Works in Nature Genetics, 1999, Vol 23, Issue 3

Results: 36

Connecting the dots.

Published in:: Nature Genetics, 1999, v. 23, n. 3, p. 249, doi. 10.1038/15410
Publication type:: Article

A bumper crop of cancer genes.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 253, doi. 10.1038/15423

By:

DePinho, Ronald A;
Jacks, Tyler

Publication type:

Article

Agouti germ line gets acquisitive.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 254, doi. 10.1038/15425

By:

John, Rosalind M;
Surani, M Azim

Publication type:

Article

The dynamics of dystroglycan.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 256, doi. 10.1038/15428

By:

Chamberlain, Jeffrey

Publication type:

Article

Modelling multiple sclerosis.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 258, doi. 10.1038/15430

By:

Ebers, George

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 1999, v. 23, n. 3, p. 261
Publication type:: Article

Colour-changing karyotyping: an alternative to M-FISH/SKY.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 263, doi. 10.1038/15437

By:

Henegariu, Octavian;
Heerema, Nyla A.;
Bray-Ward, Patricia;
Ward, David C.

Publication type:

Article

Mutations in SLC4A4 cause permanent isolated proximal renal tubular acidosis with ocular abnormalities.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 264, doi. 10.1038/15440

By:

Igarashi, Takashi;
Inatomi, Jun;
Sekine, Takashi;
Cha, Seok Ho;
Kanai, Yoshikatsu;
Kunimi, Motoei;
Tsukamoto, Kazuhisa;
Satoh, Hiroaki;
Shimadzu, Mitsunobu;
Tozawa, Fumiko;
Mori, Tetsuo;
Shiobara, Masaaki;
Seki, George;
Endou, Hitoshi

Publication type:

Article

The DNA repair gene MBD4 (MED1) is mutated in human carcinomas with microsatellite instability.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 266, doi. 10.1038/15443

By:

Riccio, Antonio;
Aaltonen, Lauri A.;
Godwin, Andrew K.;
Loukola, Anu;
Percesepe, Antonio;
Salovaara, Reijo;
Masciullo, Valeria;
Genuardi, Maurizio;
Paravatou-Petsotas, Maria;
Bassi, Daniel E.;
Ruggeri, Bruce A.;
Klein-Szanto, Andres J.P.;
Testa, Joseph R.;
Neri, Giovanni;
Bellacosa, Alfonso

Publication type:

Article

Scd1 is expressed in sebaceous glands and is disrupted in the asebia mouse.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 268, doi. 10.1038/15446

By:

Zheng, Ying;
Eilertsen, Kenneth J.;
Ge, Lan;
Zhang, Lin;
Sundberg, John P.;
Prouty, Stephen M.;
Stenn, Kurt S.;
Parimoo, Satish

Publication type:

Article

Fine-mapping of an ancestral recombination breakpoint in DCP1.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 270, doi. 10.1038/15449

By:

Farrall, Martin;
Keavney, Bernard;
McKenzie, Colin;
Delépine, Marc;
Matsuda, Fumihiko;
Lathrop, G. Mark

Publication type:

Article

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 271, doi. 10.1038/15452

By:

Merryweather-Clarke, Alison T.;
Pointon, Jennifer J.;
Shearman, Jeremy D.;
Robson, Kathryn J.H.;
Jouanolle, Anne Marie;
Mosser, Annick;
David, Véronique;
Le Gall, Jean-Yves;
Halsall, David J.;
Elsey, Terence S.;
Kelly, Alison;
Cox, Timothy M.;
Clare, Michael;
Bomford, Adrian;
Vandwalle, Jean Luc;
Rochette, Jacques;
Borot, Nicolas;
Coppin, Hélène;
Roth, Marie-Paule

Publication type:

Article

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 271, doi. 10.1038/15722

By:

Noll, Walter W.;
Belloni, Dorothy R.;
Stenzel, Timothy T.;
Grody, Wayne W.

Publication type:

Article

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 272, doi. 10.1038/15723

By:

Gomez, Patricia S.;
Parks, Sharie;
Ries, Rhonda;
Tran, Thuan C.;
Gomez, Paul F.;
Press, Richard D.

