Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Hung Yu Shih"'
Autor:
Alexa Derksen, Hung-Yu Shih, Diane Forget, Lama Darbelli, Luan T. Tran, Christian Poitras, Kether Guerrero, Sundaresan Tharun, Fowzan S. Alkuraya, Wesam I. Kurdi, Cam-Tu Emilie Nguyen, Anne-Marie Laberge, Yue Si, Marie-Soleil Gauthier, Joshua L. Bonkowsky, Benoit Coulombe, Geneviève Bernard
Publikováno v:
HGG Advances, Vol 2, Iss 3, Pp 100034- (2021)
Summary: Leukodystrophies, genetic neurodevelopmental and/or neurodegenerative disorders of cerebral white matter, result from impaired myelin homeostasis and metabolism. Numerous genes have been implicated in these heterogeneous disorders; however,
Externí odkaz:
https://doaj.org/article/5f90d21d2bce448496c47a87b96f7a5f
Autor:
Matthew D Keefe, Haille E Soderholm, Hung-Yu Shih, Tamara J Stevenson, Kathryn A Glaittli, D Miranda Bowles, Erika Scholl, Samuel Colby, Samer Merchant, Edward W Hsu, Joshua L Bonkowsky
Publikováno v:
eLife, Vol 9 (2020)
Vanishing white matter disease (VWM) is a severe leukodystrophy of the central nervous system caused by mutations in subunits of the eukaryotic initiation factor 2B complex (eIF2B). Current models only partially recapitulate key disease features, and
Externí odkaz:
https://doaj.org/article/0ee75c412d8f4dd58a470302d1887a1f
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 2; Pages: 1733
Bone morphogenetic protein (BMP) signaling regulates neural induction, neuronal specification, and neuronal differentiation. However, the role of BMP signaling in neural progenitors remains unclear. This is because interruption of BMP signaling befor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8ec67409c108c217ea8e39fd2bea6c1
Autor:
Sheng-Jia, Lin, Yin-Cheng, Huang, Hao-Yuan, Chen, Jia-You, Fang, Shu-Yuan, Hsu, Hung-Yu, Shih, Yu-Chien, Liu, Yi-Chuan, Cheng
Publikováno v:
Anticancer research. 41(12)
This study aimed to explore RGS2 as a regulator of melanoma cell growth.Effect of RGS2 over-expression was analyzed in three melanoma cell lines, and Rgs2 knockdown was performed in zebrafish.RGS2 was differentially expressed among the cell lines. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cf05b903a2aaa9592bb76243b07785d9
https://pubmed.ncbi.nlm.nih.gov/34848468
https://pubmed.ncbi.nlm.nih.gov/34848468
Autor:
Alexa, Derksen, Hung-Yu, Shih, Diane, Forget, Lama, Darbelli, Luan T, Tran, Christian, Poitras, Kether, Guerrero, Sundaresan, Tharun, Fowzan S, Alkuraya, Wesam I, Kurdi, Cam-Tu Emilie, Nguyen, Anne-Marie, Laberge, Yue, Si, Marie-Soleil, Gauthier, Joshua L, Bonkowsky, Benoit, Coulombe, Geneviève, Bernard
Publikováno v:
Human Genetics and Genomics Advances
Summary Leukodystrophies, genetic neurodevelopmental and/or neurodegenerative disorders of cerebral white matter, result from impaired myelin homeostasis and metabolism. Numerous genes have been implicated in these heterogeneous disorders; however, m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94f50963af932cd6c3c1b449d3fb22fa
https://pubmed.ncbi.nlm.nih.gov/35047835
https://pubmed.ncbi.nlm.nih.gov/35047835
Autor:
Yi-Chuan Cheng, Fu-Yu Hsieh, Ming-Chang Chiang, Paul J Scotting, Hung-Yu Shih, Sheng-Jia Lin, Hui-Lan Wu, Han-Ting Lee
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54262 (2013)
Akt1 is well known for its role in regulating cell proliferation, differentiation, and apoptosis and is implicated in tumors and several neurological disorders. However, the role of Akt1 in neural development has not been well defined. We have isolat
Externí odkaz:
https://doaj.org/article/ab9e1d9c33124f8b81ae9246eb40d3c8
Autor:
Edward W. Hsu, Erika A. Scholl, Samuel Colby, D. Miranda Bowles, Matthew D. Keefe, Joshua L. Bonkowsky, Haille E Soderholm, Samer S. Merchant, Tamara J. Stevenson, Hung-Yu Shih, Kathryn A Glaittli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64240e156e081bc2516a046ee82ea198
https://doi.org/10.7554/elife.56319.sa2
https://doi.org/10.7554/elife.56319.sa2
Autor:
Edward W. Hsu, Matthew D. Keefe, Erika A. Scholl, Joshua L. Bonkowsky, Samuel Colby, Samer S. Merchant, Tamara J. Stevenson, D. M. Bowles, Kathryn A Glaittli, Hung-Yu Shih, Haille E Soderholm
Publikováno v:
eLife, Vol 9 (2020)
eLife
eLife
Vanishing White Matter disease (VWM) is a severe leukodystrophy of the central nervous system caused by mutations in subunits of the eukaryotic initiation factor 2B complex (eIF2B). Current models only partially recapitulate key disease features, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d0503061717502e5bc0e530df3898a8
Autor:
Yin Cheng Huang, Hung Yu Shih, Tu Hsueh Yeh, Han Fang Liu, Ming-Chang Chiang, Hao Yuan Chen, Yi-Chuan Cheng, Chien Ping Wang, Yen Che Hsieh
Publikováno v:
Developmental Dynamics. 247:1264-1275
Background Many molecules and signaling pathways involved in neural development play a role in neurodegenerative diseases and brain tumor progression. Peroxisome proliferator-activated receptor (PPAR) proteins regulate the differentiation of tissues
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f8d13125b35bd36aeb67290d88623d9
https://doi.org/10.1002/dvdy.24683
https://doi.org/10.1002/dvdy.24683
Autor:
Cam-Tu Emilie Nguyen, Benoit Coulombe, Luan T. Tran, Yue Si, Christian Poitras, Sundaresan Tharun, Geneviève Bernard, Wesam Kurdi, Marie-Soleil Gauthier, Diane Forget, Fowzan S. Alkuraya, Anne-Marie Laberge, Hung-Yu Shih, Kether Guerrero, Alexa Derksen, Joshua L. Bonkowsky, Lama Darbelli
Publikováno v:
HGG Advances, Vol 2, Iss 3, Pp 100034-(2021)
Summary: Leukodystrophies, genetic neurodevelopmental and/or neurodegenerative disorders of cerebral white matter, result from impaired myelin homeostasis and metabolism. Numerous genes have been implicated in these heterogeneous disorders; however,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e42d09f648272cbb55ec4b8db6b0627b
https://doi.org/10.1016/j.xhgg.2021.100034
https://doi.org/10.1016/j.xhgg.2021.100034