Works matching IS 10614036 AND DT 1998 AND VI 19 AND IP 3

Results: 32

Privacy matters.

Published in:: 1998
Publication type:: Editorial

Weighing in on diabetes risk.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 209, doi. 10.1038/876

By:

McCarthy, Mark

Publication type:

Article

Counting on Xist.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 211, doi. 10.1038/878

By:

Carrel, Laura;
Willard, Huntington F.

Publication type:

Article

Sometimes it's hot, sometimes it's not.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 213, doi. 10.1038/881

By:

Lernmark, Åke;
Ott, Jurg

Publication type:

Article

Nuclear power and mitochondrial disease.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 214, doi. 10.1038/883

By:

DiMauro, Salvatore;
Schon, Eric A.

Publication type:

Article

It's raining SNPs, hallelujah?

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 216, doi. 10.1038/885

By:

Chakravarti, Aravinda

Publication type:

Article

Touching Base.

Published in:: Nature Genetics, 1998, v. 19, n. 3, p. 218, doi. 10.1038/888
Publication type:: Article

Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 219, doi. 10.1038/890

By:

Okano, Masaki;
Xie, Shaoping;
Li, En

Publication type:

Article

Non-invasive sexing of preimplantation stage mammalian embryos.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 220, doi. 10.1038/893

By:

Hadjantonakis, Anna-Katerina;
Gertsenstein, Marina;
Ikawa, Masahito;
Okabe, Masaru;
Nagy, Andras

Publication type:

Article

Human genome annotation ? a possible role for HUGO?

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 222, doi. 10.1038/896

By:

Little, Peter

Publication type:

Article

PTEN and inherited hamartoma-cancer syndromes.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 223, doi. 10.1038/897

By:

Eng, Charis;
Peacocke, Monica

Publication type:

Article

Mutation detection and single-molecule counting using isothermal rolling-circle amplification.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 225, doi. 10.1038/898

By:

Lizardi, Paul M.;
Huang, Xiaohua;
Zhu, Zhengrong;
Bray-Ward, Patricia;
Thomas, David C.;
Ward, David C.

Publication type:

Article

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 233, doi. 10.1038/907

By:

Nickerson, Deborah A.;
Taylor, Scott L.;
Weiss, Kenneth M.;
Clark, Andrew G.;
Hutchinson, Richard G.;
Stengård, Jari;
Salomaa, Veikko;
Vartiainen, Erkki;
Boerwinkle, Eric;
Sing, Charles F.

Publication type:

Article

Identification of the gene responsible for Best macular dystrophy.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 241, doi. 10.1038/915

By:

Petrukhin, Konstantin;
Koisti, Markus J.;
Bakall, Benjamin;
Li, Wen;
Xie, Guochun;
Marknell, Towa;
Sandgren, Ola;
Forsman, Kristina;
Holmgren, Gösta;
Andreasson, Sten;
Vujic, Mihailo;
Bergen, Arthur A. B.;
McGarty-Dugan, Valarie;
Figueroa, David;
Austin, Christopher P.;
Metzker, Michael L.;
Caskey, C.Thomas;
Wadelius, Claes

Publication type:

Article

Role of the region 3′ to Xist exon 6 in the counting process of X-chromosome inactivation.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 249, doi. 10.1038/924

By:

Clerc, Philippe;
Avner, Philip

Publication type:

Article

BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 254, doi. 10.1038/930

By:

Anderson, Stephen F.;
Schlegel, Brian P.;
Nakajima, Toshihiro;
Wolpin, Eric S.;
Parvin, Jeffrey D.

