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au.\*:("MORIZONO, H")

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The clinically variable R40H mutant ornithine carbamoyltransferase shows cytosolic degradation of the precursor protein in CHO cellsMAVINAKERE, M; MORIZONO, H; SHI, D et al.Journal of inherited metabolic disease. 2001, Vol 24, Num 6, pp 614-622, issn 0141-8955Article

Sustained correction of OTC deficiency in spfash mice using optimized self-complementary AAV2/8 vectorsWANG, L; WANG, H; MORIZONO, H et al.Gene therapy (Basingstoke). 2012, Vol 19, Num 4, pp 404-410, issn 0969-7128, 7 p.Article

GFAP mutations, age at onset, and clinical subtypes in Alexander diseasePRUST, M; WANG, J; ALBIN, R et al.Neurology. 2011, Vol 77, Num 13, pp 1287-1294, issn 0028-3878, 8 p.Article

'Late onset' ornithine transcarbamylase deficiency : function of three purified recombinant mutant enzymesMORIZONO, H; LISTROM, C. D; RAJAGOPAL, B. S et al.Human molecular genetics (Print). 1997, Vol 6, Num 6, pp 963-968, issn 0964-6906Article

The molecular basis of ornithine transcarbamylase deficiency : modelling the human enzyme and the effects of mutationsTUCHMAN, M; MORIZONO, H; REISH, O et al.Journal of medical genetics. 1995, Vol 32, Num 9, pp 680-688, issn 0022-2593Article

The biochemical and molecular spectrum of ornithine transcarbamylase deficiencyTUCHMAN, M; MORIZONO, H; RAJAGOPAL, B. S et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 40-58, issn 0141-8955, SUP1Conference Paper

Identification of 'private' mutations in patients with ornithine transcarbamylase deficiencyTUCHMAN, M; MORIZONO, H; RAJAGOPAL, B. S et al.Journal of inherited metabolic disease. 1997, Vol 20, Num 4, pp 525-527, issn 0141-8955Article

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