학술논문
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'학술논문'
에서 검색결과 61건 | 목록
1~20
Academic Journal
Whitworth, J; Smith, PS; Martin, J-E; West, H; Luchetti, A; Rodger, F; Clark, G; Carss, K; Stephens, J; Stirrups, K; Penkett, C; Mapeta, R; Ashford, S; Megy, K; Shakeel, H; Ahmed, M; Adlard, J; Barwell, J; Brewer, C; Casey, RT; Armstrong, R; Cole, T; Evans, DG; Fostira, F; Greenhalgh, L; Hanson, H; Henderson, A; Hoffman, J; Izatt, L; Kumar, A; Kwong, A; Lalloo, F; Ong, KR; Paterson, J; Park, S-M; Chen-Shtoyerman, R; Searle, C; Side, L; Skytte, A-B; Snape, K; Woodward, ER; Tischkowitz, MD; Maher, ER; Aitman, T; Alachkar, H; Ali, S; Allen, L; Allsup, D; Ambegaonkar, G; Anderson, J; Antrobus, R; Arno, G; Arumugakani, G; Astle, W; Attwood, A; Austin, S; Bacchelli, C; Bakchoul, T; Bariana, TK; Baxendale, H; Bennett, D; Bethune, C; Bibi, S; Bitner-Glindzicz, M; Bleda, M; Boggard, H; Bolton-Maggs, P; Booth, C; Bradley, JR; Brady, A; Brown, M; Browning, M; Bryson, C; Burns, S; Calleja, P; Canham, N; Carmichael, J; Caulfield, M; Chalmers, E; Chandra, A; Chinnery, P; Chitre, M; Church, C; Clement, E; Clements-Brod, N; Clowes, V; Coghlan, G; Collins, P; Cookson, V; Cooper, N; Corris, P; Creaser-Myers, A; Dacosta, R; Daugherty, L; Davies, S; Davis, J; De Vries, M; Deegan, P; Deevi, SVV; Deshpande, C; Devlin, L; Dewhurst, E; Dixon, P; Doffinger, R; Dormand, N; Drewe, E; Edgar, D; Egner, W; Erber, WN; Erwood, M; Everington, T; Favier, R; Firth, H; Fletcher, D; Flinter, F; Frary, A; Freson, K; Furie, B; Furnell, A; Gale, D; Gardham, A; Gattens, M; Ghali, N; Ghataorhe, PK; Ghurye, R; Gibbs, S; Gilmour, K; Gissen, P; Goddard, S; Gomez, K; Gordins, P; Graf, S; Gräf, S; Greene, D; Greenhalgh, A; Greinacher, A; Grigoriadou, S; Grozeva, D; Hackett, S; Hadinnapola, C; Hague, R; Haimel, M; Halmagyi, C; Hammerton, T; Hart, D; Hayman, G; Heemskerk, JWM; Henderson, R; Hensiek, A; Henskens, Y; Herwadkar, A; Holden, S; Holder, M; Holder, S; Hu, F; Veld, A; Huissoon, A; Humbert, M; Hurst, J; James, R; Jolles, S; Josifova, D; Kazmi, R; Keeling, D; Kelleher, P; Kelly, AM; Kennedy, F; Kiely, D; Kingston, N; Koziell, A; Krishnakumar, D; Kuijpers, TW; Kuijpers, T; Kumararatne, D; Kurian, M; Laffan, MA; Lambert, MP; Allen, HL; Lango-Allen, H; Lawrie, A; Lear, S; Lees, M; Lentaigne, C; Liesner, R; Linger, R; Longhurst, H; Lorenzo, L; Louka, E; Machado, R; Ross, RM; Maclaren, R; Maher, E; Maimaris, J; Mangles, S; Manson, A; Markus, HS; Martin, J; Masati, L; Mathias, M; Matser, V; Maw, A; McDermott, E; McJannet, C; Meacham, S; Meehan, S; Mehta, S; Michaelides, M; Millar, CM; Moledina, S; Moore, A; Morrell, N; Mumford, A; Murng, S; Murphy, E; Nejentsev, S; Noorani, S; Nurden, P; Oksenhendler, E; Othman, S; Ouwehand, WH; Papadia, S; Parker, A; Pasi, J; Patch, C; Payne, J; Peacock, A; Peerlinck, K; Penkett, CJ; Pepke-Zaba, J; Perry, D; Perry, DJ; Pollock, V; Polwarth, G; Ponsford, M; Qasim, W; Quinti, I; Rankin, S; Rankin, J; Raymond, FL; Rayner-Matthews, P; Rehnstrom, K; Reid, E; Rhodes, CJ; Richards, M; Richardson, S; Richter, A; Roberts, I; Rondina, M; Rosser, E; Roughley, C; Roy, N; Rue-Albrecht, K; Samarghitean, C; Sanchis-Juan, A; Sandford, R; Santra, S; Sargur, R; Savic, S; Schotte, G; Schulman, S; Schulze, H; Scott, R; Scully, M; Seneviratne, S; Sewell, C; Shamardina, O; Shipley, D; Simeoni, I; Sivapalaratnam, S; Smith, KGC; Sohal, A; Southgate, L; Staines, S; Staples, E; Stark, H; Stauss, H; Stein, P; Stock, S; Suntharalingam, J; Talks, K; Tan, Y; Thachil, J; Thaventhiran, J; Thomas, E; Thomas, M; Thompson, D; Thrasher, A; Tischkowitz, M; Titterton, C; Toh, C-H; Toshner, M; Treacy, C; Trembath, R; Tuna, S; Turek, W; Turro, E; Van Geet, C; Veltman, M; Vogt, J; Von Ziegenweldt, J; Noordegraaf, AV; Wakeling, E; Wanjiku, I; Warner, TQ; Wassmer, E; Watkins, H; Watt, C; Webster, N; Welch, S; Westbury, S; Wharton, J; Whitehorn, D; Wilkins, M; Willcocks, L; Williamson, C; Woods, G; Wort, J; Yeatman, N; Yong, P; Young, T; Yu, P
Am J Hum Genet
AMERICAN JOURNAL OF HUMAN GENETICS
NIHR BioResource Rare Diseases Consortium 2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', American journal of human genetics, vol. 103, no. 1, pp. 3-18. https://doi.org/10.1016/j.ajhg.2018.04.013
Whitworth, J, Smith, P S, Martin, J-E, West, H, Luchetti, A, Rodger, F, Clark, G, Carss, K, Stephens, J, Stirrups, K, Penkett, C, Mapeta, R, Ashford, S, Megy, K, Shakeel, H, Ahmed, M, Adlard, J, Barwell, J, Brewer, C, Casey, R T, Armstrong, R, Cole, T, Evans, D G, Fostira, F, Greenhalgh, L, Hanson, H, Henderson, A, Hoffman, J, Izatt, L, Kumar, A, Kwong, A, Lalloo, F, Ong, K R, Paterson, J, Park, S-M, Chen-Shtoyerman, R, Searle, C, Side, L, Skytte, A-B, Snape, K, Woodward, E R & NIHR BioResource Rare Diseases Consortium 2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', American Journal of Human Genetics, vol. 103, no. 1, pp. 3-18. https://doi.org/10.1016/j.ajhg.2018.04.013
2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', American Journal of Human Genetics, vol. 103, no. 1, pp. 3-18. https://doi.org/10.1016/j.ajhg.2018.04.013
2018, ' Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes ', American Journal of Human Genetics, vol. 103, no. 1, pp. 3-18 . https://doi.org/10.1016/j.ajhg.2018.04.013
NIHR BioResource Rare Diseases Consortium & Evans, D G 2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', Cell, vol. 103, no. 1. https://doi.org/10.1016/j.ajhg.2018.04.013
American Journal of Human Genetics
AMERICAN JOURNAL OF HUMAN GENETICS
NIHR BioResource Rare Diseases Consortium 2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', American journal of human genetics, vol. 103, no. 1, pp. 3-18. https://doi.org/10.1016/j.ajhg.2018.04.013
