Published in J Biol Chem on May 23, 2007
Long-chain acyl-CoA synthetases and fatty acid channeling. Future Lipidol (2007) 1.53
Mutations in the fatty acid transport protein 4 gene cause the ichthyosis prematurity syndrome. Am J Hum Genet (2009) 1.53
Biochemistry and genetics of inherited disorders of peroxisomal fatty acid metabolism. J Lipid Res (2010) 1.30
Reduced absorption of saturated fatty acids and resistance to diet-induced obesity and diabetes by ezetimibe-treated and Npc1l1-/- mice. Am J Physiol Gastrointest Liver Physiol (2008) 1.26
Hsf-1 and POB1 induce drug sensitivity and apoptosis by inhibiting Ralbp1. J Biol Chem (2008) 1.26
Presenilins are enriched in endoplasmic reticulum membranes associated with mitochondria. Am J Pathol (2009) 1.24
Regulation of C. elegans fat uptake and storage by acyl-CoA synthase-3 is dependent on NR5A family nuclear hormone receptor nhr-25. Cell Metab (2010) 1.18
Peroxisomal acyl-CoA synthetases. Biochim Biophys Acta (2012) 1.14
SLC27 fatty acid transport proteins. Mol Aspects Med (2013) 1.08
Fatty acid transport protein 4 is dispensable for intestinal lipid absorption in mice. J Lipid Res (2008) 1.03
Functional domains of the fatty acid transport proteins: studies using protein chimeras. Biochim Biophys Acta (2008) 1.02
Increased long chain acyl-Coa synthetase activity and fatty acid import is linked to membrane synthesis for development of picornavirus replication organelles. PLoS Pathog (2013) 0.98
Acyl-CoA synthetase VL3 knockdown inhibits human glioma cell proliferation and tumorigenicity. Cancer Res (2009) 0.94
Overexpressed FATP1, ACSVL4/FATP4 and ACSL1 increase the cellular fatty acid uptake of 3T3-L1 adipocytes but are localized on intracellular membranes. PLoS One (2012) 0.93
Fatty acids are rapidly delivered to and extracted from membranes by methyl-beta-cyclodextrin. J Lipid Res (2010) 0.91
Role of fatty acid transporters in epidermis: Implications for health and disease. Dermatoendocrinol (2011) 0.91
Impaired very long-chain acyl-CoA β-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction. J Biol Chem (2013) 0.90
Adipocyte-specific inactivation of Acyl-CoA synthetase fatty acid transport protein 4 (Fatp4) in mice causes adipose hypertrophy and alterations in metabolism of complex lipids under high fat diet. J Biol Chem (2011) 0.87
Epidermal hyperproliferation in mice lacking fatty acid transport protein 4 (FATP4) involves ectopic EGF receptor and STAT3 signaling. Dev Biol (2010) 0.85
Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia-response and RNA processing functions. Neuropathol Appl Neurobiol (2015) 0.84
Fatty acid transporters in skin development, function and disease. Biochim Biophys Acta (2013) 0.82
Identifying cross-category relations in gene ontology and constructing genome-specific term association networks. BMC Bioinformatics (2013) 0.82
A Novel SLC27A4 Splice Acceptor Site Mutation in Great Danes with Ichthyosis. PLoS One (2015) 0.81
Identification of a new fatty acid synthesis-transport machinery at the peroxisomal membrane. J Biol Chem (2011) 0.81
Fatty acid transport protein 1 can compensate for fatty acid transport protein 4 in the developing mouse epidermis. J Invest Dermatol (2014) 0.79
Baicalein 5,6,7-trimethyl ether activates peroxisomal but not mitochondrial fatty acid beta-oxidation. J Inherit Metab Dis (2008) 0.78
A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis. PLoS One (2012) 0.77
Mitochondria-associated ER membranes and Alzheimer disease. Curr Opin Genet Dev (2016) 0.76
Effects of hematopoietic stem cell transplantation on acyl-CoA oxidase deficiency: a sibling comparison study. J Inherit Metab Dis (2014) 0.76
Chlamydia trachomatis growth and development requires the activity of host Long-chain Acyl-CoA Synthetases (ACSLs). Sci Rep (2016) 0.76
Fatty Acid Transport Proteins: Targeting FATP2 as a Gatekeeper Involved in the Transport of Exogenous Fatty Acids. Medchemcomm (2016) 0.75
