Works matching AU Dianatpour, Mehdi

Results: 67

Biallelic TMEM251 variants in patients with severe skeletal dysplasia and extreme short stature.

Published in:

Human Mutation, 2021, v. 42, n. 1, p. 89, doi. 10.1002/humu.24139

By:

Ain, Noor U.;
Muhammad, Niaz;
Dianatpour, Mehdi;
Baroncelli, Marta;
Iqbal, Muddassar;
Fard, Mohammad A. F.;
Bukhari, Ihtisham;
Ahmed, Sufian;
Hajipour, Massoumeh;
Tabatabaie, Zahra;
Foroutan, Hamidreza;
Nilsson, Ola;
Faghihi, Mohammad A.;
Makitie, Outi;
Naz, Sadaf

Publication type:

Article

An improved control strategy for an industrial copper solvent extraction process.

Published in:

Separation Science & Technology, 2022, v. 57, n. 11, p. 1745, doi. 10.1080/01496395.2021.2007132

By:

Shahcheraghi, Seyed Hadi;
Mousavi, Seyed Majid;
Dianatpour, Mehdi

Publication type:

Article

Endometrial mesenchymal stem stromal cells in mature and immature sheep: An in vitro study.

Published in:

International Journal of Reproductive Biomedicine, 2018, v. 16, n. 2, p. 83

By:

Ghobadi, Farnaz;
Rahmanifar, Farhad;
Mehrabani, Davood;
Tamadon, Amin;
Dianatpour, Mehdi;
Zare, Shahrokh;
Jahromi, Iman Razeghian

Publication type:

Article

Finding a Proper Valproic Acid-Based Autism Spectrum Disorder Model in Zebrafish: Early and Long-term Neurobehavioral Studies.

Published in:

Iranian Journal of Psychiatry & Behavioral Sciences / Progress in Psychiatry & Behavioral Sciences, 2023, v. 17, n. 3, p. 1, doi. 10.5812/ijpbs-137118

By:

Karimi, Zahra;
Zarifkar, Asadollah;
Dianatpour, Mehdi;
Mirzaei, Esmaeil;
Dara, Mahintaj;
Aligholi, Hadi

Publication type:

Article

Acetylsalicylic acid enhanced neurotrophic profile of epidermal neural crest stem cells: a possible approach for the combination therapy.

Published in:

Physiology & Pharmacology, 2022, v. 26, n. 2, p. 200, doi. 10.52547/phypha.26.2.1

By:

Zafarmand, Seyedeh Shaghayegh;
Salehi, Mohammad Saied;
Mokhtari, Mohammad Javad;
Safari, Anahid;
Pandamooz, Sareh;
Dianatpour, Mehdi;
Borhani-Haghighi, Afshin

Publication type:

Article

B2M gene knockout in HEK293T cells by non-viral delivery of CRISPR-Cas9 system for the generation of universal cells.

Published in:

Egyptian Journal of Medical Human Genetics, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s43042-022-00267-z

By:

Ranjbar, Maryam;
Amiri, Farshid;
Nourigorji, Marjan;
Torabizadeh, Farid;
Dara, Mahintaj;
Dianatpour, Mehdi

Publication type:

Article

HLA-A gene knockout using CRISPR/Cas9 system toward overcoming transplantation concerns.

Published in:

Egyptian Journal of Medical Human Genetics, 2021, v. 22, p. 1, doi. 10.1186/s43042-021-00155-y

By:

Amiri, Farshid;
Ranjbar, Maryam;
Pirouzfar, Mohammad;
Nourigorji, Marjan;
Dianatpour, Mehdi

Publication type:

Article

HLA-A gene knockout using CRISPR/Cas9 system toward overcoming transplantation concerns.

Published in:

Egyptian Journal of Medical Human Genetics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s43042-021-00155-y

By:

Amiri, Farshid;
Ranjbar, Maryam;
Pirouzfar, Mohammad;
Nourigorji, Marjan;
Dianatpour, Mehdi

Publication type:

Article

EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review.

