2016
Case-based learning and multiple choice questioning methods favored by students.
Chéron M,
Ademi M,
Kraft F,
Löffler-Stastka H.
BMC Med Educ. 2016 Feb 2;16:41. doi: 10.1186/s12909-016-0564-x.
2016
Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity.
Fazel A,
Kashef S,
Aleyasin S,
Harsini S,
Karamizadeh Z,
Zoghi S,
Flores SK,
Boztug K,
Rezaei N.
Allergol Immunopathol (Madr). 2016 Oct 24. pii: S0301-0546(16)30116-1.
2016
DNA Methylation Dynamics of Human Hematopoietic Stem Cell Differentiation.
Farlik M,
Halbritter F,
Müller F,
Choudry FA,
Ebert P,
Klughammer J,
Farrow S,
Santoro A,
Ciaurro V,
Mathur A,
Uppal R,
Stunnenberg HG,
Ouwehand WH,
Laurenti E,
Lengauer T,
Frontini M,
Bock C.
Cell Stem Cell. 2016 Dec 1;19(6):808-822. doi: 10.1016/j.stem.2016.10.019.
2016
Genome-wide genetic screening with chemically mutagenized haploid embryonic stem cells.
Forment JV,
Herzog M,
Coates J,
Konopka T,
Gapp BV,
Nijman SM,
Adams DJ,
Keane TM,
Jackson SP.
Nat Chem Biol. 2016 Oct 31. doi: 10.1038/nchembio.2226.
2016
Crystal Structure of the Acid Sphingomyelinase-Like Phosphodiesterase SMPDL3B Provides Insights into Determinants of Substrate Specificity.
Gorelik A,
Heinz LX,
Illes K,
Superti-Furga G,
Nagar B.
J Biol Chem. 2016 Sep 28. pii: jbc.M116.755801.
2016
DNMT3A mutations promote anthracycline resistance in acute myeloid leukemia via impaired nucleosome remodeling.
Guryanova OA,
Shank K,
Spitzer B,
Luciani L,
Koche RP,
Garrett-Bakelman FE,
Ganzel C,
Durham BH,
Mohanty A,
Hoermann G,
Rivera SA,
Chramiec AG,
Pronier E,
Bastian L,
Keller MD,
Tovbin D,
Loizou E,
Weinstein AR,
Gonzalez AR,
Lieu YK,
Rowe JM,
Pastore F,
McKenney AS,
Krivtsov AV,
Sperr WR,
Cross JR,
Mason CE,
Tallman MS,
Arcila ME,
Abdel-Wahab O,
Armstrong SA,
Kubicek S,
Staber PB,
Gönen M,
Paietta EM,
Melnick AM,
Nimer SD,
Mukherjee S,
Levine RL.
Nat Med. 2016 Dec;22(12):1488-1495. doi: 10.1038/nm.4210.
2016
Defining the microbial transcriptional response to colitis through integrated host and microbiome profiling.
Ilott NE,
Bollrath J,
Danne C,
Schiering C,
Shale M,
Adelmann K,
Krausgruber T,
Heger A,
Sims D,
Powrie F.
ISME J. 2016 Oct;10(10):2389-404. doi: 10.1038/ismej.2016.40.
2016
Increased survival and cell cycle progression pathways are required for EWS/FLI1-induced malignant transformation.
Javaheri T,
Kazemi Z,
Pencik J,
Pham HT,
Kauer M,
Noorizadeh R,
Sax B,
Nivarthi H,
Schlederer M,
Maurer B,
Hofbauer M,
Aryee DN,
Wiedner M,
Tomazou EM,
Logan M,
Hartmann C,
Tuckermann JP,
Kenner L,
Mikula M,
Dolznig H,
Üren A,
Richter GH,
Grebien F,
Kovar H,
Moriggl R.
Cell Death Dis. 2016 Oct 13;7(10):e2419. doi: 10.1038/cddis.2016.268.
2016
Band 3 nullVIENNA , a novel homozygous SLC4A1 p.
Kager L,
Bruce LJ,
Zeitlhofer P,
Flatt JF,
Maia TM,
Ribeiro ML,
Fahrner B,
Fritsch G,
Boztug K,
Haas OA.
Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis. Pediatr Blood Cancer. 2016 Oct 8. doi: 10.1002/pbc.26227.
2016
The second European interdisciplinary Ewing sarcoma research summit--A joint effort to deconstructing the multiple layers of a complex disease.
Kovar H,
Amatruda J,
Brunet E,
Burdach S,
Cidre-Aranaz F,
de Alava E,
Dirksen U,
van der Ent W,
Grohar P,
Grünewald TG,
Helman L,
Houghton P,
Iljin K,
Korsching E,
Ladanyi M,
Lawlor E,
Lessnick S,
Ludwig J,
Meltzer P,
Metzler M,
Mora J,
Moriggl R,
Nakamura T,
Papamarkou T,
Radic Sarikas B,
Rédini F,
Richter GH,
Rossig C,
Schadler K,
Schäfer BW,
Scotlandi K,
Sheffield NC,
Shelat A,
Snaar-Jagalska E,
Sorensen P,
Stegmaier K,
Stewart E,
Sweet-Cordero A,
Szuhai K,
Tirado OM,
Tirode F,
Toretsky J,
Tsafou K,
Üren A,
Zinovyev A,
Delattre O.
Oncotarget. 2016 Feb 23;7(8):8613-24. doi: 10.18632/oncotarget.6937. Review.
