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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1995 | 2 |
2003 | 2 |
2005 | 2 |
2009 | 1 |
2024 | 0 |
PubMed (cited) for id: 608145
7 results
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Page 1
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling.
Hum Mol Genet. 2009 Oct 15;18(20):3805-21. doi: 10.1093/hmg/ddp324. Epub 2009 Jul 20.
Hum Mol Genet. 2009.
PMID: 19620182
Free PMC article.
A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia.
Reed JA, Wilkinson PA, Patel H, Simpson MA, Chatonnet A, Robay D, Patton MA, Crosby AH, Warner TT.
Reed JA, et al.
Neurogenetics. 2005 May;6(2):79-84. doi: 10.1007/s10048-004-0209-9. Epub 2005 Feb 12.
Neurogenetics. 2005.
PMID: 15711826
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Distinct novel mutations affecting the same base in the NIPA1 gene cause autosomal dominant hereditary spastic paraplegia in two Chinese families.
Chen S, Song C, Guo H, Xu P, Huang W, Zhou Y, Sun J, Li CX, Du Y, Li X, Liu Z, Geng D, Maxwell PH, Zhang C, Wang Y.
Chen S, et al.
Hum Mutat. 2005 Feb;25(2):135-41. doi: 10.1002/humu.20126.
Hum Mutat. 2005.
PMID: 15643603
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NIPA1 gene mutations cause autosomal dominant hereditary spastic paraplegia (SPG6).
Rainier S, Chai JH, Tokarz D, Nicholls RD, Fink JK.
Rainier S, et al.
Am J Hum Genet. 2003 Oct;73(4):967-71. doi: 10.1086/378817. Epub 2003 Sep 23.
Am J Hum Genet. 2003.
PMID: 14508710
Free PMC article.
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Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.
Chai JH, Locke DP, Greally JM, Knoll JH, Ohta T, Dunai J, Yavor A, Eichler EE, Nicholls RD.
Chai JH, et al.
Am J Hum Genet. 2003 Oct;73(4):898-925. doi: 10.1086/378816. Epub 2003 Sep 23.
Am J Hum Genet. 2003.
PMID: 14508708
Free PMC article.
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Autosomal dominant, familial spastic paraplegia, type I: clinical and genetic analysis of a large North American family.
Fink JK, Sharp GB, Lange BM, Wu CB, Haley T, Otterud B, Peacock M, Leppert M.
Fink JK, et al.
Neurology. 1995 Feb;45(2):325-31. doi: 10.1212/wnl.45.2.325.
Neurology. 1995.
PMID: 7854534
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Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.
Fink JK, Wu CT, Jones SM, Sharp GB, Lange BM, Lesicki A, Reinglass T, Varvil T, Otterud B, Leppert M.
Fink JK, et al.
Am J Hum Genet. 1995 Jan;56(1):188-92.
Am J Hum Genet. 1995.
PMID: 7825577
Free PMC article.
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