학술논문


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'학술논문' 에서 검색결과 763건 | 목록 1~20
Academic Journal
Küry, SébastienStanton, Janelle E.van Woerden, Geeske M.Bosc-Rosati, AmélieHsieh, Tzung-ChienBray, LiseOloudé, MarielleRosenfelt, CoryScott-Boyer, Marie PierMost, VictoriaWang, TianyunPapendorf, Jonas J.de Konink, CharlotteDeb, WallidVignard, VirginieStudencka-Turski, MajaBesnard, ThomasHajdukowicz, Anna M.Thiel, Franziska G.Wolfgramm, SophieFlorenceau, LaëtitiaCuinat, SilvestreMarsac, SylvainVerrès, YannDangoumau, AudreyPoirier, LéaWentzensen, Ingrid M.Tuttle, AnnabelleForster, CaraStriesow, JohannaGolnik, RichardOrtiz, DamaraJenkins, LauraRosenfeld, Jill A.Ziegler, AlbanHoudayer, ClaraBonneau, DominiqueTorti, ErinBegtrup, AmberMonaghan, Kristin G.Mullegama, Sureni V.Volker-Touw, Catharina M. L. Nienkevan Gassen, Koen L. I.Oegema, Renskede Pagter, Mirjam S.Steindl, KatharinaRauch, AnitaIvanovski, IvanMcDonald, KimberlyBoothe, EmilyDauber, AndrewBaker, JaniceFabie, Noelle Andrea V.Bernier, Raphael A.Turner, Tychele N.Srivastava, SiddharthDies, Kira A.Swanson, Lindsay C.Costin, CarrieAbdulrazak, AlaliJobling, Rebekah K.Pappas, JohnRabin, RachelNiyazov, DmitriyChun-Hui Tsai, AnneKovak, KarenBeck, David B.Malicdan, May Christine V.Adams, David R.Wolfe, LynneGanetzky, Rebecca D.Muraresku, Colleen C.Babikyan, DavitSedláček, ZdeněkHančárová, MiroslavaTimberlake, Andrew T.Saif, Hind AlNestler, BerkleyKing, KaylaHajianpour, MJCostain, GregoryPrendergast, D’ArcyLi, ChumeiGeneviève, DavidVitobello, AntonioSorlin, ArthurPhilippe, ChristopheHarel, TamarToker, OriSabir, AtafLim, DerekHamilton, Mark J.Bryson, Lisa J.Cleary, ElaineWeber, SachaHoffman, Trevor L.Cueto-González, Anna M.Tizzano, Eduardo F.Gómez-Andrés, DavidCodina-Solà, MartaVerveri, AthinaPavlidou, EfterpiLambropoulos, AlexandrosGarganis, KyriakosRio, MarlèneLevy, JonathanLangas, Sarah J.McRae, Anne M.Lessard, Mathieu K.D’Agostino, Maria DanielaDe Bie, IsabelleWegler, MeretAbou Jamra, RamiKamphausen, Susanne B.Bothe, ViktoriaPotocki, LorraineOlinger, EricSznajer, YvesWiame, ElsaThompson, Michelle L.Schroeder, Molly C.Gooch, CatherineSmith, Raphael A.Pandya, ArtiBusch, Larissa M.Völker, UweHammer, ElkeWende, KristianCogné, BenjaminIsidor, BertrandMeiler, JensRipoll, ClémentineBigou, StéphanieLaumonnier, FrédéricHildebrand, Peter W.Eichler, Evan E.McWalter, KirstyKrawitz, Peter M.Roux-Dalvai, FlorenceElgersma, YpeMarcoux, JulienBousquet, Marie-PierreDroit, ArnaudPoschmann, JeremieGrabrucker, Andreas M.Bolduc, Francois V.Bézieau, StéphaneEbstein, FrédéricKrüger, Elke
Nature Communications. 16(1)
Conference
Proceedings of the 2nd International Conference on Interaction Sciences: Information Technology, Culture and Human. :1130-1135
Academic Journal
Thomas, MintaSu, Yu-RuRosenthal, Elisabeth A.Sakoda, Lori C.Schmit, Stephanie L.Timofeeva, Maria N.Chen, ZhishanFernandez-Rozadilla, CeresLaw, Philip J.Murphy, NeilCarreras-Torres, RobertDiez-Obrero, Virginiavan Duijnhoven, Franzel J. B.Jiang, ShangqingShin, AesunWolk, AlicjaPhipps, Amanda I.Burnett-Hartman, AndreaGsur, AndreaChan, Andrew T.Zauber, Ann G.Wu, Anna H.Lindblom, AnnikaUm, Caroline Y.Tangen, Catherine M.Gignoux, ChrisNewton, ChristinaHaiman, Christopher A.Qu, ConghuiBishop, D. TimothyBuchanan, Daniel D.Crosslin, David R.Conti, David V.Kim, Dong-HyunHauser, ElizabethWhite, EmilySiegel, ErinSchumacher, Fredrick R.Rennert, GadGiles, Graham G.Hampel, HeatherBrenner, HermannOze, IsaoOh, Jae HwanLee, Jeffrey K.Schneider, Jennifer L.Chang-Claude, JennyKim, JeongseonHuyghe, Jeroen R.Zheng, JiayinHampe, JochenGreenson, JoelHopper, John