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März 2018 / RNA Biol Expanding the map of protein-RNA interaction sites via cell fusion followed by PAR-CLIP F. Hinze P. Drewe-Boss M. Milek U. Ohler M. Landthaler M. Gotthardt 01. Januar 2018 / Methods Mol Biol Systematic detection of poly(A)(+) RNA-interacting proteins and their differential binding M. Milek M. Landthaler 01. Februar 2018 / J Physiol K(2P) TASK-2 and KCNQ1/KCNE3 K(+) channels are major players contributing to intestinal anion and fluid secretion F. Julio-Kalajzić S. Villanueva J. Burgos M. Ojeda L.P. Cid T.J. Jentsch F.V. Sepúlveda 01. Februar 2018 / Mol Psychiatr De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females E.E. Palmer T. Stuhlmann S. Weinert E. Haan H. Van Esch M. Holvoet J. Boyle M. Leffler M. Raynaud C. Moraine H. van Bokhoven T. Kleefstra K. Kahrizi H. Najmabadi H.H. Ropers M.R. Delgado D. Sirsi S. Golla A. Sommer M.P. Pietryga W.K. Chung J. Wynn L. Rohena E. Bernardo D. Hamlin B.M. Faux D.K. Grange L. Manwaring J. Tolmie S. Joss J.M. Cobben F.A.M. Duijkers J.M. Goehringer T.D. Challman F. Hennig U. Fischer A. Grimme V. Suckow L. Musante J. Nicholl M. Shaw S.P. Lodh Z. Niu J.A. Rosenfeld P. Stankiewicz T.J. Jentsch J. Gecz M. Field V.M. Kalscheuer 01. Januar 2018 / Cell Mol Life Sci Dimerization leads to changes in APP (amyloid precursor protein) trafficking mediated by LRP1 and SorLA S. Eggert A.C. Gonzalez C. Thomas S. Schilling S.M. Schwarz C. Tischer V. Adam P. Strecker V. Schmidt T.E. Willnow G. Hermey C.U. Pietrzik E.H. Koo Stefan Kins 01. Februar 2018 / Mol Metab Cadm2 regulates body weight and energy homeostasis in mice X. Yan Z. Wang V. Schmidt A. Gauert T.E. Willnow M. Heinig M.N. Poy 01. Februar 2018 / Mol Metab The RhoGAP Stard13 controls insulin secretion through F-actin remodeling H. Naumann T. Rathjen M.N. Poy F.M. Spagnoli 01. Januar 2018 / Methods Mol Biol Assessment of blood brain barrier leakage with gadolinium-enhanced MRI M.C. Ku S. Waiczies T. Niendorf A. Pohlmann 01. März 2018 / Nat Genet CLCN2 chloride channel mutations in familial hyperaldosteronism type II U.I. Scholl G. Stölting J. Schewe A. Thiel H. Tan C. Nelson-Williams A.A. Vichot S.C. Jin E. Loring V. Untiet T. Yoo J. Choi S. Xu A. Wu M. Kirchner P. Mertins L.C. Rump A.M. Onder C. Gamble D. McKenney R.W. Lash D.P. Jones G. Chune P. Gagliardi M. Choi R. Gordon M. Stowasser C. Fahlke R.P. Lifton 01. März 2018 / Nat Genet A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism F.L. Fernandes-Rosa G. Daniil I.J. Orozco C. Göppner R. El Zein V. Jain S. Boulkroun X. Jeunemaitre L. Amar H. Lefebvre T. Schwarzmayr T.M. Strom T.J. Jentsch M.C. Zennaro Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
04. März 2018 / RNA Biol Expanding the map of protein-RNA interaction sites via cell fusion followed by PAR-CLIP F. Hinze P. Drewe-Boss M. Milek U. Ohler M. Landthaler M. Gotthardt
01. Januar 2018 / Methods Mol Biol Systematic detection of poly(A)(+) RNA-interacting proteins and their differential binding M. Milek M. Landthaler
01. Februar 2018 / J Physiol K(2P) TASK-2 and KCNQ1/KCNE3 K(+) channels are major players contributing to intestinal anion and fluid secretion F. Julio-Kalajzić S. Villanueva J. Burgos M. Ojeda L.P. Cid T.J. Jentsch F.V. Sepúlveda
01. Februar 2018 / Mol Psychiatr De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females E.E. Palmer T. Stuhlmann S. Weinert E. Haan H. Van Esch M. Holvoet J. Boyle M. Leffler M. Raynaud C. Moraine H. van Bokhoven T. Kleefstra K. Kahrizi H. Najmabadi H.H. Ropers M.R. Delgado D. Sirsi S. Golla A. Sommer M.P. Pietryga W.K. Chung J. Wynn L. Rohena E. Bernardo D. Hamlin B.M. Faux D.K. Grange L. Manwaring J. Tolmie S. Joss J.M. Cobben F.A.M. Duijkers J.M. Goehringer T.D. Challman F. Hennig U. Fischer A. Grimme V. Suckow L. Musante J. Nicholl M. Shaw S.P. Lodh Z. Niu J.A. Rosenfeld P. Stankiewicz T.J. Jentsch J. Gecz M. Field V.M. Kalscheuer
01. Januar 2018 / Cell Mol Life Sci Dimerization leads to changes in APP (amyloid precursor protein) trafficking mediated by LRP1 and SorLA S. Eggert A.C. Gonzalez C. Thomas S. Schilling S.M. Schwarz C. Tischer V. Adam P. Strecker V. Schmidt T.E. Willnow G. Hermey C.U. Pietrzik E.H. Koo Stefan Kins
01. Februar 2018 / Mol Metab Cadm2 regulates body weight and energy homeostasis in mice X. Yan Z. Wang V. Schmidt A. Gauert T.E. Willnow M. Heinig M.N. Poy
01. Februar 2018 / Mol Metab The RhoGAP Stard13 controls insulin secretion through F-actin remodeling H. Naumann T. Rathjen M.N. Poy F.M. Spagnoli
01. Januar 2018 / Methods Mol Biol Assessment of blood brain barrier leakage with gadolinium-enhanced MRI M.C. Ku S. Waiczies T. Niendorf A. Pohlmann
01. März 2018 / Nat Genet CLCN2 chloride channel mutations in familial hyperaldosteronism type II U.I. Scholl G. Stölting J. Schewe A. Thiel H. Tan C. Nelson-Williams A.A. Vichot S.C. Jin E. Loring V. Untiet T. Yoo J. Choi S. Xu A. Wu M. Kirchner P. Mertins L.C. Rump A.M. Onder C. Gamble D. McKenney R.W. Lash D.P. Jones G. Chune P. Gagliardi M. Choi R. Gordon M. Stowasser C. Fahlke R.P. Lifton
01. März 2018 / Nat Genet A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism F.L. Fernandes-Rosa G. Daniil I.J. Orozco C. Göppner R. El Zein V. Jain S. Boulkroun X. Jeunemaitre L. Amar H. Lefebvre T. Schwarzmayr T.M. Strom T.J. Jentsch M.C. Zennaro