Works matching IS 10614036 AND DT 2000 AND VI 24 AND IP 2

Results: 27

Aberrant CpG-island methylation has non-random and tumour-type?specific patterns.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 132, doi. 10.1038/72785

By:

Costello, Joseph F.;
Frühwald, Michael C.;
Smiraglia, Dominic J.;
Rush, Laura J.;
Robertson, Gavin P.;
Gao, Xin;
Wright, Fred A.;
Feramisco, Jamison D.;
Peltomäki, Päivi;
Lang, James C.;
Schuller, David E.;
Yu, Li;
Bloomfield, Clara D.;
Caligiuri, Michael A.;
Yates, Allan;
Nishikawa, Ryo;
Su Huang, H.-J.;
Petrelli, Nicholas J.;
Zhang, Xueli

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 2000, v. 24, n. 2, p. 105
Publication type:: Article

Flu times two.

Published in:

2000

By:

Mahy, Brian W.J.

Publication type:

Book Review

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 127, doi. 10.1038/72777

By:

Haider, Neena B.;
Jacobson, Samuel G.;
Cideciyan, Artur V.;
Swiderski, Ruth;
Streb, Luan M.;
Searby, Charles;
Beck, Gretel;
Hockey, Robin;
Hanna, David B.;
Gorman, Susan;
Duhl, David;
Carmi, Rivka;
Bennett, Jean;
Weleber, Richard G.;
Fishman, Gerald A.;
Wright, Alan F.;
Stone, Edwin M.;
Sheffield, Val C.

Publication type:

Article

Heritable and inducible genetic interference by double-stranded RNA encoded by transgenes.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 180, doi. 10.1038/72850

By:

Tavernarakis, Nektarios;
Wang, Shi L.;
Dorovkov, Maxim;
Ryazanov, Alexey;
Driscoll, Monica

Publication type:

Article

A bird's eye view of global methylation.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 101, doi. 10.1038/72730

By:

Eng, Charis;
Herman, James G;
Baylin, Stephen B

Publication type:

Article

Pushing the envelope on lipodystrophy.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 103, doi. 10.1038/72734

By:

Flier, Jeffrey S

Publication type:

Article

A take on the tectorial membrane.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 104, doi. 10.1038/72737

By:

Steel, Karen P

Publication type:

Article

Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 175, doi. 10.1038/72842

By:

Hicks, Geoffrey G.;
Singh, Nagendra;
Nashabi, Abudi;
Mai, Sabine;
Bozek, Gracjan;
Klewes, Ludger;
Arapovic, Djula;
White, Erica K.;
Koury, Mark J.;
Oltz, Eugene M.;
Van Kaer, Luc;
Ruley, H. E.

Publication type:

Article

The ethical challenges of in utero gene therapy.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 107, doi. 10.1038/72747

By:

Caplan, Arthur L.;
Wilson, James M.

Publication type:

Article

Nuclear transfer into mouse zygotes.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 108, doi. 10.1038/72749

By:

Wakayama, Teruhiko;
Tateno, Hiroyuki;
Mombaerts, Peter;
Yanagimachi, Ryuzo

Publication type:

Article

Generation of mice from wild-type and targeted ES cells by nuclear cloning.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 109, doi. 10.1038/72753

By:

Rideout, William M.;
Wakayama, Teruhiko;
Wutz, Anton;
Eggan, Kevin;
Jackson-Grusby, Laurie;
Dausman, Jessica;
Yanagimachi, Ryuzo;
Jaenisch, Rudolf

Publication type:

Article

Targeted disruption of Otog results in deafness and severe imbalance.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 139, doi. 10.1038/72793

By:

Simmler, Marie-Christine;
Cohen-Salmon, Martine;
El-Amraoui, Aziz;
Guillaud, Laurent;
Benichou, Jean-Claude;
Petit, Christine;
Panthier, Jean-Jacques

Publication type:

Article

Gene-target recognition among members of the Myc superfamily and implications for oncogenesis.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 113, doi. 10.1038/72761

By:

O'Hagan, Rónán C.;
Schreiber-Agus, Nicole;
Chen, Ken;
David, Gregory;
Engelman, Jeffrey A.;
Schwab, Richard;
Alland, Leila;
Thomson, Cole;
Ronning, Donald R.;
Sacchettini, James C.;
Meltzer, Paul;
DePinho, Ronald A.

Publication type:

Article

ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORF.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 120, doi. 10.1038/72769

By:

Engert, James C.;
Bérubé, Pierre;
Mercier, Jocelyne;
Doré, Carole;
Lepage, Pierre;
Ge, Bing;
Bouchard, Jean-Pierre;
Mathieu, Jean;
Melançon, Serge B.;
Schalling, Martin;
Lander, Eric S.;
Morgan, Kenneth;
Hudson, Thomas J.;
Richter, Andrea

Publication type:

Article

Kit/stem cell factor receptor-induced activation of phosphatidylinositol 3′-kinase is essential for male fertility.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 157, doi. 10.1038/72814

By:

Blume-Jensen, Peter;
Jiang, Guoqiang;
Hyman, Robert;
Lee, Kuo-Fen;
O'Gorman, Stephen;
Hunter, Tony

Publication type:

Article

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 153, doi. 10.1038/72807

By:

Shackleton, Sue;
Lloyd, David J.;
Jackson, Stephen N.J.;
Evans, Richard;
Niermeijer, Martinus F.;
Singh, Baldev M.;
Schmidt, Hartmut;
Brabant, Georg;
Kumar, Sudesh;
Durrington, Paul N.;
Gregory, Simon;
O'Rahilly, Stephen;
Trembath, Richard C.

