Ranum LPW - Search Results

1

Longitudinal single-cell transcriptional dynamics throughout neurodegeneration in SCA1.

Tejwani L, Ravindra NG, Lee C, Cheng Y, Nguyen B, Luttik K, Ni L, Zhang S, Morrison LM, Gionco J, Xiang Y, Yoon J, Ro H, Haidery F, Grijalva RM, Bae E, Kim K, Martuscello RT, Orr HT, Zoghbi HY, McLoughlin HS, Ranum LPW, Shakkottai VG, Faust PL, Wang S, van Dijk D, Lim J. Tejwani L, et al. Among authors: ranum lpw. Neuron. 2024 Feb 7;112(3):362-383.e15. doi: 10.1016/j.neuron.2023.10.039. Epub 2023 Nov 27. Neuron. 2024. PMID: 38016472 Free article.

2

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

Chung MY, Ranum LP, Duvick LA, Servadio A, Zoghbi HY, Orr HT. Chung MY, et al. Nat Genet. 1993 Nov;5(3):254-8. doi: 10.1038/ng1193-254. Nat Genet. 1993. PMID: 8275090

3

Mapping and cloning of the critical region for the spinocerebellar ataxia type 1 gene (SCA1) in a yeast artificial chromosome contig spanning 1.2 Mb.

Banfi S, Chung MY, Kwiatkowski TJ Jr, Ranum LP, McCall AE, Chinault AC, Orr HT, Zoghbi HY. Banfi S, et al. Genomics. 1993 Dec;18(3):627-35. doi: 10.1016/s0888-7543(05)80365-9. Genomics. 1993. PMID: 8307572

4

Dinucleotide repeat polymorphism at the D6S109 locus.

Ranum LP, Chung MY, Duvick LA, Zoghbi HY, Orr HT. Ranum LP, et al. Nucleic Acids Res. 1991 Mar 11;19(5):1171. doi: 10.1093/nar/19.5.1171-a. Nucleic Acids Res. 1991. PMID: 2020562 Free PMC article. No abstract available.

5

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

Orr HT, Chung MY, Banfi S, Kwiatkowski TJ Jr, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY. Orr HT, et al. Nat Genet. 1993 Jul;4(3):221-6. doi: 10.1038/ng0793-221. Nat Genet. 1993. PMID: 8358429

6

Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p.

Ranum LP, Duvick LA, Rich SS, Schut LJ, Litt M, Orr HT. Ranum LP, et al. Am J Hum Genet. 1991 Jul;49(1):31-41. Am J Hum Genet. 1991. PMID: 1676561 Free PMC article.

7

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

Ranum LP, Schut LJ, Lundgren JK, Orr HT, Livingston DM. Ranum LP, et al. Nat Genet. 1994 Nov;8(3):280-4. doi: 10.1038/ng1194-280. Nat Genet. 1994. PMID: 7874171

8

Nuclear localization of the spinocerebellar ataxia type 7 protein, ataxin-7.

Kaytor MD, Duvick LA, Skinner PJ, Koob MD, Ranum LP, Orr HT. Kaytor MD, et al. Hum Mol Genet. 1999 Sep;8(9):1657-64. doi: 10.1093/hmg/8.9.1657. Hum Mol Genet. 1999. PMID: 10441328

9

Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxia.

Ranum LP, Lundgren JK, Schut LJ, Ahrens MJ, Perlman S, Aita J, Bird TD, Gomez C, Orr HT. Ranum LP, et al. Am J Hum Genet. 1995 Sep;57(3):603-8. Am J Hum Genet. 1995. PMID: 7668288 Free PMC article.

10

Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred.

Ranum LP, Rich SS, Nance MA, Duvick LA, Aita JF, Orr HT, Anton-Johnson S, Schut LJ. Ranum LP, et al. Neurology. 1992 Feb;42(2):344-7. doi: 10.1212/wnl.42.2.344. Neurology. 1992. PMID: 1736163

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