Published in:

Human Genome Variation, 2023, v. 10, n. 1, p. 1, doi. 10.1038/s41439-023-00229-w

By:

Abbasi, Zahra;
Jafari Khamirani, Hossein;
Tabei, Seyed Mohammad Bagher;
Manoochehri, Jamal;
Dianatpour, Mehdi;
Dastgheib, Seyed Alireza

Publication type:

Article

Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report.

Published in:

2021

By:

Manoochehri, Jamal;
Dastgheib, Seyed Alireza;
Khamirani, Hossein Jafari;
Mollaie, Maryam;
Sharifi, Zahra;
Zoghi, Sina;
Tabei, Seyed Mohammad Bagher;
Mohammadi, Sanaz;
Dehghanian, Fatemeh;
Farbod, Zahra;
Dianatpour, Mehdi

Publication type:

Correction Notice

Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1.

Published in:

Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00171-9

By:

Alavi, Omid;
Khamirani, Hossein Jafari;
Zoghi, Sina;
Feili, Afrooz;
Dastgheib, Seyed Alireza;
Tabei, Seyed Mohammad Bagher;
Manoochehri, Jamal;
Panahandeh, Seyed Mehdi;
Kamali, Majid;
Dianatpour, Mehdi

Publication type:

Article

A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report.

Published in:

Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00164-8

By:

Manoochehri, Jamal;
Dastgheib, Seyed Alireza;
Khamirani, Hossein Jafari;
Mollaie, Maryam;
Sharifi, Zahra;
Zoghi, Sina;
Tabei, Seyed Mohammad Bagher;
Mohammadi, Sanaz;
Dehghanian, Fatemeh;
Farbod, Zahra;
Dianatpour, Mehdi

Publication type:

Article

A novel PTRH2 missense mutation causing IMNEPD: a case report.

Published in:

Human Genome Variation, 2021, v. 8, n. 1, p. 1, doi. 10.1038/s41439-021-00147-9

By:

Khamirani, Hossein Jafari;
Zoghi, Sina;
Dianatpour, Mehdi;
Jankhah, Aria;
Tabei, Seyed Sajjad;
Mohammadi, Sanaz;
Dastgheib, Seyed Alireza

Publication type:

Article

Design and synthesis of novel nitrothiazolacetamide conjugated to different thioquinazolinone derivatives as anti-urease agents.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05736-4

By:

Sohrabi, Marzieh;
Nazari Montazer, Mohammad;
Farid, Sara Moghadam;
Tanideh, Nader;
Dianatpour, Mehdi;
Moazzam, Ali;
Zomorodian, Kamiar;
Yazdanpanah, Somayeh;
Asadi, Mehdi;
Hosseini, Samanesadat;
Biglar, Mahmood;
Larijani, Bagher;
Amanlou, Massoud;
Barazandeh Tehrani, Maliheh;
Iraji, Aida;
Mahdavi, Mohammad

Publication type:

Article

The Implementation of Preconditioned Epidermal Neural Crest Stem Cells to Combat Ischemic Stroke. Comment on Othman, F.A.; Tan, S.C. Preconditioning Strategies to Enhance Neural Stem Cell-Based Therapy for Ischemic Stroke. Brain Sci. 2020, 10 , 893.

Published in:

2021

By:

Pandamooz, Sareh;
Jurek, Benjamin;
Salehi, Mohammad Saied;
Mostaghel, Mandana;
Miyan, Jaleel A.;
Dianatpour, Mehdi;
Borhani-Haghighi, Afshin;
Porzio, Umberto di

Publication type:

Letter

The beneficial effects of chick embryo extract preconditioning on hair follicle stem cells: A promising strategy to generate Schwann cells.

