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Identification of Four Novel Human Genes Amplified and Overexpressed in Breast Carcinoma and Localized to the q11-q21.3 Region of Chromosome 17

Genomics (San Diego, Calif.), 1995-08, Vol.28 (3), p.367-376

1995

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Identification of a new collagen IV chain, alpha 6(IV), by cDNA isolation and assignment of the gene to chromosome Xq22, which is the same locus for COL4A5

The Journal of biological chemistry, 1994-03, Vol.269 (10), p.7520-7526

1994

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G.O.5 Partial functionality of a Mini-dysferlin molecule identified in a patient affected with moderately severe primary dysferlinopathy

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.781-781

2008

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Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporter

Cytogenetic and genome research, 2001-01, Vol.92 (3-4), p.264-270

2001

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CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene

The Journal of immunology (1950), 1993-06, Vol.150 (12), p.5445-5456

1993

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Localization of a Novel Ryanodine Receptor Gene (RYR3) to Human Chromosome 15q14-q15 by in Situ Hybridization

Genomics (San Diego, Calif.), 1993-10, Vol.18 (1), p.163-165

1993

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Genomic organization and chromosomal localization of the murine epididymal retinoic acid-binding protein (mE-RABP) gene

Molecular reproduction and development, 1998-08, Vol.50 (4), p.387-395

1998

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Identification and in situ hybridization mapping of a mouse Tpd52l1 (D53) orthologue to chromosome 10A4-B2

Cytogenetic and genome research, 1998-01, Vol.81 (3-4), p.199-201

1998

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Cloning of Two Novel ABC Transporters Mapping on Human Chromosome 9

Genomics (San Diego, Calif.), 1994-05, Vol.21 (1), p.150-159

1994

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Cloning of the cDNA Encoding Human Tissue Inhibitor of Metalloproteinases-3 (TIMP-3) and Mapping of the TIMP3 Gene to Chromosome 22

Genomics (San Diego, Calif.), 1994-01, Vol.19 (1), p.86-90

1994

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Assignment of the Human Tear Lipocalin Gene (LCN1) to 9q34 by in Situ Hybridization

Genomics (San Diego, Calif.), 1993-10, Vol.18 (1), p.160-161

1993

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Myelin/Oligodendrocyte Glycoprotein is a Member of a Subset of the Immunoglobulin Superfamily Encoded within the Major Histocompatibility Complex

Proceedings of the National Academy of Sciences - PNAS, 1993-09, Vol.90 (17), p.7990-7994

1993

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Structure, mapping and expression of a growth factor inducible gene encoding a putative nuclear hormonal binding receptor

The EMBO journal, 1989-11, Vol.8 (11), p.3327-3335

1989

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Programmed cell death is affected in the novel mouse mutant Fused toes (Ft)

Development (Cambridge), 1994-09, Vol.120 (9), p.2601-2607

1994

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Definition of the tumor protein D52 (TPD52) gene family through cloning of D52 homologues in human (hD53) and mouse (mD52)

Genomics (San Diego, Calif.), 1996-08, Vol.35 (3), p.523-532

1996

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Molecular characterization of the mouse beta 3‐adrenergic receptor: relationship with the atypical receptor of adipocytes

The EMBO journal, 1991-12, Vol.10 (12), p.3721-3727

1991

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The characterization of the promoter of the gene encoding the p50 subunit of NF‐kappa B indicates that it participates in its own regulation

The EMBO journal, 1992-01, Vol.11 (1), p.195-203

1992

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Human Type VII Collagen: cDNA Cloning and Chromosomal Mapping of the Gene

Proceedings of the National Academy of Sciences - PNAS, 1991-08, Vol.88 (16), p.6931-6935

1991

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Assignment of Vascular Endothelial Growth Factor (VEGF) and Placenta Growth Factor (PlGF) Genes to Human Chromosome 6p12–p21 and 14q24–q31 Regions, Respectively

Genomics (San Diego, Calif.), 1996-02, Vol.32 (1), p.168-169

1996

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Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation

American journal of medical genetics. Part A, 2005-04, Vol.134A (1), p.39-44

2005

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Structural Organization of the Porcine and Human Genes Coding for a Leydig Cell-Specific Insulin-like Peptide (LEY I-L) and Chromosomal Localization of the Human Gene (INSL3)

