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The International Journal of Biochemistry & Cell Biology|March 18, 2018
The kinetic analysis of the N-methylation of 4-phenylpyridine by nicotinamide N-methyltransferase: Evidence for a novel mechanism of substrate inhibitionMatthijs J van Haren, Martin G Thomas, Davide Sartini, et al.
Brain and Behavior|September 6, 2012
Human neuronal uncoupling proteins 4 and 5 (UCP4 and UCP5): structural properties, regulation, and physiological role in protection against oxidative stress and mitochondrial dysfunctionDavid B Ramsden, Philip W-L Ho, Jessica W-M Ho, et al.
The Journal of Clinical Endocrinology and Metabolism|July 23, 2020
AMY1 Gene Copy Number Correlates With Glucose Absorption and Visceral Fat Volume, but Not with Insulin ResistanceThomas M Barber, Ahsan A Bhatti, Patrick J D Elder, et al.
Journal of the Peripheral Nervous System : JPNS|April 2, 2009
-459C>T point mutation in 5' non-coding region of human GJB1 gene is linked to X-linked Charcot-Marie-Tooth neuropathyMiaoxin Li, Tat-Sun Cheng, Philip W-L Ho, et al.
The Biochemical Journal|July 9, 2016
Nicotinamide N-methyltransferase catalyses the N-methylation of the endogenous β-carboline norharman: evidence for a novel detoxification pathwayMartin G Thomas, Davide Sartini, Monica Emanuelli, et al.
Inflammatory Bowel Diseases|July 23, 2013
Analysis of volatile organic compounds of bacterial origin in chronic gastrointestinal diseasesChristopher Walton, Dawn P Fowler, Claire Turner, et al.
Annals of Clinical and Translational Neurology|October 31, 2014
LRRK2 R1441G mice are more liable to dopamine depletion and locomotor inactivityHui-Fang Liu, Song Lu, Philip Wing-Lok Ho, et al.
FEMS Immunology and Medical Microbiology|February 8, 2012
Diversity and distribution of sulphate-reducing bacteria in human faeces from healthy subjects and patients with inflammatory bowel diseaseWenjing Jia, Rebekah N Whitehead, Lesley Griffiths, et al.
Cell Communication and Signaling : CCS|October 10, 2024
Loss of mitochondrial Ca2+ response and CaMKII/ERK activation by LRRK2R1441G mutation correlate with impaired depolarization-induced mitophagyEunice Eun-Seo Chang, Huifang Liu, Zoe Yuen-Kiu Choi, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 12, 2006
Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutationGardian C Y Fong, Ken H H Kwok, Y Q Song, et al.
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