Works matching IS 10614036 AND DT 1999 AND VI 22 AND IP 2

Results: 30

The gene mutated in bare patches and striated mice encodes a novel 3β-hydroxysteroid dehydrogenase.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 182, doi. 10.1038/9700

By:

Liu, Xiao Yu;
Dangel, Andrew W.;
Kelley, Richard I.;
Zhao, Wei;
Denny, Paul;
Botcherby, Marc;
Cattanach, Bruce;
Peters, Jo;
Hunsicker, Patricia R.;
Mallon, Ann-Marie;
Strivens, Mark A.;
Bate, Rachael;
Miller, Webb;
Rhodes, Michael;
Brown, Stephen D.M.;
Herman, Gail E.

Publication type:

Article

Breaking waves down under.

Published in:: Nature Genetics, 1999, v. 22, n. 2, p. 117, doi. 10.1038/9617
Publication type:: Article

Genetic conflicts and the private life of Peromyscus polionotus.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 131, doi. 10.1038/9640

By:

Haig, David

Publication type:

Article

A mutation in the gene encoding steroidogenic factor-1 causes XY sex reversal and adrenal failure in humans.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 125, doi. 10.1038/9629

By:

Achermann, John C.;
Ito, Masafumi;
Ito, Mika;
Hindmarsh, Peter C.;
Jameson, J. Larry

Publication type:

Article

Prospects for whole-genome linkage disequilibrium mapping of common disease genes.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 139, doi. 10.1038/9642

By:

Kruglyak, L

Publication type:

Article

Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 128, doi. 10.1038/9635

By:

Zielenski, Julian;
Corey, Mary;
Rozmahel, Richard;
Markiewicz, Danuta;
Aznarez, Isabel;
Casals, Teresa;
Larriba, Sara;
Mercier, Bernard;
Cutting, Garry R.;
Krebsova, Alice;
Macek, Milan;
Langfelder-Schwind, Elinor;
Marshall, Bruce C.;
DeCelie-Germana, J.;
Claustres, Mirreille;
Palacio, Ana;
Bal, Jerzy;
Nowakowska, Aleksandra;
Ferec, Claude

Publication type:

Article

Chips for chimps.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 119, doi. 10.1038/9619

By:

Clark, Andrew G

Publication type:

Article

Creating deaths from malaria.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 120, doi. 10.1038/9621

By:

Wahlgren, Mats

Publication type:

Article

You give me fever.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 121, doi. 10.1038/9624

By:

Valle, David

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 1999, v. 22, n. 2, p. 123
Publication type:: Article

The future of genetic counselling: an international perspective.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 133, doi. 10.1038/9641

By:

Bowles Biesecker, Barbara;
Marteau, Theresa M.

Publication type:

Article

Cloning of male mice from adult tail-tip cells.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 127, doi. 10.1038/9632

By:

Wakayama, Teruhiko;
Yanagimachi, Ryuzo

Publication type:

Article

Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 151, doi. 10.1038/9658

By:

Camacho, Jose A.;
Obie, Cassandra;
Biery, Barbara;
Goodman, Barbara K.;
Hu, Chien-An;
Almashanu, Shlomo;
Steel, Gary;
Casey, Robin;
Lambert, Marie;
Mitchell, Grant A.;
Valle, David

Publication type:

Article

An estimated frequency of endogenous insertional mutations in humans.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 130, doi. 10.1038/9638

By:

Kazazian, Haig H.

Publication type:

Article

Imprinting and monogamy.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 130, doi. 10.1038/9639

By:

Moore, Tom;
Mills, Walter

Publication type:

Article

A double-stranded RNA binding protein required for activation of repressed messages in mammalian germ cells.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 171, doi. 10.1038/9684

By:

Zhong, Jun;
Peters, Antoine H.F.M.;
Lee, Keesook;
Braun, Robert E.

