Selected publications CMMC-project - Jan. - May 2017

Selected publications related to CMMC-projects are listed in alphabetical order by the first author published  from Jan. - May 2017.

  1. Altmuller J, Haenisch B, Kawalia A, Menzen M, Nothen MM, Fier H and Molderings GJ (2017). "Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing." Immunogenetics 69(6): 359-369.

  2. Ardicli D, Gocmen R, Talim B, Sprute R, Haliloglu G, Cirak S and Topaloglu H (2017). "Congenital mirror movements in a patient with alpha-dystroglycanopathy due to a novel POMK mutation." Neuromuscul Disord 27(3): 239-242.

  3. 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 (2017). "Characterization of a splice-site mutation in the tumor suppressor gene FLCN associated with renal cancer." BMC Med Genet 18(1): 53.

  4. Batinica M, Stephan A, Steiger J, Tantcheva-Poomicronr I, Eming SA and Fabri M (2017). "Stimulus-dependent NETosis by neutrophils from a Papillon-Lefevre Syndrome patient." J Eur Acad Dermatol Venereol 31(5): e239-e241.

  5. Brauchle E, Bauer H, Fernes P, Zuk A, Schenke-Layland K and Sengle G (2017). "Raman microspectroscopy as a diagnostic tool for the non-invasive analysis of fibrillin-1 deficiency in the skin and in the in vitro skin models." Acta Biomater 52: 41-48.

  6. Brunn A, Mihelcic M, Carstov M, Feind L, Wieser EC, Schmidt J, Utermohlen O and Deckert M (2017). "Toll-Like Receptor 2, Toll-Like Receptor 4, Myeloid Differentiation Response Gene 88, and Toll-IL-1 Receptor Domain-Containing Adaptor-Inducing Interferon-gamma (TRIF) Selectively Regulate Susceptibility of P0106-125-Induced Murine Experimental Autoimmune Neuritis." Am J Pathol 187(1): 42-54.

  7. Chacon-Martinez CA, Klose M, Niemann C, Glauche I and Wickstrom SA (2017). "Hair follicle stem cell cultures reveal self-organizing plasticity of stem cells and their progeny." EMBO J 36(2): 151-164.

  8. Chaudhari U, Ellis JK, Wagh V, Nemade H, Hescheler J, Keun HC and Sachinidis A (2017). "Metabolite signatures of doxorubicin induced toxicity in human induced pluripotent stem cell-derived cardiomyocytes." Amino Acids.

  9. Colaianna M, Ilmjarv S, Peterson H, Kern I, Julien S, Baquie M, Pallocca G, Bosgra S, Sachinidis A, Hengstler JG, Leist M and Krause KH (2017). "Fingerprinting of neurotoxic compounds using a mouse embryonic stem cell dual luminescence reporter assay." Arch Toxicol 91(1): 365-391.

  10. Corallo D, Schiavinato A, Bizzotto D, Milanetto M, Guljelmovic M, Keene DR, Sengle G, Braghetta P and Bonaldo P (2017). "EMILIN3, an extracellular matrix molecule with restricted distribution in skin." Exp Dermatol 26(5): 435-438.

  11. Cruz-Molina S, Respuela P, Tebartz C, Kolovos P, Nikolic M, Fueyo R, van Ijcken WFJ, Grosveld F, Frommolt P, Bazzi H and Rada-Iglesias A (2017). "PRC2 Facilitates the Regulatory Topology Required for Poised Enhancer Function during Pluripotent Stem Cell Differentiation." Cell Stem Cell 20(5): 689-705 e689.

  12. Diao Y, Cui L, Chen Y, Burbridge TJ, Han W, Wirth B, Sestan N, Crair MC and Zhang J (2017). "Reciprocal Connections Between Cortex and Thalamus Contribute to Retinal Axon Targeting to Dorsal Lateral Geniculate Nucleus." Cereb Cortex: 1-15.

  13. Ebner K, Dafinger C, Ortiz-Bruechle N, Koerber F, Schermer B, Benzing T, Dotsch J, Zerres K, Weber LT, Beck BB and Liebau MC (2017). "Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations." Pediatr Nephrol 32(7): 1269-1273.

