Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mohammad Ali Dowlati"'
Publikováno v:
رشد و یادگیری حرکتی ورزشی, Vol 14, Iss 2, Pp 118-135 (2022)
Introduction: Brain-derived neurotrophic factor (BDNF) is a protein that is highly expressed in the structures of the central nervous system and affects synaptic plasticity and the acquisition of motor and cognitive skills. This is while val66met pol
Externí odkaz:
https://doaj.org/article/d22b74ce8dff4945b561e6067406104a
Publikováno v:
Fiyz̤, Vol 22, Iss 6, Pp 617-623 (2019)
Background: Alzheimer's disease is the most common cause of dementia in the elderly and the genetic and environmental factors interfere with its creation. The BDNF gene is responsible for producing a brain-derived neuronal factor. In this disease, th
Externí odkaz:
https://doaj.org/article/13fb6c58441b4c9db39e6979c97e22e2
Publikováno v:
Advances in Cognitive Science. 22:61-69
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6eb008a711e45c73393f865398dcd10a
https://doi.org/10.30699/icss.22.1.61
https://doi.org/10.30699/icss.22.1.61
Publikováno v:
Middle East Journal of Rehabilitation and Health Studies. 7
Background: The brain-derived neurotrophic factor (BDNF) is a neurotrophic factor in the brain associated with the growth, synaptic plasticity, learning, and cognitive processes. Objectives: The presence of val66met polymorphism in codon 66 of the BD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18babc4102674d44eb032207147e60d5
https://doi.org/10.5812/mejrh.101559
https://doi.org/10.5812/mejrh.101559
Publikováno v:
Biosciences, Biotechnology Research Asia. 13:1037-1044
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::695f1121ff7bb7f5bc188a018b00db65
https://doi.org/10.13005/bbra/2130
https://doi.org/10.13005/bbra/2130
Autor:
Farkhondeh Behjati, Ali Rashidi-Nezhad, Roxana Kariminejad, Mohammad-Ali Dowlati, Azadeh Shojaei, Pupak Derakhshandeh-Peykar, Maryam Razzaghy-Azar, Javad Tavakkoly-Bazzaz, Hasan Otukesh
Publikováno v:
Gene. 517:137-145
Terminal 7q duplication and terminal 13q deletion are two conditions with variable phenotypes including microcephaly, thumb a-/hypoplasia, cortical dysplasia, microphtalmia, intellectual disability and dysmorphic features. We describe a boy born to a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b224a5d8c8c091727ef401e96bea4b81
https://doi.org/10.1016/j.gene.2012.11.013
https://doi.org/10.1016/j.gene.2012.11.013
Autor:
Massoud Houshmand, Mohammad Ali Dowlati, Masoumeh Falah, Esmaiil Mohammadi, Azadeh Shojaei, Mohammad Farhadi, Shima Arastoo, Pupak Derakhshandeh-Peykar, Ardavan Tajdini, Javad Tavakkoly-Bazzaz
Publikováno v:
Molecular Biology Reports. 40:2689-2695
Mitochondria have essential role in cellular energy metabolism and defects in their function lead to many metabolic diseases. Mitochondrial DNA (mtDNA) mutations have been associated with number diseases such as nonsyndromic and aminoglycoside-induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c31aaa23ecfba09add282761357a41fe
https://doi.org/10.1007/s11033-012-2355-8
https://doi.org/10.1007/s11033-012-2355-8
Autor:
Mohammad Ali Dowlati, Javad Tavakkoly Bazzaz, Mohammad Farhadi, Massoud Houshmand, Azadeh Shojaei, Pupak Derakhshandeh-Peykar
Publikováno v:
Mitochondrial DNA. 24:132-136
We present a patient with non-syndromic and sensorineural hearing impairment with a novel mitochondrial DNA transition. A 7-year-old boy showed progressive deafness. He gradually lost his hearing ability and his hearing function did not improve with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8796ced03481458737cf2b0f942fdfdf
https://doi.org/10.3109/19401736.2012.717935
https://doi.org/10.3109/19401736.2012.717935