Publication type:

Article

A polymorphism that affects OCT-1 binding to the TNF promoter region is associated with severe malaria.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 145, doi. 10.1038/9649

By:

Knight, Julian C.;
Udalova, Irina;
Hill, Adrian V.S.;
Greenwood, Brian M.;
Peshu, Norbert;
Marsh, Kevin;
Kwiatkowski, Dominic

Publication type:

Article

The gene mutated in adult-onset type II citrullinaemia encodes a putative mitochondrial carrier protein.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 159, doi. 10.1038/9667

By:

Kobayashi, Keiko;
Sinasac, David S.;
Iijima, Mikio;
Boright, Andrew P.;
Begum, Laila;
Lee, Jeffrey R.;
Yasuda, Tomotsugu;
Ikeda, Sayaka;
Hirano, Ryuki;
Terazono, Hiroki;
Crackower, Michael A.;
Kondo, Ikuko;
Tsui, Lap-Chee;
Scherer, Stephen W.;
Saheki, Takeyori

Publication type:

Article

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 196, doi. 10.1038/9718

By:

Wallis, Deeann E.;
Roessler, Erich;
Hehr, Ute;
Nanni, Luisa;
Wiltshire, Tim;
Richieri-Costa, Antonio;
Gillessen-Kaesbach, Gabriele;
Zackai, Elaine H.;
Rommens, Johanna;
Muenke, Maximilian

Publication type:

Article

Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 168, doi. 10.1038/9680

By:

Drazen, Jeffrey M.;
Yandava, Chandri N.;
Dubé, Louise;
Szczerback, Natalie;
Hippensteel, Richard;
Pillari, Antonino;
Israel, Elliot;
Schork, Nicholas;
Silverman, Eric S.;
Katz, David A.;
Drajesk, Jeffrey

Publication type:

Article

Determination of ancestral alleles for human single-nucleotide polymorphisms using high-density oligonucleotide arrays.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 164, doi. 10.1038/9674

By:

Hacia, Joseph G.;
Fan, Jian-Bing;
Ryder, Oliver;
Jin, Li;
Edgemon, Keith;
Ghandour, Ghassan;
Mayer, R. Aeryn;
Sun, Bryan;
Hsie, Linda;
Robbins, Christiane M.;
Brody, Lawrence C.;
Wang, David;
Lander, Eric S.;
Lipshutz, Robert;
Fodor, Stephen P.A.;
Collins, Francis S.

Publication type:

Article

Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 175, doi. 10.1038/9691

By:

Houten, Sander M.;
Kuis, Wietse;
Duran, Marinus;
de Koning, Tom J.;
van Royen-Kerkhof, Annet;
Romeijn, Gerrit J.;
Frenkel, Joost;
Dorland, Lambertus;
de Barse, Martina M.J.;
Huijbers, Wim A.R.;
Rijkers, Ger T.;
Waterham, Hans R.;
Wanders, Ronald J.A.;
Poll-The, Bwee Tien

Publication type:

Article

Summer array.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 207, doi. 10.1038/9731

By:

Ronemus, Michael

Publication type:

Article

Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 178, doi. 10.1038/9696

By:

Drenth, Joost P.H.;
Cuisset, Laurence;
Grateau, Gilles;
Vasseur, Christian;
van de Velde-Visser, Saskia D.;
de Jong, Jan G.N.;
Beckmann, Jacques S.;
van der Meer, Jos W.M.;
Delpech & contributing members of the International Hyper-IgD Study Group, Marc

Publication type:

Article

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

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 209, doi. 10.1038/9735

By:

Lahn, Bruce T;
Page, David C

Publication type:

Article

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 209, doi. 10.1038/9738

By:

Coffee et al., Bradford

Publication type:

Article

Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 188, doi. 10.1038/9707

By:

Yamamoto, Hiroyuki;
Simon, András;
Eriksson, Ulf;
Harris, Eddie;
Berson, Eliot L.;
Dryja, Thaddeus P.

Publication type:

Article

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 192, doi. 10.1038/9713

By:

Delpire, Eric;
Lu, Jianming;
England, Roger;
Dull, Christopher;
Thorne, Tina

Publication type:

Article

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 199, doi. 10.1038/9722

By:

Stone, Edwin M.;
Lotery, Andrew J.;
Munier, Francis L.;
Héon, Elise;
Piguet, Bertrand;
Guymer, Robyn H.;
Vandenburgh, Kimberlie;
Cousin, Pascal;
Nishimura, Darryl;
Swiderski, Ruth E.;
Silvestri, Giuliana;
Mackey, David A.;
Hageman, Gregory S.;
Bird, Alan C.;
Sheffield, Val C.;
Schorderet, Daniel F.

Publication type:

Article

DNA methylation represses transcription in vivo.

Published in:

Nature Genetics, 1999, v. 22, n. 2, p. 203, doi. 10.1038/9727

By:

Siegfried, Zahava;
Eden, Sharon;
Mendelsohn, Monica;
Feng, Xu;
Tsuberi, Ben-Zion;
Cedar, Howard

Publication type:

Article