  14. Ebner K, Reintjes N, Feldkotter M, Korber F, Nagel M, Dotsch J, Hoppe B, Weber LT, Beck BB and Liebau MC (2017). "A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome." Clin Nephrol.

  15. Eckes B and Eming SA (2017). "Tissue fibrosis: a pathomechanistically unresolved challenge and scary clinical problem." Exp Dermatol 26(2): 135-136.

  16. Franko A, Kunze A, Bose M, von Kleist-Retzow JC, Paulsson M, Hartmann U and Wiesner RJ (2017). "Impaired Insulin Signaling is Associated with Hepatic Mitochondrial Dysfunction in IR+/--IRS-1+/- Double Heterozygous (IR-IRS1dh) Mice." Int J Mol Sci 18(6).

  17. Franzen J, Zirkel A, Blake J, Rath B, Benes V, Papantonis A and Wagner W (2017). "Senescence-associated DNA methylation is stochastically acquired in subpopulations of mesenchymal stem cells." Aging Cell 16(1): 183-191.

  18. Franzoso FD, Seyffert M, Vogel R, Yakimovich A, de Andrade Pereira B, Meier AF, Sutter SO, Tobler K, Vogt B, Greber UF, Buning H, Ackermann M and Fraefel C (2017). "Cell cycle-dependent expression of AAV2 Rep in HSV-1 co-infections gives rise to a mosaic of cells replicating either AAV2 or HSV-1." J Virol.

  19. Gabriel E and Gopalakrishnan J (2017). "Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders." J Vis Exp(122).

  20. Gabriel E, Ramani A, Karow U, Gottardo M, Natarajan K, Gooi LM, Goranci-Buzhala G, Krut O, Peters F, Nikolic M, Kuivanen S, Korhonen E, Smura T, Vapalahti O, Papantonis A, Schmidt-Chanasit J, Riparbelli M, Callaini G, Kronke M, Utermohlen O and Gopalakrishnan J (2017). "Recent Zika Virus Isolates Induce Premature Differentiation of Neural Progenitors in Human Brain Organoids." Cell Stem Cell 20(3): 397-406 e395.

  21. Geoerger B, Bourdeaut F, DuBois SG, Fischer M, Geller JI, Gottardo NG, Marabelle A, Pearson ADJ, Modak S, Cash T, Robinson GW, Motta M, Matano A, Bhansali SG, Dobson JR, Parasuraman S and Chi SN (2017). "A Phase I Study of the CDK4/6 Inhibitor Ribociclib (LEE011) in Pediatric Patients with Malignant Rhabdoid Tumors, Neuroblastoma, and Other Solid Tumors." Clin Cancer Res 23(10): 2433-2441.

  22. George J, Saito M, Tsuta K, Iwakawa R, Shiraishi K, Scheel AH, Uchida S, Watanabe SI, Nishikawa R, Noguchi M, Peifer M, Jang SJ, Petersen I, Buttner R, Harris CC, Yokota J, Thomas RK and Kohno T (2017). "Genomic Amplification of CD274 (PD-L1) in Small-Cell Lung Cancer." Clin Cancer Res 23(5): 1220-1226.

  23. Gioia R, Tonelli F, Ceppi I, Biggiogera M, Leikin S, Fisher S, Tenedini E, Yorgan TA, Schinke T, Tian K, Schwartz JM, Forte F, Wagener R, Villani S, Rossi A and Forlino A (2017). "The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta." Hum Mol Genet.

  24. Gkogkolou P, Hildebrandt K, Broekaert S, Metze D, Sengle G and Bohm M (2017). "Cutis laxa acquisita: novel insights into impaired elastic fibre regeneration." Br J Dermatol 176(3): 832-835.

  25. Gordon CT, Xue S, Yigit G, Filali H, Chen K, Rosin N, Yoshiura KI, Oufadem M, Beck TJ, McGowan R, Magee AC, Altmuller J, Dion C, Thiele H, Gurzau AD, Nurnberg P, Meschede D, Muhlbauer W, Okamoto N, Varghese V, Irving R, Sigaudy S, Williams D, Ahmed SF, Bonnard C, Kong MK, Ratbi I, Fejjal N, Fikri M, Elalaoui SC, Reigstad H, Bole-Feysot C, Nitschke P, Ragge N, Levy N, Tuncbilek G, Teo AS, Cunningham ML, Sefiani A, Kayserili H, Murphy JM, Chatdokmaiprai C, Hillmer AM, Wattanasirichaigoon D, Lyonnet S, Magdinier F, Javed A, Blewitt ME, Amiel J, Wollnik B and Reversade B (2017). "De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development." Nat Genet 49(2): 249-255.

