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Elevated expression of S100B and RAGE positively correlates with pro-inflammatory cytokine production that may contributie to rapid neurodegeneration in INCL.
- Published in:
- FASEB Journal, 2007, v. 21, n. 6, p. A989, doi. 10.1096/fasebj.21.6.a989
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- Publication type:
- Article
Novel anti-inflammatory peptides from the region of highest similarity between uteroglobin and lipocortin I.
- Published in:
- Nature, 1988, v. 335, n. 6192, p. 726, doi. 10.1038/335726a0
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- Publication type:
- Article
Suppression of agrin-22 production and synaptic dysfunction in Cln1<sup>-/-</sup> mice.
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- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 12, p. 1085, doi. 10.1002/acn3.261
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- Publication type:
- Article
Evaluation of disease progression in INCL by MR spectroscopy.
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- Annals of Clinical & Translational Neurology, 2015, v. 2, n. 8, p. 797, doi. 10.1002/acn3.222
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- Publication type:
- Article
Mice homozygous for c.451C>T mutation in Cln1 gene recapitulate INCL phenotype.
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- Annals of Clinical & Translational Neurology, 2014, v. 1, n. 12, p. 1006, doi. 10.1002/acn3.144
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- Publication type:
- Article
Neuroprotection and lifespan extension in Ppt1<sup>−/−</sup> mice by NtBuHA: therapeutic implications for INCL.
- Published in:
- Nature Neuroscience, 2013, v. 16, n. 11, p. 1608, doi. 10.1038/nn.3526
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- Publication type:
- Article
Molecular Characterization of Murine Pancreatic Phospholipase A[sub 2].
- Published in:
- DNA & Cell Biology, 2001, v. 20, n. 3, p. 149, doi. 10.1089/104454901300068988
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- Publication type:
- Article
Cystic Fibrosis Gene Mutation (ΔF<sub>508</sub>) Is Associated with an Intrinsic Abnormality in Ca<sup>2+</sup>-Induced Arachidonic Acid Release by Epithelial Cells.
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- DNA & Cell Biology, 1997, v. 16, n. 6, p. 749, doi. 10.1089/dna.1997.16.749
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- Publication type:
- Article
Human Uteroglobin Gene: Structure, Subchromosomal Localization, and Polymorphism.
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- DNA & Cell Biology, 1997, v. 16, n. 1, p. 73, doi. 10.1089/dna.1997.16.73
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- Publication type:
- Article
Nonradiometric ELISA-Based Quantitation and Validation of Polymerase Chain Reaction-Amplified DNA, Including Detection of Point Mutations, Without Allele-Specific Amplification, or Ligation.
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- DNA & Cell Biology, 1994, v. 13, n. 12, p. 1233, doi. 10.1089/dna.1994.13.1233
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- Publication type:
- Article
Expression of Clara Cell 10-kD Gene in the Human Endometrium and Its Relationship to Ovarian Menstrual Cycle.
- Published in:
- DNA & Cell Biology, 1994, v. 13, n. 5, p. 495, doi. 10.1089/dna.1994.13.495
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- Publication type:
- Article
Regulation of Extracellular Phospholipase A<sub>2</sub> Activity: Implications for Inflammatory Diseases.
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- DNA & Cell Biology, 1992, v. 11, n. 3, p. 233, doi. 10.1089/dna.1992.11.233
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- Publication type:
- Article
Uteroglobin is essential in preventing immunoglobulin A nephropathy in mice.
- Published in:
- Nature Medicine, 1999, v. 5, n. 9, p. 1018, doi. 10.1038/12458
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- Publication type:
- Article
Preface.
- Published in:
- Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. ix, doi. 10.1111/j.1749-6632.2000.tb05514.x
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- Publication type:
- Article
Insight into the Physiological Function(s) of Uteroglobin by Gene-Knockout and Antisense-Transgenic Approaches.
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- Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. 210, doi. 10.1111/j.1749-6632.2000.tb05532.x
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- Publication type:
- Article
Crystal Structure Analysis of Recombinant Human Uteroglobin and Molecular Modeling of Ligand Binding.
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- Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. 113, doi. 10.1111/j.1749-6632.2000.tb05523.x
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- Publication type:
- Article
Uteroglobin Binding Proteins: Regulation of Cellular Motility and Invasion in Normal and Cancer Cells.
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- Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. 234, doi. 10.1111/j.1749-6632.2000.tb05533.x
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- Publication type:
- Article
Human Uteroglobin Gene Polymorphisms and Genetic Susceptibility to Asthma.
