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M.W. Ho. Saros Seminar on the Dilemma of Knowledge, Transcript, Bristol Book Club, 1990.
£1.00
In Search of the Sublime.
M.W. Ho. Metanoia Introductory Issue, pp. 9-16, Spring,1994.
£1.00
Re-animating Nature: the Integration of Science with Human Experience.
Ho, M.W. Leonardo 24: 607-615, 1991.
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Re-animating Nature: The Integration of Science with Human Experience.
M.W. Ho. Beshara Magazine , Issue 8, 16-25, 1989.
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CATEGORY: Genetics (availability variable)
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Adult Gaucher's Disease: Kindred Studies and Demonstration of a Deficiency of Acid b-Glucosidase in Cultured Fibroblasts.
M.W. Ho, J. Seck, D. Schmidt, L. Veath, W. Johnson, R.O. Brady and J.S. O'Brien. Am. J. Hum. Genet . 24: 37-45, 1972.
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b-Galactosidase Deficiency in Hurler's Syndrome.
M. MacBrinn, S. Okada, M. Wollacott, V. Patel, M.W. Ho, A.L. Tappel and J.S. O'Brien. New Eng. J. Med . 281: 338-43, 1969.
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Ceramide Trihexoside b-Galactosidase: Kinetic Properties and Alterations in Fabry's Disease.
M.W. Ho. Fed. Proc . 31: 437, 1972.
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Chloride Ions Cancel Out Inhibition of b-Galactosidase Activity by Acid Mucopolysaccharides.
M.W. Ho and A. Fluharty. Nature (Lond) 253:660, 1975.
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Differential Effect of Chloride Ions on b-Galactosidase Isoenzymes: A Method for Separate Assay.
M.W. Ho and J.S. O'Brien. Clin. chim. Acta, 32, 223-36, 1971.
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Effects of Detergents on Ceramide-3 Hydrolysis by ?-Galactosidase
A.W. Schram, M.W. Ho, S. Cordus, M. Samson, M.H. Hamers, I. Brown, D. Rabinson and J.M. Tager. In Enzymes of Lipid Metabolism. (S. Gatt, L. Freysz and P. Mandel, eds.) pp 531-35, Plenum Press, New York, 1971.
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Fabry's Disease: Evidence for a Physically Altered b-Galactosidase.
M.W. Ho, S. Beutler, L.Tennant and J.S. O'Brien. Am. J. Hum. Genet . 24: 256-266, 1972. (Reprinted in Biochemical Basis of Inherited Human Diseases . MSS Information Corporation, NewYork, 1973.
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Ganglioside Storage Diseases.
J.S. O'Brien, S. Okada, M.W. Ho, D.L. Fillerup, M.L. Veath and K. Adams. In Lipid Storage Diseases , pp 225-273, Academic Press, New York, 1971.
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Ganglioside Storage Diseases.
J.S. O'Brien, S. Okada, M.W. Ho, D.L. Fillerup, M.L. Veath and K. Adams. Fed. Proc ., 30: 956-69, 1971.
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Gaucher's disease: Deficiency of 'Acid' b-Glucosidase and Reconstitution of Enzyme Acticity in vitro I.
M.W. Ho and J.S. O'Brien. Proc. Nat. Acad. Sci . USA, 68: 2810-13, 1971.
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Generalised Gangliosidosis: Impaired Cleavage of Galactose from a Mucopolysaccharide and a Glycoprotein.
M.C. MacBrinn, S. Okada, M.W. Ho, C.C. Hu and J.S. O'Brien. Science, 163: 964-67, 1969.
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Genetic Heterogeneity in GM S1 S Gangliosidoses.
H. Galjaard, A. Hoogeveen, W. Keijzer, H.a. de Wit-Verbeed, A.J.J. Reuser, M.W. Ho and D. Robinson. Nature (Lond) 254: 6062, 1975.
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Glucocerebrosidase: Reconstitution of Activity from Macromolecular Components.
Glucocerebrosidase: A Model of Enzyme Action in Membrane.