L.Palmer, Julie R.Visvanathan, KalaMatsuo, KeitaroMatsuda, KoichiJung, Keum JiLi, LiLe Marchand, LoicVodickova, LudmilaBujanda, LuisGunter, Marc J.Matejcic, MarcoJenkins, Mark A.Slattery, Martha L.D’Amato, MauroWang, MeilinHoffmeister, MichaelWoods, Michael O.Kim, MichelleSong, MingyangIwasaki, MotokiDu, MulongUdaltsova, NataliaSawada, NorieVodicka, PavelCampbell, Peter T.Newcomb, Polly A.Cai, QiuyinPearlman, RachelPai, Rish K.Schoen, Robert E.Steinfelder, Robert S.Haile, Robert W.Vandenputtelaar, RositaPrentice, Ross L.Küry, SébastienCastellví-Bel, SergiTsugane, ShoichiroBerndt, Sonja I.Lee, Soo ChinBrezina, StefanieWeinstein, Stephanie J.Chanock, Stephen J.Jee, Sun HaKweon, Sun-SeogVadaparampil, SusanHarrison, Tabitha A.Yamaji, TaikiKeku, Temitope O.Vymetalkova, VeronikaArndt, VolkerJia, Wei-HuaShu, Xiao-OuLin, YiAhn, Yoon-OkStadler, Zsofia K.van Guelpen, BethanyUlrich, Cornelia M.Platz, Elizabeth A.Potter, John D.Li, Christopher I.Meester, ReinierMoreno, VictorFigueiredo, Jane C.Casey, GrahamLansdorp Vogelaar, IrisDunlop, Malcolm G.Gruber, Stephen B.Hayes, Richard B.Pharoah, Paul D. P.Houlston, Richard S.Jarvik, Gail P.Tomlinson, Ian P.Zheng, WeiCorley, Douglas A.Peters, UlrikeHsu, Li
Nature Communications. 14(1)
Academic Journal
日本機械学会誌 / Journal of the Society of Mechanical Engineers. 1961, 64(504):197
Academic Journal
Uguen K; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Service de Génétique Médicale, CHU de Brest, Brest, France.; Centre de Référence Déficience Intellectuelle et Polyhandicap de causes rares, CHU de Brest, Brest, France.; Bergot T; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Currently in the Division of Structural Biology, The Institute of Cancer Research, London, England.; Scott-Boyer MP; CHU de Québec-Laval University Research Center, Quebec City, QC, Canada.; Chapalain S; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Desdouets C; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Commet S; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Zhu C; Center for Brain Repair and Rehabilitation, Institute of Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden.; Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, Institute of Neuroscience and Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.; Xu Y; Henan Key Laboratory of Child Brain Injury and Henan Pediatric Clinical Research Center, Institute of Neuroscience and Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.; Wang Y; Institutes of Biomedical Sciences and Children's Hospital, Fudan University, Shanghai, China.; Roscioli T; New South Wales Health Pathology Randwick Genomics, Prince of Wales Hospital, Sydney, NSW, Australia.; Neuroscience Research Australia (NeuRA), University of New South Wales Sydney, Sydney, NSW, Australia.; Tran-Mau-Them F; Université Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, Centre Neomics, FHU TRANSLAD, Centre de recherche Translationnelle en Médecine moléculaire-Inserm UMR1231, équipe GAD, Dijon, France.; Faivre L; Université Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Centre de référence Déficiences Intellectuelles de Causes Rares, et Centre de référence GénoPsy, Dijon, France.; Maraval J; Université Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Centre de référence Déficiences Intellectuelles de Causes Rares, et Centre de référence GénoPsy, Dijon, France.; Delanne J; Université Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Centre de référence Déficiences Intellectuelles de Causes Rares, et Centre de référence GénoPsy, Dijon, France.; Denommé-Pichon