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Human cancer growth and therapy in immunodeficient mouse models

Cold Spring Harbor protocols, 2014-07, Vol.2014 (7), p.694

2014

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Tissue-specific role of RHBDF2 in cutaneous wound healing and hyperproliferative skin disease

BMC research notes, 2017-11, Vol.10 (1), p.573-573, Article 573

2017

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Subcapsular transplantation of tissue in the kidney

Cold Spring Harbor protocols, 2014-07, Vol.2014 (7), p.737

2014

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The mouse mutation “thrombocytopenia and cardiomyopathy” (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia

Blood, 2010-02, Vol.115 (6), p.1267-1276

2010

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Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) mice

PloS one, 2013-01, Vol.8 (1), p.e53426-e53426

2013

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Continuous Glucose Monitoring in Female NOD Mice Reveals Daily Rhythms and a Negative Correlation With Body Temperature

Endocrinology (Philadelphia), 2017-09, Vol.158 (9), p.2707-2712

2017

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Antibiotic-associated Manipulation of the Gut Microbiota and Phenotypic Restoration in NOD Mice

Comparative medicine, 2017-08, Vol.67 (4), p.335-343

2017

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Accelerated Wound Healing of Alkali-Burned Corneas in MRL Mice Is Associated with a Reduced Inflammatory Signature

Investigative ophthalmology & visual science, 2005-11, Vol.46 (11), p.4097-4106

2005

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Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly

Human molecular genetics, 2003, Vol.12 (1), p.61-69

2003

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Human antibodies induce arthritis in mice deficient in the low-affinity inhibitory IgG receptor Fc gamma RIIB

The Journal of experimental medicine, 2006-02, Vol.203 (2), p.275-280

2006

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General Considerations for Mouse Survival Surgery

Current protocols in mouse biology, 2012-09, Vol.2 (3), p.263-271

2012

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The Tetratricopeptide Repeat Domain 7 Gene is Mutated in Flaky Skin Mice: A Model for Psoriasis, Autoimmunity, and Anemia

Experimental biology and medicine (Maywood, N.J.), 2005-10, Vol.230 (9), p.659-667

2005

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Deficiency of SHP-1 Protein-Tyrosine Phosphatase in "Viable Motheaten" Mice Results in Retinal Degeneration

Investigative ophthalmology & visual science, 2006-03, Vol.47 (3), p.1201-1209

2006

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Rejection of human islets and human HLA-A2.1 transgenic mouse islets by alloreactive human lymphocytes in immunodeficient NOD-scid and NOD-Rag1(null)Prf1(null) mice

Clinical immunology (Orlando, Fla.), 2004-09, Vol.112 (3), p.273

2004

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Curly bare ( cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene ( mcub) on chromosome 5

Genomics (San Diego, Calif.), 2003, Vol.81 (1), p.6-14

2003

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Mechanisms of anemia in SHP-1 protein tyrosine phosphatase-deficient “viable motheaten” mice

Experimental hematology, 2003-03, Vol.31 (3), p.234-243

2003

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Human lymphoid and myeloid cell development in NOD/LtSz-scid IL2R gamma null mice engrafted with mobilized human hemopoietic stem cells

The Journal of immunology (1950), 2005-05, Vol.174 (10), p.6477-6489

2005

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Establishment and characterization of a new osteogenic cell line (MOS-J) from a spontaneous C57BL/6J mouse osteosarcoma

In vivo (Athens), 2002-07, Vol.16 (4), p.223

2002

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T Cell Developmental Defects in ‘Viable Motheaten’ Mice Deficient in SHP-1 Protein-Tyrosine Phosphatase. Developmental Defects are Corrected in vitro in the Presence of Normal Hematopoietic-Origin Stromal Cells and in vivo by Exogenous IL-7

Journal of autoimmunity, 2002-03, Vol.18 (2), p.119-130

2002

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Absence of CD5 Dramatically Reduces Progression of Pulmonary Inflammatory Lesions in SHP-1 Protein-Tyrosine Phosphatase-Deficient ‘Viable Motheaten’ Mice