Published in:

Cell Proliferation, 2023, v. 56, n. 7, p. 1, doi. 10.1111/cpr.13397

By:

Pandamooz, Sareh;
Jurek, Benjamin;
Dianatpour, Mehdi;
Haerteis, Silke;
Limm, Katharina;
Oefner, Peter J.;
Dargahi, Leila;
Borhani‐Haghighi, Afshin;
Miyan, Jaleel A.;
Salehi, Mohammad Saied

Publication type:

Article

Fast free of acrylamide clearing tissue (FACT) for clearing, immunolabelling and three‐dimensional imaging of partridge tissues.

Published in:

Microscopy Research & Technique, 2018, v. 81, n. 12, p. 1374, doi. 10.1002/jemt.23078

By:

Mohammad Rezazadeh, Farzad;
Saedi, Saman;
Rahmanifar, Farhad;
Namavar, Mohammad Reza;
Dianatpour, Mehdi;
Tanideh, Nader;
Akhlaghi, Amir;
Niazi, Ali;
Arabi Monfared, Ali;
Tsutsui, Kazuyoshi;
Jafarzadeh Shirazi, Mohammad Reza;
Tamadon, Amin

Publication type:

Article

In utero xenotransplantation of mice bone marrow-derived stromal/stem cells into fetal rat liver: An experimental study.

Published in:

International Journal of Reproductive Biomedicine, 2020, v. 18, n. 9, p. 701, doi. 10.18502/ijrm.v13i9.7665

By:

Kasraeian, Maryam;
Ghasemi, Elahe;
Dianatpour, Mehdi;
Tanideh, Nader;
Jahromi, Iman Razeghian;
Khodabandeh, Zahra;
Dorvash, Mohammad Reza;
Zare, Shahrokh;
Hosseinabadi, Omid Koohi;
Tamadon, Amin

Publication type:

Article

CRISPR/CAS9-MEDIATED KNOCKOUT OF MLL5 ENHANCES APOPTOTIC EFFECT OF CISPLATIN IN HELA CELLS IN VITRO.

Published in:

EXCLI Journal, 2020, v. 19, p. 135, doi. 10.17179/excli2019-1957

By:

Pirouzfar, Mohammad;
Amiri, Farshid;
Dianatpour, Mehdi;
Takhshid, Mohammad Ali

Publication type:

Article

Intranasal application of stem cells and their derivatives as a new hope in the treatment of cerebral hypoxia/ischemia: a review.

Published in:

Reviews in the Neurosciences, 2022, v. 33, n. 6, p. 583, doi. 10.1515/revneuro-2021-0163

By:

Salehi, Mohammad Saied;
Jurek, Benjamin;
Karimi-Haghighi, Saeideh;
Nezhad, Nahid Jashire;
Mousavi, Seyedeh Maryam;
Hooshmandi, Etrat;
Safari, Anahid;
Dianatpour, Mehdi;
Haerteis, Silke;
Miyan, Jaleel A.;
Pandamooz, Sareh;
Borhani-Haghighi, Afshin

Publication type:

Article

Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder.

Published in:

Journal of Genetics, 2023, v. 102, n. 1, p. 1, doi. 10.1007/s12041-023-01420-2

By:

Mohammadi, Sanaz;
Jafari Khamirani, Hossein;
Zoghi, Sina;
Dastgheib, Seyed Alireza;
Tabei, Seyed Mohammad Bagher;
Talebzadeh, Mahdieh;
Adibi, Mohammad Hossein;
Dianatpour, Mehdi

Publication type:

Article

MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family.

Published in:

Journal of Genetics, 2022, v. 101, n. 1, p. 1, doi. 10.1007/s12041-022-01364-z

By:

Zeraatpisheh, Zahra;
Sichani, Ali Saber;
Kamal, Neda;
Khamirani, Hossein Jafari;
Zoghi, Sina;
Ehsani, Elham;
Mohammadi, Sanaz;
Tabei, Seyed Sajjad;
Dastgheib, Seyed Alireza;
Tabei, Seyed Mohammad Bagher;
Dianatpour, Mehdi

Publication type:

Article

Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS.

