Works by Galehdari, Hamid

Results: 127

Reduced Anticancer Potency of Carboplatin in the Presence of Sialic Acid in SH-SY5Y Cells.

Published in:

Jentashapir Journal of Cellular & Molecular Biology, 2023, v. 14, n. 3, p. 1, doi. 10.5812/jjcmb-138709

By:

Abo-Abdolah, Doa;
Galehdari, Hamid;
Shafiei, Mohammad

Publication type:

Article

Molecular Characterization of a cDNA Encoding of an Anionic Cysteine-Free Antimicrobial Peptide From the Iranian Scorpion Odontobuthus Doriae Venom Glands.

Published in:

Pharmaceutical & Biomedical Research, 2022, v. 8, n. 3, p. 199

By:

Jalali, Amir;
Mahdavinia, Masoud;
Galehdari, Hamid;
Baradaran, Masoumeh;
Valdi-Biranvand, Davood;
Soorki, Maryam Naderi

Publication type:

Article

Evaluation of Amniocentesis Results in Patients With High-Risk Cell-Free Fetal DNA.

Published in:

International Journal of Women's Health & Reproduction Sciences, 2023, v. 11, n. 4, p. 178, doi. 10.15296/ijwhr.2023.39

By:

Jafari, Raziyeh Mohammad;
Masihi, Sara;
Galehdari, Hamid;
Najafian, Mahin;
Barati, Mojgan;
Khosravani, Maryam

Publication type:

Article

Sperm miR‐26a‐5p and its target PTEN transcripts content in men with unexplained infertility.

Published in:

Andrology, 2020, v. 8, n. 5, p. 1167, doi. 10.1111/andr.12801

By:

Dorostghoal, Mehran;
Galehdari, Hamid;
Moramezi, Farideh;
Danyari, Reza

Publication type:

Article

Hematologic Parameters Cut-off Assessment of Adult Alpha-Thalassemia Patients in Iran.

Published in:

International Journal of Hematology-Oncology & Stem Cell Research, 2024, v. 18, n. 4, p. 323

By:

Keikhaei, Bijan;
Bitaraf, Saeid;
Mafakher, Ladan;
Galehdari, Hamid;
Saki-Malehi, Amal;
Bahadoram, Mohammad

Publication type:

Article

Prenatal diagnosis of different polymorphisms of β-globin gene in Ahvaz.

Published in:

International Journal of Hematology-Oncology & Stem Cell Research, 2013, v. 7, n. 2, p. 17

By:

Dehghanifard, Ali;
Shahjahani, Mohammad;
Galehdari, Hamid;
Rahim, Fakher;
Hamid, Fatemeh;
Jaseb, Kaveh;
Asnafi, Ali Amin;
Jalalifar, Mohammad Ali;
Saki, Najmaldin

Publication type:

Article

Molecular Genetics Diagnosis of Wilson Disease: the First Reported Case of ATP7B Gene Mutation at Codon 778 in Southwest Iran.

Published in:

2012

By:

Galehdari, Hamid;
Tangestani, Raheleh

Publication type:

Case Study

A Significant Upregulation of miR-886-5p in High Grade and Invasive Bladder Tumors.

Published in:

2015

By:

Khoshnevisan, Atefeh;
Parvin, Mahmoud;
Ghorbanmehr, Nasim;
Hatefi, Nasim;
Galehdari, Hamid;
Ziaee, Seyed Amir Mohsen;
Mowla, Seyed Javad

Publication type:

journal article

A Significant Upregulation of miR-886-5p in High Grade and Invasive Bladder Tumors.

Published in:

Urology Journal, 2015, v. 12, n. 3, p. 2160

By:

Khoshnevisan, Atefeh;
Parvin, Mahmoud;
Ghorbanmehr, Nasim;
Hatefi, Nasim;
Galehdari, Hamid;
Seyed Amir Mohsen Ziaee;
Mowla, Seyed Javad

Publication type:

Article

Ameliorating Effect of Osteopontin on H<sub>2</sub>O<sub>2</sub>-Induced Apoptosis of Human Oligodendrocyte Progenitor Cells.

