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Results:
1-11
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Results: 11
Authors:
Lin, L
Lobel, P
Citation: L. Lin et P. Lobel, Production and characterization of recombinant human CLN2 protein for enzyme-replacement therapy in late infantile neuronal ceroid lipofuscinosis, BIOCHEM J, 357, 2001, pp. 49-55
Authors:
Lin, L
Sohar, I
Lackland, H
Lobel, P
Citation: L. Lin et al., The human CLN2 protein/tripeptidyl-peptidase I is a serine protease that autoactivates at acidic pH, J BIOL CHEM, 276(3), 2001, pp. 2249-2255
Authors:
Millat, G
Chikh, K
Naureckiene, S
Sleat, DE
Fensom, AH
Higaki, K
Elleder, M
Lobel, P
Vanier, MT
Citation: G. Millat et al., Niemann-Pick disease type C: Spectrum of HE1 mutations and genotype/phenotype correlations in the NPC2 group, AM J HU GEN, 69(5), 2001, pp. 1013-1021
Authors:
Berry-Kravis, E
Sleat, DE
Sohar, I
Meyer, P
Donnelly, R
Lobel, P
Citation: E. Berry-kravis et al., Prenatal testing for late infantile neuronal ceroid lipofuscinosis, ANN NEUROL, 47(2), 2000, pp. 254-257
Authors:
Tyynela, J
Sohar, I
Sleat, DE
Gin, RM
Donnelly, RJ
Baumann, M
Haltia, M
Lobel, P
Citation: J. Tyynela et al., A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration, EMBO J, 19(12), 2000, pp. 2786-2792
Authors:
Naureckiene, S
Sleat, DE
Lackland, H
Fensom, A
Vanier, MT
Wattiaux, R
Jadot, M
Lobel, P
Citation: S. Naureckiene et al., Identification of HE1 as the second gene of Niemann-Pick C disease, SCIENCE, 290(5500), 2000, pp. 2298
Authors:
Sohar, I
Lin, L
Lobel, P
Citation: I. Sohar et al., Enzyme-based diagnosis of classical late infantile neuronal ceroid lipofuscinosis: comparison of tripeptidyl peptidase I and pepstatin-insensitive protease assays, CLIN CHEM, 46(7), 2000, pp. 1005-1008
Authors:
Lobel, P
Pichot, C
Blanc-Feraud, L
Barlaud, M
Louis, AK
Citation: P. Lobel et al., Image reconstruction from the 1997 Ipswich Data using a conjugate-gradientalgorithm, IEEE ANT PR, 41(1), 1999, pp. 48-51
Authors:
Sohar, I
Sleat, DE
Jadot, M
Lobel, P
Citation: I. Sohar et al., Biochemical characterization of a lysosomal protease deficient in classical late infantile neuronal ceroid lipofuscinosis (LINCL) and development of an enzyme-based assay for diagnosis and exclusion of LINCL in human specimens and animal models, J NEUROCHEM, 73(2), 1999, pp. 700-711
Authors:
Jadot, M
Lin, L
Sleat, DE
Sohar, I
Hsu, MS
Pintar, J
Dubois, F
Wattiaux-De Coninck, S
Wattiaux, R
Lobel, P
Citation: M. Jadot et al., Subcellular localization of mannose 6-phosphate glycoproteins in rat brain, J BIOL CHEM, 274(30), 1999, pp. 21104-21113
Authors:
Sleat, DE
Gin, RM
Sohar, I
Wisniewski, K
Sklower-Brooks, S
Pullarkat, RK
Palmer, DN
Lerner, TJ
Boustany, RM
Uldall, P
Siakotos, AN
Donnelly, RJ
Lobel, P
Citation: De. Sleat et al., Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder, AM J HU GEN, 64(6), 1999, pp. 1511-1523
Risultati:
1-11
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