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1
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Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

Marsh, Ashley P. L ; Héron, Delphine ; Edwards, Timothy J ; Quartier, Angélique ; Galea, Charles ; Nava, Caroline ; Rastetter, Agnès ; Moutard, Marie-Laure ; Anderson, Vicki ; Bitoun, Pierre ; Bunt, Jens ; Faudet, Anne ; Garel, Catherine ; Gillies, Greta ; Gobius, Ilan ; Guegan, Justine ; Heide, Solveig ; Keren, Boris ; Lesne, Fabien ; Lukic, Vesna ; Mandelstam, Simone A ; Mcgillivray, George ; Mcilroy, Alissandra ; Méneret, Aurélie ; Mignot, Cyril ; Morcom, Laura R ; Odent, Sylvie ; Paolino, Annalisa ; Pope, Kate ; Riant, Florence ; Robinson, Gail A ; Spencer-Smith, Megan ; Srour, Myriam ; Stephenson, Sarah E. M ; Tankard, Rick ; Trouillard, Oriane ; Welniarz, Quentin ; Wood, Amanda ; Brice, Alexis ; Rouleau, Guy ; Attie-Bitach, Tania ; Delatycki, Martin B ; Mandel, Jean-Louis ; Amor, David J ; Roze, Emmanuel ; Piton, Amélie ; Bahlo, Melanie ; Billette De Villemeur, Thierry ; Sherr, Elliott H ; Leventer, Richard J ; Richards, Linda J ; Lockhart, Paul J ; Depienne, Christel

Nature Genetics, 2017, Vol.49(4), pp.511-514 [Tạp chí có phản biện]

ISSN: 1061-4036 ; E-ISSN: 1546-1718 ; DOI: 10.1038/ng.3794

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2
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Investigation of inter- and intraspecies variation through genome sequencing of Aspergillus section Nigri

Vesth, Tammi C ; Nybo, Jane L ; Theobald, Sebastian ; Frisvad, Jens C ; Larsen, Thomas O ; Nielsen, Kristian F ; Hoof, Jakob B ; Brandl, Julian ; Salamov, Asaf ; Riley, Robert ; Gladden, John M ; Phatale, Pallavi ; Nielsen, Morten ; Lyhne, Ellen ; Kogle, Martin E ; Strasser, Kimchi ; Mcdonnell, Erin ; Barry, Kerrie ; Clum, Alicia ; Chen, Cindy ; Labutti, Kurt ; Haridas, Sajeet ; Nolan, Matt ; Sandor, Laura ; Kuo, Alan ; Lipzen, Anna ; Hainaut, Matthieu ; Drula, Elodie ; Tsang, Adrian ; Magnuson, Jon K ; Henrissat, Bernard B ; Wiebenga, Ad ; Simmons, Blake A ; Mäkelä, Miia R ; De Vries, Ronald P ; Grigoriev, Igor V ; Mortensen, Uffe H ; Baker, Scott E ; Handersen, Mikael R

Nature Genetics, December 2018, Vol.50(12), pp.1688-1695 [Tạp chí có phản biện]

ISSN: 1061-4036 ; E-ISSN: 1546-1718 ; DOI: 10.1038/s41588-018-0246-1

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3
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Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

Poirier, Karine ; Lebrun, Nicolas ; Broix, Loic ; Tian, Guoling ; Saillour, Yoann ; Boscheron, Cécile ; Parrini, Elena ; Valence, Stephanie ; Pierre, Benjamin Saint ; Oger, Madison ; Lacombe, Didier ; Geneviève, David ; Fontana, Elena ; Darra, Franscesca ; Cances, Claude ; Barth, Magalie ; Bonneau, Dominique ; Bernadina, Bernardo Dalla ; N'Guyen, Sylvie ; Gitiaux, Cyril ; Parent, Philippe ; Des Portes, Vincent ; Pedespan, Jean Michel ; Legrez, Victoire ; Castelnau-Ptakine, Laetitia ; Nitschke, Patrick ; Hieu, Thierry ; Masson, Cecile ; Zelenika, Diana ; Andrieux, Annie ; Francis, Fiona ; Guerrini, Renzo ; Cowan, Nicholas J ; Bahi-Buisson, Nadia ; Chelly, Jamel

