Omrani MD - Search Results

1

Non-coding RNAs and type 2 diabetes mellitus.

Taheri M, Eghtedarian R, Ghafouri-Fard S, Omrani MD. Taheri M, et al. Among authors: omrani md. Arch Physiol Biochem. 2023 Apr;129(2):526-535. doi: 10.1080/13813455.2020.1843498. Epub 2020 Nov 6. Arch Physiol Biochem. 2023. PMID: 33155514

2

shRNA mediated RHOXF1 silencing influences expression of BCL2 but not CASP8 in MCF-7 and MDA-MB-231 cell lines.

Ghafouri-Fard S, Abdollahi DZ, Omrani M, Azizi F. Ghafouri-Fard S, et al. Asian Pac J Cancer Prev. 2012;13(11):5865-9. doi: 10.7314/apjcp.2012.13.11.5865. Asian Pac J Cancer Prev. 2012. PMID: 23317270 Free article.

3

An Iranian family with azoospermia and premature ovarian insufficiency segregating NR5A1 mutation.

Safari S, Zare-Abdollahi D, Mirfakhraie R, Ghafouri-Fard S, Pouresmaeili F, Movafagh A, Omrani MD. Safari S, et al. Among authors: omrani md. Climacteric. 2014 Jun;17(3):301-3. doi: 10.3109/13697137.2013.847079. Epub 2013 Oct 28. Climacteric. 2014. PMID: 24067197

4

Are so-called cancer-testis genes expressed only in testis?

Ghafouri-Fard S, Rezazadeh F, Zare-Abdollahi D, Omrani MD, Movafagh A. Ghafouri-Fard S, et al. Among authors: omrani md. Asian Pac J Cancer Prev. 2014;15(18):7703-5. doi: 10.7314/apjcp.2014.15.18.7703. Asian Pac J Cancer Prev. 2014. PMID: 25292049 Free article.

5

HLA genes as modifiers of response to IFN-β-1a therapy in relapsing-remitting multiple sclerosis.

Mazdeh M, Taheri M, Sayad A, Bahram S, Omrani MD, Movafagh A, Inoko H, Akbari MT, Noroozi R, Hajilooi M, Solgi G. Mazdeh M, et al. Among authors: omrani md. Pharmacogenomics. 2016 Apr;17(5):489-98. doi: 10.2217/pgs.16.2. Epub 2016 Mar 29. Pharmacogenomics. 2016. PMID: 27020477

6

Impact of ATM and SLC22A1 Polymorphisms on Therapeutic Response to Metformin in Iranian Diabetic Patients.

Shokri F, Ghaedi H, Ghafouri Fard S, Movafagh A, Abediankenari S, Mahrooz A, Kashi Z, Omrani MD. Shokri F, et al. Among authors: omrani md. Int J Mol Cell Med. 2016 Winter;5(1):1-7. Int J Mol Cell Med. 2016. PMID: 27386433 Free PMC article.

7

FOXP3 gene variations and susceptibility to autism: A case-control study.

Safari MR, Ghafouri-Fard S, Noroozi R, Sayad A, Omrani MD, Komaki A, Eftekharian MM, Taheri M. Safari MR, et al. Among authors: omrani md. Gene. 2017 Jan 5;596:119-122. doi: 10.1016/j.gene.2016.10.019. Epub 2016 Oct 14. Gene. 2017. PMID: 27751813

8

Single nucleotide polymorphisms in the FOXP3 gene are associated with increased risk of relapsing-remitting multiple sclerosis.

Eftekharian MM, Sayad A, Omrani MD, Ghannad MS, Noroozi R, Mazdeh M, Mirfakhraie R, Movafagh A, Roshanaei G, Azimi T, Inoko H, Taheri M. Eftekharian MM, et al. Among authors: omrani md. Hum Antibodies. 2016;24(3-4):85-90. doi: 10.3233/HAB-160299. Hum Antibodies. 2016. PMID: 27792007

9

Synaptosome-Associated Protein 25 (SNAP25) Gene Association Analysis Revealed Risk Variants for ASD, in Iranian Population.

Safari MR, Omrani MD, Noroozi R, Sayad A, Sarrafzadeh S, Komaki A, Manjili FA, Mazdeh M, Ghaleiha A, Taheri M. Safari MR, et al. Among authors: omrani md. J Mol Neurosci. 2017 Mar;61(3):305-311. doi: 10.1007/s12031-016-0860-2. Epub 2016 Nov 26. J Mol Neurosci. 2017. PMID: 27888397

10

Up regulation of MMP9 gene expression in female patients with multiple sclerosis.

Hamedani SY, Taheri M, Sajjadi E, Omrani MD, Mazdeh M, Arsang-Jang S, Panah AS, Sayad A. Hamedani SY, et al. Among authors: omrani md. Hum Antibodies. 2016;24(3-4):59-64. doi: 10.3233/HAB-160292. Hum Antibodies. 2016. PMID: 28128762

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

239 results

Search Page