Works matching IS 10614036 AND DT 1999 AND VI 22 AND IP 3

Results: 25

Array data go public.

Published in:: Nature Genetics, 1999, v. 22, n. 3, p. 211, doi. 10.1038/10264
Publication type:: Article

Data analysis and integration: of steps and arrows.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 213, doi. 10.1038/10265

By:

Bittner, Michael;
Meltzer, Paul;
Trent, Jeffrey

Publication type:

Article

Architectural regulations and Hmg1.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 215, doi. 10.1038/10267

By:

Wolffe, Alan P

Publication type:

Article

Clocks, criteria and critical genes.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 217, doi. 10.1038/10270

By:

Foster, Russell G;
Lucas, Robert J

Publication type:

Article

The weed paves the way.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 219, doi. 10.1038/10274

By:

Gibbs, Richard A

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 1999, v. 22, n. 3, p. 221
Publication type:: Article

The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 223, doi. 10.1038/10279

By:

Delbridge, Margaret L.;
Lingenfelter, Patricia A.;
Disteche, Christine M.;
Graves, Jennifer A. Marshall

Publication type:

Article

RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 224, doi. 10.1038/10282

By:

Mazeyrat, Sophie;
Saut, Noëmie;
Mattei, Marie-Geneviève;
Mitchell, Michael J.

Publication type:

Article

Absence of Cd36 mutation in the original spontaneously hypertensive rats with insulin resistance.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 226, doi. 10.1038/10285

By:

Gotoda, Takanari;
Iizuka, Yoko;
Kato, Norihiro;
Osuga, Jun-ichi;
Bihoreau, Marie-Therese;
Murakami, Toru;
Yamori, Yukio;
Shimano, Hitoshi;
Ishibashi, Shun;
Yamada, Nobuhiro

Publication type:

Article

The flower, the gene, the brain and the creative process.

Published in:

1999

By:

Altaba, Ariel Ruiz i

Publication type:

Book Review

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

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 231, doi. 10.1038/10290

By:

Cargill, Michele;
Altshuler, David;
Ireland, James;
Sklar, Pamela;
Ardlie, Kristin;
Patil, Nila;
Lane, Charles R.;
Lim, Esther P.;
Kalyanaraman, Nilesh;
Nemesh, James;
Ziaugra, Liuda;
Friedland, Lisa;
Rolfe, Alex;
Warrington, Janet;
Lipshutz, Robert;
Daley, George Q.;
Lander, Eric S.

Publication type:

Article

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 239, doi. 10.1038/10297

By:

Halushka, Marc K.;
Fan, Jian-Bing;
Bentley, Kimberly;
Hsie, Linda;
Shen, Naiping;
Weder, Alan;
Cooper, Richard;
Lipshutz, Robert;
Chakravarti, Aravinda

Publication type:

Article

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 248, doi. 10.1038/10305

By:

Pierce, Eric A.;
Quinn, Tracey;
Meehan, Terrence;
McGee, Terri L.;
Berson, Eliot L.;
Dryja, Thaddeus P.

Publication type:

Article

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 255, doi. 10.1038/10314

By:

Sullivan, Lori S.;
Heckenlively, John R.;
Bowne, Sara J.;
Zuo, Jian;
Hide, Winston A.;
Gal, Andreas;
Denton, Michael;
Inglehearn, Chris F.;
Blanton, Susan H.;
Daiger, Stephen P.

Publication type:

Article

Regulation of anterior/posterior patterning of the axial skeleton by growth/differentiation factor 11.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 260, doi. 10.1038/10320

By:

McPherron, Alexandra C.;
Lawler, Ann M.;
Lee, Se-Jin

Publication type:

Article

A map for sequence analysis of the Arabidopsis thaliana genome.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 265, doi. 10.1038/10327

By:

Marra, Marco;
Kucaba, Tamara;
Sekhon, Mandeep;
Hillier, LaDeana;
Martienssen, Robert;
Chinwalla, Asif;
Crockett, Jye'mon;
Fedele, Jacqueline;
Grover, Heather;
Gund, Christopher;
McCombie, W. Richard;
McDonald, Ken;
McPherson, John;
Mudd, Nancy;
Parnell, Larry;
Schein, Jacqueline;
Seim, Ryan;
Shelby, Proteon;
Waterston, Robert

Publication type:

Article

A complete BAC-based physical map of the Arabidopsis thaliana genome.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 271, doi. 10.1038/10334

By:

Mozo, Teresa;
Dewar, Ken;
Dunn, Pat;
Ecker, Joseph R.;
Fischer, Sabine;
Kloska, Sebastian;
Lehrach, Hans;
Marra, Marco;
Martienssen, Robert;
Meier-Ewert, Sebastian;
Altmann, Thomas

Publication type:

Article

The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 276, doi. 10.1038/10338

By:

Calogero, Sabina;
Grassi, Fabio;
Aguzzi, Adriano;
Voigtländer, Till;
Ferrier, Pierre;
Ferrari, Simona;
Bianchi, Marco E.