  26. Grahammer F, Ramakrishnan SK, Rinschen MM, Larionov AA, Syed M, Khatib H, Roerden M, Sass JO, Helmstaedter M, Osenberg D, Kuhne L, Kretz O, Wanner N, Jouret F, Benzing T, Artunc F, Huber TB and Theilig F (2017). "mTOR Regulates Endocytosis and Nutrient Transport in Proximal Tubular Cells." J Am Soc Nephrol 28(1): 230-241.

  27. Hackl A, Ehren R, Kirschfink M, Zipfel PF, Beck BB, Weber LT and Habbig S (2017). "Successful discontinuation of eculizumab under immunosuppressive therapy in DEAP-HUS." Pediatr Nephrol 32(6): 1081-1087.

  28. Hackl A, Mehler K, Gottschalk I, Vierzig A, Eydam M, Hauke J, Beck BB, Liebau MC, Ensenauer R, Weber LT and Habbig S (2017). "Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease-different clinical entities and comparable perinatal renal abnormalities." Pediatr Nephrol 32(5): 791-800.

  29. Hahn M, Burckert JP, Luttenberger CA, Klebow S, Hess M, Al-Maarri M, Vogt M, Reissig S, Hallek M, Wienecke-Baldacchino A, Buch T, Muller CP, Pallasch CP, Wunderlich FT, Waisman A and Hovelmeyer N (2017). "Aberrant splicing of the tumor suppressor CYLD promotes the development of chronic lymphocytic leukemia via sustained NF-kappaB signaling." Leukemia.

  30. Hahn O, Gronke S, Stubbs TM, Ficz G, Hendrich O, Krueger F, Andrews S, Zhang Q, Wakelam MJ, Beyer A, Reik W and Partridge L (2017). "Dietary restriction protects from age-associated DNA methylation and induces epigenetic reprogramming of lipid metabolism." Genome Biol 18(1): 56.

  31. Haliloglu G, Becker K, Temucin C, Talim B, Kucuksahin N, Pergande M, Motameny S, Nurnberg P, Aydingoz U, Topaloglu H and Cirak S (2017). "Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defects." J Hum Genet 62(4): 497-501.

  32. Hamdi Y, Soucy P, Kuchenbaeker KB, Pastinen T, Droit A, Lemacon A, Adlard J, Aittomaki K, Andrulis IL, Arason A, Arnold N, Arun BK, Azzollini J, Bane A, Barjhoux L, Barrowdale D, Benitez J, Berthet P, Blok MJ, Bobolis K, Bonadona V, Bonanni B, Bradbury AR, Brewer C, Buecher B, Buys SS, Caligo MA, Chiquette J, Chung WK, Claes KB, Daly MB, Damiola F, Davidson R, De la Hoya M, De Leeneer K, Diez O, Ding YC, Dolcetti R, Domchek SM, Dorfling CM, Eccles D, Eeles R, Einbeigi Z, Ejlertsen B, Embrace, Engel C, Gareth Evans D, Feliubadalo L, Foretova L, Fostira F, Foulkes WD, Fountzilas G, Friedman E, Frost D, Ganschow P, Ganz PA, Garber J, Gayther SA, Collaborators GS, Gerdes AM, Glendon G, Godwin AK, Goldgar DE, Greene MH, Gronwald J, Hahnen E, Hamann U, Hansen TV, Hart S, Hays JL, Hebon, Hogervorst FB, Hulick PJ, Imyanitov EN, Isaacs C, Izatt L, Jakubowska A, James P, Janavicius R, Jensen UB, John EM, Joseph V, Just W, Kaczmarek K, Karlan BY, Investigators KC, Kets CM, Kirk J, Kriege M, Laitman Y, Laurent M, Lazaro C, Leslie G, Lester J, Lesueur F, Liljegren A, Loman N, Loud JT, Manoukian S, Mariani M, Mazoyer S, McGuffog L, Meijers-Heijboer HE, Meindl A, Miller A, Montagna M, Mulligan AM, Nathanson KL, Neuhausen SL, Nevanlinna H, Nussbaum RL, Olah E, Olopade OI, Ong KR, Oosterwijk JC, Osorio A, Papi L, Park SK, Pedersen IS, Peissel B, Segura PP, Peterlongo P, Phelan CM, Radice P, Rantala J, Rappaport-Fuerhauser C, Rennert G, Richardson A, Robson M, Rodriguez GC, Rookus MA, Schmutzler RK, Sevenet N, Shah PD, Singer CF, Slavin TP, Snape K, Sokolowska J, Sonderstrup IM, Southey M, Spurdle AB, Stadler Z, Stoppa-Lyonnet D, Sukiennicki G, Sutter C, Tan Y, Tea MK, Teixeira MR, Teule A, Teo SH, Terry MB, Thomassen M, Tihomirova L, Tischkowitz M, Tognazzo S, Toland AE, Tung N, van den Ouweland AM, van der Luijt RB, van Engelen K, van Rensburg EJ, Varon-Mateeva R, Wappenschmidt B, Wijnen JT, Rebbeck T, Chenevix-Trench G, Offit K, Couch FJ, Nord S, Easton DF, Antoniou AC and Simard J (2017). "Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3." Breast Cancer Res Treat 161(1): 117-134.

