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Cited by in F6Publishing
For: Palakuzhiyil SV, Christopher R, Chandra SR. Deciphering the modifiers for phenotypic variability of X-linked adrenoleukodystrophy. World J Biol Chem 2020; 11(3): 99-111 [PMID: 33274015 DOI: 10.4331/wjbc.v11.i3.99] [Cited by in CrossRef: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
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1 Golbano A, Pardo L, Menacho CM, Rierola M, Claro E, Wood LB, Masgrau R, Galea E. Defective neuritogenesis in Abcd1/2 deficient rat neurons due to intrinsic and astrocyte-dependent mechanisms.. [DOI: 10.1101/2022.09.30.510337] [Reference Citation Analysis]
2 Lu Q, Zong W, Zhang M, Chen Z, Yang Z. The Overlooked Transformation Mechanisms of VLCFAs: Peroxisomal β-Oxidation. Agriculture 2022;12:947. [DOI: 10.3390/agriculture12070947] [Reference Citation Analysis]
3 Tieu JH, Sahasrabudhe SA, Orchard PJ, Cloyd JC, Kartha RV. Translational and clinical pharmacology considerations in drug repurposing for X-linked adrenoleukodystrophy-A rare peroxisomal disorder. Br J Clin Pharmacol 2021. [PMID: 34558098 DOI: 10.1111/bcp.15090] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Campopiano R, Femiano C, Chiaravalloti MA, Ferese R, Centonze D, Buttari F, Zampatti S, Fanelli M, Amatori S, D'Alessio C, Giardina E, Fornai F, Biagioni F, Storto M, Gambardella S. A Large Family with p.Arg554His Mutation in ABCD1: Clinical Features and Genotype/Phenotype Correlation in Female Carriers. Genes (Basel) 2021;12:775. [PMID: 34069712 DOI: 10.3390/genes12050775] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]