1. A novel TECTA mutation causes ARNSHL. (January 2017) Authors: Asgharzade, Samira; Tabatabaiefar, Mohammad Amin; Modarressi, Mohammad Hossein; Ghahremani, Mohammad Hossein; Reiisi, Somayeh; Tahmasebi, Parisa; Abdollahnejad, Fatemeh; Chaleshtori, Morteza Hashemzadeh Journal: International journal of pediatric otorhinolaryngology Issue: Volume 92(2017:Jan.) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cag Pathogenicity island-dependent upregulation of matrix metalloproteinase-7 in infected patients with Helicobacter pylori. Issue 6 (2nd November 2017) Authors: Sadeghiani, Marzieh; Bagheri, Nader; Shahi, Heshmat; Reiisi, Somayeh; Rahimian, Ghorbanali; Rashidi, Reza; Mahsa, Majid; Shafigh, Mohammedhadi; Salimi, Elaheh; Rafieian-kopaei, Mahmoud; Hashemzadeh-chaleshtori, Morteza; Shirzad, Hedayatollah Journal: Journal of immunoassay & immunochemistry Issue: Volume 38:Issue 6(2017) Page Start: 595 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Contribution of hsa-miR-146a and hsa-miR-223 gene variations in patients with multiple sclerosis reveals association of rs2910164 and rs1044165 with risk of multiple sclerosis susceptibility. (21st January 2021) Authors: Shareef, Salar; Ebrahimi, Seyed Omar; Reiisi, Somayeh Journal: Journal of investigative medicine Issue: Volume 69:Number 5(2021) Page Start: 1015 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Contribution of Hsa-Mir-146A and Hsa-Mir-223 Gene Variations in Patients with Multiple Sclerosis Reveals Association of Rs2910164 and Rs1044165 with Risk of Multiple Sclerosis Susceptibility. (June 2021) Authors: Shareef, Salar; Ebrahimi, Seyed Omar; Reiisi, Somayeh Journal: Journal of investigative medicine Issue: Volume 69:Number 5(2021) Page Start: 1015 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants. (April 2018) Authors: Koohiyan, Mahbobeh; Hashemzadeh-Chaleshtori, Morteza; Salehi, Mansoor; Abtahi, Hamidreza; Reiisi, Somayeh; Pourreza, Mohammad Reza; Noori-Daloii, Mohammad Reza; Tabatabaiefar, Mohammad Amin Journal: International journal of pediatric otorhinolaryngology Issue: Volume 107(2018:Apr.) Page Start: 121 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Increased risk of polycystic ovary syndrome (PCOS) associated with CC genotype of miR-146a gene variation. (2nd September 2018) Authors: Ebrahimi, Seyed Omar; Reiisi, Somayeh; Parchami Barjui, Shahrbanou Journal: Gynecological endocrinology Issue: Volume 34:Number 9(2018) Page Start: 793 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. MiRNAs, oxidative stress, and cancer: A comprehensive and updated review. Issue 11 (11th May 2020) Authors: Ebrahimi, Seyed Omar; Reiisi, Somayeh; Shareef, Salar Journal: Journal of cellular physiology Issue: Volume 235:Issue 11(2020:Nov.) Page Start: 8812 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Study of quercetin and fisetin synergistic effect on breast cancer and potentially involved signaling pathways. (23rd October 2022) Authors: Hosseini, Seyede Saba; Ebrahimi, Seyed Omar; Haji Ghasem Kashani, Maryam; Reiisi, Somayeh Journal: Cell biology international Issue: Volume 47:Number 1(2023) Page Start: 98 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