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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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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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Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency

Human molecular genetics, 2004-09, Vol.13 (18), p.1999-2010

2004

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Studies of OC-STAMP in Osteoclast Fusion: A New Knockout Mouse Model, Rescue of Cell Fusion, and Transmembrane Topology

PloS one, 2015-06, Vol.10 (6), p.e0128275-e0128275

2015

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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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High-throughput discovery of novel developmental phenotypes

Nature (London), 2016-09, Vol.537 (7621), p.508-514

2016

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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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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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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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Spontaneous Fractures in the Mouse Mutant sfx Are Caused by Deletion of the Gulonolactone Oxidase Gene, Causing Vitamin C Deficiency

Journal of bone and mineral research, 2005-09, Vol.20 (9), p.1597-1610

2005

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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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New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice

Mammalian genome, 2004-03, Vol.15 (3), p.151-161

2004

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A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis

Journal of bone and mineral research, 2003-09, Vol.18 (9), p.1612-1621

2003

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Identification of genes required for eye development by high-throughput screening of mouse knockouts

Communications biology, 2018-01, Vol.1 (1), p.236, Article 236

2018

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Variation in Bone Biomechanical Properties, Microstructure, and Density in BXH Recombinant Inbred Mice

Journal of bone and mineral research, 2001-02, Vol.16 (2), p.206-213

2001

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Insulin-like Growth Factors and Bone: The Osteoporosis Connection

Experimental biology and medicine (Maywood, N.J.), 1994-06, Vol.206 (2), p.83-102

1994

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Chromosomal inversion discovered in C3H/HeJ mice

Genomics (San Diego, Calif.), 2006-02, Vol.87 (2), p.311-313

2006

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Ovariectomy‐Induced Bone Loss Varies Among Inbred Strains of Mice

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

Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency

Studies of OC-STAMP in Osteoclast Fusion: A New Knockout Mouse Model, Rescue of Cell Fusion, and Transmembrane Topology

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

High-throughput discovery of novel developmental phenotypes

Mutation discovery in mice by whole exome sequencing

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

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

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

Spontaneous Fractures in the Mouse Mutant sfx Are Caused by Deletion of the Gulonolactone Oxidase Gene, Causing Vitamin C Deficiency

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

New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice

A Missense Mutation in the Mouse Col2a1 Gene Causes Spondyloepiphyseal Dysplasia Congenita, Hearing Loss, and Retinoschisis

Identification of genes required for eye development by high-throughput screening of mouse knockouts

Variation in Bone Biomechanical Properties, Microstructure, and Density in BXH Recombinant Inbred Mice

Insulin-like Growth Factors and Bone: The Osteoporosis Connection

Chromosomal inversion discovered in C3H/HeJ mice

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