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Pharmaceutical Patent Analyst|April 22, 2020
Therapies for galactosemia: a patent landscapeDavid J TimsonBioscience Reports|February 27, 2019
Fructose 1,6-bisphosphatase: getting the message acrossDavid J TimsonThe FEBS Journal|November 24, 2005
Functional analysis of disease-causing mutations in human UDP-galactose 4-epimeraseDavid J TimsonInternational Journal of Food Sciences and Nutrition|November 28, 2013
Purple sweet potato colour--a potential therapy for galactosemia?David J TimsonGene|June 5, 2013
Comparison of dynamics of wildtype and V94M human UDP-galactose 4-epimerase-A computational perspective on severe epimerase-deficiency galactosemiaDavid J Timson, Steffen LindertBiochimie|November 12, 2020
The structural and molecular biology of type IV galactosemiaSamantha Banford, David J TimsonFEMS Yeast Research|January 27, 2007
Characterization of the Saccharomyces cerevisiae galactose mutarotase/UDP-galactose 4-epimerase protein, Gal10pAaron Scott, David J TimsonApplied Biochemistry and Biotechnology|October 11, 2011
N-acetylgalactosamine kinase: a naturally promiscuous small molecule kinaseHelena Kristiansson, David J TimsonJournal of Inherited Metabolic Disease|February 18, 2010
The biochemical basis of hereditary fructose intoleranceNadia Bouteldja, David J TimsonCurrent Cancer Drug Targets|September 24, 2016
UDP-N-acetyl-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase- 6 (pp-GalNAc-T6): Role in Cancer and Prospects as a Drug TargetSamantha Banford, David J TimsonPageof 15