Works matching IS 10614036 AND DT 2000 AND VI 24 AND IP 4

Results: 31

Repair affairs.

Published in:: Nature Genetics, 2000, v. 24, n. 4, p. 325, doi. 10.1038/74122
Publication type:: Article

Fly meets shotgun: shotgun wins.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 327, doi. 10.1038/74125

By:

Hartl, Daniel L

Publication type:

Article

Oct-4, Scene 1: the drama of mouse development.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 328, doi. 10.1038/74129

By:

Stewart, Colin L

Publication type:

Article

A hole in the head.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 330, doi. 10.1038/74132

By:

Ferguson, Mark W J

Publication type:

Article

Do all SINEs lead to LINEs?

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 332, doi. 10.1038/74135

By:

Weiner, Alan M

Publication type:

Article

Getting a foothold in nephrotic syndrome.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 333, doi. 10.1038/74139

By:

Somlo, Stefan;
Mundel, Peter

Publication type:

Article

Touchingbase.

Published in:: Nature Genetics, 2000, v. 24, n. 4, p. 337
Publication type:: Article

A systematic, high-resolution linkage of the cytogenetic and physical maps of the human genome.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 339, doi. 10.1038/74149

By:

Kirsch, Ilan R.;
Green, Eric D.;
Yonescu, Raluca;
Strausberg, Robert;
Carter, Nigel;
Bentley, David;
Leversha, Margaret A.;
Dunham, Ian;
Braden, Valerie V.;
Hilgenfeld, Eva;
Schuler, Greg;
Lash, Alex E.;
Shen, Grace L.;
Martelli, Maria;
Kuehl, W. Michael;
Klausner, Richard D.;
Ried, Thomas

Publication type:

Article

ISIS, the intron information system, reveals the high frequency of alternative splicing in the human genome.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 340, doi. 10.1038/74153

By:

Croft, Larry;
Schandorff, Soeren;
Clark, Francis;
Burrage, Kevin;
Arctander, Peter;
Mattick, John S.

Publication type:

Article

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 342, doi. 10.1038/74155

By:

van den Boogaard, Marie-José H.;
Dorland, Marinus;
Beemer, Frits A.;
van Amstel, Hans Kristian Ploos

Publication type:

Article

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 343, doi. 10.1038/74159

By:

Escayg, Andrew;
MacDonald, Bryan T.;
Meisler, Miriam H.;
Baulac, Stéphanie;
Huberfeld, Gilles;
An-Gourfinkel, Isabelle;
Brice, Alexis;
LeGuern, Eric;
Moulard, Bruno;
Chaigne, Denys;
Buresi, Catherine;
Malafosse, Alain

Publication type:

Article

Dolly part one: the end of the beginning in mammalian cloning?

Published in:

2000

By:

Perry, Tony;
Wakayama, Teru

Publication type:

Book Review

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 349, doi. 10.1038/74166

By:

Boute, Nicolas;
Gribouval, Olivier;
Roselli, Séverine;
Benessy, France;
Lee, Hyunjoo;
Fuchshuber, Arno;
Dahan, Karin;
Gubler, Marie-Claire;
Niaudet, Patrick;
Antignac, Corinne

Publication type:

Article

Robustness against mutations in genetic networks of yeast.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 355, doi. 10.1038/74174

By:

Wagner, Andreas

Publication type:

Article

Human LINE retrotransposons generate processed pseudogenes.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 363, doi. 10.1038/74184

By:

Esnault, Cécile;
Maestre, Joël;
Heidmann, Thierry

Publication type:

Article

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 368, doi. 10.1038/74191

By:

Gibbons, Richard J.;
McDowell, Tarra L.;
Raman, Sundhya;
O'Rourke, Delia M.;
Garrick, David;
Ayyub, Helena;
Higgs, Douglas R.

Publication type:

Article

Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 372, doi. 10.1038/74199

By:

Niwa, Hitoshi;
Miyazaki, Jun-ichi;
Smith, Austin G.

Publication type:

Article

In vivo modulation of Hmgic reduces obesity.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 377, doi. 10.1038/74207

By:

Anand, Ashim;
Chada, Kiran

Publication type:

Article

Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 381, doi. 10.1038/74215

By:

Lindblad-Toh, Kerstin;
Winchester, Ellen;
Daly, Mark J.;
Wang, David G.;
Hirschhorn, Joel N.;
Laviolette, Jean-Philippe;
Ardlie, Kristin;
Reich, David E.;
Robinson, Elizabeth;
Sklar, Pamela;
Shah, Nila;
Thomas, Daryl;
Fan, Jian-Bing;
Gingeras, Thomas;
Warrington, Janet;
Patil, Nila;
Hudson, Thomas J.;
Lander, Eric S.

