28 results on '"Roessler, Helen I"'
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2. Cantu syndrome–associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-of-function by differential mechanisms
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3. ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9
4. Cantú syndrome, the changing phenotype: a report of the two oldest Dutch patients
5. ATP-sensitive potassium channels in zebrafish cardiac and vascular smooth muscle
6. Isolation of Cardiac and Vascular Smooth Muscle Cells from Adult, Juvenile, Larval and Embryonic Zebrafish for Electrophysiological Studies
7. ATP‐sensitive potassium channels in zebrafish cardiac and vascular smooth muscle
8. Young adult with Cantú syndrome: dealing with a rare genetic skin disorder
9. Behavioral and cognitive functioning in individuals with Cantú syndrome
10. Drug Repurposing for Rare Diseases
11. Young adult with Cantú syndrome: Dealing with a rare genetic skin disorder
12. Behavioral and cognitive functioning in individuals with Cantú syndrome
13. Three‐dimensional facial morphology in Cantú syndrome
14. KATP Channels in Zebrafish Cardiovascular System: A Model to Study Cantú Syndrome
15. ATP-sensitive potassium channels in zebrafish cardiac and vascular smooth muscle.
16. ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9
17. Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry
18. ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9
19. Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry
20. Cantu syndrome-Associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-offunction by differential mechanisms
21. Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders
22. Cantú syndrome, the changing phenotype : a report of the two oldest Dutch patients
23. Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders
24. Cantu syndrome-Associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-offunction by differential mechanisms
25. Cantú syndrome, the changing phenotype: a report of the two oldest Dutch patients
26. Effective CRISPR/Cas9-based nucleotide editing in zebrafish to model human genetic cardiovascular disorders
27. Cantu syndrome-associated SUR2 (ABCC9) mutations in distinct structural domains result in KATP channel gain-of-function by differential mechanisms
28. ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9.
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