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Ovariectomy‐Induced Bone Loss Varies Among Inbred Strains of Mice

Journal of bone and mineral research, 2005-07, Vol.20 (7), p.1085-1092

2005

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Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource

Nature communications, 2012-11, Vol.3 (1), p.1218, Article 1218

2012

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Mutations in a Novel CLN6-Encoded Transmembrane Protein Cause Variant Neuronal Ceroid Lipofuscinosis in Man and Mouse

American journal of human genetics, 2002-02, Vol.70 (2), p.324-335

2002

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Mapping Quantitative Trait Loci for Vertebral Trabecular Bone Volume Fraction and Microarchitecture in Mice

Journal of bone and mineral research, 2004-04, Vol.19 (4), p.587-599

2004

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Genetic Dissection of Mouse Distal Chromosome 1 Reveals Three Linked BMD QTLs With Sex‐Dependent Regulation of Bone Phenotypes

Journal of bone and mineral research, 2007-08, Vol.22 (8), p.1187-1196

2007

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Genetically Based Influences on the Site‐Specific Regulation of Trabecular and Cortical Bone Morphology

Journal of bone and mineral research, 2004-04, Vol.19 (4), p.600-606

2004

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Low-level mechanical vibrations can influence bone resorption and bone formation in the growing skeleton

Bone (New York, N.Y.), 2006-11, Vol.39 (5), p.1059-1066

2006

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Genetically Linked Site‐Specificity of Disuse Osteoporosis

Journal of bone and mineral research, 2004-04, Vol.19 (4), p.607-613

2004

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Ultrastructural Properties in Cortical Bone Vary Greatly in Two Inbred Strains of Mice as Assessed by Synchrotron Light Based Micro‐ and Nano‐CT

Journal of bone and mineral research, 2007-10, Vol.22 (10), p.1557-1570

2007

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Genetic predisposition to low bone mass is paralleled by an enhanced sensitivity to signals anabolic to the skeleton

The FASEB journal, 2002-08, Vol.16 (10), p.1280-1282

2002

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Automated compartmental analysis for high-throughput skeletal phenotyping in femora of genetic mouse models

Bone (New York, N.Y.), 2007-10, Vol.41 (4), p.659-667

2007

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Insulin-Like Growth Factor Regulates Peak Bone Mineral Density in Mice by Both Growth Hormone-Dependent and -Independent Mechanisms

Endocrinology (Philadelphia), 2003-03, Vol.144 (3), p.929-936

2003

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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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Genetic Loci That Control the Loss and Regain of Trabecular Bone During Unloading and Reambulation

Journal of bone and mineral research, 2013-07, Vol.28 (7), p.1537-1549

2013

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Congenital Hypothyroidism, Dwarfism, and Hearing Impairment Caused by a Missense Mutation in the Mouse Dual Oxidase 2 Gene, Duox2

Molecular endocrinology (Baltimore, Md.), 2007-07, Vol.21 (7), p.1593-1602

2007

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Genetic Regulation of Cortical and Trabecular Bone Strength and Microstructure in Inbred Strains of Mice

Journal of bone and mineral research, 2000-06, Vol.15 (6), p.1126-1131

2000

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Disheveled hair and ear (Dhe), a spontaneous mouse Lmna mutation modeling human laminopathies

PloS one, 2010-04, Vol.5 (4), p.e9959-e9959

2010

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BMD regulation on mouse distal chromosome 1, candidate genes, and response to ovariectomy or dietary fat

Journal of bone and mineral research, 2011-01, Vol.26 (1), p.88-99

2011

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Generating embryonic stem cells from the inbred mouse strain DBA/2J, a model of glaucoma and other complex diseases

PloS one, 2012-11, Vol.7 (11), p.e50081-e50081

2012

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Mechanical modulation of molecular signals which regulate anabolic and catabolic activity in bone tissue

Journal of cellular biochemistry, 2005-04, Vol.94 (5), p.982-994

2005

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Genetic variations that regulate bone morphology in the male mouse skeleton do not define its susceptibility to mechanical unloading

