Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Hasan Mollanoori"'
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:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Background Kawasaki disease (KD) is a pediatric inflammatory disorder causes coronary artery complications. The disease overlapping manifestations with a set of symptomatically like diseases such as bacterial and viral infections, juvenile i
Externí odkaz:
https://doaj.org/article/0f1569ddb3464050a70344a414f62baa
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:
Ehsan Moghanloo, Hasan Mollanoori, Mohsen Talebi, Salar Pashangzadeh, Fatemeh Faraji, Farimah Hadjilooei, Habibollah Mahmoodzadeh
Publikováno v:
Translational Oncology, Vol 14, Iss 6, Pp 101070- (2021)
Cell-based immunotherapies have been selected for the front-line cancer treatment approaches. Among them, CAR-T cells have shown extraordinary effects in hematologic diseases including chemotherapy-resistant acute lymphoblastic leukemia (ALL), chroni
Externí odkaz:
https://doaj.org/article/65c3669bc92947a88c64bd9b3a9fc41e
Autor:
Hojat Shahraki, Akbar Dorgalaleh, Majid Fathi, Shadi Tabibian, Shahram Teimourian, Hasan Mollanoori, Alireza Khiabani, Farhad Zaker
Publikováno v:
International Journal of Hematology-Oncology and Stem Cell Research, Vol 14, Iss 4 (2020)
Abstract Congenital factor XIII (FXIII) deficiency is an extremely rare bleeding disorder (RBD) with estimated prevalence of one per 2 million in the general population. The disorder causes different clinical manifestations such as intracranial he
Externí odkaz:
https://doaj.org/article/4aecb31c93484d5aa343cf9a6ab2ba26
Autor:
Yazdan Rahmati, Hasan Mollanoori, Naser Kakavandi, Alireza Nateghian, Shirin Sayyahfar, Vahid Babaei, Sajad Esmaeili, Shahram Teimourian
Publikováno v:
Informatics in Medicine Unlocked, Vol 20, Iss , Pp 100423- (2020)
Kawasaki disease (KD) is an inflammatory condition in children, which has unknown etiology with an insufficiently described genetic mechanism. There is no accurate molecular diagnostic test for KD, but some genetic factors have been proposed in previ
Externí odkaz:
https://doaj.org/article/97062d877ce1409bac3f24fd5745fb71
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
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:
Naser Kakavandi, Yazdan Rahmati, Sajad Esmaeili, Alireza Nateghian, Hasan Mollanoori, Shahram Teimourian, Vahid Babaei, Shirin Sayyahfar
Publikováno v:
Informatics in Medicine Unlocked, Vol 20, Iss, Pp 100423-(2020)
Kawasaki disease (KD) is an inflammatory condition in children, which has unknown etiology with an insufficiently described genetic mechanism. There is no accurate molecular diagnostic test for KD, but some genetic factors have been proposed in previ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4778da6a1f8c9a0cf55e05a4b56c55cf
http://www.sciencedirect.com/science/article/pii/S2352914820305736
http://www.sciencedirect.com/science/article/pii/S2352914820305736
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