Published in:

Cellular & Molecular Neurobiology, 2018, v. 38, n. 4, p. 891, doi. 10.1007/s10571-017-0563-4

By:

Mazaheri, Neda;
Peymani, Maryam;
Galehdari, Hamid;
Ghaedi, Kamran;
Ghoochani, Ali;
Kiani-Esfahani, Abbas;
Nasr-Esfahani, Mohammad Hossein

Publication type:

Article

The first Molecular genetics analysis of individuals suffering from nephropatic cystinosis in the Southwestern Iran.

Published in:

Nefrologia, 2013, v. 33, n. 3, p. 308, doi. 10.3265/Nefrologia.pre2012.Sep.11558

By:

Shahkarami, Sepideh;
Galehdari, Hamid;
Ahmadzadeh, Ali;
Babaahmadi, Mahnaz;
Pedram, Mohammad

Publication type:

Article

The first survey of distribution of inherited deafness patterns in individuals referred to genetic center of Ahvaz welfare organization, Southern Iran.

Published in:

Audiology, 2011, v. 20, n. 2, p. 72

By:

Mohammad Foroughmand, Ali;
Galehdari, Hamid;
Mohammadian, Gholamreza;
Rasekh, Abdolrahman;
Ghavabesh, Jasem

Publication type:

Article

Time depended Bcl-2 inhibition might be useful for a targeted drug therapy.

Published in:

Cancer Cell International, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12935-015-0254-5

By:

Talaiezadeh, Abdolhassan;
jalali, Fateme;
Galehdari, Hamid;
Khodadadi, Ali

Publication type:

Article

The functional impact of the C/N-terminal extensions of the mouse retinal IMPDH1 isoforms: a kinetic evaluation.

Published in:

Molecular & Cellular Biochemistry, 2020, v. 465, n. 1/2, p. 155, doi. 10.1007/s11010-019-03675-9

By:

Andashti, Behnaz;
Yazdanparast, Razieh;
Barzegari, Ebrahim;
Galehdari, Hamid

Publication type:

Article

Pemphigus vegetans misdiagnosed as condylomata acuminata: A case report.

Published in:

2022

By:

Siadat, Amir Hossein;
Moeine, Reza;
Iraji, Fariba;
Galehdari, Hamid;
Shahriarirad, Reza

Publication type:

Case Study

Successful treatment of Becker's nevus with dermabrasion by sandpaper: A case report.

Published in:

2021

By:

Hafezi, Hossein;
Galehdari, Hamid;
Rezaie, Mina;
Moeini, Reza

Publication type:

Case Study

Pustular psoriasis of pregnancy in early first trimester: A case report.

Published in:

Clinical Case Reports, 2021, v. 9, n. 7, p. 1, doi. 10.1002/ccr3.4438

By:

Mohaghegh, Fatemeh;
Galehdari, Hamid;
Rezaie, Mina

Publication type:

Article

Cutaneous leukocytoclastic vasculitis secondary to COVID‐19 infection: A case report.

Published in:

Clinical Case Reports, 2021, v. 9, n. 2, p. 830, doi. 10.1002/ccr3.3596

By:

Iraji, Fariba;
Galehdari, Hamid;
Siadat, Amir Hossein;
Bokaei Jazi, Safoura

Publication type:

Article

Prenatal diagnosis of a rare de novo 1q22‐q25.1 chromosomal deletion syndrome using oligo array CGH.

Published in:

2018

By:

Shariati, Gholamreza;
Saberi, Alihossein;
Hamid, Mohammad;
Galehdari, Hamid;
Sedaghat, Alireza;
Abdorasuli, Nehzat

Publication type:

Case Study

Molecular prenatal diagnosis of megalencephalic leukoencephalopathy with subcortical cysts in a child from southwest of Iran.

