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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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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

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