Works matching IS 10614036 AND DT 2005 AND VI 37 AND IP 9

Results: 27

High-input biology.

Published in:: 2005
Publication type:: Editorial

Editor in the field: Caltech's Division of Biology.

Published in:: 2005
Publication type:: Editorial

Haplotype block structure of the cytochrome P450 CYP2C gene cluster on chromosome 10.

Published in:

2005

By:

Walton, Robert;
Kimber, Martin;
Rockett, Kirk;
Trafford, Clare;
Kwiatkowski, Dominic;
Sirugo, Giorgio

Publication type:

Letter

Reply to 'Haplotype block structure of the cytochrome P450 CYP2C gene cluster on chromosome 10'.

Published in:

2005

By:

Ahmadi, Kourosh R.;
Weale, Michael E.;
Roses, Allen D.;
Saunders, Ann M.;
Goldstein, David B.

Publication type:

Letter

Defining epigenetic states through chromatin and RNA.

Published in:

2005

By:

Schübeler, Dirk;
Elgin, Sarah C. R.

Publication type:

Report

A wonderfully diverse life.

Published in:

2005

By:

Jorde, Lynn B.

Publication type:

Book Review

Unraveling the Fanconi anemia–DNA repair connection.

Published in:

Nature Genetics, 2005, v. 37, n. 9, p. 921, doi. 10.1038/ng0905-921

By:

Thompson, Larry H.

Publication type:

Article

On being the right size.

Published in:

Nature Genetics, 2005, v. 37, n. 9, p. 923, doi. 10.1038/ng0905-923

By:

Holmes, Edward C.

Publication type:

Article

Elucidating mouse transmission ratio distortion.

Published in:

Nature Genetics, 2005, v. 37, n. 9, p. 924, doi. 10.1038/ng0905-924

By:

Lyon, Mary F.

Publication type:

Article

Prime movers of noisy gene expression.

Published in:

Nature Genetics, 2005, v. 37, n. 9, p. 925, doi. 10.1038/ng0905-925

By:

Paulsson, Johan

Publication type:

Article

Touching base.

Published in:

Nature Genetics, 2005, v. 37, n. 9, p. 927, doi. 10.1038/ng0905-927

By:

Axton, Myles;
Bahcall, Orli;
Packer, Alan

Publication type:

Article

Research Highlights.

Published in:

Nature Genetics, 2005, v. 37, n. 9, p. 929, doi. 10.1038/ng0905-929

By:

Bahcall, Orli;
Niemitz, Emily;
Packer, Alan;
Vogan, Kyle

Publication type:

Article

Dkk2 has a role in terminal osteoblast differentiation and mineralized matrix formation.

Published in:

Nature Genetics, 2005, v. 37, n. 9, p. 945, doi. 10.1038/ng1614

By:

Xiaofeng Li;
Peng Liu;
Wenzhong Liu;
Maye, Peter;
Jianghong Zhang;
Yazhou Zhang;
Marja Hurley;
Caiying Guo;
Adele Boskey;
Le Sun;
Harris, Stephen E.;
Rowe, David W.;
Hua Zhu Ke;
Dianqing Wu

Publication type:

Article

Gene duplication and exon shuffling by helitron-like transposons generate intraspecies diversity in maize.

Published in:

2005

By:

Morgante, Michele;
Brunner, Stephan;
Pea, Giorgio;
Fengler, Kevin;
Zuccolo, Andrea;
Rafalski, Antoni

Publication type:

Letter

Contributions of low molecule number and chromosomal positioning to stochastic gene expression.

Published in:

2005

By:

Becskei, Attila;
Kaufmann, Benjamin B;
van Oudenaarden, Alexander

Publication type:

Letter

The t complex–encoded GTPase-activating protein Tagap1 acts as a transmission ratio distorter in mice.

Published in:

2005

By:

Bauer, Hermann;
Willert, Jürgen;
Koschorz, Birgit;
Herrmann, Bernhard G.

Publication type:

Letter

Intragenic tandem repeats generate functional variability.

Published in:

2005

By:

Verstrepen, Kevin J.;
Jansen, An;
Lewitter, Fran;
Fink, Gerald R.

Publication type:

Letter

Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP.

Published in:

2005

By:

Lihong Zhao;
Chantal Longo-Guess;
Belinda S. Harris;
Jeong-Woong Lee;
Ackerman, Susan L.