AS; Université Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, Centre Neomics, FHU TRANSLAD, Centre de recherche Translationnelle en Médecine moléculaire-Inserm UMR1231, équipe GAD, Dijon, France.; Vitobello A; Université Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, Centre Neomics, FHU TRANSLAD, Centre de recherche Translationnelle en Médecine moléculaire-Inserm UMR1231, équipe GAD, Dijon, France.; Jost C; Université Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231, équipe GAD, FHU TRANSLAD, Centre de génétique, Centre de référence Anomalies du Développement et Syndromes Malformatifs, Centre de référence Déficiences Intellectuelles de Causes Rares, et Centre de référence GénoPsy, Dijon, France.; Planes M; Service de Génétique Médicale, CHU de Brest, Brest, France.; Centre de Référence Déficience Intellectuelle et Polyhandicap de causes rares, CHU de Brest, Brest, France.; Hiatt S; HudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.; Wheeler P; Division of Genetics, Arnold Palmer Hospital for Children-Orlando Health, Orlando, FL, USA.; Gonzaga-Jauregui C; International Laboratory for Human Genome Research, Laboratorio Internacional de Investigación sobre el Genoma Humano, Universidad Nacional Autónoma de México, Juriquilla, México.; Wang H; DDC Clinic for Special Needs Children, Middlefield, OH, USA.; Xin B; DDC Clinic for Special Needs Children, Middlefield, OH, USA.; Sency V; DDC Clinic for Special Needs Children, Middlefield, OH, USA.; Kruer MC; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.; Departments of Child Health, Neurology, Cellular & Molecular Medicine and Program in Genetics, University of Arizona College of Medicine, Phoenix, AZ, USA.; Bakhtiari S; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.; Departments of Child Health, Neurology, Cellular & Molecular Medicine and Program in Genetics, University of Arizona College of Medicine, Phoenix, AZ, USA.; Sulem P; deCODE Genetics/Amgen, Inc, Reykjavik, Iceland.; Curry C; Genetic Medicine, University of California, San Francisco, Fresno, CA, USA.; Prescott T; Department of Medical Genetics, Telemark Hospital Trust, Skien, Norway.; Strobl-Wildemann G; Department of Human Genetics, MVZ Humangenetik Ulm, Ulm, Germany.; Brunet T; Institute of Human Genetics, Klinikum Rechts der Isar, School of Medicine and Health, Technical University of Munich, Munich, Germany.; Doco Fenzy M; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Courtin T; Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, Inserm, CNRS, Paris, France.; Assistance Publique Hôpitaux de Paris, Hôpital Pitié-Salpêtrière, Département de Génétique, DMU BioGeM, Paris, France.; Poirsier C; Département de génétique médicale, CHU Reims, Reims, France.; Bjørg Hammer T; Department of Epilepsy Genetics and Personalized Treatment, The Filadelfia Danish Epilepsy Centre, Dianalund, Denmark.; Department of Clinical Genetics, Copenhagen University Hospital, Copenhagen, Denmark.; Fenger CD; Department of Epilepsy Genetics and Personalized Treatment, The Filadelfia Danish Epilepsy Centre, Dianalund, Denmark.; MacPherson M; Department of Medical Genetics, Faculty of Medicine and Dentistry, University of Alberta, Alberta Health Services, Edmonton, AB, Canada.; Izumi K; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Leonard J; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Li D; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Zackai EH; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Glass IA; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA.; Ward S; Department of Pediatrics, Division