未登录 The genome of the domesticated apple (Malus x domestica Borkh.) 驯化苹果 (Malus x domestica bokh.) 的基因组 Velasco, Riccardo; Zharkikh, Andrey; Affourtit, Jason; Dhingra, Amit; Cestaro, Alessandro; Kalyanaraman, Ananth; Fontana, Paolo; Bhatnagar, Satish K.; Troggio, Michela; Pruss, Dmitry; Salvi, Silvio; Pindo, Massimo; Baldi, Paolo; Castelletti, Sara; Cavaiuolo, Marina; Coppola, Giuseppina; Costa, Fabrizio; Cova, Valentina; Dal Ri, Antonio; Goremykin, Vadim; Komjanc, Matteo; Longhi, Sara; Magnago, Pierluigi; Malacarne, Giulia; Malnoy, Mickael; Micheletti, Diego; Moretto, Marco; Perazzolli, Michele; Si-Ammour, Azeddine; Vezzulli, Silvia; Zini, Elena; Eldredge, Glenn; Fitzgerald, Lisa M.; Gutin, Natalia; Lanchbury, Jerry; Macalma, Teresita; Mitchell, Jeff T.; Reid, Julia; Wardell, Bryan; Kodira, Chinnappa; Chen, Zhoutao; Desany, Brian; Niazi, Faheem; Palmer, Melinda; Koepke, Tyson; Jiwan, Derick; Schaeffer, Scott; Krishnan, Vandhana; Wu, Changjun; Chu, Vu T.; King, Stephen T.; Vick, Jessica; Tao, Quanzhou; Mraz, Amy; Stormo, Aimee; Stormo, Keith; Bogden, Robert; Ederle, Davide; Stella, Alessandra; Vecchietti, Alberto; Kater, Martin M.; Masiero, Simona; Lasserre, Pauline; Lespinasse, Yves; Allan, Andrew C.; Bus, Vincent; Chagne, David; Crowhurst, Ross N.; Gleave, Andrew P.; Lavezzo, Enrico; Fawcett, Jeffrey A.; Proost, Sebastian; Rouze, Pierre; Sterck, Lieven; Toppo, Stefano; Lazzari, Barbara; Hellens, Roger P.; Durel, Charles-Eric; Gutin, Alexander; Bumgarner, Roger E.; Gardiner, Susan E.; Skolnick, Mark; Egholm, Michael; Van de Peer, Yves; Salamini, Francesco; Viola, Roberto 分享 收藏
A genome wide linkage scan for dizygotic twinning in 525 families of mothers of dizygotic twins Painter, Jodie N.; Willemsen, Gonneke; Nyholt, Dale; Hoekstra, Chantal; Duffy, David L.; Henders, Anjali K.; Wallace, Leanne; Healey, Sue; Cannon-Albright, Lisa A.; Skolnick, Mark; Martin, Nicholas G.; Boomsma, Dorret I.; Montgomery, Grant W. 分享 收藏
Sequencing and assembly of highly heterozygous genome of Vitis vinifera L. cv Pinot Noir:: Problems and solutions Zharkikh, Andrey; Troggio, Michela; Pruss, Dmitry; Cestaro, Alessandro; Eldrdge, Glenn; Pindo, Massimo; Mitchell, Jeff T.; Vezzulli, Silvia; Bhatnagar, Satish; Fontana, Paolo; Viola, Roberto; Gutin, Alexander; Salamini, Francesco; Skolnick, Mark; Velasco, Riccardo 分享 收藏
Evidence for HTR1A and LHPP as interacting genetic risk factors in major depression Neff, C. D.; Abkevich, V.; Packer, J. C. L.; Chen, Y.; Potter, J.; Riley, R.; Davenport, C.; Warren, J. DeGrado; Jammulapati, S.; Bhathena, A.; Choi, W. S.; Kroeger, P. E.; Metzger, R. E.; Gutin, A.; Skolnick, M. H.; Shattuck, D.; Katz, D. A. 分享 收藏
