Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Alvin C.H. Ma"'
Autor:
Shisan Xu, Gary Tse, Fangjing Xie, Kin Fung Wong, Li Tian, Kazi Md Mahmudul Hasan, Shuk Han Cheng, Lei Sun, Alvin C.H. Ma, Yingying Lu, Jianbo Yue, Sinai H. C. Manno
Publikováno v:
npj Regenerative Medicine, Vol 6, Iss 1, Pp 1-13 (2021)
NPJ Regenerative Medicine
NPJ Regenerative Medicine
Metformin is one of the most widely used drugs for type 2 diabetes and it also exhibits cardiovascular protective activity. However, the underlying mechanism of its action is not well understood. Here, we used an adult zebrafish model of heart cryoin
Publikováno v:
Autophagy
1-phenyl 2-thiourea (PTU) is a Tyr (tyrosinase) inhibitor that is extensively used to block pigmentation and improve optical transparency in zebrafish (Danio rerio) embryo. Here, we reported a previously undescribed effect of PTU on macroautophagy/au
Autor:
Bai-Liang He, Alvin C.H. Ma, May P.L. Cheung, Toni K. Man, Nelson K. L. Ng, Yuhan Guo, Dandan Wang, Xiangguo Shi, Anskar Y.H. Leung, Bowie Yik Ling Cheng
Publikováno v:
Stem Cell Reports
Summary ADP-ribosylation factor-like 4aa (Arl4aa) is a member of the ADP-ribosylation factor family. It is expressed in hematopoietic tissue during embryonic development, but its function was unknown. Zebrafish arl4aa is preferentially expressed in t
Autophagy is an evolutionary conserved and dynamic lysosomal degradation process for cellular homeostasis and remodelling, which is essential for the development and maintenance of different hematopoietic fates. However, the roles of autophagy in def
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95ad3308d536d8ffefa73ec9582b6b38
https://doi.org/10.1101/2021.06.14.448302
https://doi.org/10.1101/2021.06.14.448302
Autor:
Gordon Tin Chun Wong, Zhen Ni Yi, Joseph Kwan, Alvin C.H. Ma, Xiang Ke Chen, Kazi Md Mahmudul Hasan, Raymond Chuen-Chung Chang
Publikováno v:
Aging Cell
Cellular senescence, a state of irreversible growth arrest triggered by various stressors, engages in a category of pathological processes, whereby senescent cells accumulate in mitotic tissues. Senolytics as novel medicine against aging and various
Publikováno v:
Alzheimer's & Dementia. 16
Autor:
Alvin C.H. Ma, Xiang Ke Chen, Gordon Tin Chun Wong, Kazi Md Mahmudul Hasan, Joseph Kwan, Zhen-Ni Yi, Raymond Chuen-Chung Chang
Background: Infiltration of macrophages into the central nervous system (CNS) is involved in many neurological disorders, such as Alzheimer’s disease (AD), amyotrophic lateral sclerosis (ALS) and autism. Despite extensive studies into neuroinflamma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91bad4c25afcbdb0e9c0f5b6692fcfc6
https://doi.org/10.21203/rs.3.rs-96577/v1
https://doi.org/10.21203/rs.3.rs-96577/v1
Autor:
Bai-Liang He, Alvin C.H. Ma, Chun Xiao Zhang, Ho Ching Leung, Stephen S. Y. Lam, Bowie Yik Ling Cheng, Cheuk Him Man, H Kwok, Chae Yin Cher, Rakesh Sharma, Grace H W Cheng, Nelson K. L. Ng, Leo Lai Hok Kan, Anskar Y.H. Leung, Ning Yang, Michelle Lu Lu Wang, Yok-Lam Kwong, Chi Wai Eric So
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 8, Pp n/a-n/a (2020)
EMBO Molecular Medicine, Vol 12, Iss 4, Pp n/a-n/a (2020)
EMBO Mol Med
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 12, Iss 4, Pp n/a-n/a (2020)
EMBO Mol Med
EMBO Molecular Medicine
Internal tandem duplication of Fms‐like tyrosine kinase 3 (FLT3/ITD) occurs in about 30% of acute myeloid leukemia (AML) and is associated with poor response to conventional treatment and adverse outcome. Here, we reported that human FLT3/ITD expre
Autor:
Steven Lim Cho Pei, Mullin H.C. Yu, Yiu-fai Cheung, Kit San Yeung, Xiangke Chen, Alvin C.H. Ma, Kazi Md Mahmudul Hasan, Brian H.Y. Chung, Dingge Ying, Christopher C.Y. Mak, Pak Cheong Chow
Publikováno v:
Circulation. Genomic and Precision Medicine
Supplemental Digital Content is available in the text.
Background: Human heterotaxy is a group of congenital disorders characterized by misplacement of one or more organs according to the left-right axis. The genetic causes of human heterotaxy a
Background: Human heterotaxy is a group of congenital disorders characterized by misplacement of one or more organs according to the left-right axis. The genetic causes of human heterotaxy a
Autor:
Carla M. Mann, Stephen C. Ekker, Karl J. Clark, Gabriel Martínez-Gálvez, Hirotaka Ata, Kyle J. Schaefbauer, Drena Dobbs, Thomas L. Ekstrom, Alexey V. Dvornikov, Alvin C.H. Ma
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 14, Iss 9, p e1007652 (2018)
PLoS Genetics, Vol 14, Iss 9, p e1007652 (2018)
One key problem in precision genome editing is the unpredictable plurality of sequence outcomes at the site of targeted DNA double stranded breaks (DSBs). This is due to the typical activation of the versatile Non-homologous End Joining (NHEJ) pathwa