of Medical Genetics and Genomic Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.; Campeau PM; Centre de Recherche Azrieli du CHU Sainte-Justine, University of Montreal, Montreal, QC, Canada.; Borroto MCH; Centre de Recherche Azrieli du CHU Sainte-Justine, University of Montreal, Montreal, QC, Canada.; Le Moigno L; Service de Pédiatrie et Unité d'Urgence Pédiatrique, Centre Hospitalier de Cornouaille, Quimper, France.; Van Esch H; Center for Human Genetics, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; De Waele L; Department of Child Neurology, University Hospitals Leuven, Herestraat 49, Leuven, Belgium.; Calame DG; Section of Pediatric Neurology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Lupski JR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Barcia G; Service de Médecine Génomique des Maladies Rares, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.; Peduto C; Service de Médecine Génomique des Maladies Rares, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.; Planté-Bordeneuve P; Service de Médecine Génomique des Maladies Rares, Hôpital Necker - Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.; Dupuis L; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.; Mendoza-Londono R; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada.; Stavropoulos DJ; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.; Gillibert-Duplantier J; VECT'UB, TBMCore, CNRS UAR 3427, INSERM US005, Université de Bordeaux, Bordeaux, France.; Besnard T; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Do Souto Ferreira L; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Cogné B; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Bézieau S; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Droit A; CHU de Québec-Laval University Research Center, Quebec City, QC, Canada.; Department of Molecular Medicine, Faculty of Medicine, Laval University, Quebec City, QC, Canada.; Corcos L; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Lippert E; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Service d'hématologie biologique, CHU de Brest, Brest, France.; CRB Santé du CHU de Brest, Brest, France.; Férec C; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Küry S; Nantes Université, CHU de Nantes, Service de Génétique médicale, Nantes, France.; Nantes Université, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Bernard DG; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France. delphine.bernard@univ-brest.fr.; CRB Santé du CHU de Brest, Brest, France. delphine.bernard@univ-brest.fr.
Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE
Academic Journal
Melnyk MI; a Institute of Pharmacology and Toxicology , National Academy of Medical Science , Kyiv , Ukraine.; b A.A. Bogomoletz Institute of Physiology , National Academy of Sciences of Ukraine , Kyiv , Ukraine.; Dryn DO; a Institute of Pharmacology and Toxicology , National Academy of Medical Science , Kyiv , Ukraine.; b A.A. Bogomoletz Institute of Physiology , National Academy of Sciences of Ukraine , Kyiv , Ukraine.; Al Kury LT; c Department of Health Sciences , Zayed University , Abu Dhabi , United Arab Emirates.; Zholos AV; b A.A. Bogomoletz Institute of Physiology , National Academy of Sciences of Ukraine , Kyiv , Ukraine.; d ESC 'Institute of Biology and Medicine' , Taras Shevchenko Kyiv National University , Kyiv , Ukraine.; Soloviev AI; a Institute of Pharmacology and Toxicology , National Academy of Medical Science , Kyiv , Ukraine.; d ESC 'Institute of Biology and Medicine' , Taras Shevchenko Kyiv National University , Kyiv , Ukraine.
