Biblio

Author Title [ Type(Desc)] Year
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Journal Article
Armanmehr A, Khamirani HJafari, Zoghi S, Dianatpour M. Analysis of DYRK1B, PPARG, and CEBPB Expression Patterns in Adipose-Derived Stem Cells from Patients Carrying DYRK1B R102C and Healthy Individuals During Adipogenesis. Metab Syndr Relat Disord. 2022.
Pandamooz S, Jurek B, Dianatpour M, Haerteis S, Limm K, Oefner PJ, Dargahi L, Borhani-Haghighi A, Miyan JA, Salehi MSaied. The beneficial effects of chick embryo extract preconditioning on hair follicle stem cells: A promising strategy to generate Schwann cells. Cell Prolif. 2023:e13397.
Bhat N, Narayanan A, Fathzadeh M, Shah K, Dianatpour M, Ziki MDAbou, Mani A. Dyrk1b promotes autophagy during skeletal muscle differentiation by upregulating 4e-bp1. Cell Signal. 2021:110186.
Abadi MKamali-Dol, Yousefi G, Dehghani F, Alizadeh AAkbar, Jangholi A, Moadab MAmin, Naseh M, Parsa S, Nasiri G, Azarpira N, et al. The Effect of Mesenchymal Stem Cells Derived-Conditioned Media in Combination with Oral Anti-Androgenic Drugs on Male Pattern Baldness: An Animal Study. Cell J. 2023;25(11):790-800.
Mehrabani D, Mahboobi R, Dianatpour M, Zare S, Tamadon A, Hosseini SEbrahim. Establishment, Culture, and Characterization of Guinea Pig Fetal Fibroblast Cell. Vet Med Int. 2014;2014:510328.
Anushiravani A, Khamirani HJafari, Mohamadkhani A, Mani A, Dianatpour M, Malekzadeh R. A Form of Metabolic-Associated Fatty Liver Disease Associated with a Novel LIPA Variant. Arch Iran Med. 2023;26(2):86-91.
Karimi-Haghighi S, Pandamooz S, Jurek B, Fattahi S, Safari A, Azarpira N, Dianatpour M, Hooshmandi E, Bayat M, Owjfard M, et al. 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. Mol Neurobiol. 2023.
Ehsani E, Khamirani HJafari, Abbasi Z, Kamal N, Zoghi S, Mohammadi S, Dianatpour M, Tabei SMohammad B, Mohamadjani O, Dastgheib SAlireza. Genotypic and phenotypic spectrum of Myofibrillar Myopathy 7 as a result of Kyphoscoliosis Peptidase deficiency: The first description of a missense mutation in KY and literature review. Eur J Med Genet. 2022:104552.
Dianatpour M, Smith E, Hashemi SBasir, Farazifard MA, Nezafat N, Razban V, Mani A. Identification of Homozygous Mutations for Hearing Loss. Gene. 2021:145464.
Tamadon A, Mehrabani D, Rahmanifar F, Jahromi ARaayat, Panahi M, Zare S, Khodabandeh Z, Jahromi IRazeghian, Tanideh N, Dianatpour M, et al. Induction of Spermatogenesis by Bone Marrow-derived Mesenchymal Stem Cells in Busulfan-induced Azoospermia in Hamster. Int J Stem Cells. 2015;8(2):134-145.
Salehi MSaied, Jurek B, Karimi-Haghighi S, Nezhad NJashire, Mousavi SMaryam, Hooshmandi E, Safari A, Dianatpour M, Haerteis S, Miyan JA, et al. Intranasal application of stem cells and their derivatives as a new hope in the treatment of cerebral hypoxia/ischemia: a review. Rev Neurosci. 2022.
Dastyafteh N, Noori M, Montazer MNazari, Zomorodian K, Yazdanpanah S, Iraji A, Ghomi MKhalili, Javanshir S, Asadi M, Dianatpour M, et al. New thioxothiazolidinyl-acetamides derivatives as potent urease inhibitors: design, synthesis, in vitro inhibition, and molecular dynamic simulation. Sci Rep. 2023;13(1):21.
Haghighi NFazelzadeh, Kamal N, Khamirani HJafari, Haghighi MFazelzadeh, Dastgheib SAlireza, Dianatpour M, Tabei SMohammad B. Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review. J Dermatol. 2023.
Shiri A, Khamirani HJafari, Kamal N, Manoochehri J, Dianatpour M, Tabei SMohammad B, Dastgheib SAlireza. Novel insight into the phenotype of microcephaly 19 in the patient with missense COPB2 mutation. Eur J Med Genet. 2023:104846.
Kamal N, Khamirani HJafari, Dara M, Dianatpour M. NRXN3 mutations cause developmental delay, movement disorder, and behavioral problems: CRISPR edited cells based WES results. Gene. 2023:147347.
Pandamooz S, Salehi MSaied, Jurek B, Meinung C-P, Azarpira N, Dianatpour M, Neumann ID. Oxytocin Receptor Expression in Hair Follicle Stem Cells: A Promising Model for Biological and Therapeutic Discovery in Neuropsychiatric Disorders. Stem Cell Rev Rep. 2023.
Khamirani HJafari, Zoghi S, Faghihi F, Dastgheib SAlireza, Hassanipour H, Tabei SMohammad B, Mohammadi S, Masoudi M, Poorang S, Ehsani E, et al. Phenotype of ST3GAL3 Deficient Patients: a Case and Review of the Literature. Eur J Med Genet. 2021:104250.
Faghihi F, Khamirani HJafari, Zoghi S, Kamal N, Yeganeh BShirazi, Dianatpour M, Tabei SMohammad B, Dastgheib SAlireza. Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1. Eur J Med Genet. 2022:104449.
Karimi-Haghighi S, Chavoshinezhad S, Safari A, Razeghian-Jahromi I, Jamhiri I, Khodabandeh Z, Khajeh S, Zare S, Borhani-Haghighi A, Dianatpour M, et al. Preconditioning with secretome of neural crest-derived stem cells enhanced neurotrophic expression in mesenchymal stem cells. Neurosci Lett. 2022:136511.
Tavakkoli Z, Salehi MSaied, Jameie F, Rahimi M, Koohpeyma F, Dianatpour M, Miyan JA, Pandamooz S. Simple Methods for Cerebrospinal Fluid Collection in Fetal, Neonatal, and Adult Rat. J Neurosci Methods. 2023:109971.
Shafieipour N, Khamirani HJafari, Kamal N, Tabei SMohammad B, Dianatpour M, Dastgheib SAlireza. The third patient of ACACA-related acetyl-CoA carboxylase deficiency with seizure and literature review. Eur J Med Genet. 2023:104707.
Khoddam S, Kamal N, Shiri A, Khamirani HJafari, Manoochehri J, Dianatpour M, Tabei SMohammad B, Dastgheib SAlireza. Two siblings with PEX11B-related peroxisome biogenesis disorder. Eur J Med Genet. 2024:104928.
Kamal N, Khamirani HJafari, Mohammadi S, Dastgheib SAlireza, Dianatpour M, Tabei SMohammad B. ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review. Eur J Med Genet. 2022:104522.