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Fatty Acid 2-Hydroxylase and 2-Hydroxylated Sphingolipids: Metabolism and Function in Health and Diseases.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 5, p. 4908, doi. 10.3390/ijms24054908
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- Article
CNS myelin protein 36K regulates oligodendrocyte differentiation through Notch.
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- Glia, 2020, v. 68, n. 3, p. 509, doi. 10.1002/glia.23732
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- Publication type:
- Article
Oligodendrocyte‐specific ceramide galactosyltransferase (CGT) expression phenotypically rescues CGT‐deficient mice and demonstrates that CGT activity does not limit brain galactosylceramide level.
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- Glia, 2005, v. 52, n. 3, p. 190, doi. 10.1002/glia.20230
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- Article
BDNF and NGF signals originating from sensory ganglia promote cranial motor axon growth.
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- Experimental Brain Research, 2020, v. 238, n. 1, p. 111, doi. 10.1007/s00221-019-05694-w
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- Article
Citrylglutamate synthase deficient male mice are subfertile with impaired histone and transition protein 2 removal in late spermatids.
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- Biochemical Journal, 2022, v. 479, n. 9, p. 953, doi. 10.1042/BCJ20210844
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- Publication type:
- Article
Identification of progesterone receptor membrane component-1 as an interaction partner and possible regulator of fatty acid 2-hydroxylase.
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- Biochemical Journal, 2018, v. 475, n. 5, p. 853, doi. 10.1042/BCJ20170963
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- Publication type:
- Article
Ceramide synthase 4 deficiency in mice causes lipid alterations in sebum and results in alopecia.
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- Biochemical Journal, 2014, v. 461, n. 1, p. 147, doi. 10.1042/BJ20131242
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- Publication type:
- Article
Vesicular uptake of N-acetylaspartylglutamate is catalysed by sialin (SLC17A5).
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- Biochemical Journal, 2013, v. 454, n. 1, p. 31, doi. 10.1042/BJ20130300
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- Publication type:
- Article
A commercial human protamine-2 antibody used in several studies to detect mouse protamine-2 recognizes mouse transition protein-2 but not protamine-2.
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- Molecular Human Reproduction, 2015, v. 21, n. 11, p. 825, doi. 10.1093/molehr/gav046
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- Article
Topography of ncam antigenic epitopes recognized by SCLC-cluster-1 antibodies. A consensus view.
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- International Journal of Cancer, 1994, v. 57, p. 27, doi. 10.1002/ijc.2910570705
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- Article
The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter.
- Published in:
- Nature Genetics, 2001, v. 28, n. 1, p. 69, doi. 10.1038/ng0501-69
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- Publication type:
- Article
Imaging of complex sulfatides SM3 and SB1a in mouse kidney using MALDI-TOF/TOF mass spectrometry.
- Published in:
- Analytical & Bioanalytical Chemistry, 2011, v. 401, n. 1, p. 53, doi. 10.1007/s00216-011-4802-0
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- Publication type:
- Article
Mice deficient in the NAAG synthetase II gene Rimkla are impaired in a novel object recognition task.
- Published in:
- Journal of Neurochemistry, 2021, v. 157, n. 6, p. 2008, doi. 10.1111/jnc.15333
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- Publication type:
- Article
Genomic organization of the murine polysialyltransferase gene ST8SiaIV (PST‐1).
- Published in:
- Glycobiology, 1998, v. 8, n. 12, p. 1165, doi. 10.1093/glycob/8.12.1165
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- Publication type:
- Article
The First Model of the Neocarzinostatin Chromophore with an Epoxide Ring and a Carbonate Moiety.
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- Angewandte Chemie International Edition, 1996, v. 35, n. 10, p. 1093, doi. 10.1002/anie.199610931
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- Publication type:
- Article
Absence of 2-Hydroxylated Sphingolipids Is Compatible with Normal Neural Development But Causes Late-Onset Axon and Myelin Sheath Degeneration.
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- Journal of Neuroscience, 2008, v. 28, n. 39, p. 9741, doi. 10.1523/JNEUROSCI.0458-08.2008
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- Publication type:
- Article
Increasing Sulfatide Synthesis in Myelin-Forming Cells of Arylsulfatase A-Deficient Mice Causes Demyelination and Neurological Symptoms Reminiscent of Human Metachromatic Leukodystrophy.