RNA-seq based detection of differentially expressed genes in the skeletal muscle of Duroc pigs with distinct lipid profiles. Sci Rep (2017) 0.75
A novel method for determining peroxisomal fatty acid β-oxidation. J Inherit Metab Dis (2016) 0.75
Glomerular-specific alterations of VEGF-A expression lead to distinct congenital and acquired renal diseases. J Clin Invest (2003) 6.44
Probiotics and antibodies to TNF inhibit inflammatory activity and improve nonalcoholic fatty liver disease. Hepatology (2003) 4.03
A simplified laminin nomenclature. Matrix Biol (2005) 3.81
CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility. Science (2003) 3.61
Role of COL4A1 in small-vessel disease and hemorrhagic stroke. N Engl J Med (2006) 3.58
Notch-deficient skin induces a lethal systemic B-lymphoproliferative disorder by secreting TSLP, a sentinel for epidermal integrity. PLoS Biol (2008) 2.98
Blocking protein farnesyltransferase improves nuclear shape in fibroblasts from humans with progeroid syndromes. Proc Natl Acad Sci U S A (2005) 2.85
Podocyte-specific deletion of dicer alters cytoskeletal dynamics and causes glomerular disease. J Am Soc Nephrol (2008) 2.69
Podocytes use FcRn to clear IgG from the glomerular basement membrane. Proc Natl Acad Sci U S A (2008) 2.12
Vascular endothelial growth factor a signaling in the podocyte-endothelial compartment is required for mesangial cell migration and survival. J Am Soc Nephrol (2006) 2.10
Revised nomenclature for the mammalian long-chain acyl-CoA synthetase gene family. J Lipid Res (2004) 2.08
Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy. J Invest Dermatol (2005) 2.06
Proteinuria precedes podocyte abnormalities inLamb2-/- mice, implicating the glomerular basement membrane as an albumin barrier. J Clin Invest (2006) 1.93
Gamma-secretase activity is dispensable for mesenchyme-to-epithelium transition but required for podocyte and proximal tubule formation in developing mouse kidney. Development (2003) 1.87
Maintenance of glomerular filtration barrier integrity requires laminin alpha5. J Am Soc Nephrol (2010) 1.73
Podocyte-specific deletion of integrin-linked kinase results in severe glomerular basement membrane alterations and progressive glomerulosclerosis. J Am Soc Nephrol (2006) 1.70
Distinct epitopes for anti-glomerular basement membrane alport alloantibodies and goodpasture autoantibodies within the noncollagenous domain of alpha3(IV) collagen: a janus-faced antigen. J Am Soc Nephrol (2005) 1.69
Quantitative trait loci influence renal disease progression in a mouse model of Alport syndrome. Am J Pathol (2002) 1.67
Bigenic mouse models of focal segmental glomerulosclerosis involving pairwise interaction of CD2AP, Fyn, and synaptopodin. J Clin Invest (2006) 1.66
Partial rescue of glomerular laminin alpha5 mutations by wild-type endothelia produce hybrid glomeruli. J Am Soc Nephrol (2007) 1.62
Beta1 integrin expression by podocytes is required to maintain glomerular structural integrity. Dev Biol (2008) 1.59
Coordinate control of axon defasciculation and myelination by laminin-2 and -8. J Cell Biol (2005) 1.56
Cellular uptake of fatty acids driven by the ER-localized acyl-CoA synthetase FATP4. J Cell Sci (2006) 1.52
Wnt/β-catenin pathway in podocytes integrates cell adhesion, differentiation, and survival. J Biol Chem (2011) 1.51
A role for genetic susceptibility in sporadic focal segmental glomerulosclerosis. J Clin Invest (2016) 1.48
Albumin-associated free fatty acids induce macropinocytosis in podocytes. J Clin Invest (2015) 1.46
Beta1-integrins are critical for cerebellar granule cell precursor proliferation. J Neurosci (2004) 1.44
Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity. Am J Pathol (2007) 1.43
A site on laminin alpha 5, AQARSAASKVKVSMKF, induces inflammatory cell production of matrix metalloproteinase-9 and chemotaxis. J Immunol (2003) 1.38
