BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Saunders CJ, Moon SH, Liu X, Thiffault I, Coffman K, LePichon JB, Taboada E, Smith LD, Farrow EG, Miller N, Gibson M, Patterson M, Kingsmore SF, Gross RW. Loss of function variants in human PNPLA8 encoding calcium-independent phospholipase A2 γ recapitulate the mitochondriopathy of the homologous null mouse. Hum Mutat 2015;36:301-6. [PMID: 25512002 DOI: 10.1002/humu.22743] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 2.9] [Reference Citation Analysis]
Number Citing Articles
1 Lin R, Du X, Peng S, Yang L, Ma Y, Gong Y, Li S. Discovering All Transcriptome Single-Nucleotide Polymorphisms and Scanning for Selection Signatures in Ducks (Anas platyrhynchos). Evol Bioinform Online 2015;11:67-76. [PMID: 26819540 DOI: 10.4137/EBO.S21545] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
2 Hara S, Yoda E, Sasaki Y, Nakatani Y, Kuwata H. Calcium-independent phospholipase A2γ (iPLA2γ) and its roles in cellular functions and diseases. Biochim Biophys Acta Mol Cell Biol Lipids 2019;1864:861-8. [PMID: 30391710 DOI: 10.1016/j.bbalip.2018.10.009] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 1.0] [Reference Citation Analysis]
3 Flex E, Niceta M, Cecchetti S, Thiffault I, Au MG, Capuano A, Piermarini E, Ivanova AA, Francis JW, Chillemi G, Chandramouli B, Carpentieri G, Haaxma CA, Ciolfi A, Pizzi S, Douglas GV, Levine K, Sferra A, Dentici ML, Pfundt RR, Le Pichon JB, Farrow E, Baas F, Piemonte F, Dallapiccola B, Graham JM Jr, Saunders CJ, Bertini E, Kahn RA, Koolen DA, Tartaglia M. Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy. Am J Hum Genet 2016;99:962-73. [PMID: 27666370 DOI: 10.1016/j.ajhg.2016.08.003] [Cited by in Crossref: 55] [Cited by in F6Publishing: 50] [Article Influence: 9.2] [Reference Citation Analysis]
4 Ramanadham S, Ali T, Ashley JW, Bone RN, Hancock WD, Lei X. Calcium-independent phospholipases A2 and their roles in biological processes and diseases. J Lipid Res 2015;56:1643-68. [PMID: 26023050 DOI: 10.1194/jlr.R058701] [Cited by in Crossref: 103] [Cited by in F6Publishing: 67] [Article Influence: 14.7] [Reference Citation Analysis]
5 Thiffault I, Farrow E, Smith L, Lowry J, Zellmer L, Black B, Abdelmoity A, Miller N, Soden S, Saunders C. PCDH19-related epileptic encephalopathy in a male mosaic for a truncating variant. Am J Med Genet A 2016;170:1585-9. [PMID: 27016041 DOI: 10.1002/ajmg.a.37617] [Cited by in Crossref: 29] [Cited by in F6Publishing: 26] [Article Influence: 4.8] [Reference Citation Analysis]
6 Shukla A, Saneto RP, Hebbar M, Mirzaa G, Girisha KM. A neurodegenerative mitochondrial disease phenotype due to biallelic loss-of-function variants in PNPLA8 encoding calcium-independent phospholipase A2γ. Am J Med Genet A 2018;176:1232-7. [PMID: 29681094 DOI: 10.1002/ajmg.a.38687] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]
7 Kohda M, Tokuzawa Y, Kishita Y, Nyuzuki H, Moriyama Y, Mizuno Y, Hirata T, Yatsuka Y, Yamashita-Sugahara Y, Nakachi Y, Kato H, Okuda A, Tamaru S, Borna NN, Banshoya K, Aigaki T, Sato-Miyata Y, Ohnuma K, Suzuki T, Nagao A, Maehata H, Matsuda F, Higasa K, Nagasaki M, Yasuda J, Yamamoto M, Fushimi T, Shimura M, Kaiho-Ichimoto K, Harashima H, Yamazaki T, Mori M, Murayama K, Ohtake A, Okazaki Y. A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies. PLoS Genet 2016;12:e1005679. [PMID: 26741492 DOI: 10.1371/journal.pgen.1005679] [Cited by in Crossref: 152] [Cited by in F6Publishing: 135] [Article Influence: 25.3] [Reference Citation Analysis]
8 Aloulou A, Rahier R, Arhab Y, Noiriel A, Abousalham A. Phospholipases: An Overview. Methods Mol Biol 2018;1835:69-105. [PMID: 30109646 DOI: 10.1007/978-1-4939-8672-9_3] [Cited by in Crossref: 27] [Cited by in F6Publishing: 22] [Article Influence: 9.0] [Reference Citation Analysis]
