关注
Laura P.W. Ranum
Laura P.W. Ranum
Kitzman Family Professor of Molecular Genetics and Microbiology, Director, Center for NeuroGenetics
在 ufl.edu 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
HT Orr, M Chung, S Banfi, TJ Kwiatkowski, A Servadio, AL Beaudet, ...
Nature genetics 4 (3), 221-226, 1993
20211993
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
CL Liquori, K Ricker, ML Moseley, JF Jacobsen, W Kress, SL Naylor, ...
Science 293 (5531), 864-867, 2001
15382001
Non-ATG–initiated translation directed by microsatellite expansions
T Zu, B Gibbens, NS Doty, M Gomes-Pereira, A Huguet, MD Stone, ...
Proceedings of the National Academy of Sciences 108 (1), 260-265, 2011
9872011
RAN proteins and RNA foci from antisense transcripts in C9ORF72 ALS and frontotemporal dementia
T Zu, Y Liu, M Bañez-Coronel, T Reid, O Pletnikova, J Lewis, TM Miller, ...
Proceedings of the National Academy of Sciences 110 (51), E4968-E4977, 2013
8732013
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
MD Koob, ML Moseley, LJ Schut, KA Benzow, TD Bird, JW Day, ...
Nature genetics 21 (4), 379-384, 1999
7131999
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I
M Chung, LPW Ranum, LA Duvick, A Servadio, HY Zoghbi, HT Orr
Nature genetics 5 (3), 254-258, 1993
5881993
RNA-mediated neuromuscular disorders
LPW Ranum, TA Cooper
Annu. Rev. Neurosci. 29, 259-277, 2006
5822006
Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum
JW Day, K Ricker, JF Jacobsen, LJ Rasmussen, KA Dick, W Kress, ...
Neurology 60 (4), 657-664, 2003
5552003
Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8
ML Moseley, T Zu, Y Ikeda, W Gao, AK Mosemiller, RS Daughters, ...
Nature genetics 38 (7), 758-769, 2006
4752006
Spectrin mutations cause spinocerebellar ataxia type 5
Y Ikeda, KA Dick, MR Weatherspoon, D Gincel, KR Armbrust, JC Dalton, ...
Nature genetics 38 (2), 184-190, 2006
4282006
C9orf72 BAC mouse model with motor deficits and neurodegenerative features of ALS/FTD
Y Liu, A Pattamatta, T Zu, T Reid, O Bardhi, DR Borchelt, AT Yachnis, ...
Neuron 90 (3), 521-534, 2016
3972016
Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11
LPW Ranum, LJ Schut, JK Lundgren, HT Orr, DM Livingston
Nature genetics 8 (3), 280-284, 1994
3811994
RAN translation in Huntington disease
M Bañez-Coronel, F Ayhan, AD Tarabochia, T Zu, BA Perez, SK Tusi, ...
Neuron 88 (4), 667-677, 2015
3782015
Genetic mapping of a second myotonic dystrophy locus
LPW Ranum, PF Rasmussen, KA Benzow, MD Koob, JW Day
Nature genetics 19 (2), 196-198, 1998
3641998
Mutant huntingtin disrupts the nuclear pore complex
JC Grima, JG Daigle, N Arbez, KC Cunningham, K Zhang, J Ochaba, ...
Neuron 94 (1), 93-107. e6, 2017
3372017
RNA gain-of-function in spinocerebellar ataxia type 8
RS Daughters, DL Tuttle, W Gao, Y Ikeda, ML Moseley, TJ Ebner, ...
PLoS genetics 5 (8), e1000600, 2009
3162009
Myotonic dystrophy: RNA pathogenesis comes into focus
LPW Ranum, JW Day
The American Journal of Human Genetics 74 (5), 793-804, 2004
3032004
Correlating phenotype and genotype in the periodic paralyses
TM Miller, MRD Da Silva, HA Miller, H Kwiecinski, JR Mendell, R Tawil, ...
Neurology 63 (9), 1647-1655, 2004
2982004
Isolation and characterization of the nitrate reductase structural gene of Chlamydomonas reinhardtii
E Fernández, R Schnell, LP Ranum, SC Hussey, CD Silflow, PA Lefebvre
Proceedings of the National Academy of Sciences 86 (17), 6449-6453, 1989
2831989
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families
ML Moseley, KA Benzow, LJ Schut, TD Bird, CM Gomez, PE Barkhaus, ...
Neurology 51 (6), 1666-1671, 1998
2731998
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