A new mutant transthyretin (Arg 10) associated with familial amyloid polyneuropathy.

Por Uemichi, T, Murrell, J R, Zeldenrust, S, Benson, M D
Publicado em 1992

Characterization of flavonol synthase and leucoanthocyanidin dioxygenase genes in Arabidopsis. Further evidence for differential regulation of "early" and "late" genes.

Por Pelletier, M K, Murrell, J R, Shirley, B W
Publicado em 1997

Tertiary structure of an amyloid immunoglobulin light chain protein: a proposed model for amyloid fibril formation.

Por Schormann, N, Murrell, J R, Liepnieks, J J, Benson, M D
Publicado em 1995

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17.

Por Murrell, J R, Koller, D, Foroud, T, Goedert, M, Spillantini, M G, Edenberg, H J, Farlow, M R, Ghetti, B
Publicado em 1997

Altered localization and functionality of TAR DNA Binding Protein 43 (TDP-43) in niemann- pick disease type C

Por Dardis, A., Zampieri, S., Canterini, S., Newell, K. L., Stuani, C., Murrell, J. R., Ghetti, B., Fiorenza, M. T., Bembi, B., Buratti, E.
Publicado no Acta Neuropathol Commun (2016)

HYPERTENSION AND INCIDENT DEMENTIA IN COMMUNITY-DWELLING ELDERLY YORUBA NIGERIANS

Por Ogunniyi, A., Lane, K.A., Baiyewu, O., Gao, S., Gureje, O., Unverzagt, F.W., Murrell, J.R., Smith-Gamble, V., Hall, K.S., Hendrie, H.C.
Publicado em 2011

Use of anticholinergics and the risk of cognitive impairment in an African American population

Por Campbell, N.L., Boustani, M.A., Lane, K.A., Gao, S., Hendrie, H., Khan, B.A., Murrell, J.R., Unverzagt, F.W., Hake, A., Smith-Gamble, V., Hall, K.
Publicado em 2010

Phenotypic variability in three families with valosin-containing protein mutation

Por Spina, S., Van Laar, A. D., Murrell, J. R., Hamilton, R. L., Kofler, J. K., Epperson, F., Farlow, M. R., Lopez, O. L., Quinlan, J., DeKosky, S. T., Ghetti, B.
Publicado em 2012