Fatty Acids

ATP binding cassette subfamily D member 1 ; Homo sapiens







26 Article(s)
Download
PMID
Title
Pub. Year
#Total Relationships
1 35013584 Structures of the human peroxisomal fatty acid transporter ABCD1 in a lipid environment. 2022 Jan 10 1
2 35053399 Structure and Function of the ABCD1 Variant Database: 20 Years, 940 Pathogenic Variants, and 3400 Cases of Adrenoleukodystrophy. 2022 Jan 14 1
3 35466195 Newborn Screening for X-Linked Adrenoleukodystrophy: Review of Data and Outcomes in Pennsylvania. 2022 Mar 23 1
4 33500543 Acyl-CoA thioesterase activity of peroxisomal ABC protein ABCD1 is required for the transport of very long-chain acyl-CoA into peroxisomes. 2021 Jan 26 1
5 34069712 A Large Family with p.Arg554His Mutation in ABCD1: Clinical Features and Genotype/Phenotype Correlation in Female Carriers. 2021 May 19 1
6 34266597 Endocrine dysfunction in adrenoleukodystrophy. 2021 1
7 34445349 Glycosphingolipids with Very Long-Chain Fatty Acids Accumulate in Fibroblasts from Adrenoleukodystrophy Patients. 2021 Aug 11 1
8 34556923 Loes Score: Clinical and Radiological Profile of 22 Patients of X-Linked Adrenoleukodystrophy: Case Series from a Single Center. 2021 Apr 1
9 34631715 The RNA N6-Methyladenosine Methyltransferase METTL3 Promotes the Progression of Kidney Cancer via N6-Methyladenosine-Dependent Translational Enhancement of ABCD1. 2021 1
10 34652380 [X-linked adrenoleukodystrophy: A case of acute childhood cerebral presentation]. 2021 Aug 1
11 32020747 Failure of intrathecal allogeneic mesenchymal stem cells to halt progressive demyelination in two boys with cerebral adrenoleukodystrophy. 2020 May 1
12 32047678 Characterization of a Pathogenic Variant in the ABCD1 Gene Through Protein Molecular Modeling. 2020 2
13 32075856 Hexacosenoyl-CoA is the most abundant very long-chain acyl-CoA in ATP binding cassette transporter D1-deficient cells. 2020 Apr 1
14 32671069 Multi-Omic Approach to Identify Phenotypic Modifiers Underlying Cerebral Demyelination in X-Linked Adrenoleukodystrophy. 2020 1
15 32923227 Chronic Progressive Spastic Paraparesis: Think of Peroxisomal Disorders - A Case Report of X-Linked Adult Onset Adrenoleukodystrophy With an Update on The Latest Treatment Strategies. 2020 Aug 9 1
16 29557549 [X-linked adrenoleukodystrophy with an atypical radiological pattern]. 2018 Apr 1 1
17 23651979 Molecular characterization of X-linked adrenoleukodystrophy in a Tunisian family: identification of a novel missense mutation in the ABCD1 gene. 2013 1
18 22045812 Identification of a new fatty acid synthesis-transport machinery at the peroxisomal membrane. 2012 Jan 2 3
19 22366764 Peroxisomal ABC transporters: structure, function and role in disease. 2012 Sep 1
20 21145416 Differential substrate specificities of human ABCD1 and ABCD2 in peroxisomal fatty acid β-oxidation. 2011 Mar 1
21 21264817 Novel exon nucleotide deletion causes adrenoleukodystrophy in a Brazilian family. 2011 Jan 18 1
22 15682271 Probing substrate-induced conformational alterations in adrenoleukodystrophy protein by proteolysis. 2005 1
23 16223892 Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage. 2005 Dec 1 2
24 8876235 A Saccharomyces cerevisiae homolog of the human adrenoleukodystrophy transporter is a heterodimer of two half ATP-binding cassette transporters. 1996 Oct 15 1
25 7597071 PXA1, a possible Saccharomyces cerevisiae ortholog of the human adrenoleukodystrophy gene. 1995 Jun 20 1
26 7668254 Altered expression of ALDP in X-linked adrenoleukodystrophy. 1995 Aug 1