90 Publications (Page 4 of 4)
1999
Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.Murrell, Jill R⋅Spillantini, Maria G⋅Zolo, P⋅Guazzelli, Mario⋅Smith, M J⋅Hasegawa, M⋅Redi, F⋅Crowther, R A⋅Pietrini, Pietro⋅Ghetti, Bernardino and Goedert, MJournal of neuropathology and experimental neurology, vol. 58, (no. 12), pp. 1207-26, 1999/Dec.
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Tau pathology in a family with dementia and a P301L mutation in tau.Mirra, Suzanne S⋅Murrell, Jill R⋅Gearing, Marla⋅Spillantini, Maria G⋅Goedert, M⋅Crowther, R A⋅Levey, Allan I⋅Jones, R⋅Green, J⋅Shoffner, J M⋅Wainer, B H⋅Schmidt, M L⋅Trojanowski, John Q and Ghetti, BernardinoJournal of Neuropathology and Experimental Neurology, vol. 58, (no. 4), pp. 335-45, 1999/Apr.
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1998
Mutation in the tau gene in familial multiple system tauopathy with presenile dementiaSpillantini, Maria G⋅Murrell, Jill R⋅Goedert, M.⋅Farlow, Martin R⋅Klug, A. and Ghetti, BernardinoProceedings of the National Academy of Sciences, USA, vol. 95, (no. 13), pp. 7737-7741, 1998.
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1997
Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filamentsSpillantini, Maria G⋅Goedert, M.⋅Crowther, RA⋅Murrell, Jill R⋅Farlow, Martin R and Ghetti, BernardinoProceedings of the National Academy of Sciences, USA, vol. 94, (no. 8), pp. 4113-4118, 1997.
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Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.Murrell, Jill R⋅Koller, D⋅Foroud, T⋅Goedert, M⋅Spillantini, M G⋅Edenberg, H J⋅Farlow, M R and Ghetti, BAmerican journal of human genetics. , vol. 61, (no. 5), pp. 1131-8, 1997/Nov.
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1995
A 500-kilobase region containing the tuberous sclerosis locus (TSC1) in a 1.7-megabase YAC and cosmid contig.Murrell, Jill R⋅Trofatter, James⋅Rutter, M⋅Cutone, S⋅Stotler, C⋅Rutter, J⋅Long, K⋅Turner, A⋅Deaven, L and Buckler, AGenomics, vol. 25, (no. 1), pp. 59-65, 1995/Jan/1.
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Tertiary structure of an amyloid immunoglobulin light chain protein: A proposed model for amyloid fibril formationSchormann, N.⋅Murrell, Jill R⋅Liepnieks, JJ and Benson, Merrill DProceedings of the National Academy of Sciences, USA, vol. 92, (no. 21), pp. 9490-9494, 1995.
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1994
Isolation of genes from complex sources of mammalian genomic DNA using exon amplification.Church, D M⋅Stotler, C J⋅Rutter, J L⋅Murrell, Jill R⋅Trofatter, James and Buckler, A JNature genetics, vol. 6, (no. 1), pp. 98-105, 1994/Jan.
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1993
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressorTrofatter, James⋅Mac Collin, Mia M⋅Rutter, JL⋅Murrell, Jill R⋅Duyao, MP⋅Parry, DM⋅Eldridge, R.⋅Kley, N.⋅Menon, Anil G⋅Pulaski, K.⋅Haase, Volker H⋅Ambrose, CM⋅Munroe, D.⋅Bove, C. and Haines, Jonathan LCell, vol. 72, (no. 5), pp. 791-800, 1993.
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A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor.Trofatter, James⋅Mac Collin, Mia M⋅Rutter, J L⋅Murrell, Jill R⋅Duyao, M P⋅Parry, D M⋅Eldridge, R⋅Kley, N⋅Menon, A G and Pulaski, KCell, vol. 75, (no. 4), pp. 826, 1993/Nov/19.
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RFLP analysis for APP 717 mutations associated with Alzheimer's disease.Zeldenrust, Steven R⋅Murrell, Jill R⋅Farlow, Martin R⋅Ghetti, Bernardino⋅Roses, Allen D and Benson, Merrill DJournal of Medical Genetics, vol. 30, (no. 6), pp. 476-478, 1993.
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Structure, function, and metabolism of transthyretin proteins (Dissertation)Murrell, Jill R (1992).