Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Fatehi, A."'
Autor:
Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
Publikováno v:
npj Genomic Medicine, Vol 9, Iss 1, Pp 1-11 (2024)
Abstract Next-generation sequencing (NGS) has been proven to be one of the most powerful diagnostic tools for rare Mendelian disorders. Several studies on the clinical application of NGS in unselected cohorts of Middle Eastern patients have reported
Externí odkaz:
https://doaj.org/article/d0de56f0485d43639ba3ed001723c22f
Autor:
Ayda Abolhassani, Zohreh Fattahi, Maryam Beheshtian, Mahsa Fadaee, Raheleh Vazehan, Fatemeh Ahangari, Shima Dehdahsi, Mehrshid Faraji Zonooz, Elham Parsimehr, Zahra Kalhor, Fatemeh Peymani, Maryam Mozaffarpour Nouri, Mojgan Babanejad, Khadijeh Noudehi, Fatemeh Fatehi, Shima Zamanian Najafabadi, Fariba Afroozan, Hilda Yazdan, Bita Bozorgmehr, Azita Azarkeivan, Shokouh Sadat Mahdavi, Pooneh Nikuei, Farzad Fatehi, Payman Jamali, Mahmoud Reza Ashrafi, Parvaneh Karimzadeh, Haleh Habibi, Kimia Kahrizi, Shahriar Nafissi, Ariana Kariminejad, Hossein Najmabadi
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101510- (2024)
Externí odkaz:
https://doaj.org/article/2b6cd8a2516d4c7dba834e7f5dd8bf1b
Autor:
Matthew Rok, Tatianna Wai Ying Wong, Eleonora Maino, Abdalla Ahmed, Grace Yang, Elzbieta Hyatt, Kyle Lindsay, Sina Fatehi, Ryan Marks, Paul Delgado-Olguín, Evgueni A. Ivakine, Ronald D. Cohn
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 30, Iss , Pp 246-258 (2023)
Duchenne muscular dystrophy (DMD) is a disease with a life-threatening trajectory resulting from mutations in the dystrophin gene, leading to degeneration of skeletal muscle and fibrosis of cardiac muscle. The overwhelming majority of mutations are m
Externí odkaz:
https://doaj.org/article/f6f44eb7d6ec40c3ab0d3efbe103235b
Autor:
Ali Khanbazi, Maryam Beheshtian, Maryam Azad, Masoume Akbari, Fariba Afrozan, Fatemeh Fatehi, Khadijeh Noudehi, Shima Zamanian Najafabadi, Ariana Kariminejad, Kimia Kahrizi, Hossein Najmabadi
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101382- (2024)
Externí odkaz:
https://doaj.org/article/3b080c4e23d84675835b4b10dfb85291
Akademický článek
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Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 20, Iss 1, Pp 1-5 (2019)
Abstract Background Colorectal cancer is the most common gastrointestinal cancer and the third most common cancer over the world. Genetic mutations in the p53 gene are associated with tumorigenesis of most cancers. So far, no study has been conducted
Externí odkaz:
https://doaj.org/article/209475190b0d40d9bc6a7c8a1cf70437
Autor:
Aliakbar Hasankhani, Abolfazl Bahrami, Negin Sheybani, Farhang Fatehi, Roxana Abadeh, Hamid Ghaem Maghami Farahani, Mohammad Reza Bahreini Behzadi, Ghazaleh Javanmard, Sadegh Isapour, Hosein Khadem, Herman W. Barkema
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Bovine respiratory disease (BRD) is the most common disease in the beef and dairy cattle industry. BRD is a multifactorial disease resulting from the interaction between environmental stressors and infectious agents. However, the molecula
Externí odkaz:
https://doaj.org/article/3fb94b0f5521400e9f0e23d70207682f
Autor:
Sina Fatehi, Ryan M. Marks, Matthew J. Rok, Lucie Perillat, Evgueni A. Ivakine, Ronald D. Cohn
Publikováno v:
Human Gene Therapy. 34:388-403
Autor:
Kiarash Jamshidi Goharrizi, Farzane Amirmahani, Foad Fatehi, Maryam Nazari, Sayyed Saeed Moosavi
Publikováno v:
Journal of Genetic Resources, Vol 5, Iss 2, Pp 72-82 (2019)
Through the exponential development in the specification of sequences and structures of proteins by genome sequencing and structural genomics approaches, there is a growing demand for valid bioinformatics methods to define these proteins function. In
Externí odkaz:
https://doaj.org/article/fe4bf152127d442082ea4a7d7518a63a
Autor:
Marzieh Khani, Hosein Shamshiri, Farzad Fatehi, Mohammad Rohani, Bahram Haghi Ashtiani, Fahimeh Haji Akhoundi, Afagh Alavi, Hamidreza Moazzeni, Hanieh Taheri, Mina Tolou Ghani, Leila Javanparast, Seyyed Saleh Hashemi, Ramona Haji‐Seyed‐Javadi, Matineh Heidari, Shahriar Nafissi, Elahe Elahi
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 7, Pp n/a-n/a (2020)
Abstract Background SPG11 mutations can cause autosomal recessive hereditary spastic paraplegia (ARHSP) and juvenile amyotrophic lateral sclerosis (JALS). Because these diseases share some clinical presentations and both can be caused by SPG11 mutati
Externí odkaz:
https://doaj.org/article/17893aa063484e249714d0aee191d73f