Publication type:

Article

Systematic determination of genetic network architecture.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 281, doi. 10.1038/10343

By:

Tavazoie, Saeed;
Hughes, Jason D.;
Campbell, Michael J.;
Cho, Raymond J.;
Church, George M.

Publication type:

Article

Mutations in a Δ8-Δ7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 286, doi. 10.1038/10350

By:

Derry, Jonathan M.J.;
Gormally, Emmanuelle;
Means, Gary D.;
Zhao, Wei;
Meindl, Alfons;
Kelley, Richard I.;
Boyd, Yvonne;
Herman, Gail E.

Publication type:

Article

Mutations in the gene encoding 3β-hydroxysteroid-Δ8,Δ7-isomerase cause X-linked dominant Conradi-Hünermann syndrome.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 291, doi. 10.1038/10357

By:

Braverman, Nancy;
Lin, Paul;
Moebius, Fabian F.;
Obie, Cassandra;
Moser, Ann;
Glossmann, Hartmut;
Wilcox, William R.;
Rimoin, David L.;
Smith, Moyra;
Kratz, Lisa;
Kelley, Richard I.;
Valle, David

Publication type:

Article

Cryptorchidism in mice mutant for Insl3.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 295, doi. 10.1038/10364

By:

Nef, Serge;
Parada, Luis F.

Publication type:

Article

Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 300, doi. 10.1038/10372

By:

Labay, Valentina;
Raz, Tal;
Baron, Dana;
Mandel, Hanna;
Williams, Hawys;
Barrett, Timothy;
Szargel, Raymonde;
McDonald, Louise;
Shalata, Adel;
Nosaka, Kazuto;
Gregory, Simon;
Cohen, Nadine

Publication type:

Article

The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 305, doi. 10.1038/10379

By:

Fleming, Judith C.;
Tartaglini, Elena;
Steinkamp, Mara P.;
Schorderet, Daniel F.;
Cohen, Nadine;
Neufeld, Ellis J.

Publication type:

Article

Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.

Published in:

Nature Genetics, 1999, v. 22, n. 3, p. 309, doi. 10.1038/10385

By:

Diaz, George A.;
Banikazemi, Maryam;
Oishi, Kimihiko;
Desnick, Robert J.;
Gelb, Bruce D.

Publication type:

Article

Works matching IS 10614036 AND DT 1999 AND VI 22 AND IP 3

Array data go public.

Data analysis and integration: of steps and arrows.

Architectural regulations and Hmg1.

Clocks, criteria and critical genes.

The weed paves the way.

TOUCHINGbase.

The candidate spermatogenesis gene RBMY has a homologue on the human X chromosome.

RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene.

Absence of Cd36 mutation in the original spontaneously hypertensive rats with insulin resistance.

The flower, the gene, the brain and the creative process.

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

Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis.

Mutations in a gene encoding a new oxygen-regulated photoreceptor protein cause dominant retinitis pigmentosa.

Mutations in a novel retina-specific gene cause autosomal dominant retinitis pigmentosa.

Regulation of anterior/posterior patterning of the axial skeleton by growth/differentiation factor 11.

A map for sequence analysis of the Arabidopsis thaliana genome.

A complete BAC-based physical map of the Arabidopsis thaliana genome.

The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice.

Systematic determination of genetic network architecture.

Mutations in a Δ<sup>8</sup>-Δ<sup>7</sup> sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata.

Mutations in the gene encoding 3β-hydroxysteroid-Δ<sup>8</sup>,Δ<sup>7</sup>-isomerase cause X-linked dominant Conradi-Hünermann syndrome.

Cryptorchidism in mice mutant for Insl3.

Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness.

The gene mutated in thiamine-responsive anaemia with diabetes and deafness (TRMA) encodes a functional thiamine transporter.

Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.