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] |
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URL: | https://www.wjgnet.com/1948-5182/full/v11/i3/99.htm |
Number | Citing Articles |
1 |
Khrystyna Shchubelka, Olga Herasymenko, Andrii Budzyn, Oleksandr Lysytsia, Anastasiia Rusyn, Olga Oleksyk, Svitlana Tynta, Taras Oleksyk. Novel ABCD1 variant causes phenotype of adrenomyeloneuropathy with cerebral involvement in Ukrainian siblings: first adult hematopoietic stem cell transplantation for ALD in Ukraine: a case report. Journal of Medical Case Reports 2024; 18(1) doi: 10.1186/s13256-023-04321-1
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2 |
Ronald J. A. Wanders, Myriam Baes, Daniela Ribeiro, Sacha Ferdinandusse, Hans R. Waterham. The physiological functions of human peroxisomes. Physiological Reviews 2023; 103(1): 957 doi: 10.1152/physrev.00051.2021
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3 |
Zhen Li, Guangrui Lai. X‑linked adrenoleukodystrophy caused by maternal ABCD1 mutation and paternal X chromosome inactivation. Experimental and Therapeutic Medicine 2022; 24(3) doi: 10.3892/etm.2022.11502
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4 |
Julianne H. Tieu, Siddhee A. Sahasrabudhe, Paul J. Orchard, James C. Cloyd, Reena V. Kartha. Translational and clinical pharmacology considerations in drug repurposing for X‐linked adrenoleukodystrophy—A rare peroxisomal disorder. British Journal of Clinical Pharmacology 2022; 88(6): 2552 doi: 10.1111/bcp.15090
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5 |
Qinyue Lu, Weicheng Zong, Mingyixing Zhang, Zhi Chen, Zhangping Yang. The Overlooked Transformation Mechanisms of VLCFAs: Peroxisomal β-Oxidation. Agriculture 2022; 12(7): 947 doi: 10.3390/agriculture12070947
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6 |
Rosa Campopiano, Cinzia Femiano, Maria Antonietta Chiaravalloti, Rosangela Ferese, Diego Centonze, Fabio Buttari, Stefania Zampatti, Mirco Fanelli, Stefano Amatori, Carmelo D’Alessio, Emiliano Giardina, Francesco Fornai, Francesca Biagioni, Marianna Storto, Stefano Gambardella. A Large Family with p.Arg554His Mutation in ABCD1: Clinical Features and Genotype/Phenotype Correlation in Female Carriers. Genes 2021; 12(5): 775 doi: 10.3390/genes12050775
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7 |
Katrin A. Dohr, Silvija Tokic, Magdalena Gastager-Ehgartner, Tatjana Stojakovic, Miroslav Dumic, Barbara Plecko, Katja K. Dumic. Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked Adrenoleukodystrophy. International Journal of Molecular Sciences 2023; 24(6): 5957 doi: 10.3390/ijms24065957
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