Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tahere Seifi"'
Autor:
Rezvan Zabihi, Mina Zamani, Majid Aminzadeh, Niloofar Chamanrou, Fatemeh Zahra Kiani, Tahere Seifi, Jawaher Zeighami, Tahere Yadegari, Alireza Sedaghat, Alihossein Saberi, Mohammad Hamid, Gholamreza Shariati, Hamid Galehdari
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction: Mucopolysaccharidoses are a group of lysosomal storage disorders that include seven types that are classified based on the enzymes that are disrupted. Malfunction of these enzymes leads to the accumulation of glycosaminoglycans (GAGs) i
Externí odkaz:
https://doaj.org/article/10be7dec0c684c42be05458add309a27
Autor:
Atefe Papi, Mina Zamani, Gholamreza Shariati, Alireza Sedaghat, Tahere Seifi, Samira Negahdari, Sahar Sadat Sedighzadeh, Jawaher Zeighami, Alihossein Saberi, Mohammad Hamid, Hamid Galehdari
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 2, Pp n/a-n/a (2023)
Abstract Background Congenital disorder of glycosylation (CDG) and Glycogen storage diseases (GSDs) are inborn metabolic disorders caused by defects in some metabolic pathways. These disorders are a heterogeneous group of diseases caused by impaired
Externí odkaz:
https://doaj.org/article/e7160f880c5e4592936d54159ff4662d
Autor:
Yuji Nakamura, Issei S. Shimada, Reza Maroofian, Henry Houlden, Micol Falabella, Masanori Fujimoto, Emi Sato, Hiroshi Takase, Shiho Aoki, Akihiko Miyauchi, Eriko Koshimizu, Satoko Miyatake, Yuko Arioka, Mizuki Honda, Takayoshi Higashi, Fuyuki Miya, Yukimune Okubo, Isamu Ogawa, Annarita Scardamaglia, Mohammad Miryounesi, Sahar Alijanpour, Farzad Ahmadabadi, Peter Herkenrath, Hormos Salimi Dafsari, Clara Velmans, Mohammed Balwi, Antonio Vitobello, Anne-Sophie Denommé-Pichon, Médéric Jeanne, Antoine Civit, Maha S. Zaki, Hossein Darvish, Somayeh Bakhtiari, Michael Kruer, Christopher J Carroll, Ehsan Ghayoor Karimiani, Rozhgar A Khailany, Talib Adil Abdulqadir, Mehmet Ozaslan, Peter Bauer, Giovanni Zifarelli, Tahere Seifi, Mina Zamani, Chadi Al Alam, Robert D S Pitceathly, Kazuhiro Haginoya, Tamihide Matsunaga, Hitoshi Osaka, Naomichi Matsumoto, Norio Ozaki, Yasuyuki Ohkawa, Shinya Oki, Tatsuhiko Tsunoda, Yoshitaka Taketomi, Makoto Murakami, Yoichi Kato, Shinji Saitoh
PNPLA8, one of the calcium-independent phospholipase A2 enzymes, is involved in various physiological processes through the maintenance of membrane phospholipids. However, little is known about its role in brain development. Here, we report 12 indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3166c6dd5bfac2bccc9f569d1910b079
https://doi.org/10.1101/2023.04.26.23288947
https://doi.org/10.1101/2023.04.26.23288947
Autor:
Mina Zamani, Gholamreza Shariati, Hamid Galehdari, Sahar Sadat Sedighzadeh, Neda Mazaheri, Alireza Sedaghat, Tahere Seifi, Jawaher Zeighami
Publikováno v:
Congenital Anomalies. 61:220-225
Mesoaxial synostotic syndactyly with phalangeal reduction (MSSD) represents a rare non-syndromic defect with an autosomal recessive pattern of inheritance. Sequence variants in the BHLHA9 gene cause MSSD and to date only a few mutations in this gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf1a2e641cf7c135cdbe2a44b9078184
https://doi.org/10.1111/cga.12439
https://doi.org/10.1111/cga.12439
Publikováno v:
Jentashapir Journal of Cellular and Molecular Biology. 13
