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
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
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
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
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
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
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
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
Contents Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 21, p. NP, doi. 10.1093/hmg/ddq437
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
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
Subscription Page.
Published in:
Human Molecular Genetics, 2010, v. 19, n. 21, p. NP, doi. 10.1093/hmg/ddq446
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