About: The hereditary spastic paraplegia-related enzyme DDHD2 is a principal brain triglyceride lipase

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About: The hereditary spastic paraplegia-related enzyme DDHD2 is a principal brain triglyceride lipase Goto Sponge NotDistinct Permalink

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description	2014年學術文章 (zh) artículu científicu espublizáu en 2014 (ast) vědecký článek publikovaný v roce 2014 (cs) 2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած (hyw) 2014 թվականի հոտեմբերին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в жовтні 2014 (uk) vedecký článok (publikovaný 2014/10/14) (sk) wetenschappelijk artikel (gepubliceerd op 2014/10/14) (nl) مقالة علمية نشرت في 14-10-2014 حول موضوع: دماغ (ar) article publié dans les Proceedings of the National Academy of Sciences of the United States of America (fr) scientific journal article (en) im Oktober 2014 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28591427-973AB425-236E-4CA9-B14D-91B319AE3A42
publication date	2014-10-14 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28591427-BD931CC5-1E7D-45E4-9DEF-0EEC77E9426D
language of work or name	English
cites work	wds:Q28591427-064B2EAC-9AD8-439F-B88D-15C44FE61F0E wds:Q28591427-0ABF1B94-3CDE-4B69-B330-9E00C95387C2 wds:Q28591427-12D56FE2-CF8F-41CB-953D-CBD8EA0848D1 wds:Q28591427-1BDE2532-AE35-43B2-836E-89670379AD59 wds:Q28591427-1D1FF089-B49B-4B71-A0E3-69A6164E7D67 wds:Q28591427-23CE151B-98C7-49B2-B424-2BADCF3CB4E7 wds:Q28591427-2424F9A6-6CA5-49F1-9DF6-5286592D47CB wds:Q28591427-2EA04D38-ECC5-41D1-94E0-F8DD82D27BC1 wds:Q28591427-315BFC0A-97BA-4598-89A9-CB67BE4C58E2 wds:Q28591427-39F18D39-7C1F-4E99-8E78-463475C4104F wds:Q28591427-3DF65A61-F26A-4323-96B3-C8157682BE3C wds:Q28591427-432531C2-DC53-4404-AFFB-DD878CA6D2AE wds:Q28591427-4D3959E1-7B06-4F3F-9A0B-05E3FA21B60E wds:Q28591427-5223F02E-2D51-4028-B221-5E24DB5936E8 wds:Q28591427-54C0C020-9F5B-46A5-A465-D1579C805CEF wds:Q28591427-54FA118C-4182-4A08-9381-1E8AD94D2331 wds:Q28591427-5B730152-8C73-440E-8AF1-BCB5C3C26A10 wds:Q28591427-5D0D984B-EC28-42AE-A7BA-396F2B540296 wds:Q28591427-61F6F3A1-8B31-4C0D-B48B-48E71800A8BB wds:Q28591427-68D9C422-7951-4620-A1A5-3A4C9E9FC010 wds:Q28591427-6ED17A55-10B7-452A-9421-F354061A8B72 wds:Q28591427-83078B38-3F64-4CC3-8209-DAFD64CE7554 wds:Q28591427-8AFD0624-EA91-46D4-864F-35EB39CCBF55 wds:Q28591427-8F26EA97-61DD-40E3-94A0-79A882097BD8 wds:Q28591427-A2FADBC4-9748-4FFB-A536-5B7B007F6184 wds:Q28591427-B03D3273-60FF-419C-AB2D-7EA3D3E49131 wds:Q28591427-B6B4AF69-8398-4B11-8254-D101BBA84C65 wds:Q28591427-BC3D61A5-3378-49CB-9C47-5359D08EAE9E wds:Q28591427-D1420F52-011B-430A-B563-29686B89421A wds:Q28591427-D4CC79E3-8B23-4E55-AF6F-D423224E7376 wds:Q28591427-DC22771B-4860-4B41-BD42-FAADFA9B4EBE wds:Q28591427-E6B2DA85-82FC-4A4F-8162-AF26B61F880B wds:Q28591427-EA75B1B7-3CB9-46A8-8CCF-9E82C7389F97 wds:Q28591427-ECE7E5E4-5081-49B6-AA71-876F8F55287D wds:Q28591427-EE63F1D0-3ECB-4717-B05E-3D7E020A329C wds:Q28591427-F14E107E-6D0F-4F03-B84C-C9BDD40C917D wds:Q28591427-F9F1D0D2-C84A-44E0-8F9F-9FE00CDDA9D2