Publisher: Informa Healthcare Country of Publication: England NLM ID: 9001952 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2394 (Electronic) Linking ISSN: 08982104 NLM ISO Abbreviation: J Liposome Res Subsets: MEDLINE
Academic Journal
Harris, Holly K.Nakayama, TojoLai, JennyZhao, BoxunArgyrou, NikoletaGubbels, Cynthia S.Soucy, AubrieGenetti, Casie A.Suslovitch, VictoriaRodan, Lance H.Tiller, George E.Lesca, GaetanGripp, Karen W.Asadollahi, RezaHamosh, AdaApplegate, Carolyn D.Turnpenny, Peter D.Simon, Marleen E. H.Volker-Touw, Catharina M. L.Gassen, Koen L. I. vanBinsbergen, Ellen vanPfundt, RolphGardeitchik, ThatjanaVries, Bert B. A. deImmken, LaDonna L.Buchanan, CatherineWilling, MarciaToler, Tomi L.Fassi, EmilyBaker, LauraVansenne, FleurWang, XiadongAmbrus, Jr., Julian L.Fannemel, MadeleinePosey, Jennifer E.Agolini, EmanueleNovelli, AntonioRauch, AnitaBoonsawat, ParanchaiFagerberg, Christina R.Larsen, Martin J.Kibaek, MariaLabalme, AudreyPoisson, AlicePayne, Katelyn K.Walsh, Laurence E.Aldinger, Kimberly A.Balciuniene, JoruneSkraban, CaraGray, ChristopherMurrell, JillBupp, Caleb P.Pascolini, GiuliaGrammatico, PaolaBroly, MartinKüry, SébastienNizon, MathildeRasool, Iqra GhulamZahoor, Muhammad YasirKraus, CorneliaReis, AndréIqbal, MuhammadUguen, KevinAudebert-Bellanger, SeverineFerec, ClaudeRedon, SylviaBaker, JaniceWu, YunhongZampino, GuiseppeSyrbe, SteffanBrosse, InesJamra, Rami AbouDobyns, William B.Cohen, Lilian L.Blomhoff, AnneMignot, CyrilKeren, BorisCourtin, ThomasAgrawal, Pankaj B.Beggs, Alan H.Yu, Timothy W.
Genetics in Medicine: Official journal of the American College of Medical Genetics and Genomics. 23(6):1028-1040
Academic Journal
Ham H; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Division of Oncology Research, Schulze Center for Novel Therapeutics, Mayo Clinic, Rochester, MN, USA.; Jing H; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Lamborn IT; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Kober MM; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Koval A; Department of Cell Physiology and Metabolism, Faculty of Medicine, Translational Research Center in Oncohaematology, University of Geneva, Geneva, Switzerland.; Berchiche YA; Laboratory of Chemical Biology and Signal Transduction, The Rockefeller University, New York, NY, USA.; Anderson DE; Advanced Mass Spectrometry Facility, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), NIH, Bethesda, MD, USA.; Druey KM; Lung and Vascular Inflammation Section, Laboratory of Allergic Diseases, DIR, NIAID, NIH, Bethesda, MD, USA.; Mandl JN; Lymphocyte Biology Section, Laboratory of Immune System Biology, DIR, NIAID, NIH, Bethesda, MD, USA.; Isidor B; Service de Génétique Médicale, CHU Nantes, Nantes Université, Nantes, France.; L'Institut du Thorax, CHU Nantes, INSERM UMR 1087/CNRS UMR 6291, Nantes Université, Nantes, France.; Ferreira CR; Skeletal Genomics Unit, Metabolic Medicine Branch, DIR, National Human Genome Research Institute (NHGRI), NIH, Bethesda, MD, USA.; Freeman AF; Laboratory of Clinical Immunology and Microbiology, DIR, NIAID, NIH, Bethesda, MD, USA.; Ganesan S; Biological Imaging Section, Research Technologies Branch, DIR, NIAID, NIH, Bethesda, MD 20892, USA.; Karsak M; Neuronal and Cellular Signal Transduction, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Mustillo PJ; Nationwide Children's Hospital, Columbus, OH, USA.; The Ohio State University College of Medicine, Columbus, OH, USA.; Teo J; Department of Haematology, The Children's Hospital Westmead, Sydney, New South Wales, Australia.; Zolkipli-Cunningham Z; Mitochondrial Medicine Frontier Program, Division of Human Genetics, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.; Chatron N; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Institut NeuroMyoGène, Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.; Lecoquierre F; Université de Rouen Normandie, INSERM U12045 and CHU Rouen, Department of Genetics and Reference Center for Developmental Disorders, FHU-G4 Génomique, Rouen, France.; Oler AJ; Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology (OCICB), NIAID, NIH, Bethesda, MD, USA.; Schmid JP; Division of Immunology, University Children's Hospital Zurich, Zurich, Switzerland.; Pediatric Immunology, University of