Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mehrdad Vakilian"'
Autor:
Zahra Koveitypour, Farnoush Panahi, Mehrdad Vakilian, Maryam Peymani, Farzad Seyed Forootan, Mohammad Hossein Nasr Esfahani, Kamran Ghaedi
Publikováno v:
Cell & Bioscience, Vol 9, Iss 1, Pp 1-14 (2019)
Abstract Colorectal cancer (CRC) is the fourth leading cause of the worldwide cancer mortality. Different molecular mechanisms have been attributed to the development and progress of CRC. In this review, we will focus on the mitogen-activated protein
Externí odkaz:
https://doaj.org/article/2ec2248996f045ab823a874e72788eb8
Publikováno v:
In Vitro Cellular & Developmental Biology - Animal. 57:587-597
Conventional methods for obtaining pancreatic β cells are based on simulating the embryonic development phase of endocrine cells via hierarchical differentiation of pluripotent stem cells (PSCs). Accordingly, we attempted to modify the protocols for
Autor:
Serkan Ismail Göktuna, Sayed Rasoul Zaker, Maryam Peymani, Mehrdad Vakilian, Maryam Keshani, Farzad Seyed Forootan, Kamran Ghaedi, Tieu-Lan Chau, Maryam Esmaeili, Mohammad Hossein Nasr Esfahani, Mohadeseh Esmaeili
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Colorectal cancer (CRC) is one of the most common types of cancer which affects the colon and the rectum. Approximately one third of annual CRC mortality occurs due to the late detection of this type of cancer. Therefore, there is an urgent need for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d87b07aa8c4dd41f0d1a001d0951650a
http://hdl.handle.net/10261/221276
http://hdl.handle.net/10261/221276
Autor:
Mehrdad Vakilian
Publikováno v:
Clinical Immunology. 234:108896
Little is known about the causes and mechanisms of ectopic immune responses, including different types of hypersensitivity, superantigens, and cytokine storms. Two of the most questionable phenomena observed in immunology are why the intensity and ex
Autor:
Maryam Peymani, Mehrdad Vakilian, Farzad Seyed Forootan, Kamran Ghaedi, Mohammad Hossein Nasr Esfahani, Zahra Koveitypour, Farnoush Panahi
Publikováno v:
Cell & Bioscience
Digital.CSIC. Repositorio Institucional del CSIC
instname
Cell & Bioscience, Vol 9, Iss 1, Pp 1-14 (2019)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Cell & Bioscience, Vol 9, Iss 1, Pp 1-14 (2019)
Colorectal cancer (CRC) is the fourth leading cause of the worldwide cancer mortality. Different molecular mechanisms have been attributed to the development and progress of CRC. In this review, we will focus on the mitogen-activated protein kinase (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c90d1d3d0435db186cc877b04b5e949
https://hdl.handle.net/10668/3153
https://hdl.handle.net/10668/3153
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Insulin is a peptide hormone responsible for stable glycemia, is entirely secreting from pancreatic β cells at the core of glucose homeostatic regulation. Upon synthesis as preproinsulin on rough endoplasmic reticulum (rER), proinsulin is directed t
Autor:
Abdelkrim Hmadcha, Vivian Capilla-González, Bernat Soria, Christian Claude Lachaud, Javier López-Beas, Natalia Escacena-Acosta, Franz Martín, Mehrdad Vakilian, Francisco J. Bedoya, Juan R. Tejedo
Publikováno v:
Essentials in Ophthalmology ISBN: 9783030013035
Recent research has shown that the most effective system of repair of the human body is represented by stem cells. By definition, stem cells are able to divide and make copies of themselves indefinitely (self-renewal). In turn, under certain physiolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::207a7bb5708f0e405c1b2aa72438da61
https://doi.org/10.1007/978-3-030-01304-2_4
https://doi.org/10.1007/978-3-030-01304-2_4
Leber's Hereditary Optic Neuropathy: The Spectrum of Mitochondrial DNA Mutations in Iranian Patients
Autor:
Sh. Lavasani, Massoud Houshmand, Mehrdad Vakilian, Fatemeh Sharifpanah, Mohammad Hossein Sanati, A. Tabasi, S. Joughehdoust
Publikováno v:
Annals of the New York Academy of Sciences. 1011:345-349
We studied 14 patients with Leber’s hereditary optic neuropathy (LHON) to investigate the mtDNA haplotypes associated with the primary mutation(s). Eleven patients carried the mitochondrial DNA (mtDNA) G11778A mutation, while one had the T14484C mu
Autor:
Jamshid Lotfi, Mohammad Hossein Sanati, Arman Ardalan, DD Farhud, M. Akuchekian, Mehrdad Vakilian, Masoud Houshmand, M. Teimori, F. Babrzadeh
Publikováno v:
Multiple sclerosis (Houndmills, Basingstoke, England). 11(6)
Background: Multiple sclerosis (MS) is an immunological inflammatory disease of the central nervous system (CNS) which is chronically observed in young adults. On the basis of earlier studies, potential relatedness between MS and mitochondrial DNA (m