Zobrazeno 1 - 10
of 151
pro vyhledávání: '"Hassan Vahidnezhad"'
Autor:
Mahmoud Amiri Roudbar, Seyed Milad Vahedi, Jin Jin, Mina Jahangiri, Hossein Lanjanian, Danial Habibi, Sajedeh Masjoudi, Parisa Riahi, Sahand Tehrani Fateh, Farideh Neshati, Asiyeh Sadat Zahedi, Maryam Moazzam-Jazi, Leila Najd-Hassan-Bonab, Seyedeh Fatemeh Mousavi, Sara Asgarian, Maryam Zarkesh, Mohammad Reza Moghaddas, Albert Tenesa, Anoshirvan Kazemnejad, Hassan Vahidnezhad, Hakon Hakonarson, Fereidoun Azizi, Mehdi Hedayati, Maryam Sadat Daneshpour, Mahdi Akbarzadeh
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-12 (2024)
Abstract This study aims to assess the effect of familial structures on the still-missing heritability estimate and prediction accuracy of Type 2 Diabetes (T2D) using pedigree estimated risk values (ERV) and genomic ERV. We used 11,818 individuals (T
Externí odkaz:
https://doaj.org/article/d1778760f30742c2868c53ce140b1d16
Autor:
Leila Youssefian, Amir Hossein Saeidian, Zahra Saffarian, Mona Ariamanesh, Fahimeh Abdollahimajd, Sara Molkara, Mohammad Shahidi-Dadras, Reem Diab, Fatemeh Vahidnezhad, Sirous Zeinali, Vivien Béziat, Emmanuelle Jouanguy, Jean-Laurent Casanova, Jouni Uitto, Hassan Vahidnezhad
Publikováno v:
JID Innovations, Vol 4, Iss 4, Pp 100278- (2024)
Most viral infections can be self-limited, with no requirement for medical intervention. However, the same viruses can cause severe diseases in patients with compromised immunity due to single-gene diseases, acquired immune deficiency syndrome, or he
Externí odkaz:
https://doaj.org/article/dc896b1c835c43f8ae7219a7ffba12b1
Autor:
Sajjad Biglari, Hassan Vahidnezhad, Mohammad Amin Tabatabaiefar, Hamid Reza Khorram Khorshid, Emran Esmaeilzadeh
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 4, Pp n/a-n/a (2024)
Abstract Background Hypomyelinating leukodystrophy‐9 (HLD‐9) is caused by biallelic pathogenic variants in RARS1, which codes for the cytoplasmic tRNA synthetase for arginine (ArgRS). This study aims to evaluate the clinical, neuroradiological, a
Externí odkaz:
https://doaj.org/article/3db4072ee00842fd85063a977604b46b
Autor:
Liaosadat Mirsafaee, Mohammad Dehghani Firouzabadi, Sayeh Parkhideh, Hassan Vahidnezhad, Fatemeh Dehghani Firouzabadi, Maryam Arab, David M. Yousem, Mersedeh Karvandi
Publikováno v:
Caspian Journal of Internal Medicine, Vol 15, Iss 1, Pp 199-201 (2024)
Multiple myeloma (MM) is characterized by the neoplastic proliferation of plasma cells, leading to the production of monoclonal immunoglobulins. High-dose chemotherapy with autologous stem cell transplant has been used in the treatment of patients wi
Externí odkaz:
https://doaj.org/article/cce37bddfb934655b46b767a82922401
Autor:
Ali Zare Dehnavi, Maryam Bemanalizadeh, Seyyed Mohammad Kahani, Mahmoud Reza Ashrafi, Mohammad Rohani, Mehran Beiraghi Toosi, Morteza Heidari, Sareh Hosseinpour, Behnam Amini, Shaghayegh Zokaei, Zahra Rezaei, Hajar Aryan, Man Amanat, Hassan Vahidnezhad, Pouria Mohammadi, Masoud Garshasbi, Ali Reza Tavasoli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-18 (2023)
Abstract Background Phospholipase-associated neurodegeneration (PLAN) caused by mutations in the PLA2G6 gene is a rare neurodegenerative disorder that presents with four sub-groups. Infantile neuroaxonal dystrophy (INAD) and PLA2G6-related dystonia-p
Externí odkaz:
https://doaj.org/article/33b08d5b1a9846ac9b6a4cfa26acdbbd
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101140- (2024)
Externí odkaz:
https://doaj.org/article/28a03d884947434da0dc0b1437d1b8d3
Autor:
Leila Youssefian, Sajjad Biglari, Atefeh Sohanforooshan Moghaddam, Amir Hossein Saeidian, Fatemeh Vahidnezhad, Hassan Vahidnezhad
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101660- (2024)
Externí odkaz:
https://doaj.org/article/30ef90709d44443f872d3c921b70457c
Autor:
Forough Shams, Hadi Bayat, Omid Mohammadian, Somayeh Mahboudi, Hassan Vahidnezhad, Mohsen Soosanabadi, Azam Rahimpour
Publikováno v:
BioImpacts, Vol 12, Iss 4, Pp 371-391 (2022)
Introduction: Clustered regularly interspaced short palindromic repeat and its associated protein (CRISPR-Cas)-based technologies generate targeted modifications in host genome by inducing site-specific double-strand breaks (DSBs) that can serve as a
Externí odkaz:
https://doaj.org/article/6fcd609d157b4f6e8b679668ed991df2
Autor:
Amir Hossein Saeidian, Leila Youssefian, Mahtab Naji, Hamidreza Mahmoudi, Samantha M. Barnada, Charles Huang, Karim Naghipoor, Amir Hozhabrpour, Jason S. Park, Flavia Manzo Margiotta, Fatemeh Vahidnezhad, Zahra Saffarian, Kambiz Kamyab-Hesari, Mohammad Tolouei, Niloofar Faraji, Seyyede Zeinab Azimi, Ghazal Namdari, Parvin Mansouri, Jean-Laurent Casanova, Vivien Béziat, Emmanuelle Jouanguy, Jouni Uitto, Hassan Vahidnezhad
Publikováno v:
JCI Insight, Vol 8, Iss 5 (2023)
HPVs are DNA viruses include approximately 450 types that are classified into 5 genera (α-, β-, γ-, μ-, and ν-HPV). The γ- and β-HPVs are present in low copy numbers in healthy individuals; however, in patients with an inborn error of immunity
Externí odkaz:
https://doaj.org/article/9e248cc04e0543ff9964e5f4094c74bd
Autor:
Leila Youssefian, Hassan Vahidnezhad, Jouni Uitto, Amir Hossein Saeidian, Rana Samii, Elnaz Kalamati, Ali Reza Tavasoli, Zahra Saffarian, John A. McGrath, Soheila Sotoudeh
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100394- (2023)
Externí odkaz:
https://doaj.org/article/5078f96175b74cb19fbe3a91056b0cad