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Epigenetic interactions and the structure of phenotypic variation in the cranium

Evolution & development, 2007-01, Vol.9 (1), p.76-91

2007

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A seven-transmembrane domain receptor involved in fusion and entry of T-cell-tropic human immunodeficiency virus type 1 strains

Journal of Virology, 1996-09, Vol.70 (9), p.6288-6295

1996

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Endogenous cellular prion protein regulates contractility of the mouse ileum

Neurogastroenterology and motility, 2012-09, Vol.24 (9), p.e412-e424

2012

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Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6

Carcinogenesis (New York), 2006-12, Vol.27 (12), p.2402-2408

2006

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Increased bone mass in male and female mice following tamoxifen administration

Genesis (New York, N.Y. : 2000), 2007-04, Vol.45 (4), p.229-235

2007

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Targeted disruption of the pituitary adenylate cyclase-activating polypeptide gene results in early postnatal death associated with dysfunction of lipid and carbohydrate metabolism

Molecular endocrinology (Baltimore, Md.), 2001-10, Vol.15 (10), p.1739-1747

2001

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Characterization and kinetic analysis of the intracellular domain of human protein tyrosine phosphatase β (HPTPβ) using synthetic phosphopeptides

Biochemical journal, 1994-03, Vol.298 (2), p.395-401

1994

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Murine Mucopolysaccharidosis Type I: Targeted Disruption of the Murine α-l-Iduronidase Gene

Human molecular genetics, 1997-04, Vol.6 (4), p.503-511

1997

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Bacterial lipopolysaccharide and inflammatory mediators augment IL-6 secretion by human endothelial cells

The Journal of immunology (1950), 1989-01, Vol.142 (1), p.144-147

1989

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Interleukin (IL)-3 and granulocyte/macrophage colony-stimulating factor, but not IL-4, induce tyrosine phosphorylation, activation, and association of SHPTP2 with Grb2 and phosphatidylinositol 3'-kinase

The Journal of biological chemistry, 1994-09, Vol.269 (38), p.23764-23768

1994

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Compound heterozygosity for Pten and SHIP augments T‐dependent humoral immune responses and cytokine production by CD4+ T cells

Immunology, 2004-07, Vol.112 (3), p.404-412

2004

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TCR activation inhibits chemotaxis toward stromal cell-derived factor-1: evidence for reciprocal regulation between CXCR4 and the TCR

The Journal of immunology (1950), 1999-01, Vol.162 (1), p.215-223

1999

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Role of DNA mismatch repair in the cytotoxicity of ionizing radiation

Cancer research (Chicago, Ill.), 1997-11, Vol.57 (22), p.5143-5147

1997

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Protein-tyrosine Phosphatase α Regulates Src Family Kinases and Alters Cell-Substratum Adhesion

The Journal of biological chemistry, 1998-11, Vol.273 (48), p.31890-31900

1998

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Defective hematopoiesis and hepatic steatosis in mice with combined deficiencies of the genes encoding Fancc and Cu/Zn superoxide dismutase

Blood, 2001-08, Vol.98 (4), p.1003-1011

2001

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Tissues of MSH2-Deficient Mice Demonstrate Hypermutability on Exposure to a DNA Methylating Agent

Proceedings of the National Academy of Sciences - PNAS, 1998-02, Vol.95 (3), p.1126-1130

1998

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Mutagenesis in PMS2- and MSH2-deficient mice indicates differential protection from transversions and frameshifts

Carcinogenesis (New York), 2000-07, Vol.21 (7), p.1291-1295

2000

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Anti‐IL‐4 treatment prevents dermal collagen deposition in the tight‐skin mouse model of scleroderma

European journal of immunology, 1998-09, Vol.28 (9), p.2619-2629

1998

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Base transitions dominate the mutational spectrum of a transgenic reporter gene in MSH2 deficient mice

Oncogene, 1997-07, Vol.15 (2), p.123-129

1997

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Mammalian SH2-Containing Protein Tyrosine Phosphatases

Cell, 1996-04, Vol.85 (1), p.15-15

1996

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Loss of a single allele of SHIP exacerbates the immunopathology of Pten heterozygous mice