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- Journal of Neuroscience, 2007, v. 27, n. 35, p. 9482, doi. 10.1523/JNEUROSCI.2287-07.2007
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- Publication type:
- Article
Sulfatide Storage in Neurons Causes Hyperexcitability and Axonal Degeneration in a Mouse Model of Metachromatic Leukodystrophy.
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- Journal of Neuroscience, 2007, v. 27, n. 34, p. 9009, doi. 10.1523/JNEUROSCI.2329-07.2007
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- Publication type:
- Article
Myelination in the absence of UDP-galactose:ceramide galactosyl-transferase and fatty acid 2 -hydroxylase.
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- 2011
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- Publication type:
- journal article
Myelination in the absence of UDP-galactose: ceramide galactosyl-transferase and fatty acid 2-hydroxylase.
- Published in:
- BMC Neuroscience, 2011, v. 12, n. 1, p. 22, doi. 10.1186/1471-2202-12-22
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- Publication type:
- Article
Absence of endogenous carnosine synthesis does not increase protein carbonylation and advanced lipoxidation end products in brain, kidney or muscle.
- Published in:
- Amino Acids, 2022, v. 54, n. 7, p. 1013, doi. 10.1007/s00726-022-03150-8
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- Publication type:
- Article
Arylsulfatase A Overexpressing Human iPSC-derived Neural Cells Reduce CNS Sulfatide Storage in a Mouse Model of Metachromatic Leukodystrophy.
- Published in:
- Molecular Therapy, 2015, v. 23, n. 9, p. 1519, doi. 10.1038/mt.2015.106
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- Publication type:
- Article
Molecular cloning and functional expression of bacteriophage PK1E--encoded endoneuraminidase Endo NE.
- Published in:
- Molecular Microbiology, 1995, v. 16, n. 3, p. 441, doi. 10.1111/j.1365-2958.1995.tb02409.x
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- Publication type:
- Article
Optical genome mapping reveals additional prognostic information compared to conventional cytogenetics in AML/MDS patients.
- Published in:
- International Journal of Cancer, 2022, v. 150, n. 12, p. 1998, doi. 10.1002/ijc.33942
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- Publication type:
- Article
Pathology and Current Treatment of Neurodegenerative Sphingolipidoses.
- Published in:
- NeuroMolecular Medicine, 2010, v. 12, n. 4, p. 362, doi. 10.1007/s12017-010-8133-7
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- Publication type:
- Article
Case Report: Hemophagocytic Lymphohistiocytosis and Non-Tuberculous Mycobacteriosis Caused by a Novel GATA2 Variant.
- Published in:
- Frontiers in Immunology, 2021, v. 11, p. N.PAG, doi. 10.3389/fimmu.2021.682934
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- Publication type:
- Article
Elevated sulfatide levels in neurons cause lethal audiogenic seizures in mice.
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- Journal of Neurochemistry, 2010, v. 112, n. 1, p. 282, doi. 10.1111/j.1471-4159.2009.06458.x
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- Publication type:
- Article
NAAG synthetase deficiency has only low influence on pathogenesis in a Canavan disease mouse model.
- Published in:
- Journal of Inherited Metabolic Disease, 2024, v. 47, n. 2, p. 230, doi. 10.1002/jimd.12693
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- Publication type:
- Article
Differential expression of (dihydro)ceramide synthases in mouse brain: oligodendrocyte-specific expression of CerS2/Lass2.
- Published in:
- Histochemistry & Cell Biology, 2008, v. 129, n. 2, p. 233, doi. 10.1007/s00418-007-0344-0
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- Publication type:
- Article
Decreased turnover of the CNS myelin protein Opalin in a mouse model of hereditary spastic paraplegia 35.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 22, p. 3616, doi. 10.1093/hmg/ddaa246
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- Publication type:
- Article
Efficacy of enzyme replacement therapy in an aggravated mouse model of metachromatic leukodystrophy declines with age.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 11, p. 2599, doi. 10.1093/hmg/dds086
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- Publication type:
- Article
BI 1356, a Novel and Selective Xanthine Based Competitive DPP-IV Inhibitor, Has a Longer Off-Rate from the DPP-IV Enzyme than Vildagliptin.
