- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
CLN6 deficiency causes selective changes in the lysosomal protein composition ; day:09 ; month:09 ; year:2021 ; extent:11
Proteomics ; (09.09.2021) (gesamt 11)
- Creator
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Tuermer, Andreas
Mausbach, Simone
Kaade, Edgar
Damme, Markus
Sylvester, Marc
Gieselmann, Volkmar
Thelen, Melanie
- DOI
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10.1002/pmic.202100043
- URN
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urn:nbn:de:101:1-2021091015122886943379
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:25 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Tuermer, Andreas
- Mausbach, Simone
- Kaade, Edgar
- Damme, Markus
- Sylvester, Marc
- Gieselmann, Volkmar
- Thelen, Melanie
Other Objects (12)
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Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology
Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome
Mitochondrial translation deficiency impairs NAD + ‐mediated lysosomal acidification
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia
Publisher Correction: Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome
Lysosomal dysfunction and microglial hyperactivation in models of progranulin deficiency
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Impairment of chaperone‐mediated autophagy leads to selective lysosomal degradation defects in the lysosomal storage disease cystinosis
Thioredoxin Reductase 2 Variant as a Cause of Micropenis, Undescended Testis, and Selective Glucocorticoid Deficiency
Hepatosteatosis from Lysosomal Acid Lipase Deficiency
Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology
Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome
Mitochondrial translation deficiency impairs NAD + ‐mediated lysosomal acidification
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia
Publisher Correction: Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome
Lysosomal dysfunction and microglial hyperactivation in models of progranulin deficiency
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Impairment of chaperone‐mediated autophagy leads to selective lysosomal degradation defects in the lysosomal storage disease cystinosis
Thioredoxin Reductase 2 Variant as a Cause of Micropenis, Undescended Testis, and Selective Glucocorticoid Deficiency
Hepatosteatosis from Lysosomal Acid Lipase Deficiency
Lysosomal lipid alterations caused by glucocerebrosidase deficiency promote lysosomal dysfunction, chaperone-mediated-autophagy deficiency, and alpha-synuclein pathology
Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome
Mitochondrial translation deficiency impairs NAD + ‐mediated lysosomal acidification
Persistent dyslipidemia in treatment of lysosomal acid lipase deficiency
Cerebellar and Midbrain Lysosomal Enzyme Deficiency in Isolated Dystonia
Publisher Correction: Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome
Lysosomal dysfunction and microglial hyperactivation in models of progranulin deficiency
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Lysosomal protease deficiency or substrate overload induces an oxidative-stress mediated STAT3-dependent pathway of lysosomal homeostasis
Impairment of chaperone‐mediated autophagy leads to selective lysosomal degradation defects in the lysosomal storage disease cystinosis