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A canine chromosome 7 locus confers compulsive disorder susceptibility

Molecular psychiatry, 2010-01, Vol.15 (1), p.8-10

2010

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Vasopressin V1b receptor knockout reduces aggressive behavior in male mice

Molecular psychiatry, 2002-01, Vol.7 (9), p.975-984

2002

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Consequences of β-glucocerebrosidase deficiency in epidermis : ultrastructure and permeability barrier alterations in Gaucher disease

The Journal of clinical investigation, 1994-04, Vol.93 (4), p.1756-1764

1994

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Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene

Nature (London), 1992-06, Vol.357 (6377), p.407-410

1992

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Disruption of sonic hedgehog signaling in Ellis-van Creveld dwarfism confers protection against bipolar affective disorder

Molecular psychiatry, 2015-10, Vol.20 (10), p.1212-1218

2015

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A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

Nature genetics, 1996-04, Vol.12 (4), p.431-435

1996

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Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher disease

Genome research, 1997-10, Vol.7 (10), p.1020-1026

1997

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Prolonged ethanol inhalation decreases gamma-aminobutyric acidA receptor alpha subunit mRNAs in the rat cerebral cortex

Molecular pharmacology, 1991-02, Vol.39 (2), p.157-163

1991

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Association of an X-chromosome dodecamer insertional variant allele with mental retardation

Molecular psychiatry, 1998-07, Vol.3 (4), p.303-309

1998

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Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish

Nature (London), 1989-11, Vol.342 (6247), p.238-243

1989

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Production of antisera selective for m1 muscarinic receptors using fusion proteins: distribution of m1 receptors in rat brain

Molecular pharmacology, 1991-05, Vol.39 (5), p.643-649

1991

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Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease

Pediatric research, 1996, Vol.39 (1), p.134-141

1996

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Mice That Lack Thrombospondin 2 Display Connective Tissue Abnormalities That Are Associated with Disordered Collagen Fibrillogenesis, an Increased Vascular Density, and a Bleeding Diathesis

The Journal of cell biology, 1998-01, Vol.140 (2), p.419-430

1998

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Transgenic Expression of Green Fluorescent Protein in Mouse Oxytocin Neurones

Journal of neuroendocrinology, 1999-12, Vol.11 (12), p.935-939

1999

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Absence of a significant linkage between Na+,K+-ATPase subunit (ATP1A3 and ATP1B3) genotypes and bipolar affective disorder in the old-order Amish

American journal of medical genetics, 2001-04, Vol.105 (3), p.291-294

2001

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Human glucocerebrosidase: heterologous expression of active site mutants in murine null cells

Glycobiology (Oxford), 2000-11, Vol.10 (11), p.1217-1224

2000

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A Triplet Repeat on 17q Accounts for Most Expansions Detected by the Repeat-Expansion–Detection Technique

American journal of human genetics, 1998-06, Vol.62 (6), p.1548-1551

1998

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Isolation, Characterization, and Proteolysis of Human Prosaposin, the Precursor of Saposins (Sphingolipid Activator Proteins)

Archives of biochemistry and biophysics, 1993-07, Vol.304 (1), p.110-116

1993

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A new gene, EVC2, is mutated in Ellis–van Creveld syndrome

Molecular genetics and metabolism, 2002-12, Vol.77 (4), p.291-295

2002

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Metaxin, a Gene Contiguous to Both Thrombospondin 3 and Glucocerebrosidase, is Required for Embryonic Development in the Mouse: Implications for Gaucher Disease

Proceedings of the National Academy of Sciences - PNAS, 1995-05, Vol.92 (10), p.4547-4551

1995

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A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease

The New England journal of medicine, 1987-03, Vol.316 (10), p.570-575

1987

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The genomic structure and developmental expression patterns of the human OPA-containing gene (HOPA)

Human genetics, 1999-07, Vol.105 (1-2), p.174-178

1999

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Biosynthesis of the lysosomal enzyme glucocerebrosidase

The Journal of biological chemistry, 1985-11, Vol.260 (26), p.14319-14324

1985

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Structure and Organization of the Human Metaxin Gene (MTX) and Pseudogene

Genomics (San Diego, Calif.), 1996-04, Vol.33 (2), p.177-184

1996

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Mice with an Aspartylglucosaminuria Mutation Similar to Humans Replicate the Pathophysiology in Patients

Human molecular genetics, 1998-02, Vol.7 (2), p.265-272

1998

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A canine chromosome 7 locus confers compulsive disorder susceptibility

Vasopressin V1b receptor knockout reduces aggressive behavior in male mice

Consequences of β-glucocerebrosidase deficiency in epidermis : ultrastructure and permeability barrier alterations in Gaucher disease

Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene

Disruption of sonic hedgehog signaling in Ellis-van Creveld dwarfism confers protection against bipolar affective disorder

A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

Identification of three additional genes contiguous to the glucocerebrosidase locus on chromosome 1q21: implications for Gaucher disease

Prolonged ethanol inhalation decreases gamma-aminobutyric acidA receptor alpha subunit mRNAs in the rat cerebral cortex

Association of an X-chromosome dodecamer insertional variant allele with mental retardation

Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish

Production of antisera selective for m1 muscarinic receptors using fusion proteins: distribution of m1 receptors in rat brain

Epidermal abnormalities may distinguish type 2 from type 1 and type 3 of Gaucher disease

Mice That Lack Thrombospondin 2 Display Connective Tissue Abnormalities That Are Associated with Disordered Collagen Fibrillogenesis, an Increased Vascular Density, and a Bleeding Diathesis

Transgenic Expression of Green Fluorescent Protein in Mouse Oxytocin Neurones

Absence of a significant linkage between Na+,K+-ATPase subunit (ATP1A3 and ATP1B3) genotypes and bipolar affective disorder in the old-order Amish

Human glucocerebrosidase: heterologous expression of active site mutants in murine null cells

A Triplet Repeat on 17q Accounts for Most Expansions Detected by the Repeat-Expansion–Detection Technique

Isolation, Characterization, and Proteolysis of Human Prosaposin, the Precursor of Saposins (Sphingolipid Activator Proteins)

A new gene, EVC2, is mutated in Ellis–van Creveld syndrome

Metaxin, a Gene Contiguous to Both Thrombospondin 3 and Glucocerebrosidase, is Required for Embryonic Development in the Mouse: Implications for Gaucher Disease

A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease

The genomic structure and developmental expression patterns of the human OPA-containing gene (HOPA)

Biosynthesis of the lysosomal enzyme glucocerebrosidase

Structure and Organization of the Human Metaxin Gene (MTX) and Pseudogene

Mice with an Aspartylglucosaminuria Mutation Similar to Humans Replicate the Pathophysiology in Patients

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