Background: Glioblastoma (GBM, known as Glioblastoma Multiforme) is one of the most common and also most aggressive solid tumors in adults. It has a poor prognosis and highly invasive behavior leading to difficulties in complete therapy. Understandin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f48754069e466c9a81bf3fd5bc6a08bd
https://doi.org/10.5812/jjcmb-130150
https://doi.org/10.5812/jjcmb-130150
Publikováno v:
Medical Journal of Tabriz University of Medical Sciences and Health Services. 42:91-96
Background: Multiple sclerosis (MS) seems to be a multifactorial disease in which the environment and genetics are involved. One of the factors associated with MS disease is the reduction in vitamin D levels and its specialized role in its pathogenic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ff4367eb87aea6a76ac49bd40b0ab93a
https://doi.org/10.34172/mj.2020.024
https://doi.org/10.34172/mj.2020.024
Autor:
Atefe Papi, Mina Zamani, Gholamreza Shariati, Alireza Sedaghat, Tahere Seifi, Samira Negahdari, Sahar Sadat Sedighzadeh, Jawaher Zeighami, Alihossein Saberi, Mohammad Hamid, Hamid Galehdari
Publikováno v:
Molecular geneticsgenomic medicineREFERENCES.
Congenital disorder of glycosylation (CDG) and Glycogen storage diseases (GSDs) are inborn metabolic disorders caused by defects in some metabolic pathways. These disorders are a heterogeneous group of diseases caused by impaired O- as well as N-glyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::913b476dc5febd988296262e75452941
https://pubmed.ncbi.nlm.nih.gov/36579437
https://pubmed.ncbi.nlm.nih.gov/36579437
Autor:
Hamid Galehdari, Gholam Reza Shariati, Jawaher Zeighami, Alireza Sedaghat, Neda Mazaheri, Reza Maroofian, Nafi Dilaver, Mina Zamani, Tahere Seifi
Ryanodine receptor 1 (RYR1) is an intracellular calcium receptor primarily expressed in skeletal muscle with a role in excitation contraction. Both dominant and recessive mutations in the RYR1 gene cause a range of RYR1-related myopathies and/or susc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f46422bdfa8323d7ac2286a9a0e8b707
https://europepmc.org/articles/PMC5803739/
https://europepmc.org/articles/PMC5803739/
Autor:
Hossein Baharvand, Abbas Kiani-Esfahani, Tahere Seifi, S Tanhaei, Kamran Ghaedi, Maryam Peymani, Fereshteh Karamali, Mohammad Hossein Nasr-Esfahani
Publikováno v:
Cellular and molecular neurobiology. 34(5)
FNDC5 (also termed PEP) gene encodes a type I membrane protein which is cleaved and secreted as Irisin hormone. We have identified mouse putative core promoter of FNDC5 and characterized its activity. FNDC5 is located within mouse chromosome 4, spans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::294a68669d9335ab9192ae0e4ae831dc
https://pubmed.ncbi.nlm.nih.gov/24706335
https://pubmed.ncbi.nlm.nih.gov/24706335
Autor:
Tahere, Seifi, Kamran, Ghaedi, Ahmad, Salamian, Sommayeh, Tanhaei, Forouzan, Safari, Zohreh, Hojati, Manuchehr, Tavassoli, Hossein, Baharvand, Mohammad-Hossein Nasr, Esfahani
Publikováno v:
Avicenna Journal of Medical Biotechnology
Background Recently, we have shown that peroxisomal protein expression was induced upon retinoic acid treatment in mouse embryonic stem cells during the process of neurogenesis. Thus, characterization of the respective promoter could elucidate the mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd46715e08f02e1aa596b79f810cbcb2
https://pubmed.ncbi.nlm.nih.gov/23408119
https://pubmed.ncbi.nlm.nih.gov/23408119