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Human Molecular Genetics|July 21, 1998
An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomesN Braverman, G Dodt, S J Gould, et al.Annals of the New York Academy of Sciences|December 27, 1996
From expressed sequence tags to peroxisome biogenesis disorder genesG Dodt, N Braverman, D Valle, et al.The Journal of Clinical Investigation|June 15, 1996
A mouse model of gyrate atrophy of the choroid and retina. Early retinal pigment epithelium damage and progressive retinal degenerationT Wang, A H Milam, G Steel, et al.Genomics|April 2, 1998
Genomic organization of the 70-kDa peroxisomal membrane protein gene (PXMP1)J Gärtner, G Jimenez-Sanchez, P Roerig, et al.Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
Correction of ornithine accumulation prevents retinal degeneration in a mouse model of gyrate atrophy of the choroid and retinaT Wang, G Steel, A H Milam, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1991
Gyrate atrophy of the choroid and retina. Long-term reduction of ornithine slows retinal degenerationM I Kaiser-Kupfer, R C Caruso, D ValleHuman Molecular Genetics|January 1, 1995
Disorders of peroxisome biogenesisN Braverman, G Dodt, S J Gould, et al.Brain Research|June 9, 1980
The development of catecholaminergic innervation in chick spinal cordH S Singer, J T Coyle, N Vernon, et al.Cell|July 1, 1979
Loss of integrated viral DNA sequences in polyomatransformed cells is associated with an active viral A functionC Basilico, S Gattoni, D Zouzias, et al.American Journal of Ophthalmology|February 1, 1980
Clinical and biochemical heterogeneity in gyrate atrophyM I Kaiser-Kupfer, D Valle, A J BronPageof 42