Whitworth, J, Smith, P S, Martin, J-E, West, H, Luchetti, A, Rodger, F, Clark, G, Carss, K, Stephens, J, Stirrups, K, Penkett, C, Mapeta, R, Ashford, S, Megy, K, Shakeel, H, Ahmed, M, Adlard, J, Barwell, J, Brewer, C, Casey, R T, Armstrong, R, Cole, T, Evans, D G, Fostira, F, Greenhalgh, L, Hanson, H, Henderson, A, Hoffman, J, Izatt, L, Kumar, A, Kwong, A, Lalloo, F, Ong, K R, Paterson, J, Park, S-M, Chen-Shtoyerman, R, Searle, C, Side, L, Skytte, A-B, Snape, K, Woodward, E R & NIHR BioResource Rare Diseases Consortium 2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', American Journal of Human Genetics, vol. 103, no. 1, pp. 3-18. https://doi.org/10.1016/j.ajhg.2018.04.013
2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', American Journal of Human Genetics, vol. 103, no. 1, pp. 3-18. https://doi.org/10.1016/j.ajhg.2018.04.013
2018, ' Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes ', American Journal of Human Genetics, vol. 103, no. 1, pp. 3-18 . https://doi.org/10.1016/j.ajhg.2018.04.013
NIHR BioResource Rare Diseases Consortium & Evans, D G 2018, 'Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes', Cell, vol. 103, no. 1. https://doi.org/10.1016/j.ajhg.2018.04.013
American Journal of Human Genetics
Academic Journal
Journal of Thrombosis and Haemostasis. Jun 01, 2015 13 Suppl 2:183-184
Academic Journal
Arno, G; Carss, KJ; Hull, S; Zihni, C; Robson, AG; Fiorentino, A; Hardcastle, AJ; Holder, GE; Cheetham, ME; Plagnol, V; Moore, AT; Raymond, FL; Matter, K; Balda, MS; Webster, AR; Black, G; Hall, G; Ingram, S; Gillespie, R; Manson, F; Sergouniotis, P; Inglehearn, C; Toomes, C; Ali, M; McKibbin, M; Poulter, J; Khan, K; Lord, E; Nemeth, A; Downes, S; Halford, S; Yu, J; Lise, S; Ponitkos, N; Michaelides, M; van Heyningen, V; Aitman, T; Alachkar, H; Ali, S; Allen, L; Allsup, D; Ambegaonkar, G; Anderson, J; Antrobus, R; Armstrong, R; Arumugakani, G; Ashford, S; Astle, W; Attwood, A; Austin, S; Bacchelli, C; Bakchoul, T; Bariana, TK; Baxendale, H; Bennett, D; Bethune, C; Bibi, S; Bitner-Glindzicz, M; Bleda, M; Boggard, H; Bolton-Maggs, P; Booth, C; Bradley, JR; Brady, A; Brown, M; Browning, M; Bryson, C; Burns, S; Calleja, P; Canham, N; Carmichael, J; Carss, K; Caulfield, M; Chalmers, E; Chandra, A; Chinnery, P; Chitre, M; Church, C; Clement, E; Clements-Brod, N; Clowes, V; Coghlan, G; Collins, P; Cooper, N; Creaser-Myers, A; DaCosta, R; Daugherty, L; Davies, S; Davis, J; De Vries, M; Deegan, P; Deevi, SVV; Deshpande, C; Devlin, L; Dewhurst, E; Doffinger, R; Dormand, N; Drewe, E; Edgar, D; Egner, W; Erber, WN; Erwood, M; Everington, T; Favier, R; Firth, H; Fletcher, D; Flinter, F; Fox, JC; Frary, A; Freson, K; Furie, B; Furnell, A; Gale, D; Gardham, A; Gattens, M; Ghali, N; Ghataorhe, PK; Ghurye, R; Gibbs, S; Gilmour, K; Gissen, P; Goddard, S; Gomez, K; Gordins, P; Gräf, S; Greene, D; Greenhalgh, A; Greinacher, A; Grigoriadou, S; Grozeva, D; Hackett, S; Hadinnapola, C; Hague, R; Haimel, M; Halmagyi, C; Hammerton, T; Hart, D; Hayman, G; Heemskerk, JWM; Henderson, R; Hensiek, A; Henskens, Y; Herwadkar, A; Holden, S; Holder, M; Holder, S; Hu, F; Huissoon, A; Humbert, M; Hurst, J; James, R; Jolles, S; Josifova, D; Kazmi, R; Keeling, D; Kelleher, P; Kelly, AM; Kennedy, F; Kiely, D; Kingston, N; Koziell, A; Krishnakumar, D; Kuijpers, TW; Kumararatne, D; Kurian, M; Laffan, MA; Lambert, MP; Allen, HL; Lawrie, A; Lear, S; Lees, M; Lentaigne, C; Liesner, R; Linger, R; Longhurst, H; Lorenzo, L; Machado, R; Mackenzie, R; MacLaren, R; Maher, E; Maimaris, J; Mangles, S; Manson, A; Mapeta, R; Markus, HS; Martin, J; Masati, L; Mathias, M; Matser, V; Maw, A; McDermott, E; McJannet, C; Meacham, S; Meehan, S; Megy, K; Mehta, S; Millar, CM; Moledina, S; Moore, A; Morrell, N; Mumford, A; Murng, S; Murphy, E; Nejentsev, S; Noorani, S; Nurden, P; Oksenhendler, E; Ouwehand, WH; Papadia, S; Park, S-M; Parker, A; Pasi, J; Patch, C; Paterson, J; Payne, J; Peacock, A; Peerlinck, K; Penkett, CJ; Pepke-Zaba, J; Perry, DJ; Pollock, V; Polwarth, G; Ponsford, M; Qasim, W; Quinti, I; Rankin, S; Rankin, J; Rehnstrom, K; Reid, E; Rhodes, CJ; Richards, M; Richardson, S; Richter, A; Roberts, I; Rondina, M; Rosser, E; Roughley, C; Rue-Albrecht, K; Samarghitean, C; Sanchis-Juan, A; Sandford, R; Santra, S; Sargur, R; Savic, S; Schulman, S; Schulze, H; Scott, R; Scully, M; Seneviratne, S; Sewell, C; Shamardina, O; Shipley, D; Simeoni, I; Sivapalaratnam, S; Smith, K; Sohal, A; Southgate, L; Staines, S; Staples, E; Stauss, H; Stein, P; Stephens, J; Stirrups, K; Stock, S; Suntharalingam, J; Tait, RC; Talks, K; Tan, Y; Thachil, J; Thaventhiran, J; Thomas, E; Thomas, M; Thompson, D; Thrasher, A; Tischkowitz, M; Titterton, C; Toh, C-H; Toshner, M; Treacy, C; Trembath, R; Tuna, S; Turek, W; Turro, E; Van Geet, C; Veltman, M; Vogt, J; von Ziegenweldt, J; Noordegraaf, AV; Wakeling, E; Wanjiku, I; Warner, TQ; Wassmer, E; Watkins, H; Webster, A; Welch, S; Westbury, S; Wharton, J; Whitehorn, D; Wilkins, M; Willcocks, L; Williamson, C; Woods, G; Wort, J; Yeatman, N; Yong, P; Young, T; Yu, P
UK Inherited Retinal Disease Consortium, NIHR BioResource Rare Diseases Consortium, NIHR BioResource Rare Diseases Consortium & NIHR Bioresource – Rare Diseases Consortium 2017, 'Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration', American journal of human genetics, vol. 100, no. 2, pp. 334-342. https://doi.org/10.1016/j.ajhg.2016.12.014
Arno, G, Carss, K J, Hull, S, Zihni, C, Robson, A G, Fiorentino, A, Hardcastle, A J, Holder, G E, Cheetham, M E, Plagnol, V, Moore, A T, Raymond, F L, Matter, K, Balda, M S, Webster, A R, Uk Inherited Retinal Disease Consortium & Black, G 2017, 'Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration', American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2016.12.014
Arno, G, Carss, K J, Hull, S, Zihni, C, Robson, A G, Fiorentino, A, Hardcastle, A J, Holder, G E, Cheetham, M E, Plagnol, V, Moore, A T, Raymond, F L, Matter, K, Balda, M S, Webster, A R, Uk Inherited Retinal Disease Consortium & Black, G 2017, 'Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration', American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2016.12.014
