Works matching IS 09646906 AND DT 2016 AND VI 25 AND IP 2

Results: 18

Dasatinib as a treatment for Duchenne muscular dystrophy.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 266, doi. 10.1093/hmg/ddv469

By:

Lipscomb, Leanne;
Piggott, Robert W.;
Emmerson, Tracy;
Winder, Steve J.

Publication type:

Article

New function of TSGA10 gene in angiogenesis and tumor metastasis: a response to a challengeable paradox.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 233, doi. 10.1093/hmg/ddv461

By:

Mansouri, Kamran;
Mostafie, Ali;
Rezazadeh, Davood;
Shahlaei, Mohsen;
Modarressi, Mohammad Hossein

Publication type:

Article

Rescue of neurodegeneration in the Fig4 null mouse by a catalytically inactive FIG4 transgene.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 340, doi. 10.1093/hmg/ddv480

By:

Lenk, Guy M.;
Frei, Christen M.;
Miller, Ashley C.;
Wallen, Rachel C.;
Mironova, Yevgeniya A.;
Giger, Roman J.;
Meisler, Miriam H.

Publication type:

Article

Preferential PPAR-α activation reduces neuroinflammation, and blocks neurodegeneration in vivo.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 317, doi. 10.1093/hmg/ddv477

By:

Esmaeili, Mohammad A.;
Yadav, Shilpi;
Gupta, Ravi Kr.;
Waggoner, Garrett R.;
Deloach, Abigail;
Calingasan, Noel Y.;
Beal, M. Flint;
Kiaei, Mahmoud

Publication type:

Article

Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 254, doi. 10.1093/hmg/ddv468

By:

Wyles, Saranya P.;
Xing Li;
Hrstka, Sybil C.;
Reyes, Santiago;
Oommen, Saji;
Beraldi, Rosanna;
Edwards, Jessica;
Terzic, Andre;
Olson, Timothy M.;
Nelson, Timothy J.

Publication type:

Article

Yeast reveals similar molecular mechanisms underlying alpha- and beta-synuclein toxicity.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 275, doi. 10.1093/hmg/ddv470

By:

Tenreiro, Sandra;
Rosado-Ramos, Rita;
Gerhardt, Ellen;
Favretto, Filippo;
Magalhães, Filipa;
Popova, Blagovesta;
Becker, Stefan;
Zweckstetter, Markus;
Braus, Gerhard H.;
Tiago Fleming Outeiro

Publication type:

Article

Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 371, doi. 10.1093/hmg/ddv462

By:

Rand, Kristin A.;
Rohland, Nadin;
Tandon, Arti;
Stram, Alex;
Xin Sheng;
Do, Ron;
Pasaniuc, Bogdan;
Allen, Alex;
Quinque, Dominique;
Mallick, Swapan;
Le Marchand, Loic;
Kaggwa, Sam;
Lubwama, Alex;
Stram, Daniel O.;
Watya, Stephen;
Henderson, Brian E.;
Conti, David V.;
Reich, David;
Haiman, Christopher A.

Publication type:

Article

Genome-wide association study identifies common and low-frequency variants at the AMH gene locus that strongly predict serum AMH levels in males.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 382, doi. 10.1093/hmg/ddv465

By:

Perry, John R. B.;
McMahon, George;
Day, Felix R.;
Ring, Susan M.;
Nelson, Scott M.;
Lawlor, Debbie A.

Publication type:

Article

Rheumatoid arthritis-associated RBPJ polymorphism alters memory CD4<sup>+</sup> T cells.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 404, doi. 10.1093/hmg/ddv474

By:

Orent, William;
Mchenry, Allison R.;
Rao, Deepak A.;
White, Charles;
Klein, Hans-Ulrich;
Bassil, Ribal;
Srivastava, Gyan;
Replogle, Joseph M.;
Raj, Towfique;
Frangieh, Michael;
Cimpean, Maria;
Cuerdon, Nicole;
Chibnik, Lori;
Khoury, Samia J.;
Karlson, Elizabeth W.;
Brenner, Michael B.;
De Jager, Philip;
Bradshaw, Elizabeth M.;
Elyaman, Wassim

Publication type:

Article

Extracellular cleavage of collagen XVII is essential for correct cutaneous basement membrane formation.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 328, doi. 10.1093/hmg/ddv478

By:

Machiko Nishimura;
Wataru Nishie;
Yoshinori Shirafuji;
Satoru Shinkuma;
Ken Natsuga;
Hideki Nakamura;
Daisuke Sawamura;
Keiji Iwatsuki;
Hiroshi Shimizu

