Works matching IS 10614036 AND DT 2001 AND VI 29 AND IP 3

Results: 31

Genomics and future biological weapons: the need for preventive action by the biomedical community.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 253, doi. 10.1038/ng763

By:

Fraser, Claire M.;
Dando, Malcolm R.

Publication type:

Article

Pharmacogenetics: more than skin deep.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 247, doi. 10.1038/ng1101-247

By:

McLeod, Howard L.

Publication type:

Article

Genes, drugs and race.

Published in:: 2001
Publication type:: Editorial

A fever gene comes in from the cold.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 241, doi. 10.1038/ng1101-241

By:

Kastner, Daniel L.;
O'Shea, John J.

Publication type:

Article

The fragility of fertility.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 243, doi. 10.1038/ng1101-243

By:

Yen, Pauline

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 2001, v. 29, n. 3, p. 249
Publication type:: Article

The replication requirement.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 244, doi. 10.1038/ng1101-244

By:

Vieland, Veronica J.

Publication type:

Article

High Oct-ane fuel powers the stem cell.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 246, doi. 10.1038/ng1101-246

By:

Donovan, Peter J.

Publication type:

Article

Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle?Wells syndrome.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 301, doi. 10.1038/ng756

By:

Hoffman, Hal M.;
Mueller, James L.;
Broide, David H.;
Wanderer, Alan A.;
Kolodner, Richard D.

Publication type:

Article

The Church of Charles Darwin (without Darwin).

Published in:

2001

By:

Balaban, Evan

Publication type:

Book Review

An Flp indicator mouse expressing alkaline phosphatase from the ROSA26 locus.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 257, doi. 10.1038/ng1101-257

By:

Awatramani, Rajeshwar;
Soriano, Philippe;
Mai, Jia Jia;
Dymecki, Susan

Publication type:

Article

Erratum: TGF-β signaling in tumor suppression and cancer progression.

Published in:

2001

By:

Derynck, R.;
Akhurst, R.J.;
Balmain, A.

Publication type:

Correction Notice

Erratum: A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2.

Published in:

2001

By:

Avner, P.;
Bruls, T.;
Poras, I.;
Eley, L.;
Gas, S.;
Ruiz, P.;
Wiles, M.V.;
Sousa-Nunes, R.;
Kettleborough, R.;
Rana, A.;
Morrisette, J.;
Bentley, L.;
Goldsworthy, M.;
Haynes, A.;
Herbert, E.;
Southam, L.;
Lehrach, H.;
Weissenbach, J.;
Manenti, G.

Publication type:

Erratum

Erratum: The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Published in:

2001

By:

Yang, Y.;
Hentati, A.;
Deng, H.-X.;
Dabbagh, O.;
Sasaki, T.;
Hirano, M.;
Hung, W.-Y.;
Ouahchi, K.;
Yan, J.;
Azim, A.C.;
Cole, N.;
Gascon, G.;
Yagmour, A.;
Ben-Hamida, M.;
Pericak-Vance, M.;
Hentati, F.;
Siddique, T.

Publication type:

Erratum

Erratum: A radiation hybrid transcript map of the mouse genome.

Published in:

2001

By:

Hadano, S.;
Hand, C.K.;
Osuga, H.;
Yanagisawa, Y.;
Otomo, A.;
Devon, R.S.;
Miyamoto, N.;
Showguchi-Miyata, J.;
Okada, Y.;
Singaraja, R.;
Figlewicz, D.A.;
Kwiatkowski, T.;
Hosler, B.A.;
Sagie, T.;
Skaug, J.;
Nasir, J.;
Brown Jr, R.H.;
Scherer, S.W.;
Rouleau, G.A.

Publication type:

Correction Notice

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 345, doi. 10.1038/ng726

By:

Verpy, Elisabeth;
Masmoudi, Saber;
Zwaenepoel, Ingrid;
Leibovici, Michel;
Hutchin, Tim P.;
Del Castillo, Ignacio;
Nouaille, Sylvie;
Blanchard, Stéphane;
Lainé, Sophie;
Popot, Jean-Luc;
Moreno, Felipe;
Mueller, Robert F.;
Petit, Christine

Publication type:

Article

Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 315, doi. 10.1038/ng744

By:

Nakano, Motoi;
Yamada, Koki;
Fain, Jennifer;
Sener, Emin C.;
Selleck, Carol J.;
Awad, Abdulaziz H.;
Zwaan, Johan;
Mullaney, Paul B.;
Bosley, Thomas M.;
Engle, Elizabeth C.

Publication type:

Article

Mutant protein in Huntington disease is resistant to proteolysis in affected brain.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 270, doi. 10.1038/ng745

By:

Dyer, Roy B.;
McMurray, Cynthia T.

Publication type:

Article

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 337, doi. 10.1038/ng746

By:

Mandel, Hanna;
Szargel, Raymonde;
Labay, Valentina;
Elpeleg, Orly;
Saada, Ann;
Shalata, Adel;
Anbinder, Yefim;
Berkowitz, Drora;
Hartman, Corina;
Barak, Mila;
Eriksson, Staffan;
Cohen, Nadine

Publication type:

Article

Replication validity of genetic association studies.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 306, doi. 10.1038/ng749

By:

Ioannidis, John P.A.;
Ntzani, Evangelia E.;
Trikalinos, Thomas A.;
Contopoulos-Ioannidis, Despina G.

