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Neuron|February 17, 2000
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLAG Schilling, J D Wood, K Duan, et al.
Journal of Physics. Condensed Matter : an Institute of Physics Journal|December 3, 2016
Interface electronic structure at the topological insulator-ferrimagnetic insulator junctionY Kubota, K Murata, J Miyawaki, et al.
Neurology|July 23, 1998
Patients with features similar to Huntington's disease, without CAG expansion in huntingtinA Rosenblatt, N G Ranen, D C Rubinsztein, et al.
Human Molecular Genetics|September 25, 1997
A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1T S Breschel, M G McInnis, R L Margolis, et al.
Human Molecular Genetics|May 18, 2000
Decreased expression of striatal signaling genes in a mouse model of Huntington's diseaseR Luthi-Carter, A Strand, N L Peters, et al.
Molecular Psychiatry|July 13, 2000
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxiaM G McInnis, T Swift-Scanlanl, A T Mahoney, et al.
The Journal of Biological Chemistry|May 16, 1998
Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tractC L Wellington, L M Ellerby, A S Hackam, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|August 15, 2016
HDQLIFE: development and assessment of health-related quality of life in Huntington disease (HD)N E Carlozzi, S G Schilling, J-S Lai, et al.
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