Malakootian M - Search Results

1

Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation.

Malakootian M, Jalilian M, Kalayinia S, Hosseini Moghadam M, Heidarali M, Haghjoo M. Malakootian M, et al. BMC Cardiovasc Disord. 2022 Feb 11;22(1):37. doi: 10.1186/s12872-022-02485-0. BMC Cardiovasc Disord. 2022. PMID: 35148685 Free PMC article.

2

MicroRNAs: roles in cardiovascular development and disease.

Kalayinia S, Arjmand F, Maleki M, Malakootian M, Singh CP. Kalayinia S, et al. Among authors: malakootian m. Cardiovasc Pathol. 2021 Jan-Feb;50:107296. doi: 10.1016/j.carpath.2020.107296. Epub 2020 Oct 3. Cardiovasc Pathol. 2021. PMID: 33022373 Review.

3

Dilated cardiomyopathy caused by a pathogenic nucleotide variant in RBM20 in an Iranian family.

Malakootian M, Bagheri Moghaddam M, Kalayinia S, Farrashi M, Maleki M, Sadeghipour P, Amin A. Malakootian M, et al. BMC Med Genomics. 2022 May 8;15(1):106. doi: 10.1186/s12920-022-01262-4. BMC Med Genomics. 2022. PMID: 35527250 Free PMC article.

4

Endothelial nitric oxide synthase Asp298Glu (894G/T) gene polymorphism as a possible risk factor for the coronary slow flow phenomenon among Iranians.

Karimi Y, Sehati F, Sarreshtedari A, Mirzad M, Khalili Y, Kiani R, Taheri Bajgan E, Hosseini Moghadam M, Mehrvarz F, Bakhshandeh H, Parham M, Malakootian M, Sadeghipour P. Karimi Y, et al. Among authors: malakootian m. BMC Cardiovasc Disord. 2022 Jun 30;22(1):300. doi: 10.1186/s12872-022-02736-0. BMC Cardiovasc Disord. 2022. PMID: 35773625 Free PMC article.

5

Mutational Spectrum of LDLR and PCSK9 Genes Identified in Iranian Patients With Premature Coronary Artery Disease and Familial Hypercholesterolemia.

Moradi A, Maleki M, Ghaemmaghami Z, Khajali Z, Noohi F, Moghadam MH, Kalyinia S, Mowla SJ, Seidah NG, Malakootian M. Moradi A, et al. Among authors: malakootian m. Front Genet. 2021 Feb 11;12:625959. doi: 10.3389/fgene.2021.625959. eCollection 2021. Front Genet. 2021. PMID: 33732287 Free PMC article.

6

Associations between low serum levels of ANRIL and some common gene SNPs in Iranian patients with premature coronary artery disease.

Taheri Bajgan E, Zahedmehr A, Shakerian F, Maleki M, Bakhshandeh H, Mowla SJ, Malakootian M. Taheri Bajgan E, et al. Among authors: malakootian m. Sci Rep. 2024 Jan 13;14(1):1244. doi: 10.1038/s41598-024-51715-2. Sci Rep. 2024. PMID: 38218954 Free PMC article.

7

Tenascin-C as a noninvasive biomarker of coronary artery disease.

Gholipour A, Shakerian F, Zahedmehr A, Oveisee M, Maleki M, Mowla SJ, Malakootian M. Gholipour A, et al. Among authors: malakootian m. Mol Biol Rep. 2022 Oct;49(10):9267-9273. doi: 10.1007/s11033-022-07760-z. Epub 2022 Aug 8. Mol Biol Rep. 2022. PMID: 35941419

8

hsa-miR-508-5p as a New Potential Player in Intervertebral Disc Degeneration.

Gholipour A, Malakootian M, Oveisee M. Gholipour A, et al. Among authors: malakootian m. Int J Mol Cell Med. 2022;11(2):137-149. doi: 10.22088/IJMCM.BUMS.11.2.137. Epub 2023 Jan 1. Int J Mol Cell Med. 2022. PMID: 37091041 Free PMC article.

9

Two lung development-related microRNAs, miR-134 and miR-187, are differentially expressed in lung tumors.

Mirzadeh Azad F, Naeli P, Malakootian M, Baradaran A, Tavallaei M, Ghanei M, Mowla SJ. Mirzadeh Azad F, et al. Among authors: malakootian m. Gene. 2016 Feb 15;577(2):221-6. doi: 10.1016/j.gene.2015.11.040. Epub 2015 Nov 28. Gene. 2016. PMID: 26642897

10

Novel spliced variants of OCT4, OCT4C and OCT4C1, with distinct expression patterns and functions in pluripotent and tumor cell lines.

Malakootian M, Mirzadeh Azad F, Naeli P, Pakzad M, Fouani Y, Taheri Bajgan E, Baharvand H, Mowla SJ. Malakootian M, et al. Eur J Cell Biol. 2017 Jun;96(4):347-355. doi: 10.1016/j.ejcb.2017.03.009. Epub 2017 Apr 10. Eur J Cell Biol. 2017. PMID: 28476334

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