Works matching IS 09646906 AND DT 2011 AND VI 20 AND IP 4

Results: 23

Increased power of mixed models facilitates association mapping of 10 loci for metabolic traits in an isolated population.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 827, doi. 10.1093/hmg/ddq510
By:
- Kenny, Eimear E.;
- Kim, Minseung;
- Gusev, Alexander;
- Lowe, Jennifer K.;
- Salit, Jacqueline;
- Smith, J. Gustav;
- Kovvali, Sirisha;
- Kang, Hyun Min;
- Newton-Cheh, Christopher;
- Daly, Mark J.;
- Stoffel, Markus;
- Altshuler, David M.;
- Friedman, Jeffrey M.;
- Eskin, Eleazar;
- Breslow, Jan L.;
- Pe'er, Itsik
Publication type:
Article
Contents Page.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. NP, doi. 10.1093/hmg/ddr002
Publication type:
Article
Ftx is a non-coding RNA which affects Xist expression and chromatin structure within the X-inactivation center region.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 705, doi. 10.1093/hmg/ddq516
By:
- Chureau, Corinne;
- Chantalat, Sophie;
- Romito, Antonio;
- Galvani, Angélique;
- Duret, Laurent;
- Avner, Philip;
- Rougeulle, Claire
Publication type:
Article
Strategies for diminishing katanin-based loss of microtubules in tauopathic neurodegenerative diseases.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 763, doi. 10.1093/hmg/ddq521
By:
- Sudo, Haruka;
- Baas, Peter W.
Publication type:
Article
Replication timing-related and gene body-specific methylation of active human genes.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 670, doi. 10.1093/hmg/ddq513
By:
- Aran, Dvir;
- Toperoff, Gidon;
- Rosenberg, Michael;
- Hellman, Asaf
Publication type:
Article
Interleukin-10 reduces the pathology of mdx muscular dystrophy by deactivating M1 macrophages and modulating macrophage phenotype.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 790, doi. 10.1093/hmg/ddq523
By:
- Villalta, S. Armando;
- Rinaldi, Chiara;
- Deng, Bo;
- Liu, Grace;
- Fedor, Brian;
- Tidball, James G.
Publication type:
Article
A window into third generation sequencing.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 853, doi. 10.1093/hmg/ddq481
By:
- Schadt, Eric E.;
- Turner, Steve;
- Kasarskis, Andrew
Publication type:
Article
Editorial Board.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. NP, doi. 10.1093/hmg/ddr006
Publication type:
Article
Collagen-related genes influence the glaucoma risk factor, central corneal thickness.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 649, doi. 10.1093/hmg/ddq511
By:
- Vithana, Eranga N.;
- Aung, Tin;
- Khor, Chiea Chuen;
- Cornes, Belinda K.;
- Tay, Wan-Ting;
- Sim, Xueling;
- Lavanya, Raghavan;
- Wu, Renyi;
- Zheng, Yingfeng;
- Hibberd, Martin L.;
- Chia, Kee Seng;
- Seielstad, Mark;
- Goh, Liang Kee;
- Saw, Seang-Mei;
- Shyong Tai, E.;
- Wong, Tien Y.
Publication type:
Article
A hypomorphic Artemis human disease allele causes aberrant chromosomal rearrangements and tumorigenesis.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 806, doi. 10.1093/hmg/ddq524
By:
- Jacobs, Cheryl;
- Huang, Ying;
- Masud, Tehmina;
- Lu, William;
- Westfield, Gerwin;
- Giblin, William;
- Sekiguchi, JoAnn M.
Publication type:
Article
Phenylbutyrate therapy for maple syrup urine disease.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 631, doi. 10.1093/hmg/ddq507
By:
- Brunetti-Pierri, Nicola;
- Lanpher, Brendan;
- Erez, Ayelet;
- Ananieva, Elitsa A.;
- Islam, Mohammad;
- Marini, Juan C.;
- Sun, Qin;
- Yu, Chunli;
- Hegde, Madhuri;
- Li, Jun;
- Wynn, R. Max;
- Chuang, David T.;
- Hutson, Susan;
- Lee, Brendan
Publication type:
Article
Cover Page.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. NP, doi. 10.1093/hmg/ddr004
Publication type:
Article
A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 820, doi. 10.1093/hmg/ddq509
By:
- Gu, Jian;
- Ye, Yuanqing;
- Spitz, Margaret R.;
- Lin, Jie;
- Kiemeney, Lambertus A.;
- Xing, Jingliang;
- Hildebrandt, Michelle A. T.;
- Ki Hong, Waun;
- Amos, Christopher I.;
- Wu, Xifeng
Publication type:
Article
miRNA-132 orchestrates chromatin remodeling and translational control of the circadian clock.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 731, doi. 10.1093/hmg/ddq519
By:
- Alvarez-Saavedra, Matías;
- Antoun, Ghadi;
- Yanagiya, Akiko;
- Oliva-Hernandez, Reynaldo;
- Cornejo-Palma, Daniel;
- Perez-Iratxeta, Carolina;
- Sonenberg, Nahum;
- Cheng, Hai-Ying M.
