Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Shu-Ting You"'
Publikováno v:
PLoS Biology, Vol 17, Iss 10, p e3000433 (2019)
Cell-to-cell heterogeneity within an isogenic population has been observed in prokaryotic and eukaryotic cells. Such heterogeneity often manifests at the level of individual protein abundance and may have evolutionary benefits, especially for organis
Externí odkaz:
https://doaj.org/article/38765a6612d945e8968d0af7c7234f54
Autor:
Hsiu Mei Hsieh-Li, Shu Ting You, Chi Wei Huang, Jian Fu Liao, Sabrina Wang, Chih Chieh Hsu, Jen Jie Chiou, Yun Fang Cheng, Ying-Chieh Tsai, Wen Chun Kuo
Publikováno v:
Brain, Behavior, and Immunity. 90:26-46
Evidence suggests that the Parkinson’s disease (PD) pathogenesis is strongly associated with bidirectional pathways in the microbiota-gut-brain axis (MGBA), and psychobiotics may inhibit PD progression. We previously reported that the novel psychob
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0118743 (2015)
The small GTPase Arf-like protein 1 (Arl1) is well known for its role in intracellular vesicular transport at the trans-Golgi network (TGN). In this study, we used differential affinity chromatography combined with mass spectrometry to identify Arf-i
Externí odkaz:
https://doaj.org/article/12801b2720f44257a6ce047dd5a2d7ce
Autor:
Jun-Yi Leu, Shu-Ting You
Publikováno v:
Evolutionary Biology—A Transdisciplinary Approach ISBN: 9783030572457
Noise is the heterogeneity in transcript or protein levels existing in an isogenic population under the same growth condition. Expression noise is unavoidable in living cells. To ensure accurate execution of cellular functions, cells have developed s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7c425d3f7428c0dcebbb4e40771cf0e
https://doi.org/10.1007/978-3-030-57246-4_16
https://doi.org/10.1007/978-3-030-57246-4_16
Autor:
Chun-Chun Li, Tsung-Sheng Wu, Chun-Fang Huang, Li-Ting Jang, Yu-Tsan Liu, Shu-Ting You, Gunn-Guang Liou, Fang-Jen S Lee
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e43552 (2012)
ARL4D, ARL4A, and ARL4C are closely related members of the ADP-ribosylation factor/ARF-like protein (ARF/ARL) family of GTPases. All three ARL4 proteins contain nuclear localization signals (NLSs) at their C-termini and are primarily found at the pla
Externí odkaz:
https://doaj.org/article/3fd353239abe4a689f782c42d6af63f0
Publikováno v:
PLoS Biology, Vol 17, Iss 10, p e3000433 (2019)
PLoS Biology
PLoS Biology
Cell-to-cell heterogeneity within an isogenic population has been observed in prokaryotic and eukaryotic cells. Such heterogeneity often manifests at the level of individual protein abundance and may have evolutionary benefits, especially for organis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::288f838aa74da3c39a3352f80dd9bc29
Autor:
Shu-Ting You, 游淑婷
107
Cell-to-cell heterogeneity in an isogenic population has been observed in prokaryotic and eukaryotic cells. Such heterogeneity is often manifested at individual protein abundance and proposed to have evolutionary benefits, especially for org
Cell-to-cell heterogeneity in an isogenic population has been observed in prokaryotic and eukaryotic cells. Such heterogeneity is often manifested at individual protein abundance and proposed to have evolutionary benefits, especially for org
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/smpefk
Autor:
Kun-Yi Chien, Rajaneesh Karimpurath Gopinath, Shu-Ting You, Jau-Song Yu, Krishna B S Swamy, Jun-Yi Leu, Scott C. Schuyler
Publikováno v:
Genome Biology and Evolution
Hsp90 is one of the most abundant and conserved proteins in the cell. Reduced levels or activity of Hsp90 causes defects in many cellular processes and also reveals genetic and nongenetic variation within a population. Despite information about Hsp90
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 3, p e0118743 (2015)
PLoS ONE, Vol 10, Iss 3, p e0118743 (2015)
The small GTPase Arf-like protein 1 (Arl1) is well known for its role in intracellular vesicular transport at the trans-Golgi network (TGN). In this study, we used differential affinity chromatography combined with mass spectrometry to identify Arf-i