Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Hamzeh Salmani"'
Autor:
Hamzeh Salmani, Mahin Yahyaei, Reza Raoofian, Shiva Irani, Iman Salahshouri Far, Seyed Mohammad Akrami
Publikováno v:
Iranian Journal of Public Health, Vol 51, Iss 2 (2022)
Background: Mutations of the epidermal growth factor receptor (EGFR) gene, predominantly in exons 18-21, have been highlighted to function as the crucial predictors of the response rate of patients with non-small cell lung cancer (NSCLC) to EGFR tyro
Externí odkaz:
https://doaj.org/article/e480239dfce244b294fc49efc83f4e99
Publikováno v:
Middle East Journal of Cancer, Vol 9, Iss 2, Pp 105-111 (2018)
Background: Breast cancer is the second leading cause of cancer death after lung cancer. Discovering molecular biomarkers is necessary for disease management that includes prognosis prediction and preventive treatment. The aim of this study is to eva
Externí odkaz:
https://doaj.org/article/ffe6ffc3b6e34f56b4f72b3b0573ef88
Autor:
Laleh Habibi, Hamzeh Salmani
Publikováno v:
Frontiers in Microbiology, Vol 8 (2017)
RNAs have long been described as the mediators of gene expression; they play a vital role in the structure and function of cellular complexes. Although the role of RNAs in the prokaryotes is mainly confined to these basic functions, the effects of th
Externí odkaz:
https://doaj.org/article/938a37a8f2034cfa89d2d29198c91dc6
Publikováno v:
Clinical Dysmorphology. 32:84-87
Publikováno v:
Human Gene. 36:201173
Publikováno v:
Journal of Clinical Laboratory Analysis
Background Waardenburg syndrome (WS) is a genetically heterogeneous syndrome with both autosomal recessive and dominant inheritance. WS causes skin and iris pigmentation accumulation and sensorineural hearing loss, in varying degrees. There are four
Autor:
Hamzeh Salmani, Arezou Karamzade, Mohammad Keramatipour, Zahra Golchehre, Seyed Ziaeddin Tabatabaie, Mohammad Reza Saberi
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 113:229-233
Objectives Waardenburg Syndrome (WS) as a congenital auditory-pigmentary syndrome is a clinically and genetically heterogeneous disorder. Based upon clinical manifestations, it can be classified into four types. Loss of function mutations in PAX3 gen
Autor:
Hamzeh Salmani, Mahin Yahyaei, Reza Raoofian, Shiva Irani, Iman Salahshouri Far, Seyed Mohammad Akrami
Publikováno v:
Iranian journal of public health. 51(2)
Background: Mutations of the epidermal growth factor receptor (EGFR) gene, predominantly in exons 18-21, have been highlighted to function as the crucial predictors of the response rate of patients with non-small cell lung cancer (NSCLC) to EGFR tyro
Autor:
Hamzeh Salmani, Hosein Mansoori, Yaser Mansoori, Ziba Nariman-Saleh-Fam, Abdolreza Daraei, Milad Bastami, Rasoul Abdollahzadeh, Farzaneh Darbeheshti, Maral Mokhtari, Mohammad Bagher Tabei, Hassan Dastsooz, Sedigheh Tahmasebi
A growing amount of evidence has revealed that long noncoding RNAs (lncRNAs) play significant roles in malignancies through different mechanisms especially the competing endogenous RNA (ceRNA). They have also been shown to have the potential diagnost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c49bcc888ec7a5af5c910b0e4393d383
http://hdl.handle.net/2318/1800278
http://hdl.handle.net/2318/1800278
Autor:
Farzaneh Darbeheshti, Hosein Mansoori, Rasoul Abdollahzadeh, Hassan Dastsooz, Abdolreza Daraei, Maral Mokhtari, Hamzeh Salmani, Mostafa Davood Abadi Farahani, Sedigheh Tahmasebi, Yaser Mansoori
Publikováno v:
Galen Medical Journal. 10:e2108
Background: Breast cancer (BC) as a major cause of cancer-related death in women shows a very complex molecular and clinical phenotype, which has reduced the effectiveness of medical interventions. Evidence suggests that long noncoding RNAs (lncRNAs)