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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 17, 2013
Female mice lacking estrogen receptor-alpha in osteoblasts have compromised bone mass and strength
Katherine M Melville, Natalie H Kelly, Sohaib A Khan, et al.
Plos Genetics
|
November 8, 2012
Interallelic and intergenic incompatibilities of the Prdm9 (Hst1) gene in mouse hybrid sterility
Petr Flachs, Ondřej Mihola, Petr Simeček, et al.
Plos Computational Biology
|
October 3, 2012
Tissue-specific functional networks for prioritizing phenotype and disease genes
Yuanfang Guan, Dmitriy Gorenshteyn, Margit Burmeister, et al.
FEBS Letters
|
September 7, 2010
The full-length isoform of the mouse pleckstrin homology domain-interacting protein (PHIP) is required for postnatal growth
Shuai Li, Adam B Francisco, Chunchun Han, et al.
The Journal of Clinical Investigation
|
February 23, 2012
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans
Claire R Hughes, Leonardo Guasti, Eirini Meimaridou, et al.
Science Advances
|
April 2, 2020
SKP1 drives the prophase I to metaphase I transition during male meiosis
Yongjuan Guan, N Adrian Leu, Jun Ma, et al.
Human Molecular Genetics
|
March 11, 2014
STAG3 is a strong candidate gene for male infertility
Elena Llano, Laura Gomez-H, Ignacio García-Tuñón, et al.
Regenerative Medicine
|
April 30, 2014
Induced pluripotent stem cells have similar immunogenic and more potent immunomodulatory properties compared with bone marrow-derived stromal cells in vitro
Lauren V Schnabel, Christian M Abratte, John C Schimenti, et al.
Molecular and Cellular Biology
|
February 13, 2013
The MCM8-MCM9 complex promotes RAD51 recruitment at DNA damage sites to facilitate homologous recombination
Jonghoon Park, David T Long, Kyung Yong Lee, et al.
BMC Developmental Biology
|
April 22, 2009
Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass
Robert J Munroe, Vinay Prabhu, Greg M Acland, et al.
Page
of 23
Search research articles
Search
Showing results (191-200 of 226) with videos related to
Sort By:
Page
of 23
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
September 17, 2013
Female mice lacking estrogen receptor-alpha in osteoblasts have compromised bone mass and strength
Katherine M Melville, Natalie H Kelly, Sohaib A Khan, et al.
Plos Genetics
|
November 8, 2012
Interallelic and intergenic incompatibilities of the Prdm9 (Hst1) gene in mouse hybrid sterility
Petr Flachs, Ondřej Mihola, Petr Simeček, et al.
Plos Computational Biology
|
October 3, 2012
Tissue-specific functional networks for prioritizing phenotype and disease genes
Yuanfang Guan, Dmitriy Gorenshteyn, Margit Burmeister, et al.
FEBS Letters
|
September 7, 2010
The full-length isoform of the mouse pleckstrin homology domain-interacting protein (PHIP) is required for postnatal growth
Shuai Li, Adam B Francisco, Chunchun Han, et al.
The Journal of Clinical Investigation
|
February 23, 2012
MCM4 mutation causes adrenal failure, short stature, and natural killer cell deficiency in humans
Claire R Hughes, Leonardo Guasti, Eirini Meimaridou, et al.
Science Advances
|
April 2, 2020
SKP1 drives the prophase I to metaphase I transition during male meiosis
Yongjuan Guan, N Adrian Leu, Jun Ma, et al.
Human Molecular Genetics
|
March 11, 2014
STAG3 is a strong candidate gene for male infertility
Elena Llano, Laura Gomez-H, Ignacio García-Tuñón, et al.
Regenerative Medicine
|
April 30, 2014
Induced pluripotent stem cells have similar immunogenic and more potent immunomodulatory properties compared with bone marrow-derived stromal cells in vitro
Lauren V Schnabel, Christian M Abratte, John C Schimenti, et al.
Molecular and Cellular Biology
|
February 13, 2013
The MCM8-MCM9 complex promotes RAD51 recruitment at DNA damage sites to facilitate homologous recombination
Jonghoon Park, David T Long, Kyung Yong Lee, et al.
BMC Developmental Biology
|
April 22, 2009
Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass
Robert J Munroe, Vinay Prabhu, Greg M Acland, et al.
Page
of 23