Zurich, Zurich, Switzerland.; Kuhns DB; Neutrophil Monitoring Lab, Applied/Developmental Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.; Xu X; Chemotaxis Signal Section, Laboratory of Immunogenetics, DIR, NIAID, NIH, Rockville, MD, USA.; Hauck F; Division of Pediatric Immunology and Rheumatology, Department of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-Universität (LMU), Munich, Germany.; Al-Herz W; Department of Pediatrics, Faculty of Medicine, Kuwait University, Kuwait City, Kuwait.; Department of Pediatrics, Al-Sabah Hospital, Kuwait City, Kuwait.; Wagner M; Institute of Human Genetics, Technical University Munich, School of Medicine and Health, Munich, Germany.; Institute of Neurogenomics, Helmholtz Zentrum München, Neuherberg, Germany.; Department of Pediatrics, Division of Pediatric Neurology, Developmental Medicine and Social Pediatrics, University Hospital of Munich, Munich, Germany.; Terhal PA; Division of Laboratories, Pharmacy and Biomedical Genetics, University Medical Centre Utrecht, Utrecht, The Netherlands.; Muurinen M; Folkhälsan Research Center, Genetics Research Program, Helsinki, Finland.; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.; Barlogis V; APHM, La Timone Children's Hospital, Department of Pediatric Hematology, Immunology, and Oncology, Marseille, France.; Aix-Marseille University, EA 3279 Research Unit, Marseille, France.; Cruz P; Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology (OCICB), NIAID, NIH, Bethesda, MD, USA.; Danielson J; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Stewart H; Oxford Centre for Genomic Medicine, Nuffield Orthopaedic Centre, Oxford University Hospitals, NHS Foundation Trust, Headington, Oxford, UK.; Loid P; Folkhälsan Research Center, Genetics Research Program, Helsinki, Finland.; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.; Rading S; Neuronal and Cellular Signal Transduction, Center for Molecular Neurobiology Hamburg (ZMNH), University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Keren B; Genetic Departement, Assistance Publique - Hôpitaux de Paris.Sorbonne University, Paris, France.; SeqOIA Laboratory, FMG2025, Paris, France.; Pfundt R; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, Netherlands.; Zarember KA; Laboratory of Clinical Immunology and Microbiology, DIR, NIAID, NIH, Bethesda, MD, USA.; Vill K; LMU University Hospital, Department of Pediatrics, Division of Pediatric Neurology, iSPZ Hauner MUC - Munich University Center for Children with Medical and Developmental Complexity, Dr. von Hauner Children's Hospital, Munich, Germany.; Potocki L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.; Olivier KN; Pulmonary Branch, Division of Intramural Research, DIR, National Heart Lung and Blood Institute (NHLBI), NIH, Bethesda, MD, USA.; Lesca G; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Institut NeuroMyoGène, Physiopathologie et Génétique du Neurone et du Muscle, CNRS UMR 5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.; Faivre L; Génétique des Anomalies du Développement (GAD), UMR 1231, INSERM, Université Bourgogne-Franche Comté, Dijon, France.; Centre de Génétique et Centre de Référence 'Anomalies du Développement et Syndromes Malformatifs de l'Inter-région Est', FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Wong M; Department of Allergy and Immunology, The Children's Hospital at Westmead, Sydney, NSW, Australia.; Puel A; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale, INSERM U1163, Paris, France.; Imagine Institute, University of Paris Cité, Paris, France.; Chou J; Division of Immunology, Boston Children's Hospital, Department of Pediatrics, Harvard Medical School, Boston, MA, United States.; Tusseau M; Genetics Department, Lyon University Hospital, Lyon, France.; The International Center of Research in Infectiology, Lyon University, INSERM U1111, CNRS UMR 5308, ENS, UCBL, Lyon, France.; Moutsopoulos NM; Oral Immunity and Infection Section, DIR, National Institute of Dental and Craniofacial Research (NIDCR), NIH, Bethesda, MD, USA.; Matthews HF; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Molecular Development of the Immune System Section, Laboratory of Immune System Biology, DIR, NIAID, NIH, Bethesda, MD, USA.; Simons C; Centre for