Publication type:

Article

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 257, doi. 10.1038/935

By:

Kohl, Susanne;
Marx, Tim;
Giddings, Ian;
Jägle, Herbert;
Jacobson, Samuel G.;
Apfelstedt-Sylla, Eckhart;
Zrenner, Eberhart;
Sharpe, Lindsay T.;
Wissinger, Bernd

Publication type:

Article

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 260, doi. 10.1038/940

By:

Strom, Tim M.;
Nyakatura, Gerald;
Apfelstedt-Sylla, Eckart;
Hellebrand, Heide;
Lorenz, Birgit;
Weber, Bernhard H. F.;
Wutz, Krisztina;
Gutwillinger, Nadja;
Rüther, Klaus;
Drescher, Bernd;
Sauer, Christian;
Zrenner, Eberhart;
Meitinger, Thomas;
Rosenthal, Andre;
Meindl, Alfons

Publication type:

Article

Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 264, doi. 10.1038/947

By:

Bech-Hansen, N. Torben;
Naylor, Margaret J.;
Maybaum, Tracy A.;
Pearce, William G.;
Koop, Ben;
Fishman, Gerald A.;
Mets, Marilyn;
Musarella, Maria A.;
Boycott, Kym M.

Publication type:

Article

Mutations in the glucokinase gene of the fetus result in reduced birth weight.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 268, doi. 10.1038/953

By:

Hattersley, Andrew T.;
Beards, Frances;
Ballantyne, Elizabeth;
Appleton, Maggie;
Harvey, Rod;
Ellard, Sian

Publication type:

Article

Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 271, doi. 10.1038/956

By:

Okawa, Akihiko;
Nakamura, Isao;
Goto, Sumio;
Moriya, Hideshige;
Nakamura, Yusuke;
Ikegawa, Shiro

Publication type:

Article

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 274, doi. 10.1038/961

By:

Kusumi, Kenro;
Sun, Eileen;
Kerrebrock, Anne W.;
Bronson, Roderick T.;
Chi, Dow-Chung;
Bulotsky, Monique;
Spencer, Jessica B.;
Birren, Bruce W.;
Frankel, Wayne N.;
Lander, Eric S.

Publication type:

Article

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 279, doi. 10.1038/966

By:

Geller, David S.;
Rodriguez-Soriano, Juan;
Boado, Alfredo V.;
Schifter, Søren;
Bayer, Milan;
Chang, Sue S.;
Lifton, Richard P.

Publication type:

Article

Renal and intestinal absorptive defects in mice lacking the NHE3 Na+/H+ exchanger.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 282, doi. 10.1038/969

By:

Schultheis, Patrick J.;
Clarke, Lane L.;
Meneton, Pierre;
Miller, Marian L.;
Soleimani, Manoocher;
Gawenis, Lara R.;
Riddle, Tara M.;
Duffy, John J.;
Doetschman, Thomas;
Wang, Tong;
Giebisch, Gerhard;
Aronson, Peter S.;
Lorenz, John N.;
Shull, Gary E.

Publication type:

Article

CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 286, doi. 10.1038/975

By:

Savukoski, Minna;
Klockars, Tuomas;
Holmberg, Ville;
Santavuori, Pirkko;
Lander, Eric S.;
Peltonen, Leena

Publication type:

Article

Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 289, doi. 10.1038/980

By:

Abdel-Majid, Raja M.;
Leong, Wey L.;
Schalkwyk, Leonard C.;
Smallman, Donald S.;
Wong, Scott T.;
Storm, Daniel R.;
Fine, Alan;
Dobson, Melanie J.;
Guernsey, Duane L.;
Neumann, Paul E.

Publication type:

Article

A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 292, doi. 10.1038/985

By:

Concannon, Patrick;
Gogolin-Ewens, Kathryn J.;
Hinds, David A.;
Wapelhorst, Beth;
Morrison, V. Annem;
Stirling, Brigid;
Mitra, Mirna;
Farmer, Jennifer;
Williams, Sloan R.;
Cox, Nancy J.;
Bell, Graeme I.;
Risch, Neil;
Spielman, Richard S.