Publication type:

Letter

Real ribozymes suggest a relaxed error threshold.

Published in:

2005

By:

Kun, Ádám;
Santos, Mauro;
Szathmáry, Eörs

Publication type:

Letter

Regulation of polarized extension and planar cell polarity in the cochlea by the vertebrate PCP pathway.

Published in:

2005

By:

Jianbo Wang;
Sharayne Mark;
Xiaohui Zhang;
Dong Qian;
Seung-Jong Yoo;
Radde-Gallwitz, Kristen;
Yanping Zhang;
Xi Lin;
Collazo, Andres;
Wynshaw-Boris, Anthony;
Ping Chen

Publication type:

Letter

Mutations in genes in the renin-angiotensin system are associated with autosomal recessive renal tubular dysgenesis.

Published in:

2005

By:

Gribouval, Olivier;
Gonzales, Marie;
Neuhaus, Thomas;
Aziza, Jacqueline;
Bieth, Eric;
Laurent, Nicole;
Bouton, Jean Marie;
Feuillet, François;
Makni, Saloua;
Amar, Hatem Ben;
Laube, Guido;
Delezoide, Anne-Lise;
Bouvier, Raymonde;
Dijoud, Frédérique;
Ollagnon-Roman, Elisabeth;
Roume, Joelle;
Joubert, Madeleine;
Antignac, Corinne;
Gubler, Marie Claire

Publication type:

Letter

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia.

Published in:

2005

By:

Levran, Orna;
Attwooll, Claire;
Henry, Rashida T.;
Milton, Kelly L.;
Neveling, Kornelia;
Rio, Paula;
Batish, Sat Dev;
Kalb, Reinhard;
Velleuer, Eunike;
Barral, Sandra;
Ott, Jurg;
Petrini, John;
Schindler, Detlev;
Hanenberg, Helmut;
Auerbach, Arleen D.

Publication type:

Letter

The DNA helicase BRIP1 is defective in Fanconi anemia complementation group J.

Published in:

2005

By:

Levitus, Marieke;
Waisfisz, Quinten;
Godthelp, Barbara C.;
Vries, Yne de;
Hussain, Shobbir;
Wiegant, Wouter W.;
Elghalbzouri-Maghrani, Elhaam;
Steltenpool, Jûrgen;
Rooimans, Martin A.;
Pals, Gerard;
Arwert, Fré;
Mathew, Christopher G.;
Zdzienicka, Małgorzata Z.;
Hiom, Kevin;
de Winter, Johan P.;
Joenje, Hans

Publication type:

Letter

A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

Published in:

2005

By:

Meetei, Amom Ruhikanta;
Medhurst, Annette L.;
Chen Ling;
Yutong Xue;
Singh, Thiyam Ramsing;
Bier, Patrick;
Steltenpool, Jurgen;
Stone, Stacie;
Dokal, Inderjeet;
Mathew, Christopher G.;
Hoatlin, Maureen;
Joenje, Hans;
de Winter, Johan P.;
Weidong Wang

Publication type:

Letter

The BRIP1 helicase functions independently of BRCA1 in the Fanconi anemia pathway for DNA crosslink repair.

Published in:

2005

By:

Bridge, Wendy L.;
Vandenberg, Cassandra J.;
Franklin, Roger J.;
Hiom, Kevin

Publication type:

Letter

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

Published in:

2005

By:

Gicquel, Christine;
Rossignol, Sylvie;
Cabrol, Sylvie;
Houang, Muriel;
Steunou, Virginie;
Barbu, Véronique;
Danton, Fabienne;
Thibaud, Nathalie;
Merrer, Martine Le;
Burglen, Lydie;
Bertrand, Anne-Marie;
Netchine, Irène;
Bouc, Yves Le

Publication type:

Letter

Genome-wide analysis of mouse transcripts using exon microarrays and factor graphs.

Published in:

2005

By:

Frey, Brendan J.;
Mohammad, Naveed;
Morris, Quaid D.;
Zhang, Wen;
Robinson, Mark D.;
Mnaimneh, Sanie;
Chang, Richard;
Pan, Qun;
Sat, Eric;
Rossant, Janet;
Bruneau, Benoit G.;
Aubin, Jane E.;
Blencowe, Benjamin J.;
Hughes, Timothy R.

Publication type:

Letter