Population Genomics, Garvan Institute of Medical Research and UNSW Sydney, Sydney, NSW, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Taft RJ; Institute for Molecular Bioscience, University of Queensland, St. Lucia, Queensland, Australia.; Illumina, San Diego, CA, USA.; Soldatos A; National Institute of Neurological Disorders and Stroke (NINDS), NIH, Bethesda, MD, USA.; Masle-Farquhar E; Immunogenomics Laboratory, Garvan Institute of Medical Research, Sydney, NSW, Australia.; School of Clinical Medicine, UNSW Sydney, Sydney, NSW, Australia.; Pittaluga S; Laboratory of Pathology, Center for Cancer Research, NCI, NIH, Bethesda, MD, USA.; Brink R; St. Vincent's Clinical School, UNSW, Sydney, NSW, Australia.; B Cell Biology Laboratory, Garvan Institute of Medical Research, Sydney, NSW, Australia.; Fink DL; Neutrophil Monitoring Lab, Applied/Developmental Research Directorate, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.; Kong HH; Cutaneous Microbiome and Inflammation Section, Dermatology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, MD, USA.; Kabat J; Biological Imaging Section, Research Technologies Branch, DIR, NIAID, NIH, Bethesda, MD 20892, USA.; Kim WS; Chemotaxis Signal Section, Laboratory of Immunogenetics, DIR, NIAID, NIH, Rockville, MD, USA.; Bierhals T; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Meguro K; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Hsu AP; Laboratory of Clinical Immunology and Microbiology, DIR, NIAID, NIH, Bethesda, MD, USA.; Gu J; Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology (OCICB), NIAID, NIH, Bethesda, MD, USA.; Stoddard J; Immunology Service, Department of Laboratory Medicine, Clinical Center, NIH, Bethesda, MD, USA.; Banos-Pinero B; Oxford Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust, Oxford, Oxfordshire, UK.; Slack M; Division of Allergy and Immunology, Department of Pediatrics, University of Rochester Medical Center and Golisano Children's Hospital, Rochester, NY, USA.; Trivellin G; Section on Endocrinology and Genetics (SEGEN), DIR, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH, Bethesda, MD, USA.; Mazel B; Centre de Génétique et Centre de Référence 'Anomalies du Développement et Syndromes Malformatifs de l'Inter-région Est', FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Centre de Référence Déficiences Intellectuelles de Causes Rares, CHU Dijon Bourgogne, Dijon, France.; Soomann M; Division of Immunology, University Children's Hospital Zurich, Zurich, Switzerland.; Li S; Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology (OCICB), NIAID, NIH, Bethesda, MD, USA.; Watts VJ; Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN, USA.; Stratakis CA; Section on Endocrinology and Genetics (SEGEN), DIR, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), NIH, Bethesda, MD, USA.; Rodriguez-Quevedo MF; Division of Oncology Research, Schulze Center for Novel Therapeutics, Mayo Clinic, Rochester, MN, USA.; Bruel AL; Génétique des Anomalies du Développement (GAD), UMR 1231, INSERM, Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Lipsanen-Nyman M; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Saultier P; APHM, La Timone Children's Hospital, Department of Pediatric Hematology, Immunology, and Oncology, Marseille, France.; Aix-Marseille University, INSERM, National Research Institute for Agriculture, Food and Environment (INRAe), Cardiovascular and Nutrition Research Center (C2VN), Marseille, France.; Jain R; Clinical Immunology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.; Lehalle D; AP-HP Sorbonne Université, UF de Génétique Clinique, Centre de Référence Maladies Rares des Anomalies du Développement et Syndromes Malformatifs, Hôpital Trousseau, Paris, France.; Torres D; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Sullivan KE; Division of Allergy and Immunology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Barbarot S; Department of Dermatology, CHU Nantes, INRAE, UMR 1280, PhAN, Nantes Université, Nantes, France.; Neu A; Department of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Duffourd Y; Génétique des Anomalies du Développement (GAD), UMR 1231, INSERM, Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Similuk M; Centralized Sequencing