Works matching IS 09646906 AND DT 2010 AND VI 19 AND IP 21

Results: 22

Estrogen and progesterone receptor status affect genome-wide DNA methylation profile in breast cancer.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4273, doi. 10.1093/hmg/ddq351

By:

Li, Lian;
Lee, Kyoung-Mu;
Han, Wonshik;
Choi, Ji-Yeob;
Lee, Ji-Young;
Kang, Gyeong Hoon;
Park, Sue Kyung;
Noh, Dong-Young;
Yoo, Keun-Young;
Kang, Daehee

Publication type:

Article

Oxidative stress by monoamine oxidases is causally involved in myofiber damage in muscular dystrophy.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4207, doi. 10.1093/hmg/ddq339

By:

Menazza, Sara;
Blaauw, Bert;
Tiepolo, Tania;
Toniolo, Luana;
Braghetta, Paola;
Spolaore, Barbara;
Reggiani, Carlo;
Di Lisa, Fabio;
Bonaldo, Paolo;
Canton, Marcella

Publication type:

Article

A humanized Smn gene containing the SMN2 nucleotide alteration in exon 7 mimics SMN2 splicing and the SMA disease phenotype.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4239, doi. 10.1093/hmg/ddq343

By:

Gladman, Jordan T.;
Bebee, Thomas W.;
Edwards, Chris;
Wang, Xueyong;
Sahenk, Zarife;
Rich, Mark M.;
Chandler, Dawn S.

Publication type:

Article

A novel SOD1 splice site mutation associated with familial ALS revealed by SOD activity analysis.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4201, doi. 10.1093/hmg/ddq338

By:

Birve, Anna;
Neuwirth, Christoph;
Weber, Markus;
Marklund, Stefan L.;
Nilsson, Ann-Charloth;
Jonsson, Per Andreas;
Andersen, Peter M.

Publication type:

Article

Editorial Board.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 21, p. NP, doi. 10.1093/hmg/ddq443
Publication type:: Article

Flt-1 haploinsufficiency ameliorates muscular dystrophy phenotype by developmentally increased vasculature in mdx mice.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4145, doi. 10.1093/hmg/ddq334

By:

Verma, Mayank;
Asakura, Yoko;
Hirai, Hiroyuki;
Watanabe, Shuichi;
Tastad, Christopher;
Fong, Guo-Hua;
Ema, Masatsugu;
Call, Jarrod A.;
Lowe, Dawn A.;
Asakura, Atsushi

Publication type:

Article

Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4296

By:

O'Seaghdha, Conall M.;
Yang, Qiong;
Glazer, Nicole L.;
Leak, Tennille S.;
Dehghan, Abbas;
Smith, Albert V.;
Kao, W.H. Linda;
Lohman, Kurt;
Hwang, Shih-Jen;
Johnson, Andrew D.;
Hofman, Albert;
Uitterlinden, Andre G.;
Chen, Yii-Der Ida;
Brown, Edward M.;
Siscovick, David S.;
Harris, Tamara B.;
Psaty, Bruce M.;
Coresh, Josef;
Gudnason, Vilmundur;
Witteman, Jacqueline C.

Publication type:

Article

Contents Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 21, p. NP, doi. 10.1093/hmg/ddq437
Publication type:: Article

A functional variant in NKX3.1 associated with prostate cancer susceptibility down-regulates NKX3.1 expression.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4265, doi. 10.1093/hmg/ddq350

By:

Akamatsu, Shusuke;
Takata, Ryo;
Ashikawa, Kyota;
Hosono, Naoya;
Kamatani, Naoyuki;
Fujioka, Tomoaki;
Ogawa, Osamu;
Kubo, Michiaki;
Nakamura, Yusuke;
Nakagawa, Hidewaki

Publication type:

Article

SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4216, doi. 10.1093/hmg/ddq340

By:

Wishart, Thomas M.;
Huang, Jack P.-W.;
Murray, Lyndsay M.;
Lamont, Douglas J.;
Mutsaers, Chantal A.;
Ross, Jenny;
Geldsetzer, Pascal;
Ansorge, Olaf;
Talbot, Kevin;
Parson, Simon H.;
Gillingwater, Thomas H.

Publication type:

Article

Subscription Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 21, p. NP, doi. 10.1093/hmg/ddq446
Publication type:: Article

The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4278, doi. 10.1093/hmg/ddq324

By:

Reed, Danielle R.;
Zhu, Gu;
Breslin, Paul A.S.;
Duke, Fujiko F.;
Henders, Anjali K.;
Campbell, Megan J.;
Montgomery, Grant W.;
Medland, Sarah E.;
Martin, Nicholas G.;
Wright, Margaret J.

