Works matching IS 10614036 AND DT 2006 AND VI 38 AND IP 10

Results: 27

Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer.

Published in:

2006

By:

Chan, Tsun Leung;
Yuen, Siu Tsan;
Kong, Chi Kwan;
Chan, Yee Wai;
Chan, Annie S. Y.;
Ng, Wai Fu;
Tsui, Wai Yin;
Lo, Michelle W. S.;
Tam, Wing Yip;
Li, Vivian S. W.;
Leung, Suet Yi

Publication type:

Letter

Touching base.

Published in:: Nature Genetics, 2006, v. 38, n. 10, p. 1107, doi. 10.1038/ng1006-1107
Publication type:: Article

Research highlights.

Published in:: Nature Genetics, 2006, v. 38, n. 10, p. 1109, doi. 10.1038/ng1006-1109
Publication type:: Article

Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1111, doi. 10.1038/ng1870

By:

Zara, Federico;
Biancheri, Roberta;
Bruno, Claudio;
Bordo, Laura;
Assereto, Stefania;
Gazzerro, Elisabetta;
Sotgia, Federica;
Wang, Xiao Bo;
Gianotti, Stefania;
Stringara, Silvia;
Pedemonte, Marina;
Uziel, Graziella;
Rossi, Andrea;
Schenone, Angelo;
Tortori-Donati, Paolo;
van der Knaap, Marjo S.;
Lisanti, Michael P.;
Minetti, Carlo

Publication type:

Article

Lamin B1 duplications cause autosomal dominant leukodystrophy.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1114, doi. 10.1038/ng1872

By:

Padiath, Quasar S.;
Saigoh, Kazumasa;
Schiffmann, Raphael;
Asahara, Hideaki;
Yamada, Takeshi;
Koeppen, Anulf;
Hogan, Kirk;
Ptáček, Louis J.;
Fu, Ying-Hui

Publication type:

Article

Minimum compliance for a microarray experiment?

Published in:: 2006
Publication type:: Editorial

Many hypotheses but no replication for the association between PDE4D and stroke.

Published in:

2006

By:

Rosand, Jonathan;
Bayley, Nick;
Rost, Natalia;
de Bakker, Paul I. W.

Publication type:

Letter

Reply to “Many hypotheses but no replication for the association between PDE4D and stroke”.

Published in:

2006

By:

Gulcher, Jeffrey R.;
Kong, Augustine;
Gretarsdottir, Solveig;
Thorleifsson, Gudmar;
Stefansson, Kari

Publication type:

Letter

The genetics of health.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1095, doi. 10.1038/ng1006-1095

By:

Nadeau, Joseph H.;
Topol, Eric J.

Publication type:

Article

A weed for one year.

Published in:

2006

By:

Packer, Alan

Publication type:

Book Review

Tiling DNA microarrays for fly genome cartography.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1101, doi. 10.1038/ng1006-1101

By:

Oliver, Brian

Publication type:

Article

(Re)modeling the transcriptional enhancer.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1102, doi. 10.1038/ng1006-1102

By:

Halfon, Marc S.

Publication type:

Article

New evidence that DNA encodes its packaging.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1104, doi. 10.1038/ng1006-1104

By:

Ercan, Sevinc;
Lieb, Jason D.

Publication type:

Article

A WNK in the kidney controls blood pressure.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1105, doi. 10.1038/ng1006-1105

By:

Coffman, Thomas M.

Publication type:

Article

Indian hedgehog is a major mediator of progesterone signaling in the mouse uterus.

Published in:

2006

By:

Lee, Kevin;
Jeong, Jae Wook;
Kwak, Inseok;
Yu, Cheng-Tai;
Lanske, Beate;
Soegiarto, Desi W.;
Toftgard, Rune;
Tsai, Ming-Jer;
Tsai, Sophia;
Lydon, John P.;
DeMayo, Francesco J.

Publication type:

Letter

Biological function of unannotated transcription during the early development of Drosophila melanogaster.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1151, doi. 10.1038/ng1875

By:

Manak, J. Robert;
Dike, Sujit;
Sementchenko, Victor;
Kapranov, Philipp;
Biemar, Frederic;
Long, Jeff;
Cheng, Jill;
Bell, Ian;
Ghosh, Srinka;
Piccolboni, Antonio;
Gingeras, Thomas R.

Publication type:

Article

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.