Program, DIR, NIAID, NIH, Bethesda, MD, USA.; McWalter K; GeneDx, Gaithersburg, MD, USA.; Blanc P; SeqOIA Laboratory, FMG2025, Paris, France.; Bézieau S; Service de Génétique Médicale, CHU Nantes, Nantes Université, Nantes, France.; L'Institut du Thorax, CHU Nantes, INSERM UMR 1087/CNRS UMR 6291, Nantes Université, Nantes, France.; Jin T; Chemotaxis Signal Section, Laboratory of Immunogenetics, DIR, NIAID, NIH, Rockville, MD, USA.; Geha RS; Division of Immunology, Boston Children's Hospital, Department of Pediatrics, Harvard Medical School, Boston, MA, United States.; Casanova JL; St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.; Laboratory of Human Genetics of Infectious Diseases, Necker Branch, Institut National de la Santé et de la Recherche Médicale, INSERM U1163, Paris, France.; Imagine Institute, University of Paris Cité, Paris, France.; Howard Hughes Medical Institute, New York, NY, USA.; Department of Pediatrics, Necker Hospital for Sick Children, Paris, France.; Makitie OM; Folkhälsan Research Center, Genetics Research Program, Helsinki, Finland.; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Research Program for Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.; Kubisch C; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Martin Zeitz Center for Rare Diseases, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; Edery P; Service de Génétique, Hospices Civils de Lyon, Lyon, France.; Centre de Recherche en Neurosciences de Lyon, Inserm U1028, UMR CNRS 5292, Université Claude Bernard Lyon 1, Lyon, France.; Christodoulou J; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Australia.; Specialty of Child and Adolescent Health, University of Sydney, Sydney, Australia.; Germain RN; Lymphocyte Biology Section, Laboratory of Immune System Biology, DIR, NIAID, NIH, Bethesda, MD, USA.; Goodnow CC; Immunogenomics Laboratory, Garvan Institute of Medical Research, Sydney, NSW, Australia.; Cellular Genomics Futures Institute, Sydney, NSW, Australia.; Sakmar TP; Laboratory of Chemical Biology and Signal Transduction, The Rockefeller University, New York, NY, USA.; Karolinska Institutet, Department of Neurobiology, Care Sciences and Society, Center for Alzheimer Research, Division of Neurogeriatrics, Stockholm, Sweden.; Billadeau DD; Division of Oncology Research, Schulze Center for Novel Therapeutics, Mayo Clinic, Rochester, MN, USA.; Küry S; Service de Génétique Médicale, CHU Nantes, Nantes Université, Nantes, France.; L'Institut du Thorax, CHU Nantes, INSERM UMR 1087/CNRS UMR 6291, Nantes Université, Nantes, France.; Katanaev VL; Department of Cell Physiology and Metabolism, Faculty of Medicine, Translational Research Center in Oncohaematology, University of Geneva, Geneva, Switzerland.; Institute of Life Sciences and Biomedicine, Far Eastern Federal University, Vladivostok, Russia.; Zhang Y; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Lenardo MJ; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.; Molecular Development of the Immune System Section, Laboratory of Immune System Biology, DIR, NIAID, NIH, Bethesda, MD, USA.; Su HC; Human Immunological Diseases Section, Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research (DIR), National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA.; Clinical Genomics Program, DIR, NIAID, NIH, Bethesda, MD, USA.; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 0404511 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1095-9203 (Electronic) Linking ISSN: 00368075 NLM ISO Abbreviation: Science Subsets: MEDLINE
Academic Journal
Banasik K; Department of Cardiology, Specialist Hospital in Chelm, Chełm, Poland. kamil1.16@o2.pl.; Kowalczyk D; Department of Cardiology, Specialist Hospital in Chelm, Chełm, Poland.; Celiński R; Department of Cardiology, Specialist Hospital in Chelm, Chełm, Poland.; Łubiarz M; Department of Cardiology, Specialist Hospital in Chelm, Chełm, Poland.; Kurys-Denis E; 2nd Department of Radiology, Medical University of Lublin, Lublin, Poland.
Publisher: Via Medica Country of Publication: Poland NLM ID: 0376352 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1897-4279 (Electronic) Linking ISSN: 00229032 NLM ISO Abbreviation: Kardiol Pol Subsets: In Process; MEDLINE
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