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

Results: 32

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
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
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
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
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
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 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
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
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
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
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
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
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.
Published in:
1998
By:
- Brais et al., Bernard
Publication type:
Erratum
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

Connect.

LISsen up!

The three faces of the WS helicase.

Casting light on focal adhesions.

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.

Alpha-2 macroglobulin is genetically associated with Alzheimer disease.

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

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

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

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

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.

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.

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

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

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

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