Detalhe da pesquisa
1.
CHCHD10S59L/+ mouse model: Behavioral and neuropathological features of frontotemporal dementia.
Neurobiol Dis
; 195: 106498, 2024 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38583639
2.
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability.
Brain
; 145(10): 3415-3430, 2022 10 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-35656794
3.
Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy.
Am J Hum Genet
; 100(1): 151-159, 2017 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-27989324
4.
Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse.
Acta Neuropathol
; 138(1): 123-145, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30874923
5.
Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases.
Neurobiol Dis
; 119: 159-171, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30092269
6.
A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.
Brain
; 137(Pt 8): 2329-45, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24934289
7.
Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.
Brain
; 139(Pt 4): e22, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26719380
8.
hMSH5 is a nucleocytoplasmic shuttling protein whose stability depends on its subcellular localization.
Nucleic Acids Res
; 38(11): 3655-71, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20185565
9.
Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.
Brain
; 138(Pt 8): e373, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25576309
10.
Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
Brain
; 138(Pt 10): e386, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25953779
11.
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.
Brain
; 138(Pt 9): e377, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25681413
12.
Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.
Brain
; 137(Pt 12): e312, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25261971
13.
Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.
Brain
; 137(Pt 12): e310, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25113788
14.
Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?
Brain
; 137(Pt 12): e314, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25348633
15.
Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice.
Mitochondrion
; 30: 126-37, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-26923168
16.
CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis.
EMBO Mol Med
; 8(1): 58-72, 2016 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26666268
17.
The human MSH5 (MutSHomolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage.
Mitochondrion
; 12(6): 654-65, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22917773
18.
CRM1-dependent nuclear export and dimerization with hMSH5 contribute to the regulation of hMSH4 subcellular localization.
Exp Cell Res
; 313(17): 3680-93, 2007 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17869244
19.
The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination.
Hum Mol Genet
; 11(15): 1697-706, 2002 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-12095912
20.
Association between MSH4 (MutS homologue 4) and the DNA strand-exchange RAD51 and DMC1 proteins during mammalian meiosis.
Mol Hum Reprod
; 10(12): 917-24, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15489243