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Human, Mouse, and Rat Calnexin cDNA Cloning: Identification of Potential Calcium Binding Motifs and Gene Localization to Human Chromosome 5

Biochemistry (Easton), 1994-03, Vol.33 (11), p.3229-3236

1994

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Cloning and expression of the murine gene and chromosomal location of the human gene encoding N-acetylglucosaminyltransferase I

Glycobiology (Oxford), 1992-08, Vol.2 (4), p.383-393

1992

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Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35

Diabetes (New York, N.Y.), 1987-04, Vol.36 (4), p.546-549

1987

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Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogene-like sequence (GLUT6)

The Journal of biological chemistry, 1990-08, Vol.265 (22), p.13276-13282

1990

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Identification of a Distinct Type IV Collagen α Chain with Restricted Kidney Distribution and Assignment of its Gene to the Locus of X Chromosome-Linked Alport Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1990-02, Vol.87 (4), p.1606-1610

1990

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Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13

Diabetes (New York, N.Y.), 1989-08, Vol.38 (8), p.1072-1075

1989

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Two chromosomal locations for human ornithine decarboxylase gene sequences and elevated expression in colorectal neoplasia

Cancer research (Chicago, Ill.), 1990-10, Vol.50 (19), p.6146-6153

1990

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Complete amino acid sequence of human cartilage link protein ( CRTL1) deduced from cDNA clones and chromosomal assignment of the gene

Genomics (San Diego, Calif.), 1990-11, Vol.8 (3), p.562-567

1990

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Sequence, Tissue Distribution, and Chromosomal Localization of mRNA Encoding a Human Glucose Transporter-Like Protein

Proceedings of the National Academy of Sciences - PNAS, 1988-08, Vol.85 (15), p.5434-5438

1988

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Chromosome mapping and organization of the human β-galactoside α2,6-sialyltransferase gene : differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

The Journal of biological chemistry, 1993-02, Vol.268 (6), p.4355-4361

1993

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Cloning of human lysyl hydroxylase: Complete cDNA-derived amino acid sequence and assignment of the gene ( PLOD) to chromosome 1p36.3→p36.2

Genomics (San Diego, Calif.), 1992-05, Vol.13 (1), p.62-69

1992

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Cloning of Human and Mouse EBI1, a Lymphoid-Specific G-Protein-Coupled Receptor Encoded on Human Chromosome 17q12-q21.2

Genomics (San Diego, Calif.), 1994-10, Vol.23 (3), p.643-650

1994

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Gastric inhibitory polypeptide: structure and chromosomal localization of the human gene

Molecular endocrinology (Baltimore, Md.), 1989-06, Vol.3 (6), p.1014-1021

1989

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Characterization of a novel tumor necrosis factor-alpha-induced endothelial primary response gene

The Journal of biological chemistry, 1992-01, Vol.267 (2), p.1317-1326

1992

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The Genes for the Lipopolysaccharide Binding Protein (LBP) and the Bactericidal Permeability Increasing Protein (BPI) Are Encoded in the Same Region of Human Chromosome 20

Genomics (San Diego, Calif.), 1993, Vol.15 (1), p.188-190

1993

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Structure of the human lipoprotein-associated coagulation inhibitor gene. Intro/exon gene organization and localization of the gene to chromosome 2

The Journal of biological chemistry, 1991-03, Vol.266 (8), p.5036-5041

1991

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Structure and chromosomal location of the human gene encoding cartilage matrix protein

The Journal of biological chemistry, 1990-11, Vol.265 (32), p.19624-19631

1990

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Cloning of human heparan sulfate proteoglycan core protein, assignment of the gene ( HSPG2) to 1p36.1→p35 and identification of a BamHI restriction fragment length polymorphism

Genomics (San Diego, Calif.), 1991-10, Vol.11 (2), p.389-396

1991

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Human collagen gene COL5A1 maps to the q34.2→q34.3 region of chromosome 9, near the locus for nail-patella syndrome

Genomics (San Diego, Calif.), 1992-04, Vol.12 (4), p.836-837

1992

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Human Metallothionein Genes are Clustered on Chromosome 16

Proceedings of the National Academy of Sciences - PNAS, 1984-09, Vol.81 (17), p.5494-5498