- Published in:
- Diabetes, 2007, v. 56, p. A543
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- Publication type:
- Article
A Highly Convergent Total Synthetic Route to Glycopeptides Carrying a High-Mannose Core Pentasaccharide Domain N-linked to a Natural Peptide Motif.
- Published in:
- Chemistry - A European Journal, 1997, v. 3, n. 10, p. 1617, doi. 10.1002/chem.19970031011
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- Publication type:
- Article
The PGRMC1 Antagonist AG-205 Inhibits Synthesis of Galactosylceramide and Sulfatide.
- Published in:
- Cells (2073-4409), 2021, v. 10, n. 12, p. 3520, doi. 10.3390/cells10123520
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- Publication type:
- Article
Unusual 5'-regulatory structure and regulation of the murine Mlc1 gene: Lack of promoter-specific functional elements.
- Published in:
- Journal of Nucleic Acids Investigation, 2011, v. 2, n. 1-3, p. 70, doi. 10.4081/jnai.2011.2314
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- Publication type:
- Article
Delay of myelin formation in arylsulphatase A-deficient mice.
- Published in:
- European Journal of Neuroscience, 2005, v. 21, n. 3, p. 711, doi. 10.1111/j.1460-9568.2005.03891.x
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- Publication type:
- Article
Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35).
- Published in:
- Human Mutation, 2010, v. 31, n. 4, p. E1251, doi. 10.1002/humu.21205
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- Publication type:
- Article
Transgenic overexpression of polysialyltransferase ST8SiaIV under the control of a neuron-specific promoter does not affect brain development but impairs exploratory behavior.
- Published in:
- Glycobiology, 2019, v. 29, n. 9, p. 657, doi. 10.1093/glycob/cwz040
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- Publication type:
- Article
Polysialyltransferase overexpression in Schwann cells mediates different effects during peripheral nerve regeneration.
- Published in:
- Glycobiology, 2012, v. 22, n. 1, p. 107, doi. 10.1093/glycob/cwr113
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- Publication type:
- Article
Sulfatide binding properties of murine and human antiganglioside antibodies.
- Published in:
- Glycobiology, 2007, v. 17, n. 11, p. 1156, doi. 10.1093/glycob/cwm095
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- Publication type:
- Article
Functional expression of the CMP-sialic acid transporter in Escherichia coli and its identification as a simple mobile carrier.
- Published in:
- Glycobiology, 2006, v. 16, n. 1, p. 73
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- Publication type:
- Article
Reversal of non-hydroxy : α-hydroxy galactosylceramide ratio and unstable myelin in transgenic mice overexpressing UDP-galactose : ceramide galactosyltransferase.
- Published in:
- Journal of Neurochemistry, 2005, v. 94, n. 2, p. 469, doi. 10.1111/j.1471-4159.2005.03221.x
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- Publication type:
- Article
A progesterone receptor membrane component 1 antagonist induces large vesicles independent of progesterone receptor membrane component 1 expression.
- Published in:
- Biological Chemistry, 2020, v. 401, n. 9, p. 1093, doi. 10.1515/hsz-2019-0417
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- Publication type:
- Article
Age-Dependent Increase in Schmidt-Lanterman Incisures and a Cadm4-Associated Membrane Skeletal Complex in Fatty Acid 2-hydroxylase Deficient Mice: a Mouse Model of Spastic Paraplegia SPG35.
- Published in:
- Molecular Neurobiology, 2022, v. 59, n. 7, p. 3969, doi. 10.1007/s12035-022-02832-4
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- Publication type:
- Article
The Role and Metabolism of Sulfatide in the Nervous System.
- Published in:
- Molecular Neurobiology, 2008, v. 37, n. 2/3, p. 93, doi. 10.1007/s12035-008-8022-3
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- Publication type:
- Article
Molecular characterization of eukaryotic polysialyltransferase-1.
- Published in:
- Nature, 1995, v. 373, n. 6516, p. 715, doi. 10.1038/373715a0
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- Publication type:
- Article
N-Acetylaspartate Synthase Deficiency Corrects the Myelin Phenotype in a Canavan Disease Mouse Model But Does Not Affect Survival Time.
- Published in:
- Journal of Neuroscience, 2015, v. 35, n. 43, p. 14501, doi. 10.1523/JNEUROSCI.1056-15.2015
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- Publication type:
- Article