Team:KIT-Kyoto/Attributions

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:1. [http://www.ncbi.nlm.nih.gov/pubmed?term=Extraction%2C%20Purification%20and%20Properties%20of%20Aequorin%2C%20a%20Bioluminescent%20Protein%20from%20the%20Luminous%20Hydromedusan%2C%20Aequorea%E2%80%A0 PMID :13911999]SHIMOMURA O, JOHNSON FH, SAIGA Y.:‘Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan, Aequorea.’(“Journal of Cellular and Comparative Physiology” 59(3) [1962.6] pp.223-39 【Z53-D30】)
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:2. [http://www.ncbi.nlm.nih.gov/pubmed/8303295 PMID:8303295]Chalfie M, Tu Y, Euskirchen G, Ward WW, Prasher DC.Green fluorescent protein as a marker for gene expression.Science. 1994 Feb 11;263(5148):802-5.
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:3. [http://www.ncbi.nlm.nih.gov/pubmed?term=Nature%20388%3A355-358 PMID:9237752]Dickson RM, Cubitt AB, Tsien RY, Moerner WE.On/off blinking and switching behaviour of single molecules of green fluorescent protein.Nature. 1997 Jul 24;388(6640):355-8.
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:4. [http://www.ncbi.nlm.nih.gov/pubmed/9368766 PMID:9368766]Elowitz MB, Surette MG, Wolf PE, Stock J, Leibler S.Curr Biol.Photoactivation turns green fluorescent protein red. 1997 Oct 1;7(10):809-12.
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:5. [http://www.ncbi.nlm.nih.gov/pubmed/2547163 PMID:2547163]Fields S, Song O.A novel genetic system to detect protein-protein interactions.Nature. 1989 Jul 20;340(6230):245-6.
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:6. [http://www.ncbi.nlm.nih.gov/pubmed?term=Nature%20388%3A882-887 PMID:9278050]Miyawaki A, Llopis J, Heim R, McCaffery JM, Adams JA, Ikura M, Tsien RY.Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin.Nature. 1997 Aug 28;388(6645):882-7.
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:7. [http://www.ncbi.nlm.nih.gov/pubmed/9330791 PMID:9330791]Persechini A, Lynch JA, Romoser VA.Novel fluorescent indicator proteins for monitoring free intracellular Ca2+.Persechini A, Lynch JA, Romoser VA.Cell Calcium. 1997 Sep;22(3):209-16.
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:8. [http://www.ncbi.nlm.nih.gov/pubmed/1347277 PMID:1347277]Prasher DC, Eckenrode VK, Ward WW, Prendergast FG, Cormier MJ.Primary structure of the Aequorea victoria green-fluorescent protein.Gene. 1992 Feb 15;111(2):229-33.
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:9. [http://www.ncbi.nlm.nih.gov/pubmed?term=J.Biol.Chem%20272%3A13270-13274 PMID:9148946]Romoser VA, Hinkle PM, Persechini A.Detection in living cells of Ca2+-dependent changes in the fluorescence emission of an indicator composed of two green fluorescent protein variants linked by a calmodulin-binding sequence. A new class of fluorescent indicators.J Biol Chem. 1997 May 16;272(20):13270-4.
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:10. [http://www.ncbi.nlm.nih.gov/pubmed?term=Curr.Biol%207%3AR606-R607 PMID:9368737]Sawin KE, Nurse P.Photoactivation of green fluorescent protein.Curr Biol. 1997 Oct 1;7(10):R606-7.
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:11. [http://www.ncbi.nlm.nih.gov/pubmed/?term=Wakana%20Sugano1%2C2%2C%20Katsuhito%20Ohno1%2C*%2C%20Noriko%20Yoneda-Kato3%2C%20Jun-ya%20Kato3%20and%20Masamitsu%20Yamaguchi1%2C2 PMID: 18199288]Sugano W, Ohno K, Yoneda-Kato N, Kato JY, Yamaguchi M.The myeloid leukemia factor interacts with COP9 signalosome subunit 3 in Drosophila melanogaster.FEBS J. 2008 Feb;275(3):588-600.Source Department of Applied Biology, Kyoto Institute of Technology, Japan.
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Latest revision as of 03:37, 6 October 2011



