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28 results on '"MacRae, Calum"'

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1. Towards Precision Cardiovascular Analysis in Zebrafish: The ZACAF Paradigm

2. Perturbational phenotyping of human blood cells reveals genetically determined latent traits associated with subsets of common diseases

3. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

4. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

5. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

6. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

7. Transcriptomic and spatial dissection of human ex vivo right atrial tissue reveals proinflammatory microvascular changes in ischemic heart disease

8. De novo variants in DENND5B cause a neurodevelopmental disorder

9. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

10. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

11. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

12. De novo variants in DENND5B cause a neurodevelopmental disorder

13. REALM-DCM: A Phase 3, Multinational, Randomized, Placebo-Controlled Trial of ARRY-371797 in Patients With Symptomatic LMNARelated Dilated Cardiomyopathy.

14. The Role of MAPRE2 and Microtubules in Maintaining Normal Ventricular Conduction

15. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

16. Investigating the replacement of carboxylates with carboxamides to modulate the safety and efficacy of platinum(II) thioether cyanide scavengers.

17. Artificial intelligence-enabled prediction of chemotherapy-induced cardiotoxicity from baseline electrocardiograms.

19. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

20. Dominant missense variants in SREBF2are associated with complex dermatological, neurological, and skeletal abnormalities

21. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

22. Transcriptomic and spatial dissection of human ex vivoright atrial tissue reveals proinflammatory microvascular changes in ischemic heart disease

23. Biallelic CRELD1variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

24. Personalized Intervention Based on Early Detection of Atherosclerosis: JACC State-of-the-Art Review.

25. Understanding activity and physiology at scale: The Apple Heart & Movement Study.

26. Characterization and natural history of patients with LMNA-related dilated cardiomyopathy in the phase 3 REALM-DCM trial.

27. REALM-DCM: A Phase 3, Multinational, Randomized, Placebo-Controlled Trial of ARRY-371797 in Patients With Symptomatic LMNA -Related Dilated Cardiomyopathy.

28. Prdm16 mutation determines sex-specific cardiac metabolism and identifies two novel cardiac metabolic regulators.

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