Figura, Kurt von 1944-
Kurt von Figura German physician
Figura, Kurt von
VIAF ID: 20182281 (Personal)
Permalink: http://viaf.org/viaf/20182281
Preferred Forms
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100 1 _ ‡a Figura, Kurt von
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100 1 _
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Figura, Kurt von
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100 1 _ ‡a Figura, Kurt von (sparse)
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100 1 _
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Figura, Kurt von
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1944-
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100 1 _
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Figura, Kurt von
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1944-
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Kurt von Figura
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German physician
4xx's: Alternate Name Forms (12)
5xx's: Related Names (1)
- 551 _ _
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Heiningen, Baden-Württemberg
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ortg
‡4
https://d-nb.info/standards/elementset/gnd#placeOfBirth
Works
| Title | Sources |
|---|---|
| Defective oligomerization of arylsulfatase a as a cause of its instability in lysosomes and metachromatic leukodystrophy |
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| Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig |
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| The disintegrin/metalloprotease ADAM 10 is essential for Notch signalling but not for alpha-secretase activity in fibroblasts |
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| Disturbed cholesterol traffic but normal proteolytic function in LAMP-1/LAMP-2 double-deficient fibroblasts |
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| Edvard Munch - Druckgraphik Kunstverein Göttingen und Kulturamt der Stadt Göttingen im Alten Rathaus, 23. November 1997 - 4. Januar 1998 ; [zur Ausstellung "Edvard Munch - Druckgraphik"] |
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| Efficacy of enzyme replacement therapy in alpha-mannosidosis mice: a preclinical animal study |
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| Expression, localization, structural, and functional characterization of pFGE, the paralog of the Calpha-formylglycine-generating enzyme |
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| Granzyme-mediated cytotoxicity does not involve the mannose 6-phosphate receptors on target cells |
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| Heparan sulfate 6-O-endosulfatases: discrete in vivo activities and functional co-operativity |
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| Horst Antes Werkverzeichnis der Radierungen |
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| The human SUMF1 gene, required for posttranslational sulfatase modification, defines a new gene family which is conserved from pro- to eukaryotes |
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| Identification of formylglycine in sulfatases by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry |
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| Identification of novel lysosomal matrix proteins by proteome analysis |
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| Involvement of cathepsin E in exogenous antigen processing in primary cultured murine microglia |
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| LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice |
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| Locating the anomalous scatterer substructures in halide and sulfur phasing |
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| Lungenfunktionsdiagnostische Untersuchungen an ehemaligen Frühgeborenen |
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| Mannose 6-phosphate receptors, Niemann-Pick C2 protein, and lysosomal cholesterol accumulation |
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| Molecular basis of multiple sulfatase deficiency, mucolipidosis II/III and Niemann-Pick C1 disease - Lysosomal storage disorders caused by defects of non-lysosomal proteins |
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| Molecular characterization of the hypothetical 66.3-kDa protein in mouse: lysosomal targeting, glycosylation, processing and tissue distribution |
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| Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C(alpha)-formylglycine generating enzyme |
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| A new type of congenital disorders of glycosylation (CDG-Ii) provides new insights into the early steps of dolichol-linked oligosaccharide biosynthesis |
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| The non-catalytic N-terminal extension of formylglycine-generating enzyme is required for its biological activity and retention in the endoplasmic reticulum |
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| Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten disease). |
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| Phosphorylation of the AP2 mu subunit by AAK1 mediates high affinity binding to membrane protein sorting signals |
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| Sanfilippo B corrective factor a N-acetyl--D-gluosaminidase |
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| Sanfilippo-B-Erkrankung: Enzymdefekt, Diagnostik und Untersuchungen zur Therapie durch Enzymsubstitution |
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| Structural requirements for interactions between leucine-sorting signals and clathrin-associated adaptor protein complex AP3 |
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| Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethality |
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| Thyroid functions of mouse cathepsins B, K, and L. |
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| The tyrosine motifs of Lamp 1 and LAP determine their direct and indirect targetting to lysosomes |
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