CCM2L and CCM2 prevent the activation of the MAP kinase MEKK3
105. Fusiform Aneurysms Are Associated with Aortic Root Dilatation in Patients with Subarachnoid Hemorrhage
106. Atypical Alexander disease with dystonia, retinopathy, and a brain mass mimicking astrocytoma
107. Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical Trial
108. Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty LMNA gene
109. Zebrafish as a Mainstream Model for In Vivo Systems Pharmacology and Toxicology
110. Prdm16mutation determines sex-specific cardiac metabolism and identifies two novel cardiac metabolic regulators
111. Cardiovascular Disease Causes Proinflammatory Microvascular Changes in the Human Right Atrium
112. RBPMS2 Is a Myocardial-Enriched Splicing Regulator Required for Cardiac Function
113. Intramuscular administration of glyoxylate rescues swine from lethal cyanide poisoning and ameliorates the biochemical sequalae of cyanide intoxication
114. Importance of external validation and subgroup analysis of artificial intelligence in the detection of low ejection fraction from electrocardiograms
115. Long-Term Efficacy and Safety of ARRY-371797 (PF-07265803) in Patients With Lamin A/C–Related Dilated Cardiomyopathy
116. A One-Page Summary Report of Genome Sequencing for the Healthy Adult
117. A Novel Clinical Expert System for Chest Pain Risk Assessment
118. Arrhythmogenic cardiomyopathy — New insights into disease mechanisms and drug discovery
119. An Ontology Driven and Bayesian Network Based Cardiovascular Decision Support Framework
120. Semantically Inspired Electronic Healthcare Records
121. Abstract P212: A Community Intervention For Hypertension Control Using Health Worker Outreach And Algorithmic Software-driven Blood Pressure Management
122. Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy
123. Network Analysis to Risk Stratify Patients With Exercise Intolerance
124. Notch signaling regulates cardiomyocyte proliferation during zebrafish heart regeneration
125. Abstract 19157: Variants of Unknown Significance in LMNA and MYBPC3 Alter RNA Splicing
126. Abstract 17178: CRISPR-mediated Insertions or Deletions of the Human LMNA Homolog in Zebrafish as a Model of Early-onset Cardiac Conduction Disease
127. Abstract 16710: Network Analysis for Diagnosis and Risk Stratification of Cardiopulmonary Patients With Exercise Dysfunction
128. Extraction of Ejection Fraction from Echocardiography Notes for Constructing a Cohort of Patients having Heart Failure with reduced Ejection Fraction (HFrEF)
129. Genomics
130. Importance of external validation and subgroup analysis in artificial-intelligence detecting low ejection fraction from electrocardiograms
131. Pulse Oximetry Values from 33,080 Participants in the Apple Heart & Movement Study
132. A novel DPH5-related diphthamide-deficiency syndrome causing embryonic lethality or profound neurodevelopmental disorder
133. Stx4 is required to regulate cardiomyocyte Ca2+ handling during vertebrate cardiac development
134. Single Cell Biology: Exploring Somatic Cell Behaviors, Competition and Selection in Chronic Disease
135. BS-513-02 GENOME-WIDE ASSOCIATION ANALYSES IDENTIFY NOVEL BRUGADA SYNDROME RISK LOCI AND HIGHLIGHT A NEW MECHANISM OF SODIUM CHANNEL REGULATION IN DISEASE SUSCEPTIBILITY
136. An In Vivo Zebrafish Screen Identifies Organophosphate Antidotes with Diverse Mechanisms of Action
137. Changing the scale and efficiency of chemical warfare countermeasure discovery using the zebrafish
138. BS-469619-002 PHARMACOLOGIC RESCUE OF LOSS-OF-FUNCTION SCN5A CHANNELOPATHY
139. Closing the Genotype-Phenotype Loop for Precision Medicine
140. A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients
141. THSD1 (Thrombospondin Type 1 Domain Containing Protein 1) Mutation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage
142. Genetics of Hypertrophic Cardiomyopathy
143. Zebrafish as tools for drug discovery
144. Management Strategy in 249 Consecutive Patients With Obstructive Hypertrophic Cardiomyopathy Referred to a Dedicated Program
145. Genetic Testing in Sudden Cardiac Arrest: the History and Physical Exam Remain Central in the Genomics Era
146. 138 - Drug Discovery for Myocardial Diseases and Cardiac Arrhythmias Using Zebrafish
147. 54 - Deep Phenotyping: Adding New Tools to Understand Disease
148. Inherited Cardiomyopathies
149. Molecular Genetics: New Mutations that Cause Familial Hypertrophic Cardiomyopathy
150. Proactive Variant Effect Mapping to Accelerate Genetic Diagnosis for Pediatric Cardiac Arrest
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