Works matching IS 10614036 AND DT 2004 AND VI 36 AND IP 4

Results: 31

Intersecting paths to cancer.

Published in:: 2004
Publication type:: Editorial

Marjorie A. Asmussen 1949-2004.

Published in:

2004

By:

Avise, John C.

Publication type:

Obituary

A rich biodiversity of explanations.

Published in:

2004

By:

Harris, Lynne M.

Publication type:

Book Review

The postgenomic shipwright.

Published in:

2004

By:

Dietrich, Michael R.

Publication type:

Book Review

Wip-ing out cancer.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 319, doi. 10.1038/ng0404-319

By:

Bernards, René

Publication type:

Article

Shutting down Wnt signal-activated cancer.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 320, doi. 10.1038/ng0404-320

By:

Taketo, M. Mark

Publication type:

Article

USF1 on trial.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 322, doi. 10.1038/ng0404-322

By:

Shoulders, Carol C.

Publication type:

Article

Phenotype matters.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 323, doi. 10.1038/ng0404-323

By:

Biesecker, Leslie G.

Publication type:

Article

A plethora of sites.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 325, doi. 10.1038/ng0404-325

By:

Euskirchen, Ghia;
Snyder, Michael

Publication type:

Article

Touchingbase.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 327, doi. 10.1038/ng0404-327

By:

Axton, Myles;
Packer, Alan;
Stebbins, Michael;
Vogan, Kyle

Publication type:

Article

Research Notes.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 329, doi. 10.1038/ng0404-329

By:

Axton, Myles;
Packer, Alan;
Stebbins, Michael;
Vogan, Kyle

Publication type:

Article

Erratum: Intense and highly localized gene conversion activity in human meiotic crossover hot spots.

Published in:

2004

By:

Jeffreys, A J;
May, C A

Publication type:

Correction Notice

Corrigendum: Gene expression-based high-throughput screening (GE-HTS) and application to leukemia differentiation.

Published in:

2004

By:

Stegmaier, K;
Ross, K N;
Colavito, S A;
O'Malley, S;
Stockwell, B R;
Golub, T R

Publication type:

Correction Notice

Corrigendum: The hyh mutation uncovers roles for aSnap in apical protein localization and control of neural cell fate.

Published in:

2004

By:

Chae, T H;
Kim, S;
Marz, K E;
Hanson, P I;
Walsh, C A

Publication type:

Correction Notice

Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK-mediated activation of the p16Ink4a-p19Arf pathway.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 343, doi. 10.1038/ng1317

By:

Bulavin, Dmitry V.;
Phillips, Crissy;
Nannenga, Bonnie;
Timofeev, Oleg;
Donehower, Larry A.;
Anderson, Carl W.;
Appella, Ettore;
Fornace Jr., Albert J.

Publication type:

Article

Rb regulates proliferation and rod photoreceptor development in the mouse retina.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 351, doi. 10.1038/ng1318

By:

Jiakun Zhang, Stephen P.;
Gray, Jonathan;
Lizhao Wu;
Leone, Gustavo;
Rowan, Sheldon;
Cepko, Constance L.;
Xuemei Zhu;
Craft, Cheryl M.;
Dyer, Michael A.

Publication type:

Article

Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 405, doi. 10.1038/ng1319

By:

King, Lily M.;
Morgan, Timothy;
Sebald, Eiman T.;
Bertolotto, Cristina;
Wachsmann-Hogiu, Sebastian;
Acuna, Dora;
Shapiro, Sandor S.;
Takafuta, Toshiro;
Aftimos, Salim;
Chong Ae Kim;
Firth, Helen;
Steiner, Carlos E.;
Cormier-Daire, Valerie;
Superti-Furga, Andrea;
Bonafe, Luisa;
Graham Jr, John M.;
Grix, Arthur;
Bacino, Carlos A.;
Allanson, Judith;
Bialer, Martin G.

