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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 22. Mai 2020 / Development The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with Dishevelled M.C. Kratzer S.F.S. Becker A. Grund A. Merks J. Harnoš V. Bryja K. Giehl J. Kashef A. Borchers 01. Juni 2020 / Curr Opin Cell Biol Evolving methodologies and concepts in 4D nucleome research T.M. Sparks I. Harabula A. Pombo 30. Juni 2020 / PLoS Genet Age-of-onset information helps identify 76 genetic variants associated with allergic disease M.A.R. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander Vi. Ullemar Y. Lu S. Grosche F. Rüschendorf R. Granell B.M. Brumpton L.G. Fritsche L. Bhatta M.E. Gabrielsen J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer N.C. Emami T.B. Cavazos J.S. Witte A. Szwajda D.A. Hinds N. Hübner S. Weidinger P.K. Magnusson E. Jorgenson R. Karlsson L. Paternoster D.I. Boomsma C. Almqvist Y.A. Lee G.H. Koppelman 23. September 2020 / Neuron SUMOylation of enzymes and ion channels in sensory neurons protects against metabolic dysfunction, neuropathy, and sensory loss in diabetes N. Agarwal F.J. Taberner D. Rangel Rojas M. Moroni D. Omberbasic C. Njoo A. Andrieux P. Gupta K.K. Bali E. Herpel F. Faghihi T. Fleming A. Dejean S.G. Lechner P.P. Nawroth G.R. Lewin R. Kuner 19. November 2020 / Nature LifeTime and improving European healthcare through cell-based interceptive medicine N. Rajewsky G. Almouzni S.A. Gorski S. Aerts I. Amit M.G. Bertero C. Bock A.L. Bredenoord G. Cavalli S. Chiocca H. Clevers B. De Strooper A. Eggert J. Ellenberg X.M. Fernández M. Figlerowicz S.M. Gasser N. Hubner J. Kjems J.A. Knoblich G. Krabbe P. Lichter S. Linnarsson J.C. Marine J. Marioni M.A. Marti-Renom M.G. Netea D. Nickel M. Nollmann H.R. Novak H. Parkinson S. Piccolo I. Pinheiro A. Pombo C. Popp W. Reik S. Roman-Roman P. Rosenstiel J.L. Schultze O. Stegle A. Tanay G. Testa D. Thanos F.J. Theis M.E. Torres-Padilla A. Valencia C. Vallot A. van Oudenaarden M. Vidal T. Voet 09. November 2020 / Neurooncol Adv Long-lived tumor-associated macrophages in glioma P.B. Georgieva T. Mathivet S. Alt W. Giese M. Riva M. Balcer H. Gerhardt 01. September 2020 / Pain William D. Willis, Jr, MD, PhD Memorial Lecture: the evolutionary history of nerve growth factor and nociception G.R. Lewin 20. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4-kinase β mutations cause nonsyndromic 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 11. November 2020 / Genes Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families J. Doll B. Vona L. Schnapp F. Rüschendorf I. Khan S. Khan N. Muhammad S. Alam Khan H. Nawaz A. Khan N. Ahmad S.M. Kolb L. Kühlewein J.D.J. Labonne L.C. Layman M.A.H. Hofrichter T. Röder M. Dittrich T. Müller T.D. Graves I.K. Kong I. Nanda H.G. Kim T. Haaf Seitennummerierung Aktuelle Seite 1 Seite 2 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
22. Mai 2020 / Development The Rho guanine nucleotide exchange factor Trio is required for neural crest cell migration and interacts with Dishevelled M.C. Kratzer S.F.S. Becker A. Grund A. Merks J. Harnoš V. Bryja K. Giehl J. Kashef A. Borchers
01. Juni 2020 / Curr Opin Cell Biol Evolving methodologies and concepts in 4D nucleome research T.M. Sparks I. Harabula A. Pombo
30. Juni 2020 / PLoS Genet Age-of-onset information helps identify 76 genetic variants associated with allergic disease M.A.R. Ferreira J.M. Vonk H. Baurecht I. Marenholz C. Tian J.D. Hoffman Q. Helmer A. Tillander Vi. Ullemar Y. Lu S. Grosche F. Rüschendorf R. Granell B.M. Brumpton L.G. Fritsche L. Bhatta M.E. Gabrielsen J.B. Nielsen W. Zhou K. Hveem A. Langhammer O.L. Holmen M. Løset G.R. Abecasis C.J. Willer N.C. Emami T.B. Cavazos J.S. Witte A. Szwajda D.A. Hinds N. Hübner S. Weidinger P.K. Magnusson E. Jorgenson R. Karlsson L. Paternoster D.I. Boomsma C. Almqvist Y.A. Lee G.H. Koppelman
23. September 2020 / Neuron SUMOylation of enzymes and ion channels in sensory neurons protects against metabolic dysfunction, neuropathy, and sensory loss in diabetes N. Agarwal F.J. Taberner D. Rangel Rojas M. Moroni D. Omberbasic C. Njoo A. Andrieux P. Gupta K.K. Bali E. Herpel F. Faghihi T. Fleming A. Dejean S.G. Lechner P.P. Nawroth G.R. Lewin R. Kuner
19. November 2020 / Nature LifeTime and improving European healthcare through cell-based interceptive medicine N. Rajewsky G. Almouzni S.A. Gorski S. Aerts I. Amit M.G. Bertero C. Bock A.L. Bredenoord G. Cavalli S. Chiocca H. Clevers B. De Strooper A. Eggert J. Ellenberg X.M. Fernández M. Figlerowicz S.M. Gasser N. Hubner J. Kjems J.A. Knoblich G. Krabbe P. Lichter S. Linnarsson J.C. Marine J. Marioni M.A. Marti-Renom M.G. Netea D. Nickel M. Nollmann H.R. Novak H. Parkinson S. Piccolo I. Pinheiro A. Pombo C. Popp W. Reik S. Roman-Roman P. Rosenstiel J.L. Schultze O. Stegle A. Tanay G. Testa D. Thanos F.J. Theis M.E. Torres-Padilla A. Valencia C. Vallot A. van Oudenaarden M. Vidal T. Voet
09. November 2020 / Neurooncol Adv Long-lived tumor-associated macrophages in glioma P.B. Georgieva T. Mathivet S. Alt W. Giese M. Riva M. Balcer H. Gerhardt
01. September 2020 / Pain William D. Willis, Jr, MD, PhD Memorial Lecture: the evolutionary history of nerve growth factor and nociception G.R. Lewin
20. Oktober 2020 / J Genet Genomics Phosphatidylinositol 4-kinase β mutations cause nonsyndromic 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
11. November 2020 / Genes Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families J. Doll B. Vona L. Schnapp F. Rüschendorf I. Khan S. Khan N. Muhammad S. Alam Khan H. Nawaz A. Khan N. Ahmad S.M. Kolb L. Kühlewein J.D.J. Labonne L.C. Layman M.A.H. Hofrichter T. Röder M. Dittrich T. Müller T.D. Graves I.K. Kong I. Nanda H.G. Kim T. Haaf