Discs-large homolog 1 regulates smooth muscle orientation in the mouse ureter. Proc Natl Acad Sci U S A (2006) 1.36
Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development. Proc Natl Acad Sci U S A (2003) 1.35
Loss of alpha3/alpha4(IV) collagen from the glomerular basement membrane induces a strain-dependent isoform switch to alpha5alpha6(IV) collagen associated with longer renal survival in Col4a3-/- Alport mice. J Am Soc Nephrol (2006) 1.35
Increased progerin expression associated with unusual LMNA mutations causes severe progeroid syndromes. Hum Mutat (2007) 1.34
Adreno-leukodystrophy: oxidative stress of mice and men. J Neuropathol Exp Neurol (2005) 1.34
Laminins promote postsynaptic maturation by an autocrine mechanism at the neuromuscular junction. J Cell Biol (2008) 1.34
Laminin alpha5 is necessary for submandibular gland epithelial morphogenesis and influences FGFR expression through beta1 integrin signaling. Dev Biol (2007) 1.33
Impaired glomerular maturation and lack of VEGF165b in Denys-Drash syndrome. J Am Soc Nephrol (2007) 1.30
A hypomorphic mutation in the mouse laminin alpha5 gene causes polycystic kidney disease. J Am Soc Nephrol (2006) 1.29
Mesangial cells organize the glomerular capillaries by adhering to the G domain of laminin alpha5 in the glomerular basement membrane. J Cell Biol (2003) 1.29
A new function for parietal epithelial cells: a second glomerular barrier. Am J Physiol Renal Physiol (2009) 1.29
Activation of NFAT signaling in podocytes causes glomerulosclerosis. J Am Soc Nephrol (2010) 1.27
The enigmatic parietal epithelial cell is finally getting noticed: a review. Kidney Int (2009) 1.24
Coordinate integrin and c-Met signaling regulate Wnt gene expression during epithelial morphogenesis. Development (2009) 1.24
Rac1 activation in podocytes induces rapid foot process effacement and proteinuria. Mol Cell Biol (2013) 1.19
Podocyte-derived BMP7 is critical for nephron development. J Am Soc Nephrol (2008) 1.19
Laminin-10 is crucial for hair morphogenesis. EMBO J (2003) 1.17
Laminin alpha5 is required for dental epithelium growth and polarity and the development of tooth bud and shape. J Biol Chem (2005) 1.17
Domain IV of mouse laminin beta1 and beta2 chains. Eur J Biochem (2002) 1.15
Epithelial laminin alpha5 is necessary for distal epithelial cell maturation, VEGF production, and alveolization in the developing murine lung. Dev Biol (2005) 1.15
Comparative biochemical studies of the murine fatty acid transport proteins (FATP) expressed in yeast. J Biol Chem (2005) 1.15
Laminin alpha 5 is required for lobar septation and visceral pleural basement membrane formation in the developing mouse lung. Dev Biol (2002) 1.12
Laminin compensation in collagen alpha3(IV) knockout (Alport) glomeruli contributes to permeability defects. J Am Soc Nephrol (2007) 1.10
Glomerular filtration is normal in the absence of both agrin and perlecan-heparan sulfate from the glomerular basement membrane. Nephrol Dial Transplant (2009) 1.09
Pathogenesis of nonimmune glomerulopathies. Annu Rev Pathol (2006) 1.08
Biophysical properties of normal and diseased renal glomeruli. Am J Physiol Cell Physiol (2010) 1.07
Stem cell therapy for Alport syndrome: the hope beyond the hype. Nephrol Dial Transplant (2008) 1.07
A mutant form of the Wilms' tumor suppressor gene WT1 observed in Denys-Drash syndrome interferes with glomerular capillary development. J Am Soc Nephrol (2002) 1.06
Laminets: laminin- and netrin-related genes expressed in distinct neuronal subsets. Mol Cell Neurosci (2002) 1.06
Update on the glomerular filtration barrier. Curr Opin Nephrol Hypertens (2009) 1.06
Nanoscale protein architecture of the kidney glomerular basement membrane. Elife (2013) 1.06
Identification of the binding site for the Lutheran blood group glycoprotein on laminin alpha 5 through expression of chimeric laminin chains in vivo. J Biol Chem (2002) 1.05