Published in:

Clinical Case Reports, 2015, v. 3, n. 2, p. 114, doi. 10.1002/ccr3.168

By:

Shariati, Gholamreza;
Mohammad Hamid;
Saberi, Alihossein;
Andashti, Behnaz;
Galehdari, Hamid

Publication type:

Article

UGT1A1 Gene Mutation due to Crigler-Najjar Syndrome in Iranian Patients: Identification of a Novel Mutation.

Published in:

2013

By:

Mohammadi Asl, Javad;
Tabatabaiefar, Mohammad Amin;
Galehdari, Hamid;
Riahi, Kourosh;
Masbi, Mohammad Hosein;
Zargar Shoshtari, Zohre;
Rahim, Fakher

Publication type:

Journal Article

UGT1A1 Gene Mutation due to Crigler-Najjar Syndrome in Iranian Patients: Identification of a Novel Mutation.

Published in:

BioMed Research International, 2013, v. 2013, p. 1, doi. 10.1155/2013/342371

By:

Asl, Javad Mohammadi;
Tabatabaiefar, Mohammad Amin;
Galehdari, Hamid;
Riahi, Kourosh;
Masbi, Mohammad Hosein;
Shoshtari, Zohre Zargar;
Rahim, Fakher

Publication type:

Article

Whole‐transcriptome sequencing identifies postzygotic ATP2A2 mutations in a patient misdiagnosed with herpes zoster, confirming the diagnosis of very late‐onset segmental Darier disease.

Published in:

Experimental Dermatology, 2022, v. 31, n. 6, p. 943, doi. 10.1111/exd.14559

By:

Mohaghegh, Fatemeh;
Youssefian, Leila;
Galehdari, Hamid;
Tavakoli, Narjes;
Vahidnezhad, Hassan;
Uitto, Jouni

Publication type:

Article

Evaluation of the relationship between serum levels of insulin, cortisol and growth hormones with wound healing in normal and diabetic rats.

Published in:

Physiology & Pharmacology, 2014, v. 18, n. 1, p. 92

By:

Zadeh, Zahra Abbasi;
Kesmati, Mahnaz;
Galehdari, Hamid;
Rezai, Anahita;
Seyednezhad, Seyed Mansor;
Torabi, Mozhgan

Publication type:

Article

Genotype–phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran.

Published in:

Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-08986-4

By:

Hamid, Mohammad;
keikhaei, Bijan;
Galehdari, Hamid;
Saberi, Alihossein;
Sedaghat, Alireza;
Shariati, Gholamreza;
Mohammadi-Anaei, Marziye

Publication type:

Article

Identification of new variants in patients with mucopolysaccharidosis in consanguineous Iranian families.

Published in:

Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1343094

By:

Zabihi, Rezvan;
Zamani, Mina;
Aminzadeh, Majid;
Chamanrou, Niloofar;
Kiani, Fatemeh Zahra;
Seifi, Tahere;
Zeighami, Jawaher;
Yadegari, Tahere;
Sedaghat, Alireza;
Saberi, Alihossein;
Hamid, Mohammad;
Shariati, Gholamreza;
Galehdari, Hamid

Publication type:

Article

Recombinant Production and Purification of Inosine 5-Mono Phosphate Dehydrogenase 1 Retinal Isoforms for Functional Studies.

Published in:

Acta Medica Iranica, 2022, v. 60, n. 12, p. 765

By:

Andashti, Behnaz;
Yazdanparast, Razieh;
Galehdari, Hamid

Publication type:

Article

Development of an indirect sandwich ELISA for detection of urinary antigen, using Legionella pneumophila PAL protein.

