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(54) Annibale, Paolo Dr. (10) Bader, Michael Prof. Dr. (50) Bähring, Sylvia Dr. (2) Bartolomaeus, Hendrik (7) Bartolomaeus, Theda (3) Baumann, Elisabeth (1) Bayram, Safak (1) Bernert, Carola (1) Berruezo Llacuna, Maria (1) Beule, Dieter Dr. (23) Birchmeier, Walter Prof. Dr. (10) Birchmeier-Kohler, Carmen Prof. Dr. (10) Birol, Melissa Dr. (2) Blachut, Susanne (3) Blankenstein, Thomas Prof. Dr. (6) Blume, Alexander Dr. (1) Blüthgen, Nils (2) Bock-Bierbaum, Tobias Dr. (4) Braeuning, Caroline (2) Bunina, Daria Dr. (2) Bunse, Mario Dr. (1) Burkert, Christian Martin (1) Cakmak-Görür, Nese Dr. (1) Cano Rincon, Elena Dr. (1) Castilho de Barros, Carlos Prof. Dr. (1) Chakrabarti, Sampurna Dr. (1) Chekulaeva, Marina Dr. (4) Chen, Wei Prof. Dr. (17) Chu, Van Trung Dr. (9) Cöl Arslan, Seda Dr. (1) Collins, Russell Thomas Dr. (1) Conrad, Thomas Dr. (3) Coralluzzo, Violeta (1) Coscia, Fabian Dr. (6) Dahlmann, Mathias Dr. (5) Dang Ngoc, Tu Dr. (1) Daniel, Peter Prof. Dr. (1) Dartsch, Josephine (3) Daumke, Oliver Prof. Dr. (14) Dechend, Ralf Priv. 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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 02. Dezember 2020 / Mol Ther CRISPR/Cas9-mediated ELANE mutation correction in hematopoietic stem and progenitor cells to treat severe congenital neutropenia N.T. Tran R. Graf A. Wulf-Goldenberg M. Stecklum G. Strauß R. Kühn C. Kocks K. Rajewsky V.T. Chu 25. Oktober 2019 / Nat Commun Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program E. Wyler V. Franke J. Menegatti C. Kocks A. Boltengagen S. Praktiknjo B. Walch-Rückheim J. Bosse N. Rajewsky F. Grässer A. Akalin M. Landthaler 22. Oktober 2019 / Mol Autism Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism H.G. Kim J.A. Rosenfeld D.A. Scott G. Bénédicte J.D. Labonne J. Brown M. McGuire S. Mahida S. Naidu J. Gutierrez G. Lesca V. des Portes A.L. Bruel A. Sorlin F. Xia Y. Capri E. Muller D. McKnight E. Torti F. Rüschendorf O. Hummel Z. Islam P.R. Kolatkar L.C. Layman D. Ryu I.K. Kong S. Madan-Khetarpal C.H. Kim 01. Januar 2020 / Cancer Res Phosphorylation of RAB7 by TBK1/IKKε regulates innate immune signaling in triple negative breast cancer J.L. Ritter Z. Zhu T.C. Thai N.R. Mahadevan P. Mertins E.H. Knelson B.P. Piel S. Han J.D. Jaffe S.A. Carr D.A. Barbie T.U. Barbie 07. November 2019 / Genes Dev Context-specific regulation of cell survival by a miRNA-controlled BIM rheostat V. Labi S. Peng F. Klironomos M. Munschauer N. Kastelic T. Chakraborty K. Schoeler E. Derudder M. Martella G. Mastrobuoni L.R. Hernandez-Miranda I. Lahmann C. Kocks C. Birchmeier S. Kempa L. Quintanilla-Martinez de Fend M. Landthaler N. Rajewsky K. Rajewsky 01. November 2019 / Front Cell Dev Biol Studying Brugada syndrome with an SCN1B variants in human-induced pluripotent stem cell-derived cardiomyocytes I. El-Battrawy J. Müller Z. Zhao L. Cyganek R. Zhong F. Zhang M. Kleinsorge H. Lan X. Li Q. Xu M. Huang Z. Liao A. Moscu-Gregor S. Albers H. Dinkel S. Lang S. Diecke W.H. Zimmermann J. Utikal T. Wieland M. Borggrefe X. Zhou I. Akin 28. September 2020 / Dev Cell Endogenous retrovirus-derived lncRNA BANCR promotes cardiomyocyte migration in humans and non-human primates K.D. Wilson M. Ameen H. Guo O.J. Abilez