Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Sheena Li"'
Autor:
Wendy Ungar, Vercancy Wu, Christian Marshall, Jackie Hwang, Robin Hayeems, Kate Tsiplova, Meredith Gillespie, Anna Szuto, Caitlin Chisholm, Dimitri Stavropoulos, Viji Venkataramanan, Bowen Xiao, Sheena Li, Gregory Costain, Melanie Beaulieu Bergeron, Sarah Sawyer, Lynette Lau, Lijia Huang, Roberto Mendoza-Londono, Brian Smith, Edward Higginbotham, Martin Somerville, Kym Boycott
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101365- (2024)
Externí odkaz:
https://doaj.org/article/3031b497e1034a96a0e6104670aa93a3
Autor:
Nicole M. Revie, Kali R. Iyer, Michelle E. Maxson, Jiabao Zhang, Su Yan, Caroline M. Fernandes, Kirsten J. Meyer, Xuefei Chen, Iwona Skulska, Meea Fogal, Hiram Sanchez, Saif Hossain, Sheena Li, Yoko Yashiroda, Hiroyuki Hirano, Minoru Yoshida, Hiroyuki Osada, Charles Boone, Rebecca S. Shapiro, David R. Andes, Gerard D. Wright, Justin R. Nodwell, Maurizio Del Poeta, Martin D. Burke, Luke Whitesell, Nicole Robbins, Leah E. Cowen
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-20 (2022)
There is an urgent need for novel strategies to combat life-threatening fungal infections. Here, Revie et al. identify a compound that induces alterations in fungal membranes, synergizes with azole antifungals against the pathogen Candida albicans, a
Externí odkaz:
https://doaj.org/article/8bca44075efb4f07a12ae3b736c09d4d
Autor:
Ivo J. H. M. de Vos, Arnette Shi Wei Wong, Jason Taslim, Sheena Li Ming Ong, Nicole C. Syder, Julian L. Goggi, Thomas J. Carney, Maurice A. M. van Steensel
Publikováno v:
Biology Open, Vol 9, Iss 12 (2020)
Frank-Ter Haar syndrome (FTHS, MIM #249420) is a rare skeletal dysplasia within the defective collagen remodelling spectrum (DECORS), which is characterised by craniofacial abnormalities, skeletal malformations and fibrotic soft tissues changes inclu
Externí odkaz:
https://doaj.org/article/fbf0145d5183405281f6adafd7b26f1b
Publikováno v:
Journal of Childhood Studies; Feb2024, Vol. 49 Issue 1, p12-30, 19p
Autor:
M. Meroshini, Sheena Li Ming Ong, Bernard A. Liu, Lucian B. Tomaz, Ee Kim Tan, Nicholas S. Tolwinski, Christopher S. Williams, Marc Leushacke, N. Ray Dunn, Anne-Claude Gingras
Mutated in Colorectal Cancer (MCC) encodes a coiled-coil protein implicated, as its name suggests, in the pathogenesis of hereditary human colon cancer. To date, however, the contributions of MCC to intestinal homeostasis remain unclear. Here, we exa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aecfea10afe60ece165bab867e19cff8
https://doi.org/10.1101/2021.07.27.453941
https://doi.org/10.1101/2021.07.27.453941
Autor:
Julian L. Goggi, Thomas J. Carney, Nicole C. Syder, Jason Taslim, Ivo J. H. M. de Vos, Sheena Li Ming Ong, Arnette Shi Wei Wong, Maurice A.M. van Steensel
Publikováno v:
Biology Open
article-version (VoR) Version of Record
Biology Open, Vol 9, Iss 12 (2020)
Open Biology, 9(12):054270. COMPANY OF BIOLOGISTS LTD
article-version (VoR) Version of Record
Biology Open, Vol 9, Iss 12 (2020)
Open Biology, 9(12):054270. COMPANY OF BIOLOGISTS LTD
Frank-Ter Haar syndrome (FTHS, MIM #249420) is a rare skeletal dysplasia within the defective collagen remodelling spectrum (DECORS), which is characterised by craniofacial abnormalities, skeletal malformations and fibrotic soft tissues changes inclu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c116903393a2e5b53ff9b907a1968a69
http://europepmc.org/articles/PMC7790187
http://europepmc.org/articles/PMC7790187
Publikováno v:
Scientific Reports
Scientific Reports, 10(1):11801. Nature Publishing Group
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, 10(1):11801. Nature Publishing Group
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Microfibril-associated glycoprotein 4 (MFAP4) is an extracellular matrix protein belonging to the fibrinogen-related protein superfamily. MFAP4 is produced by vascular smooth muscle cells and is highly enriched in the blood vessels of the heart and l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d54836f8abbbb683ee79524cff89ab92
https://research.rug.nl/en/publications/f4160b91-3b82-4783-a9a4-f12ef73ac1f6
https://research.rug.nl/en/publications/f4160b91-3b82-4783-a9a4-f12ef73ac1f6
Akademický článek
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Autor:
Sheena Li Ming Ong, Alexander P.A. Stegmann, David J. Amor, Evelyn Yaqiong Tao, Julian L. Goggi, Thomas J. Carney, Norris R. Dunn, Thomas S. Scerri, Barry J. Coull, Arnette Shi Wei Wong, Paul J. Lockhart, Melanie Bahlo, Dominic Grussu, Gabrielle R. Wilson, Maurice A.M. van Steensel, Ivo J. H. M. de Vos, Renske Janssen, Michel van Geel, Chernis Guai Mun Low
Publikováno v:
Human Molecular Genetics, 27(16), 2775-2788. Oxford University Press
Winchester syndrome (WS, MIM #277950) is an extremely rare autosomal recessive skeletal dysplasia characterized by progressive joint destruction and osteolysis. To date, only one missense mutation inMMP14, encoding the membrane-bound matrix metallopr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd43255ad9f8f58fef9c35dce662d171
https://doi.org/10.1101/281485
https://doi.org/10.1101/281485
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.