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Selected publications related to CMMC-projects are listed in alphabetical order by the first author published in Search the list of publications:. Abken H Driving CARs on the Highway to Solid Cancer: Some Considerations on the Adoptive Therapy with CAR T Cells. Hum Gene Ther 28 11 : Ahmad I, Baig SM, Abdulkareem AR, Hussain MS, Sur I, Toliat MR, Nurnberg G, Dalibor N, Moawia A, Waseem SS, Asif M, Nagra H, Sher M, Khan MMA, Hassan I, Rehman SU, Thiele H, Altmuller J, Noegel AA and Nurnberg P Genetic heterogeneity in Pakistani microcephaly families revisited.

Clin Genet 92 1 : Altmuller J, Haenisch B, Kawalia A, Menzen M, Nothen MM, Fier H and Molderings GJ Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing. Immunogenetics 69 6 : Amer W, Toth C, Vassella E, Meinrath J, Koitzsch U, Arens A, Huang J, Eischeid H, Adam A, Buettner R, Scheel A, Schaefer SC and Odenthal M Evolution analysis of heterogeneous non-small cell lung carcinoma by ultra-deep sequencing of the mitochondrial genome.

Sci Rep 7 1 : Appel S, Schulze-Edinghausen M, Kretschmer T, Storck S, Janoschek R, Bae-Gartz I, Handwerk M, Wohlfarth M, Nusken KD, Hucklenbruch-Rother E, Heykants M, Mahabir E and Dotsch J J Reprod Immunol Aradjanski M, Dogan SA, Lotter S, Wang S, Hermans S, Wibom R, Rugarli E and Trifunovic A DARS2 protects against neuroinflammation and apoptotic neuronal loss, but is dispensable for myelin producing cells.

Hum Mol Genet 26 21 : Ardicli D, Gocmen R, Talim B, Sprute R, Haliloglu G, Cirak S and Topaloglu H Congenital mirror movements in a patient with alpha-dystroglycanopathy due to a novel POMK mutation. Neuromuscul Disord 27 3 : Awazawa M, Gabel P, Tsaousidou E, Nolte H, Kruger M, Schmitz J, Ackermann PJ, Brandt C, Altmuller J, Motameny S, Wunderlich FT, Kornfeld JW, Bluher M and Bruning JC A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle.

Nat Med 23 12 : Bartram MP, Mishra T, Reintjes N, Fabretti F, Gharbi H, Adam AC, Gobel H, Franke M, Schermer B, Haneder S, Benzing T, Beck BB and Muller RU Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer.

BMC Med Genet 18 1 : Published online. Batinica M, Stephan A, Steiger J, Tantcheva-Poomicronr I, Eming SA and Fabri M Stimulus-dependent NETosis by neutrophils from a Papillon-Lefevre Syndrome patient. J Eur Acad Dermatol Venereol 31 5 : ee Bicker F, Vasic V, Horta G, Ortega F, Nolte H, Kavyanifar A, Keller S, Stankovic ND, Harter PN, Benedito R, Lutz B, Bauerle T, Hartwig J, Baumgart J, Kruger M, Radyushkin K, Alberi L, Berninger B and Schmidt MHH