Nature Genetics, 21 April 2013, Vol.45(6), pp.639-47 [Tạp chí có phản biện]

ISSN: 1061-4036 ; E-ISSN: 1546-1718 ; DOI: 10.1038/ng.2613

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4
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Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Kirby, Andrew ; Gnirke, Andreas ; Jaffe, David B ; Barešová, Veronika ; Pochet, Nathalie ; Blumenstiel, Brendan ; Ye, Chun ; Aird, Daniel ; Stevens, Christine ; Robinson, James T ; Cabili, Moran N ; Gat - Viks, Irit ; Kelliher, Edward ; Daza, Riza ; Defelice, Matthew ; Hůlková, Helena ; Sovová, Jana ; Vylet'Al, Petr ; Antignac, Corinne ; Guttman, Mitchell ; Handsaker, Robert E ; Perrin, Danielle ; Steelman, Scott ; Sigurdsson, Snaevar ; Scheinman, Steven J ; Sougnez, Carrie ; Cibulskis, Kristian ; Parkin, Melissa ; Green, Todd ; Rossin, Elizabeth ; Zody, Michael C ; Xavier, Ramnik J ; Pollak, Martin R ; Alper, Seth L ; Lindblad - Toh, Kerstin ; Gabriel, Stacey ; Hart, P Suzanne ; Regev, Aviv ; Nusbaum, Chad ; Kmoch, Stanislav ; Bleyer, Anthony J ; Lander, Eric S ; Daly, Mark J

NATURE GENETICS, 2013 [Tạp chí có phản biện]

ISSN: 1061-4036 ; DOI: 10.10.8/ng.2543

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5
Material Type:
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SUMOylation promotes de novo targeting of HP1α to pericentric heterochromatin

Maison, Christèle ; Bailly, Delphine ; Roche, Danièle ; Montes De Oca, Rocio ; Probst, Aline V ; Vassias, Isabelle ; Dingli, Florent ; Lombard, Bérengère ; Loew, Damarys ; Quivy, Jean-Pierre ; Almouzni, Geneviève

Nature Genetics, March 2011, Vol.43(3), pp.220-7 [Tạp chí có phản biện]

ISSN: 1061-4036 ; E-ISSN: 1546-1718 ; DOI: 10.1038/ng.765

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6
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The genome sequence of the orchid Phalaenopsis equestris

Cai, Jing ; Liu, Xin ; Vanneste, Kevin ; Proost, Sebastian ; Tsai, Wen - Chieh ; Liu, Ke - Wei ; Chen, Li - Jun ; He, Ying ; Xu, Qing ; Bian, Chao ; Zheng, Zhijun ; Sun, Fengming ; Liu, Weiqing ; Hsiao, Yu - Yun ; Pan, Zhao - Jun ; Hsu, Chia - Chi ; Yang, Ya - Ping ; Hsu, Yi - Chin ; Chuang, Yu - Chen ; Dievart, Anne ; Dufayard, Jean - François ; Xu, Xun ; Wang, Jun - Yi ; Wang, Jun ; Xiao, Xin - Ju ; Zhao, Xue - Min ; Du, Rong ; Zhang, Guo - Qiang ; Wang, Meina ; Su, Yong - Yu ; Xie, Gao - Chang ; Liu, Guo - Hui ; Li, Li - Qiang ; Huang, Lai - Qiang ; Luo, Yi - Bo ; Chen, Hong - Hwa ; Van De Peer, Yves ; Liu, Zhong - Jian

NATURE GENETICS, 2015 [Tạp chí có phản biện]

ISSN: 1061-4036 ; DOI: 10.10.8/ng.3149

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7
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A basic helix-loop-helix transcription factor controls cell growth and size in root hairs.(LETTERS)(Report)

