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Andreas Brodehl

medical school owl university of bielefeld

27H指数
78论文数
2.0K被引数
收录论文 32
发表时间
Mutational mapping of sequence variants within the arginine- and serine-rich domain of RNA binding motif protein 20RNA结合结构域蛋白20的精氨酸-丝氨酸富集区序列变异的突变图谱构建
err2026-07-16
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errOAAI
errJoline Groß; Caroline Wiebe; Elina Felski; Sandra Landwehr; Andreas Brodehl; Hans Ebbinghaus; Masoomeh Rezaei; Meryem Özger; Julia Blöbaum; Dorothee Staiger; Jan Gummert; Annika Hoyer; Stephan Schubert; Hendrik Milting; Anna Gärtner
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The myofibrillar myopathy–linked variant DES-p.T341P impairs desmin filament assembly与肌原纤维肌病相关的变异体DES-p.T341P损害了desmin丝状体的组装
err2026-03-25
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errAlexander Lütkemeyer; Sabrina Voß; Franziska Klag; Joline Groß; Jonas Reckmann; Anna Gärtner; Dario Anselmetti; Jan Gummert; Volker Walhorn; Hendrik Milting; Andreas Brodehl
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EPAS1 induction drives myocardial degeneration in desmoplakin-cardiomyopathyEPAS1诱导驱动desmoplakin-心肌病中心肌变性
err2025-03-01
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errKyriakopoulou, Eirini; van Kampen, Sebastiaan J.; Wehrens, Martijn; Han, Su Ji; de Ruiter, Hesther; Monshouwer-Kloots, Jantine; Marshall, Emma; Brodehl, Andreas; van der Kraak, Petra; te Riele, Anneline S. J. M.; van Aarnhem, Egidius E. H. L.; van Laake, Linda W.; Tsui, Hoyee; Boogerd, Cornelis J.
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Functional impact of the head domain variants of DES (Desmin) on filament assembly
err2025-01-01
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errVol, Sabrina; Walhorn, Volker; Holler, Stephanie; Gaertner, Anna; Pohl, Greta; Tiesmeier, Jens; Gummert, Jan; Anselmetti, Dario; Milting, Hendrik; Brodehl, Andreas
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Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy与Desmin相关的心律失常性心肌病的表型和临床结局
err2024-06-01
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PREAI
errBermudez-Jimenez, Francisco J.; Protonotarios, Alexandros; Garcia-Hernandez, Soledad; Asensio, Ana Perez; Rampazzo, Alessandra; Zorio, Esther; Brodehl, Andreas; Arias, Miguel A.; Macias-Ruiz, Rosa; Fernandez-Armenta, Juan; Perez, Paloma Remior; Munoz-Esparza, Carmen; Pilichou, Kalliopi; Bauce, Barbara; Merino, Jose L.; Moliner-Abos, Carlos; Ochoa, Juan P.; Barriales-Villa, Roberto; Garcia-Pavia, Pablo; Lopes, Luis R.; Syrris, Petros; Corrado, Domenico; Elliott, Perry M.; McKenna, William J.; Jimenez-Jaimez, Juan
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ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardiumROD2结构域细丝蛋白C错义突变表现出限制性/肥厚型心肌病和锯齿状心肌的独特心脏表型
err2023-05-01
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PREAI
errBermudez-Jimenez, Francisco; Carriel, Victor; Jose Santos-Mateo, Juan; Fernandez, Adrian; Garcia-Hernandez, Soledad; Ramos, Karina Analia; Piqueras-Flores, Jesus; Cabrera-Romero, Eva; Barriales-Villa, Roberto; Romero, Luis de la Higuera; Lopez, Juan Emilio Alcala; Blanes, Juan Ramoen Gimeno; Sanchez-Porras, David; Campos, Fernando; Alaminos, Miguel; Oyonarte-Ramirez, Jose Manuel; Alvarez, Miguel; Tercedor, Luis; Brodehl, Andreas; Jimenez-Jaimez, Juan
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The Consideration of Pseudoxanthoma Elasticum as a Progeria Syndrome
err2023-03-20
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errTiemann, Janina; Lindenkamp, Christopher; Wagner, Thomas; Brodehl, Andreas; Pluemers, Ricarda; Faust-Hinse, Isabel; Knabbe, Cornelius; Hendig, Doris
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Spatial transcriptomics unveils ZBTB11 as a regulator of cardiomyocyte degeneration in arrhythmogenic cardiomyopathy
err2022-05-16
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errBoogerd, Cornelis J.; Lacraz, Gregory P. A.; Vertesy, Abel; van Kampen, Sebastiaan J.; Perini, Ilaria; de Ruiter, Hesther; Versteeg, Danielle; Brodehl, Andreas; van der Kraak, Petra; Giacca, Mauro; de Jonge, Nicolaas; Junker, Jan Philipp; van Oudenaarden, Alexander; Vink, Aryan; van Rooij, Eva
