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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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Chemotherapy-resistant human AML stem cells home to and engraft within the bone-marrow endosteal region

Nature biotechnology, 2007-11, Vol.25 (11), p.1315-1321

2007

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Evaluation of tarsal injuries in C57BL/6J male mice

PloS one, 2023-06, Vol.18 (6), p.e0287204-e0287204

2023

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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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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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The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities

PloS one, 2020-06, Vol.15 (6), p.e0230162-e0230162

2020

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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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From “What the Thunder Said” to “Hebrew Lessons” and Other Jewish Poems

Studies in American Jewish literature (1981), 2012-09, Vol.31 (2), p.228-237

Lyons, Bonnie

2012

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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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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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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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Purified human hematopoietic stem cells contribute to the generation of cardiomyocytes through cell fusion

The FASEB journal, 2006-05, Vol.20 (7), p.950-952

2006

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Humanized NOD/LtSz-scid IL2 Receptor Common Gamma Chain Knockout Mice in Diabetes Research

Annals of the New York Academy of Sciences, 2007-04, Vol.1103 (1), p.77-89

2007

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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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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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Education and the making of a democratic people

2008

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Playing God

Shofar (West Lafayette, Ind.), 2009-04, Vol.27 (3), p.114-114

Lyons, Bonnie

2009

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Studies In American Jewish Literature
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Human cancer growth and therapy in immunodeficient mouse models

Chemotherapy-resistant human AML stem cells home to and engraft within the bone-marrow endosteal region

Evaluation of tarsal injuries in C57BL/6J male mice

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

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

The occurrence of tarsal injuries in male mice of C57BL/6N substrains in multiple international mouse facilities

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

From “What the Thunder Said” to “Hebrew Lessons” and Other Jewish Poems

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

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

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

Purified human hematopoietic stem cells contribute to the generation of cardiomyocytes through cell fusion

Humanized NOD/LtSz-scid IL2 Receptor Common Gamma Chain Knockout Mice in Diabetes Research

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

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

Education and the making of a democratic people

Playing God

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