Works matching IS 10614036 AND DT 1998 AND VI 19 AND IP 4

Results: 32

Casting light on focal adhesions.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 309, doi. 10.1038/1189

By:

Brugge, Joan S

Publication type:

Article

Connect.

Published in:: Nature Genetics, 1998, v. 19, n. 4, p. 305, doi. 10.1038/1182
Publication type:: Article

LISsen up!

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 307, doi. 10.1038/1186

By:

Walsh, Christopher A

Publication type:

Article

The three faces of the WS helicase.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 308, doi. 10.1038/1188

By:

Fry, Michael;
Loeb, Lawrence A

Publication type:

Article

Expanding the repertoire of RP genes.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 311, doi. 10.1038/1192

By:

Stone, Edwin M

Publication type:

Article

Stargazing nets new calcium channel subunit.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 313, doi. 10.1038/1194

By:

Puranam, Ram S;
McNamara, James O

Publication type:

Article

Alzheimer disease ? when and why?

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 314, doi. 10.1038/1196

By:

Price, Donald L;
Sisodia, Sangram S;
Borchelt, David R

Publication type:

Article

Sense and anti-sense ? The X-Files.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 316, doi. 10.1038/1199

By:

Goldman, Judy;
Pillinger, Michael

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 1998, v. 19, n. 4, p. 317
Publication type:: Article

Homozygotes carrying an autosomal dominant TIGR mutation do not manifest glaucoma.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 319, doi. 10.1038/1203

By:

Morissette, Jean;
Clépet, Christian;
Moisan, Steve;
Dubois, Stéphane;
Winstall, Eric;
Vermeeren, Diana;
Nguyen, Thai;
Polansky, Jon;
Côté, Gilles;
Anctil, Jean-Louis;
Amyot, Marcel;
Plante, Micheline;
Falardeau, Pierre;
Raymond, Vincent

Publication type:

Article

APOE genotype predicts when ? not whether ? one is predisposed to develop Alzheimer disease.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 321, doi. 10.1038/1206

By:

Meyer, Marion R;
Tschanz, JoAnn T;
Norton, Maria C;
Welsh-Bohmer, Kathleen A;
Steffens, David C;
Wyse, Bonita W;
Breitner, John C S

Publication type:

Article

Familial gastrointestinal stromal tumours with germline mutation of the KIT gene.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 323, doi. 10.1038/1209

By:

Nishida, Toshirou;
Hirota, Seiichi;
Taniguchi, Masahiko;
Hashimoto, Koji;
Isozaki, Koji;
Nakamura, Harumi;
Kanakura, Yuzuru;
Tanaka, Tomoyuki;
Takabayashi, Arimichi;
Matsuda, Hikaru;
Kitamura, Yukihiko

Publication type:

Article

Methylation analysis of the PWS/AS region does not support an enhancer-competition model.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 324, doi. 10.1038/1211

By:

Schumacher, Axel;
Buiting, Karin;
Zeschnigk, Michael;
Doerfler, Walter;
Horsthemke, Bernhard

Publication type:

Article

Reply to Schumacher et al.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 325, doi. 10.1038/1498

By:

Tilghman, Shirley;
Schoenherr, Chris

Publication type:

Article

Positional cloning of the gene for X-linked retinitis pigmentosa 2.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 327, doi. 10.1038/1214

By:

Schwahn, Uwe;
Lenzner, Steffen;
Dong, Juan;
Feil, Silke;
Hinzmann, Bernd;
van Duijnhoven, Gerard;
Kirschner, Renate;
Hemberger, Myriam;
Bergen, Arthur A.B.;
Rosenberg, Thomas;
Pinckers, Alfred J.L.G.;
Fundele, Reinald;
Rosenthal, André;
Cremers, Frans P.M.;
Ropers, H.-Hilger;
Berger, Wolfgang

Publication type:

Article

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 333, doi. 10.1038/1221

By:

