Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Hadideh Mabudi"'
Publikováno v:
AMB Express, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Pseudomonas aeruginosa is a commonly found Gram-negative bacterium in healthcare facilities and is renowned for its ability to form biofilms and its virulence factors that are controlled by quorum sensing (QS) systems. The increasing prevale
Externí odkaz:
https://doaj.org/article/e4879b1268b242bfbce74fde28d226a6
Publikováno v:
International Journal of Biomedicine, Vol 14, Iss 1, Pp 170-174 (2024)
Autism spectrum disorder has evolved from a rare childhood-onset disorder to a widely acknowledged, extensively researched, and heterogeneous lifelong condition. This study focuses on an Iranian pedigree affected by autism spectrum disorder. By emplo
Externí odkaz:
https://doaj.org/article/52032793fa944b49aa54b423ae2a88e6
Autor:
Mostafa Neissi, Hadideh Mabudi, Adnan Issa Al-Badran, Javad Mohammadi-Asl, Raed Abdulelah Al-Badran
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 24, Iss 1, Pp 1-6 (2023)
Abstract Background Charcot–Marie–Tooth disease comprises a large spectrum of clinically heterogeneous disorders. PLEKHG5 variants have shown an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease C and distal spinal muscular
Externí odkaz:
https://doaj.org/article/8a792d9e64214f42865d4d92d57af81d
Autor:
Raed Abdulelah Al-Badran, Adnan Issa Al-Badran, Hadideh Mabudi, Mostafa Neissi, Javad Mohammadi-Asl
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 23, Iss 1, Pp 1-5 (2022)
Abstract Background Autosomal recessive cataract (CTRCT18) is a rare type of congenital cataract that develops to complete and lifelong childhood blindness. This inherited disorder is one of the major visual health concerns in infants. Genetic studie
Externí odkaz:
https://doaj.org/article/2edf1edf35e34068b7835c34c4eb395c
Autor:
Mostafa Neissi, Husham Khirullah Abdulzahra, Motahareh Sheikh-Hosseini, Hadideh Mabudi, Javad Mohammadi-Asl, Raed Abdulelah Al-Badran
Publikováno v:
International Journal of Biomedicine, Vol 12, Iss 1, Pp 164-166 (2022)
Hereditary hearing loss is the most common sensory neural disorder, which has been revealed to have high genetic heterogeneity. Herein, we aimed to figure out the underlying genetics of the subject from an Iranian deaf family. Next-generation sequenc
Externí odkaz:
https://doaj.org/article/8514a31c6b964ce7b45b655e89ec5086
Publikováno v:
بیولوژی کاربردی, Vol 9, Iss 35, Pp 1-14 (2019)
Accurate recognition of shirbot blood parameters can be increase keeping up and breeding of these valuable fish. The goal of this study is to find the effect of different salinity stress on some electrolyte, cortisol and glucose in reared fingerling
Externí odkaz:
https://doaj.org/article/b4eae694099c4eeb82d2c50255443c7c
Publikováno v:
Clinical Case Reports, Vol 9, Iss 10, Pp n/a-n/a (2021)
Abstract This point of detected mutation could be considered as a novel mutational hotspot point that carried in patient ancestors. Moreover, the obtained results and family history suggest a precise genetic consulting and molecular prenatal evaluati
Externí odkaz:
https://doaj.org/article/20e8674bfaf2470dad3a62b2c1b596a3
Autor:
Razieh Sokooti, Mojdeh Chelemal Dezfoulnejad, Mehran Javaheri Baboli, Abolfazl Askary Sary, Hadideh Mabudi
Publikováno v:
Aquaculture Research. 53:5500-5509
Publikováno v:
Journal of Animal Physiology and Animal Nutrition. 95:599-602
Summary Ghrelin is expressed in key cells of the female reproductive organ in several species of fishes. It has a role in the control of fertility. In the present study, the histological effect of ghrelin on 48 female Barbus sharpeyi was tested. Twen