Published in:

World Journal of Microbiology & Biotechnology, 2014, v. 30, n. 5, p. 1463, doi. 10.1007/s11274-013-1560-5

By:

Gholipour, Abolfazl;
Moosavian, Mojtaba;
Makvandi, Manoochehr;
Galehdari, Hamid;
Alvandi, Amirhooshang;
Mard, Seyyed

Publication type:

Article

Alpha‐globin gene triplication and its effect in beta‐thalassemia carrier, sickle cell trait, and healthy individual.

Published in:

EJHaem, 2021, v. 2, n. 3, p. 366, doi. 10.1002/jha2.262

By:

Hamid, Mohammad;
keikhaei, Bijan;
Galehdari, Hamid;
Saberi, Alihossein;
Sedaghat, Alireza;
Shariati, Gholamreza;
Mohammadi‐Anaei, Marziye

Publication type:

Article

Hb AHVAZ [ α83(F4)Leu→Arg, C TG>C GG ( α2); HBA2: c.251T>G],A New Hemoglobin Variant of the α2-Globin Gene.

Published in:

Hemoglobin, 2013, v. 37, n. 5, p. 477, doi. 10.3109/03630269.2013.792095

By:

Hamid, Mohammad;
Shariati, Gholamreza;
Saberi, Alihossein;
Galehdari, Hamid;
Kaikhaei, Bijan;
Mohammadi-Anaei, Marziye

Publication type:

Article

Comprehensive Spectrum of the β-Thalassemia Mutations in Khuzestan, Southwest Iran.

Published in:

Hemoglobin, 2010, v. 34, n. 5, p. 461, doi. 10.3109/03630269.2010.514153

By:

Galehdari, Hamid;
Salehi, Bahaoddin;
Azmoun, Somaiyeh;
Keikhaei, Bijan;
Zandian, Khoda Morad;
Pedram, Mohammad

Publication type:

Article

A prospective study to evaluate the gender prediction of blastocysts by using cell-free DNA within a culture medium.

Published in:

International Journal of Reproductive Biomedicine, 2022, v. 20, n. 7, p. 561, doi. 10.18502/ijrm.v20i7.11558

By:

Barzanouni, Somayeh;
Moramezi, Farideh;
Zargar, Mahvash;
Galehdari, Hamid;
Hemadi, Masoud

Publication type:

Article

HOXC10 is significantly overexpressed in colorectal cancer.

Published in:

Biomedical Reports, 2020, v. 13, n. 3, p. N.PAG, doi. 10.3892/br.2020.1325

By:

Enteghami, Mahboubeh;
Ghorbani, Mahsa;
Zamani, Mina;
Galehdari, Hamid

Publication type:

Article

High incidence of AZF duplications in clan-structured Iranian populations detected through Y chromosome sequencing read depth analysis.

Published in:

Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-39069-7

By:

Hajiesmaeil, Mogge;
Ravasini, Francesco;
Risi, Flavia;
Magnarini, Giorgia;
Olivieri, Anna;
D'Atanasio, Eugenia;
Galehdari, Hamid;
Trombetta, Beniamino;
Cruciani, Fulvio

Publication type:

Article

Regression Modeling and Meta-Analysis of Diagnostic Accuracy of SNP-Based Pathogenicity Detection Tools for UGT1A1 Gene Mutation.

Published in:

Genetics Research International, 2013, p. 1, doi. 10.1155/2013/546909

By:

Rahim, Fakher;
Galehdari, Hamid;
Mohammadi-asl, Javad;
Saki, Najmaldin

Publication type:

Article

Association of HLA-DR2-Related Haplotype (HLA-DRB501-DRB11501-DQB1*0602) in Patients with Multiple Sclerosis in Khuzestan Province.

Published in:

Iranian Journal of Child Neurology, 2021, v. 15, n. 3, p. 35, doi. 10.22037/ijcn.v14i4.18795

By:

DELFAN, Nooshin;
GALEHDARI, Hamid;
GHANBARI MARDASI, Farideh;
ZABIHI, Rezvan;
LATIFI PAKDEHI, Tahereh;
SEIFI, Tahereh;
MAJDINASAB, Nastaran

Publication type:

Article

Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis.