Yi, Keke ; Menand, Benoit ; Bell, Elizabeth ; Dolan, Liam

Nature Genetics, March, 2010, Vol.42(3), p.264(6) [Tạp chí có phản biện]

ISSN: 1061-4036

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8
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Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders

Durand, Christelle M ; Betancur, Catalina ; Boeckers, Tobias M ; Bockmann, Juergen ; Chaste, Pauline ; Fauchereau, Fabien ; Nygren, Gudrun ; Rastam, Maria ; Gillberg, I Carina ; Anckarsäter, Henrik ; Sponheim, Eili ; Goubran-Botros, Hany ; Delorme, Richard ; Chabane, Nadia ; Mouren-Simeoni, Marie-Christine ; De Mas, Philippe ; Bieth, Eric ; Rogé, Bernadette ; Héron, Delphine ; Burglen, Lydie ; Gillberg, Christopher ; Leboyer, Marion ; Bourgeron, Thomas

Nature Genetics, January 2007, Vol.39(1), pp.25-7 [Tạp chí có phản biện]

ISSN: 1061-4036 ; E-ISSN: 1546-1718 ; DOI: 10.1038/ng1933

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9
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Loss-of-function mutations in ADCY3 cause monogenic severe obesity

Saeed, S ; Bonnefond, A ; Tamanini, F ; Mirza, Mu ; Manzoor, J ; Janjua, Qm ; Din, Sm ; Gaitan, J ; Milochau, A ; Durand, E ; Vaillant, E ; Haseeb, A ; De Graeve, F ; Rabearivelo, I ; Sand, O ; Queniat, G ; Boutry, R ; Schott, Da ; Ayesha, H ; Ali, M ; Khan, Wi ; Butt, Ta ; Rinne, T ; Stumpel, C ; Abderrahmani, A ; Lang, J ; Arslan, M ; Froguel, P

NATURE GENETICS, 08 January 2018 [Tạp chí có phản biện]

ISBN: 2 ; ISSN: 1061-4036 ; ISBN: 10 DOI: 10.1038/s41588-017-0023-6

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10
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Patterns of genic intolerance of rare copy number variation in 59,898 human exomes.

Ruderfer, Dm ; Hamamsy, T ; Lek, M ; Karczewski, Kj ; Kavanagh, D ; Samocha, Ke ; Exome Aggregation Consortium ; Daly, Mj ; Macarthur, Dg ; Fromer, M ; Purcell, Sm

Nature Genetics, 17 August 2016 [Tạp chí có phản biện]

ISSN: 1061-4036 DOI: 10.1038/ng.3638

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11
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Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

Waage, J ; Standl, M ; Curtin, Ja ; Jessen, L ; Thorsen, J ; The 23andme Research Team ; Aagc Collaborators ; Abdellaoui, A ; Ahluwalia, Ts ; Alves, A ; Amaral, Afs ; Anto, Jm ; Arnold, A ; Flores, C ; Baurecht, H ; Beijstervedldt, Tcem ; Bleecker, Er ; Bonas - Guarch, S ; Boomsma, D ; Brix, S ; Bunyavanich, S ; Burchard, E ; Chen, Z ; Curjuric, I ; Custovic, A ; Den Dekker, M ; Dharmage, Sc ; Dmitrieva, J ; Duijts, L ; Ege, M ; Barreto - Luis, A ; Gauderman, Wj ; Georges, M ; Gieger, C ; Gilliland, F ; Granell, R ; Gui, H ; Hansen, T ; Heinrich, J ; Henderson, J ; Hernandez - Pacheco, N ; Hinds, Da ; Holt, P ; Imboden, M ; Jaddoe, V ; Jarvelin, M ; Jarvis, D ; Jensen, Kk ; Jonsdottir, I ; Kabesch, M ; Kaprio, J ; Kumar, A ; Lee, Y ; Levin, Am ; Li, X ; Lorenz - Diaz, F ; Melen, E ; Mercader, Jm ; Meyers, Da ; Nicolae, Dl ; Nohr, E ; Palvianinen, T ; Paternoster, L ; Pennell, C ; Pershagen, G ; Pino - Yanes, M ; Probst - Hensch, Nm ; Ruschendorf, F ; Schoettler, N ; Simpson, A ; Stefansson, K ; Sunyer, J ; Sveinbjornsson, G ; Thiering, E ; Thompson, Pj ; Tian, C ; Torrent, M ; Torrents, D ; Tung, Jy ; Wang, C ; Weidinger, S ; Weiss, S ; Willemsen, G ; Williams, Lk ; Ober, C ; Ferreira, Ma ; Bisgaard, H ; Strachan, D ; Bonnelykke, K

