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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 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 19. Juni 2020 / Nat Commun Deconstructing sarcomeric structure-function relations in titin-BioID knock-in mice F. Rudolph C. Fink J. Hüttemeister M. Kirchner M.H. Radke J. Lopez Carballo E. Wagner T. Kohl S.E. Lehnart P. Mertins M. Gotthardt 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 01. Januar 2020 / Ion and Molecule Transport in Lysosomes Chloride transport across the lysosomal membrane S. Saha A. Blessing T.J. Jentsch 03. August 2020 / eLife A human ESC-based screen identifies a role for the translated lncRNA LINC00261 in pancreatic endocrine differentiation B. Gaertner S. van Heesch V. Schneider-Lunitz J.F. Schulz F. Witte S. Blachut S. Nguyen R. Wong I. Matta N. Hübner M. Sander 20. August 2020 / Sci Rep Effects of empagliflozin and target-organ damage in a novel rodent model of heart failure induced by combined hypertension and diabetes K. Kräker F. Herse M. Golic N. Reichhart S. Crespo-Garcia O. Straß J. Grune U. Kintscher M. Ebrahim M. Bader N. Alenina A. Heuser F.C. Luft D.N. Müller R. Dechend N. Haase 08. September 2020 / Cell Rep iPSC modeling of RBM20-deficient DCM identifies upregulation of RBM20 as a therapeutic strategy F. Briganti H. Sun W. Wei J. Wu C. Zhu M. Liss I. Karakikes S. Rego A. Cipriano M. Snyder B. Meder Z. Xu G. Millat M. Gotthardt M. Mercola L.M. Steinmetz 02. November 2020 / Sci Rep Assessment of nanoindentation in stiffness measurement of soft biomaterials: kidney, liver, spleen and uterus G. Wu M. Gotthardt M. Gollasch 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 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
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
19. Juni 2020 / Nat Commun Deconstructing sarcomeric structure-function relations in titin-BioID knock-in mice F. Rudolph C. Fink J. Hüttemeister M. Kirchner M.H. Radke J. Lopez Carballo E. Wagner T. Kohl S.E. Lehnart P. Mertins M. Gotthardt
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
01. Januar 2020 / Ion and Molecule Transport in Lysosomes Chloride transport across the lysosomal membrane S. Saha A. Blessing T.J. Jentsch
03. August 2020 / eLife A human ESC-based screen identifies a role for the translated lncRNA LINC00261 in pancreatic endocrine differentiation B. Gaertner S. van Heesch V. Schneider-Lunitz J.F. Schulz F. Witte S. Blachut S. Nguyen R. Wong I. Matta N. Hübner M. Sander
20. August 2020 / Sci Rep Effects of empagliflozin and target-organ damage in a novel rodent model of heart failure induced by combined hypertension and diabetes K. Kräker F. Herse M. Golic N. Reichhart S. Crespo-Garcia O. Straß J. Grune U. Kintscher M. Ebrahim M. Bader N. Alenina A. Heuser F.C. Luft D.N. Müller R. Dechend N. Haase
08. September 2020 / Cell Rep iPSC modeling of RBM20-deficient DCM identifies upregulation of RBM20 as a therapeutic strategy F. Briganti H. Sun W. Wei J. Wu C. Zhu M. Liss I. Karakikes S. Rego A. Cipriano M. Snyder B. Meder Z. Xu G. Millat M. Gotthardt M. Mercola L.M. Steinmetz
02. November 2020 / Sci Rep Assessment of nanoindentation in stiffness measurement of soft biomaterials: kidney, liver, spleen and uterus G. Wu M. Gotthardt M. Gollasch
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