Hasil Pencarian - Maria Fuller

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  1. 1
    Os Corpos de Trabalhadores e a organização do trabalho livre na província do Pará (1838-1859)

    Os Corpos de Trabalhadores e a organização do trabalho livre na província do Pará (1838-1859) oleh Claudia Maria Fuller

    Diterbitkan 2011-08-01
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  2. 2
    Functional assessment of the genetic findings indicating mucopolysaccharidosis type II in the prenatal setting

    Functional assessment of the genetic findings indicating mucopolysaccharidosis type II in the prenatal setting oleh Maria Fuller, David Ketteridge

    Diterbitkan 2021-07-01
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  3. 3
    Experience with the Urinary Tetrasaccharide Metabolite for Pompe Disease in the Diagnostic Laboratory

    Experience with the Urinary Tetrasaccharide Metabolite for Pompe Disease in the Diagnostic Laboratory oleh Jennifer T. Saville, Maria Fuller

    Diterbitkan 2021-07-01
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  4. 4
    Prevalence of lysosomal storage disorders in Australia from 2009 to 2020

    Prevalence of lysosomal storage disorders in Australia from 2009 to 2020 oleh Sharon J Chin, Maria Fuller

    Diterbitkan 2022-02-01
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  5. 5
    Metabolomics to Improve the Diagnostic Efficiency of Inborn Errors of Metabolism

    Metabolomics to Improve the Diagnostic Efficiency of Inborn Errors of Metabolism oleh Dylan Mordaunt, David Cox, Maria Fuller

    Diterbitkan 2020-02-01
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  6. 6
    Neurocognitive testing in a murine model of mucopolysaccharidosis type IIIA

    Neurocognitive testing in a murine model of mucopolysaccharidosis type IIIA oleh Kleopatra Pericleous, Chantelle McIntyre, Maria Fuller

    Diterbitkan 2023-09-01
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  7. 7
    Value of Glucosylsphingosine (Lyso-Gb1) as a Biomarker in Gaucher Disease: A Systematic Literature Review

    Value of Glucosylsphingosine (Lyso-Gb1) as a Biomarker in Gaucher Disease: A Systematic Literature Review oleh Shoshana Revel-Vilk, Maria Fuller, Ari Zimran

    Diterbitkan 2020-09-01
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  8. 8
    Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease

    Selective reduction of bis(monoacylglycero)phosphate ameliorates the storage burden in a THP-1 macrophage model of Gaucher disease oleh Leanne K. Hein, Stephen Duplock, Maria Fuller

    Diterbitkan 2013-06-01
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  9. 9
    Distribution of Heparan Sulfate Oligosaccharides in Murine Mucopolysaccharidosis Type IIIA

    Distribution of Heparan Sulfate Oligosaccharides in Murine Mucopolysaccharidosis Type IIIA oleh Kerryn Mason, Peter Meikle, John Hopwood, Maria Fuller

    Diterbitkan 2014-12-01
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  10. 10
    Aberrant Lipid Metabolism: An Emerging Diagnostic and Therapeutic Target in Ovarian Cancer

    Aberrant Lipid Metabolism: An Emerging Diagnostic and Therapeutic Target in Ovarian Cancer oleh Martin K. Oehler, Carmela Ricciardelli, Carmen E. Pyragius, Maria Fuller

    Diterbitkan 2013-04-01
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  11. 11
    Lipid composition of microdomains is altered in a cell model of Gaucher disease*

    Lipid composition of microdomains is altered in a cell model of Gaucher disease* oleh Leanne K. Hein, Stephen Duplock, John J. Hopwood, Maria Fuller

    Diterbitkan 2008-08-01
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  12. 12
    Mono-symptomatic Fabry disease in a population with mild-to-moderate left ventricular hypertrophy

    Mono-symptomatic Fabry disease in a population with mild-to-moderate left ventricular hypertrophy oleh Maria Fuller, Rebecca Perry, Madiha Saiedi, Janice M. Fletcher, Joseph B. Selvanayagam

    Diterbitkan 2020-12-01
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  13. 13
    Stearoyl-CoA Desaturase 1 Is a Key Determinant of Membrane Lipid Composition in 3T3-L1 Adipocytes.

