William F. Kaemmerer, Ph.D. - Publications

Affiliations: 
University of Minnesota, Twin Cities, Minneapolis, MN 
Area:
Stem cells

10 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Grondin R, Ge P, Chen Q, Sutherland JE, Zhang Z, Gash DM, Stiles DK, Stewart GR, Sah DW, Kaemmerer WF. Onset Time and Durability of Huntingtin Suppression in Rhesus Putamen After Direct Infusion of Antihuntingtin siRNA. Molecular Therapy. Nucleic Acids. 4: e245. PMID 26125484 DOI: 10.1038/Mtna.2015.20  0.342
2012 Grondin R, Kaytor MD, Ai Y, Nelson PT, Thakker DR, Heisel J, Weatherspoon MR, Blum JL, Burright EN, Zhang Z, Kaemmerer WF. Six-month partial suppression of Huntingtin is well tolerated in the adult rhesus striatum. Brain : a Journal of Neurology. 135: 1197-209. PMID 22252996 DOI: 10.1093/Brain/Awr333  0.392
2012 Stiles DK, Zhang Z, Ge P, Nelson B, Grondin R, Ai Y, Hardy P, Nelson PT, Guzaev AP, Butt MT, Charisse K, Kosovrasti V, Tchangov L, Meys M, Maier M, ... ... Kaemmerer WF, et al. Widespread suppression of huntingtin with convection-enhanced delivery of siRNA. Experimental Neurology. 233: 463-71. PMID 22119622 DOI: 10.1016/J.Expneurol.2011.11.020  0.365
2009 Lombardi MS, Jaspers L, Spronkmans C, Gellera C, Taroni F, Di Maria E, Donato SD, Kaemmerer WF. A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference. Experimental Neurology. 217: 312-9. PMID 19289118 DOI: 10.1016/J.Expneurol.2009.03.004  0.307
2008 Belur LR, Kaemmerer WF, McIvor RS, Low WC. Adeno-associated virus type 2 vectors: transduction and long-term expression in cerebellar Purkinje cells in vivo is mediated by the fibroblast growth factor receptor 1 : bFGFR-1 mediates AAV2 transduction of Purkinje cells. Archives of Virology. 153: 2107-10. PMID 18937030 DOI: 10.1007/S00705-008-0222-7  0.456
2008 van Bilsen PH, Jaspers L, Lombardi MS, Odekerken JC, Burright EN, Kaemmerer WF. Identification and allele-specific silencing of the mutant huntingtin allele in Huntington's disease patient-derived fibroblasts. Human Gene Therapy. 19: 710-9. PMID 18549309 DOI: 10.1089/Hum.2007.116  0.339
2002 Pan D, Gunther R, Duan W, Wendell S, Kaemmerer W, Kafri T, Verma IM, Whitley CB. Biodistribution and toxicity studies of VSVG-pseudotyped lentiviral vector after intravenous administration in mice with the observation of in vivo transduction of bone marrow. Molecular Therapy : the Journal of the American Society of Gene Therapy. 6: 19-29. PMID 12095299 DOI: 10.1006/Mthe.2002.0630  0.359
2001 Kaemmerer WF, Rodrigues CM, Steer CJ, Low WC. Creatine-supplemented diet extends Purkinje cell survival in spinocerebellar ataxia type 1 transgenic mice but does not prevent the ataxic phenotype. Neuroscience. 103: 713-24. PMID 11274790 DOI: 10.1016/S0306-4522(01)00017-3  0.486
2000 Kaemmerer WF, Reddy RG, Warlick CA, Hartung SD, McIvor RS, Low WC. In vivo transduction of cerebellar Purkinje cells using adeno-associated virus vectors. Molecular Therapy : the Journal of the American Society of Gene Therapy. 2: 446-57. PMID 11082318 DOI: 10.1006/Mthe.2000.0134  0.473
1999 Kaemmerer WF, Low WC. Cerebellar allografts survive and transiently alleviate ataxia in a transgenic model of spinocerebellar ataxia type-1. Experimental Neurology. 158: 301-11. PMID 10415138 DOI: 10.1006/Exnr.1999.7099  0.471
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