Bone (New York, N.Y.), 2004-12, Vol.35 (6), p.1353-1360

2004

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Quantitative Trait Loci for Femoral and Lumbar Vertebral Bone Mineral Density in C57BL/6J and C3H/HeJ Inbred Strains of Mice

Journal of bone and mineral research, 2001-07, Vol.16 (7), p.1195-1206

2001

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A novel spontaneous mutation of Irs1 in mice results in hyperinsulinemia, reduced growth, low bone mass and impaired adipogenesis

Journal of endocrinology, 2010-03, Vol.204 (3), p.241-253

2010

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Generation of a New Congenic Mouse Strain to Test the Relationships Among Serum Insulin‐like Growth Factor I, Bone Mineral Density, and Skeletal Morphology In Vivo

Journal of bone and mineral research, 2002-04, Vol.17 (4), p.570-579

2002

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Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth

Human molecular genetics, 2002-10, Vol.11 (22), p.2709-2721

2002

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Ovariectomy‐Induced Bone Loss Varies Among Inbred Strains of Mice

Supporting conditional mouse mutagenesis with a comprehensive cre characterization resource

Mutations in a Novel CLN6-Encoded Transmembrane Protein Cause Variant Neuronal Ceroid Lipofuscinosis in Man and Mouse

Mapping Quantitative Trait Loci for Vertebral Trabecular Bone Volume Fraction and Microarchitecture in Mice

Genetic Dissection of Mouse Distal Chromosome 1 Reveals Three Linked BMD QTLs With Sex‐Dependent Regulation of Bone Phenotypes

Genetically Based Influences on the Site‐Specific Regulation of Trabecular and Cortical Bone Morphology

Low-level mechanical vibrations can influence bone resorption and bone formation in the growing skeleton

Genetically Linked Site‐Specificity of Disuse Osteoporosis

Ultrastructural Properties in Cortical Bone Vary Greatly in Two Inbred Strains of Mice as Assessed by Synchrotron Light Based Micro‐ and Nano‐CT

Genetic predisposition to low bone mass is paralleled by an enhanced sensitivity to signals anabolic to the skeleton

Automated compartmental analysis for high-throughput skeletal phenotyping in femora of genetic mouse models

Insulin-Like Growth Factor Regulates Peak Bone Mineral Density in Mice by Both Growth Hormone-Dependent and -Independent Mechanisms

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

Genetic Loci That Control the Loss and Regain of Trabecular Bone During Unloading and Reambulation

Congenital Hypothyroidism, Dwarfism, and Hearing Impairment Caused by a Missense Mutation in the Mouse Dual Oxidase 2 Gene, Duox2

Genetic Regulation of Cortical and Trabecular Bone Strength and Microstructure in Inbred Strains of Mice

Disheveled hair and ear (Dhe), a spontaneous mouse Lmna mutation modeling human laminopathies

BMD regulation on mouse distal chromosome 1, candidate genes, and response to ovariectomy or dietary fat

Generating embryonic stem cells from the inbred mouse strain DBA/2J, a model of glaucoma and other complex diseases

Mechanical modulation of molecular signals which regulate anabolic and catabolic activity in bone tissue

Genetic variations that regulate bone morphology in the male mouse skeleton do not define its susceptibility to mechanical unloading

Quantitative Trait Loci for Femoral and Lumbar Vertebral Bone Mineral Density in C57BL/6J and C3H/HeJ Inbred Strains of Mice

A novel spontaneous mutation of Irs1 in mice results in hyperinsulinemia, reduced growth, low bone mass and impaired adipogenesis

Generation of a New Congenic Mouse Strain to Test the Relationships Among Serum Insulin‐like Growth Factor I, Bone Mineral Density, and Skeletal Morphology In Vivo

Cln3(Deltaex7/8) knock-in mice with the common JNCL mutation exhibit progressive neurologic disease that begins before birth

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