2016
Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4+ T cells into distinct effector subsets.
Ma CS,
Wong N,
Rao G,
Nguyen A,
Avery DT,
Payne K,
Torpy J,
O'Young P,
Deenick E,
Bustamante J,
Puel A,
Okada S,
Kobayashi M,
Martinez-Barricarte R,
Elliott M,
Sebnem Kilic S,
El Baghdadi J,
Minegishi Y,
Bousfiha A,
Robertson N,
Hambleton S,
Arkwright PD,
French M,
Blincoe AK,
Hsu P,
Campbell DE,
Stormon MO,
Wong M,
Adelstein S,
Fulcher DA,
Cook MC,
Stepensky P,
Boztug K,
Beier R,
Ikincioğullari A,
Ziegler JB,
Gray P,
Picard C,
Boisson-Dupuis S,
Phan TG,
Grimbacher B,
Warnatz K,
Holland SM,
Uzel G,
Casanova JL,
Tangye SG.
J Exp Med. 2016 Jul 25;213(8):1589-608. doi: 10.1084/jem.20151467.
2016
Pharmacological treats for SUMO addicts.
Licciardello MP,
Kubicek S.
Pharmacol Res. 2016 Jan 24. pii: S1043-6618(16)30009-3. doi: 10.1016/j.phrs.2016.01.004.
2016
Sustained PI3K Activation exacerbates BLM-induced Lung Fibrosis via activation of pro-inflammatory and pro-fibrotic pathways.
Kral JB,
Kuttke M,
Schrottmaier WC,
Birnecker B,
Warszawska J,
Wernig C,
Paar H,
Salzmann M,
Sahin E,
Brunner JS,
Österreicher C,
Knapp S,
Assinger A,
Schabbauer G.
Sci Rep. 2016 Mar 14;6:23034. doi: 10.1038/srep23034.
2016
Parallel reverse genetic screening in mutant human cells using transcriptomics.
Gapp BV,
Konopka T,
Penz T,
Dalal V,
Bürckstümmer T,
Bock C,
Nijman SM.
Mol Syst Biol. 2016 Aug 1;12(8):879. doi: 10.15252/msb.20166890.
2016
A human haploid gene trap collection to study lncRNAs with unusual RNA biology.
Kornienko AE,
Vlatkovic I,
Neesen J,
Barlow DP,
Pauler FM.
RNA Biol. 2016 Feb;13(2):196-220. doi: 10.1080/15476286.2015.1110676.
2016
Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans.
Kornienko AE,
Dotter CP,
Guenzl PM,
Gisslinger H,
Gisslinger B,
Cleary C,
Kralovics R,
Pauler FM,
Barlow DP.
Genome Biol. 2016 Jan 29;17(1):14. doi: 10.1186/s13059-016-0873-8.
2016
Functional crosstalk between membrane lipids and TLR biology.
Köberlin MS,
Heinz LX,
Superti-Furga G.
Curr Opin Cell Biol. 2016 Feb 16;39:28-36. doi: 10.1016/j.ceb.2016.01.010.
2016
Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia.
Kiykim A,
Garncarz W,
Karakoc-Aydiner E,
Ozen A,
Kiykim E,
Yesil G,
Boztug K,
Baris S.
Clin Immunol. 2016 Feb 23;165:1-3. doi: 10.1016/j.clim.2016.02.008.
2016
Cooperation of germline JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia.
Kapralova K,
Horvathova M,
Pecquet C,
Fialova Kucerova J,
Pospisilova D,
Leroy E,
Kralova B,
Milosevic Feenstra JD,
Schischlik F,
Kralovics R,
Constantinescu SN,
Divoky V.
Blood. 2016 Jul 7. pii: blood-2016-02-698951.
2016
Two Novel Missense Mutations and a 5bp Deletion in the Erythroid-Specific Promoter of the PKLR Gene in Two Unrelated Patients With Pyruvate Kinase Deficient Transfusion-Dependent Chronic Nonspherocytic Hemolytic Anemia.
Kager L,
Minkov M,
Zeitlhofer P,
Fahrner B,
Ratzinger F,
Boztug K,
Dossenbach-Glaninger A,
Haas OA.
Pediatr Blood Cancer. 2016 Jan 5. doi: 10.1002/pbc.25878.
