Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Elahe, Elahi"'
Autor:
Marzieh Khani, Hosein Shamshiri, Shahriar Nafissi, Najmeh Salehi, Hamidreza Moazzeni, Hanieh Taheri, Elahe Elahi
Publikováno v:
Clinical Case Reports, Vol 12, Iss 1, Pp n/a-n/a (2024)
Key Clinical Message Fazio‐Londe disease and Brown‐Vialetto‐Van Laere syndrome are rare related neurological disorders. Although SLC52A3 and SLC52A2 that encode riboflavin transporters are their only known causative genes, many patients without
Externí odkaz:
https://doaj.org/article/2726eafbefe64b43acbff02336e65555
Autor:
Ensieh Darbari, Hamid Ahmadieh, Narsis Daftarian, Mozhgan Rezaei Kanavi, Fatemeh Suri, Hamideh Sabbaghi, Elahe Elahi
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 17, Iss 1, Pp 51-58 (2022)
Abstract Purpose: Stargardt disease type 1 (STGD1) is a recessively inherited retinal disorder that can cause severe visual impairment. ABCA4 mutations are the usual cause of STGD1. ABCA4 codes a transporter protein exclusively expressed in retinal p
Externí odkaz:
https://doaj.org/article/49a6e618ea1d451496fa3fd3130670a1
Autor:
Ali Heshmati, Peyman Taghizadeh, Hamid Ahmadieh, Mehdi Yaseri, Fatemeh Suri, Mahsa Alizadeh, Marjan Dadashzadeh, Hajar Khatami, Monireh Moradkhah Navi, Parisa Zamanparvar, Hassan Behboudi, Elahe Elahi
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 16, Iss 4, Pp 574-581 (2021)
Abstract Purpose: To estimate carrier frequencies of CYP1B1 mutations p.Gly61Glu and p.Arg368His, respectively, in Talesh and the east of Guilan province in Iran with a maximum error of 2%. Previously, it was shown that these CYP1B1 mutations may be
Externí odkaz:
https://doaj.org/article/b4b18880fe45485489ffda447c4f575e
Autor:
Elahe Elahi
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 15, Pp 1-3 (2020)
Externí odkaz:
https://doaj.org/article/ef0947d0eb2844b5861203e1896089c3
Autor:
Faezeh Darki, Sahba Fekri, Shaghayegh Farhangmehr, Hamid Ahmadieh, Mohammad Hossein Dehghan, Elahe Elahi
Publikováno v:
Journal of Current Ophthalmology, Vol 31, Iss 2, Pp 172-179 (2019)
Purpose: To report the genetic analysis of an Iranian Bietti crystalline dystrophy (BCD)-affected family, and to review previously reported mutations in the gene and assess the distribution of affected amino acids in the encoded protein. Methods: The
Externí odkaz:
https://doaj.org/article/1a3a53e1739f4a9bb0e120fb798571fb
Autor:
Ali Heshmati, Peyman Taghizadeh, Hamid Ahmadieh, Mehdi Yaseri, Fatemeh Suri, Mahsa Alizadeh; Marjan Dadashzadeh; Hajar Khatami, Monireh Moradkhah Navi; Parisa Zamanparvar; Hassan Behboudi, Elahe Elahi
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 17, Iss 2, Pp 311-311 (2022)
Externí odkaz:
https://doaj.org/article/cc4bfbef2ecb4c189a434d95db40b510
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
Publikováno v:
PLoS ONE, Vol 15, Iss 10, p e0240330 (2020)
Zymomonas mobilis, as an ethanologenic microorganism with many desirable industrial features, faces crucial obstacles in the lignocellulosic ethanol production process. A significant hindrance occurs during the pretreatment procedure that not only pr
Externí odkaz:
https://doaj.org/article/f0221d85082c465bb1b3c046e7118500
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 13, Iss 4, Pp 403-410 (2018)
Purpose: To perform a population-based screening of four CYP1B1 mutations—p.Gly61Glu, p.Arg368His, p.Arg390His, and p.Arg469Trp—in the province of Gilan, Iran. Previous studies have shown that CYP1B1 is a cause of disease in approximately 70% of
Externí odkaz:
https://doaj.org/article/8fe5a16296ac49ca8d6073f22e8e4c65
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 12, Iss 4, Pp 407-412 (2017)
Purpose: We aimed to assess whether the transcription factor PAX6 affects transcription of FMNL2. PAX6 is a transcription factor with significant roles in development of the eye and eye-related functions. FMNL2 encodes a member of the formin family o
Externí odkaz:
https://doaj.org/article/230acddc14514dfe934f3e00bcb3d45b