Publication type:

Article

Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 291, doi. 10.1093/hmg/ddv471

By:

Joyce, Peter I.;
Fratta, Pietro;
Landman, Allison S.;
Mcgoldrick, Philip;
Wackerhage, Henning;
Groves, Michael;
Busam, Bharani Shiva;
Galino, Jorge;
Corrochano, Silvia;
Beskina, Olga A.;
Esapa, Christopher;
Ryder, Edward;
Carter, Sarah;
Stewart, Michelle;
Codner, Gemma;
Hilton, Helen;
Teboul, Lydia;
Tucker, Jennifer;
Lionikas, Arimantas;
Estabel, Jeanne

Publication type:

Article

NEDD4-mediated HSF1 degradation underlies α-synucleinopathy.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 211, doi. 10.1093/hmg/ddv445

By:

Eunhee Kim;
Bin Wang;
Sastry, Namratha;
Masliah, Eliezer;
Nelson, Peter T.;
Cai, Huaibin;
Liao, Francesca-Fang

Publication type:

Article

Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndrome.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 348, doi. 10.1093/hmg/ddv481

By:

Boyden, Lynn M.;
Kam, Chen Y.;
Hernández-Martín, Angela;
Jing Zhou;
Craiglow, Brittany G.;
Sidbury, Robert;
Mathes, Erin F.;
Maguiness, Sheilagh M.;
Crumrine, Debra A.;
Williams, Mary L.;
Ronghua Hu;
Lifton, Richard P.;
Elias, Peter M.;
Green, Kathleen J.;
Choate, Keith A.

Publication type:

Article

CpG methylation differences between neurons and glia are highly conserved from mouse to human.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 223, doi. 10.1093/hmg/ddv459

By:

Kessler, Noah J.;
Van Baak, Timothy E.;
Baker, Maria S.;
Laritsky, Eleonora;
Coarfa, Cristian;
Waterland, Robert A.

Publication type:

Article

The ASK1-specific inhibitors K811 and K812 prolong survival in a mouse model of amyotrophic lateral sclerosis.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 245, doi. 10.1093/hmg/ddv467

By:

Takao Fujisawa;
Motoo Takahashi;
Yuka Tsukamoto;
Namiko Yamaguchi;
Masayoshi Nakoji;
Megumi Endo;
Hiroshi Kodaira;
Yuki Hayashi;
Hideki Nishitoh;
Isao Naguro;
Kengo Homma;
Hidenori Ichijo

Publication type:

Article

Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 389, doi. 10.1093/hmg/ddv472

By:

Felix, Janine F.;
Bradfield, Jonathan P.;
Monnereau, Claire;
van der Valk, Ralf J. P.;
Stergiakouli, Evie;
Chesi, Alessandra;
Gaillard, Romy;
Feenstra, Bjarke;
Thiering, Elisabeth;
Kreiner-Møller, Eskil;
Mahajan, Anubha;
Pitkänen, Niina;
Joro, Raimo;
Cavadino, Alana;
Huikari, Ville;
Franks, Steve;
Groen-Blokhuis, Maria M.;
Cousminer, Diana L.;
Marsh, Julie A.;
Lehtimäki, Terho

Publication type:

Article

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 358, doi. 10.1093/hmg/ddv454

By:

de Vries, Paul S.;
Chasman, Daniel I.;
Sabater-Lleal, Maria;
Ming-Huei Chen;
Huffman, Jennifer E.;
Steri, Maristella;
Weihong Tang;
Teumer, Alexander;
Marioni, Riccardo E.;
Grossmann, Vera;
Hottenga, Jouke J.;
Trompet, Stella;
Müller-Nurasyid, Martina;
Jing Hua Zhao;
Brody, Jennifer A.;
Kleber, Marcus E.;
Xiuqing Guo;
Jie Jin Wang;
Auer, Paul L.;
Attia, John R.

Publication type:

Article

MRI phenotypes with high neurodegeneration are associated with peripheral blood B-cell changes.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 2, p. 308, doi. 10.1093/hmg/ddv473

By:

Comabella, Manuel;
Cantó, Ester;
Nurtdinov, Ramil;
Río, Jordi;
Villar, Luisa M.;
Picón, Carmen;
Castilló, Joaquín;
Fissolo, Nicolás;
Aymerich, Xavier;
Auger, Cristina;
Rovira, Alex;
Montalban, Xavier

Publication type:

Article