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A novel system for the production of fully deleted adenovirus vectors that does not require helper adenovirus

Gene therapy, 2001-06, Vol.8 (11), p.846-854

2001

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Evaluation of promoter strength for hepatic gene expression in vivo following adenovirus-mediated gene transfer

Gene therapy, 1996-09, Vol.3 (9), p.802

1996

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Macrophage depletion increases the safety, efficacy and persistence of adenovirus-mediated gene transfer in vivo

Gene therapy, 1997-04, Vol.4 (4), p.309-316

1997

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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

Gene therapy, 1996-03, Vol.3 (3), p.217

1996

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Gene therapy for hemophilia B: host immunosuppression prolongs the therapeutic effect of adenovirus-mediated factor IX expression

Human gene therapy, 1995-08, Vol.6 (8), p.1039-1044

1995

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Correction of obesity and diabetes in genetically obese mice by leptin gene therapy

Proceedings of the National Academy of Sciences - PNAS, 1996-12, Vol.93 (25), p.14804-14808

1996

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Gene therapy for phenylketonuria: phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer

Gene therapy, 1994-07, Vol.1 (4), p.247

1994

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A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria

Human molecular genetics, 1993-05, Vol.2 (5), p.577-581

1993

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Molecular basis of phenylketonuria and a correlation between genotype and phenotype in a heterogeneous southeastern US population

Pediatrics (Evanston), 1996-04, Vol.97 (4), p.512

1996

Volltextzugriff (PDF)

Viral vector-mediated gene therapy for hemophilia B

Thrombosis and haemostasis, 1997-07, Vol.78 (1), p.24

1997

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Molecular correlations in phenylketonuria : Mutation patterns and corresponding biochemical and clinical phenotypes in a heterogeneous California population

Pediatric research, 1999-11, Vol.46 (5), p.594-602

1999

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Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patients

European journal of pediatrics, 1993-02, Vol.152 (2), p.132-139

1993

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Updated listing of haplotypes at the human phenylalanine hydroxylase (PAH) locus

American journal of human genetics, 1992-12, Vol.51 (6), p.1445-1448

1992

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Multiple origins for phenylketonuria in Europe

American journal of human genetics, 1992-12, Vol.51 (6), p.1355-1365

1992

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Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans

American journal of human genetics, 1995, Vol.56 (1), p.278-286

1995

Volltextzugriff (PDF)

Detection of the Xmnl RFLP at the human PAH locus by PCR

Nucleic acids research, 1992-02, Vol.20 (4), p.927-927

1992

Volltextzugriff (PDF)

Haplotypes and mutations of the PAH locus in Egyptian families with PKU

European journal of human genetics : EJHG, 1999-02, Vol.7 (2), p.259-262

1999

Volltextzugriff (PDF)

A simple and efficient method for the concentration and purification of recombinant retrovirus for increased hepatocyte transduction in vivo

Human gene therapy, 1996-09, Vol.7 (14), p.1735-1742

1996

Volltextzugriff (PDF)

Somatic gene therapy for phenylketonuria and other hepatic deficiencies

Journal of inherited metabolic disease, 1996-01, Vol.19 (4), p.412-423

1996

Volltextzugriff (PDF)

Gene therapy for phenylketonuria

European journal of pediatrics, 1996-07, Vol.155 Suppl 1 (S1), p.S16-S19

1996

Volltextzugriff (PDF)

Founder Effect of a Prevalent Phenylketonuria Mutation in the Oriental Population

Proceedings of the National Academy of Sciences - PNAS, 1991-03, Vol.88 (6), p.2146-2150

1991

Volltextzugriff (PDF)

Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria

The New England journal of medicine, 1991-05, Vol.324 (18), p.1232-1238

1991

Volltextzugriff (PDF)

Gene therapy for phenylketonuria

Acta Paediatrica, 1994-12, Vol.83 (s407), p.124-129

1994

Volltextzugriff (PDF)

Population genetics of phenylketonuria

Acta Paediatrica, 1994-12, Vol.83 (s407), p.19-26

1994

Volltextzugriff (PDF)

Phenylketonuria missense mutations in the Mediterranean

Genomics (San Diego, Calif.), 1991, Vol.9 (1), p.96-103

1991

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A novel system for the production of fully deleted adenovirus vectors that does not require helper adenovirus

Evaluation of promoter strength for hepatic gene expression in vivo following adenovirus-mediated gene transfer

Macrophage depletion increases the safety, efficacy and persistence of adenovirus-mediated gene transfer in vivo

Lack of persistence of E1- recombinant adenoviral vectors containing a temperature-sensitive E2A mutation in immunocompetent mice and hemophilia B dogs

Gene therapy for hemophilia B: host immunosuppression prolongs the therapeutic effect of adenovirus-mediated factor IX expression

Correction of obesity and diabetes in genetically obese mice by leptin gene therapy

Gene therapy for phenylketonuria: phenotypic correction in a genetically deficient mouse model by adenovirus-mediated hepatic gene transfer

A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria

Molecular basis of phenylketonuria and a correlation between genotype and phenotype in a heterogeneous southeastern US population

Viral vector-mediated gene therapy for hemophilia B

Molecular correlations in phenylketonuria : Mutation patterns and corresponding biochemical and clinical phenotypes in a heterogeneous California population

Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patients

Updated listing of haplotypes at the human phenylalanine hydroxylase (PAH) locus

Multiple origins for phenylketonuria in Europe

Recurrence of the R408W mutation in the phenylalanine hydroxylase locus in Europeans

Detection of the Xmnl RFLP at the human PAH locus by PCR

Haplotypes and mutations of the PAH locus in Egyptian families with PKU

A simple and efficient method for the concentration and purification of recombinant retrovirus for increased hepatocyte transduction in vivo

Somatic gene therapy for phenylketonuria and other hepatic deficiencies

Gene therapy for phenylketonuria

Founder Effect of a Prevalent Phenylketonuria Mutation in the Oriental Population

Molecular Basis of Phenotypic Heterogeneity in Phenylketonuria

Gene therapy for phenylketonuria

Population genetics of phenylketonuria

Phenylketonuria missense mutations in the Mediterranean

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