KIAA0196: Difference between revisions
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*{{cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides |
*{{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= 171–174 |year= 1994 |pmid= 8125298 |doi=10.1016/0378-1119(94)90802-8 }} |
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*{{cite journal | author=Nagase T |
*{{cite journal | author=Nagase T |title=Prediction of the coding sequences of unidentified human genes. V. The coding sequences of 40 new genes (KIAA0161-KIAA0200) deduced by analysis of cDNA clones from human cell line KG-1 |journal=DNA Res. |volume=3 |issue= 1 |pages= 17–24 |year= 1996 |pmid= 8724849 |doi=10.1093/dnares/3.1.17 | author-separator=, | author2=Seki N | author3=Ishikawa K | display-authors=3 | last4=Tanaka | first4=A | last5=Nomura | first5=N }} |
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*{{cite journal | author=Suzuki Y |
*{{cite journal | author=Suzuki Y |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library |journal=Gene |volume=200 |issue= 1–2 |pages= 149–156 |year= 1997 |pmid= 9373149 |doi=10.1016/S0378-1119(97)00411-3 | author-separator=, | author2=Yoshitomo-Nakagawa K | author3=Maruyama K | display-authors=3 | last4=Suyama | first4=A | last5=Sugano | first5=S }} |
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*{{cite journal | author=Hedera P |
*{{cite journal | author=Hedera P |title=Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q |journal=Am. J. Hum. Genet. |volume=64 |issue= 2 |pages= 563–569 |year= 1999 |pmid= 9973294 |doi=10.1086/302258 | pmc=1377766 | author-separator=, | author2=Rainier S | author3=Alvarado D | display-authors=3 | last4=Zhao | first4=X | last5=Williamson | first5=J | last6=Otterud | first6=B | last7=Leppert | first7=M | last8=Fink | first8=J }} |
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*{{cite journal | author=Strausberg RL |
*{{cite journal | author=Strausberg RL |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= 16899–16903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 | author-separator=, | author2=Feingold EA | author3=Grouse LH | display-authors=3 | last4=Derge | first4=JG | last5=Klausner | first5=RD | last6=Collins | first6=FS | last7=Wagner | first7=L | last8=Shenmen | first8=CM | last9=Schuler | first9=GD }} |
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*{{cite journal | author=Gevaert K |
*{{cite journal | author=Gevaert K |title=Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides |journal=Nat. Biotechnol. |volume=21 |issue= 5 |pages= 566–569 |year= 2004 |pmid= 12665801 |doi= 10.1038/nbt810 | author-separator=, | author2=Goethals M | author3=Martens L | display-authors=3 | last4=Van Damme | first4=Jozef | last5=Staes | first5=An | last6=Thomas | first6=Grégoire R. | last7=Vandekerckhove | first7=Joël }} |
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*{{cite journal | author=Porkka KP, Tammela TL, Vessella RL, Visakorpi T |title=RAD21 and KIAA0196 at 8q24 are amplified and overexpressed in prostate cancer |
*{{cite journal | author=Porkka KP, Tammela TL, Vessella RL, Visakorpi T |title=RAD21 and KIAA0196 at 8q24 are amplified and overexpressed in prostate cancer |journal=Genes Chromosomes Cancer |volume=39 |issue= 1 |pages= 1–10 |year= 2004 |pmid= 14603436 |doi= 10.1002/gcc.10289 }} |
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*{{cite journal | author=Gerhard DS |
*{{cite journal | author=Gerhard DS |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–2127 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 | author-separator=, | author2=Wagner L | author3=Feingold EA | display-authors=3 | last4=Shenmen | first4=CM | last5=Grouse | first5=LH | last6=Schuler | first6=G | last7=Klein | first7=SL | last8=Old | first8=S | last9=Rasooly | first9=R }} |
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*{{cite journal | author=Kimura K |
*{{cite journal | author=Kimura K |title=Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes |journal=Genome Res. |volume=16 |issue= 1 |pages= 55–65 |year= 2006 |pmid= 16344560 |doi= 10.1101/gr.4039406 | pmc=1356129 | author-separator=, | author2=Wakamatsu A | author3=Suzuki Y | display-authors=3 | last4=Ota | first4=T | last5=Nishikawa | first5=T | last6=Yamashita | first6=R | last7=Yamamoto | first7=J | last8=Sekine | first8=M | last9=Tsuritani | first9=K }} |
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*{{cite journal | author=Valdmanis PN |
*{{cite journal | author=Valdmanis PN |title=Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia |journal=Am. J. Hum. Genet. |volume=80 |issue= 1 |pages= 152–161 |year= 2007 |pmid= 17160902 |doi= 10.1086/510782 | pmc=1785307 | author-separator=, | author2=Meijer IA | author3=Reynolds A | display-authors=3 | last4=Lei | first4=Adrienne | last5=MacLeod | first5=Patrick | last6=Schlesinger | first6=David | last7=Zatz | first7=Mayana | last8=Reid | first8=Evan | last9=Dion | first9=Patrick A. }} |
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{{refend}} |
{{refend}} |
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Revision as of 04:10, 20 June 2011
Template:PBB KIAA0196 is a human gene.[1]
External Links
- GeneReviews/NCBI/NIH/UW entry on Spastic Paraplegia 8 and the involvement of the protein strumpellin
References
Further reading
 | This article on a gene on human chromosome 8 is a stub. You can help Wikipedia by expanding it. |