cites work	p125 is a novel mammalian Sec23p-interacting protein with structural similarity to phospholipid-modifying proteins A novel phospholipase A1 with sequence homology to a mammalian Sec23p-interacting protein, p125. Memory deficits associated with senescence: A neurophysiological and behavioral study in the rat Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms Large-scale analysis of the yeast proteome by multidimensional protein identification technology Fate of fat: the role of adipose triglyceride lipase in lipolysis Defective lipolysis and altered energy metabolism in mice lacking adipose triglyceride lipase Thematic review series: glycerolipids. DGAT enzymes and triacylglycerol biosynthesis XCMS: processing mass spectrometry data for metabolite profiling using nonlinear peak alignment, matching, and identification Fat mobilization in adipose tissue is promoted by adipose triglyceride lipase The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy Neuropathy target esterase gene mutations cause motor neuron disease Human neuropathy target esterase catalyzes hydrolysis of membrane lipids Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis DGAT enzymes are required for triacylglycerol synthesis and lipid droplets in adipocytes Activity-based proteomics of enzyme superfamilies: serine hydrolases as a case study Assignment of endogenous substrates to enzymes by global metabolite profiling Therapeutic strategies for metabolic diseases: Small-molecule diacylglycerol acyltransferase (DGAT) inhibitors Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders Neutral lipid storage disease: genetic disorders caused by mutations in adipose triglyceride lipase/PNPLA2 or CGI-58/ABHD5. Detection of the abundance of diacylglycerol and triacylglycerol molecular species in cells using neutral loss mass spectrometry Structural characterization of triacylglycerols as lithiated adducts by electrospray ionization mass spectrometry using low-energy collisionally activated dissociation on a triple stage quadrupole instrument The main triglyceride-lipase from the insect fat body is an active phospholipase A(1): identification and characterization Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders ABHD12 controls brain lysophosphatidylserine pathways that are deregulated in a murine model of the neurodegenerative disease PHARC Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations. Lipidomics at the interface of structure and function in systems biology Quantitative comparison of the fasted and re-fed mouse liver phosphoproteomes using lower pH reductive dimethylation. Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54). Development of small-molecule inhibitors targeting adipose triglyceride lipase Adipose triglyceride lipase affects triacylglycerol metabolism at brain barriers. Roles of SAM and DDHD domains in mammalian intracellular phospholipase A1 KIAA0725p. Imaging lipid droplets by electron microscopy Cloning of a phosphatidic acid-preferring phospholipase A1 from bovine testis. Development and optimization of piperidyl-1,2,3-triazole ureas as selective chemical probes of endocannabinoid biosynthesis
author name string	wds:Q28591427-669C4E20-CD38-4564-ADEB-249793181620 wds:Q28591427-81E5F73B-32A0-4B4B-99E1-3A9CE93B6EF0 wds:Q28591427-81ED4808-359E-41E2-91CE-31CCB5C60EF0 wds:Q28591427-981C2D93-7EDB-42EC-991C-E24EF1A66715 wds:Q28591427-A01D6CF8-910D-4358-B3D1-FE04162C34FE wds:Q28591427-F4E8E337-4C3E-4469-906F-EB06E0C264BA
OpenCitations bibliographic resource ID	wds:Q28591427-393E5817-9953-4456-9AF6-64DCE7B05EEF
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/4772297
author name string	Andreu Viader

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