  33. Herling M, Rengstl B, Scholtysik R, Hartmann S, Kuppers R, Hansmann ML, Diebner HH, Roeder I, Abken H, Newrzela S and Kirberg J (2017). "Concepts in mature T-cell lymphomas - highlights from an international joint symposium on T-cell immunology and oncology." Leuk Lymphoma 58(4): 788-796.

  34. Hos D, Tuac O, Schaub F, Stanzel TP, Schrittenlocher S, Hellmich M, Bachmann BO and Cursiefen C (2017). "Incidence and Clinical Course of Immune Reactions after Descemet Membrane Endothelial Keratoplasty: Retrospective Analysis of 1000 Consecutive Eyes." Ophthalmology 124(4): 512-518.

  35. Hosel M, Huber A, Bohlen S, Lucifora J, Ronzitti G, Puzzo F, Boisgerault F, Hacker UT, Kwanten WJ, Kloting N, Bluher M, Gluschko A, Schramm M, Utermohlen O, Bloch W, Mingozzi F, Krut O and Buning H (2017). "Autophagy determines efficiency of liver-directed gene therapy with adeno-associated viral vectors." Hepatology.

  36. Ising C and Brinkkoetter PT (2017). "Prohibitin Signaling at the Kidney Filtration Barrier." Adv Exp Med Biol 982: 563-575.

  37. Jaco I, Annibaldi A, Lalaoui N, Wilson R, Tenev T, Laurien L, Kim C, Jamal K, Wicky John S, Liccardi G, Chau D, Murphy JM, Brumatti G, Feltham R, Pasparakis M, Silke J and Meier P (2017). "MK2 Phosphorylates RIPK1 to Prevent TNF-Induced Cell Death." Mol Cell 66(5): 698-710 e695.

  38. Kalimuthu P, Belaidi AA, Schwarz G and Bernhardt PV (2017). "Mediated Catalytic Voltammetry of Holo and Heme-Free Human Sulfite Oxidases." Chemelectrochem 4(4): 947-956.

  39. Kamper M, Paulsson M and Zaucke F (2017). "Absence of collagen IX accelerates hypertrophic differentiation in the embryonic mouse spine through a disturbance of the Ihh-PTHrP feedback loop." Cell Tissue Res 367(2): 359-367.

  40. Karaoglu P, Quizon N, Pergande M, Wang H, Polat AI, Ersen A, Ozer E, Willkomm L, Hiz Kurul S, Heredia R, Yis U, Selcen D and Cirak S (2017). "Dropped head congenital muscular dystrophy caused by de novo mutations in LMNA." Brain Dev 39(4): 361-364.

  41. Khan AO, Becirovic E, Betz C, Neuhaus C, Altmuller J, Maria Riedmayr L, Motameny S, Nurnberg G, Nurnberg P and Bolz HJ (2017). "A deep intronic CLRN1 (USH3A) founder mutation generates an aberrant exon and underlies severe Usher syndrome on the Arabian Peninsula." Sci Rep 7(1): 1411.

