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Parham Habibzadeh

Showing results (51-60 of 60) with videos related to

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BMC Medical Genetics|February 5, 2020
Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT geneParham Habibzadeh, Zahra Tabatabaei, Mohammad Ali Farazi Fard, et al.
Acta Biomaterialia|February 18, 2025
Subcutaneous liposomal delivery improves monoclonal antibody pharmacokinetics in vivoMaryam Karimi, Arash Aslanabadi, Ben Atkinson, et al.
Journal of Inherited Metabolic Disease|February 13, 2020
Expanding the molecular and clinical phenotypes of FUT8-CDGBobby G Ng, Hassan Dastsooz, Mohammad Silawi, et al.
Brain Communications|November 3, 2021
High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian E Alecu, Barbara Brechmann, et al.
American Journal of Human Genetics|April 2, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
A comprehensive engineering strategy improves potency and manufacturability of a near pan-neutralizing antibody against HIVMohammad M Sajadi, Abdolrahim Abbasi, Zahra Rikhtegaran Tehrani, et al.
American Journal of Human Genetics|June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Structure (London, England : 1993)|May 15, 2025
A comprehensive engineering strategy improves potency and manufacturability of a near pan-neutralizing antibody against HIVMohammad M Sajadi, Abdolrahim Abbasi, Zahra Rikhtegaran Tehrani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2021
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorderDaniel L Polla, Mohammad Ali Farazi Fard, Zahra Tabatabaei, et al.
Brain : a Journal of Neurology|September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
BMC Medical Genetics|February 5, 2020
Pre-implantation genetic diagnosis in an Iranian family with a novel mutation in MUT geneParham Habibzadeh, Zahra Tabatabaei, Mohammad Ali Farazi Fard, et al.
Acta Biomaterialia|February 18, 2025
Subcutaneous liposomal delivery improves monoclonal antibody pharmacokinetics in vivoMaryam Karimi, Arash Aslanabadi, Ben Atkinson, et al.
Journal of Inherited Metabolic Disease|February 13, 2020
Expanding the molecular and clinical phenotypes of FUT8-CDGBobby G Ng, Hassan Dastsooz, Mohammad Silawi, et al.
Brain Communications|November 3, 2021
High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian E Alecu, Barbara Brechmann, et al.
American Journal of Human Genetics|April 2, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Biorxiv : the Preprint Server for Biology|October 28, 2024
A comprehensive engineering strategy improves potency and manufacturability of a near pan-neutralizing antibody against HIVMohammad M Sajadi, Abdolrahim Abbasi, Zahra Rikhtegaran Tehrani, et al.
American Journal of Human Genetics|June 8, 2019
Truncating Mutations in UBAP1 Cause Hereditary Spastic ParaplegiaMohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, et al.
Structure (London, England : 1993)|May 15, 2025
A comprehensive engineering strategy improves potency and manufacturability of a near pan-neutralizing antibody against HIVMohammad M Sajadi, Abdolrahim Abbasi, Zahra Rikhtegaran Tehrani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 7, 2021
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorderDaniel L Polla, Mohammad Ali Farazi Fard, Zahra Tabatabaei, et al.
Brain : a Journal of Neurology|September 26, 2020
Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegiaDarius Ebrahimi-Fakhari, Julian Teinert, Robert Behne, et al.
Pageof 6