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Author/Creator Sham, Pak C.

1. Amelioration of X-Linked Related Autophagy Failure in Danon Disease With DNA Methylation Inhibitor. Issue 18 (1st November 2016)

Authors:
Ng, Kwong-Man; Mok, Pamela Y.; Butler, Amy W.; Ho, Jenny C.Y.; Choi, Shing-Wan; Lee, Yee-Ki; Lai, Wing-Hon; Au, Ka-Wing; Lau, Yee-Man; Wong, Lai-Yung; Esteban, Miguel A.; Siu, Chung-Wah; Sham, Pak C.; Colman, Alan; Tse, Hung-Fat
Journal:
Circulation
Issue:
Volume 134:Issue 18(2016)
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Record Type:
Journal Article
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3. CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis. Issue 1 (13th November 2016)

Authors:
Leung, Gordon K. C.; Ying, Dingge; Mak, Christopher C. Y.; Chen, Xin‐Ying; Xu, Weiyi; Yeung, Kit‐San; Wong, Wai‐Lap; Chu, Yoyo W. Y.; Mok, Gary T. K.; Chau, Christy S. K.; McLuskey, Jenna; Ong, Winnie P. T.; Leong, Huey‐Yin; Chan, Kelvin Y. K.; Yang, Wanling; Chen, Jeng‐Haur; Li, Albert M.; Sham,...
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 5:Issue 1(2017)
Page Start:
40
Record Type:
Journal Article
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5. Dysfunction of Myosin Light‐Chain 4 (MYL4) Leads to Heritable Atrial Cardiomyopathy With Electrical, Contractile, and Structural Components: Evidence From Genetically‐Engineered Rats. Issue 11 (28th October 2017)

Authors:
Peng, Wenhui; Li, Miaoxin; Li, Hailing; Tang, Kai; Zhuang, Jianhui; Zhang, Jianguo; Xiao, Jingjing; Jiang, Hui; Li, Dali; Yu, Yongchun; Sham, Pak C.; Nattel, Stanley; Xu, Yawei
Journal:
Journal of the American Heart Association
Issue:
Volume 6:Issue 11(2017)
Page Start:
n/a
Record Type:
Journal Article
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6. Early intervention and evaluation for adult‐onset psychosis: the JCEP study rationale and design. Issue 3 (28th February 2013)

Authors:
Hui, Christy L.M.; Chang, Wing C.; Chan, Sherry K.W.; Lee, Edwin H.M.; Tam, Wendy W.Y.; Lai, Dik C.; Wong, Gloria H.Y.; Tang, Jennifer Y.M.; Li, Frendi W.S.; Leung, Kwok F.; McGhee, Sarah M.; Sham, Pak C.; Chen, Eric Y.H.
Journal:
Early intervention in psychiatry
Issue:
Volume 8:Issue 3(2014:Aug.)
Page Start:
261
Record Type:
Journal Article
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7. Exome Sequencing Identifies a Novel Frameshift Mutation of MYO6 as the Cause of Autosomal Dominant Nonsyndromic Hearing Loss in a Chinese Family. (17th September 2014)

Authors:
Cheng, Jing; Zhou, Xueya; Lu, Yu; Chen, Jing; Han, Bing; Zhu, Yuhua; Liu, Liyang; Choy, Kwong‐Wai; Han, Dongyi; Sham, Pak C.; Zhang, Michael Q.; Zhang, Xuegong; Yuan, Huijun
Journal:
Annals of human genetics
Issue:
Volume 78:Number 6(2014:Nov.)
Page Start:
410
Record Type:
Journal Article
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9. High risk Epstein‐Barr virus variants characterized by distinct polymorphisms in the EBER locus are strongly associated with nasopharyngeal carcinoma. Issue 12 (7th January 2019)

Authors:
Hui, Kwai Fung; Chan, Tsz Fung; Yang, Wanling; Shen, Jiangshan Jane; Lam, Ki Pui; Kwok, Hin; Sham, Pak C.; Tsao, Sai Wah; Kwong, Dora L.; Lung, Maria Li; Chiang, Alan Kwok Shing
Journal:
International journal of cancer
Issue:
Volume 144:Issue 12(2019)
Page Start:
3031
Record Type:
Journal Article
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