Authors
This author contributed to 35 pathways:
This author contributed to 35 pathways:
Ash iyer
Aishwarya Iyer - Maastricht University
- GitHub: ashviyer
- ORCiD: https://orcid.org/0000-0003-2878-4049
- Google Scholar: https://scholar.google.com/citations?user=_NcxvCAAAAAJ&hl=en
- Email: [email protected]
Communities
Pathways
This author contributed to 35 pathways:
This author contributed to 35 pathways:
- CAMKK2 pathway - WP4874 (Homo sapiens)
- Omega-9 fatty acid synthesis - WP4351 (Mus musculus)
- Mitochondrial fission and fusion - WP4318 (Homo sapiens)
- Aerobic glycolysis - augmented - WP4628 (Homo sapiens)
- ROS in COVID-19 endothelial dysfunction - WP5258 (Homo sapiens)
- Mitochondrial fatty acid oxidation disorders - WP5123 (Homo sapiens)
- Heart development - WP1591 (Homo sapiens)
- Vitamin B12 metabolism - WP1533 (Homo sapiens)
- EGFR tyrosine kinase inhibitor resistance - WP4806 (Homo sapiens)
- Sphingolipid metabolism overview - WP4725 (Homo sapiens)
- TGF-beta signaling in thyroid cells for epithelial-mesenchymal transition - WP3859 (Homo sapiens)
- ERK pathway in Huntington's disease - WP3853 (Homo sapiens)
- Electron transport chain: OXPHOS system in mitochondria - WP111 (Homo sapiens)
- Markers of kidney cell lineage - WP5236 (Homo sapiens)
- Development of ureteric derived collecting system - WP5053 (Homo sapiens)
- GDNF/RET signaling axis - WP4830 (Homo sapiens)
- Affected pathways in Duchenne muscular dystrophy - WP5356 (Homo sapiens)
- Ergosterol biosynthesis - WP5354 (Saccharomyces cerevisiae)
- Orexin receptor pathway - WP5094 (Homo sapiens)
- 3q29 copy number variation syndrome - WP4906 (Homo sapiens)
- Vitamin A1 and A5/X pathways - WP5397 (Homo sapiens)
- Macrophage-stimulating protein (MSP) signaling - WP5353 (Homo sapiens)
- 16p11.2 proximal deletion syndrome - WP4949 (Homo sapiens)
- Network map of SARS-CoV-2 signaling - WP5115 (Homo sapiens)
- Proximal tubule transport - WP4917 (Homo sapiens)
- SARS coronavirus and innate immunity - WP4912 (Homo sapiens)
- Purinergic signaling - WP4900 (Homo sapiens)
- Smith-Magenis and Potocki-Lupski syndrome copy number variation - WP5381 (Homo sapiens)
- 11p11.2 copy number variation syndrome - WP5348 (Homo sapiens)
- 1p36 copy number variation syndrome - WP5345 (Homo sapiens)
- Oxylipins pathways - WP5140 (Mus musculus)
- Metabolic epileptic disorders - WP5355 (Homo sapiens)
- 7-oxo-C and 7-beta-HC pathways - WP5064 (Homo sapiens)
- EPAC1 and PKA reduction of retinal inflammation - WP5440 (Homo sapiens)
- Primary ovarian insufficiency - WP5316 (Homo sapiens)