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- Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. 303, doi. 10.1111/j.1749-6632.2000.tb05538.x
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- Publication type:
- Article
A Novel In Situ Method of SV40 Transfection for the Establishment of Immortal Pulmonary Alveolar Type II Cell Lines.
- Published in:
- Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. 325, doi. 10.1111/j.1749-6632.2000.tb05543.x
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- Publication type:
- Article
Amino Acid Residues in α-Helix-3 of Human Uteroglobin Are Critical for Its Phospholipase A<sub>2</sub> Inhibitory Activity.
- Published in:
- Annals of the New York Academy of Sciences, 2000, v. 923, n. 1, p. 307, doi. 10.1111/j.1749-6632.2000.tb05539.x
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- Publication type:
- Article
RAGE signaling contributes to neuroinflammation in infantile neuronal ceroid lipofuscinosis
- Published in:
- FEBS Letters, 2008, v. 582, n. 27, p. 3823, doi. 10.1016/j.febslet.2008.10.015
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- Publication type:
- Article
ROLE OF UTEROGLOBIN AND TRANSGLUTAMINASE IN SELF AND NON-SELF RECOGNITION DURING REPRODUCTION IN THE RABBIT.
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- Annals of the New York Academy of Sciences, 1982, v. 392, n. 1, p. 401, doi. 10.1111/j.1749-6632.1982.tb36138.x
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- Publication type:
- Article
DNA Synthesis during Meiotic Prophase in Male Mice.
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- Nature, 1968, v. 219, n. 5153, p. 489, doi. 10.1038/219489a0
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- Publication type:
- Article
Cln1 gene disruption in mice reveals a common pathogenic link between two of the most lethal childhood neurodegenerative lysosomal storage disorders.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 19, p. 5416, doi. 10.1093/hmg/ddv266
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- Publication type:
- Article
The blood-brain barrier is disrupted in a mouse model of infantile neuronal ceroid lipofuscinosis: amelioration by resveratrol.
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- Human Molecular Genetics, 2012, v. 21, n. 10, p. 2233, doi. 10.1093/hmg/dds038
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- Publication type:
- Article
Disruption of adaptive energy metabolism and elevated ribosomal p-S6K1 levels contribute to INCL pathogenesis: partial rescue by resveratrol.
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- Human Molecular Genetics, 2011, v. 20, n. 6, p. 1111, doi. 10.1093/hmg/ddq555
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- Publication type:
- Article
ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones.
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- Human Molecular Genetics, 2008, v. 17, n. 4, p. 469, doi. 10.1093/hmg/ddm324
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- Publication type:
- Article
Production of lysophosphatidylcholine by cPLA2 in the brain of mice lacking PPT1 is a signal for phagocyte infiltration.
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- Human Molecular Genetics, 2007, v. 16, n. 7, p. 837, doi. 10.1093/hmg/ddm029
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- Publication type:
- Article
Endoplasmic reticulum stress-induced caspase-4 activation mediates apoptosis and neurodegeneration in INCL.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 11, p. 1826, doi. 10.1093/hmg/ddl105
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- Publication type:
- Article
Palmitoyl-protein thioesterase-1 deficiency leads to the activation of caspase-9 and contributes to rapid neurodegeneration in INCL.
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- Human Molecular Genetics, 2006, v. 15, n. 10, p. 1580, doi. 10.1093/hmg/ddl078
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- Publication type:
- Article
Misrouting of v-ATPase subunit V0a1 dysregulates lysosomal acidification in a neurodegenerative lysosomal storage disease model.
- Published in:
- Nature Communications, 2017, v. 8, n. 3, p. 14612, doi. 10.1038/ncomms14612
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- Publication type:
- Article
In a Model of Batten Disease, Palmitoyl Protein Thioesterase-1 Deficiency Is Associated with Brown Adipose Tissue and Thermoregulation Abnormalities.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0048733
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- Publication type:
- Article
Lysosomal ceroid depletion by drugs: Therapeutic implications for a hereditary neurodegenerative disease of childhood.
- Published in:
- Nature Medicine, 2001, v. 7, n. 4, p. 478, doi. 10.1038/86554
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- Publication type:
- Article
Interaction of Osteopontin with Fibronectin and Other Extracellular Matrix Molecules<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1995, v. 760, n. 1, p. 201, doi. 10.1111/j.1749-6632.1995.tb44631.x
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- Publication type:
- Article
Development of Novel, Sensitive, Nonradioactive, Quantitative ELISA-PCR Methods Potentially Applicable to the Detection of Fetal Cells in Maternal Circulation.
