Pages that link to "Q36566796"
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The following pages link to A mouse model for X-linked adrenoleukodystrophy (Q36566796):
Displaying 50 items.
- ATP-binding cassette, sub-family D (ALD), member 1 (Q14912816) (← links)
- Restoration of PEX2 peroxisome assembly defects by overexpression of PMP70 (Q22003909) (← links)
- Adrenoleukodystrophy-related protein can compensate functionally for adrenoleukodystrophy protein deficiency (X-ALD): implications for therapy (Q22009167) (← links)
- Progression of abnormalities in adrenomyeloneuropathy and neurologically asymptomatic X-linked adrenoleukodystrophy despite treatment with "Lorenzo's oil" (Q24673003) (← links)
- Peroxisomes in brain development and function (Q26774697) (← links)
- Astrocytes are central in the pathomechanisms of vanishing white matter (Q27330146) (← links)
- Sterol carrier protein-2 (Q28138468) (← links)
- X-linked adrenoleukodystrophy: role of very long-chain acyl-CoA synthetases (Q28505196) (← links)
- Mouse very long-chain acyl-CoA synthetase in X-linked adrenoleukodystrophy (Q28507035) (← links)
- ABHD12 controls brain lysophosphatidylserine pathways that are deregulated in a murine model of the neurodegenerative disease PHARC (Q28509608) (← links)
- Functional Characterization of IPSC-Derived Brain Cells as a Model for X-Linked Adrenoleukodystrophy (Q28551048) (← links)
- C26:0-Carnitine Is a New Biomarker for X-Linked Adrenoleukodystrophy in Mice and Man (Q28551663) (← links)
- Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissues (Q28590214) (← links)
- Absence of spontaneous peroxisome proliferation in enoyl-CoA Hydratase/L-3-hydroxyacyl-CoA dehydrogenase-deficient mouse liver. Further support for the role of fatty acyl CoA oxidase in PPARalpha ligand metabolism (Q28591221) (← links)
- Mirror expression of adrenoleukodystrophy and adrenoleukodystrophy related genes in mouse tissues and human cell lines (Q32064197) (← links)
- The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage (Q33270660) (← links)
- The neurobiology of X-linked adrenoleukodystrophy, a demyelinating peroxisomal disorder (Q33544235) (← links)
- On the front of X-linked adrenoleukodystrophy (Q33607731) (← links)
- X-linked adrenoleukodystrophy: genes, mutations, and phenotypes (Q33607735) (← links)
- X-linked adrenoleukodystrophy enigma: how does the ALD peroxisomal transporter mutation affect CNS glia? (Q33811095) (← links)
- Adrenomyeloneuropathy: a neuropathologic review featuring its noninflammatory myelopathy (Q33882324) (← links)
- Interferons, signal transduction pathways, and the central nervous system (Q33988186) (← links)
- Human peroxisomal disorders (Q34196103) (← links)
- Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice (Q34257373) (← links)
- PEX11 beta deficiency is lethal and impairs neuronal migration but does not abrogate peroxisome function (Q34280995) (← links)
- ABCD2 alters peroxisome proliferator-activated receptor α signaling in vitro, but does not impair responses to fenofibrate therapy in a mouse model of diet-induced obesity (Q34360091) (← links)
- Pathophysiology of X-linked adrenoleukodystrophy (Q34390414) (← links)
- Nonalcoholic steatosis and steatohepatitis. III. Peroxisomal beta-oxidation, PPAR alpha, and steatohepatitis (Q34436747) (← links)
- Liver X receptor alpha interferes with SREBP1c-mediated Abcd2 expression. Novel cross-talk in gene regulation. (Q34462811) (← links)
- Pathomechanisms underlying X-adrenoleukodystrophy: a three-hit hypothesis. (Q34491978) (← links)
- The mousetrap: what we can learn when the mouse model does not mimic the human disease (Q34578759) (← links)
- Antioxidants halt axonal degeneration in a mouse model of X-adrenoleukodystrophy. (Q34631169) (← links)
- Peroxisomal dysfunction in inflammatory childhood white matter disorders: an unexpected contributor to neuropathology (Q34801173) (← links)
- Role of ALDP (ABCD1) and mitochondria in X-linked adrenoleukodystrophy (Q34811374) (← links)
- Histone deacetylase inhibitor upregulates peroxisomal fatty acid oxidation and inhibits apoptotic cell death in abcd1-deficient glial cells (Q34907267) (← links)
- Autophagy induction halts axonal degeneration in a mouse model of X-adrenoleukodystrophy. (Q35092638) (← links)
- Oxidative damage compromises energy metabolism in the axonal degeneration mouse model of X-adrenoleukodystrophy (Q35193956) (← links)
- Loss of AMP-activated protein kinase induces mitochondrial dysfunction and proinflammatory response in unstimulated Abcd1-knockout mice mixed glial cells. (Q35227024) (← links)
- ABCD1 deletion-induced mitochondrial dysfunction is corrected by SAHA: implication for adrenoleukodystrophy (Q35417932) (← links)
- Mammalian peroxisomal ABC transporters: from endogenous substrates to pathology and clinical significance. (Q35636076) (← links)
- The Myelin Mutants as Models to Study Myelin Repair in the Leukodystrophies (Q35648148) (← links)
- Deletion of a single allele of the Pex11β gene is sufficient to cause oxidative stress, delayed differentiation and neuronal death in mouse brain (Q35665063) (← links)
- Functional genomic analysis unravels a metabolic-inflammatory interplay in adrenoleukodystrophy (Q35750216) (← links)
- Evaluation of therapy of X-linked adrenoleukodystrophy (Q35771255) (← links)
- Pioglitazone halts axonal degeneration in a mouse model of X-linked adrenoleukodystrophy (Q35997389) (← links)
- Activation of sirtuin 1 as therapy for the peroxisomal disease adrenoleukodystrophy. (Q36288305) (← links)
- Oxidative stress modulates mitochondrial failure and cyclophilin D function in X-linked adrenoleukodystrophy (Q36474703) (← links)
- Dietary rescue of altered metabolism gene reveals unexpected Drosophila mating cues (Q36617475) (← links)
- The peroxisomal ABC transporter family (Q36622676) (← links)
- Experimental models of spontaneous autoimmune disease in the central nervous system. (Q36849410) (← links)