BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

51 related articles for article (PubMed ID: 37021679)

  • 1. CHCHD2 and CHCHD10 regulate mitochondrial dynamics and integrated stress response.
    Ruan Y; Hu J; Che Y; Liu Y; Luo Z; Cheng J; Han Q; He H; Zhou Q
    Cell Death Dis; 2022 Feb; 13(2):156. PubMed ID: 35173147
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Aberrant CHCHD2-associated mitochondriopathy in Kii ALS/PDC astrocytes.
    Leventoux N; Morimoto S; Ishikawa M; Nakamura S; Ozawa F; Kobayashi R; Watanabe H; Supakul S; Okamoto S; Zhou Z; Kobayashi H; Kato C; Hirokawa Y; Aiba I; Takahashi S; Shibata S; Takao M; Yoshida M; Endo F; Yamanaka K; Kokubo Y; Okano H
    Acta Neuropathol; 2024 May; 147(1):84. PubMed ID: 38750212
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Disruption of Mitophagy Flux through the PARL-PINK1 Pathway by CHCHD10 Mutations or CHCHD10 Depletion.
    Liu T; Wetzel L; Zhu Z; Kumaraguru P; Gorthi V; Yan Y; Bukhari MZ; Ermekbaeva A; Jeon H; Kee TR; Woo JA; Kang DE
    Cells; 2023 Dec; 12(24):. PubMed ID: 38132101
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CHCHD10
    Genin EC; di Borgo PP; Lorivel T; Hugues S; Farinelli M; Mauri-Crouzet A; Lespinasse F; Godin L; Paquis-Flucklinger V; Petit-Paitel A
    Neurobiol Dis; 2024 Jun; 195():106498. PubMed ID: 38583639
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Generation of a human iPSC line from a Parkinson's disease patient with a novel CHCHD2 mutation (p.R145Q).
    Chen X; Sun J; Wang T; Tang Q; Su L; Sun Y; Chen L; Seo H; Cheng T; Wang J; Song B
    Stem Cell Res; 2024 Jun; 77():103419. PubMed ID: 38631182
    [TBL] [Abstract][Full Text] [Related]  

  • 6. High fat diet ameliorates mitochondrial cardiomyopathy in CHCHD10 mutant mice.
    Southwell N; Manzo O; Bacman S; Zhao D; Sayles NM; Dash J; Fujita K; D'Aurelio M; Di Lorenzo A; Manfredi G; Kawamata H
    EMBO Mol Med; 2024 Jun; 16(6):1352-1378. PubMed ID: 38724625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. High fat diet ameliorates mitochondrial cardiomyopathy in CHCHD10 mutant mice.
    Southwell N; Manzo O; Zhao D; Sayles NM; Dash J; Fujita K; D'Aurelio M; Di Lorenzo A; Manfredi G; Kawamata H
    bioRxiv; 2023 Dec; ():. PubMed ID: 36865125
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Editorial: Molecular links between mitochondrial damage and human neurodegenerative disorders, volume II.
    Imai Y
    Front Cell Dev Biol; 2024; 12():1417802. PubMed ID: 38742140
    [No Abstract]   [Full Text] [Related]  

  • 9. What is the role of CHCHD2 in adrenal tumourigenesis?
    Karapanagioti A; Nasiri-Ansari N; Moustogiannis A; Trigas GC; Zografos G; Aggeli C; Kyriakopoulos G; Choreftaki T; Philippou A; Kaltsas G; Kassi E; Angelousi A
    Endocrine; 2023 Aug; 81(2):357-367. PubMed ID: 37221428
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Elevated CHCHD4 orchestrates mitochondrial oxidative phosphorylation to disturb hypoxic pulmonary hypertension.
    Wang Y; Zeng Z; Zeng Z; Chu G; Shan X
    J Transl Med; 2023 Jul; 21(1):464. PubMed ID: 37438854
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The impacts of the mitochondrial myopathy-associated G58R mutation on the dynamic structural properties of CHCHD10.
    Alici H; Uversky VN; Kang DE; Woo JA; Coskuner-Weber O
    J Biomol Struct Dyn; 2024 Jul; 42(11):5607-5616. PubMed ID: 37349880
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Modulating Golgi Stress Signaling Ameliorates Cell Morphological Phenotypes Induced by CHMP2B with Frontotemporal Dementia-Associated p.Asp148Tyr.
    Fukatsu S; Okawa M; Okabe M; Cho M; Isogai M; Yokoi T; Shirai R; Oizumi H; Yamamoto M; Ohbuchi K; Miyamoto Y; Yamauchi J
    Curr Issues Mol Biol; 2024 Feb; 46(2):1398-1412. PubMed ID: 38392208
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lowered oxidative capacity in spinal muscular atrophy, Jokela type; comparison with mitochondrial muscle disease.
    Ratia N; Palu E; Lantto H; Ylikallio E; Luukkonen R; Suomalainen A; Auranen M; Piirilä P
    Front Neurol; 2023; 14():1277944. PubMed ID: 38020590
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signature.
    Shammas MK; Nie Y; Gilsrud A; Huang X; Narendra DP; Chinnery PF
    Hum Mol Genet; 2023 Dec; 33(1):91-101. PubMed ID: 37815936
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The identification of high-performing antibodies for Coiled-coil-helix-coiled-coil-helix domain containing protein 10 (CHCHD10) for use in Western Blot, immunoprecipitation and immunofluorescence.
    Ayoubi R; Alshafie W; Southern K; McPherson PS; Laflamme C;
    F1000Res; 2023; 12():403. PubMed ID: 37767023
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Case report: Asp194Ala variant in MFN2 is associated with ALS-FTD in an Italian family.
    Vinciguerra C; Di Fonzo A; Monfrini E; Ronchi D; Cuoco S; Piscosquito G; Barone P; Pellecchia MT
    Front Genet; 2023; 14():1235887. PubMed ID: 37547466
    [No Abstract]   [Full Text] [Related]  

  • 17. CHCHD2 and CHCHD10-related neurodegeneration: molecular pathogenesis and the path to precision therapy.
    Shammas MK; Huang TH; Narendra DP
    Biochem Soc Trans; 2023 Apr; 51(2):797-809. PubMed ID: 37021679
    [TBL] [Abstract][Full Text] [Related]  

  • 18. ALS and Parkinson's disease genes CHCHD10 and CHCHD2 modify synaptic transcriptomes in human iPSC-derived motor neurons.
    Harjuhaahto S; Rasila TS; Molchanova SM; Woldegebriel R; Kvist J; Konovalova S; Sainio MT; Pennonen J; Torregrosa-Muñumer R; Ibrahim H; Otonkoski T; Taira T; Ylikallio E; Tyynismaa H
    Neurobiol Dis; 2020 Jul; 141():104940. PubMed ID: 32437855
    [TBL] [Abstract][Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.