Published in:

Journal of Genetics, 2021, v. 100, n. 2, p. 1, doi. 10.1007/s12041-021-01315-0

By:

Khamirani, Hossein Jafari;
Zoghi, Sina;
Sichani, Ali Saber;
Dianatpour, Mehdi;
Mohammadi, Sanaz;
Tabei, Seyed Mohammad Bagher;
Dastgheib, Seyed Alireza

Publication type:

Article

Optimized Method for High‐Quality RNA Extraction from Formalin‐Fixed Paraffin‐Embedded Tissues.

Published in:

ChemistrySelect, 2024, v. 9, n. 16, p. 1, doi. 10.1002/slct.202400369

By:

Dara, Mahintaj;
Dianatpour, Mehdi;
Omidifar, Navid;
Azarpira, Negar;
Nili‐Ahmadabadi, Amir

Publication type:

Article

Design, Synthesis, and Molecular Dynamics Simulation Studies of New Chalcone‐Based 2‐Arylidene‐1,3‐indandiones as Tyrosinase Inhibitors.

Published in:

ChemistrySelect, 2023, v. 8, n. 33, p. 1, doi. 10.1002/slct.202302192

By:

Najafi, Zahra;
Rafiei, Farshideh;
Ghafouri‐Khosrowshahi, Abolfazl;
Mahdavi, Mohammad;
Dianatpour, Mehdi;
Iraji, Aida

Publication type:

Article

A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease.

Published in:

Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.1021037

By:

Khamirani, Hossein Jafari;
Palicharla, Vivek Reddy;
Dastgheib, Seyed Alireza;
Dianatpour, Mehdi;
Imanieh, Mohammad Hadi;
Tabei, Seyed Sajjad;
Besse, Whitney;
Mukhopadhyay, Saikat;
Liem Jr., Karel F.

Publication type:

Article

Caprine Endometrial Mesenchymal Stromal Stem Cell: Multilineage Potential, Characterization, and Growth Kinetics in Breeding and Anestrous Stages.

Published in:

Veterinary Medicine International, 2017, p. 1, doi. 10.1155/2017/5052801

By:

Tamadon, Amin;
Mehrabani, Davood;
Zarezadeh, Younes;
Rahmanifar, Farhad;
Dianatpour, Mehdi;
Zare, Shahrokh

Publication type:

Article

Establishment, Culture, and Characterization of Guinea Pig Fetal Fibroblast Cell.

Published in:

Veterinary Medicine International, 2014, p. 1, doi. 10.1155/2014/510328

By:

Mehrabani, Davood;
Mahboobi, Reza;
Dianatpour, Mehdi;
Zare, Shahrokh;
Tamadon, Amin;
Hosseini, Seyed Ebrahim

Publication type:

Article

Dystrophin gene editing by CRISPR/Cas9 system in human skeletal muscle cell line (HSkMC).

Published in:

Iranian Journal of Basic Medical Sciences, 2021, v. 24, n. 8, p. 1153, doi. 10.22038/IJBMS.2021.54711.12269

By:

Dara, Mahintaj;
Razban, Vahid;
Mazloomrezaei, Mohsen;
Ranjbar, Maryam;
Nourigorji, Marjan;
Dianatpour, Mehdi

Publication type:

Article

Use of dual-transfection for programmed death cell protein 1 disruption mediated by CRISPR-Cas9 in human peripheral blood mononuclear cells.

Published in:

Iranian Journal of Basic Medical Sciences, 2021, v. 24, n. 1, p. 44, doi. 10.22038/ijbms.2020.48566.11146

By:

Alambeladi, SeyedAli;
Hosseiny, SeyedEbrahim;
Jafarinia, Mojtaba;
Dianatpour, Mehdi

Publication type:

Article

Wi-Fi (2.4 GHz) affects anti-oxidant capacity, DNA repair genes expression and, apoptosis in pregnant mouse placenta.

