BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Capel E, Vatier C, Cervera P, Stojkovic T, Disse E, Cottereau AS, Auclair M, Verpont MC, Mosbah H, Gourdy P, Barraud S, Miquel A, Züchner S, Bonnefond A, Froguel P, Christin-Maitre S, Delemer B, Fève B, Laville M, Robert J, Tenenbaum F, Lascols O, Vigouroux C, Jéru I. MFN2-associated lipomatosis: Clinical spectrum and impact on adipose tissue. J Clin Lipidol 2018;12:1420-35. [PMID: 30158064 DOI: 10.1016/j.jacl.2018.07.009] [Cited by in Crossref: 24] [Cited by in F6Publishing: 20] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Chapman J, Ng YS, Nicholls TJ. The Maintenance of Mitochondrial DNA Integrity and Dynamics by Mitochondrial Membranes. Life (Basel) 2020;10:E164. [PMID: 32858900 DOI: 10.3390/life10090164] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
2 Mann JP, Savage DB. What lipodystrophies teach us about the metabolic syndrome. J Clin Invest 2019;129:4009-21. [PMID: 31380809 DOI: 10.1172/JCI129190] [Cited by in Crossref: 30] [Cited by in F6Publishing: 13] [Article Influence: 10.0] [Reference Citation Analysis]
3 Maresca A, Carelli V. Molecular Mechanisms behind Inherited Neurodegeneration of the Optic Nerve. Biomolecules 2021;11:496. [PMID: 33806088 DOI: 10.3390/biom11040496] [Reference Citation Analysis]
4 Jéru I. Genetics of lipodystrophy syndromes. Presse Med 2021;50:104074. [PMID: 34562561 DOI: 10.1016/j.lpm.2021.104074] [Reference Citation Analysis]
5 Ng MYW, Wai T, Simonsen A. Quality control of the mitochondrion. Dev Cell 2021;56:881-905. [PMID: 33662258 DOI: 10.1016/j.devcel.2021.02.009] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
6 Lim K, Haider A, Adams C, Sleigh A, Savage DB. Lipodistrophy: a paradigm for understanding the consequences of "overloading" adipose tissue. Physiol Rev 2021;101:907-93. [PMID: 33356916 DOI: 10.1152/physrev.00032.2020] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
7 Sollier C, Vatier C, Capel E, Lascols O, Auclair M, Janmaat S, Fève B, Jéru I, Vigouroux C. Lipodystrophic syndromes: From diagnosis to treatment. Ann Endocrinol (Paris) 2020;81:51-60. [PMID: 31982105 DOI: 10.1016/j.ando.2019.10.003] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 2.3] [Reference Citation Analysis]
8 Bruno A, Di Sano C, Simon HU, Chanez P, Patti AM, Di Vincenzo S, Dino P, D'Esposito V, Formisano P, Beguinot F, Pace E. Leptin and TGF-β1 Downregulate PREP1 Expression in Human Adipose-Derived Mesenchymal Stem Cells and Mature Adipocytes. Front Cell Dev Biol 2021;9:700481. [PMID: 34327205 DOI: 10.3389/fcell.2021.700481] [Reference Citation Analysis]
9 Chen K, Wan X, Zhao L, Zhao S, Peng L, Yang W, Yuan J, Zhu L, Mo Z. Cbl Proto-Oncogene B (CBLB) c.197A>T Mutation Induces Mild Metabolic Dysfunction in Partial Type I Multiple Symmetric Lipomatosis (MSL). Diabetes Metab Syndr Obes 2020;13:3535-49. [PMID: 33116705 DOI: 10.2147/DMSO.S273780] [Reference Citation Analysis]
10 Brandão BB, Poojari A, Rabiee A. Thermogenic Fat: Development, Physiological Function, and Therapeutic Potential. Int J Mol Sci 2021;22:5906. [PMID: 34072788 DOI: 10.3390/ijms22115906] [Reference Citation Analysis]
