Brodehl A - Search Results

1

The Consideration of Pseudoxanthoma Elasticum as a Progeria Syndrome.

Tiemann J, Lindenkamp C, Wagner T, Brodehl A, Plümers R, Faust-Hinse I, Knabbe C, Hendig D. Tiemann J, et al. Among authors: brodehl a. Front Biosci (Landmark Ed). 2023 Mar 20;28(3):55. doi: 10.31083/j.fbl2803055. Front Biosci (Landmark Ed). 2023. PMID: 37005749 Free article.

2

Restrictive Cardiomyopathy is Caused by a Novel Homozygous Desmin (DES) Mutation p.Y122H Leading to a Severe Filament Assembly Defect.

Brodehl A, Pour Hakimi SA, Stanasiuk C, Ratnavadivel S, Hendig D, Gaertner A, Gerull B, Gummert J, Paluszkiewicz L, Milting H. Brodehl A, et al. Genes (Basel). 2019 Nov 11;10(11):918. doi: 10.3390/genes10110918. Genes (Basel). 2019. PMID: 31718026 Free PMC article.

3

Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants.

Brodehl A, Hedde PN, Dieding M, Fatima A, Walhorn V, Gayda S, Šarić T, Klauke B, Gummert J, Anselmetti D, Heilemann M, Nienhaus GU, Milting H. Brodehl A, et al. J Biol Chem. 2012 May 4;287(19):16047-57. doi: 10.1074/jbc.M111.313841. Epub 2012 Mar 8. J Biol Chem. 2012. PMID: 22403400 Free PMC article.

4

Genetic Animal Models for Arrhythmogenic Cardiomyopathy.

Gerull B, Brodehl A. Gerull B, et al. Among authors: brodehl a. Front Physiol. 2020 Jun 24;11:624. doi: 10.3389/fphys.2020.00624. eCollection 2020. Front Physiol. 2020. PMID: 32670084 Free PMC article. Review.

5

Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia.

Bermúdez-Jiménez FJ, Carriel V, Brodehl A, Alaminos M, Campos A, Schirmer I, Milting H, Abril BÁ, Álvarez M, López-Fernández S, García-Giustiniani D, Monserrat L, Tercedor L, Jiménez-Jáimez J. Bermúdez-Jiménez FJ, et al. Among authors: brodehl a. Circulation. 2018 Apr 10;137(15):1595-1610. doi: 10.1161/CIRCULATIONAHA.117.028719. Epub 2017 Dec 6. Circulation. 2018. PMID: 29212896 Free article.

6

The N-Terminal Part of the 1A Domain of Desmin Is a Hot Spot Region for Putative Pathogenic DES Mutations Affecting Filament Assembly.

Brodehl A, Holler S, Gummert J, Milting H. Brodehl A, et al. Cells. 2022 Dec 2;11(23):3906. doi: 10.3390/cells11233906. Cells. 2022. PMID: 36497166 Free PMC article.

7

Altered Expression of TMEM43 Causes Abnormal Cardiac Structure and Function in Zebrafish.

Zink M, Seewald A, Rohrbach M, Brodehl A, Liedtke D, Williams T, Childs SJ, Gerull B. Zink M, et al. Among authors: brodehl a. Int J Mol Sci. 2022 Aug 23;23(17):9530. doi: 10.3390/ijms23179530. Int J Mol Sci. 2022. PMID: 36076925 Free PMC article.

8

In vitro analysis of arrhythmogenic cardiomyopathy associated desmoglein-2 (DSG2) mutations reveals diverse glycosylation patterns.

Debus JD, Milting H, Brodehl A, Kassner A, Anselmetti D, Gummert J, Gaertner-Rommel A. Debus JD, et al. Among authors: brodehl a. J Mol Cell Cardiol. 2019 Apr;129:303-313. doi: 10.1016/j.yjmcc.2019.03.014. Epub 2019 Mar 15. J Mol Cell Cardiol. 2019. PMID: 30885746 Free article.

9

Cardiomyopathy related desmocollin-2 prodomain variants affect the intracellular cadherin transport and processing.

Pohl GM, Göz M, Gaertner A, Brodehl A, Cimen T, Saguner AM, Schulze-Bahr E, Walhorn V, Anselmetti D, Milting H. Pohl GM, et al. Among authors: brodehl a. Front Cardiovasc Med. 2023 May 19;10:1127261. doi: 10.3389/fcvm.2023.1127261. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37273868 Free PMC article.

10

The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy.

Gaertner A, Bloebaum J, Brodehl A, Klauke B, Sielemann K, Kassner A, Fox H, Morshuis M, Tiesmeier J, Schulz U, Knoell R, Gummert J, Milting H. Gaertner A, et al. Among authors: brodehl a. Genes (Basel). 2021 Jun 8;12(6):883. doi: 10.3390/genes12060883. Genes (Basel). 2021. PMID: 34201072 Free PMC article.

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