OTX1: Difference between revisions
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*{{cite journal | author=Simeone A |title=A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo |journal=EMBO J. |volume=12 |issue= 7 |pages= 2735–47 |year= 1993 |pmid= 8101484 |doi= | pmc=413524 | |
*{{cite journal | author=Simeone A |title=A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo |journal=EMBO J. |volume=12 |issue= 7 |pages= 2735–47 |year= 1993 |pmid= 8101484 |doi= | pmc=413524 |name-list-format=vanc| author2=Acampora D | author3=Mallamaci A | display-authors=3 | last4=Stornaiuolo | first4=A | last5=d'Apice | first5=MR | last6=Nigro | first6=V | last7=Boncinelli | first7=E }} |
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*{{cite journal | author=Acampora D |title=Epilepsy and brain abnormalities in mice lacking the Otx1 gene |journal=Nat. Genet. |volume=14 |issue= 2 |pages= 218–22 |year= 1996 |pmid= 8841200 |doi= 10.1038/ng1096-218 | |
*{{cite journal | author=Acampora D |title=Epilepsy and brain abnormalities in mice lacking the Otx1 gene |journal=Nat. Genet. |volume=14 |issue= 2 |pages= 218–22 |year= 1996 |pmid= 8841200 |doi= 10.1038/ng1096-218 |name-list-format=vanc| author2=Mazan S | author3=Avantaggiato V | display-authors=3 | last4=Barone | first4=Paolo | last5=Tuorto | first5=Francesca | last6=Lallemand | first6=Yvan | last7=Brûlet | first7=Philippe | last8=Simeone | first8=Antonio }} |
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*{{cite journal | author=Nagao T |title=Developmental rescue of Drosophila cephalic defects by the human Otx genes |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 7 |pages= 3737–42 |year= 1998 |pmid= 9520436 |doi=10.1073/pnas.95.7.3737 | pmc=19906 | |
*{{cite journal | author=Nagao T |title=Developmental rescue of Drosophila cephalic defects by the human Otx genes |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 7 |pages= 3737–42 |year= 1998 |pmid= 9520436 |doi=10.1073/pnas.95.7.3737 | pmc=19906 |name-list-format=vanc| author2=Leuzinger S | author3=Acampora D | display-authors=3 | last4=Simeone | first4=A | last5=Finkelstein | first5=R | last6=Reichert | first6=H | last7=Furukubo-Tokunaga | first7=K }} |
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*{{cite journal | author=Weimann JM |title=Cortical neurons require Otx1 for the refinement of exuberant axonal projections to subcortical targets |journal=Neuron |volume=24 |issue= 4 |pages= 819–31 |year= 2000 |pmid= 10624946 |doi=10.1016/S0896-6273(00)81030-2 | |
*{{cite journal | author=Weimann JM |title=Cortical neurons require Otx1 for the refinement of exuberant axonal projections to subcortical targets |journal=Neuron |volume=24 |issue= 4 |pages= 819–31 |year= 2000 |pmid= 10624946 |doi=10.1016/S0896-6273(00)81030-2 |name-list-format=vanc| author2=Zhang YA | author3=Levin ME | display-authors=3 | last4=Devine | first4=W.Patrick | last5=Brûlet | first5=Philippe | last6=McConnell | first6=Susan K }} |
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*{{cite journal | author=Francks C |title=Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1 |journal=Psychiatr. Genet. |volume=12 |issue= 1 |pages= 35–41 |year= 2002 |pmid= 11901358 |doi=10.1097/00041444-200203000-00005 | |
*{{cite journal | author=Francks C |title=Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1 |journal=Psychiatr. Genet. |volume=12 |issue= 1 |pages= 35–41 |year= 2002 |pmid= 11901358 |doi=10.1097/00041444-200203000-00005 |name-list-format=vanc| author2=Fisher SE | author3=Olson RK | display-authors=3 | last4=Pennington | first4=Bruce F. | last5=Smith | first5=Shelley D. | last6=Defries | first6=John C. | last7=Monaco | first7=Anthony P. }} |
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*{{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= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 | |
*{{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= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |name-list-format=vanc| 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=Ota T |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 | |
*{{cite journal | author=Ota T |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |name-list-format=vanc| author2=Suzuki Y | author3=Nishikawa T | display-authors=3 | last4=Otsuki | first4=Tetsuji | last5=Sugiyama | first5=Tomoyasu | last6=Irie | first6=Ryotaro | last7=Wakamatsu | first7=Ai | last8=Hayashi | first8=Koji | last9=Sato | first9=Hiroyuki }} |
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*{{cite journal | author=Puelles E |title=Otx2 regulates the extent, identity and fate of neuronal progenitor domains in the ventral midbrain |journal=Development |volume=131 |issue= 9 |pages= 2037–48 |year= 2004 |pmid= 15105370 |doi= 10.1242/dev.01107 | |
*{{cite journal | author=Puelles E |title=Otx2 regulates the extent, identity and fate of neuronal progenitor domains in the ventral midbrain |journal=Development |volume=131 |issue= 9 |pages= 2037–48 |year= 2004 |pmid= 15105370 |doi= 10.1242/dev.01107 |name-list-format=vanc| author2=Annino A | author3=Tuorto F | display-authors=3 | last4=Usiello | first4=A | last5=Acampora | first5=D | last6=Czerny | first6=T | last7=Brodski | first7=C | last8=Ang | first8=SL | last9=Wurst | first9=W }} |
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*{{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= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 | |
*{{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= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 |name-list-format=vanc| 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=Hillier LW |title=Generation and annotation of the DNA sequences of human chromosomes 2 and 4 |journal=Nature |volume=434 |issue= 7034 |pages= 724–31 |year= 2005 |pmid= 15815621 |doi= 10.1038/nature03466 | |
*{{cite journal | author=Hillier LW |title=Generation and annotation of the DNA sequences of human chromosomes 2 and 4 |journal=Nature |volume=434 |issue= 7034 |pages= 724–31 |year= 2005 |pmid= 15815621 |doi= 10.1038/nature03466 |name-list-format=vanc| author2=Graves TA | author3=Fulton RS | display-authors=3 | last4=Fulton | first4=Lucinda A. | last5=Pepin | first5=Kymberlie H. | last6=Minx | first6=Patrick | last7=Wagner-Mcpherson | first7=Caryn | last8=Layman | first8=Dan | last9=Wylie | first9=Kristine }} |
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*{{cite journal | author=Rual JF |title=Towards a proteome-scale map of the human protein-protein interaction network |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 | |
*{{cite journal | author=Rual JF |title=Towards a proteome-scale map of the human protein-protein interaction network |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209 |name-list-format=vanc| author2=Venkatesan K | author3=Hao T | display-authors=3 | last4=Hirozane-Kishikawa | first4=Tomoko | last5=Dricot | first5=Amélie | last6=Li | first6=Ning | last7=Berriz | first7=Gabriel F. | last8=Gibbons | first8=Francis D. | last9=Dreze | first9=Matija }} |
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Revision as of 14:05, 27 July 2015
Template:PBB Homeobox protein OTX1 is a protein that in humans is encoded by the OTX1 gene.[1][2]
References
- ^ Kastury K, Druck T, Huebner K, Barletta C, Acampora D, Simeone A, Faiella A, Boncinelli E (Dec 1994). "Chromosome locations of human EMX and OTX genes". Genomics. 22 (1): 41–5. doi:10.1006/geno.1994.1343. PMID 7959790.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: OTX1 orthodenticle homeobox 1".
Further reading
External links
- OTX1+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.