Academic Journal
Sivapalaratnam, S; Westbury, SK; Stephens, JC; Greene, D; Downes, K; Kelly, AM; Lentaigne, C; Astle, WJ; Huizinga, EG; Nurden, P; Papadia, S; Peerlinck, K; Penkett, CJ; Perry, DJ; Roughley, C; Simeoni, I; Stirrups, K; Hart, DP; Tait, RC; Mumford, AD; NIHR BioResource; Laffan, MA; Freson, K; Ouwehand, WH; Kunishima, S; Turro, E
Blood. 129:520-524
Academic Journal
Goubau, C; Devriendt, K; Van der Aa, N; Wieczorek, D; Kleefstra, T; Rauch, A; Tzschach, A; Buyse, G; Van Geet, C; Freson, K
Journal of Thrombosis and Haemostasis. Jul 01, 2013 11 Suppl 2:455-455
Academic Journal
Journal of Thrombosis and Haemostasis. Jul 01, 2013 11 Suppl 2:159-159
Academic Journal
Di Michele, M; Goubau, C; Waelkens, E; Thys, C; Overbergh, L; Buyse, G; Casaer, P; Van Geet, C; Freson, K
Journal of Thrombosis and Haemostasis. Jul 01, 2013 11 Suppl 2:160-160
Academic Journal
Albers, C A; Paul, D S; Schulze, H; Freson, K; Stephens, J C; Smethurst, P A; Jolley, J D; Cvejic, A; Kostadima, M; Bertone, P; Breuning, M H; Debili, N; Deloukas, P; Favier, R; Fiedler, J; Hobbs, C M; Huang, N; Hurles, M E; Kiddle, G; Krapels, I; Nurden, P; Ruivenkamp, C AL; Sambrook, J G; Smith, K; Stemple, D L; Strauss, G; Thys, C; van Geet, C; Newbury-Ecob, R; Ouwehand, W H; Ghevaert, C
British Journal of Haematology. Apr 01, 2012 157 Suppl. 1:9-9
New variant of platelet type von Willebrand disease due to increased expression of GPib/V/IX complex
Academic Journal
Haemophilia. Jul 01, 2002 8(4):509-509
Academic Journal
Haemophilia. Jul 01, 2002 8(4):504-504
Academic Journal
Wei, W; Tuna, S; Keogh, MJ; Smith, KR; Aitman, TJ; Beales, PL; Bennett, DL; Gale, DP; Bitner-Glindzicz, MAK; Black, GC; Brennan, P; Elliott, P; Flinter, FA; Floto, RA; Houlden, H; Irving, M; Koziell, A; Maher, ER; Markus, HS; Morrell, NW; Newman, WG; Roberts, I; Sayer, JA; Smith, KGC; Taylor, JC; Watkins, H; Webster, AR; Wilkie, AOM; Williamson, C; Attwood, A; Brown, M; Brod, NC; Crisp-Hihn, A; Davis, J; Deevi, SVV; Dewhurst, EF; Edwards, K; Erwood, M; Fox, J; Frary, AJ; Hu, F; Jolley, J; Kingston, N; Linger, R; Mapeta, R; Martin, J; Meacham, S; Papadia, S; Rayner-Matthews, PJ; Samarghitean, C; Shamardina, O; Simeoni, I; Staines, S; Staples, E; Stark, H; Stephens, J; Titterton, C; Von Ziegenweidt, J; Watt, C; Whitehorn, D; Wood, Y; Yates, K; Yu, P; James, R; Ashford, S; Penkett, CJ; Stirrups, KE; Bariana, T; Lentaigne, C; Sivapalaratnam, S; Westbury, SK; Allsup, DJ; Bakchoul, T; Biss, T; Boyce, S; Collins, J; Collins, PW; Curry, NS; Downes, K; Dutt, T; Erber, WN; Evans, G; Everington, T; Favier, R; Gomez, K; Greene, D; Gresele, P; Hart, D; Kazmi, R; Kelly, AM; Lambert, M; Madan, B; Mangles, S; Mathias, M; Millar, C; Obaji, S; Peerlinck, K; Roughley, C; Schulman, S; Scully, M; Shapiro, SE; Sibson, K; Sims, MC; Tait, RC; Talks, K; Thys, C; Toh, C-H; Van