  42. Khan AO, Budde BS, Nurnberg P, Kawalia A, Lenzner S and Bolz HJ (2017). "Genome-wide linkage and sequence analysis challenge CCDC66 as a human retinal dystrophy candidate gene and support a distinct NMNAT1-related fundus phenotype." Clin Genet.

  43. Koehler S, Brahler S, Braun F, Hagmann H, Rinschen MM, Spath MR, Hohne M, Wunderlich FT, Schermer B, Benzing T and Brinkkoetter PT (2017). "Construction of a viral T2A-peptide based knock-in mouse model for enhanced Cre recombinase activity and fluorescent labeling of podocytes." Kidney Int 91(6): 1510-1517.

  44. Koitzsch U, Heydt C, Attig H, Immerschitt I, Merkelbach-Bruse S, Fammartino A, Buttner RH, Kong Y and Odenthal M (2017). "Use of the GeneReader NGS System in a clinical pathology laboratory: a comparative study." J Clin Pathol.

  45. Kondylis V, Kumari S, Vlantis K and Pasparakis M (2017). "The interplay of IKK, NF-kappaB and RIPK1 signaling in the regulation of cell death, tissue homeostasis and inflammation." Immunol Rev 277(1): 113-127.

  46. Kraal KC, Bleeker GM, van Eck-Smit BL, van Eijkelenburg NK, Berthold F, van Noesel MM, Caron HN and Tytgat GA (2017). "Feasibility, toxicity and response of upfront metaiodobenzylguanidine therapy therapy followed by German Pediatric Oncology Group Neuroblastoma 2004 protocol in newly diagnosed stage 4 neuroblastoma patients." Eur J Cancer 76: 188-196.

  47. Kuczkowski A and Brinkkoetter PT (2017). "Metabolism and homeostasis in the kidney: metabolic regulation through insulin signaling in the kidney." Cell Tissue Res.

  48. Lang F, Aravamudhan S, Nolte H, Tuerk C, Holper S, Muller S, Gunther S, Blaauw B, Braun T and Kruger M (2017). "Dynamic changes in the skeletal muscle proteome during denervation-induced atrophy." Dis Model Mech.

  49. Loos S, Aulbert W, Hoppe B, Ahlenstiel-Grunow T, Kranz B, Wahl C, Staude H, Humberg A, Benz K, Krause M, Pohl M, Liebau MC, Schild R, Lemke J, Beringer O, Muller D, Hartel C, Wigger M, Vester U, Konrad M, Haffner D, Pape L, Oh J and Kemper MJ (2017). "Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4." Clin Infect Dis 64(12): 1637-1643.

  50. Lucas T, Schafer F, Muller P, Eming SA, Heckel A and Dimmeler S (2017). "Light-inducible antimiR-92a as a therapeutic strategy to promote skin repair in healing-impaired diabetic mice." Nat Commun 8: 15162.

  51. Ludwig KU, Bohmer AC, Bowes J, Nikolic M, Ishorst N, Wyatt N, Hammond NL, Golz L, Thieme F, Barth S, Schuenke H, Klamt J, Spielmann M, Aldhorae K, Rojas-Martinez A, Nothen MM, Rada-Iglesias A, Dixon MJ, Knapp M and Mangold E (2017). "Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip +/- cleft palate and cleft palate only." Hum Mol Genet 26(4): 829-842.

  52. Mescher M, Jeong P, Knapp SK, Rubsam M, Saynisch M, Kranen M, Landsberg J, Schlaak M, Mauch C, Tuting T, Niessen CM and Iden S (2017). "The epidermal polarity protein Par3 is a non-cell autonomous suppressor of malignant melanoma." J Exp Med 214(2): 339-358.

