Works matching IS 10614036 AND DT 1999 AND VI 22 AND IP 1

Results: 33

Freely associating.

Published in:: Nature Genetics, 1999, v. 22, n. 1, p. 1, doi. 10.1038/8702
Publication type:: Article

Branching out with BRCA1.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 10, doi. 10.1038/8714

By:

Dennis, Carina

Publication type:

Article

c-MYC interacts with INI1/hSNF5 and requires the SWI/SNF complex for transactivation function.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 102, doi. 10.1038/8811

By:

Cheng, S.-W. Grace;
Davies, Kelvin P.;
Yung, Eric;
Beltran, Ralph J.;
Yu, Jin;
Kalpana, Ganjam V.

Publication type:

Article

Evolution of neoplastic cell lineages in Barrett oesophagus.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 106, doi. 10.1038/8816

By:

Barrett, Michael T.;
Sanchez, Carissa A.;
Prevo, Laura J.;
Wong, David J.;
Galipeau, Patricia C.;
Paulson, Thomas G.;
Rabinovitch, Peter S.;
Reid, Brian J.

Publication type:

Article

TOUCHINGbase.

Published in:: Nature Genetics, 1999, v. 22, n. 1, p. 11
Publication type:: Article

Synphilin-1 associates with α-synuclein and promotes the formation of cytosolic inclusions.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 110, doi. 10.1038/8820

By:

Engelender, Simone;
Kaminsky, Zachary;
Guo, Xin;
Sharp, Alan H.;
Amaravi, Ravi K.;
Kleiderlein, John J.;
Margolis, Russell L.;
Troncoso, Juan C.;
Lanahan, Anthony A.;
Worley, Paul F.;
Dawson, Valina L.;
Dawson, Ted M.;
Ross, Christopher A.

Publication type:

Article

PML induces a novel caspase-independent cell death process.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 115, doi. 10.1038/8706

By:

Quignon, Fredérique

Publication type:

Article

A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 13, doi. 10.1038/8719

By:

Merienne, Karine;
Jacquot, Sylvie;
Pannetier, Solange;
Zeniou, Maria;
Bankier, Agnes;
Gecz, Jozef;
Mandel, Jean-Louis;
Mulley, John;
Sassone-Corsi, Paolo;
Hanauer, André

Publication type:

Article

Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 15, doi. 10.1038/8722

By:

Tsai, Ting-Fen;
Armstrong, Dawna;
Beaudet, Arthur L.

Publication type:

Article

α-2 macroglobulin polymorphism and Alzheimer disease risk in the UK.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 16, doi. 10.1038/8724

By:

Dow, David J.;
Lindsey, Nicola;
Cairns, Nigel J.;
Brayne, Carol;
Robinson, Damian;
Huppert, Felicia A.;
Paykel, Eugene S.;
Xuereb, John;
Wilcock, Gordon;
Whittaker, Joanne L.;
Rubinsztein, David C.

Publication type:

Article

α-2 macroglobulin gene and Alzheimer disease.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 17, doi. 10.1038/8726

By:

Rudrasingham, Varuni;
Wavrant-De Vrièze, Fabienne;
Lambert, Jean-Charles;
Chakraverty, Sumi;
Kehoe, Patrick;
Crook, Richard;
Amouyel, Philippe;
Wu, William;
Rice, Frances;
Pérez-Tur, Jordi;
Frigard, Bernard;
Morris, John C.;
Carty, Stephanie;
Petersen, Ronald;
Cottel, Dominique;
Tunstall, Nigel;
Holmans, Peter;
Lovestone, Simon;
Chartier-Harlin, Marie-Christine

Publication type:

Article

An α-2-macroglobulin insertion-deletion polymorphism in Alzheimer disease.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 19, doi. 10.1038/8729

By:

Rogaeva, Ekaterina A.;
Premkumar, Smita;
Grubber, Janet;
Serneels, Lutgarde;
Scott, William K.;
Kawarai, Toshitaka;
Song, Youqiang;
Hill, De'Lisa M.;
Abou-Donia, Suzanne M.;
Martin, Eden R.;
Vance, Jeffrey J.;
Yu, Gang;
Orlacchio, Antonio;
Pei, York;
Nishimura, Masaki;
Supala, Agres;
Roberge, Brenda;
Saunders, Ann M.;
Roses, Allen D.

Publication type:

Article

In reply.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 21, doi. 10.1038/8732

By:

Blacker, Deborah;
Crystal, Adam S.;
Wilcox, Marsha A.;
Laird, Nan M.;
Tanzi, Rudolph E.

