# Clueless with fewer cues from endothelin. Commentary: Venous endothelin guides sympathetic innervation of the developing mouse heart

**Authors:** Cedric Viero

PMC · DOI: 10.3389/fcell.2015.00054 · Frontiers in Cell and Developmental Biology · 2015-09-24

## Full-text entities

- **Genes:** Th (tyrosine hydroxylase) [NCBI Gene 21823], Slc18a3 (solute carrier family 18 (vesicular monoamine), member 3) [NCBI Gene 20508] {aka VAChT, VAT}, Ednra (endothelin receptor type A) [NCBI Gene 13617] {aka AEA001, ET-AR, ETa, Gpcr10, Mhdaaea1}, Chat (choline O-acetyltransferase) [NCBI Gene 12647] {aka B230380D24Rik, CHOACTase}, Tyro3 (TYRO3 protein tyrosine kinase 3) [NCBI Gene 22174] {aka Brt, Dtk, Etk-2, Rse, Sky, TK19-2}, Tek (TEK receptor tyrosine kinase) [NCBI Gene 21687] {aka Cd202b, Hyk, STK1, Tie-2, Tie2}, EDN1 (endothelin 1) [NCBI Gene 1906] {aka ARCND3, ET1, HDLCQ7, PPET1, QME}, Edn1 (endothelin 1) [NCBI Gene 13614] {aka ET-1, PPET1, preproET}, Tbx18 (T-box18) [NCBI Gene 76365] {aka 2810012F10Rik, 2810404D13Rik}, Ngf (nerve growth factor) [NCBI Gene 18049] {aka Ngfb, beta-NGF}
- **Diseases:** heart failure (MESH:D006333), hypertrophy (MESH:D006984), congenital syndromes (MESH:D008209), DiGeorge syndrome (MESH:D004062), Chagas' disease (MESH:D014355), dilated cardiomyopathy (MESH:D002311), arrhythmia (MESH:D001145), sudden cardiac death (MESH:D016757), aortic arch malformations (MESH:D001015), myocardial infarction (MESH:D009203), cardiovascular diseases (MESH:D002318), hypertension (MESH:D006973), ventricular septal defect (MESH:D006345), cholinergic (MESH:C535672), Pierre-Robin syndrome (MESH:D010855), Parkinson's disease (MESH:D010300)
- **Chemicals:** noradrenaline (MESH:D009638), amphetamine (MESH:D000661)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC4585226/full.md

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Source: https://tomesphere.com/paper/PMC4585226