TBC1D1 is a candidate for a severe obesity gene and evidence for a gene/gene interaction in obesity predisposition Stone, Steven; Abkevich, Victor; Russell, Deanna L.; Riley, Robyn; Timms, Kirsten; Tran, Thanh; Trem, Deborah; Frank, David; Jammulapati, Srikanth; Neff, Chris D.; Iliev, Diana; Gress, Richard; He, Gongping; Frech, Georges C.; Adams, Ted D.; Skolnick, Mark H.; Lanchbury, Jerry S.; Gutin, Alexander; Hunt, Steven C.; Shattuck, Donna 分享 收藏
Variants in Apaf-1 segregating with major depression promote apoptosome function Harlan, J; Chen, Y; Gubbins, E; Mueller, R; Roch, JM; Walter, K; Lake, M; Olsen, T; Metzger, P; Dorwin, S; Ladror, U; Egan, DA; Severin, J; Johnson, RW; Holzman, TF; Voelp, K; Davenport, C; Beck, A; Potter, J; Gopalakrishnan, M; Hahn, A; Spear, BB; Halbert, DN; Sullivan, JP; Abkevich, V; Neff, CD; Skolnick, MH; Shattuck, D; Katz, DA 分享 收藏
A mutation in PCSK9 causing autosomal-dominant hypercholesterolemia in a Utah pedigree PCSK9突变导致犹他州家系常染色体显性高胆固醇血症 Timms, KM; Wagner, S; Samuels, ME; Forbey, K; Goldfine, H; Jammulapati, S; Skolnick, MH; Hopkins, PN; Hunt, SC; Shattuck, DM 分享 收藏
Predisposition locus for major depression at chromosome 12q22-12q23.2 Abkevich, V; Camp, NJ; Hensel, CH; Neff, CD; Russell, DL; Hughes, DC; Plenk, AM; Lowry, MR; Richards, RL; Carter, C; Frech, GC; Stone, S; Rowe, K; Chau, CA; Cortado, K; Hunt, A; Luce, K; O'Neil, G; Poarch, J; Potter, J; Poulsen, GH; Saxton, H; Bernat-Sestak, M; Thompson, V; Gutin, A; Skolnick, MH; Shattuck, D; Cannon-Albright, L 分享 收藏
A candidate prostate cancer susceptibility gene at chromosome 17p Tavtigian, SV; Simard, J; Teng, DHF; Abtin, V; Baumgard, M; Beck, A; Camp, NJ; Carillo, AR; Chen, Y; Dayananth, P; Desrochers, M; Dumont, M; Farnham, JM; Frank, D; Frye, C; Ghaffari, S; Gupte, JS; Hu, R; Iliev, D; Janecki, T; Kort, EN; Laity, KE; Leavitt, A; Leblanc, G; McArthur-Morrison, J; Pederson, A; Penn, B; Peterson, KT; Reid, JE; Richards, S; Schroeder, M; Smith, R; Snyder, SC; Swedlund, B; Swensen, J; Thomas, A; Tranchant, M; Woodland, AM; Labrie, F; Skolnick, MH; Neuhausen, S; Rommens, J; Cannon-Albright, LA 分享 收藏
Evidence of linkage of familial hypoalphalipoproteinemia to a novel locus on chromosome 11q23 Kort, EN; Ballinger, DG; Ding, W; Hunt, SC; Bowen, BR; Abkevich, V; Bulka, K; Campbell, B; Capener, C; Gutin, A; Harshman, K; McDermott, M; Thorne, T; Wang, H; Wardell, B; Wong, J; Hopkins, PN; Skolnick, M; Samuels, M 分享 收藏
A broad role for the zinc finger protein ZNF202 in human lipid metabolism Wagner, S; Hess, MA; Ormonde-Hanson, P; Malandro, J; Hu, HP; Chen, M; Kehrer, R; Frodsham, M; Schumacher, C; Beluch, M; Honer, C; Skolnick, M; Ballinger, D; Bowen, BR 分享 收藏
Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred Hunt, SC; Hopkins, PN; Bulka, K; McDermott, MT; Thorne, TL; Wardell, BB; Bowen, BR; Ballinger, DG; Skolnick, MH; Samuels, ME 分享 收藏
Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1 Rahman, N; Abidi, F; Ford, D; Arbour, L; Rapley, E; Tonin, P; Barton, D; Batcup, G; Berry, J; Cotter, F; Davison, V; Gerrard, M; Gray, E; Grundy, R; Hanafy, M; King, D; Lewis, I; Luethy, AR; Madlensky, L; Mann, J; O'Meara, A; Oakhill, T; Skolnick, M; Strong, L; Variend, D; Narod, S; Schwartz, C; Pritchard-Jones, K; Stratton, MR 分享 收藏
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Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13 Couch, FJ; Rommens, JM; Neuhausen, SL; Belanger, C; Dumont, M; Abel, K; Bell, R; Berry, S; Bogden, R; CannonAbright, L; Farid, L; Frye, C; Hattier, T; Janecki, T; Jiang, P; Kehrer, R; Leblanc, JF; McArthurMorrison, J; McSweeney, D; Miki, Y; Peng, Y; Samson, C; Schroeder, M; Snyder, SC; Stringfellow, M; Stroup, C; Swedlund, B; Swensen, J; Teng, D; Thakur, S; Tran, T; Tranchant, I; WelverFeldhaus, J; Wong, AKC; Shizuya, H; Labrie, F; Skolnick, MH; Goldgar, DE; Kamb, A; Weber, BL; Tavtigian, SV; Simard, J 分享 收藏
Low incidence of BRCA2 mutations in breast carcinoma and other cancers Teng, DHF; Bogden, R; Mitchell, J; Baumgard, M; Bell, R; Berry, S; Davis, T; Ha, PC; Kehrer, R; Jammulapati, S; Chen, QA; Offit, K; Skolnick, MH; Tavtigian, SV; Jhanwar, S; Swedlund, B; Wong, AKC; Kamb, A 分享 收藏
Germline BRCA1 185delAG mutations in Jewish women with breast cancer Offit, K; Gilewski, T; McGuire, P; Schluger, A; Hampel, H; Brown, K; Swensen, J; Neuhausen, S; Skolnick, M; Norton, L; Goldgar, D 分享 收藏
Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer Neuhausen, S; Gilewski, T; Norton, L; Tran, T; McGuire, P; Swensen, J; Hampel, H; Borgen, P; Brown, K; Skolnick, M; ShattuckEidens, D; Jhanwar, S; Goldgar, D; Offit, K 分享 收藏
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The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds Tavtigian, SV; Simard, J; Rommens, J; Couch, F; ShattuckEidens, D; Neuhausen, S; Merajver, S; Thorlacius, S; Offit, K; StoppaLyonnet, D; Belanger, C; Bell, R; Berry, S; Bogden, R; Chen, Q; Davis, T; Dumont, M; Frye, C; Hattier, T; Jammulapati, S; Janecki, T; Jiang, P; Kehrer, R; Leblanc, JF; Mitchell, JT; McArthurMorrison, J; Nguyen, K; Peng, Y; Samson, C; Schroeder, M; Snyder, SC; Steele, L; Stringfellow, M; Stroup, C; Swedlund, B; Swensen, J; Teng, D; Thomas, A; Tran, T; Tran, T; Tranchant, M; WeaverFeldhaus, J; Wong, AKC; Shizuya, H; Eyfjord, JE; CannonAlbright, L; Labrie, F; Skolnick, MH; Weber, B; Kamb, A; Goldgar, DE 分享 收藏
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