Publication type:

Article

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 371, doi. 10.1038/ng1320

By:

Pajukanta, Päivi;
Lilja, Heidi E.;
Sinsheimer, Janet S.;
Cantor, Rita M.;
Gentile, Massimiliano;
Lusis, Aldons J.;
Duan, Xiaoqun Joyce;
Soro-Paavonen, Aino;
Naukkarinen, Jussi;
Saarela, Janna;
Laakso, Markku;
Ehnholm, Christian;
Taskinen, Marja-Riitta;
Peltonen, Leena

Publication type:

Article

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 411, doi. 10.1038/ng1321

By:

Ng, David;
Thakker, Nalin;
Corcoran, Connie M.;
Donnai, Dian;
Perveen, Rahat;
Schneider, Adele;
Hadley, Donald W.;
Tifft, Cynthia;
Zhang, Liqun;
Wilkie, Andrew O. M.;
van der Smagt, Jasper J.;
Gorlin, Robert J.;
Burgess, Shawn M.;
Bardwell, Vivian J.;
Black, Graeme C. M.;
Biesecker, Leslie G.

Publication type:

Article

Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 361, doi. 10.1038/ng1322

By:

Inoue, Ken;
Khajavi, Mehrdad;
Ohyama, Tomoko;
Hirabayashi, Shin-ichi;
Wilson, John;
Reggin, James D.;
Mancias, Pedro;
Butler, Ian J.;
Wilkinson, Miles F.;
Wegner, Michael;
Lupski, James R.

Publication type:

Article

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 337, doi. 10.1038/ng1323

By:

Bottini, Nunzio Bottini;
Musumeci, Lucia;
Alonso, Andres;
Rahmouni, Souad;
Nika, Konstantina;
Rostamkhani, Masoud;
MacMurray, James;
Meloni, Gian Franco;
Lucarelli, Paola;
Pellecchia, Maurizio;
Eisenbarth, George S.;
Comings, David;
Mustelin, Tomas

Publication type:

Article

Pervasive joint influence of epistasis and plasticity on mutational effects in Escherichia coli.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 423, doi. 10.1038/ng1324

By:

Lenski, Richard E.;
Remold, Susanna K.

Publication type:

Article

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 400, doi. 10.1038/ng1325

By:

Gissen, Paul;
Johnson, Colin A.;
Morgan, Neil V.;
Stapelbroek, Janneke M.;
Forshew, Tim;
Cooper, Wendy N.;
McKiernan, Patrick J.;
Klomp, Leo W. J.;
Morris, Andrew A. M.;
Wraith, James E.;
McClean, Patricia;
Lynch, Sally A.;
Thompson, Richard J.;
Lo, Bryan;
Quarrell, Oliver W.;
Di Rocco, Maja;
Trembath, Richard C.;
Mandel, Hanna;
Wali, S.;
Karet, Fiona E.

Publication type:

Article

Limited number of patrilines in horse domestication.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 335, doi. 10.1038/ng1326

By:

Lindgren, Gabriella;
Backström, Niclas;
Swinburne, June;
Hellborg, Linda;
Einarsson, Annika;
Sandberg, Kaj;
Cothran, Gus;
Vilà, Carles;
Binns, Matthew;
Ellegren, Hans

Publication type:

Article

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 339, doi. 10.1038/ng1327

By:

Mnatzakanian, Gevork N.;
Lohi, Hannes;
Munteanu, Iulia;
Alfred, Simon E.;
Yamada, Takahiro;
MacLeod, Patrick J. M.;
Jones, Julie R.;
Scherer, Stephen W.;
Schanen, N. Carolyn;
Friez, Michael J.;
Vincent, John B.;
Minassian, Berge A.

