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The Journal of Biological Chemistry|November 25, 1982
ATP-dependent lysosomal cystine efflux is defective in cystinosisA J Jonas, M L Smith, J A SchneiderClinica Chimica Acta; International Journal of Clinical Chemistry|April 23, 1982
Measurement of intracellular amino acids in cultured fibroblastsA J Jonas, S A Smith, N Gochman, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1982
Cystine accumulation and loss in normal, heterozygous, and cystinotic fibroblastsA J Jonas, A A Greene, M L Smith, et al.Pediatric Research|December 1, 1981
Cystinotic fibroblasts are depleted of free-cystine by acid pH mediumD G Ritchie, A J Jonas, R G Oshima, et al.In Vitro|January 1, 1984
Renal cell culture using autopsy material from children with cystinosisO L Pellett, M L Smith, J G Thoene, et al.The Journal of Biological Chemistry|October 10, 1983
Proton-translocating ATPase and lysosomal cystine transportA J Jonas, M L Smith, W S Allison, et al.Kidney International|January 1, 1989
Urine glyceraldehyde excretion is elevated in the renal Fanconi syndromeA J Jonas, S N Lin, S B Conley, et al.Biochemical and Biophysical Research Communications|May 29, 1986
Studies of lysosomal sialic acid metabolism: retention of sialic acid by Salla disease lysosomesA J JonasPediatric Research|November 1, 1985
Lysosomal cystine storage in cystinosis and mucolipidosis type IIA A Greene, A J Jonas, E Harms, et al.Pageof 20