Publication type:

Article

Epigenetic silencing of CD4 in T cells committed to the cytotoxic lineage.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 332, doi. 10.1038/ng750

By:

Zou, Yong-Rui;
Sunshine, Mary-Jean;
Taniuchi, Ichiro;
Hatam, Farah;
Killeen, Nigel;
Littman, Dan R.

Publication type:

Article

Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 342, doi. 10.1038/ng751

By:

Saada, Ann;
Shaag, Avraham;
Mandel, Hanna;
Nevo, Yoram;
Eriksson, Staffan;
Elpeleg, Orly

Publication type:

Article

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 310

By:

Birkenhäger, Ralf;
Otto, Edgar;
Schürmann, Maria J.;
Vollmer, Martin;
Ruf, Eva-Maria;
Maier-Lutz, Irina;
Beekmann, Frank;
Fekete, Andrea;
Omran, Heymut;
Feldmann, Delphine;
Milford, David V.;
Jeck, Nicola;
Konrad, Martin;
Landau, Daniel;
Knoers, Nine V.A.M.;
Antignac, Corinne;
Sudbrak, Ralf;
Kispert, Andreas;
Hildebrandt, Friedhelm

Publication type:

Article

A 1.5 million?base pair inversion polymorphism in families with Williams-Beuren syndrome.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 321, doi. 10.1038/ng753

By:

Osborne, Lucy R.;
Li, Martin;
Pober, Barbara;
Chitayat, David;
Bodurtha, Joann;
Mandel, Ariane;
Costa, Teresa;
Grebe, Theresa;
Cox, Sarah;
Tsui, Lap-Chee;
Scherer, Stephen W.

Publication type:

Article

Assembly of microarrays for genome-wide measurement of DNA copy number.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 263, doi. 10.1038/ng754

By:

Snijders, Antoine M.;
Nowak, Norma;
Segraves, Richard;
Blackwood, Stephanie;
Brown, Nils;
Conroy, Jeffrey;
Hamilton, Greg;
Hindle, Anna Katherine;
Huey, Bing;
Kimura, Karen;
Law, Sindy;
Myambo, Ken;
Palmer, Joel;
Ylstra, Bauke;
Yue, Jingzhu Pearl;
Gray, Joe W.;
Jain, Ajay N.;
Pinkel, Daniel;
Albertson, Donna G.

Publication type:

Article

Bioinformatic identification of potential autocrine signaling loops in cancers from gene expression profiles.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 295, doi. 10.1038/ng755

By:

Graeber, Thomas G.;
Eisenberg, David

Publication type:

Article

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 279, doi. 10.1038/ng757

By:

Kuroda-Kawaguchi, Tomoko;
Skaletsky, Helen;
Brown, Laura G.;
Minx, Patrick J.;
Cordum, Holland S.;
Waterston, Robert H.;
Wilson, Richard K.;
Silber, Sherman;
Oates, Robert;
Rozen, Steve;
Page, David C.

Publication type:

Article

Mutations at the mitochondrial DNA polymerase (POLG) locus associated with male infertility.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 261, doi. 10.1038/ng759

By:

Rovio, Anja T.;
Marchington, David R.;
Donat, Susanne;
Schuppe, Hans-Christian;
Abel, Josef;
Fritsche, Ellen;
Elliott, David J.;
Laippala, Pekka;
Ahola, Arja L.;
McNay, David;
Harrison, Robert F.;
Hughes, Barbara;
Barrett, Thomas;
Bailey, David M.D.;
Mehmet, Denise;
Jequier, Anne M.;
Hargreave, Tim B.;
Kao, Shu-Huei;
Cummins, James M.

Publication type:

Article

Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 326, doi. 10.1038/ng758

By:

Zhao, Xinping;
Alvarado, David;
Rainier, Shirley;
Lemons, Rosemary;
Hedera, Peter;
Weber, Christian H.;
Tukel, Turgut;
Apak, Memnune;
Heiman-Patterson, Terry;
Ming, Lei;
Bui, Melanie;
Fink, John K.

Publication type:

Article

MID1, mutated in Opitz syndrome, encodes an ubiquitin ligase that targets phosphatase 2A for degradation.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 287, doi. 10.1038/ng762

By:

Trockenbacher, Alexander;
Suckow, Vanessa;
Foerster, John;
Winter, Jennifer;
Krauß, Sybille;
Ropers, Hans-Hilger;
Schneider, Rainer;
Schweiger, Susann

Publication type:

Article

Population genetic structure of variable drug response.

Published in:

Nature Genetics, 2001, v. 29, n. 3, p. 265, doi. 10.1038/ng761

By:

Wilson, James F.;
Weale, Michael E.;
Smith, Alice C.;
Gratrix, Fiona;
Fletcher, Benjamin;
Thomas, Mark G.;
Bradman, Neil;
Goldstein, David B.

Publication type:

Article