5.9
CiteScore
5.9
Impact Factor

2012 Vol. 39, No. 6

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Editorial
Beyond Mice: Genetically Modifying Larger Animals to Model Human Diseases
Xiao-Jiang Li, Wei Li
2012, 39(6): 237-238. doi: 10.1016/j.jgg.2012.05.006
Abstract (84) HTML PDF (0)
Abstract:
Review
Influence of Species Differences on the Neuropathology of Transgenic Huntington's Disease Animal Models
Xiao-Jiang Li, Shihua Li
2012, 39(6): 239-245. doi: 10.1016/j.jgg.2012.05.002
Abstract (84) HTML PDF (0)
Abstract:
Transgenic animal models have revealed much about the pathogenesis of age-dependent neurodegenerative diseases and proved to be a useful tool for uncovering therapeutic targets. Huntington's disease is a well-characterized neurodegenerative disorder that is caused by expansion of a CAG repeat, which...
Transgenic Nonhuman Primate Models for Human Diseases: Approaches and Contributing Factors
Yongchang Chen, Yuyu Niu, Weizhi Ji
2012, 39(6): 247-251. doi: 10.1016/j.jgg.2012.04.007
Abstract (112) HTML PDF (0)
Abstract:
Nonhuman primates (NHPs) provide powerful experimental models to study human development, cognitive functions and disturbances as well as complex behavior, because of their genetic and physiological similarities to humans. Therefore, NHPs are appropriate models for the study of human diseases, such ...
Pluripotent Stem Cells Models for Huntington's Disease: Prospects and Challenges
Richard L. Carter, Anthony W.S. Chan
2012, 39(6): 253-259. doi: 10.1016/j.jgg.2012.04.006
Abstract (88) HTML PDF (0)
Abstract:
Pluripotent cellular models have shown great promise in the study of a number of neurological disorders. Several advantages of using a stem cell model include the potential for cells to derive disease relevant neuronal cell types, providing a system for researchers to monitor disease progression dur...
Retake the Center Stage – New Development of Rat Genetics
Sushuang Zheng, Kindiya Geghman, Sushila Shenoy, Chenjian Li
2012, 39(6): 261-268. doi: 10.1016/j.jgg.2012.05.003
Abstract (96) HTML PDF (0)
Abstract:
The rat is a powerful model for the study of human physiology and diseases, and is preferred by physiologists, neuroscientists and toxicologists. However, the lack of robust genetic modification tools has severely limited the generation of rat genetic models over the last two decades. In the last fe...
Targeted Genome Editing by Recombinant Adeno-Associated Virus (rAAV) Vectors for Generating Genetically Modified Pigs
Yonglun Luo, Emil Kofod-Olsen, Rikke Christensen, Charlotte Brandt Sørensen, Lars Bolund
2012, 39(6): 269-274. doi: 10.1016/j.jgg.2012.05.004
Abstract (105) HTML PDF (0)
Abstract:
Recombinant adeno-associated virus (rAAV) vectors have been extensively used for experimental gene therapy of inherited human diseases. Several advantages, such as simple vector construction, high targeting frequency by homologous recombination, and applicability to many cell types, make rAAV an att...
Original research
Rapid and Cost-Effective Gene Targeting in Rat Embryonic Stem Cells by TALENs
Chang Tong, Guanyi Huang, Charles Ashton, Hongping Wu, Hexin Yan, Qi-Long Ying
2012, 39(6): 275-280. doi: 10.1016/j.jgg.2012.04.004
Abstract (113) HTML PDF (1)
Abstract:
The rat is the preferred animal model in many areas of biomedical research and drug development. Genetic manipulation in rats has lagged behind that in mice due to the lack of efficient gene targeting tools. Previously, we generated a knockout rat via conventional homologous recombination in rat emb...
Production of Brown/Yellow Patches in the SLC7A11 Transgenic Sheep via Testicular Injection of Transgene
Xin He, Hongtao Li, Zhiyong Zhou, Zongsheng Zhao, Wei Li
2012, 39(6): 281-285. doi: 10.1016/j.jgg.2012.04.005
Abstract (69) HTML PDF (0)
Abstract:
The gene, SLC7A11, which encodes the solute carrier family 7 member 11 (anionic amino acid transporter light chain, xCT), has been reported to be implicated in multiple processes such as in pheomelanin production, cell proliferation and migration, Kaposi's sarcoma herpesvirus (KSHV) entry into the h...
Automated Behavioral Phenotyping Reveals Presymptomatic Alterations in a SCA3 Genetrap Mouse Model
Jeannette Hübener, Nicolas Casadei, Peter Teismann, Mathias W. Seeliger, Maria Björkqvist, Stephan von Hörsten, Olaf Riess, Huu Phuc Nguyen
2012, 39(6): 287-299. doi: 10.1016/j.jgg.2012.04.009
Abstract (69) HTML PDF (0)
Abstract:
Characterization of disease models of neurodegenerative disorders requires a systematic and comprehensive phenotyping in a highly standardized manner. Therefore, automated high-resolution behavior test systems such as the homecage based LabMaster system are of particular interest. We demonstrate the...