X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
about
Current and future pharmacological treatment strategies in X-linked adrenoleukodystrophyPeroxisomes in brain development and functionThe genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosisFunctional Characterization of IPSC-Derived Brain Cells as a Model for X-Linked AdrenoleukodystrophyThe ABC transporter gene family of Daphnia pulex.Immunohistochemical localization of mitochondrial fatty acid β-oxidation enzymes in rat testis.Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolismCD1 gene polymorphisms and phenotypic variability in X-linked adrenoleukodystrophy.Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient miceNo evidence for the reversal of adrenal failure after hematopoietic cell transplantation in X-linked adrenoleukodystrophyPathophysiology of X-linked adrenoleukodystrophy.Lipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models.Evaluation of retinoids for induction of the redundant gene ABCD2 as an alternative treatment option in X-linked adrenoleukodystrophy.ABCD1 deletion-induced mitochondrial dysfunction is corrected by SAHA: implication for adrenoleukodystrophy.Deletion of a single allele of the Pex11β gene is sufficient to cause oxidative stress, delayed differentiation and neuronal death in mouse brainHereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity.Spinal cord trauma and the molecular point of no returnBrain endothelial dysfunction in cerebral adrenoleukodystrophy.The gene expression profiles of induced pluripotent stem cells from individuals with childhood cerebral adrenoleukodystrophy are consistent with proposed mechanisms of pathogenesisClinical reasoning: a 56-year-old man with progressive spasticityClinical manifest x-linked recessive adrenoleukodystrophy in a female.Mutations in the Arabidopsis peroxisomal ABC transporter COMATOSE allow differentiation between multiple functions in planta: insights from an allelic series.Rapid Induction of Cerebral Organoids From Human Induced Pluripotent Stem Cells Using a Chemically Defined Hydrogel and Defined Cell Culture Medium.Adrenoleukodystrophy and the mitochondrial connection: clues for supplementing Lorenzo's oil.Glutathione imbalance in patients with X-linked adrenoleukodystrophyAn ABCD1 Mutation (c.253dupC) Caused Diverse Phenotypes of Adrenoleukodystrophy in an Iranian Consanguineous Pedigree.Peroxisomes, myelination, and axonal integrity in the CNS.Multiple sclerosis in an adrenoleukodystrophy carrier.Expanded newborn screening by mass spectrometry: New tests, future perspectives.Oxidative Stress in Patients with X-Linked Adrenoleukodystrophy.Protein transport into peroxisomes: Knowns and unknowns.X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes.Substrate specificity overlap and interaction between adrenoleukodystrophy protein (ALDP/ABCD1) and adrenoleukodystrophy-related protein (ALDRP/ABCD2).Clinical, biochemical, neuroimaging and molecular findings of X-linked Adrenoleukodystrophy patients in South China.Genome-wide analysis of the ATP-binding cassette (ABC) transporter gene family in the silkworm, Bombyx mori.Genome-wide analysis of ATP-binding cassette (ABC) transporters in the sweetpotato whitefly, Bemisia tabaci.Early diagnosis of cerebral X-linked adrenoleukodystrophy in boys with Addison's disease improves survival and neurological outcomes.The ABC transporter PXA1 and peroxisomal beta-oxidation are vital for metabolism in mature leaves of Arabidopsis during extended darkness.Beam Me In: Thyroid Hormone Analog Targets Alternative Transporter in Mouse Model of X-Linked AdrenoleukodystrophyOverexpression of PGC-1α increases peroxisomal activity and mitochondrial fatty acid oxidation in human primary myotubes.
P2860
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P2860
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
name
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@ast
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@en
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@nl
type
label
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@ast
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@en
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@nl
prefLabel
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@ast
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@en
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.
@nl
P1476
X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects
@en
P2093
Jutta Gärtner
P304
P356
10.1016/J.BBAMCR.2006.07.010
P407
P577
2006-07-26T00:00:00Z