Works matching IS 10614036 AND DT 2009 AND VI 41 AND IP 8

Results: 22

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 936, doi. 10.1038/ng.405
By:
- Schwarz, Klaus;
- Iolascon, Achille;
- Verissimo, Fatima;
- Trede, Nikolaus S.;
- Horsley, Wyatt;
- Wen Chen;
- Paw, Barry H.;
- Hopfner, Karl-Peter;
- Holzmann, Karlheinz;
- Russo, Roberta;
- Esposito, Maria Rosaria;
- Spano, Daniela;
- De Falco, Luigia;
- Heinrich, Katja;
- Joggerst, Brigitte;
- Rojewski, Markus T.;
- Perrotta, Silverio;
- Denecke, Jonas;
- Pannicke, Ulrich;
- Delaunay, Jean
Publication type:
Article
H3.3/H2A.Z double variant–containing nucleosomes mark 'nucleosome-free regions' of active promoters and other regulatory regions.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 941, doi. 10.1038/ng.409
By:
- Chunyuan Jin;
- Chongzhi Zang;
- Gang Wei;
- Kairong Cui;
- Weiqun Peng;
- Keji Zhao;
- Felsenfeld, Gary
Publication type:
Article
A transposon-based chromosomal engineering method to survey a large cis-regulatory landscape in mice.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 946, doi. 10.1038/ng.397
By:
- Kokubu, Chikara;
- Horie, Kyoji;
- Abe, Koichiro;
- Ikeda, Ryuji;
- Mizuno, Sumi;
- Uno, Yoshihiro;
- Ogiwara, Sanae;
- Ohtsuka, Masato;
- Isotani, Ayako;
- Okabe, Masaru;
- Imai, Kenji;
- Takeda, Junji
Publication type:
Article
What's so funny about peace, love and understanding?
Published in:
2009
Publication type:
Editorial
Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 873, doi. 10.1038/ng.419
By:
- Skibola, Christine F.;
- Bracci, Paige M.;
- Halperin, Eran;
- Conde, Lucia;
- Craig, David W.;
- Agana, Luz;
- Iyadurai, Kelly;
- Becker, Nikolaus;
- Brooks-Wilson, Angela;
- Curry, John D.;
- Spinelli, John J.;
- Holly, Elizabeth A.;
- Riby, Jacques;
- Luoping Zhang;
- Nieters, Alexandra;
- Smith, Martyn T.;
- Brown, Kevin M.
Publication type:
Article
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 879, doi. 10.1038/ng.416
By:
- Benjamin, Emelia J.;
- Rice, Kenneth M.;
- Arking, Dan E.;
- Pfeufer, Arne;
- van Noord, Charlotte;
- Smith, Albert V.;
- Schnabel, Renate B.;
- Bis, Joshua C.;
- Boerwinkle, Eric;
- Sinner, Moritz F.;
- Dehghan, Abbas;
- Lubitz, Steven A.;
- D'Agostino Sr, Ralph B.;
- Lumley, Thomas;
- Ehret, Georg B.;
- Heeringa, Jan;
- Aspelund, Thor;
- Newton-Cheh, Christopher;
- Larson, Martin G.;
- Marciante, Kristin D.