    Stearoyl-CoA Desaturase 1 Is a Key Determinant of Membrane Lipid Composition in 3T3-L1 Adipocytes. oleh Sergio Rodriguez-Cuenca, Lauren Whyte, Rachel Hagen, Antonio Vidal-Puig, Maria Fuller

    Diterbitkan 2016-01-01
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  14. 14
    Evaluation of Multiple Methods for Quantification of Glycosaminoglycan Biomarkers in Newborn Dried Blood Spots from Patients with Severe and Attenuated Mucopolysaccharidosis-I

    Evaluation of Multiple Methods for Quantification of Glycosaminoglycan Biomarkers in Newborn Dried Blood Spots from Patients with Severe and Attenuated Mucopolysaccharidosis-I oleh Zackary M. Herbst, Leslie Urdaneta, Terri Klein, Maria Fuller, Michael H. Gelb

    Diterbitkan 2020-08-01
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  15. 15
    Chondroitin sulfate disaccharide is a specific and sensitive biomarker for mucopolysaccharidosis type IVA

    Chondroitin sulfate disaccharide is a specific and sensitive biomarker for mucopolysaccharidosis type IVA oleh Sharon J. Chin, Jennifer T. Saville, Belinda K. McDermott, Andreas Zankl, Janice M. Fletcher, Maria Fuller

    Diterbitkan 2020-09-01
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  16. 16
    Elevation of gangliosides in four brain regions from Parkinson’s disease patients with a GBA mutation

    Elevation of gangliosides in four brain regions from Parkinson’s disease patients with a GBA mutation oleh Shani Blumenreich, Tamar Nehushtan, Or B. Barav, Jennifer T. Saville, Tamir Dingjan, John Hardy, Maria Fuller, Anthony H. Futerman

    Diterbitkan 2022-08-01
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  17. 17
    Evaluation of Two Methods for Quantification of Glycosaminoglycan Biomarkers in Newborn Dried Blood Spots from Patients with Severe and Attenuated Mucopolysaccharidosis Type II

    Evaluation of Two Methods for Quantification of Glycosaminoglycan Biomarkers in Newborn Dried Blood Spots from Patients with Severe and Attenuated Mucopolysaccharidosis Type II oleh Zackary M. Herbst, Leslie Urdaneta, Terri Klein, Barbara K. Burton, Khaja Basheeruddin, Hsuan-Chieh Liao, Maria Fuller, Michael H. Gelb

    Diterbitkan 2022-01-01
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  18. 18
    The Ckd. Qld fabRy Epidemiology (aCQuiRE) study protocol: identifying the prevalence of Fabry disease amongst patients with kidney disease in Queensland, Australia

    The Ckd. Qld fabRy Epidemiology (aCQuiRE) study protocol: identifying the prevalence of Fabry disease amongst patients with kidney disease in Queensland, Australia oleh Andrew Mallett, Phoebe Kearey, Anne Cameron, Helen Healy, Charles Denaro, Mark Thomas, Vincent W. Lee, Samantha Stark, Maria Fuller, Wendy E. Hoy

    Diterbitkan 2020-02-01
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  19. 19
    Autologous, lentivirus‐modified, T‐rapa cell “micropharmacies” for lysosomal storage disorders

    Autologous, lentivirus‐modified, T‐rapa cell “micropharmacies” for lysosomal storage disorders oleh Murtaza S Nagree, Tania C Felizardo, Mary L Faber, Jitka Rybova, C Anthony Rupar, S Ronan Foley, Maria Fuller, Daniel H Fowler, Jeffrey A Medin

    Diterbitkan 2022-04-01
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  20. 20
    Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells

    Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells oleh Rebecca J. Lehmann, Lachlan A. Jolly, Brett V. Johnson, Megan S. Lord, Ha Na Kim, Jennifer T. Saville, Maria Fuller, Sharon Byers, Ainslie L.K. Derrick-Roberts

    Diterbitkan 2021-12-01
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