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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1991 | 1 |
1994 | 1 |
1998 | 1 |
1999 | 1 |
2000 | 1 |
2004 | 1 |
2006 | 1 |
2023 | 0 |
PubMed (OMIM) for id: 155705
7 results
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Page 1
Spectrin mutations cause spinocerebellar ataxia type 5.
Nat Genet. 2006 Feb;38(2):184-90. doi: 10.1038/ng1728. Epub 2006 Jan 22.
Nat Genet. 2006.
PMID: 16429157
Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.
Bürk K, Zühlke C, König IR, Ziegler A, Schwinger E, Globas C, Dichgans J, Hellenbroich Y.
Bürk K, et al.
Neurology. 2004 Jan 27;62(2):327-9. doi: 10.1212/01.wnl.0000103293.63340.c1.
Neurology. 2004.
PMID: 14745083
Review.
Item in Clipboard
Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1.
Lin X, Antalffy B, Kang D, Orr HT, Zoghbi HY.
Lin X, et al.
Nat Neurosci. 2000 Feb;3(2):157-63. doi: 10.1038/72101.
Nat Neurosci. 2000.
PMID: 10649571
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Clinical and MRI findings in spinocerebellar ataxia type 5.
Stevanin G, Herman A, Brice A, Dürr A.
Stevanin G, et al.
Neurology. 1999 Oct 12;53(6):1355-7. doi: 10.1212/wnl.53.6.1355.
Neurology. 1999.
PMID: 10522902
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A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles.
Stankewich MC, Tse WT, Peters LL, Ch'ng Y, John KM, Stabach PR, Devarajan P, Morrow JS, Lux SE.
Stankewich MC, et al.
Proc Natl Acad Sci U S A. 1998 Nov 24;95(24):14158-63. doi: 10.1073/pnas.95.24.14158.
Proc Natl Acad Sci U S A. 1998.
PMID: 9826670
Free PMC article.
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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
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The defect in Marfan syndrome.
McKusick VA.
McKusick VA.
Nature. 1991 Jul 25;352(6333):279-81. doi: 10.1038/352279a0.
Nature. 1991.
PMID: 1852198
No abstract available.
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