Publication type:

Article

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 387, doi. 10.1038/74224

By:

Wilkie, Andrew O.M.;
Tang, Zequn;
Elanko, Navaratnam;
Walsh, Sinead;
Twigg, Stephen R.F.;
Hurst, Jane A.;
Wall, Steven A.;
Chrzanowska, Krystyna H.;
Maxson, Robert E.

Publication type:

Article

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 391, doi. 10.1038/74231

By:

Satokata, Ichiro;
Ma, Liang;
Ohshima, Hayato;
Bei, Marianna;
Woo, Ian;
Nishizawa, Kazumichi;
Maeda, Takeyasu;
Takano, Yoshiro;
Uchiyama, Makoto;
Heaney, Shaun;
Peters, Heiko;
Tang, Zequn;
Maxson, Robert;
Maas, Richard

Publication type:

Article

The direction of microsatellite mutations is dependent upon allele length.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 396, doi. 10.1038/74238

By:

Xu, Xin;
Peng, Mei;
Fang, Zhian;
Xu, Xiping

Publication type:

Article

Heterogeneous mutation processes in human microsatellite DNA sequences.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 400, doi. 10.1038/74249

By:

Ellegren, Hans

Publication type:

Article

Abnormal adaptations to stress and impaired cardiovascular function in mice lacking corticotropin-releasing hormone receptor-2.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 403, doi. 10.1038/74255

By:

Coste, Sarah C.;
Kesterson, Robert A.;
Heldwein, Kurt A.;
Stevens, Susan L.;
Heard, Amanda D.;
Hollis, Jacob H.;
Murray, Susan E.;
Hill, Jennifer K.;
Pantely, George A.;
Hohimer, Alan R.;
Hatton, Daniel C.;
Phillips, Tamara J.;
Finn, Deborah A.;
Low, Malcolm J.;
Rittenberg, Marvin B.;
Stenzel, Peter;
Stenzel-Poore, Mary P.

Publication type:

Article

Mice deficient for corticotropin-releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stress.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 410, doi. 10.1038/74263

By:

Bale, Tracy L.;
Contarino, Angelo;
Smith, George W.;
Chan, Raymond;
Gold, Lisa H.;
Sawchenko, Paul E.;
Koob, George F.;
Vale, Wylie W.;
Lee, Kuo-Fen

Publication type:

Article

Deletion of Crhr2 reveals an anxiolytic role for corticotropin-releasing hormone receptor-2.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 415, doi. 10.1038/74271

By:

Kishimoto, Toshimitsu;
Radulovic, Jelena;
Radulovic, Marko;
Lin, Chijen R.;
Schrick, Christina;
Hooshmand, Farideh;
Hermanson, Ola;
Rosenfeld, Michael G.;
Spiess, Joachim

Publication type:

Article

The SH2 tyrosine phosphatase Shp2 is required for mammalian limb development.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 420, doi. 10.1038/74279

By:

Saxton, Tracy M.;
Ciruna, Brian G.;
Holmyard, Doug;
Kulkarni, Sarang;
Harpal, Ken;
Rossant, Janet;
Pawson, Tony

Publication type:

Article

Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin α8β1.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 424, doi. 10.1038/74286

By:

Littlewood Evans, Amanda;
Müller, Ulrich

Publication type:

Article

The homeobox gene mirror links EGF signalling to embryonic dorso-ventral axis formation through Notch activation.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 429, doi. 10.1038/74294

By:

Jordan, Katherine C.;
Clegg, Nigel J.;
Blasi, Jennifer A.;
Morimoto, Alyssa M.;
Sen, Jonaki;
Stein, David;
McNeill, Helen;
Deng, Wu-Min;
Tworoger, Michael;
Ruohola-Baker, Hannele

Publication type:

Article

Mutations in Sox18 underlie cardiovascular and hair follicle defects in ragged mice.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 434, doi. 10.1038/74301

By:

Pennisi, David;
Gardner, Jennifer;
Chambers, Doreen;
Hosking, Brett;
Peters, Josephine;
Muscat, George;
Abbott, Catherine;
Koopman, Peter

Publication type:

Article

Mutations in the human Delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis.

Published in:

Nature Genetics, 2000, v. 24, n. 4, p. 438, doi. 10.1038/74307

By:

Bulman, Michael P.;
Kusumi, Kenro;
Frayling, Timothy M.;
McKeown, Carole;
Garrett, Christine;
Lander, Eric S.;
Krumlauf, Robb;
Hattersley, Andrew T.;
Ellard, Sian;
Turnpenny, Peter D.

Publication type:

Article