Published in:

Iranian Journal of Basic Medical Sciences, 2020, v. 23, n. 6, p. 833, doi. 10.22038/ijbms.2020.40184.9512

By:

Vafaei, Homeira;
Kavari, Ghazal;
Izadi, Hamid Reza;
Dorahi, Zahra Zare;
Dianatpour, Mehdi;
Daneshparvar, Afrooz;
Jamhiri, Iman

Publication type:

Article

Spermatogenesis after transplantation of adipose tissue-derived mesenchymal stem cells in busulfan-induced azoospermic hamster.

Published in:

Iranian Journal of Basic Medical Sciences, 2018, v. 21, n. 7, p. 660

By:

Karimaghai, Negar;
Tamadon, Amin;
Rahmanifar, Farhad;
Mehrabani, Davood;
Jahromi, Alireza Raayat;
Zare, Shahrokh;
Khodabandeh, Zahra;
Jahromi, Iman Razeghian;
Koohi-Hoseinabadi, Omid;
Dianatpour, Mehdi

Publication type:

Article

Intrauterine xenotransplantation of human Wharton jellyderived mesenchymal stem cells into the liver of rabbit fetuses: A preliminary study for in vivo expression of the human liver genes.

Published in:

Iranian Journal of Basic Medical Sciences, 2018, v. 21, n. 1, p. 89, doi. 10.22038/IJBMS.2017.24501.6098

By:

Rezaeian, Leila;
Hosseini, Seyed Ebrahim;
Dianatpour, Mehdi;
Edalatmanesh, Mohammad Amin;
Tanideh, Nader;
Mogheiseh, Asghar;
Tamadon, Amin

Publication type:

Article

Emergence of signs of neural cells after exposure of bone marrow-derived mesenchymal stem cells to fetal brain extract.

Published in:

Iranian Journal of Basic Medical Sciences, 2017, v. 20, n. 3, p. 301, doi. 10.22038/ijbms.2017.8360

By:

Jahromi, Iman Razeghian;
Mehrabani, Davood;
Mohammadi, Ali;
Seno, Mohammad Mahdi Ghahramani;
Dianatpour, Mehdi;
Zare, Shahrokh;
Tamadon, Amin

Publication type:

Article

Histomorphometric evaluation of treatment of rat azoospermic seminiferous tubules by allotransplantation of bone marrow-derived mesenchymal stem cells.

Published in:

Iranian Journal of Basic Medical Sciences, 2016, v. 19, n. 6, p. 653

By:

Farhad Rahmanifar;
Amin Tamadon;
Davood Mehrabani;
Shahrokh Zare;
Sorush Abasi;
Saeideh Keshavarz;
Mehdi Dianatpour;
Zahra Khodabandeh;
Iman Raze ghian Jahromi;
Omid Koohi-Hoseinabadi

Publication type:

Article

A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA Variant.

Published in:

Archives of Iranian Medicine (AIM), 2023, v. 26, n. 2, p. 86, doi. 10.34172/aim.2023.14

By:

Anushiravani, Amir;
Khamirani, Hossein Jafari;
Mohamadkhani, Ashraf;
Mani, Arya;
Dianatpour, Mehdi;
Malekzadeh, Reza

Publication type:

Article

From Hair to the Brain: The Short-Term Therapeutic Potential of Human Hair Follicle-Derived Stem Cells and Their Conditioned Medium in a Rat Model of Stroke.

Published in:

Molecular Neurobiology, 2023, v. 60, n. 5, p. 2587, doi. 10.1007/s12035-023-03223-z

By:

Karimi-Haghighi, Saeideh;
Pandamooz, Sareh;
Jurek, Benjamin;
Fattahi, Sadegh;
Safari, Anahid;
Azarpira, Negar;
Dianatpour, Mehdi;
Hooshmandi, Etrat;
Bayat, Mahnaz;
Owjfard, Maryam;
Zafarmand, Seyedeh Shaghayegh;
Mostaghel, Mandana;
Mousavi, Seyedeh Maryam;
Jashire Nezhad, Nahid;
Eraghi, Vida;
Fadakar, Nima;
Rahimi Jaberi, Abbas;
Garcia-Esperon, Carlos;
Spratt, Neil;
Levi, Christopher

Publication type:

Article

A simple model for predicting optimal weight recovery of industrial iron ore processing – case study: Iranian iron ore mines.