Nature Genetics August 2018 [Tạp chí có phản biện]

ISSN: 1061-4036 ; ISBN: 10 DOI: 10.1038/s41588-018-0157-1

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12
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Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease

Zhao, W ; Rasheed, A ; Tikkanen, E ; Lee, J - J ; Butterworth, As ; Howson, Jmm ; Assimes, Tl ; Chowdhury, R ; Orho - Melander, M ; Damrauer, S ; Small, A ; Asma, S ; Imamura, M ; Yamauch, T ; Chambers, Jc ; Chen, P ; Sapkota, Br ; Shah, N ; Jabeen, S ; Surendran, P ; Lu, Y ; Zhang, W ; Imran, A ; Abbas, S ; Majeed, F ; Trindade, K ; Qamar, N ; Mallick, Nh ; Yaqoob, Z ; Saghir, T ; Rizvi, Snh ; Memon, A ; Rasheed, Sz ; Memon, F - U - R ; Mehmood, K ; Ahmed, N ; Qureshi, Ih ; Tanveer - Us - Salam ; Iqbal, W ; Malik, U ; Mehra, N ; Kuo, Jz ; Sheu, Wh - H ; Guo, X ; Hsiung, Ca ; Juang, J - Mj ; Taylor, Kd ; Hung, Y - J ; Lee, W - J ; Quertermous, T ; Lee, I - T ; Hsu, C - C ; Bottinger, Ep ; Ralhan, S ; Teo, Yy ; Wang, T - D ; Alam, Ds ; Di Angelantonio, E ; Epstein, S ; Nielsen, Sf ; Nordestgaard, Bg ; Tybjaerg - Hansen, A ; Young, R ; Benn, M ; Frikke - Schmidt, R ; Kamstrup, Pr ; Biobank, M ; Jukema, Jw ; Sattar, N ; Smit, R ; Chung, R - H ; Liang, K - W ; Anand, S ; Sanghera, Dk ; Ripatti, S ; Loos, Rjf ; Kooner, Js ; Tai, Es ; Rotter, Ji ; Chen, Y - Di ; Frossard, P ; Maeda, S ; Kadowaki, T ; Reilly, M ; Pare, G ; Melander, O ; Salomaa, V ; Rader, Dj ; Danesh, J ; Voight, Bf ; Saleheen, D

Nature Genetics, 04 September 2017 [Tạp chí có phản biện]

ISSN: 1061-4036 DOI: 10.1038/ng.3943

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13
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Expression of 24,426 human alternative splicing events and predicted cis regulation in 48 tissues and cell lines.(Clinical report)

Castle, John C. ; Zhang, Chaolin ; Shah, Jyoti K. ; Kulkarni, Amit V. ; Kalsotra, Auinash ; Cooper, Thomas A. ; Johnson, Jason M.

Nature Genetics, Dec, 2008, Vol.40(12), p.1416(10) [Tạp chí có phản biện]

ISSN: 1061-4036

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14
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Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome

Leitch, Carmen C ; Zaghloul, Norann A ; Davis, Erica E ; Stoetzel, Corinne ; Diaz-Font, Anna ; Rix, Suzanne ; Alfadhel, Majid ; Lewis, Richard Alan ; Eyaid, Wafaa ; Banin, Eyal ; Dollfus, Helene ; Beales, Philip L ; Badano, Jose L ; Katsanis, Nicholas

Nature Genetics, April 2008, Vol.40(4), pp.443-8 [Tạp chí có phản biện]

