학술논문
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'학술논문'
에서 검색결과 128건 | 목록
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Academic Journal
Hathazi, D; Griffin, H; Jennings, MJ; Giunta, M; Powell, C; Pearce, SF; Munro, B; Wei, W; Boczonadi, V; Poulton, J
EMBO JOURNAL. 39(23)
lllumination Power, Stability, and Linearity Measurements for Confocal and Widefield Microscopes V .2
Academic Journal
Gaudreault, N.; Ali, R.; Avilov, S.; Bagley, S.; Bammann, R.; Barachati, F.; Barna, L.; Berno, V.; Bertocchi, C.; Boczonadi, V.; Boehm, U.; Bosch, M.; Brideau, C.; Carvalho, N.; Chatterjee, N.; Colarusso, P.; Cole, R.; Darwish-Miranda, N.; Dervish, S.; Dietzel, R.; Duwé, S.; Eismann, F.; Faklaris, O.; Felscher, A.; Ferdous, Z.; Guilbert, T.; Gonnert, M.; Grunwald, D.; Hoffmann, B.; Kirchner, M.; Krens, G.; Laude, A.; LeDue, J.; Liu, P.; Lorentz, P.; Martins, G.; Mezzana Robinson, V.; Mitovski, M.; Nelson, M.; Nitschke, R.; Payne-Dwyer, A.; Pimente Cabrera, J.; Podder, S.; Schroth-Diez, B.; Schwartz, S.; Srinivasan, S.; Theunauer, R.; van der Oord, K.; Taatjes, D.; van Oostende-Triplet, C.; Wee, T.; Weiss, K.; Gelman, L.
protocols.io
Academic Journal
Olsen RKJ; Konarikova E; Giancaspero TA; Mosegaard S; Boczonadi V; Matakovic L; Veauville Merllie A; Terrile C; Schwarzmayr T; Haack TB; Auranen M; Leone P; GALLUCCIO, Michele; Imbard A; Gutierrez Rios P; Palmfeldt J; Graf E; Vianey Saban C; Oppenheim M; Schiff M; Pichard S; Rigal O; Pyle A; Chinnery PF; Konstantopoulou V; Moslinger D; Feichtinger RG; Talim B; Topaloglu H; Coskun T; Gucer S; Botta A; Pegoraro E; Malena A; Vergani L; Mazza D; Zollino M; Ghezzi D; Acquaviva C; Tyni T; Boneh A; Meitinger T; Strom TM; Gregersen N; Mayr JA; Horvath R; Barile M; Prokisch H.
Am J Hum Genet
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
instname
Am. J. Hum. Genet. 98, 1130-1145 (2016)
Olsen, R K J, Koňaříková, E, Giancaspero, T A, Mosegaard, S,Boczonadi , V , Mataković, L, Veauville-Merllié, A, Terrile, C, Schwarzmayr, T, Haack, T B, Auranen, M, Leone, P, Galluccio, M, Imbard, A, Gutierrez-Rios, P, Palmfeldt, J, Graf, E, Vianey-Saban, C, Oppenheim, M, Schiff, M, Pichard, S, Rigal, O, Pyle, A, Chinnery, P F, Konstantopoulou, V , Möslinger, D, Feichtinger, R G, Talim, B, Topaloglu, H, Coskun, T, Gucer, S, Botta, A, Pegoraro, E, Malena, A, Vergani, L, Mazzà, D, Zollino, M, Ghezzi, D, Acquaviva, C, Tyni, T, Boneh, A, Meitinger, T, Strom, T M, Gregersen, N, Mayr, J A, Horvath, R, Barile, M & Prokisch, H 2016, 'Riboflavin-Responsive and-Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency', American Journal of Human Genetics, vol. 98, no. 6, pp. 1130-45. https://doi.org/10.1016/j.ajhg.2016.04.006
American Journal of Human Genetics
Digital.CSIC. Repositorio Institucional del CSIC
Consejo Superior de Investigaciones Científicas (CSIC)
instname
Am. J. Hum. Genet. 98, 1130-1145 (2016)
Olsen, R K J, Koňaříková, E, Giancaspero, T A, Mosegaard, S,
American Journal of Human Genetics
Academic Journal
Kurzawa-Akanbi M; Whitfield P; Burte F; Bertelli PM; Pathak V; Doherty M; Hilgen B; Gliaudelyte L; Platt M; Queen R; Coxhead J; Porter A; Oberg M; Fabrikova D; Davey T; Beh CS; Georgiou M; Collin J; Boczonadi V; Hartlova A; Taggart M; Al-Aama J; Korolchuk VI; Morris CM; Guduric-Fuchs J; Steel DH; Medina RJ; Armstrong L; Lako M
J Extracell Vesicles
Journal of Extracellular Vesicles, Vol 11, Iss 12, Pp n/a-n/a (2022)
Kurzawa-Akanbi, M, Whitfield, P, Burté, F, Bertelli, P M, Pathak,V , Doherty, M, Hilgen, B, Gliaudelytė, L, Platt, M, Queen, R, Coxhead, J, Porter, A, Öberg, M, Fabrikova, D, Davey, T, Beh, C S, Georgiou, M, Collin, J, Boczonadi , V , Härtlova, A, Taggart, M, Al-Aama, J, Korolchuk, V I, Morris, C M, Guduric-Fuchs, J, Steel, D H, Medina, R J, Armstrong, L & Lako, M 2022, 'Retinal pigment epithelium extracellular vesicles are potent inducers of age-related macular degeneration disease phenotype in the outer retina', Journal of Extracellular Vesicles, vol. 11, no. 12, 12295. https://doi.org/10.1002/jev2.12295
Journal of Extracellular Vesicles, Vol 11, Iss 12, Pp n/a-n/a (2022)
Kurzawa-Akanbi, M, Whitfield, P, Burté, F, Bertelli, P M, Pathak,
Academic Journal
Boczonadi V.; Meyer K.; Gonczarowska-Jorge H.; Griffin H.; Roos A.; Bartsakoulia M.; Bansagi B.; Ricci G.; Palinkas F.; Zahedi R. P.; Bruni F.; Kaspar B.; Lochmuller H.; Boycott K. M.; Muller J. S.; Horvath R.
