2015
Differential DNA Methylation Analysis without a Reference Genome.
Klughammer J,
Datlinger P,
Printz D,
Sheffield NC,
Farlik M,
Hadler J,
Fritsch G,
Bock C.
Cell Rep. 2015 Dec 7. pii: S2211-1247(15)01324-8. doi: 10.1016/j.celrep.2015.11.024.
2015
ChIPmentation: fast, robust, low-input ChIP-seq for histones and transcription factors.
Schmidl C,
Rendeiro AF,
Sheffield NC,
Bock C.
Nat Methods. 2015 Aug 17. doi: 10.1038/nmeth.3542.
2015
Impaired microbial killing by neutrophils from patients with protein kinase C delta deficiency.
Szilagyi K,
Gazendam RP,
van Hamme JL,
Tool AT,
van Houdt M,
Vos WA,
Verkuijlen P,
Janssen H,
Belot A,
Juillard L,
Förster-Waldl E,
Boztug K,
Kraal G,
de Winther MP,
Kuijpers TW,
van den Berg TK.
J Allergy Clin Immunol. 2015 Nov;136(5):1404-1407.e10. doi: 10.1016/j.jaci.2015.06.016. Epub 2015 Jul 30.
2015
Arenavirus Glycan Shield Promotes Neutralizing Antibody Evasion and Protracted Infection.
Sommerstein R,
Flatz L,
Remy MM,
Malinge P,
Magistrelli G,
Fischer N,
Sahin M,
Bergthaler A,
Igonet S,
Ter Meulen J,
Rigo D,
Meda P,
Rabah N,
Coutard B,
Bowden TA,
Lambert PH,
Siegrist CA,
Pinschewer DD.
PLoS Pathog. 2015 Nov 20;11(11):e1005276. doi: 10.1371/journal.ppat.1005276. eCollection 2015 Nov.
2015
LOLA: Enrichment analysis for genomic region sets and regulatory elements in R and Bioconductor.
Sheffield NC,
Bock C.
Bioinformatics. 2015 Oct 27. pii: btv612.
2015
Long-term remission after allogeneic hematopoietic stem cell transplantation in LPS-responsive beige-like anchor (LRBA) deficiency.
Seidel MG,
Hirschmugl T,
Gamez-Diaz L,
Schwinger W,
Serwas N,
Deutschmann A,
Gorkiewicz G,
Zenz W,
Windpassinger C,
Grimbacher B,
Urban C,
Boztug K.
J Allergy Clin Immunol. 2015 May;135(5):1384-90.e1-8. doi: 10.1016/j.jaci.2014.10.048. Epub 2014 Dec 22.
2015
Immune Dysregulation Syndromes (IPEX, CD27 Deficiency, and Others): Always Doomed from the Start? J Clin Immunol.
Seidel MG,
Boztug K,
Haas OA.
2015 Dec 10.
2015
Efficacy of ruxolitinib in myeloid neoplasms with PCM1-JAK2 fusion gene.
Rumi E,
Milosevic JD,
Selleslag D,
Casetti I,
Lierman E,
Pietra D,
Cavalloni C,
Bellini M,
Milanesi C,
Dambruoso I,
Astori C,
Kralovics R,
Vandenberghe P,
Cazzola M.
Ann Hematol. 2015 Nov;94(11):1927-8. doi: 10.1007/s00277-015-2451-7. Epub 2015 Jul 23.
2015
Mutations in the heat-shock protein A9 (HSPA9) gene cause the EVEN-PLUS syndrome of congenital malformations and skeletal dysplasia.
Royer-Bertrand B,
Castillo-Taucher S,
Moreno-Salinas R,
Cho TJ,
Chae JH,
Choi M,
Kim OH,
Dikoglu E,
Campos-Xavier B,
Girardi E,
Superti-Furga G,
Bonafé L,
Rivolta C,
Unger S,
Superti-Furga A.
Sci Rep. 2015 Nov 24;5:17154. doi: 10.1038/srep17154.
2015
SLC38A9: a lysosomal amino acid transporter at the core of the amino acid-sensing machinery that controls MTORC1.
Rebsamen M,
Superti-Furga G.
Autophagy. 2015 Oct 2:0.
