Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Bita Hassani"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract Recently, it has been identified that circRNAs can act as miRNA sponge to regulate gene expression in various types of cancers, associating them with cancer initiation and progression. The present study aims to identify colorectal cancer-rel
Externí odkaz:
https://doaj.org/article/b33aee25ad834ce099517d951d416484
Publikováno v:
Genes and Diseases, Vol 8, Iss 2, Pp 146-156 (2021)
Duchenne muscular dystrophy is an X-linked recessive hereditary monogenic disorder caused by inability to produce dystrophin protein. In most patients, the expression of dystrophin lost due to disrupting mutations in open reading frame. Despite the e
Externí odkaz:
https://doaj.org/article/9bf6e940b10a4f5aaec4904f8baddeb6
Autor:
Bita Hassani, Mohammad Taheri, Yazdan Asgari, Ali Zekri, Ali Sattari, Soudeh Ghafouri-Fard, Farkhondeh Pouresmaeili
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Breast cancer is the most common neoplasm among females. Estrogen receptor (ESR) signaling has a prominent impact in the pathogenesis of breast cancer. Among the transcription factors associated with ESR signaling, FOXM1, GATA3, FOXA1 and ESR1 have b
Externí odkaz:
https://doaj.org/article/6d0d371d2488460a8e25a408cdb05258
Autor:
Mojtaba SAFFARI, Mohammad Hossein MODARRESSI, Reza SHIRKOOHI, Bita HASSANI, Mandana AFSHARPAD, Gholamreza RAFIEI, Gholamreza ABROODI, Mir Saeed YEKANINEJAD, Jamal ARFAEE, Seyed Mohammad AKRAMI
Publikováno v:
Iranian Journal of Public Health, Vol 48, Iss 9 (2019)
Plasma 5-miRNA as Biomarkers for Identifying Prostate Cancer Patients
Externí odkaz:
https://doaj.org/article/07c79bcd608c42489647ba5672a49293
Publikováno v:
Genes and Diseases, Vol 8, Iss 2, Pp 146-156 (2021)
Genes & Diseases
Genes & Diseases
Duchenne muscular dystrophy is an X-linked recessive hereditary monogenic disorder caused by inability to produce dystrophin protein. In most patients, the expression of dystrophin lost due to disrupting mutations in open reading frame. Despite the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb9930242d3f85750e14011a77daa70c
https://doi.org/10.1016/j.gendis.2019.12.007
https://doi.org/10.1016/j.gendis.2019.12.007
Autor:
Soudeh Ghafouri-Fard, Yazdan Asgari, Farkhondeh Pouresmaeili, Ali Sattari, Mohammad Taheri, Bita Hassani, Ali Zekri
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Frontiers in Oncology
Frontiers in Oncology
Breast cancer is the most common neoplasm among females. Estrogen receptor (ESR) signaling has a prominent impact in the pathogenesis of breast cancer. Among the transcription factors associated with ESR signaling, FOXM1, GATA3, FOXA1 and ESR1 have b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57bdd49e5a69407390c280601c332f37
https://www.frontiersin.org/articles/10.3389/fonc.2021.671418/full
https://www.frontiersin.org/articles/10.3389/fonc.2021.671418/full
Publikováno v:
Gene Reports. 26:101510
Background. Luminal tumors are the utmost frequent subtype of breast cancer (BC). Despite luminal BC has relatively good prognosis, in a subset of patients, disease relapse occurs to endocrine therapy ;hence, there is a critical need to identify new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bc4ae7aebf0b0d4b50fea2af8ea96f3
https://doi.org/10.1016/j.genrep.2022.101510
https://doi.org/10.1016/j.genrep.2022.101510
Autor:
Gholamreza Abroodi, Gholamreza Rafiei, Bita Hassani, Mandana Afsharpad, Mojtaba Saffari, Mir Saeed Yekaninejad, Reza Shirkoohi, Seyed Mohammad Akrami, Jamal Arfaee, Mohammad Hossein Modarressi
Publikováno v:
Iranian Journal of Public Health, Vol 48, Iss 9 (2019)
Iranian Journal of Public Health
Europe PubMed Central
Scopus-Elsevier
Iranian Journal of Public Health
Europe PubMed Central
Scopus-Elsevier
Plasma 5-miRNA as Biomarkers for Identifying Prostate Cancer Patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24e501e2f0b7caad322e51c839166683
https://doi.org/10.18502/ijph.v48i9.3038
https://doi.org/10.18502/ijph.v48i9.3038
Autor:
Soheila Sotoudeh, Anna Isaian, Hasan Mollanoori, Vahid Babaei, Shahram Teimourian, Mansoureh Shariat, Arghavan Ziaali, Bita Hassani
Publikováno v:
International Journal of Dermatology. 57:1485-1491
BACKGROUND Filaggrin is a key structural epidermal protein in terminal differentiation and formation of skin barrier. The important role of filaggrin and its effects in various cutaneous and noncutaneous disorders initiated a cascade of considerable
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5cf029902cf93b74d3fc7946766c3ba
https://doi.org/10.1111/ijd.14213
https://doi.org/10.1111/ijd.14213
Publikováno v:
Gene Reports. 12:122-127
Background In humans mutations in the PLN gene, a crucial Ca 2+ cycling protein, have been associated with idiopathic dilated cardiomyopathy with prevalence depending on the population. In Iran, the prevalence of PLN mutations in dilated cardiomyopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01464b0133198be2cc380dc78611644c
https://doi.org/10.1016/j.genrep.2018.06.014
https://doi.org/10.1016/j.genrep.2018.06.014