Publication type:

Article

A point of entry into genomics.

Published in:

1999

By:

Bork, Peer;
Huynen, Martijn

Publication type:

Book Review

Protecting communities in research: current guidelines and limits of extrapolation.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 275, doi. 10.1038/15455

By:

Weijer, Charles;
Goldsand, Gary;
Emanuel, Ezekiel J.

Publication type:

Article

Diverse and dynamic functions of the Sir silencing complex.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 281, doi. 10.1038/15458

By:

Guarente, L

Publication type:

Article

A RA-dependent, tumour-growth suppressive transcription complex is the target of the PML-RARα and T18 oncoproteins.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 287, doi. 10.1038/15463

By:

Zhong, Sue;
Delva, Laurent;
Rachez, Christophe;
Cenciarelli, Cristina;
Gandini, Domenica;
Zhang, Hui;
Kalantry, Sundeep;
Freedman, Leonard P.;
Pandolfi, Pier Paolo

Publication type:

Article

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 296, doi. 10.1038/15472

By:

Hazan, Jamilé;
Fonknechten, Nùria;
Mavel, Delphine;
Paternotte, Caroline;
Samson, Delphine;
Artiguenave, François;
Davoine, Claire-Sophie;
Cruaud, Corinne;
Dürr, Alexandra;
Wincker, Patrick;
Brottier, Philippe;
Cattolico, Laurence;
Barbe, Valérie;
Burgunder, Jean-Marc;
Prud'homme, Jean-François;
Brice, Alexis;
Fontaine, Bertrand;
Heilig, Roland;
Weissenbach, Jean

Publication type:

Article

Differential methylation of genes and retrotransposons facilitates shotgun sequencing of the maize genome.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 305, doi. 10.1038/15479

By:

Rabinowicz, Pablo D.;
Schutz, Kristin;
Dedhia, Neilay;
Yordan, Cristina;
Parnell, Laurence D.;
Stein, Lincoln;
McCombie, W. Richard;
Martienssen, Robert A.

Publication type:

Article

A shotgun optical map of the entire Plasmodium falciparum genome.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 309, doi. 10.1038/15484

By:

Lai, Zhongwu;
Jing, Junping;
Aston, Christopher;
Clarke, Virginia;
Apodaca, Jennifer;
Dimalanta, Eileen T.;
Carucci, Daniel J.;
Gardner, Malcolm J.;
Mishra, Bud;
Anantharaman, Thomas S.;
Paxia, Salvatore;
Hoffman, Stephen L.;
Venter, J. Craig;
Huff, Edward J.;
Schwartz, David C.

Publication type:

Article

Epigenetic inheritance at the agouti locus in the mouse.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 314, doi. 10.1038/15490

By:

Morgan, Hugh D.;
Sutherland, Heidi G.E.;
Martin, David I.K.;
Whitelaw, Emma

Publication type:

Article

CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndrome.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 319, doi. 10.1038/15496

By:

Marcelino, Jose;
Carpten, John D.;
Suwairi, Wafaa M.;
Gutierrez, Orlando M.;
Schwartz, Stuart;
Robbins, Christiane;
Sood, Raman;
Makalowska, Izabela;
Baxevanis, Andy;
Johnstone, Brian;
Laxer, Ronald M.;
Zemel, Lawrence;
Kim, Chong Ae;
Herd, J. Kenneth;
Ihle, Johannes;
Williams, Cal;
Johnson, Mark;
Raman, Vidya;
Alonso, Luís Garcia

Publication type:

Article

Mutations in NEUROD1 are associated with the development of type 2 diabetes mellitus.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 323, doi. 10.1038/15500

By:

Malecki, Maciej T.;
Jhala, Ulupi S.;
Antonellis, Anthony;
Fields, Liz;
Doria, Alessandro;
Orban, Tihamer;
Saad, Mohammed;
Warram, James H.;
Montminy, Marc;
Krolewski, Andrzej S.

