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Results: 1-9 |
Results: 9
METABOLIC ENGINEERING AS THERAPY FOR INBORN-ERRORS OF METABOLISM - DEVELOPMENT OF MICE WITH PHENYLALANINE-HYDROXYLASE EXPRESSION IN MUSCLE
Authors: HARDING CO WILD K CHANG D MESSING A WOLFF JA
Citation: Co. Harding et al., METABOLIC ENGINEERING AS THERAPY FOR INBORN-ERRORS OF METABOLISM - DEVELOPMENT OF MICE WITH PHENYLALANINE-HYDROXYLASE EXPRESSION IN MUSCLE, Gene therapy, 5(5), 1998, pp. 677-683
RENAL-TRANSPLANTATION IN A PATIENT WITH METHYLMALONIC ACIDEMIA
Authors: VANCALCAR SC HARDING CO LYNE P HOGAN K BANERJEE R SOLLINGER H RIESELBACH RE WOLFF JA
Citation: Sc. Vancalcar et al., RENAL-TRANSPLANTATION IN A PATIENT WITH METHYLMALONIC ACIDEMIA, Journal of inherited metabolic disease, 21(7), 1998, pp. 729-737
FRIEDREICHS ATAXIA - A FRATAXIN MEDIATED MITOCHONDRIAL DISEASE
Authors: GALLAGHER CL WACLAWIK AJ SALAMAT SM LOTZ BP FADIC R HARDING CO JOHNS DR BEINLICH BR
Citation: Cl. Gallagher et al., FRIEDREICHS ATAXIA - A FRATAXIN MEDIATED MITOCHONDRIAL DISEASE, Neurology, 50(4), 1998, pp. 6127-6127
THE MURINE MUTATION GGT(ENUL) IS CAUSED BY REPLACEMENT OF A LEUCINE WITH A STOP CODON IN THE FIRST CODING EXON OF THE GAMMA-GLUTAMYL-TRANSFERASE (GGT) MESSENGER-RNA
Authors: JEAN JC HARDING CO OAKES SM YU Q JOYCEBRADY M
Citation: Jc. Jean et al., THE MURINE MUTATION GGT(ENUL) IS CAUSED BY REPLACEMENT OF A LEUCINE WITH A STOP CODON IN THE FIRST CODING EXON OF THE GAMMA-GLUTAMYL-TRANSFERASE (GGT) MESSENGER-RNA, Molecular biology of the cell, 8, 1997, pp. 1992-1992
FUNCTIONAL METHIONINE SYNTHASE DEFICIENCY DUE TO CBLG DISORDER - A REPORT OF 2 PATIENTS AND A REVIEW
Authors: HARDING CO ARNOLD G BARNESS LA WOLFF JK ROSENBLATT DS
Citation: Co. Harding et al., FUNCTIONAL METHIONINE SYNTHASE DEFICIENCY DUE TO CBLG DISORDER - A REPORT OF 2 PATIENTS AND A REVIEW, American journal of medical genetics, 71(4), 1997, pp. 384-390
LONG-TERM SURVIVAL IN TYPICAL THANATOPHORIC DYSPLASIA TYPE-1
Authors: BAKER KM OLSON DS HARDING CO PAULI RM
Citation: Km. Baker et al., LONG-TERM SURVIVAL IN TYPICAL THANATOPHORIC DYSPLASIA TYPE-1, American journal of medical genetics, 70(4), 1997, pp. 427-436
MICE WITH GENETIC GAMMA-GLUTAMYL-TRANSPEPTIDASE DEFICIENCY EXHIBIT GLUTATHIONURIA, SEVERE GROWTH FAILURE, REDUCED LIFE SPANS, AND INFERTILITY
Authors: HARDING CO WILLIAMS P WAGNER E CHANG DS WILD K COLWELL RE WOLFF JA
Citation: Co. Harding et al., MICE WITH GENETIC GAMMA-GLUTAMYL-TRANSPEPTIDASE DEFICIENCY EXHIBIT GLUTATHIONURIA, SEVERE GROWTH FAILURE, REDUCED LIFE SPANS, AND INFERTILITY, The Journal of biological chemistry, 272(19), 1997, pp. 12560-12567
THE MOUSE MUTATION SARCOSINEMIA (SAR) MAPS TO CHROMOSOME-2 IN A REGION HOMOLOGOUS TO HUMAN-9Q33-Q34
Authors: BRUNIALTI ALB HARDING CO WOLFF JA GUENET JL
Citation: Alb. Brunialti et al., THE MOUSE MUTATION SARCOSINEMIA (SAR) MAPS TO CHROMOSOME-2 IN A REGION HOMOLOGOUS TO HUMAN-9Q33-Q34, Genomics, 36(1), 1996, pp. 182-184
SAR - A GENETIC MOUSE MODEL FOR HUMAN SARCOSINEMIA GENERATED BY ETHYLNITROSOUREA MUTAGENESIS
Authors: HARDING CO WILLIAMS P PFLANZER DM COLWELL RE LYNE PW WOLFF JA
Citation: Co. Harding et al., SAR - A GENETIC MOUSE MODEL FOR HUMAN SARCOSINEMIA GENERATED BY ETHYLNITROSOUREA MUTAGENESIS, Proceedings of the National Academy of Sciences of the United Statesof America, 89(7), 1992, pp. 2644-2648
Risultati: 1-9 |