M.W. Ho. In Enzyme Therapy and Lysosomal Storage Diseases (Eds, J.M. Tager, G.J.M. Hooghwinkel and W.Th. Daems) pp 239-246, 1974.
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Glucocerebrosidase: Reconstitution from Mutliple components Depends on Acidic Phospholipids.
M.W. Ho and N.D. Light, Biochem. J. 136 821823. 1973.
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Glucocerebrosidase: Stiochiometry of Association between Effector and Catalytic Proteins.
M.W. Ho and M. Rigby. Biochem. Biophys. Acta . 396, 267-73, 1975.
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Glycophingolipid Storage Disease: Biochemistry and Genetics.
M.W. Ho, A.G.W. Norden and J.A. Alhadeff. Mol. Cell. Biochem . 17: 125138, 1977.
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GM-S1 S Gangliosidosis Type II.
J.S. O'Brien, M.W. Ho, M.L. Veath, J.F. Wilson, G. Myers, J.M. Optiz, G.M. Zurheim, J.W. Spranger, H.A. Hartman, B. Haneberg and F.R. Grosse. Clin. Genet . 3: 411-434, 1974.
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Human Lactase and the Molecular Basis of Lactase Persistence.
J. Potter, H.W. Ho, H. Bolton, A. Furth, D. Swallow and B. Griffiths. Biochem. Genetics 23: 423-39, 1985.
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Hurler's Syndrome: Deficiency of a Specific b-Galactosidase Isoenzyme.
M.W. Ho and J.S. O'Brien. Science, 165:611-13, 1969.
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Hydrolysis of Ceramide Trihexoside by a Specific b-Galactosidase from Human Liver.
M.W. Ho, Biochem. J . 133: 1-10, 1973.
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Hydrolysis of GM S1 S galglioside by Human Liver b-Galactrosidase Isoenzymes.
M.W.Ho, P. Cheetham and D. Robinson, Biochem. J . 136: 351-59, 1973.
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I-cell Disease: Biochemical Studies.
J.G. Leroy, M.W. Ho, M.C. MacBrinn, K. Zielke, J. Jacob and J.S. O'Brien. Ped. Res . 1972.
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Identity of Acid b-Glucosidase and Glucocerebrosidase in Human Spleen.
M.W. Ho, Biochem. J . 136: 721-29, 1973.
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Isolation of a cDNA probe for a Human Jejunal Brush-border Hydrolase, Sucrase- isomaltase and Assignment of the Gene Locus to Chromosome 3
Green, F., Edwards, Y., Hauri, H.P., Povey, S., Ho, M.W., Pinto, M. and Swallow, D. Gene 57:101-10, 1987.
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Lactase Polymorphism in Adult British Natives. Estimating Allele Frequencies by Enzyme Assays.
M.W. Ho, S. Povey and D. Swallow. Am. J. Human Genetics 34; 650-657, 1982.
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Mosaic Pattern of Lactase Expression by Villous Enterocytes in Human Adult-type Hypolactasia.
Maiuri, L., Raia, V., Potter, J., Swallow, D., Ho, M.W., Fiocca, R., Finzi, G., Cornaggia, M., Capella, D., Quaroni, D. and Auricchio, S.Gastroenterology 100: 359-69, 1991.
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Preparation of a Monoclonal Antibody to Human Lactase.
D. Swallow, J. Potter, F. Green and M.W. Ho. J. Immunol. Methods 77: 139-45, 1985.
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Specificity of Low Molecular Weight Glycoprotein Effector of Lipid Glycosidase.
M.W. Ho. FEBS Letters . 53: 243-47, 1975.
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Sphinolipidoses: Detection of Heterozygotes and Homozygotes.
J.S. O'Brien, M.W. Ho, S. Okada, K. Zielke, M.L. Veath and L. Tennant. In Shingolipids, Shingolipidoses and Allied Disorders , pp 581-97, Plenum Publishing Corp, New York, 1972.
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Stimulation of Acid b-Galactosidase Activity By Chloride Ions.
M.W. Ho and J.S. O'Brien.Clin. Chim. Acta , 30: 531-34, 1970.
