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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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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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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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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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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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Identification of a new endothelial cell growth factor receptor tyrosine kinase

Oncogene, 1991-09, Vol.6 (9), p.1677-1683

1991

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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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Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses

Human molecular genetics, 1996-10, Vol.5 (10), p.1547-1557

1996

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Human monocyte ARG-serpin cDNA: sequence, chromosomal assignment, and homology to plasminogen activator-inhibitor

The Journal of experimental medicine, 1987-07, Vol.166 (1), p.77-94

1987

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Molecular genetics of Alport syndrome

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

1993

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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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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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Intrachromosomal genomic instability in human sporadic colorectal cancer measured by genome-wide allelotyping and inter-(simple sequence repeat) PCR

Cancer research (Chicago, Ill.), 2001-11, Vol.61 (22), p.8274-8283

2001

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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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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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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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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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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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Rearrangement and overexpression of D11S287E, a candidate oncogene on chromosome 11q13 in benign parathyroid tumors

Oncogene, 1991-03, Vol.6 (3), p.449-453

1991

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Harold P. Klinger, 1929–2004

Cytogenetic and genome research, 2005-01, Vol.109 (4), p.409-413

2005

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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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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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EGR3, a novel member of the Egr family of genes encoding immediate-early transcription factors

Oncogene, 1991-06, Vol.6 (6), p.917-928

1991

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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

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

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

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

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

Identification of a new endothelial cell growth factor receptor tyrosine kinase

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

Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses

Human monocyte ARG-serpin cDNA: sequence, chromosomal assignment, and homology to plasminogen activator-inhibitor

Molecular genetics of Alport syndrome

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

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

Intrachromosomal genomic instability in human sporadic colorectal cancer measured by genome-wide allelotyping and inter-(simple sequence repeat) PCR

MAGOH Interacts with a Novel RNA-Binding Protein

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

Bestrophin Gene Mutations in Patients with Best Vitelliform Macular Dystrophy

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

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

Rearrangement and overexpression of D11S287E, a candidate oncogene on chromosome 11q13 in benign parathyroid tumors

Harold P. Klinger, 1929–2004

A Model System to Study Genomic Imprinting of Human Genes

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

EGR3, a novel member of the Egr family of genes encoding immediate-early transcription factors

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