Keratinocyte-specific expression of fatty acid transport protein 4 rescues the wrinkle-free phenotype in Slc27a4/Fatp4 mutant mice. J Biol Chem (2007) 1.05
Bromocriptine administration reduces hyperphagia and adiposity and differentially affects dopamine D2 receptor and transporter binding in leptin-receptor-deficient Zucker rats and rats with diet-induced obesity. Neuroendocrinology (2008) 1.05
The LG1-3 tandem of laminin alpha5 harbors the binding sites of Lutheran/basal cell adhesion molecule and alpha3beta1/alpha6beta1 integrins. J Biol Chem (2007) 1.04
The acyl-CoA synthetase "bubblegum" (lipidosin): further characterization and role in neuronal fatty acid beta-oxidation.. J Biol Chem (2003) 1.04
Molecular dissection of laminin alpha 5 in vivo reveals separable domain-specific roles in embryonic development and kidney function. Dev Biol (2006) 1.04
Participation of two members of the very long-chain acyl-CoA synthetase family in bile acid synthesis and recycling. J Biol Chem (2002) 1.04
The fatty acid transport protein (FATP) family: very long chain acyl-CoA synthetases or solute carriers? J Mol Neurosci (2007) 1.03
A missense LAMB2 mutation causes congenital nephrotic syndrome by impairing laminin secretion. J Am Soc Nephrol (2011) 1.03
Fatty acid transport protein 4 is dispensable for intestinal lipid absorption in mice. J Lipid Res (2008) 1.03
Revisiting the glomerular charge barrier in the molecular era. Curr Opin Nephrol Hypertens (2008) 1.03
The glomerular basement membrane as a barrier to albumin. Nat Rev Nephrol (2013) 1.00
Dystroglycan does not contribute significantly to kidney development or function, in health or after injury. Am J Physiol Renal Physiol (2011) 1.00
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders. Am J Hum Genet (2002) 1.00
A potent HIV protease inhibitor, darunavir, does not inhibit ZMPSTE24 or lead to an accumulation of farnesyl-prelamin A in cells. J Biol Chem (2008) 0.99
Laminin alpha 5 influences the architecture of the mouse small intestine mucosa. J Cell Sci (2008) 0.99
X-linked adrenoleukodystrophy: ABCD1 de novo mutations and mosaicism. Mol Genet Metab (2011) 0.99
Increased long chain acyl-Coa synthetase activity and fatty acid import is linked to membrane synthesis for development of picornavirus replication organelles. PLoS Pathog (2013) 0.98
Mouse very long-chain Acyl-CoA synthetase 3/fatty acid transport protein 3 catalyzes fatty acid activation but not fatty acid transport in MA-10 cells. J Biol Chem (2004) 0.98
A chemotactic peptide from laminin alpha 5 functions as a regulator of inflammatory immune responses via TNF alpha-mediated signaling. J Immunol (2005) 0.97
Abnormalities in neural crest cell migration in laminin alpha5 mutant mice. Dev Biol (2005) 0.97
The expression and function of fatty acid transport protein-2 and -4 in the murine placenta. PLoS One (2011) 0.96
Defining kidney biology to understand renal disease. Clin J Am Soc Nephrol (2013) 0.96
Feasibility of repairing glomerular basement membrane defects in Alport syndrome. J Am Soc Nephrol (2013) 0.94
Acyl-CoA synthetase VL3 knockdown inhibits human glioma cell proliferation and tumorigenicity. Cancer Res (2009) 0.94
Review: Lutheran/B-CAM: a laminin receptor on red blood cells and in various tissues. Connect Tissue Res (2005) 0.93
Human fatty acid transport protein 2a/very long chain acyl-CoA synthetase 1 (FATP2a/Acsvl1) has a preference in mediating the channeling of exogenous n-3 fatty acids into phosphatidylinositol. J Biol Chem (2011) 0.92
Role of fatty acid transporters in epidermis: Implications for health and disease. Dermatoendocrinol (2011) 0.91
A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy. Hum Mol Genet (2003) 0.90
Role of the polarity protein Scribble for podocyte differentiation and maintenance. PLoS One (2012) 0.90
Laminin β2 gene missense mutation produces endoplasmic reticulum stress in podocytes. J Am Soc Nephrol (2013) 0.90