Works matching IS 10614036 AND DT 2001 AND VI 27 AND IP 3

Results: 32

Harvesting the fruits of the human genome.

Published in:: 2001
Publication type:: Editorial

The end of all human DNA maps?

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 229, doi. 10.1038/85766

By:

Little, Peter

Publication type:

Article

BACking up the promises.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 230, doi. 10.1038/85769

By:

Antonarakis, Stylianos E

Publication type:

Article

Chipping away at the transcriptome.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 232, doi. 10.1038/85772

By:

Burge, Christopher B

Publication type:

Article

Variation is the spice of life.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 234, doi. 10.1038/85776

By:

Kruglyak, Leonid;
Nickerson, Deborah A

Publication type:

Article

γ-H2AX illuminates meiosis.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 236, doi. 10.1038/85781

By:

Hunter, Neil;
Valentin Börner, G;
Lichten, Michael;
Kleckner, Nancy

Publication type:

Article

Deconstructing DiGeorge syndrome.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 238, doi. 10.1038/85784

By:

Schinke, Martina;
Izumo, Seigo

Publication type:

Article

Chipping away at chromatin.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 240, doi. 10.1038/85787

By:

Martienssen, Robert

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 2001, v. 27, n. 3, p. 243
Publication type:: Article

Alzheimer genetics, part I.

Published in:

2001

By:

Buxbaum, Joseph D

Publication type:

Book Review

DNA double-strand breaks: signaling, repair and the cancer connection.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 247, doi. 10.1038/85798

By:

Khanna, Kum Kum;
Jackson, Stephen P.

Publication type:

Article

Evolution of imprinting mechanisms: the battle of the sexes begins in the zygote.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 255, doi. 10.1038/85804

By:

Reik, Wolf;
Walter, Jörn

Publication type:

Article

Selection for transgene homozygosity in embryonic stem cells results in extensive loss of heterozygosity.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 257, doi. 10.1038/85808

By:

Lefebvre, Louis;
Dionne, Nancy;
Karaskova, Jana;
Squire, Jeremy A.;
Nagy, Andras

Publication type:

Article

Multigenic control of Listeria monocytogenes susceptibility in mice.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 259, doi. 10.1038/85812

By:

Boyartchuk, Victor L.;
Broman, Karl W.;
Mosher, Rebecca E.;
D'Orazio, Sarah E.F.;
Starnbach, Michael N.;
Dietrich, William F.

Publication type:

Article

SPTLC1 is mutated in hereditary sensory neuropathy, type 1.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 261, doi. 10.1038/85817

By:

Bejaoui, Khemissa;
Wu, Chenyan;
Scheffler, Margaret D.;
Haan, Geoffry;
Ashby, Peter;
Wu, Lianchan;
de Jong, Peter;
Brown, Robert H.

Publication type:

Article

Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-α (C/EBPα), in acute myeloid leukemia.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 263, doi. 10.1038/85820

By:

Pabst, Thomas;
Mueller, Beatrice U.;
Zhang, Pu;
Radomska, Hanna S.;
Narravula, Sailaja;
Schnittger, Susanne;
Behre, Gerhard;
Hiddemann, Wolfgang;
Tenen, Daniel G.

Publication type:

Article

Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 309, doi. 10.1038/85879

By:

Dawkins, Jennifer L.;
Hulme, Dennis J.;
Brahmbhatt, Sonal B.;
Auer-Grumbach, Michaela;
Nicholson, Garth A.

Publication type:

Article

Recombinational DNA double-strand breaks in mice precede synapsis.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 271, doi. 10.1038/85830

By:

Mahadevaiah, Shantha K.;
Turner, James M.A.;
Baudat, Frédéric;
Rogakou, Emmy P.;
de Boer, Peter;
Blanco-Rodríguez, Josefa;
Jasin, Maria;
Keeney, Scott;
Bonner, William M.;
Burgoyne, Paul S.

Publication type:

Article

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 286, doi. 10.1038/85845

By:

Jerome, Loydie A.;
Papaioannou, Virginia E.

Publication type:

Article

Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 293, doi. 10.1038/85855

By:

Guris, Deborah L.;
Fantes, Judith;
Tara, David;
Druker, Brian J.;
Imamoto, Akira

Publication type:

Article

A temperature-sensitive disorder in basal transcription and DNA repair in humans.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 299, doi. 10.1038/85864

By:

Vermeulen, Wim;
Rademakers, Suzanne;
Jaspers, Nicolaas G.J.;
Appeldoorn, Esther;
Raams, Anja;
Klein, Binie;
Kleijer, Wim J.;
Kjærsgård Hansen, Lars;
Hoeijmakers, Jan H.J.

