Items where Division is "Faculty of Medicine > Basic Sciences Academic Groups > Department of Biochemistry and Genetics" and Year is 2015

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Creators | Item Type | No Grouping
Jump to: A | F | R | S | Y
Number of items: 6.

A

Amini Sarteshnizi, Neamatollah. and Teimori, Hossein. and Zahri, Saber. and Mobini Dehkordi, Mohsen. and Khosravi, Somayeh. and Amini Sarteshnizi, Roghayeh. (2015) Effect of Chrysin on AGS human gastric cancer cell line. Journal of Gorgan University of Medical Sciences, 16 (4).

F

Fouladi, Bahman. and Yadegari, Mohammad Hossein. and Rajabibazl, Masoumeh. and Fazaeli, Asghar. and Hashemzadeh-Chaleshtori, Morteza. (2015) Identification of candida species in patients with vulvovaginitis presenting different clinical symptoms. Journal of Zanjan University of Medical Sciences and Health Services, 23 (98). pp. 57-68.

R

Rad, F.R. and Mobasheri, M.B. and Modarressi, M.H. (2015) TSGA10, as a cancer/testis gene: Review article. Tehran University Medical Journal, 73 (4). pp. 231-242.

Rouhi-Boroujeni, Hojjat and Rouhi-Boroujeni, Hamid and Heidarian, E. and Mohammadizadeh, F. and Rafieian-Kopaei, M. (2015) Herbs with anti-lipid effects and their interactions with statins as a chemical anti-hyperlipidemia group drugs: A systematic review. ARYA atherosclerosis, 11 (4).

S

Sadrizade, N. and Parchami Barjui, Shahrbanoo. and Reiisi, Somayeh. and Hashemzadeh-Chaleshtori, Morteza. and Hajhashemi, M. (2015) Screening BRCA1 and BRCA2 Mutation Frequencies In Breast Cancer Patients Of West Iran Reveals a Novel Polymorphism In BRCA1 Gene «L’indagine sulla frequenza di mutazione dei BRCA1 e BRCA2 in pazienti con tumore mammario dell’Iran occidentale evidenzia un nuovo polimorfismo del gene BRCA1». European Journal of Oncology, 20 (2). pp. 94-99.

Y

Yazdanpanahi, Nasrin. and Tabatabaiefar, Mohammad Amin. and Bagheri, Nader. and Azadegan-Dehkordi, Fatemeh. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. (2015) The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness. INTERNATIONAL JOURNAL OF AUDIOLOGY, 54 (2). pp. 124-130.

This list was generated on Mon May 21 01:02:16 2018 IRDT.