Genomics (San Diego, Calif.), 1994-03, Vol.20 (1), p.13-19

1994

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Cloning of Human Striatin cDNA (STRN), Gene Mapping to 2p22–p21, and Preferential Expression in Brain

Genomics (San Diego, Calif.), 1998-07, Vol.51 (1), p.136-139

1998

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Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation: Unusual Phenotype With Progressive Vertebral Fusion

American journal of medical genetics. Part A, 2005-04, Vol.134A (1), p.39-44

2005

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Characterization of cDNAs Encoding Human Leukosialin and Localization of the Leukosialin Gene to Chromosome 16

Proceedings of the National Academy of Sciences - PNAS, 1989-02, Vol.86 (4), p.1328-1332

1989

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Localization of new genes and markers to the distal part of the human major histocompatibility complex (MHC) region and comparison with the mouse: new insights into the evolution of mammalian genomes

Genomics (San Diego, Calif.), 1995-03, Vol.26 (1), p.9-20

1995

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Identification of Four Novel Human Genes Amplified and Overexpressed in Breast Carcinoma and Localized to the q11-q21.3 Region of Chromosome 17

Identification of a new collagen IV chain, alpha 6(IV), by cDNA isolation and assignment of the gene to chromosome Xq22, which is the same locus for COL4A5

G.O.5 Partial functionality of a Mini-dysferlin molecule identified in a patient affected with moderately severe primary dysferlinopathy

Comparative analysis of the promoter structure and genomic organization of the human and mouse ABCA7 gene encoding a novel ABCA transporter

CTLA-8, cloned from an activated T cell, bearing AU-rich messenger RNA instability sequences, and homologous to a herpesvirus saimiri gene

Localization of a Novel Ryanodine Receptor Gene (RYR3) to Human Chromosome 15q14-q15 by in Situ Hybridization

Genomic organization and chromosomal localization of the murine epididymal retinoic acid-binding protein (mE-RABP) gene

Identification and in situ hybridization mapping of a mouse Tpd52l1 (D53) orthologue to chromosome 10A4-B2

Cloning of Two Novel ABC Transporters Mapping on Human Chromosome 9

Cloning of the cDNA Encoding Human Tissue Inhibitor of Metalloproteinases-3 (TIMP-3) and Mapping of the TIMP3 Gene to Chromosome 22

Assignment of the Human Tear Lipocalin Gene (LCN1) to 9q34 by in Situ Hybridization

Myelin/Oligodendrocyte Glycoprotein is a Member of a Subset of the Immunoglobulin Superfamily Encoded within the Major Histocompatibility Complex

Structure, mapping and expression of a growth factor inducible gene encoding a putative nuclear hormonal binding receptor

Programmed cell death is affected in the novel mouse mutant Fused toes (Ft)

Definition of the tumor protein D52 (TPD52) gene family through cloning of D52 homologues in human (hD53) and mouse (mD52)

Molecular characterization of the mouse beta 3‐adrenergic receptor: relationship with the atypical receptor of adipocytes

The characterization of the promoter of the gene encoding the p50 subunit of NF‐kappa B indicates that it participates in its own regulation

Human Type VII Collagen: cDNA Cloning and Chromosomal Mapping of the Gene

Assignment of Vascular Endothelial Growth Factor (VEGF) and Placenta Growth Factor (PlGF) Genes to Human Chromosome 6p12–p21 and 14q24–q31 Regions, Respectively

Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation

Structural Organization of the Porcine and Human Genes Coding for a Leydig Cell-Specific Insulin-like Peptide (LEY I-L) and Chromosomal Localization of the Human Gene (INSL3)

Cloning of Human Striatin cDNA (STRN), Gene Mapping to 2p22–p21, and Preferential Expression in Brain

Unusual phenotype with progressive vertebral fusion in a girl with an apparently balanced t(10;20)(p11;p13) translocation: Unusual Phenotype With Progressive Vertebral Fusion

Characterization of cDNAs Encoding Human Leukosialin and Localization of the Leukosialin Gene to Chromosome 16

Localization of new genes and markers to the distal part of the human major histocompatibility complex (MHC) region and comparison with the mouse: new insights into the evolution of mammalian genomes

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