Publication type:
Article
Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 840, doi. 10.1093/hmg/ddq518
By:
- Jarick, Ivonne;
- Vogel, Carla I.G.;
- Scherag, Susann;
- Schäfer, Helmut;
- Hebebrand, Johannes;
- Hinney, Anke;
- Scherag, André
Publication type:
Article
Subscription Page.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. NP, doi. 10.1093/hmg/ddr008
Publication type:
Article
Satellite cell loss and impaired muscle regeneration in selenoprotein N deficiency.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 694, doi. 10.1093/hmg/ddq515
By:
- Castets, Perrine;
- Bertrand, Anne T.;
- Beuvin, Maud;
- Ferry, Arnaud;
- Le Grand, Fabien;
- Castets, Marie;
- Chazot, Guillaume;
- Rederstorff, Mathieu;
- Krol, Alain;
- Lescure, Alain;
- Romero, Norma B.;
- Guicheney, Pascale;
- Allamand, Valérie
Publication type:
Article
Impaired muscle growth and response to insulin-like growth factor 1 in dysferlin-mediated muscular dystrophy.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 779, doi. 10.1093/hmg/ddq522
By:
- Demonbreun, Alexis R.;
- Fahrenbach, John P.;
- Deveaux, Kieran;
- Earley, Judy U.;
- Pytel, Peter;
- McNally, Elizabeth M.
Publication type:
Article
Intravenous scAAV9 delivery of a codon-optimized SMN1 sequence rescues SMA mice.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 681, doi. 10.1093/hmg/ddq514
By:
- Dominguez, Elisa;
- Marais, Thibaut;
- Chatauret, Nicolas;
- Benkhelifa-Ziyyat, Sofia;
- Duque, Sandra;
- Ravassard, Philippe;
- Carcenac, Romain;
- Astord, Stéphanie;
- de Moura, Aurélie Pereira;
- Voit, Thomas;
- Barkats, Martine
Publication type:
Article
Human germ cell differentiation from fetal- and adult-derived induced pluripotent stem cells.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 752, doi. 10.1093/hmg/ddq520
By:
- Panula, Sarita;
- Medrano, Jose V.;
- Kee, Kehkooi;
- Bergström, Rosita;
- Nguyen, Ha Nam;
- Byers, Blake;
- Wilson, Kitchener D.;
- Wu, Joseph C.;
- Simon, Carlos;
- Hovatta, Outi;
- Reijo Pera, Renee A.
Publication type:
Article
Electroconvulsive shock ameliorates disease processes and extends survival in huntingtin mutant mice.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 659, doi. 10.1093/hmg/ddq512
By:
- Mughal, Mohamed R.;
- Baharani, Akanksha;
- Chigurupati, Srinivasulu;
- Son, Tae Gen;
- Chen, Edmund;
- Yang, Peter;
- Okun, Eitan;
- Arumugam, Thiruma;
- Chan, Sic L.;
- Mattson, Mark P.
Publication type:
Article
Impaired minor tri-snRNP assembly generates differential splicing defects of U12-type introns in lymphoblasts derived from a type I SMA patient.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 641, doi. 10.1093/hmg/ddq508
By:
- Boulisfane, Nawal;
- Choleza, Maria;
- Rage, Florence;
- Neel, Henry;
- Soret, Johann;
- Bordonné, Rémy
Publication type:
Article
Decreased catalytic activity and altered activation properties of PDE6C mutants associated with autosomal recessive achromatopsia.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 4, p. 719, doi. 10.1093/hmg/ddq517
By:
- Grau, Tanja;
- Artemyev, Nikolai O.;
- Rosenberg, Thomas;
- Dollfus, Hélène;
- Haugen, Olav H.;
- Cumhur Sener, E.;
- Jurklies, Bernhard;
- Andreasson, Sten;
- Kernstock, Christoph;
- Larsen, Michael;
- Zrenner, Eberhart;
- Wissinger, Bernd;
- Kohl, Susanne
Publication type:
Article