Zeinab Fazlali
Affiliations: | Institute for Research in Fundamental Sciences (IPM), Tehran, Tehran Province, Iran |
Area:
Neuromodulation, Sensory processing, Whisker barrel system, Cortical states, Neural codingGoogle:
"Zeinab Fazlali"Mean distance: 14.98 (cluster 17) | S | N | B | C | P |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Ranjbar-Slamloo Y, Fazlali Z. (2019) Dopamine and Noradrenaline in the Brain; Overlapping or Dissociate Functions? Frontiers in Molecular Neuroscience. 12: 334 |
| Fazlali Z, Ranjbar-Slamloo Y, Adibi M, et al. (2016) Correlation between Cortical State and Locus Coeruleus Activity: Implications for Sensory Coding in Rat Barrel Cortex. Frontiers in Neural Circuits. 10: 14 |
| Salimi S, Saravani M, Yaghmaei M, et al. (2015) The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms. Archives of Gynecology and Obstetrics. 291: 1303-12 |
| Ghazavi F, Fazlali Z, Banihosseini SS, et al. (2011) PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 80-9 |
| Shojaee S, Fazlali Z, Ghazavi F, et al. (2009) Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patients. Neuroscience Letters. 467: 53-7 |
| Narooie-Nejad M, Paylakhi SH, Shojaee S, et al. (2009) Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma. Human Molecular Genetics. 18: 3969-77 |
| Shojaee S, Sina F, Farboodi N, et al. (2009) A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 1023-7 |