Education
M.D., 1957, Saint Louis University
Research Interests
Areas of research include: (i) experimental approaches to treatment of murine beta-glucuronidase deficiency mucopolysaccharidosis (Sly syndrome), (ii) biochemical and molecular genetics of human deficiencies of beta-glucuronidase and carbonic anhydrases, and (iii) developing transgenic mice and mouse models of human disease by targeted mutagenesis.
Recent Publications
  • Carbonic anhydrase XII functions in health and disease.
    Waheed A, Sly WS. Gene. (2017) Apr 19 [Epub ahead of print].
  • Raine Syndrome (OMIM #259775), caused By FAM20C mutation, is congenital sclerosing osteomalacia with cerebral calcification (OMIM 259660).
    Whyte MP, McAlister WH, Fallon MD, Pierpont ME, Bijanki VN, Duan S, Otaify GA, Sly WS, Mumm S. J Bone Miner Res. (2016) 32(4):757-769.
  • Carbonic anhydrase enzymes II, VII, IX and XII in colorectal carcinomas.
    ViikilŠ P, KivelŠ AJ, Mustonen H, Koskensalo S, Waheed A, Sly WS, Pastorek J, Pastorekova S, Parkkila S, Haglund C. World J Gastroenterol. (2016) 22(36):8168-8177.
  • Loss of carbonic anhydrase XII function in individuals with elevated sweat chloride concentration and pulmonary airway disease.
    Lee M, Vecchio-Pag‡n B, Sharma N, Waheed A, Li X, Raraigh KS, Robbins S, Han ST, Franca AL, Pellicore MJ, Evans TA, Arcara KM, Nguyen H, Luan S, Belchis D, Hertecant J, Zabner J, Sly WS, Cutting GR. Hum Mol Genet. (2016) 25(10):1923-1933.
  • Clinical course of sly syndrome.
    Montano AM, Lock-Hock N, et al. J Med Genet. (2016) 53(6):403-418.
  • Pharmacologic manipulation of lysosomal enzyme transport across the blood-brain barrier.
    Urayama A, Grubb JH, Sly WS, Banks WA. J Cereb Blood Flow Metab. (2016) 36(3):476-486.
  • Large scale analysis of the mutational landscape in β-glucuronidase: A major player of mucopolysaccharidosis type VII.
    Khan FI, Shahbaaz M, Bisetty K, Waheed A, Sly WS, Ahmad F, Hassan MI. Gene. (2016) 576(1 Pt 1):36-44.