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Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong 01. Mai 2014 / Leukemia Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A F. Auer F. Rueschendorf M. Gombert P. Husemann S. Ginzel S. Izraeli M. Harit M. Weintraub O.Y. Weinstein I. Lerer P. Stepensky A. Borkhardt J. Hauer 01. August 2013 / J Allergy Clin Immunol A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis J. Esparza-Gordillo H. Schaarschmidt L. Liang W. Cookson A. Bauerfeind M.A. Lee-Kirsch K. Nemat J. Henderson L. Paternoster J.L. Harper E. Mangold M.M. Nothen F. Rüschendorf T. Kerscher I. Marenholz A. Matanovic S. Lau T. Keil C.P. Bauer M. Kurek A. Ciechanowicz M. Macek A. Franke M. Kabesch N. Hubner G. Abecasis S. Weidinger M. Moffatt Y.A. Lee 30. Mai 2013 / PLoS ONE Active suppression induced by repetitive self-epitopes protects against EAE development F. Puentes K. Dickhaut M. Hofstätter K. Falk O. Roetzschke 11. Juni 2022 / Cancers Evidence for recombinant GRP78, CALR, PDIA3 and GPI as mediators of genetic instability in human CD34+ cells A. Fabarius V. Samra O. Drews H. Mörz M. Bierbaum A. Darwich C. Weiss S. Brendel H. Kleiner W. Seifarth W. Greffrath W.K. Hofmann C.A. Schmitt H.D. Popp 15. Dezember 2016 / Blood Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma L. Mansouri D. Noerenberg E. Young E. Mylonas M. Abdulla M. Frick F. Asmar V. Ljungstroem M. Schneider K. Yoshida A. Skaftason T. Pandzic B. Gonzalez A. Tasidou N. Waldhueter A. Rivas-Delgado M. Angelopoulou M. Ziepert C.M. Arends L. Couronne D. Lenze C.D. Baldus C. Bastard J. Okosun J. Fitzgibbon B. Doerken H.G. Drexler D. Roos-Weil C.A. Schmitt H.D. Munch-Petersen T. Zenz M.L. Hansmann J.C. Strefford G. Enblad O.A. Bernard E. Ralfkiaer M. Erlanson P. Korkolopoulou M. Hultdin T. Papadaki K. Gronbaek A. Lopez-Guillermo S. Ogawa R. Kueppers K. Stamatopoulos N. Stavroyianni G. Kanellis A. Rosenwald E. Campo R.M. Amini G. Ott T.P. Vassilakopoulos M. Hummel R. Rosenquist F. Damm 07. Oktober 2016 / Nat Commun Bimodal antagonism of PKA signalling by ARHGAP36 R.L. Eccles M.T. Czajkowski C. Barth P.M. Müller E. McShane S. Grunwald P. Beaudette N. Mecklenburg R. Volkmer K. Zühlke G. Dittmar M. Selbach A. Hammes O. Daumke E. Klussmann S. Urbé O. Rocks 05. Januar 2017 / Blood Pharmacological restoration and therapeutic targeting of the B-cell phenotype in classical Hodgkin's lymphoma J. Du M. Neuenschwander Y. Yu J.H.M. Däbritz N.R. Neuendorff K. Schleich A. Bittner M. Milanovic G. Beuster S. Radetzki E. Specker M. Reimann F. Rosenbauer S. Mathas P. Lohneis M. Hummel B. Dörken J.P. von Kries S. Lee C.A. Schmitt 01. Oktober 2022 / Hum Mutat Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function S.J. Lin B. Vona H.M. Porter M. Izadi K. Huang Y. Lacassie J.A. Rosenfeld S. Khan C. Petree T.A. Ali N. Muhammad S.A. Khan N. Muhammad P. Liu M.L. Haymon F. Rüschendorf I.K. Kong L. Schnapp N. Shur L. Chorich L. Layman T. Haaf E. Pourkarimi H.G. Kim G.K. Varshney 12. Juli 2022 / J Vis Exp Simultaneous imaging and flow-cytometry-based detection of multiple fluorescent senescence markers in therapy-induced senescent cancer cells E. Dovjak M. Mairhofer C. Wöß J. Qi D.N.Y. Fan C.A. Schmitt Y. Yu Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
28. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation X. Su Y. Feng S.A. Rahman S. Wu G. Li F. Rüschendorf L. Zhao H. Cui J. Liang L. Fang H. Hu S. Froehler Y. Yu G. Patone O. Hummel Q. Chen K. Raile F.C. Luft S. Bähring K. Hussain W. Chen J. Zhang M. Gong
01. Mai 2014 / Leukemia Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A F. Auer F. Rueschendorf M. Gombert P. Husemann S. Ginzel S. Izraeli M. Harit M. Weintraub O.Y. Weinstein I. Lerer P. Stepensky A. Borkhardt J. Hauer
01. August 2013 / J Allergy Clin Immunol A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis J. Esparza-Gordillo H. Schaarschmidt L. Liang W. Cookson A. Bauerfeind M.A. Lee-Kirsch K. Nemat J. Henderson L. Paternoster J.L. Harper E. Mangold M.M. Nothen F. Rüschendorf T. Kerscher I. Marenholz A. Matanovic S. Lau T. Keil C.P. Bauer M. Kurek A. Ciechanowicz M. Macek A. Franke M. Kabesch N. Hubner G. Abecasis S. Weidinger M. Moffatt Y.A. Lee
30. Mai 2013 / PLoS ONE Active suppression induced by repetitive self-epitopes protects against EAE development F. Puentes K. Dickhaut M. Hofstätter K. Falk O. Roetzschke
11. Juni 2022 / Cancers Evidence for recombinant GRP78, CALR, PDIA3 and GPI as mediators of genetic instability in human CD34+ cells A. Fabarius V. Samra O. Drews H. Mörz M. Bierbaum A. Darwich C. Weiss S. Brendel H. Kleiner W. Seifarth W. Greffrath W.K. Hofmann C.A. Schmitt H.D. Popp
15. Dezember 2016 / Blood Frequent NFKBIE deletions are associated with poor outcome in primary mediastinal B-cell lymphoma L. Mansouri D. Noerenberg E. Young E. Mylonas M. Abdulla M. Frick F. Asmar V. Ljungstroem M. Schneider K. Yoshida A. Skaftason T. Pandzic B. Gonzalez A. Tasidou N. Waldhueter A. Rivas-Delgado M. Angelopoulou M. Ziepert C.M. Arends L. Couronne D. Lenze C.D. Baldus C. Bastard J. Okosun J. Fitzgibbon B. Doerken H.G. Drexler D. Roos-Weil C.A. Schmitt H.D. Munch-Petersen T. Zenz M.L. Hansmann J.C. Strefford G. Enblad O.A. Bernard E. Ralfkiaer M. Erlanson P. Korkolopoulou M. Hultdin T. Papadaki K. Gronbaek A. Lopez-Guillermo S. Ogawa R. Kueppers K. Stamatopoulos N. Stavroyianni G. Kanellis A. Rosenwald E. Campo R.M. Amini G. Ott T.P. Vassilakopoulos M. Hummel R. Rosenquist F. Damm
07. Oktober 2016 / Nat Commun Bimodal antagonism of PKA signalling by ARHGAP36 R.L. Eccles M.T. Czajkowski C. Barth P.M. Müller E. McShane S. Grunwald P. Beaudette N. Mecklenburg R. Volkmer K. Zühlke G. Dittmar M. Selbach A. Hammes O. Daumke E. Klussmann S. Urbé O. Rocks
05. Januar 2017 / Blood Pharmacological restoration and therapeutic targeting of the B-cell phenotype in classical Hodgkin's lymphoma J. Du M. Neuenschwander Y. Yu J.H.M. Däbritz N.R. Neuendorff K. Schleich A. Bittner M. Milanovic G. Beuster S. Radetzki E. Specker M. Reimann F. Rosenbauer S. Mathas P. Lohneis M. Hummel B. Dörken J.P. von Kries S. Lee C.A. Schmitt
01. Oktober 2022 / Hum Mutat Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function S.J. Lin B. Vona H.M. Porter M. Izadi K. Huang Y. Lacassie J.A. Rosenfeld S. Khan C. Petree T.A. Ali N. Muhammad S.A. Khan N. Muhammad P. Liu M.L. Haymon F. Rüschendorf I.K. Kong L. Schnapp N. Shur L. Chorich L. Layman T. Haaf E. Pourkarimi H.G. Kim G.K. Varshney
12. Juli 2022 / J Vis Exp Simultaneous imaging and flow-cytometry-based detection of multiple fluorescent senescence markers in therapy-induced senescent cancer cells E. Dovjak M. Mairhofer C. Wöß J. Qi D.N.Y. Fan C.A. Schmitt Y. Yu