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Oncology Letters
|
June 29, 2012
A novel animal model for bone metastasis in human lung cancer
Mi Li, Mingliang Zhou, Meng Gong, et al.
Genetics
|
August 25, 2005
Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice
Yan Jiao, Jian Yan, Yu Zhao, et al.
Photodiagnosis and Photodynamic Therapy
|
July 23, 2014
Early apoptotic responses in transgenic mouse mammary carcinoma for photodynamic therapy
Heinrich Walt, Marius Nap, Ann M Dorward, et al.
Genomics
|
November 29, 2005
Chromosomal inversion discovered in C3H/HeJ mice
Ellen C Akeson, Leah Rae Donahue, Wesley G Beamer, et al.
Genomics
|
January 20, 2009
Quantitative trait loci, genes, and polymorphisms that regulate bone mineral density in mouse
Qing Xiong, Yan Jiao, Karen A Hasty, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 31, 2003
Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains
Daniel L Koller, Jennifer Schriefer, Qiwei Sun, et al.
The Journal of Biological Chemistry
|
March 5, 2011
The heparin-binding domain of IGFBP-2 has insulin-like growth factor binding-independent biologic activity in the growing skeleton
Masanobu Kawai, Anne C Breggia, Victoria E DeMambro, et al.
Neuroscience Letters
|
December 19, 2006
Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse
Jian Yan, Yan Jiao, Feng Jiao, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 4, 2011
An essential role for the association of CD47 to SHPS-1 in skeletal remodeling
Laura A Maile, Victoria E DeMambro, Christine Wai, et al.
Human Molecular Genetics
|
November 13, 2004
Urogenital and caudal dysgenesis in adrenocortical dysplasia (acd) mice is caused by a splicing mutation in a novel telomeric regulator
Catherine E Keegan, Janna E Hutz, Tobias Else, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 55) with videos related to
Sort By:
Page
of 6
Oncology Letters
|
June 29, 2012
A novel animal model for bone metastasis in human lung cancer
Mi Li, Mingliang Zhou, Meng Gong, et al.
Genetics
|
August 25, 2005
Carbonic anhydrase-related protein VIII deficiency is associated with a distinctive lifelong gait disorder in waddles mice
Yan Jiao, Jian Yan, Yu Zhao, et al.
Photodiagnosis and Photodynamic Therapy
|
July 23, 2014
Early apoptotic responses in transgenic mouse mammary carcinoma for photodynamic therapy
Heinrich Walt, Marius Nap, Ann M Dorward, et al.
Genomics
|
November 29, 2005
Chromosomal inversion discovered in C3H/HeJ mice
Ellen C Akeson, Leah Rae Donahue, Wesley G Beamer, et al.
Genomics
|
January 20, 2009
Quantitative trait loci, genes, and polymorphisms that regulate bone mineral density in mouse
Qing Xiong, Yan Jiao, Karen A Hasty, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 31, 2003
Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains
Daniel L Koller, Jennifer Schriefer, Qiwei Sun, et al.
The Journal of Biological Chemistry
|
March 5, 2011
The heparin-binding domain of IGFBP-2 has insulin-like growth factor binding-independent biologic activity in the growing skeleton
Masanobu Kawai, Anne C Breggia, Victoria E DeMambro, et al.
Neuroscience Letters
|
December 19, 2006
Effects of carbonic anhydrase VIII deficiency on cerebellar gene expression profiles in the wdl mouse
Jian Yan, Yan Jiao, Feng Jiao, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
June 4, 2011
An essential role for the association of CD47 to SHPS-1 in skeletal remodeling
Laura A Maile, Victoria E DeMambro, Christine Wai, et al.
Human Molecular Genetics
|
November 13, 2004
Urogenital and caudal dysgenesis in adrenocortical dysplasia (acd) mice is caused by a splicing mutation in a novel telomeric regulator
Catherine E Keegan, Janna E Hutz, Tobias Else, et al.
Page
of 6