Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hamed Heidary"'
Publikováno v:
Iranian Journal of Public Health, Vol 50, Iss 9 (2021)
Cystinuria is an autosomal recessive disorder in which the renal reabsorption of cystine, arginine, lysine and ornithine are disturbed. The two genes, the pathogenic forms of which are responsible for the disorder, are SLC7A9 and SLC3A1. In this stud
Externí odkaz:
https://doaj.org/article/f582e678398b4fa0856f56a242a86edb
Publikováno v:
Iranian Journal of Public Health, Vol 50, Iss 6 (2021)
Alopecia universalis (AU) congenital, known as generalized atrichia, is a severe form of autosomal recessive alopecia that results in complete hair loss of scalp and body. Mutations in the human hairless gene (HR) are associated with the phenotype of
Externí odkaz:
https://doaj.org/article/8809b564664b4775afebe4dfbff675fb
Publikováno v:
Iranian Journal of Public Health, Vol 50, Iss 9 (2021)
Iranian Journal of Public Health
Iranian Journal of Public Health
Cystinuria is an autosomal recessive disorder in which the renal reabsorption of cystine, arginine, lysine and ornithine are disturbed. The two genes, the pathogenic forms of which are responsible for the disorder, are SLC7A9 and SLC3A1. In this stud
Autor:
Mir Davood Omrani, Reza Mirfakhraie, Hamid Ghaedi, Fereidoun Azizi, Hamed Heidary, Hajar Yaghoobi, Farkhondeh Pouresmaeili, Shadi Sayban
Publikováno v:
Meta Gene. 18:58-61
Bachground The premature ovarian failure (POF) is a reason of infertility that affects about 1–4% of women before age 40. The importance of telomeres' length in different diseases has been explored before. This study examines the association betwee
Autor:
Hamed Heidary, Parisa Moeinian, Mansoureh Akouchekian, Mitra Hakim Shooshtari, Fateme Zahedi Abghari
Publikováno v:
International Journal of Neuroscience. 129:10-15
Purpose Autism spectrum disorders (ASD) consist of a group of neurodevelopmental disorders that include autistic behavior, Asperger's syndrome and pervasive developmental disabilities. According to the increasing observations that patients with mitoc
Autor:
Hamed Heidary, Mahdi Vafadar, Gholam Reza Bahoosh, Shahrbanoo Nakhaei, Farzaneh Rohani, Aliasghar Rahimian, Davoud Amirkashani
Publikováno v:
Iranian Biomedical Journal
Chanarin-Dorfman syndrome (CDS) is a rare autosomal recessive metabolic disorder caused by mutations in gene encoding the domain-5 of α/β-hydrolase enzyme (ABHD5). It is known as a natural lipid storage disorder arising from impaired lipid metaboli
Publikováno v:
Archives of Medical Science - Civilization Diseases. 3:87-91
Autor:
Hamed, Heidary, Farkhondeh, Pouresmaeili, Reza, Mirfakhraie, Mir Davood, Omrani, Hamid, Ghaedi, Zahra, Fazeli, Shadi, Sayban, Soudeh, Ghafouri-Fard, Eznollah, Azargashb, Fazlollah, Shokri
Publikováno v:
Iranian Biomedical Journal
Background: Telomeres are evolutionary, specialized terminal structures at the ends of eukaryotic chromosomes containing TTAGGG repeats in human. Several human diseases have been known to be associated with dramatic changes in telomere length. The ai
Publikováno v:
مدیریت راهبردی دانش سازمانی, Vol 3, Iss 3, Pp 87-112 (2020)
The Covid Crisis has affected many sections of human society, including organizations, because they are home to so many people. Due to the emergence of this crisis, access to the right knowledge and information can lead to a principled and safe expos
Externí odkaz:
https://doaj.org/article/01d55f3d8d0a4c209f0a28135a8425b5