1984

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The TCF8 gene encoding a zinc finger protein (Nil-2-a) resides on human chromosome 10p11.2

Genomics (San Diego, Calif.), 1992-09, Vol.14 (1), p.194-196

1992

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The human T-cell leukemia virus-related endogenous sequence ( HRES1) is located on chromosome 1 at q42

Genomics (San Diego, Calif.), 1991-12, Vol.11 (4), p.1172-1173

1991

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Cloning of a Portion of the Chromosomal Gene and cDNA for Human β-Fodrin, the Nonerythroid Form of β-Spectrin

Genomics (San Diego, Calif.), 1993-08, Vol.17 (2), p.287-293

1993

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Sialidosis and Galactosialidosis: Chromosomal Assignment of Two Genes Associated with Neuraminidase-Deficiency Disorders

Proceedings of the National Academy of Sciences - PNAS, 1986-03, Vol.83 (6), p.1817-1821

1986

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A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs

American journal of human genetics, 1991-04, Vol.48 (4), p.687-695

1991

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Human, Mouse, and Rat Calnexin cDNA Cloning: Identification of Potential Calcium Binding Motifs and Gene Localization to Human Chromosome 5

Cloning and expression of the murine gene and chromosomal location of the human gene encoding N-acetylglucosaminyltransferase I

Polymorphic human glucose transporter gene (GLUT) is on chromosome 1p31.3----p35

Human facilitative glucose transporters. Isolation, functional characterization, and gene localization of cDNAs encoding an isoform (GLUT5) expressed in small intestine, kidney, muscle, and adipose tissue and an unusual glucose transporter pseudogene-like sequence (GLUT6)

Identification of a Distinct Type IV Collagen α Chain with Restricted Kidney Distribution and Assignment of its Gene to the Locus of X Chromosome-Linked Alport Syndrome

Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13

Two chromosomal locations for human ornithine decarboxylase gene sequences and elevated expression in colorectal neoplasia

Complete amino acid sequence of human cartilage link protein ( CRTL1) deduced from cDNA clones and chromosomal assignment of the gene

Sequence, Tissue Distribution, and Chromosomal Localization of mRNA Encoding a Human Glucose Transporter-Like Protein

Chromosome mapping and organization of the human β-galactoside α2,6-sialyltransferase gene : differential and cell-type specific usage of upstream exon sequences in B-lymphoblastoid cells

Cloning of human lysyl hydroxylase: Complete cDNA-derived amino acid sequence and assignment of the gene ( PLOD) to chromosome 1p36.3→p36.2

Cloning of Human and Mouse EBI1, a Lymphoid-Specific G-Protein-Coupled Receptor Encoded on Human Chromosome 17q12-q21.2

Gastric inhibitory polypeptide: structure and chromosomal localization of the human gene

Characterization of a novel tumor necrosis factor-alpha-induced endothelial primary response gene

The Genes for the Lipopolysaccharide Binding Protein (LBP) and the Bactericidal Permeability Increasing Protein (BPI) Are Encoded in the Same Region of Human Chromosome 20

Structure of the human lipoprotein-associated coagulation inhibitor gene. Intro/exon gene organization and localization of the gene to chromosome 2

Structure and chromosomal location of the human gene encoding cartilage matrix protein

Cloning of human heparan sulfate proteoglycan core protein, assignment of the gene ( HSPG2) to 1p36.1→p35 and identification of a BamHI restriction fragment length polymorphism

Human collagen gene COL5A1 maps to the q34.2→q34.3 region of chromosome 9, near the locus for nail-patella syndrome

Human Metallothionein Genes are Clustered on Chromosome 16

The TCF8 gene encoding a zinc finger protein (Nil-2-a) resides on human chromosome 10p11.2

The human T-cell leukemia virus-related endogenous sequence ( HRES1) is located on chromosome 1 at q42

Cloning of a Portion of the Chromosomal Gene and cDNA for Human β-Fodrin, the Nonerythroid Form of β-Spectrin

Sialidosis and Galactosialidosis: Chromosomal Assignment of Two Genes Associated with Neuraminidase-Deficiency Disorders

A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs

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