Hirotsune, Shinji;
Fleck, Mark W.;
Gambello, Michael J.;
Bix, Gregory J.;
Chen, Amy;
Clark, Gary D.;
Ledbetter, David H.;
McBain, Chris J.;
Wynshaw-Boris, Anthony

Publication type:

Article

The mouse stargazer gene encodes a neuronal Ca2+-channel γ subunit.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 340, doi. 10.1038/1228

By:

Letts, Verity A.;
Felix, Ricardo;
Biddlecome, Gloria H.;
Arikkath, Jyothi;
Mahaffey, Connie L.;
Valenzuela, Alicia;
Bartlett, Frederick S.;
Mori, Yasuo;
Campbell, Kevin P.;
Frankel, Wayne N.

Publication type:

Article

Pten is essential for embryonic development and tumour suppression.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 348, doi. 10.1038/1235

By:

Cristofano, Antonio D.;
Pesce, Barbara;
Cordon-Cardo, Carlos;
Pandolfi, Pier P.

Publication type:

Article

A mouse model of Greig cephalapolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene.

Published in:

1998

By:

Hui, Chi-chung;
Joyner, Alexandra L.

Publication type:

Erratum

Cardiovascular anomaly, impaired actin bundling and resistance to Src-induced transformation in mice lacking p130Cas.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 361, doi. 10.1038/1246

By:

Honda, Hiroaki;
Oda, Hideaki;
Nakamoto, Tetsuya;
Honda, Zen-ichiro;
Sakai, Ryuichi;
Suzuki, Takahiro;
Saito, Toshiki;
Nakamura, Kenji;
Nakao, Kazuki;
Ishikawa, Takatoshi;
Katsuki, Motoya;
Yazaki, Yoshio;
Hirai, Hisamaru

Publication type:

Article

Replication focus-forming activity 1 and the Werner syndrome gene product.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 375, doi. 10.1038/1263

By:

Yan, Hong;
Chen, Chin-Yi;
Kobayashi, Ryuji;
Newport, John

Publication type:

Article

A retinoblastoma-binding protein that affects cell-cycle control and confers transforming ability.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 371, doi. 10.1038/1258

By:

Woitach, Joseph T.;
Zhang, Minghuang;
Niu, Chien-Hua;
Thorgeirsson, Snorri S.

Publication type:

Article

Missense mutations in desmin associated with familial cardiac and skeletal myopathy.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 402, doi. 10.1038/1300

By:

Goldfarb, Lev G.;
Park, Kye-Yoon;
Cervenáková, Larisa;
Gorokhova, Svetlana;
Lee, Hee-Suk;
Vasconcelos, Olavo;
Nagle, James W.;
Semino-Mora, Christina;
Sivakumar, Kumaraswamy;
Dalakas, Marinos C.

Publication type:

Article

Alpha-2 macroglobulin is genetically associated with Alzheimer disease.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 357, doi. 10.1038/1243

By:

Blacker, Deborah;
Wilcox, Marsha A.;
Laird, Nan M.;
Rodes, Linda;
Horvath, Steven M.;
Go, Rodney C.P.;
Perry, Rodney;
Watson, Bracie;
Bassett, Susan S.;
McInnis, Melvin G.;
Albert, Marilyn S.;
Hyman, Bradley T.;
Tanzi, Rudolph E.

Publication type:

Article

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.

Published in:

1998

By:

Brais et al., Bernard

Publication type:

Erratum

Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 366, doi. 10.1038/1252

By:

Wallace, Robyn H.;
Wang, Dao W.;
Singh, Rita;
Scheffer, Ingrid E.;
George, Alfred L.;
Phillips, Hilary A.;
Saar, Kathrin;
Reis, Andre;
Johnson, Eric W.;
Sutherland, Grant R.;
Berkovic, Samuel F.;
Mulley, John C.