Published in:

2023

By:

Shahcheraghi, Seyed Hadi;
Najafzadeh, Mohammad;
Dianatpour, Mehdi;
Mirzadeh, Iman

Publication type:

Letter

LIMA1 Gene Knockout by CRISPR/Cas9 System Using Lentiviruses as an in Vitro Model for Reducing Cholesterol Absorption.

Published in:

International Cardiovascular Research Journal, 2022, v. 16, n. 4, p. 129

By:

Talebzadeh, Mahdieh;
Razban, Vahid;
Dara, Mahintaj;
Khamirani, Hossein Jafari;
Ranjbar, Maryam;
Nourigorji, Marjan;
Torabizadeh, Farid;
Dianatpour, Mehdi

Publication type:

Article

A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness.

Published in:

Annals of Human Genetics, 2023, v. 87, n. 4, p. 147, doi. 10.1111/ahg.12501

By:

Mohammadi, Sanaz;
Jafari Khamirani, Hossein;
Baneshi, Maryam;
Kamal, Neda;
Manoocheri, Jamal;
Saffar, Mahsa;
Dianatpour, Mehdi;
Tabei, Seyed Mohammad Bagher;
Dastgheib, Seyed Alireza

Publication type:

Article

Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature.

Published in:

Annals of Human Genetics, 2022, v. 86, n. 1, p. 52, doi. 10.1111/ahg.12448

By:

Khamirani, Hossein Jafari;
Zoghi, Sina;
Namdar, Zahra Mehdipour;
Kamal, Neda;
Dianatpour, Mehdi;
Tabei, Seyed Mohammad Bagher;
Mohammadi, Sanaz;
Dehghanian, Fatemeh;
Farbod, Zahra;
Dastgheib, Seyed Alireza

Publication type:

Article

A Comprehensive Overview of NF1 Mutations in Iranian Patients.

Published in:

NeuroMolecular Medicine, 2024, v. 26, n. 1, p. 1, doi. 10.1007/s12017-024-08790-5

By:

Savad, Shahram;
Modarressi, Mohammad-Hossein;
Younesi, Sarang;
Seifi-Alan, Mahnaz;
Samadaian, Niusha;
Masoomy, Mona;
Dianatpour, Mehdi;
Norouzi, Shima;
Amidi, Saloomeh;
Boroumand, Amirreza;
Ashrafi, Mahmoud Reza;
Ronagh, Alireza;
Eslami, Maryam;
Hashemnejad, Maryam;
Nourian, Shahab;
Mohammadi, Sanaz;
Taheri Amin, Mohammad Mahdi;
Heidari, Morteza;
Seifi-Alan, Mahin;
Shojaaldini Ardakani, Hossein

Publication type:

Article

Therapeutic potential of hair follicle-derived stem cell intranasal transplantation in a rat model of ischemic stroke.

Published in:

BMC Neuroscience, 2022, v. 23, n. 1, p. 1, doi. 10.1186/s12868-022-00732-w

By:

Mousavi, Seyedeh Maryam;
Akbarpour, Bijan;
Karimi-Haghighi, Saeideh;
Pandamooz, Sareh;
Belém-Filho, Ivaldo Jesus Almeida;
Masís-Calvo, Marianella;
Salimi, Haniye;
Lashanizadegan, Ramin;
Pouramini, Alireza;
Owjfard, Maryam;
Hooshmandi, Etrat;
Bayat, Mahnaz;
Zafarmand, Seyedeh Shaghayegh;
Dianatpour, Mehdi;
Salehi, Mohammad Saied;
Borhani-Haghighi, Afshin

Publication type:

Article

"Effect of Sunset Yellow on Testis: Molecular Evaluation, and Protective Role of Coenzyme Q10 in Male Sprague-Dawley Rats".

