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For: Basel D. Mitochondrial DNA Depletion Syndromes. Clinics in Perinatology 2020;47:123-41. [DOI: 10.1016/j.clp.2019.10.008] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Picard M. Blood mitochondrial DNA copy number: What are we counting? Mitochondrion 2021;60:1-11. [PMID: 34157430 DOI: 10.1016/j.mito.2021.06.010] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
2 Kashiki T, Kido J, Momosaki K, Kusunoki S, Ozasa S, Nomura K, Imai-Okazaki A, Tsuruoka T, Murayama K, Koga Y, Nakamura K. Mitochondrial DNA depletion syndrome with a mutation in SLC25A4 developing epileptic encephalopathy: A case report. Brain Dev 2021:S0387-7604(21)00155-8. [PMID: 34452803 DOI: 10.1016/j.braindev.2021.08.005] [Reference Citation Analysis]
3 Longchamps RJ, Yang SY, Castellani CA, Shi W, Lane J, Grove ML, Bartz TM, Sarnowski C, Liu C, Burrows K, Guyatt AL, Gaunt TR, Kacprowski T, Yang J, De Jager PL, Yu L, Bergman A, Xia R, Fornage M, Feitosa MF, Wojczynski MK, Kraja AT, Province MA, Amin N, Rivadeneira F, Tiemeier H, Uitterlinden AG, Broer L, Van Meurs JBJ, Van Duijn CM, Raffield LM, Lange L, Rich SS, Lemaitre RN, Goodarzi MO, Sitlani CM, Mak ACY, Bennett DA, Rodriguez S, Murabito JM, Lunetta KL, Sotoodehnia N, Atzmon G, Ye K, Barzilai N, Brody JA, Psaty BM, Taylor KD, Rotter JI, Boerwinkle E, Pankratz N, Arking DE. Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation. Hum Genet 2021. [PMID: 34859289 DOI: 10.1007/s00439-021-02394-w] [Reference Citation Analysis]
4 Gilea AI, Ceccatelli Berti C, Magistrati M, di Punzio G, Goffrini P, Baruffini E, Dallabona C. Saccharomyces cerevisiae as a Tool for Studying Mutations in Nuclear Genes Involved in Diseases Caused by Mitochondrial DNA Instability. Genes (Basel) 2021;12:1866. [PMID: 34946817 DOI: 10.3390/genes12121866] [Reference Citation Analysis]
5 Marco-Hernández AV, Tomás-Vila M, Montoya-Filardi A, Barranco-González H, Vilchez Padilla JJ, Azorín I, Smeyers Dura P, Monfort-Membrado S, Pitarch-Castellano I, Martínez-Castellano F. Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene. Clin Genet 2021. [PMID: 34842280 DOI: 10.1111/cge.14093] [Reference Citation Analysis]
6 Wikramanayake TC, Chéret J, Sevilla A, Birch-Machin M, Paus R. Targeting mitochondria in dermatological therapy: Beyond oxidative damage and skin aging. Expert Opin Ther Targets 2022. [PMID: 35249436 DOI: 10.1080/14728222.2022.2049756] [Reference Citation Analysis]
7 Moretti R, Caruso P. Small Vessel Disease: Ancient Description, Novel Biomarkers. Int J Mol Sci 2022;23:3508. [PMID: 35408867 DOI: 10.3390/ijms23073508] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Pellino G, Faggioli R, Galuppi A, Leon A, Fusco C, Tugnoli V, Suppiej A. Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders. Mitochondrion 2021;61:159-64. [PMID: 34600155 DOI: 10.1016/j.mito.2021.09.011] [Reference Citation Analysis]