  53. Minnerop M, Kurzwelly D, Wagner H, Soehn AS, Reichbauer J, Tao F, Rattay TW, Peitz M, Rehbach K, Giorgetti A, Pyle A, Thiele H, Altmuller J, Timmann D, Karaca I, Lennarz M, Baets J, Hengel H, Synofzik M, Atasu B, Feely S, Kennerson M, Stendel C, Lindig T, Gonzalez MA, Stirnberg R, Sturm M, Roeske S, Jung J, Bauer P, Lohmann E, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Carloni P, Brustle O, Klopstock T, Mathews KD, Shy ME, de Jonghe P, Chinnery PF, Horvath R, Kohlhase J, Schmitt I, Wolf M, Greschus S, Amunts K, Maier W, Schols L, Nurnberg P, Zuchner S, Klockgether T, Ramirez A and Schule R (2017). "Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia." Brain 140(6): 1561-1578.

  54. Mollaoglu G, Guthrie MR, Bohm S, Bragelmann J, Can I, Ballieu PM, Marx A, George J, Heinen C, Chalishazar MD, Cheng H, Ireland AS, Denning KE, Mukhopadhyay A, Vahrenkamp JM, Berrett KC, Mosbruger TL, Wang J, Kohan JL, Salama ME, Witt BL, Peifer M, Thomas RK, Gertz J, Johnson JE, Gazdar AF, Wechsler-Reya RJ, Sos ML and Oliver TG (2017). "MYC Drives Progression of Small Cell Lung Cancer to a Variant Neuroendocrine Subtype with Vulnerability to Aurora Kinase Inhibition." Cancer Cell 31(2): 270-285.

  55. Muranen TA, Greco D, Blomqvist C, Aittomaki K, Khan S, Hogervorst F, Verhoef S, Pharoah PDP, Dunning AM, Shah M, Luben R, Bojesen SE, Nordestgaard BG, Schoemaker M, Swerdlow A, Garcia-Closas M, Figueroa J, Dork T, Bogdanova NV, Hall P, Li J, Khusnutdinova E, Bermisheva M, Kristensen V, Borresen-Dale AL, Investigators N, Peto J, Dos Santos Silva I, Couch FJ, Olson JE, Hillemans P, Park-Simon TW, Brauch H, Hamann U, Burwinkel B, Marme F, Meindl A, Schmutzler RK, Cox A, Cross SS, Sawyer EJ, Tomlinson I, Lambrechts D, Moisse M, Lindblom A, Margolin S, Hollestelle A, Martens JWM, Fasching PA, Beckmann MW, Andrulis IL, Knight JA, Investigators K, Anton-Culver H, Ziogas A, Giles GG, Milne RL, Brenner H, Arndt V, Mannermaa A, Kosma VM, Chang-Claude J, Rudolph A, Devilee P, Seynaeve C, Hopper JL, Southey MC, John EM, Whittemore AS, Bolla MK, Wang Q, Michailidou K, Dennis J, Easton DF, Schmidt MK and Nevanlinna H (2017). "Genetic modifiers of CHEK2*1100delC-associated breast cancer risk." Genet Med 19(5): 599-603.

  56. Neidhardt G, Becker A, Hauke J, Horvath J, Bogdanova Markov N, Heilmann-Heimbach S, Hellebrand H, Thiele H, Altmuller J, Nurnberg P, Meindl A, Rhiem K, Blumcke B, Wappenschmidt B, Schmutzler RK and Hahnen E (2017). "The RAD51C exonic splice-site mutations c.404G>C and c.404G>T are associated with familial breast and ovarian cancer." Eur J Cancer Prev 26(2): 165-169.

  57. Neuhaus JF, Baris OR, Kittelmann A, Becker K, Rothschild MA and Wiesner RJ (2017). "Catecholamine Metabolism Induces Mitochondrial DNA Deletions and Leads to Severe Adrenal Degeneration during Aging." Neuroendocrinology 104(1): 72-84.

  58. Nikolic M, Papantonis A and Rada-Iglesias A (2017). "GARLIC: a bioinformatic toolkit for aetiologically connecting diseases and cell type-specific regulatory maps." Hum Mol Genet 26(4): 742-752.

  59. Pajtler KW, Sadowski N, Ackermann S, Althoff K, Schonbeck K, Batzke K, Schafers S, Odersky A, Heukamp L, Astrahantseff K, Kunkele A, Deubzer HE, Schramm A, Sprussel A, Thor T, Lindner S, Eggert A, Fischer M and Schulte JH (2017). "The GSK461364 PLK1 inhibitor exhibits strong antitumoral activity in preclinical neuroblastoma models." Oncotarget 8(4): 6730-6741.

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