9 Chao H, Liu Y, Fu X, Xu X, Bao Z, Lin C, Li Z, Liu Y, Wang X, You Y, Liu N, Ji J. Lowered iPLA2γ activity causes increased mitochondrial lipid peroxidation and mitochondrial dysfunction in a rotenone-induced model of Parkinson's disease. Experimental Neurology 2018;300:74-86. [DOI: 10.1016/j.expneurol.2017.10.031] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
10 Xiao C, Rossignol F, Vaz FM, Ferreira CR. Inherited disorders of complex lipid metabolism: A clinical review. J Inherit Metab Dis 2021;44:809-25. [PMID: 33594685 DOI: 10.1002/jimd.12369] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
11 Elimam H, Papillon J, Guillemette J, Navarro-Betancourt JR, Cybulsky AV. Genetic Ablation of Calcium-independent Phospholipase A2γ Exacerbates Glomerular Injury in Adriamycin Nephrosis in Mice. Sci Rep 2019;9:16229. [PMID: 31700134 DOI: 10.1038/s41598-019-52834-x] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
12 Murakami M, Sato H, Taketomi Y. Updating Phospholipase A2 Biology. Biomolecules 2020;10:E1457. [PMID: 33086624 DOI: 10.3390/biom10101457] [Cited by in Crossref: 17] [Cited by in F6Publishing: 15] [Article Influence: 8.5] [Reference Citation Analysis]
13 Kasahara T, Kubota-Sakashita M, Nagatsuka Y, Hirabayashi Y, Hanasaka T, Tohyama K, Kato T. Cardiolipin is essential for early embryonic viability and mitochondrial integrity of neurons in mammals. FASEB J 2020;34:1465-80. [PMID: 31914590 DOI: 10.1096/fj.201901598R] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
14 Lamari F, Saudubray J, Mitchell GA. Disorders of Intracellular Triglyceride and Phospholipid Metabolism. In: Saudubray J, Baumgartner MR, Walter J, editors. Inborn Metabolic Diseases. Berlin: Springer Berlin Heidelberg; 2016. pp. 477-91. [DOI: 10.1007/978-3-662-49771-5_34] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.2] [Reference Citation Analysis]
15 Yaginuma S, Kawana H, Aoki J. Current Knowledge on Mammalian Phospholipase A1, Brief History, Structures, Biochemical and Pathophysiological Roles. Molecules 2022;27:2487. [DOI: 10.3390/molecules27082487] [Reference Citation Analysis]
16 Bello SM, Smith CL, Eppig JT. Allele, phenotype and disease data at Mouse Genome Informatics: improving access and analysis. Mamm Genome 2015;26:285-94. [PMID: 26162703 DOI: 10.1007/s00335-015-9582-y] [Cited by in Crossref: 26] [Cited by in F6Publishing: 21] [Article Influence: 3.7] [Reference Citation Analysis]
17 Kunz E, Rothammer S, Pausch H, Schwarzenbacher H, Seefried FR, Matiasek K, Seichter D, Russ I, Fries R, Medugorac I. Confirmation of a non-synonymous SNP in PNPLA8 as a candidate causal mutation for Weaver syndrome in Brown Swiss cattle. Genet Sel Evol 2016;48:21. [PMID: 26992691 DOI: 10.1186/s12711-016-0201-5] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 3.3] [Reference Citation Analysis]
18 Murakami M. Lipoquality control by phospholipase A2 enzymes. Proc Jpn Acad Ser B Phys Biol Sci 2017;93:677-702. [PMID: 29129849 DOI: 10.2183/pjab.93.043] [Cited by in Crossref: 31] [Cited by in F6Publishing: 24] [Article Influence: 7.8] [Reference Citation Analysis]
19 Vogel P, Read RW, Hansen GM, Powell DR. Histopathology is required to identify and characterize myopathies in high-throughput phenotype screening of genetically engineered mice. Vet Pathol 2021;:3009858211030541. [PMID: 34269122 DOI: 10.1177/03009858211030541] [Reference Citation Analysis]
20 Masih S, Moirangthem A, Phadke SR. Homozygous Missense Variation in PNPLA8 Causes Prenatal-Onset Severe Neurodegeneration. Mol Syndromol 2021;12:174-8. [PMID: 34177434 DOI: 10.1159/000513524] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]