Peter J. Detloff
Affiliations: | 1993- | Biochemistry and Molecular Genetics | University of Alabama, Birmingham, Birmingham, AL, United States |
Area:
Genetics, BiochemistryWebsite:
https://www.uab.edu/medicine/biochem/faculty/detloffGoogle:
"Peter J Detloff"Mean distance: 6635.5
Parents
Sign in to add mentorThomas D. Petes | grad student | 1991 | Chicago (Cell Biology Tree) | |
(DNA repair during meiotic recombination in Saccharomyces Cerevisiae.) | ||||
Oliver Smithies | post-doc | 1990-1993 | UNC Chapel Hill |
Children
Sign in to add traineeJamie A. Cearley | grad student | 2001 | UAB |
Chin-Hsing Lin | grad student | 2001 | UAB |
Oon T. Ang | grad student | 2002 | UAB |
Karen T. Dixon | grad student | 2004 | UAB |
Andrew B. Crouse | grad student | 2005 | UAB |
BETA: Related publications
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Publications
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Cao JK, Detloff PJ, Gardner RG, et al. (2017) Sex-Dependent Behavioral Impairments in the HdhQ350/+ Mouse Line. Behavioural Brain Research |
Garland H, Wood NI, Skillings EA, et al. (2017) Characterisation of progressive motor deficits in whisker movements in R6/2, Q175 and Hdh knock-in mouse models of Huntington's disease. Journal of Neuroscience Methods |
Kumar A, Zhang J, Tallaksen-Greene S, et al. (2016) Allelic Series of Huntington's Disease Knock-in Mice Reveals Expression Discorrelates. Human Molecular Genetics |
Ciamei A, Detloff PJ, Morton AJ. (2015) Progression of behavioural despair in R6/2 and Hdh knock-in mouse models recapitulates depression in Huntington's disease. Behavioural Brain Research. 291: 140-6 |
Jin J, Peng Q, Hou Z, et al. (2015) Early white matter abnormalities, progressive brain pathology and motor deficits in a novel knock-in mouse model of Huntington's disease. Human Molecular Genetics. 24: 2508-27 |
Sathasivam K, Neueder A, Gipson TA, et al. (2013) Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease. Proceedings of the National Academy of Sciences of the United States of America. 110: 2366-70 |
Dougherty SE, Reeves JL, Lesort M, et al. (2013) Purkinje cell dysfunction and loss in a knock-in mouse model of Huntington disease. Experimental Neurology. 240: 96-102 |
Kumar A, Kneynsberg A, Tucholski J, et al. (2012) Tissue transglutaminase overexpression does not modify the disease phenotype of the R6/2 mouse model of Huntington's disease. Experimental Neurology. 237: 78-89 |
Heng MY, Detloff PJ, Paulson HL, et al. (2010) Early alterations of autophagy in Huntington disease-like mice. Autophagy. 6: 1206-8 |
Heng MY, Duong DK, Albin RL, et al. (2010) Early autophagic response in a novel knock-in model of Huntington disease. Human Molecular Genetics. 19: 3702-20 |