Published in:

2006

By:

Ramirez, Alfredo;
Heimbach, André;
Gründemann, Jan;
Stiller, Barbara;
Hampshire, Dan;
Cid, L. Pablo;
Goebel, Ingrid;
Mubaidin, Ammar F.;
Wriekat, Abdul-Latif;
Roeper, Jochen;
Al-Din, Amir;
Hillmer, Axel M.;
Karsak, Meliha;
Liss, Birgit;
Woods, C. Geoffrey;
Behrens, Maria I.;
Kubisch, Christian

Publication type:

Letter

Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking.

Published in:

2006

By:

Boyadjiev, Simeon A.;
Fromme, J. Christopher;
Ben, Jin;
Chong, Samuel S.;
Nauta, Christopher;
Hur, David J.;
Zhang, George;
Hamamoto, Susan;
Schekman, Randy;
Ravazzola, Mariella;
Orci, Lelio;
Eyaid, Wafaa

Publication type:

Letter

Wnk4 controls blood pressure and potassium homeostasis via regulation of mass and activity of the distal convoluted tubule.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1124, doi. 10.1038/ng1877

By:

Lalioti, Maria D.;
Zhang, Junhui;
Volkman, Heather M.;
Kahle, Kristopher T.;
Hoffmann, Kristin E.;
Toka, Hakan R.;
Nelson-Williams, Carol;
Ellison, David H.;
Flavell, Richard;
Booth, Carmen J.;
Lu, Yin;
Geller, David S.;
Lifton, Richard P.

Publication type:

Article

iASPP preferentially binds p53 proline-rich region and modulates apoptotic function of codon 72–polymorphic p53.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1133, doi. 10.1038/ng1879

By:

Bergamaschi, Daniele;
Samuels, Yardena;
Sullivan, Alexandra;
Zvelebil, Marketa;
Breyssens, Hilde;
Bisso, Andrea;
Del Sal, Giannino;
Syed, Nelofer;
Smith, Paul;
Gasco, Milena;
Crook, Tim;
Lu, Xin

Publication type:

Article

Secretory COPII coat component Sec23a is essential for craniofacial chondrocyte maturation.

Published in:

2006

By:

Lang, Michael R.;
Lapierre, Lynne A.;
Frotscher, Michael;
Goldenring, James R.;
Knapik, Ela W.

Publication type:

Letter

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

Published in:

2006

By:

de Bakker, Paul I. W.;
McVean, Gil;
Sabeti, Pardis C.;
Miretti, Marcos M.;
Green, Todd;
Marchini, Jonathan;
Ke, Xiayi;
Monsuur, Alienke J.;
Whittaker, Pamela;
Delgado, Marcos;
Morrison, Jonathan;
Richardson, Angela;
Walsh, Emily C.;
Gao, Xiaojiang;
Galver, Luana;
Hart, John;
Hafler, David A.;
Pericak-Vance, Margaret;
Todd, John A.;
Daly, Mark J.

Publication type:

Letter

Nucleosome positions predicted through comparative genomics.

Published in:

2006

By:

Ioshikhes, Ilya P.;
Albert, Istvan;
Zanton, Sara J.;
Pugh, B. Franklin

Publication type:

Letter

Quantitative and predictive model of transcriptional control of the Drosophila melanogaster even skipped gene.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1159, doi. 10.1038/ng1886

By:

Janssens, Hilde;
Hou, Shuling;
Jaeger, Johannes;
Kim, Ah-Ram;
Myasnikova, Ekaterina;
Sharp, David;
Reinitz, John

Publication type:

Article

Mammalian ultraconserved elements are strongly depleted among segmental duplications and copy number variants.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1216, doi. 10.1038/ng1888

By:

Derti, Adnan;
Roth, Frederick P.;
Church, George M.;
Wu, C-ting

Publication type:

Article

Delineation of a Fat tumor suppressor pathway.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1142, doi. 10.1038/ng1887

By:

Cho, Eunjoo;
Feng, Yongqiang;
Rauskolb, Cordelia;
Maitra, Sushmita;
Fehon, Rick;
Irvine, Kenneth D.

Publication type:

Article

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration.

Published in:

Nature Genetics, 2006, v. 38, n. 10, p. 1173, doi. 10.1038/ng1890

By:

Hughes, Anne E.;
Orr, Nick;
Esfandiary, Hossein;
Diaz-Torres, Martha;
Goodship, Timothy;
Chakravarthy, Usha

Publication type:

Article