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The Dual Specificity Phosphatases M3/6 and MKP-3 Are Highly Selective for Inactivation of Distinct Mitogen-activated Protein Kinases

The Journal of biological chemistry, 1996-11, Vol.271 (44), p.27205-27208

1996

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A Second Promoter Provides an Alternative Target for Therapeutic up-Regulation of Utrophin in Duchenne Muscular Dystrophy

Proceedings of the National Academy of Sciences - PNAS, 1999-11, Vol.96 (24), p.14025-14030

1999

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The Mitogen-activated Protein Kinase Phosphatase-3 N-terminal Noncatalytic Region Is Responsible for Tight Substrate Binding and Enzymatic Specificity

The Journal of biological chemistry, 1998-04, Vol.273 (15), p.9323-9329

1998

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Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy

European journal of human genetics : EJHG, 1998-09, Vol.6 (5), p.467-474

1998

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Genetic analysis of autoimmune type 1 diabetes mellitus in mice

Nature (London), 1991-06, Vol.351 (6327), p.542-547

1991

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Crosses of NOD mice with the related NON strain. A polygenic model for IDDM

Diabetes (New York, N.Y.), 1995-10, Vol.44 (10), p.1186-1195

1995

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Linkage on Chromosome 3 of Autoimmune Diabetes and Defective Fc Receptor for IgG in NOD Mice

Science (American Association for the Advancement of Science), 1993-04, Vol.260 (5108), p.695-698

1993

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Analysis of mutations in the tudor domain of the survival motor neuron protein SMN

European journal of human genetics : EJHG, 1999-07, Vol.7 (5), p.519-525

1999

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Pillars Article: Genetic Analysis of Autoimmune Type 1 Diabetes Mellitus in Mice. Nature. 1991. 351: 542-547

The Journal of immunology (1950), 2014-07, Vol.193 (1), p.7-12

2014

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Missense mutation clustering in the survival motor neuron gene : a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?

Human molecular genetics, 1997-03, Vol.6 (3), p.497-500

1997

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Reactivity of Cytosine and Thymine in Single-Base-Pair Mismatches with Hydroxylamine and Osmium Tetroxide and Its Application to the Study of Mutations

Proceedings of the National Academy of Sciences - PNAS, 1988-06, Vol.85 (12), p.4397-4401

1988

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Genetic analysis of autoimmune type 1 diabetes mellitus in mice. 1991

The Journal of immunology (1950), 2014-07, Vol.193 (1), p.7-12

2014

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Syntenic Organization of the Mouse Distal Chromosome 7 Imprinting Cluster and the Beckwith-Wiedemann Syndrome Region in Chromosome 11p15.5

Human molecular genetics, 1998-07, Vol.7 (7), p.1149-1159

1998

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Gene deletions in spinal muscular atrophy

Journal of medical genetics, 1996-02, Vol.33 (2), p.93-96

1996

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Linkage analysis of 84 microsatellite markers in intra- and interspecific backcrosses

Mammalian genome, 1992, Vol.3 (8), p.457-460

1992

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Characterization of Ngef, a Novel Member of the Dbl Family of Genes Expressed Predominantly in the Caudate Nucleus

Genomics (San Diego, Calif.), 2000-04, Vol.65 (1), p.53-61

2000

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Molecular characterization of the HLA‐linked steroid 21‐hydroxylase B gene from an individual with congenital adrenal hyperplasia

The EMBO journal, 1987-06, Vol.6 (6), p.1653-1661

1987

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Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype

Neuromuscular disorders : NMD, 1997-05, Vol.7 (3), p.198-201

1997

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Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy

Journal of medical genetics, 1996-12, Vol.33 (12), p.1019-1021

1996

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Prenatal diagnosis of spinal muscular atrophy by gene deletion analysis

The Lancet (British edition), 1995-04, Vol.345 (8956), p.1049-1049

1995

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Molecular Genetics of Autosomal Recessive Spinal Muscular Atrophy

Molecular medicine (Cambridge, Mass.), 1996-07, Vol.2 (4), p.400-404, Article 400

1996

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Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele

Journal of medical genetics, 1995-02, Vol.32 (2), p.93-96

1995

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Mouse chromosome 3

Mammalian genome, 1993, Vol.4 (S1), p.S47-S57

1993

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THE HUMAN CYTOCHROME P-450 21-HYDROXYLASE GENES

RODRIGUES, NANDA R

1987

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Mouse chromosome 3

Mammalian genome, 1992, Vol.3 Spec No (S1), p.S44-S54

1992

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The Dual Specificity Phosphatases M3/6 and MKP-3 Are Highly Selective for Inactivation of Distinct Mitogen-activated Protein Kinases

A Second Promoter Provides an Alternative Target for Therapeutic up-Regulation of Utrophin in Duchenne Muscular Dystrophy

The Mitogen-activated Protein Kinase Phosphatase-3 N-terminal Noncatalytic Region Is Responsible for Tight Substrate Binding and Enzymatic Specificity

Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy

Genetic analysis of autoimmune type 1 diabetes mellitus in mice

Crosses of NOD mice with the related NON strain. A polygenic model for IDDM

Linkage on Chromosome 3 of Autoimmune Diabetes and Defective Fc Receptor for IgG in NOD Mice

Analysis of mutations in the tudor domain of the survival motor neuron protein SMN

Pillars Article: Genetic Analysis of Autoimmune Type 1 Diabetes Mellitus in Mice. Nature. 1991. 351: 542-547

Missense mutation clustering in the survival motor neuron gene : a role for a conserved tyrosine and glycine rich region of the protein in RNA metabolism?

Reactivity of Cytosine and Thymine in Single-Base-Pair Mismatches with Hydroxylamine and Osmium Tetroxide and Its Application to the Study of Mutations

Genetic analysis of autoimmune type 1 diabetes mellitus in mice. 1991

Syntenic Organization of the Mouse Distal Chromosome 7 Imprinting Cluster and the Beckwith-Wiedemann Syndrome Region in Chromosome 11p15.5

Gene deletions in spinal muscular atrophy

Linkage analysis of 84 microsatellite markers in intra- and interspecific backcrosses

Characterization of Ngef, a Novel Member of the Dbl Family of Genes Expressed Predominantly in the Caudate Nucleus

Molecular characterization of the HLA‐linked steroid 21‐hydroxylase B gene from an individual with congenital adrenal hyperplasia

Gene conversion at the SMN locus in autosomal recessive spinal muscular atrophy does not predict a mild phenotype

Evidence for compound heterozygosity causing mild and severe forms of autosomal recessive spinal muscular atrophy

Prenatal diagnosis of spinal muscular atrophy by gene deletion analysis

Molecular Genetics of Autosomal Recessive Spinal Muscular Atrophy

Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele

Mouse chromosome 3

THE HUMAN CYTOCHROME P-450 21-HYDROXYLASE GENES

Mouse chromosome 3

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