Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Marzieh Mazinani"'
Autor:
Marzieh Mazinani, Fatemeh Rahbarizadeh
Publikováno v:
Biomarker Research, Vol 11, Iss 1, Pp 1-27 (2023)
Abstract Chimeric antigen receptor (CAR) T cell therapy, in which a patient’s own T lymphocytes are engineered to recognize and kill cancer cells, has achieved striking success in some hematological malignancies in preclinical and clinical trials,
Externí odkaz:
https://doaj.org/article/cec663ad28c94658aa3b018f9ee00f33
Autor:
Marzieh Mazinani, Fatemeh Rahbarizadeh
Publikováno v:
Biomarker Research, Vol 10, Iss 1, Pp 1-24 (2022)
Abstract Chimeric antigen receptor (CAR) T cell therapy, in which a patient’s own T lymphocytes are engineered to recognize and kill cancer cells, has achieved remarkable success in some hematological malignancies in preclinical and clinical trials
Externí odkaz:
https://doaj.org/article/3a98e70b40af4bb08e2d55c83add8a9b
Autor:
Sahar Rostami Hir, Zahra Alizadeh, Marzieh Mazinani, Maryam Mahlooji Rad, Mohammad Reza Fazlollahi, Anoushiravan Kazemnejad, Ahmad Zavaran Hosseini, Mostafa Moin
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 2 (2021)
Exosomes are extracellular vesicles that are involved in intracellular communication and different biological processes. Recently, the importance of microRNAs (miRNAs) in exosomes has been considered as biomarkers in asthma diagnosis. This study aime
Externí odkaz:
https://doaj.org/article/d40f042369e348b490b4d7e77f87eec5
Autor:
Zahra Alizadeh, Parisa Dashti, Marzieh Mazinani, Maryam Nourizadeh, Leila Shakerian, Shaghayegh Tajik, Masoud Movahedi, Setareh Mamishi, Zahra Pourpak, Mohammad Reza Fazlollahi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 3 (2020)
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency caused by genetic defects in the Bruton tyrosine kinase (Btk) gene. XLA is characterized as an antibody deficiency by recurrent bacterial infections, the absence of peripheral B cells, a
Externí odkaz:
https://doaj.org/article/382b27b517b24a61bcf9f51aa21d0bd2
Autor:
Maryam Vahidi, Mohsen Badalzadeh, Masoomeh Jannesar, Marzieh Mazinani, Mohammad Reza Fazlollahi, Nazanin Khodayari Namini, Massoud Houshmand, Amir Ali Hamidieh, Leila Moradi, Zahra Pourpak, Mostafa Moin
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 18, Iss 5 (2019)
Familial haemophagocytic lymphohistiocytosis (FHL) is a rare disorder of immune dysregulation. FHL inherited in an autosomal recessive pattern is classified into five subtypes based on underlying genetic defects. Mutations in four genes including PRF
Externí odkaz:
https://doaj.org/article/dfae81c8de3f4f6098e01614efbad261
Autor:
Mohsen Badalzadeh, Marzieh Mazinani, Zahra Pourpak, Hassan Heidarnazhad, Esmaeil Mortaz, Mostafa Moin, Ali Farazmand
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 18, Iss 4 (2019)
In this study, we first tried to determine whether the expression level of 9 miRNAs in the peripheral blood CD8+ T cells of asthmatic patients varies from that of controls, and secondly, we investigated the effects of fluticasone furoate and vilanter
Externí odkaz:
https://doaj.org/article/5afdaf3ea7c94b5eb6c7eac0dbb15e79
Autor:
Ahmad Bahrami, Zahra Soltani, Mohammad Reza Fazlollahi, Farzaneh Rahmani, Massoud Houshmand, Marzieh Mazinani, Nima Rezaei
Publikováno v:
Acta Medica Iranica, Vol 56, Iss 12 (2019)
CD40 deficiency yield to an autosomal recessive subtype of hyper-immunoglobulin M syndrome (HGIM type 3), presenting with an almost identical clinical picture to X-linked CD40L deficiency (HIGM type 1) with profound T-cell dysfunction yielding to opp
Externí odkaz:
https://doaj.org/article/0d1f0adeae39404eb61b84a4607fbb35
Autor:
Zahra Alizadeh, Marzieh Mazinani, Esmaeil Mortaz, Mohammad Reza Fazlollahi, Ian Adcock, Mostafa Moein
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 17, Iss 1 (2018)
Different phenotypes of asthma from mild to severe are categorized based on diverse clinical features. A guideline for the recognition and treatment of asthma has been provided by Global Initiative for Asthma (GINA). To control symptoms and prevent a
Externí odkaz:
https://doaj.org/article/7f001acc451540d285f7492acb9b1368
Autor:
Zahra Alizadeh, Mohammad Reza Fazlollahi, Marzieh Mazinani, Mohsen Badalzadeh, Hanieh Heydarlou, Raphael Carapito, Anne Molitor, Andrés Caballero Garcia de Oteyza, Michele Proietti, Maryam Soleimani bavani, Mansoureh Shariat, Morteza Fallahpour, Masoud Movahedi, Leila Moradi, Bodo Grimbacher, Siamak Bahram, Zahra Pourpak
Purpose Severe combined immunodeficiency (SCID) is one of the severe inborn errors of the immune system associated with life-threatening infections. This disorder is characterized by diminished cellular and humoral immunity. A variable phenotype, inc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65842a4a889a452418fad22a67ad46e0
https://doi.org/10.21203/rs.3.rs-1728908/v1
https://doi.org/10.21203/rs.3.rs-1728908/v1
Autor:
Zahra Pourpak, Zahra Alizadeh, Mohammad Reza Fazlollahi, Susan Nabilou, Masoud Houshmand, Amir Ali Hamidieh, Marzieh Mazinani, Shaghayegh Tajik
Publikováno v:
Scandinavian Journal of Immunology. 93
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efe41076c593366e5e1ec51a7dc299ec
https://doi.org/10.1111/sji.12966
https://doi.org/10.1111/sji.12966