AAAAAA
Results: 1-25/28
Authors:
Costa, RM
Yang, T
Huynh, DP
Pulst, SM
Viskochil, DH
Silva, AJ
Brannan, CI
Citation: Rm. Costa et al., Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1, NAT GENET, 27(4), 2001, pp. 399-405
Authors:
Gutmann, DH
Haipek, CA
Burke, SP
Sun, CX
Scoles, DR
Pulst, SM
Citation: Dh. Gutmann et al., The NF2 interactor, hepatocyte growth factor-regulated tyrosine kinase substrate (HRS), associates with merlin in the 'open' conformation and suppresses cell growth and motility, HUM MOL GEN, 10(8), 2001, pp. 825-834
Authors:
Bruder, CEG
Hirvela, C
Tapia-Paez, I
Fransson, I
Segraves, R
Hamilton, G
Zhang, XX
Evans, DG
Wallace, AJ
Baser, ME
Zucman-Rossi, J
Hergersberg, M
Boltshauser, E
Papi, L
Rouleau, GA
Poptodorov, G
Jordanova, A
Rask-Andersen, H
Kluwe, L
Mautner, V
Sainio, M
Hung, G
Mathiesen, T
Moller, C
Pulst, SM
Harder, H
Heiberg, A
Honda, M
Miimura, M
Sahlen, S
Blennow, E
Albertson, DG
Pinkel, D
Dumanski, JP
Citation: Ceg. Bruder et al., High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH, HUM MOL GEN, 10(3), 2001, pp. 271-282
Authors:
Kiehl, TR
Shibata, H
Vo, T
Huynh, DP
Pulst, SM
Citation: Tr. Kiehl et al., Identification and expression of a mouse ortholog of A2BP1, MAMM GENOME, 12(8), 2001, pp. 595-601
Authors:
Huynh, DP
Dy, M
Nguyen, D
Kiehl, TR
Pulst, SM
Citation: Dp. Huynh et al., Differential expression and tissue distribution of parkin isoforms during mouse development, DEV BRAIN R, 130(2), 2001, pp. 173-181
Authors:
So, YT
Zu, L
Barraza, C
Figueroa, KP
Pulst, SM
Citation: Yt. So et al., Rippling muscle disease: Evidence for phenotypic and genetic heterogeneity, MUSCLE NERV, 24(3), 2001, pp. 340-344
Authors:
Sobrido, MJ
Cholfin, JA
Perlman, S
Pulst, SM
Geschwind, DH
Citation: Mj. Sobrido et al., SCA8 repeat expansions in ataxia: A controversial association, NEUROLOGY, 57(7), 2001, pp. 1310-1312
Authors:
Konakova, M
Huynh, DP
Yong, W
Pulst, SM
Citation: M. Konakova et al., Cellular distribution of torsin A and torsin B in normal human brain, ARCH NEUROL, 58(6), 2001, pp. 921-927
Authors:
Pulst, SM
Citation: Sm. Pulst, Genomes, neuroscience, and neurology, ARCH NEUROL, 58(11), 2001, pp. 1755-1757
Authors:
Cholfin, JA
Sobrido, MJ
Perlman, S
Pulst, SM
Geschwind, DH
Citation: Ja. Cholfin et al., The SCA12 mutation as a rare cause of spinocerebellar ataxia, ARCH NEUROL, 58(11), 2001, pp. 1833-1835
Authors:
Figueroa, KP
Chan, P
Schols, L
Tanner, C
Riess, O
Perlman, SL
Geschwind, DH
Pulst, SM
Citation: Kp. Figueroa et al., Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia, ARCH NEUROL, 58(10), 2001, pp. 1649-1653
Authors:
Matsuura, T
Yamagata, T
Burgess', DL
Rasmussen, A
Grewal, RP
Watase, K
Khajavi, M
McCall, AE
Davis, CF
Zu, L
Achari, M
Pulst, SM
Alonso, E
Noebels, JL
Nelson, DL
Zoghbi, HY
