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A Maternally Methylated CpG Island in KvLQT1 Is Associated with an Antisense Paternal Transcript and Loss of Imprinting in Beckwith-Wiedemann Syndrome

Proceedings of the National Academy of Sciences - PNAS, 1999-07, Vol.96 (14), p.8064-8069

1999

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Human Laminin M Chain (Merosin): Complete Primary Structure, Chromosomal Assignment, and Expression of the M and A Chain in Human Fetal Tissues

The Journal of cell biology, 1994-02, Vol.124 (3), p.381-394

1994

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NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia

Cancer research (Chicago, Ill.), 1998-10, Vol.58 (19), p.4269-4273

1998

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The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons

The Journal of neuroscience, 1995-07, Vol.15 (7), p.4762-4785

1995

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A Truncated Laminin Chain Homologous to the B2 Chain: Structure, Spatial Expression, and Chromosomal Assignment

The Journal of cell biology, 1992-11, Vol.119 (3), p.679-693

1992

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Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues

The Journal of biological chemistry, 1988-10, Vol.263 (30), p.15245-15248

1988

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A Human Amphotropic Retrovirus Receptor is a Second Member of the Gibbon Ape Leukemia Virus Receptor Family

Proceedings of the National Academy of Sciences - PNAS, 1994-02, Vol.91 (3), p.1168-1172

1994

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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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Fine Structure Analysis of the WT1 Gene in Sporadic Wilms Tumors

Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3554-3558

1994

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A Model System to Study Genomic Imprinting of Human Genes

Proceedings of the National Academy of Sciences - PNAS, 1998-12, Vol.95 (25), p.14857-14862

1998

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Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa

Biology of reproduction, 2000-08, Vol.63 (2), p.469-481

2000

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The human neurokinin A (substance K) receptor. Molecular cloning of the gene, chromosome localization, and isolation of cDNA from tracheal and gastric tissues

The Journal of biological chemistry, 1990-11, Vol.265 (33), p.20455-20462

1990

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Molecular Cloning, Sequencing, and Mapping of EGR2, a Human Early Growth Response Gene Encoding a Protein with ``Zinc-Binding Finger'' Structure

Proceedings of the National Academy of Sciences - PNAS, 1988-10, Vol.85 (19), p.7164-7168

1988

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Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma

The Journal of clinical investigation, 1989-06, Vol.83 (6), p.2034-2040

1989

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Brn-3b: a POU domain gene expressed in a subset of retinal ganglion cells

Neuron (Cambridge, Mass.), 1993-10, Vol.11 (4), p.689-701

1993

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Molecular genetics of Alport syndrome

Kidney international, 1993-01, Vol.43 (1), p.38-44

1993

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Bestrophin Gene Mutations in Patients with Best Vitelliform Macular Dystrophy

Genomics (San Diego, Calif.), 1999-05, Vol.58 (1), p.98-101

1999

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MAGOH Interacts with a Novel RNA-Binding Protein

Genomics (San Diego, Calif.), 2000-01, Vol.63 (1), p.145-148

2000

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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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Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus

American journal of respiratory cell and molecular biology, 1997-03, Vol.16 (3), p.232-241

1997

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cDNA cloning and chromosomal assignment of the gene encoding endothelin 3

The Journal of biological chemistry, 1989-10, Vol.264 (30), p.18156-18161

1989

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Structural Organization and Chromosomal Assignment of the Gene Encoding Endothelin

The Journal of biological chemistry, 1989-06, Vol.264 (18), p.10851-10857

1989

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Cloning of a novel tumor necrosis factor-alpha-inducible primary response gene that is differentially expressed in development and capillary tube-like formation in vitro

The Journal of immunology (1950), 1992-05, Vol.148 (10), p.3302-3312

1992

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A zinc finger-encoding gene coregulated with c-fos during growth and differentiation, and after cellular depolarization

Cell, 1988-04, Vol.53 (1), p.37-43

1988

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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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A Maternally Methylated CpG Island in KvLQT1 Is Associated with an Antisense Paternal Transcript and Loss of Imprinting in Beckwith-Wiedemann Syndrome

Human Laminin M Chain (Merosin): Complete Primary Structure, Chromosomal Assignment, and Expression of the M and A Chain in Human Fetal Tissues

NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia

The Brn-3 family of POU-domain factors: primary structure, binding specificity, and expression in subsets of retinal ganglion cells and somatosensory neurons

A Truncated Laminin Chain Homologous to the B2 Chain: Structure, Spatial Expression, and Chromosomal Assignment

Evidence for a family of human glucose transporter-like proteins. Sequence and gene localization of a protein expressed in fetal skeletal muscle and other tissues

A Human Amphotropic Retrovirus Receptor is a Second Member of the Gibbon Ape Leukemia Virus Receptor Family

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)

Fine Structure Analysis of the WT1 Gene in Sporadic Wilms Tumors

A Model System to Study Genomic Imprinting of Human Genes

Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa

The human neurokinin A (substance K) receptor. Molecular cloning of the gene, chromosome localization, and isolation of cDNA from tracheal and gastric tissues

Molecular Cloning, Sequencing, and Mapping of EGR2, a Human Early Growth Response Gene Encoding a Protein with ``Zinc-Binding Finger'' Structure

Molecular cloning and chromosomal mapping of DNA rearranged with the parathyroid hormone gene in a parathyroid adenoma

Brn-3b: a POU domain gene expressed in a subset of retinal ganglion cells

Molecular genetics of Alport syndrome

Bestrophin Gene Mutations in Patients with Best Vitelliform Macular Dystrophy

MAGOH Interacts with a Novel RNA-Binding Protein

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

Chromosomal localization of a human mucin gene (MUC8) and cloning of the cDNA corresponding to the carboxy terminus

cDNA cloning and chromosomal assignment of the gene encoding endothelin 3

Structural Organization and Chromosomal Assignment of the Gene Encoding Endothelin

Cloning of a novel tumor necrosis factor-alpha-inducible primary response gene that is differentially expressed in development and capillary tube-like formation in vitro

A zinc finger-encoding gene coregulated with c-fos during growth and differentiation, and after cellular depolarization

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

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