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

Results: 22

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
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
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
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
Contents Page.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 24, p. NP, doi. 10.1093/hmg/ddt590
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
Editorial Board.
Published in:
Human Molecular Genetics, 2013, v. 22, n. 24, p. NP, doi. 10.1093/hmg/ddt592
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
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
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
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
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
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
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
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
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
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
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
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