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Iranian Biomedical Journal
|
April 21, 2020
Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia
Ata Bushehri, Davood Zare-Abdollahi, Hesam Hashemian, et al.
Indian Journal of Clinical Biochemistry : IJCB
|
October 30, 2012
Isolation and purification of rat islet cells by flow cytometry
Azim Akbarzadeh, Dariush Norouzian, Ali Farhangi, et al.
The Journal of Gene Medicine
|
February 20, 2020
Ellis-van Creveld syndrome: Report of a case and recurrent variant
Mitra Eftekhariyazdi, Mahshid Meshkani, Alireza Moslem, et al.
International Journal of Molecular and Cellular Medicine
|
June 4, 2020
Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa
Ata Bushehri, Davood Zare-Abdollahi, Afagh Alavi, et al.
Medical Oncology (Northwood, London, England)
|
November 20, 2013
Intact expression status of RASSF1A in acute myeloid leukemia
Davood Zare-Abdollahi, Shamsi Safari, Abolfazl Movafagh, et al.
Medical Oncology (Northwood, London, England)
|
April 19, 2014
The expression analysis of LATS2 gene in de novo AML patients
Milad Gholami, Reza Mirfakhraie, Abolfazl Movafagh, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 22, 2026
Introducing a novel variant in the FTH1 gene; A closer look at FTH1-related neuroferritinopathy as a neurodegeneration with brain iron accumulation (NBIA) disorder
Mohammad Rohani, Moez Ravanbod, Davood Zare-Abdollahi, et al.
Inflammopharmacology
|
July 16, 2025
Exploring the role of inflammatory regulatory effects of probiotics as adjuvants in cancer development management with considering possible challenges: a comprehensive review
Mehran Mahooti, Fatemeh Safaei, Faezeh Firuzpour, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
July 13, 2022
The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects
Fatemeh Arab, Nima Rezaei, Forough Taheri, et al.
Leukemia & Lymphoma
|
December 6, 2013
MST1/2 and YAP1 gene expression in acute myeloid leukemia
Shamsi Safari, Abolfazl Movafagh, Davood Zare-Adollahi, et al.
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Search research articles
Search
Showing results (31-40 of 58) with videos related to
Sort By:
Page
of 6
Iranian Biomedical Journal
|
April 21, 2020
Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia
Ata Bushehri, Davood Zare-Abdollahi, Hesam Hashemian, et al.
Indian Journal of Clinical Biochemistry : IJCB
|
October 30, 2012
Isolation and purification of rat islet cells by flow cytometry
Azim Akbarzadeh, Dariush Norouzian, Ali Farhangi, et al.
The Journal of Gene Medicine
|
February 20, 2020
Ellis-van Creveld syndrome: Report of a case and recurrent variant
Mitra Eftekhariyazdi, Mahshid Meshkani, Alireza Moslem, et al.
International Journal of Molecular and Cellular Medicine
|
June 4, 2020
Identification of PROS1 as a Novel Candidate Gene for Juvenile Retinitis Pigmentosa
Ata Bushehri, Davood Zare-Abdollahi, Afagh Alavi, et al.
Medical Oncology (Northwood, London, England)
|
November 20, 2013
Intact expression status of RASSF1A in acute myeloid leukemia
Davood Zare-Abdollahi, Shamsi Safari, Abolfazl Movafagh, et al.
Medical Oncology (Northwood, London, England)
|
April 19, 2014
The expression analysis of LATS2 gene in de novo AML patients
Milad Gholami, Reza Mirfakhraie, Abolfazl Movafagh, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 22, 2026
Introducing a novel variant in the FTH1 gene; A closer look at FTH1-related neuroferritinopathy as a neurodegeneration with brain iron accumulation (NBIA) disorder
Mohammad Rohani, Moez Ravanbod, Davood Zare-Abdollahi, et al.
Inflammopharmacology
|
July 16, 2025
Exploring the role of inflammatory regulatory effects of probiotics as adjuvants in cancer development management with considering possible challenges: a comprehensive review
Mehran Mahooti, Fatemeh Safaei, Faezeh Firuzpour, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
July 13, 2022
The Clinical and Molecular Assessment of Iranian Families with Severe Congenital Neutropenia, Identification of HYOU1 and SHOC2 as Potential Novel Gene Defects
Fatemeh Arab, Nima Rezaei, Forough Taheri, et al.
Leukemia & Lymphoma
|
December 6, 2013
MST1/2 and YAP1 gene expression in acute myeloid leukemia
Shamsi Safari, Abolfazl Movafagh, Davood Zare-Adollahi, et al.
Page
of 6