Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 24

Results: 22

Methylomics of gene expression in human monocytes.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5065, doi. 10.1093/hmg/ddt356

By:

Liu, Yongmei;
Ding, Jingzhong;
Reynolds, Lindsay M.;
Lohman, Kurt;
Register, Thomas C.;
De La Fuente, Alberto;
Howard, Timothy D.;
Hawkins, Greg A.;
Cui, Wei;
Morris, Jessica;
Smith, Shelly G.;
Barr, R. Graham;
Kaufman, Joel D.;
Burke, Gregory L.;
Post, Wendy;
Shea, Steven;
Mccall, Charles E.;
Siscovick, David;
Jacobs, David R.;
Tracy, Russell P.

Publication type:

Article

Cover Page.

Published in:: Human Molecular Genetics, 2013, v. 22, n. 24, p. NP, doi. 10.1093/hmg/ddt591
Publication type:: Article

Targeted loss of the ATR-X syndrome protein in the limb mesenchyme of mice causes brachydactyly.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5015, doi. 10.1093/hmg/ddt351

By:

Solomon, Lauren A.;
Russell, Bailey A.;
Watson, L. Ashley;
Beier, Frank;
Bérubé, Nathalie G.

Publication type:

Article

Subscription Page.

Published in:: Human Molecular Genetics, 2013, v. 22, n. 24, p. NP, doi. 10.1093/hmg/ddt593
Publication type:: Article

LRRK2 secretion in exosomes is regulated by 14-3-3.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4988, doi. 10.1093/hmg/ddt346

By:

Fraser, Kyle B.;
Moehle, Mark S.;
Daher, João P.L.;
Webber, Philip J.;
Williams, Jeri Y.;
Stewart, Carrie A.;
Yacoubian, Talene A.;
Cowell, Rita M.;
Dokland, Terje;
Ye, Tong;
Chen, Dongquan;
Siegal, Gene P.;
Galemmo, Robert A.;
Tsika, Elpida;
Moore, Darren J.;
Standaert, David G.;
Kojima, Kyoko;
Mobley, James A.;
West, Andrew B.

Publication type:

Article

The SNM1B/APOLLO DNA nuclease functions in resolution of replication stress and maintenance of common fragile site stability.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4901, doi. 10.1093/hmg/ddt340

By:

Mason, Jennifer M.;
Das, Ishita;
Arlt, Martin;
Patel, Neil;
Kraftson, Stephanie;
Glover, Thomas W.;
Sekiguchi, JoAnn M.

Publication type:

Article

Epigenetic signature and enhancer activity of the human APOE gene.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5036, doi. 10.1093/hmg/ddt354

By:

Yu, Chang-En;
Cudaback, Eiron;
Foraker, Jessica;
Thomson, Zachary;
Leong, Lesley;
Lutz, Franziska;
Gill, James Anthony;
Saxton, Aleen;
Kraemer, Brian;
Navas, Patrick;
Keene, C. Dirk;
Montine, Thomas;
Bekris, Lynn M.

Publication type:

Article

Combining genetic mapping with genome-wide expression in experimental autoimmune encephalomyelitis highlights a gene network enriched for T cell functions and candidate genes regulating autoimmunity.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4952, doi. 10.1093/hmg/ddt343

By:

Thessen Hedreul, Melanie;
Möller, Steffen;
Stridh, Pernilla;
Gupta, Yask;
Gillett, Alan;
Daniel Beyeen, Amennai;
Öckinger, Johan;
Flytzani, Sevasti;
Diez, Margarita;
Olsson, Tomas;
Jagodic, Maja

Publication type:

Article

Contents Page.

Published in:: Human Molecular Genetics, 2013, v. 22, n. 24, p. NP, doi. 10.1093/hmg/ddt590
Publication type:: Article

Editorial Board.

Published in:: Human Molecular Genetics, 2013, v. 22, n. 24, p. NP, doi. 10.1093/hmg/ddt592
Publication type:: Article

Micro-dystrophin and follistatin co-delivery restores muscle function in aged DMD model.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4929, doi. 10.1093/hmg/ddt342

By:

Rodino-Klapac, Louise R.;
Janssen, Paul M. L.;
Shontz, Kimberly M.;
Canan, Benjamin;
Montgomery, Chrystal L.;
Griffin, Danielle;
Heller, Kristin;
Schmelzer, Leah;
Handy, Chalonda;
Clark, K. Reed;
Sahenk, Zarife;
Mendell, Jerry R.;
Kaspar, Brian K.