Publication type:

Article

A genome-wide survey of RAS transformation targets.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 144, doi. 10.1038/72799

By:

Zuber, Johannes;
Tchernitsa, Oleg I.;
Hinzmann, Bernd;
Schmitz, Anne-Chantal;
Grips, Martin;
Hellriegel, Martin;
Sers, Christine;
Rosenthal, André;
Schäfer, Reinhold

Publication type:

Article

Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 163, doi. 10.1038/72822

By:

Moreira, Eloisa S.;
Wiltshire, Tim J.;
Faulkner, Georgine;
Nilforoushan, Antje;
Vainzof, Mariz;
Suzuki, Oscar T.;
Valle, Giorgio;
Reeves, Roger;
Zatz, Mayana;
Passos-Bueno, M. R.;
Jenne, Dieter E.

Publication type:

Article

A role for Smad6 in development and homeostasis of the cardiovascular system.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 171, doi. 10.1038/72835

By:

Galvin, Katherine M.;
Donovan, Michael J.;
Lynch, Catherine A.;
Meyer, Ronald I.;
Paul, Richard J.;
Lorenz, John N.;
Fairchild-Huntress, Victoria;
Dixon, Kristen L.;
Dunmore, Judy H.;
Gimbrone, Michael A.;
Falb, Dean;
Huszar, Dennis

Publication type:

Article

A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 167, doi. 10.1038/72829

By:

Zemni, Ramzi;
Bienvenu, Thierry;
Vinet, Marie C.;
Sefiani, Aziz;
Carrié, Alain;
Billuart, Pierre;
McDonell, Nathalie;
Couvert, Philippe;
Francis, Fiona;
Chafey, Philippe;
Fauchereau, Fabien;
Friocourt, Gaelle;
Portes, Vincent des;
Cardona, Anna;
Frints, Suzanna;
Meindl, Alfonse;
Brandau, Oliver;
Ronce, Nathalie;
Moraine, Claude

Publication type:

Article

Localization to Xq27 of a susceptibility gene for testicular germ-cell tumours.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 197, doi. 10.1038/72877

By:

Rapley, Elizabeth A.;
Crockford, Gillian P.;
Teare, Dawn;
Biggs, Patrick;
Seal, Sheila;
Barfoot, Rita;
Edwards, Sandra;
Hamoudi, Rifat;
Heimdal, Ketil;
Fosså, Sophie D.;
Tucker, Kathy;
Donald, Jenny;
Collins, Felicity;
Friedlander, Michael;
Hogg, David;
Goss, Paul;
Heidenreich, Axel;
Ormiston, Wilma;
Daly, Peter A.

Publication type:

Article

Census, race and science.

Published in:: Nature Genetics, 2000, v. 24, n. 2, p. 97, doi. 10.1038/72884
Publication type:: Article

Giving in to the blues.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 99, doi. 10.1038/72887

By:

Cepko, Connie

Publication type:

Article

Fosl1 is a transcriptional target of c-Fos during osteoclast differentiation.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 184, doi. 10.1038/72855

By:

Matsuo, Koichi;
Owens, Jane M.;
Tonko, Martin;
Elliott, Candace;
Chambers, Timothy J.;
Wagner, Erwin F.

Publication type:

Article

Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 192, doi. 10.1038/72869

By:

Orsó, Evelyn;
Broccardo, Cyril;
Kaminski, Wolfgang E.;
Böttcher, Alfred;
Liebisch, Gerhard;
Drobnik, Wolfgang;
Götz, Alexandra;
Chambenoit, Olivier;
Diederich, Wendy;
Langmann, Thomas;
Spruss, Thilo;
Luciani, Marie-Francoise;
Rothe, Gregor;
Lackner, Karl J.;
Chimini, Giovanna;
Schmitz, Gerd

Publication type:

Article

Mutations in the gene encoding peroxisomal α-methylacyl-CoA racemase cause adult-onset sensory motor neuropathy.

Published in:

Nature Genetics, 2000, v. 24, n. 2, p. 188, doi. 10.1038/72861

By:

Ferdinandusse, Sacha;
Denis, Simone;
Clayton, Peter T.;
Graham, Andrew;
Rees, John E.;
Allen, John T.;
McLean, Brendan N.;
Brown, Ann Y.;
Vreken, Peter;
Waterham, Hans R.;
Wanders, Ronald J.A.

Publication type:

Article