Genes and immunity, 2003-01, Vol.4 (1), p.60-66

2003

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The Src Homology 2 (SH2) Domain of SH2-containing Inositol Phosphatase (SHIP) Is Essential for Tyrosine Phosphorylation of SHIP, Its Association with Shc, and Its Induction of Apoptosis

The Journal of biological chemistry, 1997-04, Vol.272 (14), p.8983-8988

1997

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Molecular Cloning of the cDNA and Chromosomal Localization of the Gene for a Putative Seven-Transmembrane Segment (7-TMS) Receptor Isolated from Human Spleen

Genomics (San Diego, Calif.), 1993-06, Vol.16 (3), p.707-712

1993

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Characterization of protein tyrosine phosphatase SH-PTP2. Study of phosphopeptide substrates and possible regulatory role of SH2 domains

The Journal of biological chemistry, 1994-02, Vol.269 (8), p.5602-5611

1994

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Absence of Disease Phenotype and Intergenerational Stability of the Cag Repeat in Transgenic Mice Expressing the Human Huntington Disease Transcript

Human molecular genetics, 1996-02, Vol.5 (2), p.177-185

1996

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Epigenetic interactions and the structure of phenotypic variation in the cranium

A seven-transmembrane domain receptor involved in fusion and entry of T-cell-tropic human immunodeficiency virus type 1 strains

Endogenous cellular prion protein regulates contractility of the mouse ileum

Differing patterns of genetic instability in mice deficient in the mismatch repair genes Pms2, Mlh1, Msh2, Msh3 and Msh6

Increased bone mass in male and female mice following tamoxifen administration

Targeted disruption of the pituitary adenylate cyclase-activating polypeptide gene results in early postnatal death associated with dysfunction of lipid and carbohydrate metabolism

Characterization and kinetic analysis of the intracellular domain of human protein tyrosine phosphatase β (HPTPβ) using synthetic phosphopeptides

Murine Mucopolysaccharidosis Type I: Targeted Disruption of the Murine α-l-Iduronidase Gene

Bacterial lipopolysaccharide and inflammatory mediators augment IL-6 secretion by human endothelial cells

Interleukin (IL)-3 and granulocyte/macrophage colony-stimulating factor, but not IL-4, induce tyrosine phosphorylation, activation, and association of SHPTP2 with Grb2 and phosphatidylinositol 3'-kinase

Compound heterozygosity for Pten and SHIP augments T‐dependent humoral immune responses and cytokine production by CD4+ T cells

TCR activation inhibits chemotaxis toward stromal cell-derived factor-1: evidence for reciprocal regulation between CXCR4 and the TCR

Role of DNA mismatch repair in the cytotoxicity of ionizing radiation

Protein-tyrosine Phosphatase α Regulates Src Family Kinases and Alters Cell-Substratum Adhesion

Defective hematopoiesis and hepatic steatosis in mice with combined deficiencies of the genes encoding Fancc and Cu/Zn superoxide dismutase

Tissues of MSH2-Deficient Mice Demonstrate Hypermutability on Exposure to a DNA Methylating Agent

Mutagenesis in PMS2- and MSH2-deficient mice indicates differential protection from transversions and frameshifts

Anti‐IL‐4 treatment prevents dermal collagen deposition in the tight‐skin mouse model of scleroderma

Base transitions dominate the mutational spectrum of a transgenic reporter gene in MSH2 deficient mice

Mammalian SH2-Containing Protein Tyrosine Phosphatases

Loss of a single allele of SHIP exacerbates the immunopathology of Pten heterozygous mice

The Src Homology 2 (SH2) Domain of SH2-containing Inositol Phosphatase (SHIP) Is Essential for Tyrosine Phosphorylation of SHIP, Its Association with Shc, and Its Induction of Apoptosis

Molecular Cloning of the cDNA and Chromosomal Localization of the Gene for a Putative Seven-Transmembrane Segment (7-TMS) Receptor Isolated from Human Spleen

Characterization of protein tyrosine phosphatase SH-PTP2. Study of phosphopeptide substrates and possible regulatory role of SH2 domains

Absence of Disease Phenotype and Intergenerational Stability of the Cag Repeat in Transgenic Mice Expressing the Human Huntington Disease Transcript

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