Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Edson Luck, Gonzales"'
Autor:
Gaeun Park, Wooyoung Eric Jang, Seoyeon Kim, Edson Luck Gonzales, Jungeun Ji, Seunghwan Choi, Yujin Kim, Ji Hwan Park, Hazara Begum Mohammad, Geul Bang, Minkyung Kang, Soobin Kim, Se Jin Jeon, Jin Young Kim, Kwang Pyo Kim, Chan Young Shin, Joon-Yong An, Min-Sik Kim, Yong-Seok Lee
Publikováno v:
Experimental and Molecular Medicine, Vol 55, Iss 8, Pp 1783-1794 (2023)
Abstract Autism spectrum disorder (ASD) is a neurodevelopmental disorder associated with impaired social behavior and communication, repetitive behaviors, and restricted interests. In addition to genetic factors, environmental factors such as prenata
Externí odkaz:
https://doaj.org/article/c8519af411c745c6bc546c4f406e0f20
Autor:
Yujeong Kim, Se Jin Jeon, Edson Luck Gonzales, Dongpil Shin, Chilly Gay Remonde, TaeJin Ahn, Chan Young Shin
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-11 (2022)
Abstract Fragile X syndrome (FXS) is a neurodevelopmental disorder that is caused by the loss of Fragile X-linked mental retardation protein (FMRP), an RNA binding protein that can bind and recognize different RNA structures and regulate the target m
Externí odkaz:
https://doaj.org/article/edcf42ab03b441d7bf4c4a5217a9b232
Autor:
Kyung-Jun, Boo, Edson Luck, Gonzales, Chilly Gay, Remonde, Jae Young, Seong, Se Jin, Jeon, Yeong-Min, Park, Byung-Joo, Ham, Chan Young, Shin
Publikováno v:
Biomolecules & Therapeutics. 31:161-167
Despite the various medications used in clinics, the efforts to develop more effective treatments for depression continue to increase in the past decades mainly because of the treatment-resistant population, and the testing of several hypotheses- and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc46c71121c4bffaf395a5177a0775eb
https://doi.org/10.4062/biomolther.2022.073
https://doi.org/10.4062/biomolther.2022.073
Publikováno v:
Toxicological Research. 39:37-51
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bd878578a8133bc3abf2230ec3f2c89
https://doi.org/10.1007/s43188-022-00145-1
https://doi.org/10.1007/s43188-022-00145-1
Publikováno v:
Biomolecules & Therapeutics
Astrocytes play various important roles such as maintaining brain homeostasis, supporting neurons, and secreting inflammatory mediators to protect the brain cells. In aged subjects, astrocytes show diversely changed phenotypes and dysfunctions. But,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e200730bdcd954d32f1071cbc49fc418
http://europepmc.org/articles/PMC7921865
http://europepmc.org/articles/PMC7921865
Autor:
Keremkleroo Jym Adil, Chilly Gay Remonde, Edson Luck Gonzales, Kyung-Jun Boo, Kyong Ja Kwon, Dong Hyun Kim, Hee Jin Kim, Jae Hoon Cheong, Chan Young Shin, Se Jin Jeon
Publikováno v:
Biomoleculestherapeutics. 30(4)
Neurodevelopmental disorders are complex conditions that pose difficulty in the modulation of proper motor, sensory and cognitive function due to dysregulated neuronal development. Previous studies have reported that an imbalance in the excitation/ i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01f526c83db7c3083bd6127e6d4d8119
https://pubmed.ncbi.nlm.nih.gov/35135902
https://pubmed.ncbi.nlm.nih.gov/35135902
Autor:
Se Jin Jeon, Huiyoung Kwon, Ho Jung Bae, Edson Luck Gonzales, Junhyeong Kim, Hye Jin Chung, Dong Hyun Kim, Jong Hoon Ryu, Chan Young Shin
Publikováno v:
Neuropharmacology. 219:109234
Fragile X syndrome (FXS) is the most common heritable form of neurodevelopmental disorder, which is caused by the loss of fragile X mental retardation protein (FMRP) expression. Despite the unceasing efforts to develop therapeutic agents against FXS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f64337147a3ecd167ab7fb5bc7ee2ac
https://doi.org/10.1016/j.neuropharm.2022.109234
https://doi.org/10.1016/j.neuropharm.2022.109234
Autor:
Keremkleroo Jym Adil, Edson Luck Gonzales, Chilly Gay Remonde, Kyung-Jun Boo, Se Jin Jeon, Chan Young Shin
Publikováno v:
Biomoleculestherapeutics. 30(3)
Autism spectrum disorder (ASD) having core characteristics of social interaction problems and repetitive behaviors and interests affects individuals at varying degrees and comorbidities, making it difficult to determine the precise etiology underlyin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e77f55afba6fcdafe60925846e41673b
https://pubmed.ncbi.nlm.nih.gov/34702791
https://pubmed.ncbi.nlm.nih.gov/34702791
Publikováno v:
Biomolecules & Therapeutics
Brain aging is an inevitable process characterized by structural and functional changes and is a major risk factor for neurodegenerative diseases. Most brain aging studies are focused on neurons and less on astrocytes which are the most abundant cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::651fbd2c8b9d60dafaa9c616c1f12861
https://doi.org/10.4062/biomolther.2019.151
https://doi.org/10.4062/biomolther.2019.151
Autor:
Chan Young Shin, ChiHye Chung, Hana Seung, Edson Luck Gonzales, Mee Jung Ko, Hyun Ah Oh, Ji-Woon Kim, Ri Jin Kang, Kwanghoon Park, Jae Hoon Cheong
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports
Scientific Reports
Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by social communication deficits and repetitive/restricted behaviors. Although gene-environment interactions may explain the heterogeneous etiology of ASD, it is still larg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4121f886b3c4dfc441337b4b5065dc95
http://link.springer.com/article/10.1038/s41598-019-47680-w
http://link.springer.com/article/10.1038/s41598-019-47680-w