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Januar 2014 / Am J Hum Genet Reponse to De Leeuw and Houge A.K. Arndt C.A. Macrae S. Klaassen 01. Januar 2002 / J Cell Biochem Smoothelin contains a novel actin cytoskeleton localization sequence with similarity to troponin T C. Quensel J. Kraemer M.C. Cardoso H. Leonhardt 01. Juli 2002 / Basic Res Cardiol Angiotensin II type 1 receptor expression in human coronary arteries with variable degrees of atherosclerosis C.M. Gross S. Gerbaulet C. Quensel J. Kraemer H.O. Mittelmeier F.C. Luft R. Dietz 01. Juli 2001 / Nat Genet Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease R.C. Betz B.G.H. Schoser D. Kasper K. Ricker A. Ramirez V. Stein T. Torbergsen Y.A. Lee M.M. Nothen T.F. Wienker J.P. Malin P. Propping A. Reis W. Mortier T.J. Jentsch M. Vorgerd C. Kubisch 01. Juni 2003 / Am J Med Genet A Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients S. Sasse-Klaassen B. Gerull E. Oechslin R. Jenni L. Thierfelder 01. Februar 2002 / Nat Genet Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy B. Gerull M. Gramlich J. Atherton M. McNabb K. Trombitas S. Sasse-Klaassen J.G. Seidman C. Seidman H. Granzier S. Labeit M. Frenneaux L. Thierfelder 18. Mai 2020 / J Am Heart Assoc Familial recurrent myocarditis triggered by exercise in patients with a truncating variant of the desmoplakin gene W. Poller J. Haas K. Klingel J. Kühnisch M. Gast Z. Kaya F. Escher E. Kayvanpour F. Degener B. Opgen-Rhein F. Berger H.C. Mochmann C. Skurk B. Heidecker H.P. Schultheiss L. Monserrat B. Meder U. Landmesser S. Klaassen 15. Mai 2020 / Commun Biol Cryo-EM structure of the volume-regulated anion channel LRRC8D isoform identifies features important for substrate permeation R. Nakamura T. Numata G. Kasuya T. Yokoyama T. Nishizawa T. Kusakizako T. Kato T. Hagino N. Dohmae M. Inoue K. Watanabe H. Ichijo M. Kikkawa M. Shirouzu T.J. Jentsch R. Ishitani Y. Okada O. Nureki 01. Januar 2020 / Ion and Molecule Transport in Lysosomes Chloride transport across the lysosomal membrane S. Saha A. Blessing T.J. Jentsch 01. März 2021 / Can J Cardiol Left ventricular noncompaction is a myocardial phenotype: cardiomyopathy - yes or no? E. Oechslin R. Jenni S. Klaassen Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
01. Januar 2002 / J Cell Biochem Smoothelin contains a novel actin cytoskeleton localization sequence with similarity to troponin T C. Quensel J. Kraemer M.C. Cardoso H. Leonhardt
01. Juli 2002 / Basic Res Cardiol Angiotensin II type 1 receptor expression in human coronary arteries with variable degrees of atherosclerosis C.M. Gross S. Gerbaulet C. Quensel J. Kraemer H.O. Mittelmeier F.C. Luft R. Dietz
01. Juli 2001 / Nat Genet Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease R.C. Betz B.G.H. Schoser D. Kasper K. Ricker A. Ramirez V. Stein T. Torbergsen Y.A. Lee M.M. Nothen T.F. Wienker J.P. Malin P. Propping A. Reis W. Mortier T.J. Jentsch M. Vorgerd C. Kubisch
01. Juni 2003 / Am J Med Genet A Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients S. Sasse-Klaassen B. Gerull E. Oechslin R. Jenni L. Thierfelder
01. Februar 2002 / Nat Genet Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy B. Gerull M. Gramlich J. Atherton M. McNabb K. Trombitas S. Sasse-Klaassen J.G. Seidman C. Seidman H. Granzier S. Labeit M. Frenneaux L. Thierfelder
18. Mai 2020 / J Am Heart Assoc Familial recurrent myocarditis triggered by exercise in patients with a truncating variant of the desmoplakin gene W. Poller J. Haas K. Klingel J. Kühnisch M. Gast Z. Kaya F. Escher E. Kayvanpour F. Degener B. Opgen-Rhein F. Berger H.C. Mochmann C. Skurk B. Heidecker H.P. Schultheiss L. Monserrat B. Meder U. Landmesser S. Klaassen
15. Mai 2020 / Commun Biol Cryo-EM structure of the volume-regulated anion channel LRRC8D isoform identifies features important for substrate permeation R. Nakamura T. Numata G. Kasuya T. Yokoyama T. Nishizawa T. Kusakizako T. Kato T. Hagino N. Dohmae M. Inoue K. Watanabe H. Ichijo M. Kikkawa M. Shirouzu T.J. Jentsch R. Ishitani Y. Okada O. Nureki
01. Januar 2020 / Ion and Molecule Transport in Lysosomes Chloride transport across the lysosomal membrane S. Saha A. Blessing T.J. Jentsch
01. März 2021 / Can J Cardiol Left ventricular noncompaction is a myocardial phenotype: cardiomyopathy - yes or no? E. Oechslin R. Jenni S. Klaassen