Publication type:
Article
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 876, doi. 10.1038/ng.417
By:
- Gudbjartsson, Daniel F.;
- Holm, Hilma;
- Gretarsdottir, Solveig;
- Thorleifsson, Gudmar;
- Walters, G. Bragi;
- Thorgeirsson, Gudmundur;
- Gulcher, Jeffrey;
- Mathiesen, Ellisiv B.;
- Njølstad, Inger;
- Nyrnes, Audhild;
- Wilsgaard, Tom;
- Hald, Erin M.;
- Hveem, Kristian;
- Stoltenberg, Camilla;
- Kucera, Gayle;
- Stubblefield, Tanya;
- Carter, Shannon;
- Roden, Dan;
- Ng, Maggie C. Y.;
- Baum, Larry
Publication type:
Article
The 8q24 cancer risk variant rs6983267 shows long-range interaction with MYC in colorectal cancer.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 882, doi. 10.1038/ng.403
By:
- Pomerantz, Mark M.;
- Ahmadiyeh, Nasim;
- Jia, Li;
- Herman, Paula;
- Verzi, Michael P.;
- Doddapaneni, Harshavardhan;
- Beckwith, Christine A.;
- Chan, Jennifer A.;
- Hills, Adam;
- Davis, Matt;
- Yao, Keluo;
- Kehoe, Sarah M.;
- Lenz, Heinz-Josef;
- Haiman, Christopher A.;
- Chunli Yan;
- Henderson, Brian E.;
- Frenkel, Baruch;
- Barretina, Jordi;
- Bass, Adam;
- Tabernero, Josep
Publication type:
Article
The common colorectal cancer predisposition SNP rs6983267 at chromosome 8q24 confers potential to enhanced Wnt signaling.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 885, doi. 10.1038/ng.406
By:
- Tuupanen, Sari;
- Turunen, Mikko;
- Lehtonen, Rainer;
- Hallikas, Outi;
- Vanharanta, Sakari;
- Kivioja, Teemu;
- Björklund, Mikael;
- Gonghong Wei;
- Jian Yan;
- Niittymäki, Iina;
- Mecklin, Jukka-Pekka;
- Järvinen, Heikki;
- Ristimäki, Ari;
- Di-Bernardo, Mariachiara;
- East, Phil;
- Carvajal-Carmona, Luis;
- Houlston, Richard S.;
- Tomlinson, Ian;
- Palin, Kimmo;
- Ukkonen, Esko
Publication type:
Article
A mouse model of ATR-Seckel shows embryonic replicative stress and accelerated aging.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 891, doi. 10.1038/ng.420
By:
- Murga, Matilde;
- Bunting, Samuel;
- Montaña, Maria F.;
- Soria, Rebeca;
- Mulero, Francisca;
- Cañamero, Marta;
- Youngsoo Lee;
- McKinnon, Peter J.;
- Nussenzweig, Andre;
- Fernandez-Capetillo, Oscar
Publication type:
Article
Genome-wide association study identifies five susceptibility loci for glioma.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 899, doi. 10.1038/ng.407
By:
- Shete, Sanjay;
- Hosking, Fay J.;
- Robertson, Lindsay B.;
- Dobbins, Sara E.;
- Sanson, Marc;
- Malmer, Beatrice;
- Simon, Matthias;
- Marie, Yannick;
- Boisselier, Blandine;
- Delattre, Jean-Yves;
- Khe Hoang-Xuan;
- El Hallani, Soufiane;
- Idbaih, Ahmed;
- Zelenika, Diana;
- Andersson, Ulrika;
- Henriksson, Roger;
- Bergenheim, A. Tommy;
- Feychting, Maria;
- Lönn, Stefan;
- Ahlbom, Anders
Publication type:
Article
Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia.
Published in:
2009
By:
- Kurth, Ingo;
- Klopocki, Eva;
- Stricker, Sigmar;
- van Oosterwijk, Jolieke;
- Vanek, Sebastian;
- Altmann, Jens;
- Santos, Heliosa G.;
- van Harssel, Jeske J. T.;
- de Ravel, Thomy;
- Wilkie, Andrew O. M.;
- Gal, Andreas;
- Mundlos, Stefan
Publication type:
Letter
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 905, doi. 10.1038/ng.408
By:
- Wrensch, Margaret;
- Jenkins, Robert B.;
- Chang, Jeffrey S.;
- Ru-Fang Yeh;
- Yuanyuan Xiao;
- Decker, Paul A.;
- Ballman, Karla V.;
- Berger, Mitchel;
- Buckner, Jan C.;
- Chang, Susan;
- Giannini, Caterina;
- Halder, Chandralekha;
- Kollmeyer, Thomas M.;
- Kosel, Matthew L.;
- LaChance, Daniel H.;
- McCoy, Lucie;
- O'Neill, Brian P.;
- Patoka, Joe;
- Pico, Alexander R.;
- Prados, Michael
Publication type:
Article
New common variants affecting susceptibility to basal cell carcinoma.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 909, doi. 10.1038/ng.412
By:
- Stacey, Simon N.;
- Sulem, Patrick;
- Masson, Gisli;
- Gudjonsson, Sigurjon A.;
- Thorleifsson, Gudmar;
- Jakobsdottir, Margret;
- Sigurdsson, Asgeir;
- Gudbjartsson, Daniel F.;
- Sigurgeirsson, Bardur;
- Benediktsdottir, Kristrun R.;
- Thorisdottir, Kristin;
- Ragnarsson, Rafn;
- Scherer, Dominique;
- Hemminki, Kari;
- Rudnai, Peter;
- Gurzau, Eugene;
- Koppova, Kvetoslava;
- Botella-Estrada, Rafael;
- Soriano, Virtudes;
- Juberias, Pablo
Publication type:
Article
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 915, doi. 10.1038/ng.410
By:
- Falchi, Mario;
- Bataille, Veronique;
- Hayward, Nicholas K.;
- Duffy, David L.;
- Bishop, Julia A. Newton;
- Pastinen, Tomi;
- Cervino, Alessandra;
- Zhao, Zhen Z.;
- Deloukas, Panos;
- Soranzo, Nicole;
- Elder, David E.;
- Barrett, Jennifer H.;
- Martin, Nicholas G.;
- Bishop, D. Timothy;
- Montgomery, Grant W.;
- Spector, Timothy D.