Journal of autoimmunity, 2002-03, Vol.18 (2), p.105-117

2002

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Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1 Mice

PloS one, 2013-01, Vol.8 (1), p.e53426

2013

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Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1

PloS one, 2013-01, Vol.8 (1), p.e53426

2013

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Ascorbate stimulation of PAT cells causes an increase in transcription rates and a decrease in degradation rates of procollagen mRNA

Nucleic acids research, 1984-03, Vol.12 (5), p.2569-2579

1984

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The Mouse Mutation “Thrombocytopenia and Cardiomyopathy” (trac) Is within the ABCG5 Gene: A Single Gene Model for Human Mediterranean Macrothrombocytopenia

Blood, 2007-11, Vol.110 (11), p.98-98

2007

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Thrombocytopenia and Cardiomyopathy (trac): A New Single Gene Mutation Resulting in Severe Platelet and Heart Abnormalities in Mice

Blood, 2005-11, Vol.106 (11), p.734-734

2005

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Human cancer growth and therapy in immunodeficient mouse models

Tissue-specific role of RHBDF2 in cutaneous wound healing and hyperproliferative skin disease

Subcapsular transplantation of tissue in the kidney

The mouse mutation “thrombocytopenia and cardiomyopathy” (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia

Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) mice

Continuous Glucose Monitoring in Female NOD Mice Reveals Daily Rhythms and a Negative Correlation With Body Temperature

Antibiotic-associated Manipulation of the Gut Microbiota and Phenotypic Restoration in NOD Mice

Accelerated Wound Healing of Alkali-Burned Corneas in MRL Mice Is Associated with a Reduced Inflammatory Signature

Mutations at the mouse ichthyosis locus are within the lamin B receptor gene: a single gene model for human Pelger-Huët anomaly

Human antibodies induce arthritis in mice deficient in the low-affinity inhibitory IgG receptor Fc gamma RIIB

General Considerations for Mouse Survival Surgery

The Tetratricopeptide Repeat Domain 7 Gene is Mutated in Flaky Skin Mice: A Model for Psoriasis, Autoimmunity, and Anemia

Deficiency of SHP-1 Protein-Tyrosine Phosphatase in "Viable Motheaten" Mice Results in Retinal Degeneration

Rejection of human islets and human HLA-A2.1 transgenic mouse islets by alloreactive human lymphocytes in immunodeficient NOD-scid and NOD-Rag1(null)Prf1(null) mice

Curly bare ( cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene ( mcub) on chromosome 5

Mechanisms of anemia in SHP-1 protein tyrosine phosphatase-deficient “viable motheaten” mice

Human lymphoid and myeloid cell development in NOD/LtSz-scid IL2R gamma null mice engrafted with mobilized human hemopoietic stem cells

Establishment and characterization of a new osteogenic cell line (MOS-J) from a spontaneous C57BL/6J mouse osteosarcoma

T Cell Developmental Defects in ‘Viable Motheaten’ Mice Deficient in SHP-1 Protein-Tyrosine Phosphatase. Developmental Defects are Corrected in vitro in the Presence of Normal Hematopoietic-Origin Stromal Cells and in vivo by Exogenous IL-7

Absence of CD5 Dramatically Reduces Progression of Pulmonary Inflammatory Lesions in SHP-1 Protein-Tyrosine Phosphatase-Deficient ‘Viable Motheaten’ Mice

Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1 Mice

Retrotransposon Insertion in the T-cell Acute Lymphocytic Leukemia 1

Ascorbate stimulation of PAT cells causes an increase in transcription rates and a decrease in degradation rates of procollagen mRNA

The Mouse Mutation “Thrombocytopenia and Cardiomyopathy” (trac) Is within the ABCG5 Gene: A Single Gene Model for Human Mediterranean Macrothrombocytopenia

Thrombocytopenia and Cardiomyopathy (trac): A New Single Gene Mutation Resulting in Severe Platelet and Heart Abnormalities in Mice

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