Ashizawa, T
Citation: T. Matsuura et al., Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10, NAT GENET, 26(2), 2000, pp. 191-194
Authors:
Huynh, DP
Figueroa, K
Hoang, N
Pulst, SM
Citation: Dp. Huynh et al., Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human, NAT GENET, 26(1), 2000, pp. 44-50
Authors:
Shibata, H
Huynh, DP
Pulst, SM
Citation: H. Shibata et al., A novel protein with RNA-binding motifs interacts with ataxin-2, HUM MOL GEN, 9(9), 2000, pp. 1303-1313
Authors:
Hayes, S
Turecki, G
Brisebois, K
Lopes-Cendes, I
Gaspar, C
Riess, O
Ranum, LPW
Pulst, SM
Rouleau, GA
Citation: S. Hayes et al., CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2), HUM MOL GEN, 9(12), 2000, pp. 1753-1758
Authors:
Shibata, H
Huynh, DP
Pulst, SM
Citation: H. Shibata et al., A novel protein with RNA-binding motifs interacts with ataxin-2 (vol 9, pg1303, 2000), HUM MOL GEN, 9(12), 2000, pp. 1903-1903
Authors:
Scoles, DR
Huynh, DP
Chen, MS
Burke, SP
Gutmann, DH
Pulst, SM
Citation: Dr. Scoles et al., The neurofibromatosis 2 tumor suppressor protein interacts with hepatocytegrowth factor-regulated tyrosine kinase substrate, HUM MOL GEN, 9(11), 2000, pp. 1567-1574
Authors:
Kiehl, TR
Shibata, H
Pulst, SM
Citation: Tr. Kiehl et al., The ortholog of human ataxin-2 is essential for early embryonic patterningin C-elegans, J MOL NEURO, 15(3), 2000, pp. 231-241
Authors:
Huynh, DP
Scoles, DR
Ho, TH
Del Bigio, MR
Pulst, SM
Citation: Dp. Huynh et al., Parkin is associated with actin filaments in neuronal and nonneural cells, ANN NEUROL, 48(5), 2000, pp. 737-744
Authors:
Lim, DJ
Rubenstein, AE
Evans, DG
Jacks, T
Seizinger, BG
Baser, ME
Beebe, D
Brackmann, DE
Chiocca, EA
Fehon, RG
Giovannini, M
Glazer, R
Gusella, JF
Gutmann, DH
Korf, B
Lieberman, F
Martuza, R
McClatchey, AI
Parry, DM
Pulst, SM
Ramesh, V
Ramsey, WJ
Ratner, N
Rutkowski, JL
Ruttledge, M
Weinstein, DE
Citation: Dj. Lim et al., Advances in neurofibromatosis 2 (NF2): A workshop report, J NEUROGEN, 14(2), 2000, pp. 63-106
Authors:
Pulst, SM
Citation: Sm. Pulst, Ethical issues in DNA testing, MUSCLE NERV, 23(10), 2000, pp. 1503-1507
Authors:
Pulst, SM
Citation: Sm. Pulst, NF2 in monozygotic twins, SURG NEUROL, 53(1), 2000, pp. 95-95
Authors:
Pulst, SM
Filla, A
Citation: Sm. Pulst et A. Filla, Ataxias on the march from Quebec to Tunisia, NEUROLOGY, 54(7), 2000, pp. 1400-1401
Authors:
Huynh, DP
Del Bigio, MR
Ho, DH
Pulst, SM
Citation: Dp. Huynh et al., Expression of ataxin-2 in brains from normal individuals and patients withAlzheimer's disease and spinocerebellar ataxia 2, ANN NEUROL, 45(2), 1999, pp. 232-241
Authors:
Simon, DK
Pulst, SM
Sutton, JP
Browne, SE
Beal, MF
Johns, DR
Citation: Dk. Simon et al., Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation, NEUROLOGY, 53(8), 1999, pp. 1787-1793