Publication type:
Article
Genome-wide association study identifies three loci associated with melanoma risk.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 920, doi. 10.1038/ng.411
By:
- Bishop, D. Timothy;
- Demenais, Florence;
- Iles, Mark M.;
- Harland, Mark;
- Taylor, John C.;
- Corda, Eve;
- Randerson-Moor, Juliette;
- Aitken, Joanne F.;
- Avril, Marie-Francoise;
- Azizi, Esther;
- Bakker, Bert;
- Bianchi-Scarrà, Giovanna;
- Paillerets, Brigitte Bressac-de;
- Calista, Donato;
- Cannon-Albright, Lisa A.;
- Chin-A-Woeng, Thomas;
- Dębniak, Tadeusz;
- Galore-Haskel, Gilli;
- Ghiorzo, Paola;
- Gut, Ivo
Publication type:
Article
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 926, doi. 10.1038/ng.404
By:
- Thorleifsson, Gudmar;
- Holm, Hilma;
- Edvardsson, Vidar;
- Walters, G. Bragi;
- Styrkarsdottir, Unnur;
- Gudbjartsson, Daniel F.;
- Sulem, Patrick;
- Halldorsson, Bjarni V.;
- de Vegt, Femmie;
- d'Ancona, Frank C. H.;
- den Heijer, Martin;
- Franzson, Leifur;
- Christiansen, Claus;
- Alexandersen, Peter;
- Rafnar, Thorunn;
- Kristjansson, Kristleifur;
- Sigurdsson, Gunnar;
- Kiemeney, Lambertus A.;
- Bodvarsson, Magnus;
- Indridason, Olafur S.
Publication type:
Article
De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 931, doi. 10.1038/ng.415
By:
- Greenway, Steven C.;
- Pereira, Alexandre C.;
- Lin, Jennifer C.;
- DePalma, Steven R.;
- Israel, Samuel J.;
- Mesquita, Sonia M.;
- Ergul, Emel;
- Conta, Jessie H.;
- Korn, Joshua M.;
- McCarroll, Steven A.;
- Gorham, Joshua M.;
- Gabriel, Stacey;
- Altshuler, David M.;
- Quintanilla-Dieck, Maria de Lourdes;
- Artunduaga, Maria Alexandra;
- Eavey, Roland D.;
- Plenge, Robert M.;
- Shadick, Nancy A.;
- Weinblatt, Michael E.;
- De Jager, Philip L.
Publication type:
Article
Labile H3.3+H2A.Z nucleosomes mark 'nucleosome-free regions'.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 865, doi. 10.1038/ng0809-865
By:
- Henikoff, Steven
Publication type:
Article
Life can be stressful without ATR.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 866, doi. 10.1038/ng0809-866
By:
- O'Driscoll, Mark
Publication type:
Article
Elucidating the role of 8q24 in colorectal cancer.
Published in:
Nature Genetics, 2009, v. 41, n. 8, p. 868, doi. 10.1038/ng0809-868
By:
- Harismendy, Olivier;
- Frazer, Kelly A.
Publication type:
Article
Research highlights.
Published in:
2009
By:
- Bahcall, Orli;
- Colosimo, Pamela;
- Niemitz, Emily;
- Vogan, Kyle
Publication type:
Abstract