Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Taravat Talebi"'
Autor:
Avisa Tabib, Taravat Talebi, Serwa Ghasemi, Maryam Pourirahim, Niloofar Naderi, Majid Maleki, Samira Kalayinia
Publikováno v:
European Journal of Medical Research, Vol 27, Iss 1, Pp 1-16 (2022)
Abstract Background Congenital heart defects (CHDs) are the most common congenital malformations, including structural malformations in the heart and great vessels. CHD complications such as low birth weight, prematurity, pregnancy termination, morta
Externí odkaz:
https://doaj.org/article/81e4cb87de9b4d5bb69d250fdee36d66
Autor:
Taravat Talebi, Tannaz Masoumi, Katayoun Heshmatzad, Mahshid Hesami, Majid Maleki, Samira Kalayinia
Publikováno v:
Genetics Research, Vol 2023 (2023)
Background. Health and economies are both affected by the coronavirus disease-19 (COVID-19) global pandemic. Angiotensin-converting enzyme 2 (ACE2) is a polymorphic enzyme that is a part of the renin-angiotensin system, and it plays a crucial role in
Externí odkaz:
https://doaj.org/article/7411e6cf8cc14739a79f04e2bbdf393d
Autor:
Taravat Talebi, Alireza Biglari, Mohammad Shahroeei, Majid Changi-Ashtiani, Hossein Dinmohammadi, Shadi Sadat Navabi, Nima Parvaneh, Xavier Bossuyt, Tina Shahani, Hassan Rokni-Zadeh
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 1 (2020)
Severe combined immunodeficiency (SCID) comprises a heterogeneous group of genetic disorders caused by early defects in the development and function of T cells. Other lymphocyte lineages (B and/or natural killer cells) are variably affected. With a w
Externí odkaz:
https://doaj.org/article/25733ff347694435b9b970dd526aa7ab
Autor:
Majid Maleki, Neda Mohsen-Pour, Maryam Hosseini Moghadam, Niloofar Naderi, Samira Kalayinia, Taravat Talebi
Publikováno v:
Current Molecular Medicine. 22:385-400
Background: Inversion of chromosome 9 (inv[9]) is known as one of the most common structural balanced chromosomal variations. Chromosome 9 is highly susceptible to structural rearrangements, specifically to pericentric inversions. Various investigato
Autor:
Taravat Talebi, Hermann Behling, Kamaledin Alizadeh, Behnam Hamzeh'ee, A. Shirvany, Elias Ramezani
Publikováno v:
Palynology, 45(1), 15-26. Taylor & Francis Group
Palynological analysis and radiocarbon dating of a short sediment core from a high-altitude mire in the Arasbaran area of northwestern Iran reveals long-term vegetation dynamics, climate change and anthropogenic impact. Our findings indicate the prev
Publikováno v:
The journal of maternal-fetalneonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 35(25)
Assisted reproductive technology (ART), an effective treatment modality for infertility, is associated with a higher prevalence of congenital anomalies such as congenital heart defects (CHDs). The present study aimed to evaluate data linking CHDs in
Autor:
Daan Raemaekers, Taravat Talebi Seyyedsaran, Özge Demirci, Mans Schepers, Canan Çakirlar, Safoora Kamjan, Hans Huisman, Hans Peeters
Publikováno v:
Open Archaeology, 7, 658-670. De Gruyter
Open Archaeology, Vol 7, Iss 1, Pp 658-670 (2021)
Open Archaeology, Vol 7, Iss 1, Pp 658-670 (2021)
This article presents an overview of the current evidence on the process of Neolithisation in the Dutch wetlands. Over the years, several models have been proposed with different perspectives on the timing and pace of the process: a long transition,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbb9df458a9e7e25e7e496ce4a299abe
https://research.rug.nl/en/publications/db7eeb6e-8aad-4b55-a3c0-936db0688fd2
https://research.rug.nl/en/publications/db7eeb6e-8aad-4b55-a3c0-936db0688fd2
Autor:
Nima Parvaneh, Taravat Talebi, Majid Changi-Ashtiani, Xavier Bossuyt, Hossein Dinmohammadi, Mohammad Shahroeei, Hassan Rokni-Zadeh, Shadi Sadat Navabi, Tina Shahani, Alirezai Biglari
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 19, Iss 1 (2020)
Severe combined immunodeficiency (SCID) comprises a heterogeneous group of genetic disorders caused by early defects in the development and function of T cells. Other lymphocyte lineages (B and/or natural killer cells) are variably affected. With a w