Mansour Heidari - Search Results

Year	Number of Results
2002	1
2008	1
2009	3
2010	1
2011	1
2012	3
2013	9
2014	6
2015	6
2016	7
2017	5
2018	3
2019	2
2020	1
2021	4
2022	2
2023	3
2024	2

1

Identification of a Novel Homozygous Mutation in PRDM12 Gene in a Patient with Hereditary Sensory and Autonomic Neuropathy Type VIII.

Ebrahimi AH, Bolhassani M, Zarei MR, Heidari M, ArdeshirDavani A, Mehrtash AH, Shiri Z, Heidari M, Soleyman-Nejad M, Taskhiri MH, Norouzbeigi A, Heidari M. Ebrahimi AH, et al. Among authors: heidari m. Arch Iran Med. 2024 Apr 1;27(4):223-226. doi: 10.34172/aim.2024.32. Arch Iran Med. 2024. PMID: 38685849 Free article.

2

Retraction Notice to "Possible involvement of CREB/BDNF signaling pathway in neuroprotective effects of topiramate against methylphenidate induced apoptosis, oxidative stress and inflammation in hippocampus of rats: Molecular, biochemical and histological evidences" [Brain. Res. Bull. 132 (2017) 82-98].

Motaghinejad M, Motevalian M, Babalouei F, Abdollahi M, Heidari M, Madjd Z. Motaghinejad M, et al. Among authors: heidari m. Brain Res Bull. 2024 Apr 27:110956. doi: 10.1016/j.brainresbull.2024.110956. Online ahead of print. Brain Res Bull. 2024. PMID: 38679545 Free article. No abstract available.

3

Transcriptional Regulation of the Colorectal Cancer Stem Cell Markers, Nanog and Oct4, Induced by a Thermodynamic-Based Therapy Approach.

Ghorbani Z, Heidari M, Jafarinia M, Rohani M, Akbari A. Ghorbani Z, et al. Among authors: heidari m. Iran J Public Health. 2023 Apr;52(4):848-856. doi: 10.18502/ijph.v52i4.12458. Iran J Public Health. 2023. PMID: 37551178 Free PMC article.

4

Prevalence of Chromosomal Abnormalities in Iranian Patients with Infertility.

Abbaspour S, Isazadeh A, Heidari M, Heidari M, Hajazimian S, Soleyman-Nejad M, Taskhiri MH, Bolhassani M, Ebrahimi AH, Keshavarz P, Shiri Z, Heidari M. Abbaspour S, et al. Among authors: heidari m. Arch Iran Med. 2023 Feb 1;26(2):110-116. doi: 10.34172/aim.2023.17. Arch Iran Med. 2023. PMID: 37543931 Free PMC article.

5

The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian men.

Jafari L, Safinejad K, Nasiri M, Heidari M, Houshmand M. Jafari L, et al. Among authors: heidari m. Genes Genomics. 2023 Apr;45(4):519-529. doi: 10.1007/s13258-022-01300-6. Epub 2022 Aug 18. Genes Genomics. 2023. PMID: 35982373

6

Induction of Apoptosis in the U937 Cell Line Co-cultured with Adipose-derived Stem Cells Secreting Bone Morphogenetic Protein-4.

Ghorban Khan Tafreshi M, Mazaheri Z, Heidari M, Babaei N, Doosti A. Ghorban Khan Tafreshi M, et al. Among authors: heidari m. Int J Mol Cell Med. 2021 Fall;10(4):265-275. doi: 10.22088/IJMCM.BUMS.10.4.265. Epub 2022 Jun 6. Int J Mol Cell Med. 2021. PMID: 35875334 Free PMC article.

7

The prevalence of common CFTR gene mutations and polymorphisms in infertile Iranian men with very severe oligozoospermia.

Jafari L, Safinejad K, Nasiri M, Heidari M, Houshmand M. Jafari L, et al. Among authors: heidari m. J Med Life. 2022 Apr;15(4):547-556. doi: 10.25122/jml-2021-0261. J Med Life. 2022. PMID: 35646184 Free PMC article.

8

Identification of Two Novel Mutations in PKHD1 Gene from Two Families with Polycystic Kidney Disease by Whole Exome Sequencing.

Heidari M, Gharshasbi H, Isazadeh A, Soleyman-Nejad M, Taskhiri MH, Shapouri J, Bolhassani M, Sadighi N, Heidari M. Heidari M, et al. Curr Genomics. 2021 Oct 18;22(3):232-236. doi: 10.2174/1389202922666210219111810. Curr Genomics. 2021. PMID: 34975292 Free PMC article.

9

Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin-deficient congenital muscular dystrophy type 1A.

Khorrami A, Goleij P, Karamad V, Taheri E, Shadman B, Emami P, Jahangirzadeh G, Hajazimian S, Isazadeh A, Baradaran B, Heidari M. Khorrami A, et al. Among authors: heidari m. J Clin Lab Anal. 2021 Nov;35(11):e23930. doi: 10.1002/jcla.23930. Epub 2021 Sep 16. J Clin Lab Anal. 2021. PMID: 34528292 Free PMC article.

10

Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing.

Heidari M, Soleyman-Nejad M, Isazadeh A, Taskiri MH, Bolhassani M, Sadighi N, Shiri Z, Karimi Z, Heidari M. Heidari M, et al. Iran J Basic Med Sci. 2021 Feb;24(2):191-195. doi: 10.22038/IJBMS.2020.44487.10405. Iran J Basic Med Sci. 2021. PMID: 33953858 Free PMC article.

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