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