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Dezember 2005 / BMC Struct Biol X-ray structure of engineered human Aortic Preferentially Expressed Protein-1 (APEG-1) B.A. Manjasetty F.H. Niesen C. Scheich Y. Roske F. Goetz J. Behlke V. Sievert U. Heinemann K. Buessow Juni 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder 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 2006 Structural studies of the human tethering complex TRAPP involved in vesicular transport D. Kuemmel A.P. Turnbull J.J. Mueller Y. Roske U. Heinemann 15. Juni 2007 / J Mol Biol Optimized Variants of the Cold Shock Protein from in Vitro Selection: Structural Basis of Their High Thermostability K.E. Max M. Wunderlich Y. Roske F.X. Schmid U. Heinemann 26. Oktober 2007 / J Mol Biol Optimization of the Gbeta1 domain by computational design and by in vitro evolution: structural and energetic basis of stabilization M. Wunderlich K.E. Max Y. Roske U. Mueller U. Heinemann F.X. Schmid November 2004 / Nat Genet Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy B. Gerull A. Heuser T. Wichter M. Paul C.T. Basson D.A. McDermott B.B. Lerman S.M. Markowitz P.T. Ellinor C.A. MacRae S. Peters K.S. Grossmann J. Drenckhahn B. Michely S. Sasse-Klaassen W. Birchmeier R. Dietz G. Breithardt E. Schulze-Bahr L. Thierfelder 02. November 2004 / Am J Med Genet Response to correspondence by Dr. Finsterer and Dr. Stoellberger: Heterogenous myopathic background of left ventricular hypertrabeculation/noncompaction L. Thierfelder S. Sasse-Klaassen B. Gerull R. Jenni E. Oechslin 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 11. April 2024 / Nat Commun Pathogenic mutations of human phosphorylation sites affect protein–protein interactions T. Rrustemi K. Meyer Y. Roske B. Uyar A. Akalin K. Imami Y. Ishihama O. Daumke M. Selbach Seitennummerierung Erste Seite « First Vorherige Seite ‹ Previous Seite 1 Aktuelle Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
14. Dezember 2005 / BMC Struct Biol X-ray structure of engineered human Aortic Preferentially Expressed Protein-1 (APEG-1) B.A. Manjasetty F.H. Niesen C. Scheich Y. Roske F. Goetz J. Behlke V. Sievert U. Heinemann K. Buessow
Juni 2006 / J Mol Med Identification of a novel frameshift mutation in the giant muscle filament titin in a large Australian family with dilated cardiomyopathy B. Gerull J. Atherton A. Geupel S. Sasse-Klaassen A. Heuser M. Frenneaux M. McNabb H. Granzier S. Labeit L. Thierfelder
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
2006 Structural studies of the human tethering complex TRAPP involved in vesicular transport D. Kuemmel A.P. Turnbull J.J. Mueller Y. Roske U. Heinemann
15. Juni 2007 / J Mol Biol Optimized Variants of the Cold Shock Protein from in Vitro Selection: Structural Basis of Their High Thermostability K.E. Max M. Wunderlich Y. Roske F.X. Schmid U. Heinemann
26. Oktober 2007 / J Mol Biol Optimization of the Gbeta1 domain by computational design and by in vitro evolution: structural and energetic basis of stabilization M. Wunderlich K.E. Max Y. Roske U. Mueller U. Heinemann F.X. Schmid
November 2004 / Nat Genet Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy B. Gerull A. Heuser T. Wichter M. Paul C.T. Basson D.A. McDermott B.B. Lerman S.M. Markowitz P.T. Ellinor C.A. MacRae S. Peters K.S. Grossmann J. Drenckhahn B. Michely S. Sasse-Klaassen W. Birchmeier R. Dietz G. Breithardt E. Schulze-Bahr L. Thierfelder
02. November 2004 / Am J Med Genet Response to correspondence by Dr. Finsterer and Dr. Stoellberger: Heterogenous myopathic background of left ventricular hypertrabeculation/noncompaction L. Thierfelder S. Sasse-Klaassen B. Gerull R. Jenni E. Oechslin
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
11. April 2024 / Nat Commun Pathogenic mutations of human phosphorylation sites affect protein–protein interactions T. Rrustemi K. Meyer Y. Roske B. Uyar A. Akalin K. Imami Y. Ishihama O. Daumke M. Selbach