Correction of obesity and diabetes in genetically obese mice by leptin gene therapy von Muzzin, Patrick, Eisensmith, Randy C., Copeland, Kenneth C., Savio L. C. Woo

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Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria von Okano, Yoshiyuki, Eisensmith, Randy C, Güttler, Flemming, Lichter-Konecki, Uta, Konecki, David S, Trefz, Friedrich K, Dasovich, Mary, Wang, Tao, Henriksen, Karen, Lou, Hans, Woo, Savio L.C

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Hepatic Insulin Gene Expression as Treatment for Type 1 Diabetes Mellitus in Rats von Muzzin, Patrick, Eisensmith, Randy C, Copeland, Kenneth C, Woo, Savio L. C

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IFN-gamma sensitization of prostate cancer cells to Fas-mediated death: a gene therapy approach von Selleck, William A, Canfield, Steven E, Hassen, Waleed A, Meseck, Marcia, Kuzmin, Alexei I, Eisensmith, Randy C, Chen, Shu-Hsia, Hall, Simon J

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An Immunomodulatory Procedure That Stabilizes Transgene Expression and Permits Readministration of E1-Deleted Adenovirus Vectors von Kuzmin, Alexei I., Galenko, Oxana, Eisensmith, Randy C.

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Molecular basis of phenylketonuria and a correlation between genotype and phenotype in a heterogeneous southeastern US population von EISENSMITH, R. C, MARTINEZ, D. R, KUZMIN, A. I, GOLTSOV, A. A, BROWN, A, RANI SINGH, ELSAS, L. J, WOO, S. L. C

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The Hyperphenylalaninemias of Man and Mouse von Scriver, C R, Eisensmith, R C, Woo, S L C, Kaufman, S

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Stabilization of transgenes delivered by recombinant adenovirus vectors through extrachromosomal replication von Krougliak, Valeri A., Krougliak, Natalia, Eisensmith, Randy C.

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Molecular correlations in phenylketonuria : Mutation patterns and corresponding biochemical and clinical phenotypes in a heterogeneous California population von ENNS, G. M, MARTINEZ, D. R, KUZMIN, A. I, KOCH, R, WAKEEM, C. K, WOO, S. L. C, EISENSMITH, R. C, PACKMAN, S

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A simple and efficient method for the concentration and purification of recombinant retrovirus for increased hepatocyte transduction in vivo von Bowles, N E, Eisensmith, R C, Mohuiddin, R, Pyron, M, Woo, S L

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Associations between mutations and a VNTR in the human phenylalanine hydroxylase gene von Goltsov, A A, Eisensmith, R C, Konecki, D S, Lichter-Konecki, U, Woo, S L

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A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria von Goltsov, Alexei A., Eisensmith, Randy C., Naughton, Eileen R., Jin, Li, Charkraborty, Ranajit, Woo, Savio L.C.

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In vivo gene therapy for hyperlipidemia: phenotypic correction in Watanabe rabbits by hepatic delivery of the rabbit LDL receptor gene von Li, J, Fang, B, Eisensmith, R C, Li, X H, Nasonkin, I, Lin-Lee, Y C, Mims, M P, Hughes, A, Montgomery, C D, Roberts, J D

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Molecular basis of phenylketonuria and related hyperphenylalaninemias: Mutations and polymorphisms in the human phenylalanine hydroxylase gene von Eisensmith, Randy C., Woo, Savio L. C.

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IFN-[gamma] Sensitization of Prostate Cancer Cells to Fas-Mediated Death: A Gene Therapy Approach von Selleck, William A, Canfield, Steven E, Hassen, Waleed A, Meseck, Marcia, Kuzmin, Alexei I, Eisensmith, Randy C, Chen, Shu-hsia, Hall, Simon J

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Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans von EISENSMITH, R. C, GOLTSOV, A. A, GÜTTLER, F, GULDBERG, P, EIKEN, H. G, APOLD, J, SVENSSON, E, NAUGHTEN, E, CAHALANE, S. F, CROKE, D. T, COCKBURN, F, WOO, S. L. C, O'NEILL, C, TYFIELD, L. A, SCHWARTZ, E. I, KUZMIN, A. I, BARANOVSKAYA, S. S, TSUKERMAN, G. L, TREACY, E, SCRIVER, C. R

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Phenylketonuria missense mutations in the Mediterranean von Okano, Yoshiyuki, Wang, Tao, Eisensmith, Randy C., Longhi, Riccardo, Riva, Enrica, Giovannini, Marcello, Cerone, Roberto, Romano, Cesare, Woo, Savio L.C.

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Founder Effect of a Prevalent Phenylketonuria Mutation in the Oriental Population von Wang, Tao, Okano, Yoshiyuki, Eisensmith, Randy C., Harvey, Michele L., Wilson H. Y. Lo, Huang, Shu-Zhen, Zeng, Yi-Tao, Yuan, Li-Fang, Furuyama, Jun-Ichi, Oura, Toshiaki, Sommer, Steve S., Savio L. C. Woo

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A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria von Eisensmith, Randy C., Goltsov, Alexei A., Woo, Savio L. C.

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Recurrent mutation on the human phenylalanine hydroxylase gene von OKANO, Y, WANG, T, EISENSMITH, R. C, GÜTTLER, F, WOO, S. L. C

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