Published in:

Iranian Journal of Child Neurology, 2019, v. 13, n. 2, p. 155

By:

Hashemian, Somayyeh;
Eshraghi, Peyman;
Dilaver, Nafi;
Galehdari, Hamid;
Shalbafan, Bita;
Vakili, Rahim;
Ghaemi, Nosrat;
Ahangari, Najmeh;
Varaghchi, Jamileh Rezazadeh;
Zeighami, Jawaher;
Sedaghat, Alireza;
Aminzadeh, Majid;
Hamid, Mohammad;
Saberi, Alihossein;
Ashtari, Fereshteh;
Karimiani, Ehsan Ghayoor;
Shariati, Gholamreza

Publication type:

Article

Putative founder effect of Arg338* AP4M1 (SPG50) variant causing severe intellectual disability, epilepsy and spastic paraplegia: Report of three families.

Published in:

Clinical Genetics, 2023, v. 103, n. 3, p. 346, doi. 10.1111/cge.14264

By:

Becker, Aurélie;
Felici, Charlotte;
Lambert, Laëtitia;
de Saint Martin, Anne;
Abi‐Warde, Marie‐Thérèse;
Schaefer, Elise;
Zix, Christian;
Zamani, Mina;
Sadeghian, Saeid;
Zeighami, Jawaher;
Seifi, Tahereh;
Azizimalamiri, Reza;
Shariati, Gholamreza;
Galehdari, Hamid;
Selig, Mareike;
Ding, Can;
Duerinckx, Sarah;
Pirson, Isabelle;
Abramowicz, Marc;
Clément, Guillemette

Publication type:

Article

The Effect of Platelet-Rich Plasma on the Osteoblastic Differentiation of Human Adipose Tissue-Derived Mesenchymal Stromal Cells.

Published in:

Clinical Laboratory, 2023, v. 69, n. 7, p. 1467, doi. 10.7754/Clin.Lab.2022.221206

By:

Darabi, Mehrnaz Karimi;
Pezeshki, Seyedeh Pardis;
Nazeri, Zahra;
Zarezadeh, Vahid;
Dariuni, Hossein Azizi;
Kheirollah, Alireza;
Galehdari, Hamid;
Azizidoost, Shirin;
Cheraghzadeh, Maryam

Publication type:

Article

Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics.

Published in:

Brain: A Journal of Neurology, 2024, v. 147, n. 5, p. 1751, doi. 10.1093/brain/awad427

By:

Pace, Raffaella De;
Maroofian, Reza;
Paimboeuf, Adeline;
Zamani, Mina;
Zaki, Maha S;
Sadeghian, Saeid;
Azizimalamiri, Reza;
Galehdari, Hamid;
Zeighami, Jawaher;
Williamson, Chad D;
Fleming, Emily;
Zhou, Dihong;
Gannon, Jennifer L;
Thiffault, Isabelle;
Roze, Emmanuel;
Suri, Mohnish;
Zifarelli, Giovanni;
Bauer, Peter;
Houlden, Henry;
Severino, Mariasavina

Publication type:

Article

Biallelic MCM3AP mutations cause Charcot-Marie-Tooth neuropathy with variable clinical presentation.

Published in:

2017

By:

Karakaya, Mert;
Mazaheri, Neda;
Polat, Ipek;
Bharucha-Goebel, Diana;
Donkervoort, Sandra;
Maroofian, Reza;
Shariati, Gholamreza;
Hoelker, Irmgard;
Monaghan, Kristin;
Winchester, Sara;
Zori, Robert;
Galehdari, Hamid;
Bönnemann, Carsten G.;
Yis, Uluc;
Wirth, Brunhilde

Publication type:

Letter

Lack of association between the -839C/T polymorphism in the SLC6A3 gene promoter and schizophrenia in the Iranian population.