Publication type:

Article

A mouse model for hereditary thyroid dysgenesis and cleft palate.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 395, doi. 10.1038/1289

By:

De Felice, Mario;
Ovitt, Catherine;
Biffali, Elio;
Rodriguez-Mallon, Alina;
Arra, Claudio;
Anastassiadis, Konstantinos;
Macchia, Paolo Emidio;
Mattei, Marie-Genevieve;
Mariano, Angela;
Schöler, Hans;
Macchia, Vincenzo;
Di Lauro, Roberto

Publication type:

Article

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 399, doi. 10.1038/1294

By:

Clifton-Bligh, Roderick J.;
Wentworth, John M.;
Heinz, Peter;
Crisp, Michele S.;
John, Rhys;
Lazarus, John H.;
Ludgate, Marian;
Chatterjee, V. Krishna

Publication type:

Article

Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 379, doi. 10.1038/1270

By:

Korinek, Vladimir;
Barker, Nick;
Moerer, Petra;
van Donselaar, Elly;
Huls, Gerwin;
Peters, Peter J.;
Clevers, Hans

Publication type:

Article

Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 384, doi. 10.1038/1277

By:

Shimodaira, Hideki;
Filosi, Nicole;
Shibata, Hiroyuki;
Suzuki, Takao;
Radice, Paolo;
Kanamaru, Ryunosuke;
Friend, Stephen H.;
Kolodner, Richard D.;
Ishioka, Chikashi

Publication type:

Article

Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice.

Published in:

Nature Genetics, 1998, v. 19, n. 4, p. 390, doi. 10.1038/1284

By:

Street, Valerie A.;
McKee-Johnson, Jennifer W.;
Fonseca, Rosalia C.;
Tempel, Bruce L.;
Noben-Trauth, Konrad

Publication type:

Article

Bleomycin hydrolase is associated with risk of sporadic Alzheimer's disease.

Published in:

1998

By:

Montoya et al., Susana E.

Publication type:

Erratum

Works matching IS 10614036 AND DT 1998 AND VI 19 AND IP 4

Casting light on focal adhesions.

Connect.

LISsen up!

The three faces of the WS helicase.

Expanding the repertoire of RP genes.

Stargazing nets new calcium channel subunit.

Alzheimer disease ? when and why?

Sense and anti-sense ? The X-Files.

TOUCHINGbase.

Homozygotes carrying an autosomal dominant TIGR mutation do not manifest glaucoma.

APOE genotype predicts when ? not whether ? one is predisposed to develop Alzheimer disease.

Familial gastrointestinal stromal tumours with germline mutation of the KIT gene.

Methylation analysis of the PWS/AS region does not support an enhancer-competition model.

Reply to Schumacher et al.

Positional cloning of the gene for X-linked retinitis pigmentosa 2.

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality.

The mouse stargazer gene encodes a neuronal Ca<sup>2+</sup>-channel γ subunit.

Pten is essential for embryonic development and tumour suppression.

A mouse model of Greig cephalapolysyndactyly syndrome: the extra-toes<sup>J</sup> mutation contains an intragenic deletion of the Gli3 gene.

Cardiovascular anomaly, impaired actin bundling and resistance to Src-induced transformation in mice lacking p130<sup>Cas</sup>.

Replication focus-forming activity 1 and the Werner syndrome gene product.

A retinoblastoma-binding protein that affects cell-cycle control and confers transforming ability.

Missense mutations in desmin associated with familial cardiac and skeletal myopathy.

Alpha-2 macroglobulin is genetically associated with Alzheimer disease.

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.

Febrile seizures and generalized epilepsy associated with a mutation in the Na<sup>+</sup>-channel ß1 subunit gene SCN1B.

A mouse model for hereditary thyroid dysgenesis and cleft palate.

Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia.

Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4.

Functional analysis of human MLH1 mutations in Saccharomyces cerevisiae.

Mutations in a plasma membrane Ca<sup>2+</sup>-ATPase gene cause deafness in deafwaddler mice.

Bleomycin hydrolase is associated with risk of sporadic Alzheimer's disease.