Works matching IS 10614036 AND DT 1999 AND VI 21 AND IP 4

Results: 29

Publishing paradigms.

Published in:: 1999
Publication type:: Editorial

Anti-Xistentialism.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 343, doi. 10.1038/7661

By:

Heard, Edith;
Lovell-Badge, Robin;
Avner, Philip

Publication type:

Article

Mediating immunity to mycobacteria.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 345, doi. 10.1038/7663

By:

Foote, Simon

Publication type:

Article

A vital role for vitamin A.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 346, doi. 10.1038/7665

By:

Eichele, Gregor

Publication type:

Article

Making sense out of sound.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 347, doi. 10.1038/7668

By:

Griffith, Andrew J;
Friedman, Thomas B

Publication type:

Article

Touchingbase.

Published in:: Nature Genetics, 1999, v. 21, n. 4, p. 351
Publication type:: Article

A common nonsense mutation results in α-actinin-3 deficiency in the general population.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 353, doi. 10.1038/7675

By:

North, Kathryn N.;
Yang, Nan;
Wattanasirichaigoon, Duangrurdee;
Mills, Michelle;
Easteal, Simon;
Beggs, Alan H.

Publication type:

Article

A mutation in NRL is associated with autosomal dominant retinitis pigmentosa.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 355, doi. 10.1038/7678

By:

Bessant, David A.R.;
Payne, Annette M.;
Mitton, Kenneth P.;
Wang, Qing-Liang;
Swain, Prabodha K.;
Plant, Catherine;
Bird, Alan C.;
Zack, Donald J.;
Swaroop, Anand;
Bhattacharya, Shomi S.

Publication type:

Article

Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISH.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 357, doi. 10.1038/7681

By:

Erdel, Martin;
Hubalek, Michael;
Lingenhel, Arno;
Kofler, Kurt;
Duba, Hans-C;
Utermann, Gerd

Publication type:

Article

Atm haploinsufficiency results in increased sensitivity to sublethal doses of ionizing radiation in mice.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 359, doi. 10.1038/7684

By:

Barlow, Carrolee;
Eckhaus, Michael A.;
Schäffer, Alejandro A.;
Wynshaw-Boris, Anthony

Publication type:

Article

Loss of information due to ambiguous haplotyping of SNPs.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 360, doi. 10.1038/7687

By:

Hodge, Susan E.;
Boehnke, Michael;
Spence, M. Anne

Publication type:

Article

Genetic determinism and the overprotection of human subjects.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 362, doi. 10.1038/7692

By:

Wilcox, Allen J.;
Taylor, Jack A.;
Sharp, Richard R.;
London, Stephanie J.

Publication type:

Article

A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 363, doi. 10.1038/7693

By:

Yasunaga, Shin'ichiro;
Grati, M'hamed;
Cohen-Salmon, Martine;
El-Amraoui, Aziz;
Mustapha, Mirna;
Salem, Nabiha;
El-Zir, Elie;
Loiselet, Jacques;
Petit, Christine

Publication type:

Article

A human IFNGR1 small deletion hotspot associated with dominant susceptibility to mycobacterial infection.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 370, doi. 10.1038/7701

By:

Jouanguy, Emmanuelle;
Lamhamedi-Cherradi, Salma;
Lammas, David;
Dorman, Susan E.;
Fondanèche, Marie-Claude;
Dupuis, Stéphanie;
Döffinger, Rainer;
Altare, Frédéric;
Girdlestone, John;
Emile, Jean-François;
Ducoulombier, Henri;
Edgar, David;
Clarke, Jane;
Oxelius, Vivi-Anne;
Brai, Melchiorre;
Novelli, Vas;
Heyne, Klaus;
Fischer, Alain;
Holland, Steven M

Publication type:

Article

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8).

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 379, doi. 10.1038/7710

By:

Koob, Michael D.;
Moseley, Melinda L.;
Schut, Lawrence J.;
Benzow, Kellie A.;
Bird, Thomas D.;
Day, John W.;
Ranum, Laura P.W.

