[HTML][HTML] Neurodegeneration-associated mitochondrial proteins, CHCHD2 and CHCHD10–what distinguishes the two?
A Ikeda, Y Imai, N Hattori - Frontiers in Cell and Developmental …, 2022 - frontiersin.org
Coiled-coil-helix-coiled-coil-helix domain containing 2 (CHCHD2) and Coiled-coil-helix-
coiled-coil-helix domain containing 10 (CHCHD10) are mitochondrial proteins that are …
coiled-coil-helix domain containing 10 (CHCHD10) are mitochondrial proteins that are …
CHCHD2 and CHCHD10-related neurodegeneration: molecular pathogenesis and the path to precision therapy
MK Shammas, TH Huang… - Biochemical Society …, 2023 - portlandpress.com
In the last decade, dominant mutations in the mitochondrial protein CHCHD10 (p. R15L and
p. S59L) and its paralog CHCHD2 (p. T61I) were shown to cause familial amyotrophic lateral …
p. S59L) and its paralog CHCHD2 (p. T61I) were shown to cause familial amyotrophic lateral …
High fat diet ameliorates mitochondrial cardiomyopathy in CHCHD10 mutant mice
N Southwell, O Manzo, S Bacman, D Zhao… - EMBO Molecular …, 2024 - embopress.org
Mutations in CHCHD10, a mitochondrial protein with undefined functions, are associated
with autosomal dominant mitochondrial diseases. Chchd10 knock-in mice harboring a …
with autosomal dominant mitochondrial diseases. Chchd10 knock-in mice harboring a …
[HTML][HTML] Implications of TDP-43 in non-neuronal systems
H Ke, K Liu, B Jiao, L Zhao - Cell Communication and Signaling, 2023 - Springer
Abstract TAR DNA-binding protein 43 (TDP-43) is a versatile RNA/DNA-binding protein with
multifaceted processes. While TDP-43 has been extensively studied in the context of …
multifaceted processes. While TDP-43 has been extensively studied in the context of …
[HTML][HTML] Elevated CHCHD4 orchestrates mitochondrial oxidative phosphorylation to disturb hypoxic pulmonary hypertension
Y Wang, Z Zeng, Z Zeng, G Chu, X Shan - Journal of Translational …, 2023 - Springer
Background Pulmonary arterial hypertension (PAH) is a highly prevalent cardiopulmonary
disorder characterized by vascular remodeling and increased resistance in pulmonary …
disorder characterized by vascular remodeling and increased resistance in pulmonary …
Loss of mitochondrial Chchd10 or Chchd2 in zebrafish leads to an ALS‐like phenotype and Complex I deficiency independent of the mitochondrial integrated stress …
V Petel Légaré, CJ Rampal… - Developmental …, 2023 - Wiley Online Library
Mutations in CHCHD10 and CHCHD2, encoding two paralogous mitochondrial proteins,
have been identified in cases of amyotrophic lateral sclerosis, frontotemporal lobar …
have been identified in cases of amyotrophic lateral sclerosis, frontotemporal lobar …
A Mendelian randomization study identifies the causal association between plasma mitochondrial CHCHD proteins and polycystic ovary syndrome
S Wei, Y Wang, N Liu, R Zhao - medRxiv, 2024 - medrxiv.org
Purpose: The objective of this research was to examine the causal link between PCOS and
plasma mitochondrial coiled-coil-helix-coiled-coil-helix domain (CHCHD) proteins using a …
plasma mitochondrial coiled-coil-helix-coiled-coil-helix domain (CHCHD) proteins using a …
The impacts of the mitochondrial myopathy-associated G58R mutation on the dynamic structural properties of CHCHD10
The mitochondria are responsible for producing energy within the cell, and in mitochondrial
myopathy, there is a defect in the energy production process. The CHCHD10 gene codes for …
myopathy, there is a defect in the energy production process. The CHCHD10 gene codes for …
Mitochondrial Dysfunction and Stress Responses in CHCHD10 Myopathy and Neurodegeneration
M Shammas - 2024 - repository.cam.ac.uk
In the last decade, dominant mutations in the mitochondrial protein CHCHD10 and its
paralogue CHCHD2 were shown to cause familial amyotrophic lateral sclerosis and …
paralogue CHCHD2 were shown to cause familial amyotrophic lateral sclerosis and …
Modelling diseases associated with mitochondrial proteins CHCHD10 and CHCHD2 in zebrafish
V Petel Légaré - 2023 - escholarship.mcgill.ca
Les paralogues mitochondriaux CHCHD10 et CHCHD2 sont associés à plusieurs maladies
neurodégénératives, notamment la sclérose latérale amyotrophique (SLA) et la maladie de …
neurodégénératives, notamment la sclérose latérale amyotrophique (SLA) et la maladie de …