Geet, C; Westwood, J-P; Mumford, AD; Ouwehand, WH; Freson, K; Laffan, MA; Tan, RYY; Harkness, K; Mehta, S; Muir, KW; Hassan, A; Traylor, M; Drazyk, AM; Parry, D; Ahmed, M; Kazkaz, H; Vandersteen, AM; Ormondroyd, E; Thomson, K; Dent, T; Buchan, RJ; Bueser, T; Carr-White, G; Cook, S; Daniels, MJ; Harper, AR; Ware, JS; Dixon, PH; Chambers, J; Cheng, F; Estiu, MC; Hague, WM; Marschall, H-U; Vazquez-Lopez, M; Arno, G; French, CE; Michaelides, M; Moore, AT; Sanchis-Juan, A; Carss, K; Raymond, FL; Chinnery, PF; Griffiths, P; Horvath, R; Hudson, G; Jurkute, N; Pyle, A; Yu-Wai-Man, P; Whitworth, J; Adlard, J; Armstrong, R; Brewer, C; Casey, R; Cole, TRP; Evans, DG; Greenhalgh, L; Hanson, HL; Hoffman, J; Izatt, L; Kumar, A; Lalloo, F; Ong, KR; Park, S-M; Searle, C; Side, L; Snape, K; Woodward, E; Tischkowitz, M; Grozeva, D; Kurian, MA; Themistocleous, AC; Gosal, D; Marshall, A; Matthews, E; McCarthy, MI; Renton, T; Rice, ASC; Vale, T; Walker, SM; Woods, CG; Thaventhiran, JE; Allen, HL; Savic, S; Alachkar, H; Antrobus, R; Baxendale, HE; Browning, MJ; Buckland, MS; Cooper, N; Edgar, JDM; Egner, W; Gilmour, KC; Goddard, S; Gordins, P; Grigoriadou, S; Hackett, S; Hague, R; Hayman, G; Herwadkar, A; Huissoon, AP; Jolles, S; Kelleher, P; Kumararatne, D; Longhurst, H; Lorenzo, LE; Lyons, PA; Maimaris, J; Noorani, S; Richter, A; Sargur, RB; Sewell, WAC; Thomas, D; Thomas, MJ; Worth, A; Yong, PFK; Kuijpers, TW; Thrasher, AJ; Levine, AP; Sadeghi-Alavijeh, O; Wong, EKS; Cook, HT; Chan, MMY; Hall, M; Harris, C; McAlinden, P; Marchbank, KJ; Marks, S; Maxwell, H; Mozere, M; Wessels, J; Johnson, SA; Bleda, M; Hadinnapola, C; Haimel, M; Swietlik, E; Bogaard, H; Church, C; Coghlan, G; Condliffe, R; Corris, P; Danesino, C; Eyries, M; Gall, H; Ghofrani, H-A; Gibbs, JSR; Girerd, B; Holden, S; Houweling, A; Howard, LS; Humbert, M; Kiely, DG; Kovacs, G; Lawrie, A; Ross, RVM; Moledina, S; Montani, D; Newnham, M; Olschewski, A; Olschewski, H; Peacock, A; Pepke-Zaba, J; Scelsi, L; Seeger, W; Soubrier, F; Suntharalingam, J; Toshner, M; Treacy, C; Trembath, R; Noordegraaf, AV; Waisfisz, Q; Wharton, J; Wilkins, MR; Wort, SJ; Graf, S; Louka, E; Roy, NB; Rao, A; Ancliff, P; Babbs, C; Layton, DM; Mead, AJ; O'Sullivan, J; Okoli, S; Saleem, M; Bierzynska, A; Diz, CB; Colby, E; Ekani, MN; Satchell, S; Fowler, T; Rendon, A; Scott, R; Smedley, D; Thomas, E; Caulfield, M; Abbs, S; Burrows, N; Chitre, M; Gattens, M; Gurnell, M; Kelsall, W; Poole, KES; Ross-Russell, R; Spasic-Boskovic, O; Twiss, P; Wagner, A; Banka, S; Clayton-Smith, J; Douzgou, S; Abulhoul, L; Aurora, P; Bockenhauer, D; Cleary, M; Dattani, M; Ganesan, V; Pilkington, C; Rahman, S; Shah, N; Wedderburn, L; Compton, CJ; Deshpande, C; Fassihi, H; Haque, E; Josifova, D; Mohammed, SN; Robert, L; Rose, SJ; Ruddy, DM; Sarkany, RN; Sayer, G; Shaw, AC; Campbell, C; Gibson, K; Koelling, N; Lester, T; Nemeth, AH; Palles, C; Patel, S; Sen, A; Taylor, J; Tomlinson, IP; Malka, S; Browning, AC; Burn, J; De Soyza, A; Graham, J; Pearce, S; Quinton, R; Schaefer, AM; Wilson, BT; Wright, M; Simpson, M; Syrris, P; Bradley, JR; Turro, E