Publication type:

Article

A search for type 1 diabetes susceptibility genes in families from the United Kingdom.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 297, doi. 10.1038/991

By:

Mein, CharlesA.;
Esposito, Laura;
Dunn, Michael G.;
Johnson, Gillian C. L.;
Timms, Andrew E.;
Goy, Juliet V.;
Smith, Annabel N.;
Sebag-Montefiore, Liam;
Merriman, Marilyn E.;
Wilson, Amanda J.;
Pritchard, Lynn E.;
Cucca, Francesco;
Barnett, Anthony H.;
Bain, Stephen C.;
Todd, John A.

Publication type:

Article

A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients.

Published in:

Nature Genetics, 1998, v. 19, n. 3, p. 301, doi. 10.1038/995

By:

Cucca, Francesco;
Goy, Juliet V.;
Kawaguchi, Yoshihiko;
Esposito, Laura;
Merriman, Marilyn E.;
Wilson, Amanda J.;
Cordell, Heather J.;
Bain, Stephen C.;
Todd, John A.

Publication type:

Article

A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

Published in:

1998

By:

Reiter, Lawrence;
Murakami, Tatsufumi;
Koeuth, Thearith;
Pentao, Liu;
Muzny, Donna;
Gibbs, Richard;
Lupski, James

Publication type:

Erratum

Vertebrate genome evolution and the zebrafish gene map.

Published in:

1998

By:

Postlethwait, John;
Yan, Yi-Lin;
Gates, Michael;
Horne, Sally;
Amores, Angel;
Brownlie, Alison;
Donovan, Adriana;
Egan, Elizabeth;
Force, Allan;
Gong, Zhiyuan;
Goutel, Carole;
Fritz, Andreas;
Kelsh, Robert;
Knapik, Ela;
Liao, Eric;
Paw, Barry;
Ransom, David;
Singer, Amy;
Thomson, Margaret

Publication type:

Erratum

Mutations in GDI1 are responsible for X-linked non-specific mental retardation.

Published in:

1998

By:

D'Adamo, Patrizia;
Menegon, Andrea;
Lo Nigro, Cristiana;
Grasso, Marina;
Gulisano, Massimo;
Tamanini, Filippo;
Bienvenu, Thierry;
Gedeon, Agi;
Oostra, Ben;
Wu, Shih-Kwang;
Tandon, Anurag;
Valtorta, Flavia;
Balch, William;
Chelly, Jamel;
Toniolo, Daniela

Publication type:

Erratum

Works matching IS 10614036 AND DT 1998 AND VI 19 AND IP 3

Privacy matters.

Weighing in on diabetes risk.

Counting on Xist.

Sometimes it's hot, sometimes it's not.

Nuclear power and mitochondrial disease.

It's raining SNPs, hallelujah?

Touching Base.

Cloning and characterization of a family of novel mammalian DNA (cytosine-5) methyltransferases.

Non-invasive sexing of preimplantation stage mammalian embryos.

Human genome annotation ? a possible role for HUGO?

PTEN and inherited hamartoma-cancer syndromes.

Mutation detection and single-molecule counting using isothermal rolling-circle amplification.

DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.

Identification of the gene responsible for Best macular dystrophy.

Role of the region 3′ to Xist exon 6 in the counting process of X-chromosome inactivation.

BRCA1 protein is linked to the RNA polymerase II holoenzyme complex via RNA helicase A.

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel.

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.

Loss-of-function mutations in a calcium-channel α<sub>1</sub>-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.

Mutations in the glucokinase gene of the fetus result in reduced birth weight.

Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine.

The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries.

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I.

Renal and intestinal absorptive defects in mice lacking the NHE3 Na<sup>+</sup>/H<sup>+</sup> exchanger.

CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.

Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex.

A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus.

A search for type 1 diabetes susceptibility genes in families from the United Kingdom.

A male-female bias in type 1 diabetes and linkage to chromosome Xp in MHC HLA-DR3-positive patients.

A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element.

Vertebrate genome evolution and the zebrafish gene map.

Mutations in GDI1 are responsible for X-linked non-specific mental retardation.