Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Afshin Bahramy"'
Autor:
Alireza Soltani Khaboushan, Seyedeh Nazanin Salimian, Saghar Mehraban, Afshin Bahramy, Narges Zafari, Abdol-Mohammad Kajbafzadeh, Joshua Johnson, Masoumeh Majidi Zolbin
Publikováno v:
Heliyon, Vol 10, Iss 16, Pp e35202- (2024)
Introduction: Ovarian cancer is the seventh most prevalent cancer among women. It has high mortality and morbidity and imposes a great burden on healthcare systems worldwide. Unraveling the mechanisms behind the Epithelial-Mesenchymal Transition and
Externí odkaz:
https://doaj.org/article/884c7d8cf27b460ca270083c51248b5f
Autor:
Mohammad Farid Mohammadi, Sahand Tehrani Fateh, Hadi Aghajani, Afshin Bahramy, Seyed Mohammad Salar Zaheryani, Javad Behroozi, Seyyed Mohammad Kahani, Pouria Mohammadi, Masoud Garshasbi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 10, Pp n/a-n/a (2023)
Key Clinical Message Congenital myasthenic syndromes‐5 (CMS5) is a rare autosomal recessive heterogeneous disorder, caused by pathogenic variants in the COLQ that lead to skeletal muscle weakness and abnormal fatigability. The onset is usually from
Externí odkaz:
https://doaj.org/article/df4b91691d194b778f63d76417dd44d8
Autor:
Hassan Yousefi, Afshin Bahramy, Narges Zafari, Mahsa Rostamian Delavar, Khoa Nguyen, Atousa Haghi, Tahmineh Kandelouei, Cecilia Vittori, Parham Jazireian, Sajad Maleki, Danyal Imani, Amin Moshksar, Amirreza Bitaraf, Sadegh Babashah
Publikováno v:
BMC Cancer, Vol 22, Iss 1, Pp 1-21 (2022)
Abstract Breast cancer is a complex disease exhibiting a great degree of heterogeneity due to different molecular subtypes. Notch signaling regulates the differentiation of breast epithelial cells during normal development and plays a crucial role in
Externí odkaz:
https://doaj.org/article/0ae73e25bf964666a4a44040a63225dd
Autor:
Farzaneh Darbeheshti, Sepideh Kadkhoda, Mahsa Keshavarz-Fathi, Sepideh Razi, Afshin Bahramy, Yaser Mansoori, Nima Rezaei
Publikováno v:
BMC Cancer, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract The concept of the ‘BRCAness’ phenotype implies the properties that some sporadic breast cancers (BC) share with BRCA1/2-mutation carriers with hereditary BC. Breast tumors with BRCAness have deficiencies in homologous recombination repa
Externí odkaz:
https://doaj.org/article/804416d74d9948aea4860378b970df2c
Autor:
Afshin Bahramy, Narges Zafari, Fatemeh Rajabi, Amirhossein Aghakhani, Ahmad Jayedi, Alireza Soltani Khaboushan, Masoumeh Majidi Zolbin, Mir Saeed Yekaninejad
Publikováno v:
Frontiers in Molecular Biosciences, Vol 10 (2023)
Background: Breast cancer (BC) is the most common cancer in women. The incidence and morbidity of BC are expected to rise rapidly. The stage at which BC is diagnosed has a significant impact on clinical outcomes. When detected early, an overall 5-yea
Externí odkaz:
https://doaj.org/article/c27ae1ec3c4c46e294e8f749c8e5b7d7
Autor:
Pouria Mohammadi, Elham Salehi Siavashani, Mohammad Farid Mohammadi, Afshin Bahramy, Navid Almadani, Masoud Garshasbi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background 3MC syndrome type 3 is an autosomal recessive disorder caused by mutations in the COLEC10 gene besides other genes like COLEC11 and MASP1. This disorder is characterized by facial dysmorphism, cleft lip and palate, postnatal growt
Externí odkaz:
https://doaj.org/article/b254f6852b004605bdd1d7c988df9aa8
Publikováno v:
Chronic Diseases Journal, Vol 6, Iss 3, Pp 113-119 (2019)
BACKGROUND: Female genital mutilation (FGM) is defined as an injury of the external female genitalia for cultural or non-therapeutic reasons. The aim of this study was to evaluate the prevalence of FGM and related factor among women in Kamyaran, Iran
Externí odkaz:
https://doaj.org/article/14e5d6270cd5405aaf126211ba546cc8
Autor:
Pantea Izadi, Fatemeh Soleymani, Saeideh Kavousi, Mehrdad Noruzinia, Afshin Bahramy, Narges Zafari
Publikováno v:
BioMed Research International, Vol 2021 (2021)
BioMed Research International
BioMed Research International
Background. Endometriosis is the most prevalent gynecological disease with elusive etiology. The mysterious entity and the lack of noninvasive diagnostic methods affect women’s lives negatively. This study is aimed at finding the relationship betwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09c8db16a7f00f1b85dabd240f4e010c
https://doi.org/10.1155/2021/5298006
https://doi.org/10.1155/2021/5298006
Autor:
Ali Moheb-Alian, Pantea Izadi, Narges Zafari, Mehrdad Noruzinia, Azam Tarafdari, Afshin Bahramy, Mir Saead Yekaninejad
Publikováno v:
Reproductive Sciences. 28:991-999
The objective of this study was to investigate whether the combination of miR-224-5p, miR-199-3p, and let-7d-3p is a suitable diagnostic panel for endometriosis. Twenty-five women with endometriosis (case) and twenty-five women without any sign of en
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d3a5fac08a143aeea744a83b5cf648e
https://doi.org/10.1007/s43032-020-00415-z
https://doi.org/10.1007/s43032-020-00415-z
Autor:
Afshin Bahramy, Masoud Garshasbi, Mohammad Farid Mohammadi, Navid Almadani, Pouria Mohammadi, Elham Salehi Siavashani
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Background 3MC syndrome type 3 is an autosomal recessive disorder caused by mutations in the COLEC10 gene besides other genes like COLEC11 and MASP1. This disorder is characterized by facial dysmorphism, cleft lip and palate, postnatal growth deficie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0144a130f7420dae0cfb9d54794c734
http://europepmc.org/articles/PMC8606204
http://europepmc.org/articles/PMC8606204