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Human transcription factor GATA-2. Evidence for regulation of preproendothelin-1 gene expression in endothelial cells

The Journal of biological chemistry, 1992-01, Vol.267 (2), p.1279-1285

1992

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Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11

The Journal of biological chemistry, 1992-05, Vol.267 (13), p.9281-9288

1992

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Human neutrophil cytochrome b light chain (p22-phox) : gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

The Journal of clinical investigation, 1990-11, Vol.86 (5), p.1729-1737

1990

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Amyloid $\beta $ Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage near the Alzheimer Locus

Science (American Association for the Advancement of Science), 1987-02, Vol.235 (4791), p.880-884

1987

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Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene

Science (American Association for the Advancement of Science), 1990-11, Vol.250 (4983), p.1000-1002

1990

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The Major Human Erythroid DNA-Binding Protein (GF-1): Primary Sequence and Localization of the Gene to the X Chromosome

Proceedings of the National Academy of Sciences - PNAS, 1990-01, Vol.87 (2), p.668-672

1990

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Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1

Journal of medical genetics, 2005-08, Vol.42 (8), p.666-672

2005

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Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

Nature (London), 1990-02, Vol.343 (6260), p.774-778

1990

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X-Linked Retinitis Pigmentosa: Mutation Spectrum of the RPGR and RP2 Genes and Correlation with Visual Function

Investigative ophthalmology & visual science, 2000-08, Vol.41 (9), p.2712-2721

2000

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Role for the Wilms Tumor Gene in Genital Development?

Proceedings of the National Academy of Sciences - PNAS, 1990-07, Vol.87 (14), p.5383-5386

1990

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Isolation, characterization, and mapping to chromosome 19 of the human apolipoprotein E gene

The Journal of biological chemistry, 1985-05, Vol.260 (10), p.6240-6247

1985

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Molecular Characterization of Sialophorin (CD43), the Lymphocyte Surface Sialoglycoprotein Defective in Wiskott-Aldrich Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1989-04, Vol.86 (8), p.2819-2823

1989

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Human profilin. Molecular cloning, sequence comparison, and chromosomal analysis

The Journal of biological chemistry, 1988-04, Vol.263 (12), p.5910-5915

1988

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Human Von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal Localization

Science (American Association for the Advancement of Science), 1985-06, Vol.228 (4706), p.1401-1406

1985

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Human complement factor I: analysis of cDNA-derived primary structure and assignment of its gene to chromosome 4

The Journal of biological chemistry, 1987-07, Vol.262 (21), p.10065-10071

1987

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Human Inhibitor of the First Component of Complement, C1: Characterization of cDNA Clones and Localization of the Gene to Chromosome 11

Proceedings of the National Academy of Sciences - PNAS, 1986-05, Vol.83 (10), p.3161-3165

1986

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Homozygosity of chromosome 13 in retinoblastoma

The New England journal of medicine, 1984-03, Vol.310 (9), p.550-553

1984

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The genomic organization and expression of the WT1 gene

Genomics (San Diego, Calif.), 1992-04, Vol.12 (4), p.807-813

1992

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Microdeletions in patients with Gusher-associated, X-linked mixed deafness (DFN3)

American journal of human genetics, 1992-07, Vol.51 (1), p.38-44

1992

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Report of the committee on the genetic constitution of chromosome 1

Cytogenetic and genome research, 1989-01, Vol.51 (1-4), p.67-90

1989

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Human serum amyloid P component. cDNA isolation, complete sequence of pre-serum amyloid P component, and localization of the gene to chromosome 1

The Journal of biological chemistry, 1985-06, Vol.260 (12), p.7752-7756

1985

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The β -subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus

Nature (London), 1986-06, Vol.321 (6073), p.882-887

1986

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Isolation and characterization of a cDNA that encodes the peptide core of the secretory granule proteoglycan of human promyelocytic leukemia HL-60 cells

The Journal of biological chemistry, 1988-05, Vol.263 (15), p.7287-7291

1988

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A complement receptor locus: genes encoding C3b/C4b receptor and C3d/Epstein-Barr virus receptor map to 1q32

The Journal of immunology (1950), 1987-01, Vol.138 (1), p.312-315

1987

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The Gene Encoding the ε Subunit of the T3/T-Cell Receptor Complex Maps to Chromosome 11 in Humans and to Chromosome 9 in Mice

Proceedings of the National Academy of Sciences - PNAS, 1987-03, Vol.84 (6), p.1664-1668

1987

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Human transcription factor GATA-2. Evidence for regulation of preproendothelin-1 gene expression in endothelial cells

Cloning and characterization of two human skeletal muscle alpha-actinin genes located on chromosomes 1 and 11

Human neutrophil cytochrome b light chain (p22-phox) : gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease

Amyloid $\beta $ Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage near the Alzheimer Locus

Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene

The Major Human Erythroid DNA-Binding Protein (GF-1): Primary Sequence and Localization of the Gene to the X Chromosome

Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1

Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping

X-Linked Retinitis Pigmentosa: Mutation Spectrum of the RPGR and RP2 Genes and Correlation with Visual Function

Role for the Wilms Tumor Gene in Genital Development?

Isolation, characterization, and mapping to chromosome 19 of the human apolipoprotein E gene

Molecular Characterization of Sialophorin (CD43), the Lymphocyte Surface Sialoglycoprotein Defective in Wiskott-Aldrich Syndrome

Human profilin. Molecular cloning, sequence comparison, and chromosomal analysis

Human Von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal Localization

Human complement factor I: analysis of cDNA-derived primary structure and assignment of its gene to chromosome 4

Human Inhibitor of the First Component of Complement, C1: Characterization of cDNA Clones and Localization of the Gene to Chromosome 11

Homozygosity of chromosome 13 in retinoblastoma

The genomic organization and expression of the WT1 gene

Microdeletions in patients with Gusher-associated, X-linked mixed deafness (DFN3)

Report of the committee on the genetic constitution of chromosome 1

Human serum amyloid P component. cDNA isolation, complete sequence of pre-serum amyloid P component, and localization of the gene to chromosome 1

The β -subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus

Isolation and characterization of a cDNA that encodes the peptide core of the secretory granule proteoglycan of human promyelocytic leukemia HL-60 cells

A complement receptor locus: genes encoding C3b/C4b receptor and C3d/Epstein-Barr virus receptor map to 1q32

The Gene Encoding the ε Subunit of the T3/T-Cell Receptor Complex Maps to Chromosome 11 in Humans and to Chromosome 9 in Mice

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