Published in:

Cell Biochemistry & Biophysics, 2024, v. 82, n. 3, p. 2827, doi. 10.1007/s12013-024-01398-3

By:

Dara, Mahintaj;
Nazari, Fatemeh;
Dianatpour, Mehdi;
Karimi, Fatemeh;
Alaee, Sanaz;
Shirazi, Reza;
khodabandeh, Zahra

Publication type:

Article

Therapeutic effects of nanosilibinin in valproic acid‐zebrafish model of autism spectrum disorder: Focusing on Wnt signaling pathway and autism spectrum disorder‐related cytokines.

Published in:

International Journal of Developmental Neuroscience, 2024, v. 84, n. 5, p. 454, doi. 10.1002/jdn.10348

By:

Karimi, Zahra;
Zarifkar, Asadollah;
Mirzaei, Esmaeil;
Dianatpour, Mehdi;
Dara, Mahintaj;
Aligholi, Hadi

Publication type:

Article

Engineering a DYRK1B R102C mutation: insights into metabolic syndrome pathogenesis through lentiviral gene delivery.

Published in:

Medical Laboratory Journal, 2024, v. 18, n. 5, p. 34, doi. 10.29252/mlj.18.5.34

By:

Daneshparvar, Afrooz;
Jamhiri, Iman;
Razban, Vahid;
Fallahi, Jafar;
Hamidizadeh, Nasrin;
Moghtaderi, Behnam;
Dianatpour, Mehdi

Publication type:

Article

The Effect of Mesenchymal Stem Cells Derived-Conditioned Media in Combination with Oral Anti-Androgenic Drugs on Male Pattern Baldness: An Animal Study.

Published in:

Cell Journal (Yakhteh), 2023, v. 25, n. 11, p. 790, doi. 10.22074/CELLJ.2023.2008138.1377

By:

Abadi, Majid Kamali-Dolat;
Yousefi, Gholamhossein;
Dehghani, Farzaneh;
Alizadeh, Ali Akbar;
Jangholi, Abolfazl;
Moadab, Mohammad Amin;
Naseh, Maryam;
Parsa, Shima;
Nasiri, Golara;
Azarpira, Negar;
Dianatpour, Mehdi

Publication type:

Article

Preventive Effects of Intrauterine Injection of Bone Marrow-Derived Mesenchymal Stromal Cell-Conditioned Media on Uterine Fibrosis Immediately after Endometrial Curettage in Rabbit.

Published in:

Stem Cells International, 2020, p. 1, doi. 10.1155/2020/8849537

By:

Bazoobandi, Sanaz;
Tanideh, Nader;
Rahmanifar, Farhad;
Zare, Shahrokh;
Koohi-Hosseinabadi, Omid;
Razeghian-Jahromi, Iman;
Dianatpour, Mehdi;
Ahmadi, Masoumeh;
Khoradmehr, Arezoo;
Nabipour, Iraj;
Khodabandeh, Zahra;
Tamadon, Amin

Publication type:

Article

The association between estrogen receptor 2 gene polymorphism and complexity of coronary artery disease: an analysis in elective percutaneous coronary intervention patients.

Published in:

2021

By:

Foroughinia, Farzaneh;
Dehghani, Pooyan;
Dianatpour, Mehdi;
Amiri, Arghavan;
Jamhiri, Iman;
Ghasemiyeh, Parisa

Publication type:

journal article

Clinical Features of Okur-Chung Neurodevelopmental Syndrome: Case Report and Literature Review.

Published in:

Molecular Syndromology, 2022, v. 13, n. 5, p. 381, doi. 10.1159/000522353

By:

Jafari Khamirani, Hossein;
Zoghi, Sina;
Motealleh, Ali;
Dianatpour, Mehdi;
Tabei, Seyed Mohammad Bagher;
Mohammadi, Sanaz;
Dastgheib, Seyed Alireza

Publication type:

Article