Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Wei Chieh Chiang"'
Publikováno v:
Disease Models & Mechanisms, Vol 17, Iss 7 (2024)
Externí odkaz:
https://doaj.org/article/2552e55609d44f88920526ff4f1c8c6e
Autor:
Seiji Takahashi, Yi-Min Huang, Jhy-Jyi Sze, Tung-Ting Wu, Fu-Sheng Guo, Wei-Cheng Hsu, Tung-Hsiung Tseng, King Liao, Chin-Chia Kuo, Tzu-Hsiang Chen, Wei-Chieh Chiang, Chun-Hao Chuang, Keng-Yu Chou, Chi-Hsien Chung, Kuo-Yu Chou, Chien-Hsien Tseng, Chuan-Joung Wang, Dun-Nien Yaung
Publikováno v:
Sensors, Vol 17, Iss 12, p 2816 (2017)
A submicron pixel’s light and dark performance were studied by experiment and simulation. An advanced node technology incorporated with a stacked CMOS image sensor (CIS) is promising in that it may enhance performance. In this work, we demonstrated
Externí odkaz:
https://doaj.org/article/e943c9552b8649ad8783b651839b2c7f
Autor:
Wei-Chieh Chiang, R. Luke Wiseman, Joseph Carroll, Amanda Nguyen, Julia M. D. Grandjean, Heike Kroeger, Jennifer Okalova, Jonathan H. Lin, Neil Grimsey, Evan T. Powers, Michel Michaelides, Jeffery W. Kelly, Daphne S. Bindels, Rebecca Mastey
Dysregulation of the endoplasmic reticulum (ER) Unfolded Protein Response (UPR) is implicated in the pathology of many human diseases associated with ER stress. Inactivating genetic variants in the UPR regulator Activating Transcription Factor 6 (ATF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::913b5b7d900ab5ff510d3883f7ce149e
https://doi.org/10.1101/2020.10.04.325019
https://doi.org/10.1101/2020.10.04.325019
Autor:
Daniel L. Chao, Jonathan H. Lin, Anthony T. Moore, Isabelle Audo, Rebecca Mastey, Chloe Xiaoke Bi, Dorota Skowronska-Krawczyk, Britta Baumann, Kyle Kim, Leon Chea, Wei-Chieh Chiang, Susanne Kohl, R. Luke Wiseman, Joseph Carroll, Eun-Jin Lee, Scott R. Lambert, Heike Kroeger, Julia M. D. Grandjean, Stephen H. Tsang
Publikováno v:
JCI Insight
Achromatopsia (ACHM) is an autosomal recessive disease that results in severe visual loss. Symptoms of ACHM include impaired visual acuity, nystagmus, and photoaversion starting from infancy; furthermore, ACHM is associated with bilateral foveal hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07103649fff10916483bdc2183095dca
https://doi.org/10.1172/jci.insight.136041
https://doi.org/10.1172/jci.insight.136041
Autor:
Daphne S. Bindels, Amanda Nguyen, Jonathan H. Lin, Julia M. D. Grandjean, Wei-Chieh Chiang, Rebecca Mastey, Michel Michaelides, Evan T. Powers, Jeffery W. Kelly, Joseph Carroll, Heike Kroeger, R. Luke Wiseman, Jennifer Okalova, Neil Grimsey
Publikováno v:
SSRN Electronic Journal.
Dysregulation of the endoplasmic reticulum (ER) Unfolded Protein Response (UPR) is implicated in the pathology of many human diseases associated with ER stress. Inactivating genetic variants in the UPR regulator Activating Transcription Factor 6 (ATF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecf0e3fc0f7e1e9394554248171388bb
https://doi.org/10.2139/ssrn.3746623
https://doi.org/10.2139/ssrn.3746623
Publikováno v:
Adv Exp Med Biol
Retinal Degenerative Diseases ISBN: 9783030273774
Retinal Degenerative Diseases ISBN: 9783030273774
Activating transcription factor 6 (ATF6) is a key regulator of the unfolded protein response (UPR). In response to endoplasmic reticulum (ER) stress, ATF6 is transported from the ER to the Golgi apparatus where it is cleaved by intramembrane proteoly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::872c5a8482318315905f89b0775dec2d
https://pubmed.ncbi.nlm.nih.gov/31884629
https://pubmed.ncbi.nlm.nih.gov/31884629
Publikováno v:
The FEBS Journal. 286:399-412
The human eye is the organ that is able to react to light in order to provide sharp three-dimensional and colored images. Unfortunately, the health of the eye can be impacted by various stimuli that can lead to vision loss, such as environmental chan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccaf6abef2ee12ed247c63b4795e5aa3
https://doi.org/10.1111/febs.14522
https://doi.org/10.1111/febs.14522
Autor:
Katarzyna Wicher, Bernd Wissinger, Anna Wawrocka, Dorota Pojda-Wilczek, Anna Skorczyk-Werner, Wei-Chieh Chiang, Magdalena Kostrzewska-Poczekaj, Aleksander Jamsheer, Nicole Weisschuh, Jonathan H. Lin, Rafał Płoski, Malgorzata Jarmuz-Szymczak, Małgorzata Rydzanicz, Susanne Kohl, Maciej R Krawczyński
Publikováno v:
European Journal of Human Genetics. 25:1210-1216
Inherited retinal dystrophies (IRDs) are clinically and genetically highly heterogeneous, making clinical diagnosis difficult. The advances in high-throughput sequencing (ie, panel, exome and genome sequencing) have proven highly effective on definin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dce4cd91af1a93f9c3e4f502bdd2a52
https://doi.org/10.1038/ejhg.2017.131
https://doi.org/10.1038/ejhg.2017.131
Publikováno v:
Brain Research. 1648:538-541
Photoreceptors are specialized sensory neurons essential for light detection in the human eye. Photoreceptor cell dysfunction and death cause vision loss in many eye diseases such as retinitis pigmentosa and achromatopsia. Endoplasmic reticulum (ER)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48e560a143296f9d87a237a63eb8cb92
https://doi.org/10.1016/j.brainres.2016.04.021
https://doi.org/10.1016/j.brainres.2016.04.021
Autor:
Priscilla Chan, Wei-Chieh Chiang, R. Luke Wiseman, Jonathan H. Lin, Jeffery W. Kelly, Ryan J Paxman
Publikováno v:
The FASEB Journal. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecbf7730858a2865d08471134cc3e1bd
https://doi.org/10.1096/fasebj.2018.32.1_supplement.816.3
https://doi.org/10.1096/fasebj.2018.32.1_supplement.816.3