L. Tian M.R. Mumbach S. Diecke X. Qin Y. Liu H. Yang N. Ma S. Gaddam N.J. Cunningham M. Gu E. Neofytou M. Prado T.B. Hildebrandt I. Karakikes H.Y. Chang J.C. Wu 13. Oktober 2020 / Cell Rep 4EHP and GIGYF1/2 mediate translation-coupled messenger RNA decay R. Weber M.Y. Chung C. Keskeny U. Zinnall M. Landthaler E. Valkov E. Izaurralde C. Igreja 18. November 2020 / Cell Syst Pairwise stimulations of pathogen-sensing pathways predict immune responses to multi-adjuvant combinations S. Pandey A. Gruenbaum T. Kanashova P. Mertins P. Cluzel N. Chevrier 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
02. Dezember 2020 / Mol Ther CRISPR/Cas9-mediated ELANE mutation correction in hematopoietic stem and progenitor cells to treat severe congenital neutropenia N.T. Tran R. Graf A. Wulf-Goldenberg M. Stecklum G. Strauß R. Kühn C. Kocks K. Rajewsky V.T. Chu
25. Oktober 2019 / Nat Commun Single-cell RNA-sequencing of herpes simplex virus 1-infected cells connects NRF2 activation to an antiviral program E. Wyler V. Franke J. Menegatti C. Kocks A. Boltengagen S. Praktiknjo B. Walch-Rückheim J. Bosse N. Rajewsky F. Grässer A. Akalin M. Landthaler
22. Oktober 2019 / Mol Autism Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism H.G. Kim J.A. Rosenfeld D.A. Scott G. Bénédicte J.D. Labonne J. Brown M. McGuire S. Mahida S. Naidu J. Gutierrez G. Lesca V. des Portes A.L. Bruel A. Sorlin F. Xia Y. Capri E. Muller D. McKnight E. Torti F. Rüschendorf O. Hummel Z. Islam P.R. Kolatkar L.C. Layman D. Ryu I.K. Kong S. Madan-Khetarpal C.H. Kim
01. Januar 2020 / Cancer Res Phosphorylation of RAB7 by TBK1/IKKε regulates innate immune signaling in triple negative breast cancer J.L. Ritter Z. Zhu T.C. Thai N.R. Mahadevan P. Mertins E.H. Knelson B.P. Piel S. Han J.D. Jaffe S.A. Carr D.A. Barbie T.U. Barbie
07. November 2019 / Genes Dev Context-specific regulation of cell survival by a miRNA-controlled BIM rheostat V. Labi S. Peng F. Klironomos M. Munschauer N. Kastelic T. Chakraborty K. Schoeler E. Derudder M. Martella G. Mastrobuoni L.R. Hernandez-Miranda I. Lahmann C. Kocks C. Birchmeier S. Kempa L. Quintanilla-Martinez de Fend M. Landthaler N. Rajewsky K. Rajewsky
01. November 2019 / Front Cell Dev Biol Studying Brugada syndrome with an SCN1B variants in human-induced pluripotent stem cell-derived cardiomyocytes I. El-Battrawy J. Müller Z. Zhao L. Cyganek R. Zhong F. Zhang M. Kleinsorge H. Lan X. Li Q. Xu M. Huang Z. Liao A. Moscu-Gregor S. Albers H. Dinkel S. Lang S. Diecke W.H. Zimmermann J. Utikal T. Wieland M. Borggrefe X. Zhou I. Akin
28. September 2020 / Dev Cell Endogenous retrovirus-derived lncRNA BANCR promotes cardiomyocyte migration in humans and non-human primates K.D. Wilson M. Ameen H. Guo O.J. Abilez L. Tian M.R. Mumbach S. Diecke X. Qin Y. Liu H. Yang N. Ma S. Gaddam N.J. Cunningham M. Gu E. Neofytou M. Prado T.B. Hildebrandt I. Karakikes H.Y. Chang J.C. Wu
13. Oktober 2020 / Cell Rep 4EHP and GIGYF1/2 mediate translation-coupled messenger RNA decay R. Weber M.Y. Chung C. Keskeny U. Zinnall M. Landthaler E. Valkov E. Izaurralde C. Igreja
18. November 2020 / Cell Syst Pairwise stimulations of pathogen-sensing pathways predict immune responses to multi-adjuvant combinations S. Pandey A. Gruenbaum T. Kanashova P. Mertins P. Cluzel N. Chevrier