Publication type:

Article

Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granules.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4160, doi. 10.1093/hmg/ddq335

By:

Bosco, Daryl A.;
Lemay, Nathan;
Ko, Hae Kyung;
Zhou, Hongru;
Burke, Chris;
Kwiatkowski, Thomas J.;
Sapp, Peter;
McKenna-Yasek, Diane;
Brown, Robert H.;
Hayward, Lawrence J.

Publication type:

Article

Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4286

By:

Briggs, Farren B.S.;
Bartlett, Selena E.;
Goldstein, Benjamin A.;
Wang, Joanne;
McCauley, Jacob L.;
Zuvich, Rebecca L.;
De Jager, Philip L.;
Rioux, John D.;
Ivinson, Adrian J.;
Compston, Alastair;
Hafler, David A.;
Hauser, Stephen L.;
Oksenberg, Jorge R.;
Sawcer, Stephen J.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.;
Barcellos, Lisa F.

Publication type:

Article

Kismet/CHD7 regulates axon morphology, memory and locomotion in a Drosophila model of CHARGE syndrome.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4253, doi. 10.1093/hmg/ddq348

By:

Melicharek, David J.;
Ramirez, Laura C.;
Singh, Sukhdeep;
Thompson, Rhea;
Marenda, Daniel R.

Publication type:

Article

A single-nucleotide variation in a p53-binding site affects nutrient-sensitive human SIRT1 expression.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4123, doi. 10.1093/hmg/ddq331

By:

Naqvi, Asma;
Hoffman, Timothy A.;
DeRicco, Jeremy;
Kumar, Ajay;
Kim, Cuk-Seong;
Jung, Saet-Byel;
Yamamori, Tohru;
Kim, Young-Rae;
Mehdi, Fardeen;
Kumar, Santosh;
Rankinen, Tuomo;
Ravussin, Eric;
Irani, Kaikobad

Publication type:

Article

Molecular signature of primary retinal pigment epithelium and stem-cell-derived RPE cells.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4229, doi. 10.1093/hmg/ddq341

By:

Liao, Jo-Ling;
Yu, Juehua;
Huang, Kevin;
Hu, Jane;
Diemer, Tanja;
Ma, Zhicheng;
Dvash, Tamar;
Yang, Xian-Jie;
Travis, Gabriel H.;
Williams, David S.;
Bok, Dean;
Fan, Guoping

Publication type:

Article

New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4304, doi. 10.1093/hmg/ddq349

By:

Vitart, Veronique;
Benčić, Goran;
Hayward, Caroline;
Škunca Herman, Jelena;
Huffman, Jennifer;
Campbell, Susan;
Bućan, Kajo;
Navarro, Pau;
Gunjaca, Grgo;
Marin, Josipa;
Zgaga, Lina;
Kolčić, Ivana;
Polašek, Ozren;
Kirin, Mirna;
Hastie, Nicholas D.;
Wilson, James F.;
Rudan, Igor;
Campbell, Harry;
Vatavuk, Zoran;
Fleck, Brian

Publication type:

Article

DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4176, doi. 10.1093/hmg/ddq336

By:

Ollikainen, Miina;
Smith, Katherine R.;
Joo, Eric Ji-Hoon;
Ng, Hong Kiat;
Andronikos, Roberta;
Novakovic, Boris;
Abdul Aziz, Nur Khairunnisa;
Carlin, John B.;
Morley, Ruth;
Saffery, Richard;
Craig, Jeffrey M.

Publication type:

Article

Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4189, doi. 10.1093/hmg/ddq337

By:

Visser, W. Edward;
Swagemakers, Sigrid M.A.;
Őzgűr, Zeliha;
Schot, Rachel;
Verheijen, Frans W.;
van Ijcken, Wilfred F.J.;
van der Spek, Peter J.;
Visser, Theo J.

Publication type:

Article

Cover Page.

Published in:: Human Molecular Genetics, 2010, v. 19, n. 21, p. NP, doi. 10.1093/hmg/ddq440
Publication type:: Article

Ancestral paternal genotype controls body weight and food intake for multiple generations.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 21, p. 4134, doi. 10.1093/hmg/ddq332

By:

Yazbek, Soha N.;
Spiezio, Sabrina H.;
Nadeau, Joseph H.;
Buchner, David A.

Publication type:

Article