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Identification of the gene responsible for Best macular dystrophy

Nature genetics, 1998-07, Vol.19 (3), p.241-247

1998

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Evaluation of 13 short tandem repeat loci for use in personal identification applications

American journal of human genetics, 1994-07, Vol.55 (1), p.175-189

1994

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A New Adenoviral Vector: Replacement of All Viral Coding Sequences with 28 kb of DNA Independently Expressing Both Full-Length Dystrophin and β -Galactosidase

Proceedings of the National Academy of Sciences - PNAS, 1996-06, Vol.93 (12), p.5731-5736

1996

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Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses

Human molecular genetics, 1995-01, Vol.4 (1), p.1-8

1995

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In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes

Gene therapy, 1996-11, Vol.3 (11), p.965

1996

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Hyperuricemia and urate nephropathy in urate oxidase-deficient mice

Proceedings of the National Academy of Sciences - PNAS, 1994-01, Vol.91 (2), p.742-746

1994

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Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats

Nature (London), 1993-08, Vol.364 (6439), p.717-721

1993

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DNA typing and genetic mapping with trimeric and tetrameric tandem repeats

American journal of human genetics, 1991-10, Vol.49 (4), p.746-756

1991

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Novel Proteins with Binding Specificity for DNA CTG Repeats And RNA Cug Repeats: Implications for Myotonic Dystrophy

Human molecular genetics, 1996-01, Vol.5 (1), p.115-121

1996

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Monitoring expression of genes involved in drug metabolism and toxicology using DNA microarrays

Physiological genomics, 2001-04, Vol.5 (4), p.161-170

2001

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Alu Polymerase Chain Reaction: A Method for Rapid Isolation of Human-Specific Sequences from Complex DNA Sources

Proceedings of the National Academy of Sciences - PNAS, 1989-09, Vol.86 (17), p.6686-6690

1989

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Identification of Urotensin II as the Endogenous Ligand for the Orphan G-Protein-Coupled Receptor GPR14

Biochemical and biophysical research communications, 1999-12, Vol.266 (1), p.174-178

1999

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Absence of expression of the FMR-1 gene in fragile X syndrome

Cell, 1991-08, Vol.66 (4), p.817-822

1991

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Cell, 1991-12, Vol.67 (6), p.1047-1058

1991

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Urate Oxidase: Primary Structure and Evolutionary Implications

Proceedings of the National Academy of Sciences - PNAS, 1989-12, Vol.86 (23), p.9412-9416

1989

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Rescue, Propagation, and Partial Purification of a Helper Virus-Dependent Adenovirus Vector

Proceedings of the National Academy of Sciences - PNAS, 1995-04, Vol.92 (9), p.3854-3858

1995

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An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy

Science (American Association for the Advancement of Science), 1992-03, Vol.255 (5049), p.1256-1258

1992

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Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies

Human genetics, 1999-06, Vol.104 (6), p.449-453

1999

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Characterization of the human cysteinyl leukotriene CysLT1 receptor

Nature (London), 1999-06, Vol.399 (6738), p.789-793

1999

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Triplet Repeat Mutations in Human Disease

Science (American Association for the Advancement of Science), 1992-05, Vol.256 (5058), p.784-789

1992

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Triplet repeat disorders: discussion of molecular mechanisms

Cellular and molecular life sciences : CMLS, 1999-08, Vol.55 (11), p.1432-1447

1999

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Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent

American journal of human genetics, 1995, Vol.56 (1), p.114-122

1995

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Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms

American journal of human genetics, 1991-11, Vol.49 (5), p.951-960

1991

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Identification of receptors for neuromedin U and its role in feeding

Nature (London), 2000-07, Vol.406 (6791), p.70-74

2000

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Decreased Expression of Myotonin-Protein Kinase Messenger RNA and Protein in Adult Form of Myotonic Dystrophy

Science (American Association for the Advancement of Science), 1993-04, Vol.260 (5105), p.235-238

1993

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Identification of the gene responsible for Best macular dystrophy

Evaluation of 13 short tandem repeat loci for use in personal identification applications

A New Adenoviral Vector: Replacement of All Viral Coding Sequences with 28 kb of DNA Independently Expressing Both Full-Length Dystrophin and β -Galactosidase

Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses

In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes

Hyperuricemia and urate nephropathy in urate oxidase-deficient mice

Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats

DNA typing and genetic mapping with trimeric and tetrameric tandem repeats

Novel Proteins with Binding Specificity for DNA CTG Repeats And RNA Cug Repeats: Implications for Myotonic Dystrophy

Monitoring expression of genes involved in drug metabolism and toxicology using DNA microarrays

Alu Polymerase Chain Reaction: A Method for Rapid Isolation of Human-Specific Sequences from Complex DNA Sources

Identification of Urotensin II as the Endogenous Ligand for the Orphan G-Protein-Coupled Receptor GPR14

Absence of expression of the FMR-1 gene in fragile X syndrome

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Urate Oxidase: Primary Structure and Evolutionary Implications

Rescue, Propagation, and Partial Purification of a Helper Virus-Dependent Adenovirus Vector

An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular Dystrophy

Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies

Characterization of the human cysteinyl leukotriene CysLT1 receptor

Triplet Repeat Mutations in Human Disease

Triplet repeat disorders: discussion of molecular mechanisms

Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent

Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms

Identification of receptors for neuromedin U and its role in feeding

Decreased Expression of Myotonin-Protein Kinase Messenger RNA and Protein in Adult Form of Myotonic Dystrophy

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