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NIHR BioResource-Rare Diseases, 100,000 Genomes Project–Rare Diseases Pilot, Wei, W, Tuna, S, Keogh, M J, Smith, K R, Aitman, T J, Beales, P L, Bennett, D L, Gale, D P, Bitner-Glindzicz, M A K, Black, G C, Brennan, P, Elliott, P, Flinter, F A, Floto, R A, Houlden, H, Irving, M, Koziell, A, Maher, E R, Markus, H S, Morrell, N W, Newman, W G, Roberts, I, Sayer, J A, Smith, K G C, Taylor, J C, Watkins, H, Webster, A R, Wilkie, A O M, Williamson, C, Ashford, S, Penkett, C J, Stirrups, K E, Rendon, A, Ouwehand, W H, Bradley, J R, Raymond, F L, Caulfield, M, Turro, E & Chinnery, P F 2019, 'Germline selection shapes human mitochondrial DNA diversity', Science (New York, N.Y.), vol. 364, no. 6442, pp. 1-13. https://doi.org/10.1126/science.aau6520
Science
NIHR BioResource-Rare Diseases, 100,000 Genomes Project–Rare Diseases Pilot, Wei, W, Tuna, S, Keogh, M J, Smith, K R, Aitman, T J, Beales, P L, Bennett, D L, Gale, D P, Bitner-Glindzicz, M A K, Black, G C, Brennan, P, Elliott, P, Flinter, F A, Floto, R A, Houlden, H, Irving, M, Koziell, A, Maher, E R, Markus, H S, Morrell, N W, Newman, W G, Roberts, I, Sayer, J A, Smith, K G C, Taylor, J C, Watkins, H, Webster, A R, Wilkie, A O M, Williamson, C, Ashford, S, Penkett, C J, Stirrups, K E, Rendon, A, Ouwehand, W H, Bradley, J R, Raymond, F L, Caulfield, M, Turro, E & Chinnery, P F 2019, 'Germline selection shapes human mitochondrial DNA diversity', Science (New York, N.Y.), vol. 364, no. 6442, pp. 1-13. https://doi.org/10.1126/science.aau6520
Science
Academic Journal
Ito, Y; Carss, KJ; Duarte, ST; Hartley, T; Keren, B; Kurian, MA; Marey, I; Charles, P; Mendonça, C; Nava, C; Pfundt, R; Sanchis-Juan, A; van Bokhoven, H; van Essen, A; van Ravenswaaij-Arts, C; Aitman, T; Bennett, D; Caulfield, M; Chinnery, P; Gale, D; Koziell, A; Kuijpers, TW; Laffan, MA; Maher, E; Markus, HS; Morrell, NW; Ouwehand, WH; Perry, DJ; Raymond, FL; Roberts, I; Smith, KGC; Thrasher, A; Watkins, H; Williamson, C; Woods, G; Ashford, S; Bradley, JR; Fletcher, D; Hammerton, T; James, R; Kingston, N; Penkett, CJ; Stirrups, K; Veltman, M; Young, T; Brown, M; Clements-Brod, N; Davis, J; Dewhurst, E; Dolling, H; Erwood, M; Frary, A; Linger, R; Martin, JM; Papadia, S; Rehnstrom, K; Stark, H; Allsup, D; Austin, S; Bakchoul, T; Bariana, TK; Bolton-Maggs, P; Chalmers, E; Collins, J; Collins, P; Erber, WN; Everington, T; Favier, R; Freson, K; Furie, B; Gattens, M; Gebhart, J; Gomez, K; Greene, D; Greinacher, A; Gresele, P; Hart, D; Heemskerk, JWM; Henskens, Y; Kazmi, R; Keeling, D; Kelly, AM; Lambert, MP; Lentaigne, C; Liesner, R; Makris, M; Mangles, S; Mathias, M; Millar, CM; Mumford, A; Nurden, P; Payne, J; Pasi, J; Peerlinck, K; Revel-Vilk, S
Academic Journal
Heremans J; Department of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.; Freson K; Department of Cardiovascular Sciences, Center for Molecular and Vascular Biology, KU Leuven, Leuven, Belgium.
Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 101300213 Publication Model: Print Cited Medium: Internet ISSN: 1751-553X (Electronic) Linking ISSN: 17515521 NLM ISO Abbreviation: Int J Lab Hematol Subsets: MEDLINE
Academic Journal
Jacquemin M; Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.; Laboratorium Geneeskunde, UZ Leuven, Leuven, Belgium.; Vanlinthout I; Laboratorium Geneeskunde, UZ Leuven, Leuven, Belgium.; Van Horenbeeck I; Laboratorium Geneeskunde, UZ Leuven, Leuven, Belgium.; Debasse M; Laboratorium Geneeskunde, UZ Leuven, Leuven, Belgium.; Toelen J; Laboratorium Geneeskunde, UZ Leuven, Leuven, Belgium.; Schoeters J; Laboratorium Geneeskunde, UZ Leuven, Leuven, Belgium.; Lavend'homme R; Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.; Freson K; Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.; Peerlinck K; Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.; Vascular Medicine and Haemostasis, UZ Leuven, Leuven, Belgium.
Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 101300213 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1751-553X (Electronic) Linking ISSN: 17515521 NLM ISO Abbreviation: Int J Lab Hematol Subsets: MEDLINE
Academic Journal
Pauwels S; 1Department of Public Health and Primary Care, Environment and Health,KU Leuven- University of Leuven,Leuven,Belgium.; Truijen I; 1Department of Public Health and Primary Care, Environment and Health,KU Leuven- University of Leuven,Leuven,Belgium.; Ghosh M; 1Department of Public Health and Primary Care, Environment and Health,KU Leuven- University of Leuven,Leuven,Belgium.; Duca RC; 1Department of Public Health and Primary Care, Environment and Health,KU Leuven- University of Leuven,Leuven,Belgium.; Langie SAS; 2Unit Environmental Risk and Health,Flemish Institute of Technological Research (VITO),Mol,Belgium.; Bekaert B; 4Department of Imaging & Pathology,KU Leuven - University of Leuven,Leuven,Belgium.; Freson K; 6Center for Molecular and Vascular Biology,KU Leuven - University of Leuven,Leuven,Belgium.; Huybrechts I; 7Dietary Exposure Assessment Group,International Agency for Research on Cancer,Lyon,France.; Koppen G; 2Unit Environmental Risk and Health,Flemish Institute of Technological Research (VITO),Mol,Belgium.; Devlieger R; 8Department of Development and Regeneration,KU Leuven-University of Leuven,Leuven,Belgium.; Godderis L; 1Department of Public Health and Primary Care, Environment and Health,KU Leuven- University of Leuven,Leuven,Belgium.
Publisher: Cambridge University Press Country of Publication: England NLM ID: 101517692 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2040-1752 (Electronic) Linking ISSN: 20401744 NLM ISO Abbreviation: J Dev Orig Health Dis Subsets: MEDLINE
Conference
Simoni, I; Sivapalaratnam, S; Greene, D; Laffan, M; Mumford, A; Megy, K; Freson, K; Gomez, K; Ouwehand, W; Turro, E
21st Congress of the European Hematology Association
Academic Journal
Vangeel EB; Genetic Research about Stress and Psychiatry (GRASP), Department of Neurosciences, Leuven, Belgium.; Center for Molecular and Vascular Biology (CMVB), Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.; Izzi B; Center for Molecular and Vascular Biology (CMVB), Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.; Hompes T; Genetic Research about Stress and Psychiatry (GRASP), Department of Neurosciences, Leuven, Belgium.; University Psychiatric Center, University of Leuven, Leuven, Belgium.; Vansteelandt K; University Psychiatric Center, University of Leuven, Leuven, Belgium.; Lambrechts D; Laboratory of Translational Genetics, Department of Oncology, University of Leuven, Leuven, Belgium.; Vesalius Research Center (VRC), VIB, Leuven, Belgium.; Freson K; Center for Molecular and Vascular Biology (CMVB), Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.; Claes S; Genetic Research about Stress and Psychiatry (GRASP), Department of Neurosciences, Leuven, Belgium.; University Psychiatric Center, University of Leuven, Leuven, Belgium.
Publisher: Munksgaard Country of Publication: England NLM ID: 101129617 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1601-183X (Electronic) Linking ISSN: 1601183X NLM ISO Abbreviation: Genes Brain Behav Subsets: MEDLINE
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