ISSN: 1061-4036 ; E-ISSN: 1546-1718 ; DOI: 10.1038/ng.97

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15
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Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response

Gerdes, Jantje M ; Liu, Yangfan ; Zaghloul, Norann A ; Leitch, Carmen C ; Lawson, Shaneka S ; Kato, Masaki ; Beachy, Philip A ; Beales, Philip L ; Demartino, George N ; Fisher, Shannon ; Badano, Jose L ; Katsanis, Nicholas

Nature Genetics, November 2007, Vol.39(11), pp.1350-60 [Tạp chí có phản biện]

ISSN: 1061-4036 ; E-ISSN: 1546-1718 ; DOI: 10.1038/ng.2007.12

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16
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Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration

Curtis, J ; Luo, Y ; Zenner, Hl ; Cuchet - Lourenco, D ; Wu, C ; Lo, K ; Maes, M ; Alisaac, A ; Stebbings, E ; Liu, Jz ; Kopanitsa, L ; Ignatyeva, O ; Balabanova, Y ; Nikolayevskyy, V ; Baessmann, I ; Thye, T ; Meyer, Cg ; Nuernberg, P ; Horstmann, Rd ; Drobniewski, F ; Plagnol, V ; Barrett, Jc ; Nejentsev, S

Nature Genetics, 16 March 2015 [Tạp chí có phản biện]

ISSN: 1546-1718 DOI: 10.1038/ng.3248

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17
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Genome-wide association study identifies eight loci associated with blood pressure

Newton - Cheh, C ; Johnson, T ; Gateva, V ; Tobin, Md ; Bochud, M ; Coin, L ; Najjar, Ss ; Zhao, Jh ; Heath, Sc ; Eyheramendy, S ; Papadakis, K ; Voight, Bf ; Scott, Lj ; Zhang, F ; Farrall, M ; Tanaka, T ; Wallace, C ; Chambers, Jc ; Khaw, K - T ; Nilsson, P ; Van Der Harst, P ; Polidoro, S ; Grobbee, De ; Onland - Moret, Nc ; Bots, Ml ; Wain, Lv ; Elliott, Ks ; Teumer, A ; Luan, J ; Lucas, G ; Kuusisto, J ; Burton, Pr ; Hadley, D ; Mcardle, Wl ; Brown, M ; Dominiczak, A ; Newhouse, Sj ; Samani, Nj ; Webster, J ; Zeggini, E ; Beckmann, Js ; Bergmann, S ; Lim, N ; Song, K ; Vollenweider, P ; Waeber, G ; Waterworth, Dm ; Yuan, X ; Groop, L ; Orho - Melander, M ; Allione, A ; Di Gregorio, A ; Guarrera, S ; Panico, S ; Ricceri, F ; Romanazzi, V ; Sacerdote, C ; Vineis, P ; Barroso, I ; Sandhu, Ms ; Luben, Rn ; Crawford, Gj ; Jousilahti, P ; Perola, M ; Boehnke, M ; Bonnycastle, Ll ; Collins, Fs ; Jackson, Au ; Mohlke, Kl ; Stringham, Hm ; Valle, Tt ; Willer, Cj ; Bergman, Rn ; Morken, Ma ; Doering, A ; Gieger, C ; Illig, T ; Meitinger, T ; Org, E ; Pfeufer, A ; Wichmann, He ; Kathiresan, S ; Marrugat, J ; O'Donnell, Cj ; Schwartz, Sm ; Siscovick, Ds ; Subirana, I ; Freimer, Nb ; Hartikainen, A - L ; Mccarthy, Mi ; O'Reilly, Pf ; Peltonen, L ; Pouta, A ; De Jong, Pe ; Snieder, H ; Van Gilst, Wh ; Clarke, R ; Goel, A ; Hamsten, A ; Peden, Jf ; Seedorf, U ; Syvanen, A - C ; Tognoni, G ; Lakatta, Eg ; Sanna, S ; Scheet, P ; Schlessinger, D ; Scuteri, A ; Doerr, M ; Ernst, F ; Felix, Sb ; Homuth, G ; Lorbeer, R ; Reffelmann, T ; Rettig, R ; Voelker, U ; Galan, P ; Gut, Ig ; Hercberg, S ; Lathrop, Gm ; Zelenika, D ; Deloukas, P ; Soranzo, N ; Williams, Fm ; Zhai, G ; Salomaa, V ; Laakso, M ; Elosua, R ; Forouhi, Ng ; Volzke, H ; Uiterwaal, Cs ; Van Der Schouw, Yt ; Numans, Me ; Matullo, G ; Navis, G ; Berglund, G ; Bingham, Sa ; Kooner, Js ; Connell, Jm ; Bandinelli, S ; Ferrucci, L ; Watkins, H ; Spector, Td ; Tuomilehto, J ; Altshuler, D ; Strachan, Dp ; Laan, M ; Meneton, P ; Wareham, Nj ; Uda, M ; Jarvelin, M - R ; Mooser, V ; Melander, O ; Loos, Rjf ; Elliott, P ; Abecasis, Gr ; Caulfield, M ; Munroe, Pb; Medical Research Council (MRC) ; Medical Research Council (MRC)

