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Ishii, K
Lippa, C
Tomiyama, T
Miyatake, F
Ozawa, K
Tamaoka, A
Hasegawa, T
Fraser, PE
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Nee, LE
Pollen, DA
St George-Hyslop, PH
Ii, K
Ohtake, T
Kalaria, RN
Rossor, MN
Lantos, PL
Cairns, NJ
Farrer, LA
Mori, H
Citation: K. Ishii et al., Distinguishable effects of Presenilin-1 and APP717 mutations on amyloid plaque deposition, NEUROBIOL A, 22(3), 2001, pp. 367-376
Authors:
Higgins, JJ
Loveless, JM
Goswami, S
Nee, LE
Cozzo, C
De Biase, A
Rosen, DR
Citation: Jj. Higgins et al., An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia, NEUROLOGY, 56(11), 2001, pp. 1482-1485
Authors:
Baskin, F
Rosenberg, RN
Iyer, L
Schellenberg, GD
Hynan, L
Nee, LE
Citation: F. Baskin et al., Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation, J NEUR SCI, 183(1), 2001, pp. 85-88
Citation: Le. Nee et Cf. Lippa, Alzheimer's disease in 22 twin pairs 13-year follow-up: Hormonal, infectious and traumatic factors, DEMENT G C, 10(2), 1999, pp. 148-151
Authors:
Higgins, JJ
Litvan, I
Nee, LE
Loveless, JM
Citation: Jj. Higgins et al., A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration, NEUROLOGY, 52(2), 1999, pp. 404-406
Authors:
Imafuku, I
Masaki, T
Waragai, M
Takeuchi, S
Kawabata, M
Hirai, SI
Ohno, S
Nee, LE
Lippa, CF
Kanazawa, I
Imagawa, M
Okazawa, H
Citation: I. Imafuku et al., Presenilin 1 suppresses the function of c-jun homodimers via interaction with QM/Jif-1, J CELL BIOL, 147(1), 1999, pp. 121-133