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Attributions

1. [http://www.ncbi.nlm.nih.gov/pubmed?term=Extraction%2C%20Purification%20and%20Properties%20of%20Aequorin%2C%20a%20Bioluminescent%20Protein%20from%20the%20Luminous%20Hydromedusan%2C%20Aequorea%E2%80%A0 PMID :13911999]SHIMOMURA O, JOHNSON FH, SAIGA Y.:‘Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan, Aequorea.’(“Journal of Cellular and Comparative Physiology” 59(3) [1962.6] pp.223-39 【Z53-D30】)


2. [http://www.ncbi.nlm.nih.gov/pubmed/8303295 PMID:8303295]Chalfie M, Tu Y, Euskirchen G, Ward WW, Prasher DC.Green fluorescent protein as a marker for gene expression.Science. 1994 Feb 11;263(5148):802-5.


3. [http://www.ncbi.nlm.nih.gov/pubmed?term=Nature%20388%3A355-358 PMID:9237752]Dickson RM, Cubitt AB, Tsien RY, Moerner WE.On/off blinking and switching behaviour of single molecules of green fluorescent protein.Nature. 1997 Jul 24;388(6640):355-8.


4. [http://www.ncbi.nlm.nih.gov/pubmed/9368766 PMID:9368766]Elowitz MB, Surette MG, Wolf PE, Stock J, Leibler S.Curr Biol.Photoactivation turns green fluorescent protein red. 1997 Oct 1;7(10):809-12.


5. [http://www.ncbi.nlm.nih.gov/pubmed/2547163 PMID:2547163]Fields S, Song O.A novel genetic system to detect protein-protein interactions.Nature. 1989 Jul 20;340(6230):245-6.


6. [http://www.ncbi.nlm.nih.gov/pubmed?term=Nature%20388%3A882-887 PMID:9278050]Miyawaki A, Llopis J, Heim R, McCaffery JM, Adams JA, Ikura M, Tsien RY.Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin.Nature. 1997 Aug 28;388(6645):882-7.


7. [http://www.ncbi.nlm.nih.gov/pubmed/9330791 PMID:9330791]Persechini A, Lynch JA, Romoser VA.Novel fluorescent indicator proteins for monitoring free intracellular Ca2+.Persechini A, Lynch JA, Romoser VA.Cell Calcium. 1997 Sep;22(3):209-16.


8. [http://www.ncbi.nlm.nih.gov/pubmed/1347277 PMID:1347277]Prasher DC, Eckenrode VK, Ward WW, Prendergast FG, Cormier MJ.Primary structure of the Aequorea victoria green-fluorescent protein.Gene. 1992 Feb 15;111(2):229-33.


9. [http://www.ncbi.nlm.nih.gov/pubmed?term=J.Biol.Chem%20272%3A13270-13274 PMID:9148946]Romoser VA, Hinkle PM, Persechini A.Detection in living cells of Ca2+-dependent changes in the fluorescence emission of an indicator composed of two green fluorescent protein variants linked by a calmodulin-binding sequence. A new class of fluorescent indicators.J Biol Chem. 1997 May 16;272(20):13270-4.


10. [http://www.ncbi.nlm.nih.gov/pubmed?term=Curr.Biol%207%3AR606-R607 PMID:9368737]Sawin KE, Nurse P.Photoactivation of green fluorescent protein.Curr Biol. 1997 Oct 1;7(10):R606-7.


11. [http://www.ncbi.nlm.nih.gov/pubmed/?term=Wakana%20Sugano1%2C2%2C%20Katsuhito%20Ohno1%2C*%2C%20Noriko%20Yoneda-Kato3%2C%20Jun-ya%20Kato3%20and%20Masamitsu%20Yamaguchi1%2C2 PMID: 18199288]Sugano W, Ohno K, Yoneda-Kato N, Kato JY, Yamaguchi M.The myeloid leukemia factor interacts with COP9 signalosome subunit 3 in Drosophila melanogaster.FEBS J. 2008 Feb;275(3):588-600.Source Department of Applied Biology, Kyoto Institute of Technology, Japan.