A novel system for the production of fully deleted adenovirus vectors that does not require helper adenovirus
CHESHENKO, N, KROUGLIAK, N, EISENSMITH, R. C, KROUGLIAK, V. A
Published in Gene therapy (01.06.2001)
Published in Gene therapy (01.06.2001)
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Lack of persistence of E1- recombinant adenoviral vectors containing a temperature-sensitive E2A mutation in immunocompetent mice and hemophilia B dogs
Fang, B, Wang, H, Gordon, G, Bellinger, D A, Read, M S, Brinkhous, K M, Woo, S L, Eisensmith, R C
Published in Gene therapy (01.03.1996)
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Published in Gene therapy (01.03.1996)
Journal Article
Gene therapy for hemophilia B: host immunosuppression prolongs the therapeutic effect of adenovirus-mediated factor IX expression
Fang, B, Eisensmith, R C, Wang, H, Kay, M A, Cross, R E, Landen, C N, Gordon, G, Bellinger, D A, Read, M S, Hu, P C
Published in Human gene therapy (01.08.1995)
Published in Human gene therapy (01.08.1995)
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Journal Article
A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria
Goltsov, A A, Eisensmith, R C, Naughton, E R, Jin, L, Chakraborty, R, Woo, S L
Published in Human molecular genetics (01.05.1993)
Published in Human molecular genetics (01.05.1993)
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Journal Article
Molecular basis of phenylketonuria and a correlation between genotype and phenotype in a heterogeneous southeastern US population
Eisensmith, R C, Martinez, D R, Kuzmin, A I, Goltsov, A A, Brown, A, Singh, R, Elsas LJ, I I, Woo, S L
Published in Pediatrics (Evanston) (01.04.1996)
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Published in Pediatrics (Evanston) (01.04.1996)
Journal Article
Haplotypes and mutations of the PAH locus in Egyptian families with PKU
Effat, L, Kuzmin, A, Kasem, N, Meguid, N A, Kotb, S, Eisensmith, R C, Temtamy, S A, Rushdi, S, Woo, S, el-Awady, M
Published in European journal of human genetics : EJHG (01.02.1999)
Published in European journal of human genetics : EJHG (01.02.1999)
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Journal Article
Multiple origins for phenylketonuria in Europe
EISENSMITH, R. C, OKANO, Y, HAGENFELDT, L, REY, F, MUNNICH, A, LYONNET, S, COCKBURN, F, CONNOR, J. M, PEMBREY, M. E, SMITH, I, GITZELMAN, R, STEINMANN, B, DASOVICH, M, APOLD, J, EIKEN, H. G, GIOVANNINI, M, RIVA, E, LONGHI, R, ROMANO, C, CERONE, R, NAUGHTEN, E. R, MULLINS, C, CAHALANE, S, WANG, T, OZALP, I, FEKETE, G, SCHULER, D, BERENCSI, G. Y, GÜTTLER, F, NASZ, I, BRDICKA, R, KAMARYT, J, PIJACKOVA, A, CABALSKA, B, BOSZKOWA, K, SCHWARTZ, E, KALININ, V. N, JIN, L, CHAKRABORTY, R, LOU, H, WOO, S. L. C, GULDBERG, P, LICHTER-KONECKI, U, KONECKI, D. S, SVENSSON, E
Published in American journal of human genetics (01.12.1992)
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Published in American journal of human genetics (01.12.1992)
Journal Article
Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans
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
Published in American journal of human genetics (1995)
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Published in American journal of human genetics (1995)
Journal Article
Molecular correlations in phenylketonuria : Mutation patterns and corresponding biochemical and clinical phenotypes in a heterogeneous California population
ENNS, G. M, MARTINEZ, D. R, KUZMIN, A. I, KOCH, R, WAKEEM, C. K, WOO, S. L. C, EISENSMITH, R. C, PACKMAN, S
Published in Pediatric research (01.11.1999)
Published in Pediatric research (01.11.1999)
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Journal Article
Gene therapy for phenylketonuria
Eisensmith, R C, Woo, S L
Published in Acta pædiatrica (Oslo, Norway : 1992). Supplement (01.12.1994)
Published in Acta pædiatrica (Oslo, Norway : 1992). Supplement (01.12.1994)
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Journal Article
Founder Effect of a Prevalent Phenylketonuria Mutation in the Oriental Population
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
Published in Proceedings of the National Academy of Sciences - PNAS (15.03.1991)
Published in Proceedings of the National Academy of Sciences - PNAS (15.03.1991)
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