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Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation

Human molecular genetics, 2003-11, Vol.12 (22), p.2895-2907

2003

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The Treacher Collins Syndrome (TCOF1) Gene Product, Treacle, is Targeted to the Nucleolus by Signals in Its C-Terminus

Human molecular genetics, 1998-11, Vol.7 (12), p.1947-1952

1998

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A prospective trial of telepathology for intraoperative consultation (frozen sections)

Human pathology, 2000-07, Vol.31 (7), p.781-785

2000

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Role of transforming growth factor-β in maintenance of function of cultured neonatal cardiac myocytes : autocrine action and reversal of damaging effects of interleukin-1

The Journal of clinical investigation, 1992-11, Vol.90 (5), p.2056-2062

1992

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Recombinant latent transforming growth factor beta 1 has a longer plasma half-life in rats than active transforming growth factor beta 1, and a different tissue distribution

The Journal of clinical investigation, 1990-12, Vol.86 (6), p.1976-1984

1990

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The Evolutionary Distribution and Structural Organization of the Homeobox-Containing Repeat D4Z4 Indicates a Functional Role for the Ancestral Copy in the FSHD Region

Human molecular genetics, 1996-10, Vol.5 (10), p.1567-1575

1996

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Cell, 1994-07, Vol.78 (2), p.335-342

1994

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Actinin-Associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs

The Journal of cell biology, 1997-10, Vol.139 (2), p.507-515

1997

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Inhibition of protein phosphatases blocks myogenesis by first altering MyoD binding activity

The Journal of biological chemistry, 1992-07, Vol.267 (21), p.15140-15145

1992

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An initial trial of a prototype telepathology system featuring static imaging with discrete control of the remote microscope

American journal of clinical pathology, 1998-07, Vol.110 (1), p.43-49

1998

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Expression of transforming growth factor-βs 1–4 in chicken embryo chondrocytes and myocytes

Developmental biology, 1991, Vol.143 (1), p.135-148

1991

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Case Report: Pineocytoma in a Male Fischer 344 Rat

Toxicologic pathology, 1998-03, Vol.26 (2), p.294-297

1998

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High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q

Human molecular genetics, 1994-10, Vol.3 (10), p.1801-1805

1994

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Evaluation of DNA ploidy in dysplastic and Spitz nevi by flow cytometry

Journal of cutaneous pathology, 1990-12, Vol.17 (6), p.342-347

1990

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Overexpression of transforming growth factor-beta in transgenic mice carrying the human T-cell lymphotropic virus type I tax gene

Molecular and Cellular Biology, 1991-10, Vol.11 (10), p.5222-5228

1991

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MTrasT24, a Metallothionein-ras Fusion Gene, Modulates Expression in Cultured Rat Liver Cells of Two Genes Associated with in vivo Liver Cancer

Proceedings of the National Academy of Sciences - PNAS, 1988, Vol.85 (2), p.344-348

1988

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Hyperthermia induces expression of transforming growth factor-βs in rat cardiac cells in vitro and in vivo

The Journal of clinical investigation, 1993-07, Vol.92 (1), p.404-410

1993

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Expression of sulfated glycoprotein 2 is associated with carcinogenesis induced by N-nitroso-N-methylurea in rat prostate and seminal vesicle

Cancer research (Chicago, Ill.), 1993-04, Vol.53 (7), p.1480-1483

1993

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Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus

Genomics (San Diego, Calif.), 1993-05, Vol.16 (2), p.479-485

1993

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A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD)

American journal of human genetics, 1993-10, Vol.53 (4), p.874-880

1993

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The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region

Human molecular genetics, 1997-03, Vol.6 (3), p.502-502

1997

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The distribution of somatic H1 subtypes is non-random on active vs. inactive chromatin: distribution in human fetal fibroblasts

Chromosome research, 2000-01, Vol.8 (5), p.405-424

2000

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Regional synthesis of monohydroxy eicosanoids by the kidney

The Journal of biological chemistry, 1981-10, Vol.256 (20), p.10221-10223

1981

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YAC Contigs for 4q35 in the Region of the Facioscapulohumeral Muscular Dystrophy (FSHD) Gene

Genomics (San Diego, Calif.), 1994-02, Vol.19 (3), p.532-541

1994

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Cardiomyopathy in a carrier of duchenne’s muscular dystrophy

The Journal of heart and lung transplantation, 2001-07, Vol.20 (7), p.781-784

2001

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Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation

The Treacher Collins Syndrome (TCOF1) Gene Product, Treacle, is Targeted to the Nucleolus by Signals in Its C-Terminus

A prospective trial of telepathology for intraoperative consultation (frozen sections)

Role of transforming growth factor-β in maintenance of function of cultured neonatal cardiac myocytes : autocrine action and reversal of damaging effects of interleukin-1

Recombinant latent transforming growth factor beta 1 has a longer plasma half-life in rats than active transforming growth factor beta 1, and a different tissue distribution

The Evolutionary Distribution and Structural Organization of the Homeobox-Containing Repeat D4Z4 Indicates a Functional Role for the Ancestral Copy in the FSHD Region

Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

Actinin-Associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs

Inhibition of protein phosphatases blocks myogenesis by first altering MyoD binding activity

An initial trial of a prototype telepathology system featuring static imaging with discrete control of the remote microscope

Expression of transforming growth factor-βs 1–4 in chicken embryo chondrocytes and myocytes

Case Report: Pineocytoma in a Male Fischer 344 Rat

High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q

Evaluation of DNA ploidy in dysplastic and Spitz nevi by flow cytometry

Overexpression of transforming growth factor-beta in transgenic mice carrying the human T-cell lymphotropic virus type I tax gene

MTrasT24, a Metallothionein-ras Fusion Gene, Modulates Expression in Cultured Rat Liver Cells of Two Genes Associated with in vivo Liver Cancer

Hyperthermia induces expression of transforming growth factor-βs in rat cardiac cells in vitro and in vivo

Expression of sulfated glycoprotein 2 is associated with carcinogenesis induced by N-nitroso-N-methylurea in rat prostate and seminal vesicle

Genetic Mapping of Human Heart-Skeletal Muscle Adenine Nucleotide Translocator and Its Relationship to the Facioscapulohumeral Muscular Dystrophy Locus

A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD)

The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region

The distribution of somatic H1 subtypes is non-random on active vs. inactive chromatin: distribution in human fetal fibroblasts

Regional synthesis of monohydroxy eicosanoids by the kidney

YAC Contigs for 4q35 in the Region of the Facioscapulohumeral Muscular Dystrophy (FSHD) Gene

Cardiomyopathy in a carrier of duchenne’s muscular dystrophy

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