Publikationen von Angelika Kuhl

Hedberg, C.; Melberg, A.; Kuhl, A.; Jenne, D. E.; Oldfors, A.: Functional characterization of desmin mutant p.P419S Reply [Letter]. European journal of human genetics 21 (6), S. 590 - 590 (2013)

Hedberg, C.; Melberg, A.; Kuhl, A.; Jenne, D. E.; Oldfors, A.: Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7 is caused by a DES mutation. European journal of human genetics 20 (9), S. 984 - 985 (2012)

Kuhl, A.; Korkmaz, B.; Utecht, B.; Kniepert, A.; Schonermarck, U.; Specks, U.; Jenne, D. E.: Mapping of Conformational Epitopes on Human Proteinase 3, the Autoantigen of Wegener's Granulomatosis. Journal of Immunology 185 (1), S. 387 - 399 (2010)

Korkmaz, B.; Kuhl, A.; Bayat, B.; Santoso, S.; Jenne, D. E.: A Hydrophobic Patch on Proteinase 3, the Target of Autoantibodies in Wegener Granulomatosis, Mediates Membrane Binding via NB1 Receptors. Journal of Biological Chemistry 283 (51), S. 35976 - 35982 (2008)

Kuhl, A.; Melberg, A.; Meinl, E.; Nürnberg, G.; Nürnberg, P.; Kehrer-Sawatzki, H.; Jenne, D. E.: Myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy 7: Corroboration and narrowing of the critical region on 10q22.3. European Journal of Human Genetics 16, S. 367 - 373 (2008)

Jenne, D. E.; Kuhl, A.: Production and applications of recombinant proteinase 3, Wegener's autoantigen: Problems and perspectives. Clinical Nephrology 66 (3), S. 153 - 159 (2006)