Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Inna Loutaev"'
Autor:
R. Michelle Saré, Alex Song, Merlin Levine, Abigail Lemons, Inna Loutaev, Carrie Sheeler, Christine Hildreth, Angel Mfon, Carolyn Beebe Smith
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
Sleep is critical for brain development and synaptic plasticity. In male wild-type mice, chronic sleep restriction during development results in long-lasting impairments in behavior including hypoactivity, decreased sociability, and increased repetit
Externí odkaz:
https://doaj.org/article/88efeb2f05f9464cb903aef19ec664d5
Publikováno v:
Neurobiology of Disease, Vol 148, Iss , Pp 105213- (2021)
SHANK3 is a postsynaptic scaffolding protein that plays a critical role in synaptic development and brain function. Mutations in SHANK3 are implicated in Phelan-McDermid syndrome (PMS), a neurodevelopmental disorder characterized by autistic-like beh
Externí odkaz:
https://doaj.org/article/ec1330e02d8b458b948697369089c17b
Publikováno v:
Neurobiology of Disease, Vol 143, Iss , Pp 104978- (2020)
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Fragile X mental retardation protein (FMRP), a putative translation suppressor, is absent or significantly reduced in FXS. One prevailing hypothesis is that rates
Externí odkaz:
https://doaj.org/article/607311faf2cf4cb7a573b2072f003399
Autor:
Rachel Michelle Saré, Alex Song, Merlin Levine, Abigail Lemons, Inna Loutaev, Carrie Sheeler, Christine Hildreth, Angel Mfon, Spencer Cooke, Carolyn Beebe Smith
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 13 (2019)
Sleep abnormalities are prevalent in autism spectrum disorders (ASD). Moreover, the severity of ASD symptoms are correlated with the degree of disturbed sleep. We asked if disturbed sleep during brain development itself could lead to ASD-like symptom
Externí odkaz:
https://doaj.org/article/43056dd9d493466a91fd0ed2827e997d
Autor:
Rachel M. Saré, Alex Song, Inna Loutaev, Anna Cook, Isabella Maita, Abigail Lemons, Carrie Sheeler, Carolyn B. Smith
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 10 (2018)
Fragile X syndrome (FXS), the most common form of inherited intellectual disability, is also highly associated with autism spectrum disorders (ASD). It is caused by expansion of a CGG repeat sequence on the X chromosome resulting in silencing of the
Externí odkaz:
https://doaj.org/article/17f5607b23d4422c8deb27121733bada
Autor:
Rachel Michelle Saré, Christopher Figueroa, Abigail Lemons, Inna Loutaev, Carolyn Beebe Smith
Publikováno v:
Brain Sciences, Vol 9, Iss 1, p 13 (2019)
Fragile X syndrome (FXS) is caused by silencing of the FMR1 gene leading to loss of the protein product fragile X mental retardation protein (FMRP). FXS is the most common monogenic cause of intellectual disability. There are two known mammalian para
Externí odkaz:
https://doaj.org/article/3742287e08b74c718e2ab0adb3563d6e
Autor:
Kathleen C Schmidt, Inna Loutaev, Thomas V Burlin, Audrey Thurm, Carrie Sheeler, Carolyn Beebe Smith
Publikováno v:
Journal of Cerebral Blood Flow & Metabolism. 42:1666-1675
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Fragile X mental retardation protein, a putative translation suppressor, is significantly reduced in FXS. The prevailing hypothesis is that rates of cerebral prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f277076c0538508afc00041e21f1766
https://doi.org/10.1177/0271678x221090997
https://doi.org/10.1177/0271678x221090997
Autor:
Kathleen C, Schmidt, Inna, Loutaev, Thomas V, Burlin, Audrey, Thurm, Carrie, Sheeler, Carolyn Beebe, Smith
Publikováno v:
J Cereb Blood Flow Metab
Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. Fragile X mental retardation protein, a putative translation suppressor, is significantly reduced in FXS. The prevailing hypothesis is that rates of cerebral prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f4ef634f2d5813ae77e6c7e3f91f8c45
https://pubmed.ncbi.nlm.nih.gov/35350914
https://pubmed.ncbi.nlm.nih.gov/35350914
Autor:
Dante, Picchioni, Kathleen C, Schmidt, Inna, Loutaev, Adriana J, Pavletic, Carrie, Sheeler, Shrinivas, Bishu, Thomas J, Balkin, Carolyn B, Smith
Publikováno v:
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism. 43(1)
During sleep, reduced brain energy demands provide an opportunity for biosynthetic processes like protein synthesis. Sleep is required for some forms of memory consolidation which requires
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb1a6dc02a9764c5e3831bb38022df7a
https://pubmed.ncbi.nlm.nih.gov/36071616
https://pubmed.ncbi.nlm.nih.gov/36071616
Publikováno v:
eNeuro.
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder that results in intellectual disability and, in ∼50% of patients, autism spectrum disorder. The protein products that are altered in TSC (TSC1 and TSC2) form a complex to inhibit th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9642fb4325ff004d06d70caf24482582
https://pubmed.ncbi.nlm.nih.gov/35851298
https://pubmed.ncbi.nlm.nih.gov/35851298