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Results: 1-7 |
Results: 7

Authors: LITJENS T BIELICKI J ANSON DS FRIDERICI K JONES MZ HOPWOOD JJ
Citation: T. Litjens et al., EXPRESSION, PURIFICATION AND CHARACTERIZATION OF RECOMBINANT CAPRINE N-ACETYLGLUCOSAMINE-6-SULFATASE, Biochemical journal, 327, 1997, pp. 89-94

Authors: YOGALINGAM G LITJENS T BIELICKI J CRAWLEY AC MULLER V ANSON DS HOPWOOD JJ
Citation: G. Yogalingam et al., FELINE MUCOPOLYSACCHARIDOSIS TYPE-VI - CHARACTERIZATION OF RECOMBINANT N-ACETYLGALACTOSAMINE 4-SULFATASE AND IDENTIFICATION OF A MUTATION CAUSING THE DISEASE, The Journal of biological chemistry, 271(44), 1996, pp. 27259-27265

Authors: LITJENS T BROOKS DA PETERS C GIBSON GJ HOPWOOD JJ
Citation: T. Litjens et al., IDENTIFICATION, EXPRESSION, AND BIOCHEMICAL-CHARACTERIZATION OF N-ACETYLGALACTOSAMINE-4-SULFATASE MUTATIONS AND RELATIONSHIP WITH CLINICAL PHENOTYPE IN MPS-VI PATIENTS, American journal of human genetics, 58(6), 1996, pp. 1127-1134

Authors: BROOKS DA ROBERTSON DA BINDLOSS C LITJENS T ANSON DS PETERS C MORRIS CP HOPWOOD JJ
Citation: Da. Brooks et al., 2 SITE-DIRECTED MUTATIONS ABROGATE ENZYME-ACTIVITY BUT HAVE DIFFERENTEFFECTS ON THE CONFORMATION AND CELLULAR CONTENT OF THE N-ACETYLGALACTOSAMINE 4-SULFATASE PROTEIN, Biochemical journal, 307, 1995, pp. 457-463

Authors: SCOTT HS NELSON PV LITJENS T HOPWOOD JJ MORRIS CP
Citation: Hs. Scott et al., MULTIPLE POLYMORPHISMS WITHIN THE ALPHA-L-IDURONIDASE GENE (IDUA) - IMPLICATIONS FOR A ROLE IN MODIFICATION OF MPS-I DISEASE PHENOTYPE, Human molecular genetics, 2(9), 1993, pp. 1471-1473

Authors: HOPWOOD JJ VELLODI A SCOTT HS MORRIS CP LITJENS T CLEMENTS PR BROOKS DA COOPER A WRAITH JE
Citation: Jj. Hopwood et al., LONG-TERM CLINICAL-PROGRESS IN BONE-MARROW TRANSPLANTED MUCOPOLYSACCHARIDOSIS TYPE-I PATIENTS WITH A DEFINED GENOTYPE, Journal of inherited metabolic disease, 16(6), 1993, pp. 1024-1033

Authors: SCOTT HS LITJENS T NELSON PV THOMPSON PR BROOKS DA HOPWOOD JJ MORRIS CP
Citation: Hs. Scott et al., IDENTIFICATION OF MUTATIONS IN THE ALPHA-L-IDURONIDASE GENE (IDUA) THAT CAUSE HURLER AND SCHEIE SYNDROMES, American journal of human genetics, 53(5), 1993, pp. 973-986
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