Publication type:

Article

Distribution and early development of microarray technology in Europe.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 22, doi. 10.1038/8734

By:

Vente, Andreas;
Korn, Bernd;
Zehetner, Günther;
Poustka, Annemarie;
Lehrach, Hans

Publication type:

Article

Status, sale and patenting of human genetic material: an international survey.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 23, doi. 10.1038/8735

By:

Knoppers, Bartha Maria

Publication type:

Article

A radiation hybrid map of the rat genome containing 5,255 markers.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 27, doi. 10.1038/8737

By:

Watanabe, Takeshi K.;
Bihoreau, Marie-Therese;
McCarthy, Linda C.;
Kiguwa, Susanna L.;
Hishigaki, Haretsugu;
Tsuji, Atsushi;
Browne, Julie;
Yamasaki, Yuki;
Mizoguchi-Miyakita, Ayako;
Oga, Keiko;
Ono, Toshihide;
Okuno, Shiro;
Kanemoto, Naohide;
Takahashi, Ei-ichi;
Tomita, Kazuhiro;
Hayashi, Hiromi;
Adachi, Masakazu;
Webber, Caleb;
Davis, Marie

Publication type:

Article

Rattus norvegicus and the Industrial Revolution.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 3, doi. 10.1038/8703

By:

Nadeau, Joseph H

Publication type:

Article

Conditional mutation of Brca1 in mammary epithelial cells results in blunted ductal morphogenesis and tumour formation.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 37, doi. 10.1038/8743

By:

Xu, Xiaoling;
Wagner, Kay-Uwe;
Larson, Denise;
Weaver, Zoë;
Li, Cuiling;
Ried, Thomas;
Hennighausen, Lothar;
Wynshaw-Boris, Anthony;
Deng, Chu-Xia

Publication type:

Article

The shuffling of a mortal coil.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 4, doi. 10.1038/8705

By:

Rothstein, Rodney;
Gangloff, Serge

Publication type:

Article

Loss of Cdk4 expression causes insulin-deficient diabetes and Cdk4 activation results in β-islet cell hyperplasia.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 44, doi. 10.1038/8751

By:

Rane, Sushil G.;
Dubus, Pierre;
Mettus, Richard V.;
Galbreath, Elizabeth J.;
Boden, Guenther;
Reddy, E. Premkumar;
Barbacid, Mariano

Publication type:

Article

Action of BTN1, the yeast orthologue of the gene mutated in Batten disease.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 55, doi. 10.1038/8861

By:

Pearce, David A.;
Ferea, Tracy;
Nosel, Seth A.;
Das, Biswadip;
Sherman, Fred

Publication type:

Article

Sequence variation in the human angiotensin converting enzyme.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 59, doi. 10.1038/8760

By:

Rieder, Mark J.;
Taylor, Scott L.;
Clark, Andrew G.;
Nickerson, Deborah A.

Publication type:

Article

The House & Garden guide to chromatin remodelling.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 6, doi. 10.1038/8708

By:

Martienssen, Rob;
Henikoff, Steve

Publication type:

Article

Inactivating mutations and overexpression of BCL10, a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32).

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 63, doi. 10.1038/8767

By:

Zhang, Quangeng;
Siebert, Reiner;
Yan, Minhong;
Hinzmann, Bernd;
Cui, Xiaoli;
Xue, Liquan;
Rakestraw, Karen M.;
Naeve, Clayton W.;
Beckmann, Georg;
Weisenburger, Dennis D.;
Sanger, Warren G.;
Nowotny, Hadwiga;
Vesely, Michael;
Callet-Bauchu, Evelyne;
Salles, Gilles;
Dixit, Vishva M.;
Rosenthal, André;
Schlegelberger, Brigitte;
Morris, Stephan W.

Publication type:

Article

Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 69, doi. 10.1038/8773

By:

Miettinen, Päivi J.;
Chin, Jennie R.;
Shum, Lillian;
Slavkin, Harold C.;
Shuler, Charles F.;
Derynck, Rik;
Werb, Zena

Publication type:

Article

Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-κb-inducing kinase.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 74, doi. 10.1038/8780

By:

Shinkura, Reiko;
Kitada, Kazuhiro;
Matsuda, Fumihiko;
Tashiro, Kei;
Ikuta, Koichi;
Suzuki, Misao;
Kogishi, Katsumi;
Serikawa, Tadao;
Honjo, Tasuku

Publication type:

Article

DNA sequence variation in a non-coding region of low recombination on the human X chromosome.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 78, doi. 10.1038/8785

By:

Kaessmann, Henrik;
Heißig, Florian;
Haeseler, Arndt von;
Pääbo, Svante

Publication type:

Article

Transmutation of tRNA over time.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 8, doi. 10.1038/8711

By:

Brosius, Jürgen

Publication type:

Article

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 82, doi. 10.1038/8788

By:

Kitao, Saori;
Shimamoto, Akira;
Goto, Makoto;
Miller, Robert W.;
Smithson, William A.;
Lindor, Noralane M.;
Furuichi, Yasuhiro

Publication type:

Article

Sox9 is required for cartilage formation.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 85, doi. 10.1038/8792

By:

Bi, Weimin;
Deng, Jian Min;
Zhang, Zhaoping;
Behringer, Richard R.;
de Crombrugghe, Benoit

Publication type:

Article

Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 90, doi. 10.1038/8798

By:

Hayashi, Takaaki;
Motulsky, Arno G.;
Deeb, Samir S.

Publication type:

Article

Maintenance of genomic methylation requires a SWI2/SNF2-like protein.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 94, doi. 10.1038/8803

By:

Jeddeloh, Jeffrey A.;
Stokes, Trevor L.;
Richards, Eric J.

Publication type:

Article

Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells.

Published in:

Nature Genetics, 1999, v. 22, n. 1, p. 98, doi. 10.1038/8807

By:

Coffee, Bradford;
Zhang, Fuping;
Warren, Stephen T.;
Reines, Daniel

Publication type:

Article