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A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers
Wangler, Michael F, Hubert, Leroy, Donti, Taraka R, Ventura, Meredith J, Miller, Marcus J, Braverman, Nancy, Gawron, Kelly, Bose, Mousumi, Moser, Ann B, Jones, Richard O, Rizzo, William B, Sutton, V Reid, Sun, Qin, Kennedy, Adam D, Elsea, Sarah H
Published in Genetics in medicine (01.10.2018)
Published in Genetics in medicine (01.10.2018)
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Journal Article
Detection of unusual very-long-chain fatty acid and ether lipid derivatives in the fibroblasts and plasma of patients with peroxisomal diseases using liquid chromatography-mass spectrometry
Takashima, Shigeo, Toyoshi, Kayoko, Itoh, Takahiro, Kajiwara, Naomi, Honda, Ayako, Ohba, Akiko, Takemoto, Shoko, Yoshida, Satoshi, Shimozawa, Nobuyuki
Published in Molecular genetics and metabolism (01.03.2017)
Published in Molecular genetics and metabolism (01.03.2017)
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Journal Article
Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities
Wang, Xiao-Ming, Yik, Wing Yan, Zhang, Peilin, Lu, Wange, Huang, Ning, Kim, Bo Ram, Shibata, Darryl, Zitting, Madison, Chow, Robert H., Moser, Ann B., Steinberg, Steven J., Hacia, Joseph G.
Published in Stem cell research & therapy (29.08.2015)
Published in Stem cell research & therapy (29.08.2015)
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Journal Article
Characterization of Severity in Zellweger Spectrum Disorder by Clinical Findings: A Scoping Review, Meta-Analysis and Medical Chart Review
Bose, Mousumi, Yergeau, Christine, D’Souza, Yasmin, Cuthbertson, David D., Lopez, Melisa J., Smolen, Alyssa K., Braverman, Nancy E.
Published in Cells (Basel, Switzerland) (10.06.2022)
Published in Cells (Basel, Switzerland) (10.06.2022)
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Journal Article
Elevated urinary excretion of nitric oxide metabolites in young infants with Zellweger syndrome
Surdacki, Andrzej, Tsikas, Dimitrios, Mayatepek, Ertan, Frölich, Jürgen C
Published in Clinica chimica acta (01.08.2003)
Published in Clinica chimica acta (01.08.2003)
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Journal Article
Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls
Moser, Ann B., Kreiter, Nancy, Bezman, Lena, Lu, Shou-En, Raymond, Gerald V., Naidu, Sakkubai, Moser, Hugo W.
Published in Annals of neurology (01.01.1999)
Published in Annals of neurology (01.01.1999)
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Journal Article
Zellweger syndrome
Published in Oxford Dictionary of Biochemistry and Molecular Biology
(01.01.2006)
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Reference
Metabolism of prostaglandin F2 alpha in Zellweger syndrome. Peroxisomal beta-oxidation is a major importance for in vivo degradation of prostaglandins in humans
Diczfalusy, U, Kase, B F, Alexson, S E, Björkhem, I
Published in The Journal of clinical investigation (01.09.1991)
Published in The Journal of clinical investigation (01.09.1991)
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Journal Article
Biosynthesis and Maturation of Peroxisomal β -oxidation Enzymes in Fibroblasts in Relation to the Zellweger Syndrome and Infantile Refsum Disease
Schram, André W., Strijland, Anneke, Hashimoto, Takashi, Ronald J. A. Wanders, Ruud B. H. Schutgens, Van Den Bosch, Henk, Tager, Joseph M.
Published in Proceedings of the National Academy of Sciences - PNAS (01.08.1986)
Published in Proceedings of the National Academy of Sciences - PNAS (01.08.1986)
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Journal Article
Absence of functional peroxisomes does not lead to deficiency of enzymes involved in cholesterol biosynthesis
Hogenboom, Sietske, Romeijn, Gerrit Jan, Houten, Sander M., Baes, Myriam, Wanders, Ronald J.A., Waterham, Hans R.
Published in Journal of lipid research (01.01.2002)
Published in Journal of lipid research (01.01.2002)
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Journal Article
Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts
Wiemer, E A, Brul, S, Just, W W, Van Driel, R, Brouwer-Kelder, E, Van Den Berg, M, Weijers, P J, Schutgens, R B, Van Den Bosch, H, Schram, A
Published in European journal of cell biology (01.12.1989)
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Published in European journal of cell biology (01.12.1989)
Journal Article
Histochemistry of peroxisomal enzyme activities: a tool in the diagnosis of Zellweger syndrome
Frederiks, W M, Bosch, K S, Ankum, M, Wanders, R J
Published in Journal of inherited metabolic disease (01.11.1993)
Published in Journal of inherited metabolic disease (01.11.1993)
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Journal Article
Therapeutic developments in peroxisome biogenesis disorders
McGuinness, M C, Wei, H, Smith, K D
Published in Expert opinion on investigational drugs (01.09.2000)
Published in Expert opinion on investigational drugs (01.09.2000)
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Journal Article
Acyl-CoA oxidase, peroxisomal thiolase and dihydroxyacetone phosphate acyltransferase: aberrant subcellular localization in Zellweger syndrome
van Roermund, C W, Brul, S, Tager, J M, Schutgens, R B, Wanders, R J
Published in Journal of inherited metabolic disease (01.01.1991)
Published in Journal of inherited metabolic disease (01.01.1991)
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Journal Article
Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes
Nagase, Tomoko, Shimozawa, Nobuyuki, Takemoto, Yasuhiko, Suzuki, Yasuyuki, Komori, Masayuki, Kondo, Naomi
Published in Biochimica et biophysica acta (17.03.2004)
Published in Biochimica et biophysica acta (17.03.2004)
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Journal Article