Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Jenn-Yah Yu"'
Autor:
Yi-Chia Huang, Kuan-Han Chen, Yu-Yang Chen, Liang-Hsuan Tsao, Tsung‐Han Yeh, Yu-Chia Chen, Ping-Yen Wu, Tsu-Wei Wang, Jenn-Yah Yu
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 11, Iss 9 (2021)
AbstractDuring oogenesis, a group of specialized follicle cells, known as stretched cells (StCs), flatten drastically from cuboidal to squamous shape. While morphogenesis of epithelia is critical for organogenesis, genes and signaling pathways involv
Externí odkaz:
https://doaj.org/article/f85e4c64cc65484a9f4a4285736bdeae
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Abstract The Hippo pathway is conserved and plays important roles in organ size control. The core components of the Hippo pathway are two kinases Hippo (Hpo), Warts (Wts), and a transcription-co-activator Yorkie (Yki). Yki activity is regulated by ph
Externí odkaz:
https://doaj.org/article/50deaebf4e6b45aeb7d648fe64ee7dbb
Autor:
Ming-Yang Li, Xiu-Li Yang, Chia-Chi Chung, Yun-Ju Lai, Jui-Cheng Tsai, Ya-Lin Kuo, Jenn-Yah Yu, Tsu-Wei Wang
Publikováno v:
FASEB Journal; 3/15/2024, Vol. 38 Issue 5, p1-20, 20p
Publikováno v:
Developmental Dynamics. 251:846-863
The Hippo pathway is conserved through evolution and plays critical roles in development, tissue homeostasis and tumorigenesis. Yes-associated protein (YAP) is a transcriptional coactivator downstream of the Hippo pathway. Previous studies have demon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a368bb2cac662a10e418a0c827b4f857
https://doi.org/10.1002/dvdy.448
https://doi.org/10.1002/dvdy.448
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 19; Pages: 11891
Leber’s hereditary optic neuropathy (LHON) is a maternally transmitted disease caused by mitochondria DNA (mtDNA) mutation. It is characterized by acute and subacute visual loss predominantly affecting young men. The mtDNA mutation is transmitted t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3449ff7c5eca46471a5b437d63de0aa9
https://pubmed.ncbi.nlm.nih.gov/36233195
https://pubmed.ncbi.nlm.nih.gov/36233195
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-10 (2018)
Chinese herbal medicines (CHMs) have been used to treat human diseases for thousands of years. Among them, Ginkgo biloba is reported to be beneficial to the nervous system and a potential treatment of neurological disorders. Since the presence of adu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04f0847dff68917c412524bba4fdce63
https://doi.org/10.1038/s41598-018-32960-8
https://doi.org/10.1038/s41598-018-32960-8
Publikováno v:
Developmental Dynamics. 244:852-865
Background: Tousled-like kinase (Tlk) is a conserved serine/threonine kinase regulating DNA replication, chromatin assembly, and DNA repair. Previous studies have suggested that Tlk is involved in cell morphogenesis in vitro. In addition, tlk genetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b663629968acb041de10ad8933c84a57
https://doi.org/10.1002/dvdy.24292
https://doi.org/10.1002/dvdy.24292
Autor:
Tsu Wei Wang, Yuchio Yanagawa, Pei-Lin Cheng, Jin Wu Tsai, Wan Shan Yang, Yuan Hsuan Liu, Jenn Yah Yu, Jia Long Chen, Pei Ching Chang, David L. Turner
Publikováno v:
Scientific Reports
During development, cortical interneurons generated from the ventral telencephalon migrate tangentially into the dorsal telencephalon. Although Achaete-scute family bHLH transcription factor 1 (Ascl1) plays important roles in the developing telenceph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07dd2a5901c89945c853ad9aa5bf6f5f
Publikováno v:
Genetics. 198:1087-1099
The Hippo pathway is a key signaling cascade in controlling organ size. The core components of this pathway are two kinases, Hippo (Hpo) and Warts (Wts), and a transcriptional coactivator, Yorkie (Yki). Yes-associated protein (YAP, a Yki homolog in m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::145f58b1b4cf5173eb6e47b63f434733
https://doi.org/10.1534/genetics.114.167346
https://doi.org/10.1534/genetics.114.167346
Publikováno v:
Developmental Neurobiology. 74:723-738
Mutations of the transcription factor FOXP2 in humans cause a severe speech and language disorder. Disruption of Foxp2 in songbirds or mice also leads to deficits in song learning or ultrasonic vocalization, respectively. These data suggest that Foxp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::234b5ae165d1c58d6eff32c32e0e3f1c
https://doi.org/10.1002/dneu.22166
https://doi.org/10.1002/dneu.22166