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Mehrdad A Estiar

Showing results (1-10 of 31) with videos related to

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European Journal of Pharmacology|January 28, 2021
Assessment of the role of non-coding RNAs in the pathophysiology of Parkinson's diseaseOmidvar Rezaei, Saeedeh Nateghinia, Mehrdad A Estiar, et al.
Clinical Laboratory|February 27, 2018
Analysis of miRNA-221 Expression Level in Tumors and Marginal Biopsies from Patients with Breast Cancer (Cross-Sectional Observational Study)Atefe Abak, Sima Amini, Mehrdad A Estiar, et al.
Clinical Laboratory|May 9, 2018
Expression Analysis of MicroRNA-222 in Breast CancerSima Amini, Atefeh Abak, Mehrdad A Estiar, et al.
Clinical Laboratory|February 7, 2017
Analysis of the Association between MDM4 rs4245739 Single Nucleotide Polymorphism and Breast Cancer SusceptibilityNegar Pedram, Nasser Pouladi, Mohammad A Hosseinpour Feizi, et al.
Molecular Genetics & Genomic Medicine|January 17, 2020
Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotypeMehrdad A Estiar, Etienne Leveille, Dan Spiegelman, et al.
Movement Disorders Clinical Practice|May 5, 2025
Hereditary Spastic Paraplegia in Alberta: Lessons from a Well-Defined Cohort Including the Indigenous PopulationEkhlas Assaedi, Setareh Ashtiani, Mehrdad A Estiar, et al.
Anti-Cancer Drugs|July 8, 2016
The molecular signature of breast cancer metastasis to boneTayyeb Bahrami, Sharareh Mokmeli, Hossien Hossieni, et al.
Clinical Parkinsonism & Related Disorders|November 24, 2021
Hereditary spastic paraplegia initially diagnosed as cerebral palsyOksana Suchowersky, Setareh Ashtiani, Ping-Yee Billie Au, et al.
Clinical Genetics|March 13, 2021
GCH1 mutations in hereditary spastic paraplegiaParizad Varghaei, Grace Yoon, Mehrdad A Estiar, et al.
Journal of Human Genetics|September 14, 2019
SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegiaEtienne Leveille, Mehrdad A Estiar, Lynne Krohn, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
European Journal of Pharmacology|January 28, 2021
Assessment of the role of non-coding RNAs in the pathophysiology of Parkinson's diseaseOmidvar Rezaei, Saeedeh Nateghinia, Mehrdad A Estiar, et al.
Clinical Laboratory|February 27, 2018
Analysis of miRNA-221 Expression Level in Tumors and Marginal Biopsies from Patients with Breast Cancer (Cross-Sectional Observational Study)Atefe Abak, Sima Amini, Mehrdad A Estiar, et al.
Clinical Laboratory|May 9, 2018
Expression Analysis of MicroRNA-222 in Breast CancerSima Amini, Atefeh Abak, Mehrdad A Estiar, et al.
Clinical Laboratory|February 7, 2017
Analysis of the Association between MDM4 rs4245739 Single Nucleotide Polymorphism and Breast Cancer SusceptibilityNegar Pedram, Nasser Pouladi, Mohammad A Hosseinpour Feizi, et al.
Molecular Genetics & Genomic Medicine|January 17, 2020
Clinical and genetic analysis of ATP13A2 in hereditary spastic paraplegia expands the phenotypeMehrdad A Estiar, Etienne Leveille, Dan Spiegelman, et al.
Movement Disorders Clinical Practice|May 5, 2025
Hereditary Spastic Paraplegia in Alberta: Lessons from a Well-Defined Cohort Including the Indigenous PopulationEkhlas Assaedi, Setareh Ashtiani, Mehrdad A Estiar, et al.
Anti-Cancer Drugs|July 8, 2016
The molecular signature of breast cancer metastasis to boneTayyeb Bahrami, Sharareh Mokmeli, Hossien Hossieni, et al.
Clinical Parkinsonism & Related Disorders|November 24, 2021
Hereditary spastic paraplegia initially diagnosed as cerebral palsyOksana Suchowersky, Setareh Ashtiani, Ping-Yee Billie Au, et al.
Clinical Genetics|March 13, 2021
GCH1 mutations in hereditary spastic paraplegiaParizad Varghaei, Grace Yoon, Mehrdad A Estiar, et al.
Journal of Human Genetics|September 14, 2019
SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegiaEtienne Leveille, Mehrdad A Estiar, Lynne Krohn, et al.
Pageof 4