Publication type:

Article

Chromatin profiling using targeted DNA adenine methyltransferase.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 304, doi. 10.1038/85871

By:

van Steensel, Bas;
Delrow, Jeffrey;
Henikoff, Steven

Publication type:

Article

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-κB signaling.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 277

By:

Döffinger, Rainer;
Smahi, Asma;
Bessia, Christine;
Geissmann, Frédéric;
Feinberg, Jacqueline;
Durandy, Anne;
Bodemer, Christine;
Kenwrick, Sue;
Dupuis-Girod, Sophie;
Blanche, Stéphane;
Wood, Philip;
Rabia, Smail Hadj;
Headon, Denis J.;
Overbeek, Paul A.;
Le Deist, Françoise;
Holland, Steven M.;
Belani, Kiran;
Kumararatne, Dinakantha S.;
Fischer, Alain

Publication type:

Article

Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 313, doi. 10.1038/85886

By:

Devriendt, Koenraad;
Kim, Annette S.;
Mathijs, Gert;
Frints, Suzanna G.M.;
Schwartz, Marianne;
Van den Oord, Joost J.;
Verhoef, Gregor E.G.;
Boogaerts, Marc A.;
Fryns, Jean-Pierre;
You, Daoqi;
Rosen, Michael K.;
Vandenberghe, Peter

Publication type:

Article

Episodic evolution of pyrin in primates: human mutations recapitulate ancestral amino acid states.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 318, doi. 10.1038/85893

By:

Schaner, Philip;
Richards, Neil;
Wadhwa, Anish;
Aksentijevich, Ivona;
Kastner, Daniel;
Tucker, Priscilla;
Gumucio, Deborah

Publication type:

Article

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 322, doi. 10.1038/85899

By:

Guy, Jacky;
Hendrich, Brian;
Holmes, Megan;
Martin, Joanne E.;
Bird, Adrian

Publication type:

Article

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 327, doi. 10.1038/85906

By:

Chen, Richard Z.;
Akbarian, Schahram;
Tudor, Matthew;
Jaenisch, Rudolf

Publication type:

Article

Open-reading-frame sequence tags (OSTs) support the existence of at least 17,300 genes in C. elegans.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 332, doi. 10.1038/85913

By:

Reboul, Jérôme;
Vaglio, Philippe;
Tzellas, Nia;
Thierry-Mieg, Nicolas;
Moore, Troy;
Jackson, Cindy;
Shin-i, Tadasu;
Kohara, Yuji;
Thierry-Mieg, Danielle;
Thierry-Mieg, Jean;
Lee, Hongmei;
Hitti, Joseph;
Doucette-Stamm, Lynn;
Hartley, James L.;
Temple, Gary F.;
Brasch, Michael A.;
Vandenhaute, Jean;
Lamesch, Philippe E.;
Hill, David E.

Publication type:

Article

Homology-based annotation yields 1,042 new candidate genes in the Drosophila melanogaster genome.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 337, doi. 10.1038/85922

By:

Gopal, Shuba;
Schroeder, Mark;
Pieper, Ursula;
Sczyrba, Alexander;
Aytekin-Kurban, Gulriz;
Bekiranov, Stefan;
Eduardo Fajardo, J.;
Eswar, Narayanan;
Sanchez, Roberto;
Sali, Andrej;
Gaasterland, Terry

Publication type:

Article

Maternal methylation imprints on human chromosome 15 are established during or after fertilization.

Published in:

Nature Genetics, 2001, v. 27, n. 3, p. 341, doi. 10.1038/85927

By:

El-Maarri, Osman;
Buiting, Karin;
Peery, Edwin G.;
Kroisel, Peter M.;
Balaban, Basak;
Wagner, Klaus;
Urman, Bulent;
Heyd, Julia;
Lich, Christina;
Brannan, Camilynn I.;
Walter, Jörn;
Horsthemke, Bernhard

Publication type:

Article

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.

Published in:: Nature Genetics, 2001, v. 27, n. 3, p. 345
Publication type:: Article

Linkage disequilibrium of a type 1 diabetes susceptibility gene with regulatory IL12B alleles.

Published in:: Nature Genetics, 2001, v. 27, n. 3, p. 346
Publication type:: Article