NSK Haque, P Borghesani, O Isacson - Molecular Medicine Today, 1997 - cell.com
A mutation on chromosome 4p16. 3 with an expanded polyglutamine tract has been identified as the cause of Huntington's disease (HD). The neuroscience and clinical …
CM Kosinski, JH Cha, AB Young, F Persichetti… - Experimental …, 1997 - Elsevier
Huntington's disease is caused by a mutation of the gene encoding the protein huntingtin. Features of the human disease, characterized by selective loss of neurons from the …
G Figueredo-Cardenas, Q Chen, A Reiner - Experimental neurology, 1997 - Elsevier
Some authors have reported greater sparing of neurons containing somatostatin (SS)– neuropeptide Y (NPY)–NADPH-diaphorase (NADPHd) than projection neurons after …
SP Knight, MM Richardson, AP Osmand… - Journal of the …, 1997 - Elsevier
Utilizing an affinity-purified antiserum directed against the carboxyl terminal region of atrophin-1/drplap (residues 1170–1185), we have examined the expression and distribution …