Concepedia

Beth McInnes

BM

14

Publications

463

Citations

12

H-Index

1988

Active since

Affiliations

Hospital for Sick Children(Current)

University of Toronto

Monash University

Ontario Brain Institute

Beth McInnes is an author at Hospital for Sick Children specializing in medicine, gene expression, and molecular genetics.

Top concepts

MedicineGene ExpressionMolecular GeneticsGeneticsPathologyNatural SciencesCell BiologyMolecular BiologyImmunologyLysosomal Storage Disease

Publications per year

1988–1998

14

Publications

14

Structure and distribution of an Alu-type deletion mutation in Sandhoff disease.

Kuldeep Neote, Beth McInnes, Don J. Mahuran et al. · Journal of Clinical Investigation · 1990 · 81 citations · Full text

Genetics, Sandhoff Disease, Pathology +16

An unusual splicing mutation in the HEXB gene is associated with dramatically different phenotypes in patients from different racial backgrounds.

Beth McInnes, Nobuaki Wakamatsu, S. Melançon et al. · Journal of Clinical Investigation · 1992 · 58 citations · Full text

Developmental Anomaly, Mendelian Disorder, Unusual Splicing Mutation +15

Transgenic expression of a CD46 (membrane cofactor protein) minigene: Studies of xenotransplantation and measles virus infection

Bruce Thorley, Julie Milland, Dale Christiansen et al. · European Journal of Immunology · 1997 · 55 citations

Structure–Function Studies of Interferons-α: Amino Acid Substitutions at the Conserved Residue Tyrosine 123 in Human Interferon-α <sub>1</sub>

Beth McInnes, Paul J. Chambers, B.F. Cheetham et al. · Journal of Interferon Research · 1989 · 37 citations

Functional significance of amino acid residues within conserved hydrophilic regions in human interferons-α

Martin J. Tymms, Beth McInnes, Gary J. Waine et al. · Antiviral Research · 1989 · 33 citations

Human Interferons-α, Hydrophilic Regions, Protein Function +8

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