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Zeinab Fazlali

Showing results (1-10 of 10) with videos related to

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Frontiers in Molecular Neuroscience|February 11, 2020
Dopamine and Noradrenaline in the Brain; Overlapping or Dissociate Functions?Yadollah Ranjbar-Slamloo, Zeinab Fazlali
Frontiers in Neural Circuits|April 6, 2016
Correlation between Cortical State and Locus Coeruleus Activity: Implications for Sensory Coding in Rat Barrel CortexZeinab Fazlali, Yadollah Ranjbar-Slamloo, Mehdi Adibi, et al.
Archives of Gynecology and Obstetrics|December 7, 2014
The early-onset preeclampsia is associated with MTHFR and FVL polymorphismsSaeedeh Salimi, Mohsen Saravani, Minoo Yaghmaei, et al.
Cognitive Neurodynamics|January 27, 2023
Generalised exponential-Gaussian distribution: a method for neural reaction time analysisFernando Marmolejo-Ramos, Carlos Barrera-Causil, Shenbing Kuang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2009
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patientsSeyedmehdi Shojaee, Farzad Sina, Niloofar Farboodi, et al.
Neuroscience Letters|October 6, 2009
Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patientsSeyedmehdi Shojaee, Zeinab Fazlali, Farzaneh Ghazavi, et al.
Human Molecular Genetics|August 7, 2009
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucomaMehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee, et al.
Molecular Psychiatry|January 21, 2022
Developmental impact of glutamate transporter overexpression on dopaminergic neuron activity and stereotypic behaviorMuhammad O Chohan, Jared M Kopelman, Hannah Yueh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 16, 2011
PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutationsFarzaneh Ghazavi, Zeinab Fazlali, Setareh Sadat Banihosseini, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
Diversity of ancestral brainstem noradrenergic neurons across species and multiple biological factorsMichael A Kelberman, Ellen Rodberg, Ehsan Arabzadeh, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Frontiers in Molecular Neuroscience|February 11, 2020
Dopamine and Noradrenaline in the Brain; Overlapping or Dissociate Functions?Yadollah Ranjbar-Slamloo, Zeinab Fazlali
Frontiers in Neural Circuits|April 6, 2016
Correlation between Cortical State and Locus Coeruleus Activity: Implications for Sensory Coding in Rat Barrel CortexZeinab Fazlali, Yadollah Ranjbar-Slamloo, Mehdi Adibi, et al.
Archives of Gynecology and Obstetrics|December 7, 2014
The early-onset preeclampsia is associated with MTHFR and FVL polymorphismsSaeedeh Salimi, Mohsen Saravani, Minoo Yaghmaei, et al.
Cognitive Neurodynamics|January 27, 2023
Generalised exponential-Gaussian distribution: a method for neural reaction time analysisFernando Marmolejo-Ramos, Carlos Barrera-Causil, Shenbing Kuang, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 9, 2009
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patientsSeyedmehdi Shojaee, Farzad Sina, Niloofar Farboodi, et al.
Neuroscience Letters|October 6, 2009
Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patientsSeyedmehdi Shojaee, Zeinab Fazlali, Farzaneh Ghazavi, et al.
Human Molecular Genetics|August 7, 2009
Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucomaMehrnaz Narooie-Nejad, Seyed Hassan Paylakhi, Seyedmehdi Shojaee, et al.
Molecular Psychiatry|January 21, 2022
Developmental impact of glutamate transporter overexpression on dopaminergic neuron activity and stereotypic behaviorMuhammad O Chohan, Jared M Kopelman, Hannah Yueh, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 16, 2011
PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutationsFarzaneh Ghazavi, Zeinab Fazlali, Setareh Sadat Banihosseini, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
Diversity of ancestral brainstem noradrenergic neurons across species and multiple biological factorsMichael A Kelberman, Ellen Rodberg, Ehsan Arabzadeh, et al.
Pageof 1