Narendra DP - Search Results

1

DELE1 promotes translation-associated homeostasis, growth, and survival in mitochondrial myopathy.

Lin HP, Petersen JD, Gilsrud AJ, Madruga A, D'Silva TM, Huang X, Shammas MK, Randolph NP, Li Y, Jones DR, Pacold ME, Narendra DP. Lin HP, et al. Among authors: narendra dp. bioRxiv [Preprint]. 2024 Feb 29:2024.02.29.582673. doi: 10.1101/2024.02.29.582673. bioRxiv. 2024. PMID: 38529505 Free PMC article. Preprint.

2

Loss of CHCHD2 and CHCHD10 activates OMA1 peptidase to disrupt mitochondrial cristae phenocopying patient mutations.

Liu YT, Huang X, Nguyen D, Shammas MK, Wu BP, Dombi E, Springer DA, Poulton J, Sekine S, Narendra DP. Liu YT, et al. Among authors: narendra dp. Hum Mol Genet. 2020 Jun 3;29(9):1547-1567. doi: 10.1093/hmg/ddaa077. Hum Mol Genet. 2020. PMID: 32338760 Free PMC article.

3

Mt-Keima detects PINK1-PRKN mitophagy in vivo with greater sensitivity than mito-QC.

Liu YT, Sliter DA, Shammas MK, Huang X, Wang C, Calvelli H, Maric DS, Narendra DP. Liu YT, et al. Among authors: narendra dp. Autophagy. 2021 Nov;17(11):3753-3762. doi: 10.1080/15548627.2021.1896924. Epub 2021 Mar 8. Autophagy. 2021. PMID: 33685343 Free PMC article.

4

Comment on "mt-Keima detects PINK1-PRKN mitophagy in vivo with greater sensitivity than mito-QC".

Liu YT, Sliter DA, Shammas MK, Huang X, Wang C, Calvelli H, Maric DS, Narendra DP. Liu YT, et al. Among authors: narendra dp. Autophagy. 2021 Dec;17(12):4484-4485. doi: 10.1080/15548627.2021.1909999. Epub 2021 Apr 23. Autophagy. 2021. PMID: 33890546 Free PMC article. No abstract available.

5

Sorting out Parkinson's disease: one cell at a time.

Lin HP, Narendra DP. Lin HP, et al. Among authors: narendra dp. Brain. 2022 Apr 29;145(3):811-813. doi: 10.1093/brain/awac071. Brain. 2022. PMID: 35301526 No abstract available.

6

OMA1 mediates local and global stress responses against protein misfolding in CHCHD10 mitochondrial myopathy.

Shammas MK, Huang X, Wu BP, Fessler E, Song IY, Randolph NP, Li Y, Bleck CK, Springer DA, Fratter C, Barbosa IA, Powers AF, Quirós PM, Lopez-Otin C, Jae LT, Poulton J, Narendra DP. Shammas MK, et al. Among authors: narendra dp. J Clin Invest. 2022 Jul 15;132(14):e157504. doi: 10.1172/JCI157504. J Clin Invest. 2022. PMID: 35700042 Free PMC article.

7

CHCHD2 and CHCHD10-related neurodegeneration: molecular pathogenesis and the path to precision therapy.

Shammas MK, Huang TH, Narendra DP. Shammas MK, et al. Among authors: narendra dp. Biochem Soc Trans. 2023 Apr 26;51(2):797-809. doi: 10.1042/BST20221365. Biochem Soc Trans. 2023. PMID: 37021679 Review.

8

CHCHD10 mutations induce tissue-specific mitochondrial DNA deletions with a distinct signature.

Shammas MK, Nie Y, Gilsrud A, Huang X, Narendra DP, Chinnery PF. Shammas MK, et al. Among authors: narendra dp. Hum Mol Genet. 2023 Dec 12;33(1):91-101. doi: 10.1093/hmg/ddad161. Hum Mol Genet. 2023. PMID: 37815936 Free PMC article.

9

How to treat a "sweetheart" in mitochondrial cardiomyopathy.

Lin HP, Narendra DP. Lin HP, et al. Among authors: narendra dp. EMBO Mol Med. 2024 May 9. doi: 10.1038/s44321-024-00070-w. Online ahead of print. EMBO Mol Med. 2024. PMID: 38724624 Free article. No abstract available.

10

CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10.

Huang X, Wu BP, Nguyen D, Liu YT, Marani M, Hench J, Bénit P, Kozjak-Pavlovic V, Rustin P, Frank S, Narendra DP. Huang X, et al. Among authors: narendra dp. Hum Mol Genet. 2018 Nov 15;27(22):3881-3900. doi: 10.1093/hmg/ddy270. Hum Mol Genet. 2018. PMID: 30084972 Free PMC article.

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