Converging pathways and principles in heart development and disease: CV@CSH

Cell

Volumn 110, Issue 2, 2002, Pages 153-162

  Chien, Kenneth R ^a   Olson, Eric N ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOGENIC FACTOR; VASCULOTROPIN;

ANGIOGENESIS; ARRHYTHMOGENESIS; CARDIOVASCULAR DISEASE; CELL LINEAGE; CONFERENCE PAPER; CONGENITAL HEART DISEASE; FISH GENETICS; HEART DEVELOPMENT; HEART MUSCLE CONDUCTION SYSTEM; HEART VENTRICLE; HEART VENTRICLE HYPERTROPHY; HEART VENTRICLE REMODELING; HYPERTENSION; KIDNEY CELL; NEURAL CREST; NONHUMAN; PRIORITY JOURNAL; STEM CELL; ZEBRA FISH;

DANIO RERIO;

EID: 0037178779     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(02)00834-6     Document Type: Conference Paper

References (49)

1. Fgf8 is Required For Pharyngeal Arch and Cardiovascular Development in the Mouse
2. MLP-deficient mice exhibit a disruption of cardiac cytoarchitectural organization, dilated cardiomyopathy, and heart failure
3. Role of Id proteins in embryonic and tumor angiogenesis
4. A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease
5. Stress pathways and heart failure
6. Genomic circuits and the integrative biology of cardiac diseases
7. Stritated muscle cytoarchitecture:an intricate web of form and function
8. An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy
9. An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome
10. Decoding calcium signals involved in cardiac growth and function
11. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
12. Smooth muscle cells, but not myocytes, of host origin in transplanted human hearts
13. Conducting the embryonic heart: Orchestrating development of specialized cardiac tissues
14. Mixed signals in heart failure: Cancer rules
15. Chronic Inhibition of Heart Failure Progression by a pseudophosphorylated Mutant of Phospholamban via Cardiac rAAV Gene Delivery
16. Rat genetics: Attaching physiology and pharmacology to the genome
17. DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
18. Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease
19. Identification of an angiogenic mitogen selective for endocrine gland endothelium
20. Calcineurin inhibition and cardiac hypertrophy: A matter of balance
21. Molecular mechanisms of human hypertension
22. Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice
23. Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5
24. Signal-dependent nuclear export of a histone deacetylase regulates muscle differentiation
25. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome
26. Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy
27. A calcineurin-dependent transcriptional pathway for cardiac hypertrophy
28. Mechanisms of embryonic coronary artery development
29. Transcriptional activity of MEF2 during mouse embryogenesis monitored with a MEF2-dependent transgene
30. A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages
31. Bone marrow cells regenerate infarcted myocardium
32. Adult mice deficient in actinin-associated LIM-domain protein reveal a developmental pathway for right ventricular cardiomyopathy
33. Gata5 is required for the development of the heart and endoderm in zebrafish
34. Visualization and functional characterization of the developing murine cardiac conduction system
35. Neuregulin-1 Promotes Formation of the Murine Cardiac Conduction System
36. Congenital heart disease caused by mutations in the transcription factor NKX2-5
37. The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms
38. From Zebrafish to Humans: Modular Medical Models
39. Signalling pathways in cardiac myocyte hypertrophy
40. Therapeutic angiogenesis. A single intraarterial bolus of vascular endothelial growth factor augments revascularization in a rabbit ischemic hind limb model
41. A genetic link between Tbx1 and Fibroblast Growth Factor signaling
42. UDP-glucose dehydrogenase required for cardiac valve formation in zebrafish
43. Activation of cardiac gene expression by myocardin, a transcriptional cofactor for serum response factor
44. Cardiomyopathy in zebrafish due to mutation in an alternatively spliced exon of titin
45. Vascular-specific growth factors and blood vessel formation
46. Requirement of CDC45 for postimplantation mouse development
47. Gridlock signalling pathway fashions the first embryonic artery
48. Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C
49. Ablation of Cypher, a PDZ-LIM domain Z-line protein, causes a severe form of congenital myopathy