Publication type:

Article

Patched1 is required in neural crest cells for the prevention of orofacial clefts.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5026, doi. 10.1093/hmg/ddt353

By:

Metzis, Vicki;
Courtney, Andrew D.;
Kerr, Markus C.;
Ferguson, Charles;
Rondón Galeano, Maria C.;
Parton, Robert G.;
Wainwright, Brandon J.;
Wicking, Carol

Publication type:

Article

A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5056, doi. 10.1093/hmg/ddt355

By:

Pooley, Karen A.;
Bojesen, Stig E.;
Weischer, Maren;
Nielsen, Sune F.;
Thompson, Deborah;
Amin Al Olama, Ali;
Michailidou, Kyriaki;
Tyrer, Jonathan P.;
Benlloch, Sara;
Brown, Judith;
Audley, Tina;
Luben, Robert;
Khaw, K-T;
Neal, David E.;
Hamdy, Freddie C.;
Donovan, Jenny L.;
Kote-Jarai, Zsofia;
Baynes, Caroline;
Shah, Mitul;
Bolla, Manjeet K.

Publication type:

Article

SCG10 promotes non-amyloidogenic processing of amyloid precursor protein by facilitating its trafficking to the cell surface.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4888, doi. 10.1093/hmg/ddt339

By:

Wang, Jingjing;
Shan, Chunyan;
Cao, Wenyuan;
Zhang, Chen;
Teng, Junlin;
Chen, Jianguo

Publication type:

Article

Transcriptome study of differential expression in schizophrenia.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5001, doi. 10.1093/hmg/ddt350

By:

Sanders, Alan R.;
Göring, Harald H. H.;
Duan, Jubao;
Drigalenko, Eugene I.;
Moy, Winton;
Freda, Jessica;
He, Deli;
Shi, Jianxin;
Gejman, Pablo V.

Publication type:

Article

Fine-mapping of genome-wide association study-identified risk loci for colorectal cancer in African Americans.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5048, doi. 10.1093/hmg/ddt337

By:

Wang, Hansong;
Haiman, Christopher A.;
Burnett, Terrilea;
Fortini, Barbara K.;
Kolonel, Laurence N.;
Henderson, Brian E.;
Signorello, Lisa B.;
Blot, William J.;
Keku, Temitope O.;
Berndt, Sonja I.;
Newcomb, Polly A.;
Pande, Mala;
Amos, Christopher I.;
West, Dee W.;
Casey, Graham;
Sandler, Robert S.;
Haile, Robert;
Stram, Daniel O.;
Le Marchand, Loïc

Publication type:

Article

Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 5075, doi. 10.1093/hmg/ddt357

By:

Whiffin, Nicola;
Dobbins, Sara E.;
Hosking, Fay J.;
Palles, Claire;
Tenesa, Albert;
Wang, Yufei;
Farrington, Susan M.;
Jones, Angela M.;
Broderick, Peter;
Campbell, Harry;
Newcomb, Polly A.;
Casey, Graham;
Conti, David V.;
Schumacher, Fred;
Gallinger, Steve;
Lindor, Noralane M.;
Hopper, John;
Jenkins, Mark;
Dunlop, Malcolm G.;
Tomlinson, Ian P.

Publication type:

Article

Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4978, doi. 10.1093/hmg/ddt345

By:

Marston, Steven;
Memo, Massimiliano;
Messer, Andrew;
Papadaki, Maria;
Nowak, Kristen;
McNamara, Elyshia;
Ong, Royston;
El-Mezgueldi, Mohammed;
Li, Xiaochuan;
Lehman, William

Publication type:

Article

Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4871, doi. 10.1093/hmg/ddt338

By:

Gispert, Suzana;
Parganlija, Dajana;
Klinkenberg, Michael;
Dröse, Stefan;
Wittig, Ilka;
Mittelbronn, Michel;
Grzmil, Pawel;
Koob, Sebastian;
Hamann, Andrea;
Walter, Michael;
Büchel, Finja;
Adler, Thure;
Hrabé de Angelis, Martin;
Busch, Dirk H.;
Zell, Andreas;
Reichert, Andreas S.;
Brandt, Ulrich;
Osiewacz, Heinz D.;
Jendrach, Marina;
Auburger, Georg

Publication type:

Article

Highly efficient in vivo delivery of PMO into regenerating myotubes and rescue in laminin-α2 chain-null congenital muscular dystrophy mice.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4914, doi. 10.1093/hmg/ddt341

By:

Aoki, Yoshitsugu;
Nagata, Tetsuya;
Yokota, Toshifumi;
Nakamura, Akinori;
Wood, Matthew J.A.;
Partridge, Terence;
Takeda, Shin'ichi

Publication type:

Article

MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4967, doi. 10.1093/hmg/ddt344

By:

Ha, Kyungsoo;
Buchan, Jillian G.;
Alvarado, David M.;
Mccall, Kevin;
Vydyanath, Anupama;
Luther, Pradeep K.;
Goldsmith, Matthew I.;
Dobbs, Matthew B.;
Gurnett, Christina A.

Publication type:

Article

Reducing CTGF/CCN2 slows down mdx muscle dystrophy and improves cell therapy.

Published in:

Human Molecular Genetics, 2013, v. 22, n. 24, p. 4938, doi. 10.1093/hmg/ddt352

By:

Morales, Maria Gabriela;
Gutierrez, Jaime;
Cabello-Verrugio, Claudio;
Cabrera, Daniel;
Lipson, Kenneth E.;
Goldschmeding, Roel;
Brandan, Enrique

Publication type:

Article