E-LIB Suche - Ergebnisse für: Perrot, Andreas

1

Human Genetics of Defects of Situs:

, In: Advances in Experimental Medicine and Biology; Congenital Heart Diseases: The Broken Heart,

Perrot, Andreas ; Rickert-Sperling, Silke - p. 705-717 , 2024

Link: https://doi.org/10.1007/..

2

Human Genetics of Tetralogy of Fallot and Double-Outlet Rig..:

, In: Advances in Experimental Medicine and Biology; Congenital Heart Diseases: The Broken Heart,

Dorn, Cornelia ; Perrot, Andreas ; Grunert, Marcel. - p. 629-644 , 2024

Link: https://doi.org/10.1007/..

3

Human Genetics of Ventricular Septal Defect:

, In: Advances in Experimental Medicine and Biology; Congenital Heart Diseases: The Broken Heart,

Perrot, Andreas ; Rickert-Sperling, Silke - p. 505-534 , 2024

Link: https://doi.org/10.1007/..

4

Nonsense mediated decay factor UPF3B is associated with cMy..:

Burkart, Valentin ; Kowalski, Kathrin ; Disch, Alina...
Journal of Molecular and Cellular Cardiology. 185 (2023) - p. 26-37 , 2023

Link: https://doi.org/10.1016/..

5

AQUA Mutant Protein Quantification of Endomyocardial Biopsy..:

Becker, Edgar ; Francino, Antonio ; Pich, Andreas...
Frontiers in Cardiovascular Medicine. 9 (2022) - p. , 2022

Link: https://doi.org/10.3389/..

6

Identification of a novel titin-cap/telethonin mutation in ..:

Toste, Alexandra ; Perrot, Andreas ; Özcelik, Cemil.
Revista Portuguesa de Cardiologia. 39 (2020) 6 - p. 317-327 , 2020

Link: https://doi.org/10.1016/..

7

Identification of MYOM2 as a candidate gene in hypertrophic..:

Auxerre-Plantié, Emilie ; Nielsen, Tanja ; Grunert, Marcel...
Disease Models & Mechanisms. 13 (2020) 12 - p. , 2020

Link: https://doi.org/10.1242/..

8

Identification of a novel titin-cap/telethonin mutation in ..:

Toste, Alexandra ; Perrot, Andreas ; Özcelik, Cemil.
Revista Portuguesa de Cardiologia (English Edition). 39 (2020) 6 - p. 317-327 , 2020

Link: https://doi.org/10.1016/..

9

TIP30 counteracts cardiac hypertrophy and failure by inhibi..:

Grund, Andrea ; Szaroszyk, Malgorzata ; Korf‐Klingebiel, Mortimer...
EMBO Molecular Medicine. 11 (2019) 10 - p. , 2019

Link: https://doi.org/10.15252..

10

Burst-Like Transcription of Mutant and Wildtype MYH7-Allele..:

Montag, Judith ; Kowalski, Kathrin ; Makul, Mirza...
Frontiers in Physiology. 9 (2018) - p. , 2018

Link: https://doi.org/10.3389/..

11

Intrinsic MYH7 expression regulation contributes to tissue ..:

Montag, Judith ; Syring, Mandy ; Rose, Julia...
Journal of Muscle Research and Cell Motility. 38 (2017) 3-4 - p. 291-302 , 2017

Link: https://doi.org/10.1007/..

12

Severe DCM phenotype of patient harboring RBM20 mutation S6..:

Streckfuss-Bömeke, Katrin ; Tiburcy, Malte ; Fomin, Andrey...
Journal of Molecular and Cellular Cardiology. 113 (2017) - p. 9-21 , 2017

Link: https://doi.org/10.1016/..

13

Hypertrophic remodelling in cardiac regulatory myosin light..:

Claes, Godelieve R.F. ; van Tienen, Florence H.J. ; Lindsey, Patrick...
European Heart Journal. 37 (2015) 23 - p. 1815-1822 , 2015

Link: https://doi.org/10.1093/..

14

A promoter polymorphism -945C>G in the connective tissue gr..:

Posch, Maximilian G. ; Schmidt, Gunther ; Steinhoff, Laura...
European Journal of Cardio-Thoracic Surgery. 47 (2014) 1 - p. e29-e33 , 2014

Link: https://doi.org/10.1093/..

15

CCN1 Mutation is Associated with Atrial Septal Defect:

Perrot, Andreas ; Schmitt, Katharina R. ; Roth, Eva-Maria G....
Pediatric Cardiology. 36 (2014) 2 - p. 295-299 , 2014

Link: https://doi.org/10.1007/..