Hum Mol Genet
Academic Journal
Dorgau B; Collin J; Rozanska A; boczonadi V; Molina MM; Unsworth A; Hussain r; Coxhead J; Dhanaseelan T; Armstrong L; Queen R; Lako M
iScience
iScience, Vol 27, Iss 4, Pp 109397-(2024)
iScience, Vol 27, Iss 4, Pp 109397-(2024)
Academic Journal
Podmanicky O; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, Ed Adrian Building, Robinson Way, Cambridge, CB2 0PY, United Kingdom.; Gao F; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, Ed Adrian Building, Robinson Way, Cambridge, CB2 0PY, United Kingdom.; Munro B; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, Ed Adrian Building, Robinson Way, Cambridge, CB2 0PY, United Kingdom.; Jennings MJ; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, Ed Adrian Building, Robinson Way, Cambridge, CB2 0PY, United Kingdom.; Department of Neurology, Columbia University, 630 West 168th St, New York, NY 10032, United States.; Boczonadi V; Biosciences Institute, International Centre for Life, Faculty of Medical Sciences, Newcastle University, Central Parkway, Newcastle upon Tyne, NE1 3BZ, United Kingdom.; Hathazi D; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, Ed Adrian Building, Robinson Way, Cambridge, CB2 0PY, United Kingdom.; Mueller JS; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, Ed Adrian Building, Robinson Way, Cambridge, CB2 0PY, United Kingdom.; Dubowitz Neuromuscular Centre, Department of Neuropathology, Institute of Neurology, Queen Square, London, WC1N 3BG, United Kingdom.; Horvath R; Department of Clinical Neurosciences, John Van Geest Centre for Brain Repair, University of Cambridge, Ed Adrian Building, Robinson Way, Cambridge, CB2 0PY, United Kingdom.
Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Academic Journal
The International Journal of Biochemistry & Cell Biology. 63:32-40
Academic Journal
Queen R; Bioinformatics Support Unit, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Crosier M; Human Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Eley L; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Kerwin J; Human Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Turner JE; Human Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Yu J; Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland, United States of America.; Alqahtani A; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Dhanaseelan T; Human Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Overman L; Human Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Soetjoadi H; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Baldock R; MRC Human Genetics Unit, Institute of Genetics and Cancer, Edinburgh University, United Kingdom.; Coxhead J; Genomics Core Facility, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Boczonadi V; Bioimaging Unit, Faculty of medical Sciences, Newcastle University, United Kingdom.; Laude A; Bioimaging Unit, Faculty of medical Sciences, Newcastle University, United Kingdom.; Cockell SJ; School of Biomedical, Nutritional and Sport Sciences, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Kane MA; Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, Baltimore, Maryland, United States of America.; Lisgo S; Human Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Henderson DJ; Human Developmental Biology Resource, Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.; Biosciences Institute, Faculty of Medical Sciences, Newcastle University, United Kingdom.
Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE
Academic Journal
Journal of Inherited Metabolic Disease. 38:427-435
Academic Journal
Boczonadi, V.; King, M. S.; Smith, A. C.; Olahova, M.; Bansagi, B.; Roos, A.; Eyassu, F.; Borchers, C.; Ramesh, V.; Lochmüller, H.; Polvikoski, T.; Whittaker, R. G.; Pyle, A.; Griffin, H.; Taylor, R. W.; Chinnery, P. F.; Robinson, A. J.; Kunji, E. R. S.; Horvath, R.
Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 21(9):2163-2164
Academic Journal
Boczonadi, V; Gillespie, R; Keenan, I; Ramsbottom, SA; Donald-Wilson, C; Al Nazer, M; Humbert, P; Schwarz, RJ; Chaudhry, B; Henderson, DJ
Cardiovasc Res
Boczonadi , V , Taylor, R L, Keenan, I, Ramsbottom, S, Donald-Wilson, C, Al-Nazer, M, Humbert, P, Schwartz, R J, Chaudhry, B & Henderson, D J 2014, 'Scrib:Rac1 interactions are required for the morphogenesis of the ventricular myocardium', Cardiovascular research, vol. 104, no. 1, 104, pp. 103. https://doi.org/10.1093/cvr/cvu193
Academic Journal
Journal of cell science, 2006, Vol.119(24), pp.5147-5159 [Peer Reviewed Journal]
P47Conditional deletion of Scrib gene in the developing myocardium leads to congenital heart defects
Academic Journal
Cardiovascular Research. Mar 15, 2012 93(suppl_1 Suppl 1):S9-S45
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[검색어] Boczonadi, V.
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