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- Annals of the New York Academy of Sciences, 1994, v. 731, n. 1, p. 246, doi. 10.1111/j.1749-6632.1994.tb55777.x
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- Publication type:
- Article
Palmitoyl-protein thioesterase-1 deficiency mediates the activation of the unfolded protein response and neuronal apoptosis in INCL.
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- Human Molecular Genetics, 2006, v. 15, n. 2, p. 337, doi. 10.1093/hmg/ddi451
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- Publication type:
- Article
Emerging new roles of the lysosome and neuronal ceroid lipofuscinoses.
- Published in:
- Molecular Neurodegeneration, 2019, v. 14, n. 1, p. N.PAG, doi. 10.1186/s13024-018-0300-6
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- Publication type:
- Article
Stable, Long-Term Bacterial Production of Soluble, Dimeric, Disulfide-Bonded Protein Pharmaceuticals without Antibiotic Selection.
- Published in:
- Biotechnology Progress, 2000, v. 16, n. 1, p. 17, doi. 10.1021/bp990129g
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- Publication type:
- Article
Ppt1‐deficiency dysregulates lysosomal Ca<sup>++</sup> homeostasis contributing to pathogenesis in a mouse model of CLN1 disease.
- Published in:
- Journal of Inherited Metabolic Disease, 2022, v. 45, n. 3, p. 635, doi. 10.1002/jimd.12485
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- Publication type:
- Article
In a mouse model of INCL reduced S‐palmitoylation of cytosolic thioesterase APT1 contributes to microglia proliferation and neuroinflammation.
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- Journal of Inherited Metabolic Disease, 2021, v. 44, n. 4, p. 1051, doi. 10.1002/jimd.12379
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- Publication type:
- Article
Cln1‐mutations suppress Rab7‐RILP interaction and impair autophagy contributing to neuropathology in a mouse model of infantile neuronal ceroid lipofuscinosis.
- Published in:
- Journal of Inherited Metabolic Disease, 2020, v. 43, n. 5, p. 1082, doi. 10.1002/jimd.12242
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- Publication type:
- Article
Cln3‐mutations underlying juvenile neuronal ceroid lipofuscinosis cause significantly reduced levels of Palmitoyl‐protein thioesterases‐1 (Ppt1)‐protein and Ppt1‐enzyme activity in the lysosome.
- Published in:
- Journal of Inherited Metabolic Disease, 2019, v. 42, n. 5, p. 944, doi. 10.1002/jimd.12106
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- Publication type:
- Article
Arachidonic acid release from NIH 3T3 cells by group-I phospholipase A<sub>2</sub>: Involvement of a receptor-mediated mechanism.
- Published in:
- Journal of Cellular Physiology, 1995, v. 165, n. 3, p. 566, doi. 10.1002/jcp.1041650315
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- Publication type:
- Article
Uteroglobin interacts with the heparin-binding site of fibronectin and prevents fibronectin–IgA complex formation found in IgA-nephropathy
- Published in:
- FEBS Letters, 2008, v. 582, n. 5, p. 611, doi. 10.1016/j.febslet.2008.01.025
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- Publication type:
- Article
Uteroglobin suppresses allergen-induced T<sub>H</sub>2 differentiation by down-regulating the expression of serum amyloid A and SOCS-3 genes
- Published in:
- FEBS Letters, 2006, v. 580, n. 25, p. 6022, doi. 10.1016/j.febslet.2006.09.059
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- Publication type:
- Article
Mice lacking uteroglobin are highly susceptible to developing pulmonary fibrosis
- Published in:
- FEBS Letters, 2006, v. 580, n. 18, p. 4515, doi. 10.1016/j.febslet.2006.07.031
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- Publication type:
- Article
Palmitoyl protein thioesterase-1 deficiency impairs synaptic vesicle recycling at nerve terminals, contributing to neuropathology in humans and mice.
- Published in:
- 2008
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- Publication type:
- journal article
Crystallization and characterization of the recombinant human Clara cell 10-kDa protein.
- Published in:
- Proteins, 1994, v. 20, n. 2, p. 191, doi. 10.1002/prot.340200209
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- Publication type:
- Article
Evaluation of Neurodegeneration in a Mouse Model of Infantile Batten Disease by Magnetic Resonance Imaging and Magnetic Resonance Spectroscopy.
- Published in:
- Neurodegenerative Diseases, 2012, v. 9, n. 4, p. 159, doi. 10.1159/000334838
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- Publication type:
- Article