Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nasrin Alipour Olyaei"'
Autor:
Maryam Eghbali, Kiyana Sadat Fatemi, Shadab Salehpour, Maryam Abiri, Hassan Saei, Saeed Talebi, Nasrin Alipour Olyaei, Vahid Reza Yassaee, Mohammad Hossein Modarressi
Publikováno v:
Frontiers in Genetics, Vol 11 (2021)
Glycogen storage diseases (GSDs) are the heterogeneous group of disorders caused by mutations in at least 30 different genes. Different types of GSDs, especially liver GSDs, take overlapping symptoms and can be clinically indistinguishable. This surv
Externí odkaz:
https://doaj.org/article/d0fbfc0c01d64d0daf92024e91a3ee2a
Autor:
Reza Mazhari, Reza Mirfakhraie, Mojgan Asadi, Nasrin Alipour Olyaei, Hamidreza Kheiri, Elham Moslemi, Mahnaz Khanmohamadi, Elham Tohidnejad, Vahid Reza Yasaee
Publikováno v:
Novelty in Biomedicine, Vol 4, Iss 4, Pp 173-180 (2016)
Background: Type II diabetes is known as one of the most important, prevalent, and expensive diseases of mankind. Late diagnosis and subsequent delayed initiation of treatment or surveillance of patients create a variety of problems for affected indi
Externí odkaz:
https://doaj.org/article/b19b03ec82194321892cb724360ccc1f
Autor:
Mohadese-sadat Musavi Khorshidi, Yoann Seeleuthner, Zahra Chavoshzadeh, Maryam Behfar, Amir Ali Hamidieh, Hosein Alimadadi, Roya Sherkat, Tooba Momen, Nasrin Behniafard, Shabnam Eskandarzadeh, Mahboubeh Mansouri, Mahdiyeh Behnam, Mohadese Mahdavi, Maryam Heydarazad Zadeh, Mehdi Shokri, Fatemeh Alizadeh, Mahshid Movahedi, Mana Momenilandi, Nasrin Alipour Olyaei, Mohammad Keramatipour, Jean-Laurent Casanova, Aurélie Cobat, Laurent Abel, Mohammad Shahrooei, Nima Parvaneh
Purpose: Major histocompatibility complex class II (MHC-II) deficiency is a rare inborn error of immunity (IEI). Impaired antigen presentation to CD4+ T-cells results in combined immunodeficiency. Patients typically present with severe respiratory an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6072caa82b518377b09220678cb3af7c
https://doi.org/10.21203/rs.3.rs-2726912/v1
https://doi.org/10.21203/rs.3.rs-2726912/v1
Autor:
Ilad Alavi Darazam, Mohammad Shahrooei, Atousa Hakamifard, Nasrin Alipour Olyaei, Farahnaz Bidari Zerehpoosh, Farid Javandoust Gharehbagh, Firouze Hatami, Legha Lotfollahi, Nahal Mansouri, Jean-Laurent Casanova, Davood Mansouri
Major histocompatibility complexes class I (MHC- I) deficiency, also known as bare lymphocyte syndrome type 1 (BLS-1), is a rare autosomal recessively inherited immunodeficiency disorder with remarkable clinical and biological heterogeneity. Transpor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::119c1ab51809620b10ba709373761c74
https://doi.org/10.21203/rs.3.rs-1294904/v1
https://doi.org/10.21203/rs.3.rs-1294904/v1
Autor:
Ilad Alavi Darazam, Atousa Hakamifard, Mana Momenilandi, Marie Materna, Farid Javandoust Gharehbagh, Mohammad Shahrooei, Nasrin Alipour Olyaei, Farahnaz Bidari Zerehpoosh, Antoine Fayand, Firouze Hatami, Legha Lotfollahi, Nahal Mansouri, Jean-Laurent Casanova, Vivien Béziat, Davood Mansouri
Publikováno v:
Journal of clinical immunology.
Major histocompatibility complex class I (MHC-I) deficiency, also known as bare lymphocyte syndrome type 1 (BLS-1), is a rare autosomal recessively inherited immunodeficiency disorder with remarkable clinical and biological heterogeneity. Transporter
Autor:
Mohammad Hashemi, Amir Izadi, Elham Moslemi, Nasrin Alipour Olyaei, Seyed Mohammad Poorhosseini, Zeinab Ravesh, Vahid Reza Yassaee, Hamid Reza Kheiri, Feyzollah Hashemi-Gorji
Publikováno v:
Asian Pacific Journal of Cancer Prevention. 17:155-160
Breast cancer (BC) is the second most common cancer in the world and by far the most frequent cancer among women, with an estimated 1.67 million new cancer cases diagnosed in 2012 (25% of all cancers). Polygene expression analysis is used to predict