Published in:

Journal of Genetics, 2009, v. 88, n. 3, p. 321, doi. 10.1007/s12041-009-0046-6

By:

GALEHDARI, HAMID;
HOSSEINI, SHIVA;
FOROUGHMAND, ALI MOHAMMAD;
MUSAVIUN, MOHSEN;
KHATAMI, SAEEDREZA;
POORYASIN, ATEFEH;
AJAM, TAHEREH;
HAIDARI, MARYAM

Publication type:

Article

HOTAIR/MIR1 AXIS ACTS AS A POTENTIAL CHEMOTHERAPY TARGET IN GASTRIC.

Published in:

Genetika (0534-0012), 2023, v. 55, n. 1, p. 71, doi. 10.2298/GENSR2301071G

By:

GHANADPOUR, Morteza;
KAZEMI NEZHAD, Seyed Reza;
GALEHDARI, Hamid;
HAJJARI, Mohammadreza

Publication type:

Article

Cloning and periplasmic expression of peptidoglycan-associated lipoprotein (PAL) protein of Legionella pneumophila in Escherichia coli.

Published in:

Jundishapur Journal of Microbiology, 2010, v. 3, n. 1, p. 1

By:

Gholipour, Abolfazl;
Moosavian, Mojtaba;
Galehdari, Hamid;
Makvandi, Manoochehr;
Memari, Hamid Rajabi;
Alvandi, Amirhoushang

Publication type:

Article

Cloning of poly (3-Hydroxybutyrate) synthesis genes from Azotobacter vinelandii into Escherichia coli.

Published in:

Jundishapur Journal of Microbiology, 2009, v. 2, n. 1, p. 31

By:

Galehdari, Hamid;
Alaee, Sara;
Mirzaee, Maisam

Publication type:

Article

Cloning and Expression of Thermus aquaticus DNA polymerase in Escherichia coli.

Published in:

Jundishapur Journal of Microbiology, 2008, v. 1, n. 1, p. 1

By:

Roayaei, Mohammad;
Galehdari, Hamid

Publication type:

Article

Association Between the G1001C Polymorphism in the GRIN1 Gene Promoter and Schizophrenia in the Iranian Population.

Published in:

Journal of Molecular Neuroscience, 2009, v. 38, n. 2, p. 178, doi. 10.1007/s12031-008-9148-5

By:

Galehdari, Hamid

Publication type:

Article

Association Between the G1001C Polymorphism in the GRIN1 Gene Promoter and Schizophrenia in the Iranian Population.

Published in:

2009

By:

Galehdari, Hamid;
Pooryasin, Atefeh;
Foroughmand, Alimohammad;
Daneshmand, Setareh;
Saadat, Mostafa

Publication type:

Correction Notice

Genotypic variants of the tetrahydrobiopterin (BH4) biosynthesis genes in patients with hyperphenylalaninemia from different regions of Iran.

Published in:

Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 1, p. 1, doi. 10.1002/mgg3.2294

By:

Nezhad, Seyed Reza Kazemi;
Aligoodarzi, Pegah Namdar;
Rostami, Golale;
Shariati, Gholamreza;
Galehdari, Hamid;
Saberi, Alihossein;
Sedaghat, Alireza;
Hamid, Mohammad

Publication type:

Article

Whole exome sequencing reveals several novel variants in congenital disorders of glycosylation and glycogen storage diseases in seven patients from Iran.

Published in:

Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 2, p. 1, doi. 10.1002/mgg3.2099

By:

Papi, Atefe;
Zamani, Mina;
Shariati, Gholamreza;
Sedaghat, Alireza;
Seifi, Tahere;
Negahdari, Samira;
Sedighzadeh, Sahar Sadat;
Zeighami, Jawaher;
Saberi, Alihossein;
Hamid, Mohammad;
Galehdari, Hamid

Publication type:

Article