Publication type:

Article

Comparative genomes of Chlamydia pneumoniae and C. trachomatis.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 385, doi. 10.1038/7716

By:

Kalman, Sue;
Mitchell, Wayne;
Marathe, Rekha;
Lammel, Claudia;
Fan, Jun;
Hyman, Richard W;
Olinger, Lynn;
Grimwood, Jane;
Davis, Ronald W;
Stephens, Richard

Publication type:

Article

Independent regulation of the two Pax5 alleles during B-cell development.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 390, doi. 10.1038/7720

By:

Nutt, Stephen L;
Vambrie, Susanne;
Steinlein, Peter;
Kozmik, Zbynek;
Rolink, Antonius;
Weith, Andreas;
Busslinger, Meinrad

Publication type:

Article

Transferrin receptor is necessary for development of erythrocytes and the nervous system.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 396, doi. 10.1038/7727

By:

Levy, Joanne E.;
Jin, Ou;
Fujiwara, Yuko;
Kuo, Frank;
Andrews, Nancy

Publication type:

Article

Tsix, a gene antisense to Xist at the X-inactivation centre.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 400, doi. 10.1038/7734

By:

Lee, Jeannie;
Davidow, Lance S;
Warshawsky, David

Publication type:

Article

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 405, doi. 10.1038/7741

By:

Chang, Bo;
Smith, Richard S;
Hawes, Norman L;
Anderson, Michael G;
Zabaleta, Adriana;
Savinova, Olga;
Roderick, Thomas H;
Heckenlively, John R.;
Davisson, Muriel T;
John, Simon W M

Publication type:

Article

A common human skin tumour is caused by activating mutations in β-catenin.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 410, doi. 10.1038/7747

By:

Chan, Edward;
Gat, Uri;
McNiff, Jennifer M;
Fuchs, Elaine

Publication type:

Article

The complete family of genes encoding G proteins of Caenorhabditis elegans.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 414, doi. 10.1038/7753

By:

Jansen, Gert;
Thijssen, Karen L;
Werner, Pia;
van derHorst, Marieke;
Hazendonk, Esther;
Plasterk, Ronald H A

Publication type:

Article

Identification of the gene responsible for gelatinous drop-like corneal dystrophy.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 420, doi. 10.1038/7759

By:

Tsujikawa, Motokazu;
Kurahashi, Hiroki;
Tanaka, Toshihiro;
Nishida, Kohji;
Shimomura, Yoshikazu;
Tano, Yasuo;
Nakamura, Yusuke

Publication type:

Article

A novel endothelial-derived lipase that modulates HDL metabolism.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 424, doi. 10.1038/7766

By:

Jaye, Michael;
Lynch, Kevin J.;
Krawiec, John;
Marchadier, Dawn;
Maugeais, Cyrille;
Doan, Kim;
South, Victoria;
Amin, Dilip;
Perrone, Mark;
Rader, Daniel J.

Publication type:

Article

Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 429, doi. 10.1038/7771

By:

Lahn, Bruce T;
Page, David C

Publication type:

Article

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 434, doi. 10.1038/7777

By:

Gogos, Joseph;
Santha, Miklos;
Takacs, Zoltan;
Beck, Kevin D;
Luine, Victoria;
Lucas, Louis R;
Nadler, J. Victor;
Karayiorgou, Maria

Publication type:

Article

The Pendred syndrome gene encodes a chloride-iodide transport protein.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 440, doi. 10.1038/7783

By:

Scott, Daryl A.;
Wang, Rong;
Kreman, Trisha M;
Sheffield, Val C.;
Karniski, Lawrence P

Publication type:

Article

Embryonic retinoic acid synthesis is essential for early mouse post-implantation development.

Published in:

Nature Genetics, 1999, v. 21, n. 4, p. 444, doi. 10.1038/7788

By:

Niederreither, Karen;
Subbarayan, Vemparala;
Dollé, Pascal;
Chambon, Pierre

Publication type:

Article

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

Published in:

1999

By:

Verhoeven, Kristien

Publication type:

Erratum