Výsledky vyhledávání - "Marco Chi-Chung Lau"

Suppl Figure 4 from FSTL1 Promotes Metastasis and Chemoresistance in Esophageal Squamous Cell Carcinoma through NFκB–BMP Signaling Cross-talk

Autor: Stephanie Ma, Xin-Yuan Guan, Wen Ning, Kwok Wah Chan, Yan-Ru Qin, Annie L. Cheung, Nikki P. Lee, Simon Law, Xiao-Yan Ming, Terence K. Lee, Man Tong, Tin Lok Wong, Kai Yu Ng, Marco Chi-Chung Lau

Quantification of number of cells that migrated through a membrane, invaded through a Matrigel-coated membrane, formed spheroids or formed colonies in (A) KYSE150-Luc cells co-cultured with conditioned medium collected from EV or FSTL1 OE cells; or (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53c922ae9b5681fbcf923cae91911931
https://doi.org/10.1158/0008-5472.22418481.v1

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Suppl Figure 5 from FSTL1 Promotes Metastasis and Chemoresistance in Esophageal Squamous Cell Carcinoma through NFκB–BMP Signaling Cross-talk

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0638cfefe44debc43078bbfb4d4a7bbb
https://doi.org/10.1158/0008-5472.22418478

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Data from FSTL1 Promotes Metastasis and Chemoresistance in Esophageal Squamous Cell Carcinoma through NFκB–BMP Signaling Cross-talk

Esophageal squamous cell carcinoma (ESCC) has a generally poor prognosis, and molecular markers to improve early detection and predict outcomes are greatly needed. Here, we report that the BMP-binding follistatin-like protein FSTL1 is overexpressed i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::076db88967306ba77bb8c2afc0707b4d
https://doi.org/10.1158/0008-5472.c.6510141.v1

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Restoration of polr1c in Early Embryogenesis Rescues the Type 3 Treacher Collins Syndrome Facial Malformation Phenotype in Zebrafish

Autor: Jeff Cheuk Hin Ho, May Su You, William Ka Fai Tse, Yun Jin Jiang, Marco Chi Chung Lau, Ernest Man Lok Kwong

Publikováno v: The American Journal of Pathology. 188:336-342

Treacher Collins syndrome (TCS) is a rare congenital birth disorder (1 in 50,000 live births) characterized by severe craniofacial defects. Recently, the authors' group unfolded the pathogenesis of polr1c Type 3 TCS by using the zebrafish model. Faci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af19304c78958ce8c53c6547374a28d3
https://doi.org/10.1016/j.ajpath.2017.10.004

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Pathogenesis of POLR1C-dependent Type 3 Treacher Collins Syndrome revealed by a zebrafish model

Autor: Ting-Fung Chan, Jing-Woei Li, Keng Po Lai, Ernest Man Lok Kwong, Jeff Cheuk Hin Ho, Marco Chi Chung Lau, Yun Jin Jiang, Chris K C Wong, William Ka Fai Tse

Publikováno v: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1862:1147-1158

Treacher Collins Syndrome (TCS) is a rare congenital birth disorder (1 in 50,000 live births) characterized by severe craniofacial defects, including the downward slanting palpebral fissures, hypoplasia of the facial bones, and cleft palate (CP). Ove

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f74c57b0caac742db926f8846eb8069a
https://doi.org/10.1016/j.bbadis.2016.03.005

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Osmotic stress transcription factor 1b (Ostf1b) promotes migration properties with the modulation of epithelial mesenchymal transition (EMT) phenotype in human embryonic kidney cell

Autor: Alice Y.S. Law, Chris K C Wong, Marco Chi Chung Lau, William Ka Fai Tse, Keng Po Lai, Yoshio Takei

Publikováno v: The International Journal of Biochemistry & Cell Biology. 45:1921-1926

Osmoregulation is an essential mechanism for euryhaline fish. Gill cells undergo rapid mechanism to maintain the cellular homeostasis during osmotic stress. Reports have suggested that gill cells may be able to migrate between primary filament and se

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2152070e3dc04906d784e9f0808c56c1
https://doi.org/10.1016/j.biocel.2013.05.023

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