Nature Genetics, 10 May 2009 [Tạp chí có phản biện]

ISSN: 1061-4036 DOI: 10.1038/ng.361

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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity

Turcot, V ; Lu, Y ; Highland, Hm ; Schurmann, C ; Justice, Ae ; Fine, Rs ; Bradfield, Jp ; Esko, T ; Giri, A ; Graff, M ; Guo, X ; Hendricks, Ae ; Karaderi, T ; Lempradl, A ; Locke, Ae ; Mahajan, A ; Marouli, E ; Sivapalaratnam, S ; Young, Kl ; Alfred, T ; Feitosa, Mf ; Masca, Ngd ; Manning, Ak ; Medina - Gomez, C ; Mudgal, P ; Ng, Mcy ; Reiner, Ap ; Vedantam, S ; Willems, Sm ; Winkler, Tw ; Abecasis, G ; Aben, Kk ; Alam, Ds ; Alharthi, Se ; Allison, M ; Amouyel, P ; Asselbergs, Fw ; Auer, Pl ; Balkau, B ; Bang, Le ; Barroso, I ; Bastarache, L ; Benn, M ; Bergmann, S ; Bielak, Lf ; Bluher, M ; Boehnke, M ; Boeing, H ; Boerwinkle, E ; Boger, Ca ; Bork - Jensen, J ; Bots, Ml ; Bottinger, Ep ; Bowden, Dw ; Brandslund, I ; Breen, G ; Brilliant, Mh ; Broer, L ; Brumat, M ; Burt, Aa ; Butterworth, As ; Campbell, Pt ; Cappellani, S ; Carey, Dj ; Catamo, E ; Caulfield, Mj ; Chambers, Jc ; Chasman, Di ; Chen, Y - Di ; Chowdhury, R ; Christensen, C ; Chu, Ay ; Cocca, M ; Collins, Fs ; Cook, Jp ; Corley, J ; Galbany, Jc ; Cox, Aj ; Crosslin, Ds ; Cuellar - Partida, G ; D'Eustacchio, A ; Danesh, J ; Davies, G ; Bakker, Piw ; Groot, Mch ; Mutsert, R ; Deary, Ij ; Dedoussis, G ; Demerath, Ew ; Heijer, M ; Hollander, Ai ; Ruijter, Hm ; Dennis, Jg ; Denny, Jc ; Di Angelantonio, E ; Drenos, F ; Du, M ; Dube, M - P ; Dunning, Am ; Easton, Df ; Edwards, Tl ; Ellinghaus, D ; Ellinor, Pt ; Elliott, P ; Evangelou, E ; Farmaki, A - E ; Farooqi, Is ; Faul, Jd ; Fauser, S ; Feng, S ; Ferrannini, E ; Ferrieres, J ; Florez, Jc ; Ford, I ; Fornage, M ; Franco, Oh ; Franke, A ; Franks, Pw ; Friedrich, N ; Frikke - Schmidt, R ; Galesloot, Te ; Gan, W ; Gandin, I ; Gasparini, P ; Gibson, J ; Giedraitis, V ; Gjesing, Ap ; Gordon - Larsen, P ; Gorski, M ; Grabe, H - J ; Grant, Sfa ; Grarup, N ; Griffiths, Hl ; Grove, Ml ; Gudnason, V ; Gustafsson, S ; Haessler, J ; Hakonarson, H ; Hammerschlag, Ar ; Hansen, T ; Harris, Km ; Harris, Tb ; Hattersley, At ; Have, Ct ; Hayward, C ; He, L ; Heard - Costa, Nl ; Heath, Ac ; Heid, Im ; Helgeland, O ; Hernesniemi, J ; Hewitt, Aw ; Holmen, Ol ; Hovingh, Gk ; Howson, Jmm ; Hu, Y ; Huang, Pl ; Huffman, Je ; Ikram, Ma ; Ingelsson, E ; Jackson, Au ; Jansson, J - H ; Jarvik, Gp ; Jensen, Gb ; Jia, Y ; Johansson, S ; Jorgensen, Me ; Jorgensen, T ; Jukema, Jw ; Kahali, B ; Kahn, Rs ; Kahonen, M ; Kamstrup, Pr ; Kanoni, S ; Kaprio, J ; Karaleftheri, M ; Kardia, Slr ; Karpe, F ; Kathiresan, S ; Kee, F ; Kiemeney, La ; Kim, E ; Kitajima, H ; Komulainen, P ; Kooner, Js ; Kooperberg, C ; Korhonen, T ; Kovacs, P ; Kuivaniemi, H ; Kutalik, Z ; Kuulasmaa, K ; Kuusisto, J ; Laakso, M ; Lakka, Ta ; Lamparter, D ; Lange, Em ; Lange, La ; Langenberg, C ; Larson, Eb ; Lee, Nr ; Lehtimaki, T ; Lewis, Ce ; Li, H ; Li, J ; Li - Gao, R ; Lin, H ; Lin, K - H ; Lin, L - A ; Lin, X ; Lind, L ; Lindstrom, J ; Linneberg, A ; Liu, C - T ; Liu, Dj ; Liu, Y ; Lo, Ks ; Lophatananon, A ; Lotery, Aj ; Loukola, A ; Luan, J ; Lubitz, Sa ; Lyytikainen, L - P ; Mannisto, S ; Marenne, G ; Mazul, Al ; Mccarthy, Mi ; Mckean - Cowdin, R ; Medland, Se ; Meidtner, K ; Milani, L ; Mistry, V ; Mitchell, P ; Mohlke, Kl ; Moilanen, L ; Moitry, M ; Montgomery, Gw ; Mook - Kanamori, Do ; Moore, C ; Mori, Ta ; Morris, Ad ; Morris, Ap ; Mueller - Nurasyid, M ; Munroe, Pb ; Nalls, Ma ; Narisu, N ; Nelson, Cp ; Neville, M ; Nielsen, Sf ; Nikus, K ; Njolstad, Pr

Nature Genetics, 01 July 2019 [Tạp chí có phản biện]

ISSN: 1061-4036 ; ISBN: 10 DOI: 10.1038/s41588-017-0011-x

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Excitatory amino acids, monoamine, and nitric oxide synthase systems in organotypic cultures: biochemical and immunohistochemical analysis.(Author abstract)

Herrera - Marschitz, M. ; Kohlhauser, C. ; Gomez - Urquijo, S. ; Ubink, R. ; Goiny, M. ; Hokfelt, T.

Amino Acids, August, 2000, Vol.19(1), p.33 [Tạp chí có phản biện]

ISSN: 0939-4451

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theo tác giả:

  1. Katsanis, Nicholas
  2. Zelenika, Diana
  3. Daly, Mark J
  4. Lu, Yingchang
  5. Bergmann, Sven

theo chủ đề:

  1. Biology
  2. Humans
  3. Genomes
  4. Genetics
  5. Female

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