11 Dorn GW 2nd. Mitofusin 2 Dysfunction and Disease in Mice and Men. Front Physiol 2020;11:782. [PMID: 32733278 DOI: 10.3389/fphys.2020.00782] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
12 Lemaitre M, Chevalier B, Jannin A, Bourry J, Espiard S, Vantyghem MC. Multiple symmetric and multiple familial lipomatosis. Presse Med 2021;50:104077. [PMID: 34687914 DOI: 10.1016/j.lpm.2021.104077] [Reference Citation Analysis]
13 Araújo de Melo Campos JT, Dantas de Medeiros JL, Cardoso de Melo ME, Alvares da Silva M, Oliveira de Sena M, Sales Craveiro Sarmento A, Fassarella Agnez Lima L, de Freitas Fregonezi GA, Gomes Lima J. Endoplasmic reticulum stress and muscle dysfunction in congenital lipodystrophies. Biochim Biophys Acta Mol Basis Dis 2021;1867:166120. [PMID: 33713793 DOI: 10.1016/j.bbadis.2021.166120] [Reference Citation Analysis]
14 Gautheron J, Morisseau C, Chung WK, Zammouri J, Auclair M, Baujat G, Capel E, Moulin C, Wang Y, Yang J, Hammock BD, Cerame B, Phan F, Fève B, Vigouroux C, Andreelli F, Jeru I. EPHX1 mutations cause a lipoatrophic diabetes syndrome due to impaired epoxide hydrolysis and increased cellular senescence. Elife 2021;10:e68445. [PMID: 34342583 DOI: 10.7554/eLife.68445] [Reference Citation Analysis]
15 Chen KK, Ni LS, Yu WH. Madelung disease: A case report. World J Clin Cases 2021; 9(8): 1983-1988 [PMID: 33748250 DOI: 10.12998/wjcc.v9.i8.1983] [Cited by in CrossRef: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Nadeau E, Mezei MM, Cresswell M, Zhao S, Bosdet T, Sin DD, Guenette JA, Dupuis I, Allin E, Clarke DC, Mattman A. Self-initiated lifestyle interventions lead to potential insight into an effective, alternative, non-surgical therapy for mitochondrial disease associated multiple symmetric lipomatosis. Mitochondrion 2020;52:183-9. [PMID: 32234544 DOI: 10.1016/j.mito.2020.03.009] [Reference Citation Analysis]
17 Fernández-Pombo A, Sánchez-Iglesias S, Cobelo-Gómez S, Hermida-Ameijeiras Á, Araújo-Vilar D. Familial partial lipodystrophy syndromes. Presse Med 2021;50:104071. [PMID: 34610417 DOI: 10.1016/j.lpm.2021.104071] [Reference Citation Analysis]
18 Sharma G, Pfeffer G, Shutt TE. Genetic Neuropathy Due to Impairments in Mitochondrial Dynamics. Biology (Basel) 2021;10:268. [PMID: 33810506 DOI: 10.3390/biology10040268] [Reference Citation Analysis]
19 Foss-Freitas MC, Akinci B, Luo Y, Stratton A, Oral EA. Diagnostic strategies and clinical management of lipodystrophy. Expert Rev Endocrinol Metab 2020;15:95-114. [PMID: 32368944 DOI: 10.1080/17446651.2020.1735360] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
20 Lemaitre M, Aubert S, Chevalier B, Jannin A, Bourry J, Prévost G, Lefebvre H, Vantyghem MC. Rare Forms of Lipomatosis: Dercum's Disease and Roch-Leri Mesosomatous Lipomatosis. J Clin Med 2021;10:1292. [PMID: 33800991 DOI: 10.3390/jcm10061292] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Ng YS, Lim AZ, Panagiotou G, Turnbull DM, Walker M. Endocrine manifestations and new developments in mitochondrial disease. Endocr Rev 2021:bnab036. [PMID: 34644386 DOI: 10.1210/endrev/bnab036] [Reference Citation Analysis]