Publication type:

Article

The pallid gene encodes a novel, syntaxin 13-interacting protein involved in platelet storage pool deficiency.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 329, doi. 10.1038/15507

By:

Huang, Liping;
Kuo, Yien-Ming;
Gitschier, Jane

Publication type:

Article

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 333, doi. 10.1038/15513

By:

Papadopoulou, Lefkothea C.;
Sue, Carolyn M.;
Davidson, Mercy M.;
Tanji, Kurenai;
Nishino, Ichizo;
Sadlock, James E.;
Krishna, Sindu;
Walker, Winsome;
Selby, Jeanette;
Glerum, D. Moira;
Coster, Rudy Van;
Lyon, Gilles;
Scalais, Emmanuel;
Lebel, Roger;
Kaplan, Paige;
Shanske, Sara;
De Vivo, Darryl C.;
Bonilla, Eduardo;
Hirano, Michio

Publication type:

Article

Chimaeric mice deficient in dystroglycans develop muscular dystrophy and have disrupted myoneural synapses.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 338

By:

Côté, Patrice D.;
Moukhles, Hakima;
Lindenbaum, Michael;
Carbonetto, Salvatore

Publication type:

Article

A humanized model for multiple sclerosis using HLA-DR2 and a human T-cell receptor.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 343, doi. 10.1038/15525

By:

Madsen, Lars S.;
Andersson, Ellen Christina;
Jansson, Liselotte;
Krogsgaard, Michelle;
Andersen, Claus B.;
Engberg, Jan;
Strominger, Jack L.;
Svejgaard, Arne;
Hjorth, Jens Peter;
Holmdahl, Rikard;
Wucherpfennig, Kai W.;
Fugger, Lars

Publication type:

Article

Leukaemia disease genes: large-scale cloning and pathway predictions.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 348, doi. 10.1038/15531

By:

Li, Jiayin;
Shen, Haifa;
Himmel, Karen L.;
Dupuy, Adam J.;
Largaespada, David A.;
Nakamura, Takuro;
Shaughnessy, John D.;
Jenkins, Nancy A.;
Copeland, Neal G.

Publication type:

Article

Perlecan is essential for cartilage and cephalic development.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 354, doi. 10.1038/15537

By:

Arikawa-Hirasawa, Eri;
Watanabe, Hideto;
Takami, Hiroya;
Hassell, John R.;
Yamada, Yoshihiko

Publication type:

Article

HNPCC-like cancer predisposition in mice through simultaneous loss of Msh3 and Msh6 mismatch-repair protein functions.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 359, doi. 10.1038/15544

By:

Wind, Niels de;
Dekker, Marleen;
Claij, Nanna;
Jansen, Léon;
Klink, Yvonne van;
Radman, Miroslav;
Riggins, Greg;
Valk, Martin van der;
van 't Wout, Karin;
Riele, Hein te

Publication type:

Article

Mammalian (cytosine-5) methyltransferases cause genomic DNA methylation and lethality in Drosophila.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 363, doi. 10.1038/15551

By:

Lyko, Frank;
Ramsahoye, Bernard H.;
Kashevsky, Helena;
Tudor, Matthew;
Mastrangelo, Mary-Ann;
Orr-Weaver, Terry L.;
Jaenisch, Rudolf

Publication type:

Article

Meiotic instability of human minisatellite CEB1 in yeast requires DNA double-strand breaks.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 367

By:

Debrauwère, Hélène;
Buard, Jérôme;
Tessier, Jacques;
Aubert, Dominique;
Vergnaud, Gilles;
Nicolas, Alain

Publication type:

Article

Characterization of single-nucleotide polymorphisms in coding regions of human genes.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 373, doi. 10.1038/15564

By:

Cargill, Michele

Publication type:

Article

Griscelli disease maps to chromocome 15q and is associated with mutations in the Myosin-Va gene.

Published in:

Nature Genetics, 1999, v. 23, n. 3, p. 373, doi. 10.1038/15565

By:

Pastural, Elodie

Publication type:

Article

Suppression of the novel growth inhibitor p33<sup>ING1</sup> promotes neoplastic transformation.

Published in:

1999

By:

Garkavtsev, Igor

Publication type:

Erratum