Atlastin-1: Difference between revisions

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Revision as of 23:48, 27 September 2008

Template:PBB Spastic paraplegia 3A (autosomal dominant), also known as SPG3A, is a human gene.^[1]

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References

^ "Entrez Gene: SPG3A spastic paraplegia 3A (autosomal dominant)".

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 | citations =
 *{{cite journal  | author=Gispert S, Santos N, Damen R, ''et al.'' |title=Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity. |journal=Am. J. Hum. Genet. |volume=56 |issue= 1 |pages= 183–7 |year= 1995 |pmid= 7825576 |doi=  }}
-*{{cite journal  | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=  }}
+*{{cite journal  | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8  }}
 *{{cite journal  | author=Hazan J, Lamy C, Melki J, ''et al.'' |title=Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. |journal=Nat. Genet. |volume=5 |issue= 2 |pages= 163–7 |year= 1994 |pmid= 8252041 |doi= 10.1038/ng1093-163 }}
 *{{cite journal  | author=Andersson B, Wentland MA, Ricafrente JY, ''et al.'' |title=A "double adaptor" method for improved shotgun library construction. |journal=Anal. Biochem. |volume=236 |issue= 1 |pages= 107–13 |year= 1996 |pmid= 8619474 |doi= 10.1006/abio.1996.0138 }}
 *{{cite journal  | author=Yu W, Andersson B, Worley KC, ''et al.'' |title=Large-scale concatenation cDNA sequencing. |journal=Genome Res. |volume=7 |issue= 4 |pages= 353–8 |year= 1997 |pmid= 9110174 |doi=  }}
-*{{cite journal  | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, ''et al.'' |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=  }}
+*{{cite journal  | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, ''et al.'' |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3  }}
 *{{cite journal  | author=Zhao X, Alvarado D, Rainier S, ''et al.'' |title=Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. |journal=Nat. Genet. |volume=29 |issue= 3 |pages= 326–31 |year= 2001 |pmid= 11685207 |doi= 10.1038/ng758 }}
 *{{cite journal  | author=Muglia M, Magariello A, Nicoletti G, ''et al.'' |title=Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia. |journal=Ann. Neurol. |volume=51 |issue= 6 |pages= 794–5 |year= 2002 |pmid= 12112092 |doi= 10.1002/ana.10185 }}
-*{{cite journal  | author=Luan Z, Zhang Y, Liu A, ''et al.'' |title=A novel GTP-binding protein hGBP3 interacts with NIK/HGK. |journal=FEBS Lett. |volume=530 |issue= 1-3 |pages= 233–8 |year= 2002 |pmid= 12387898 |doi=  }}
+*{{cite journal  | author=Luan Z, Zhang Y, Liu A, ''et al.'' |title=A novel GTP-binding protein hGBP3 interacts with NIK/HGK. |journal=FEBS Lett. |volume=530 |issue= 1-3 |pages= 233–8 |year= 2002 |pmid= 12387898 |doi=10.1016/S0014-5793(02)03467-1  }}
 *{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
 *{{cite journal  | author=Tessa A, Casali C, Damiano M, ''et al.'' |title=SPG3A: An additional family carrying a new atlastin mutation. |journal=Neurology |volume=59 |issue= 12 |pages= 2002–5 |year= 2003 |pmid= 12499504 |doi=  }}
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 *{{cite journal  | author=Dalpozzo F, Rossetto MG, Boaretto F, ''et al.'' |title=Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation. |journal=Neurology |volume=61 |issue= 4 |pages= 580–1 |year= 2004 |pmid= 12939451 |doi=  }}
 *{{cite journal  | author=Zhu PP, Patterson A, Lavoie B, ''et al.'' |title=Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin. |journal=J. Biol. Chem. |volume=278 |issue= 49 |pages= 49063–71 |year= 2004 |pmid= 14506257 |doi= 10.1074/jbc.M306702200 }}
-*{{cite journal  | author=Wilkinson PA, Hart PE, Patel H, ''et al.'' |title=SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia. |journal=J. Neurol. Sci. |volume=216 |issue= 1 |pages= 43–5 |year= 2004 |pmid= 14607301 |doi=  }}
+*{{cite journal  | author=Wilkinson PA, Hart PE, Patel H, ''et al.'' |title=SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia. |journal=J. Neurol. Sci. |volume=216 |issue= 1 |pages= 43–5 |year= 2004 |pmid= 14607301 |doi=10.1016/S0022-510X(03)00210-7  }}
 *{{cite journal  | author=Sauter SM, Engel W, Neumann LM, ''et al.'' |title=Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus. |journal=Hum. Mutat. |volume=23 |issue= 1 |pages= 98 |year= 2004 |pmid= 14695538 |doi= 10.1002/humu.9205 }}
 *{{cite journal  | author=D'Amico A, Tessa A, Sabino A, ''et al.'' |title=Incomplete penetrance in an SPG3A-linked family with a new mutation in the atlastin gene. |journal=Neurology |volume=62 |issue= 11 |pages= 2138–9 |year= 2004 |pmid= 15184642 |doi=  }}

Revision as of 23:48, 27 September 2008

References

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