Zobrazeno 1 - 10
of 89
pro vyhledávání: '"Jiann-Jou Yang"'
Publikováno v:
ACS Omega, Vol 9, Iss 5, Pp 5919-5931 (2024)
Externí odkaz:
https://doaj.org/article/3b0d662fa6ef4da6b8a06a563629d230
Autor:
Chun-Hung Su, Shih-Pin Chen, Li-You Chen, Jiann-Jou Yang, Yi-Chia Lee, Shiuan-Shinn Lee, Hsin-Hung Chen, Yan-Yan Ng, Yu-Hsiang Kuan
Publikováno v:
Ecotoxicology and Environmental Safety, Vol 228, Iss , Pp 112962- (2021)
Fluoranthene, a high-molecular-weight polycyclic aromatic hydrocarbon (PAH), is widely present in air pollutants, including fine inhalable particulate matter. 3-Bromofluoranthene (3-BrFlu), which is a brominated fluoranthene and halogenated PAH, is g
Externí odkaz:
https://doaj.org/article/c11625813d6c4bababff5cabc9fca5b5
Publikováno v:
Cells, Vol 11, Iss 5, p 894 (2022)
KCNQ2 mutations can cause benign familial neonatal convulsions (BFNCs), epileptic encephalopathy (EE), and mild-to-profound neurodevelopmental disabilities. Mutations in the KCNQ2 selectivity filter (SF) are critical to neurodevelopmental outcomes. T
Externí odkaz:
https://doaj.org/article/05ecdea7263a4e3897d01e8bf15aff11
Publikováno v:
Antioxidants, Vol 11, Iss 1, p 39 (2021)
The antioxidant defense system is involved in the pathogenesis of neonatal hypoxic-ischemic encephalopathy (HIE). To analyze the relationship between first serum blood glucose levels and outcomes in neonatal HIE, seventy-four patients were divided, b
Externí odkaz:
https://doaj.org/article/22a269f3fc244984818fa79d300e69de
Publikováno v:
Journal of the Formosan Medical Association, Vol 116, Iss 9, Pp 711-719 (2017)
Pediatric epilepsy caused by a KCNQ2 gene mutation usually manifests as benign familial neonatal seizures (BFNS) during the 1st week of life. However, the exact mechanism, phenotype, and genotype of the KCNQ2 mutation are unclear. Methods: We studied
Externí odkaz:
https://doaj.org/article/90603507e8334bfebd26fde09d329458
Publikováno v:
Journal of Functional Foods, Vol 28, Iss , Pp 157-167 (2017)
Ferulic acid (FA) derivatives have applied in American clinical trials for preventing and treating auditory dysfunctions. However, the effects of FA on neomycin-mediated sensorineural hearing loss are still unknown. We developed a transgenic zebrafis
Externí odkaz:
https://doaj.org/article/e8f65ab3634f452aa0d9330a29790450
Publikováno v:
Pediatrics and Neonatology, Vol 56, Iss 6, Pp 408-414 (2015)
Lenticulostriate vasculopathy is associated with various disorders, in particular cytomegalovirus infection, which can cause neurological consequences. We wanted to evaluate the association of lenticulostriate vasculopathy and cytomegalovirus infecti
Externí odkaz:
https://doaj.org/article/c5093fb9222e4fc4a06c368d6e77fde0
Publikováno v:
Cells, Vol 9, Iss 5, p 1291 (2020)
Nonsyndromic hearing loss (NSHL) is of great clinical importance, and mutations in the GJB2 gene and the encoded human CONNEXIN 26 (CX26) protein play important roles in the genetic pathogenesis. The CX26 p.R184Q mutation was shown to be a dominant-n
Externí odkaz:
https://doaj.org/article/4290ff575bba4636992c4cdf207ef320
Autor:
Chun-Ching Chiu, Ya-Fang Shi, Jiann-Jou Yang, Yuan-Chao Hsiao, Bor-Show Tzang, Tsai-Ching Hsu
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e107970 (2014)
As is widely recognized, human parvovirus B19 (B19) and human bocavirus (HBoV) are important human pathogens. Obviously, both VP1 unique region (VP1u) of B19 and HBoV exhibit the secreted phospholipase A2 (sPLA2)-like enzymatic activity and are recog
Externí odkaz:
https://doaj.org/article/f57f9fb5c2414033a425190c1e9a528e
Autor:
Yu-Fan Hsieh, Guang-Yaw Liu, Yi-Ju Lee, Jiann-Jou Yang, Katalin Sándor, Zsolt Sarang, Angela Bononi, Paolo Pinton, László Tretter, Zsuzsa Szondy, Gregory J Tsay
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e81516 (2013)
Transglutaminase 2 (TG2) is a protein cross-linking enzyme known to be associated with the in vivo apoptosis program of T cells. However, its role in the T cell apoptosis program was not investigated yet.Here we report that timed overexpression of bo
Externí odkaz:
https://doaj.org/article/c8794956117d4999ad9a1c648a9b1ddb