Graham B. Sinclair, Ph.D. - Publications

Affiliations: 
2001 University of Victoria, Victoria, British Columbia, Canada 
Area:
Molecular Biology

5 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Tarailo-Graovac M, Sinclair G, Stockler-Ipsiroglu S, Van Allen M, Rozmus J, Shyr C, Biancheri R, Oh T, Sayson B, Lafek M, Ross CJ, Robinson WP, Wasserman WW, Rossi A, van Karnebeek CD. The genotypic and phenotypic spectrum of PIGA deficiency. Orphanet Journal of Rare Diseases. 10: 23. PMID 25885527 DOI: 10.1186/s13023-015-0243-8  0.316
2006 Sinclair G, Pfeifer TA, Grigliatti TA, Choy FY. Secretion of human glucocerebrosidase from stable transformed insect cells using native signal sequences. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 84: 148-56. PMID 16609695 DOI: 10.1139/O05-165  0.351
2002 Sinclair G, Choy FY. Synonymous codon usage bias and the expression of human glucocerebrosidase in the methylotrophic yeast, Pichia pastoris. Protein Expression and Purification. 26: 96-105. PMID 12356476 DOI: 10.1016/S1046-5928(02)00526-0  0.354
2001 Sinclair G, Choy FYM, Ferreira P. Heterologous expression and characterization of a rare Gaucher disease mutation (c.481C > T) from a Canadian aboriginal population using archival tissue samples. Molecular Genetics and Metabolism. 74: 345-352. PMID 11708865 DOI: 10.1006/Mgme.2001.3215  0.396
1998 Sinclair G, Choy FYM, Humphries L. A Novel Complex Allele And Two New Point Mutations In Type 2 (Acute Neuronopathic) Gaucher Disease Blood Cells Molecules and Diseases. 24: 420-427. PMID 9851895 DOI: 10.1006/Bcmd.1998.0210  0.34
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