Publication type:

Article

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 382, doi. 10.1038/ng1329

By:

Bienengraeber, Martin;
Olson, Timothy M.;
Selivanov, Vitaliy A.;
Kathmann, Eva C.;
O'Cochlain, Fearghas;
Gao, Fan;
Karger, Amy B.;
Ballew, Jeffrey D.;
Hodgson, Denice M.;
Zingman, Leonid V.;
Pang, Yuan-Ping;
Alekseev, Alexey E.;
Terzic, Andre

Publication type:

Article

Allele-specific repression of lymphotoxin-a by activated B cell factor-1.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 394, doi. 10.1038/ng1331

By:

Knight, Julian C.;
Keating, Brendan J.;
Kwiatkowski, Dominic P.

Publication type:

Article

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 377, doi. 10.1038/ng1332

By:

Watts, Giles D. J.;
Wymer, Jill;
Kovach, Margaret J.;
Mehta, Sarju G.;
Mumm, Steven;
Darvish, Daniel;
Pestronk, Alan;
Whyte, Michael P.;
Kimonis, Virginia E.

Publication type:

Article

Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 331, doi. 10.1038/ng1335

By:

Johansson, Bertil;
Mertens, Fredrik;
Mitelman, Felix

Publication type:

Article

Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 417, doi. 10.1038/ng1330

By:

Suzuki, Hiromu;
Watkins, D. Neil;
Jair, Kam-Wing;
Schuebel, Kornel E.;
Markowitz, Sanford D.;
Chen, Wei Dong;
Pretlow, Theresa P.;
Yang, Bin;
Akiyama, Yoshimitsu;
van Engeland, Manon;
Toyota, Minoru;
Tokino, Takashi;
Hinoda, Yuji;
Imai, Kohzoh;
Herman, James G.;
Baylin, Stephen B.

Publication type:

Article

Assessing the impact of population stratification on genetic association studies.

Published in:

Nature Genetics, 2004, v. 36, n. 4, p. 388, doi. 10.1038/ng1333

By:

Freedman, Matthew L.;
Reich, David;
Penney, Kathryn L.;
McDonald, Gavin J.;
Mignault, Andre A.;
Patterson, Nick;
Gabriel, Stacey B.;
Topol, Eric J.;
Smoller, Jordan W.;
Pato, Carlos N.;
Pato, Michele T.;
Petryshen, Tracey L.;
Kolonel, Laurence N.;
Lander, Eric S.;
Sklar, Pamela;
Henderson, Brian;
Hirschhorn, Joel N.;
Altshuler, David

Publication type:

Article

Works matching IS 10614036 AND DT 2004 AND VI 36 AND IP 4

Intersecting paths to cancer.

Marjorie A. Asmussen 1949-2004.

A rich biodiversity of explanations.

The postgenomic shipwright.

Wip-ing out cancer.

Shutting down Wnt signal-activated cancer.

USF1 on trial.

Phenotype matters.

A plethora of sites.

Touchingbase.

Research Notes.

Erratum: Intense and highly localized gene conversion activity in human meiotic crossover hot spots.

Corrigendum: Gene expression-based high-throughput screening (GE-HTS) and application to leukemia differentiation.

Corrigendum: The hyh mutation uncovers roles for aSnap in apical protein localization and control of neural cell fate.

Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK-mediated activation of the p16<sup>Ink4a</sup>-p19<sup>Arf</sup> pathway.

Rb regulates proliferation and rod photoreceptor development in the mouse retina.

Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR.

Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations.

A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes.

Pervasive joint influence of epistasis and plasticity on mutational effects in Escherichia coli.

Mutations in VPS33B, encoding a regulator of SNARE-dependent membrane fusion, cause arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome.

Limited number of patrilines in horse domestication.

A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome.

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic K<sub>ATP</sub> channel gating.

Allele-specific repression of lymphotoxin-a by activated B cell factor-1.

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein.

Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer.

Epigenetic inactivation of SFRP genes allows constitutive WNT signaling in colorectal cancer.

Assessing the impact of population stratification on genetic association studies.