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

Results: 31

A rich biodiversity of explanations.
Published in:
2004
By:
- Harris, Lynne M.
Publication type:
Book Review
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
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
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
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
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
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
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
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
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

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

A rich biodiversity of explanations.

Intersecting paths to cancer.

Marjorie A. Asmussen 1949-2004.

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.

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

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.

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.

Assessing the impact of population stratification on genetic association studies.

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.

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

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