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The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3Desmin突变DES-c.735G>C通过诱导Exon-3的帧内跳跃引起严重的限制性心肌病
err2021-10-05
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errBrodehl, Andreas; Hain, Carsten; Flottmann, Franziska; Ratnavadivel, Sandra; Gaertner, Anna; Klauke, Baerbel; Kalinowski, Joern; Koerperich, Hermann; Gummert, Jan; Paluszkiewicz, Lech; Deutsch, Marcus-Andre; Milting, Hendrik
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The Novel Desmin Variant p.Leu115IIe Is Associated With a Unique Form of Biventricular Arrhythmogenic Cardiomyopathy
err2021-06-01
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errProtonotarios, Alexandros; Brodehl, Andreas; Asimaki, Angeliki; Jager, Joanna; Quinn, Ellie; Stanasiuk, Caroline; Ratnavadivel, Sandra; Futema, Marta; Akhtar, Mohammed M.; Gossios, Thomas D.; Ashworth, Michael; Savvatis, Konstantinos; Walhorn, Volker; Anselmetti, Dario; Elliott, Perry M.; Syrris, Petros; Milting, Hendrik; Lopes, Luis R.
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Functional characterization of novel alpha-helical rod domain desmin (DES) pathogenic variants associated with dilated cardiomyopathy, atrioventricular block and a risk for sudden cardiac death
err2021-04-01
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PREAI
errFischer, Bjoern; Dittmann, Sven; Brodehl, Andreas; Unger, Andreas; Stallmeyer, Birgit; Paul, Matthias; Seebohm, Guiscard; Kayser, Anne; Peischard, Stefan; Linke, Wolfgang A.; Milting, Hendrik; Schulze-Bahr, Eric
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Cardiomyopathy-associated mutations in the RS domain affect nuclear localization of RBM20
err2020-09-09
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errGaertner, Anna; Klauke, Baerbel; Felski, Elina; Kassner, Astrid; Brodehl, Andreas; Gerdes, Desiree; Stanasiuk, Caroline; Ebbinghaus, Hans; Schulz, Uwe; Dubowy, Karl-Otto; Tiesmeier, Jens; Laser, Kai-Thorsten; Bante, Hendrik; Bergau, Leonard; Sommer, Philipp; Fox, Henrik; Morshuis, Michiel; Gummert, Jan; Milting, Hendrik
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Genetic Animal Models for Arrhythmogenic Cardiomyopathy
err2020-06-24
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errGerull, Brenda; Brodehl, Andreas
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A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy
err2020-04-01
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errBrodehl, Andreas; Weiss, Juergen; Debus, Jana Davina; Stanasiuk, Caroline; Klauke, Baerbel; Deutsch, Marcus Andre; Fox, Henrik; Bax, Joerdis; Ebbinghaus, Hans; Gaertner, Anna; Tiesmeier, Jens; Laser, Thorsten; Peterschroeder, Andreas; Gerull, Brenda; Gummert, Jan; Paluszkiewicz, Lech; Milting, Hendrik
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Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction
err2020-03-29
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errKubanek, Milos; Schimerova, Tereza; Piherova, Lenka; Brodehl, Andreas; Krebsova, Alice; Ratnavadivel, Sandra; Stanasiuk, Caroline; Hansikova, Hana; Zeman, Jiri; Palecek, Tomas; Houstek, Josef; Drahota, Zdenek; Nuskova, Hana; Mikesova, Jana; Zamecnik, Josef; Macek, Milan, Jr.; Ridzon, Petr; Maluskova, Jana; Stranecky, Viktor; Melenovsky, Vojtech; Milting, Hendrik; Kmoch, Stanislav
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Mutations in ILK, encoding integrin-linked kinase, are associated with arrhythmogenic cardiomyopathy
err2019-06-01
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errBrodehl, Andreas; Rezazadeh, Saman; Williams, Tatjana; Munsie, Nicole M.; Liedtke, Daniel; Oh, Tracey; Ferrier, Raechel; Shen, Yaoqing; Jones, Steven J. M.; Stiegler, Amy L.; Boggon, Titus J.; Duff, Henry J.; Friedman, Jan M.; Gibson, William T.; Boycott, K.; Friedman, J.; Michaud, J.; Bernier, F.; Brudno, M.; Fernandez, B.; Knoppers, B.; Samuels, M.; Scherer, S.; Childs, Sarah J.; Gerull, Brenda
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