Suchergebnisse - "NDUFC2 protein, human"

PubPharm (11)

1

NDUFC2 deficiency exacerbates endothelial mesenchymal transformation during ischemia-reperfusion via NLRP3

enthalten in: Neuroreport | 2023

von Chen, J. | Liu, X. | Bi, R. | +2

2

Polymorphic variants at NDUFC2, encoding a mitochondrial complex I subunit, associate with cardiac hypertrophy in human hypertension

enthalten in: Molecular medicine (Cambridge, Mass.) | 2023

von Gallo, G. | Forte, M. | Cotugno, M. | +11

3

Mass Spectrometry-Based Quantitative Proteomics Analysis for Better Understanding of Telomeric Zinc Finger-Associated Protein-Induced Pathogenesis in Cardiomyocytes

enthalten in: International heart journal | 2022

von Sun, S. | Lv, T. | Li, S. | +4

4

The m6A methyltransferase METTL3 modifies PGC-1α mRNA promoting mitochondrial dysfunction and oxLDL-induced inflammation in monocytes

enthalten in: The Journal of biological chemistry | 2021

von Zhang, X. | Li, X. | Jia, H. | +2

5

Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex I

enthalten in: EMBO molecular medicine | 2020

von Alahmad, A. | Nasca, A. | Heidler, J. | +16

6

Complex I deficiency and Leigh syndrome through the eyes of a clinician

enthalten in: EMBO molecular medicine | 2020

von Reinson, K. | Õunap, K.

7

The reduction of NDUFC2 expression is associated with mitochondrial impairment in circulating mononuclear cells of patients with acute coronary syndrome

enthalten in: International journal of cardiology | 2019

von Raffa, S. | Chin, X. | Stanzione, R. | +12

CommentIn: Int J Cardiol. 2019 Jul 1;286:134-135. - PMID 30905519

8

Deficiency of NDUFC2 : Cause or bystander in acute coronary syndromes?

enthalten in: International journal of cardiology | 2019

von Madonna, R. | Vitulli, P. | Pierdomenico, S. | +1

CommentOn: Int J Cardiol. 2019 Jul 1;286:127-133. - PMID 30808603

9

In vitro characterization of mitochondrial function and structure in rat and human cells with a deficiency of the NADH : ubiquinone oxidoreductase Ndufc2 subunit

enthalten in: Human molecular genetics | 2017

von Raffa, S. | Scrofani, C. | Valente, S. | +9

10

Ndufc2 Gene Inhibition Is Associated With Mitochondrial Dysfunction and Increased Stroke Susceptibility in an Animal Model of Complex Human Disease

enthalten in: Journal of the American Heart Association | 2016

von Rubattu, S. | Di Castro, S. | Schulz, H. | +19