Self-eating in skeletal development: Implications for lysosomal storage disorders
نویسندگان
چکیده
منابع مشابه
Treatments for lysosomal storage disorders.
There are over 70 human diseases that are caused by defects in various aspects of lysosomal function. Until 20 years ago, the only specific therapy available for lysosomal storage disorders was allogeneic haemopoietic stem cell transplantation. Over the last two decades, there has been remarkable progress and there are now licensed treatments for seven of these diseases. In some cases, a choice...
متن کاملAutophagy in lysosomal storage disorders
Lysosomes are ubiquitous intracellular organelles that have an acidic internal pH, and play crucial roles in cellular clearance. Numerous functions depend on normal lysosomes, including the turnover of cellular constituents, cholesterol homeostasis, downregulation of surface receptors, inactivation of pathogenic organisms, repair of the plasma membrane and bone remodeling. Lysosomal storage dis...
متن کاملSelf-Regulation in Eating Disorders and Obesity – Implications for Treatment
Zusammenfassung Die Forschung hat gezeigt, dass die Behandlung einzelner Essstörungen wie z.B. der Anorexia nervosa und ungünstigen Essverhaltens bei Adipositas nur begrenzt effektiv ist bzw. dass auch nach Behandlung der Essstörungssymptomatik eine erhöhte Psychopathologie bestehen kann. Daraus ergibt sich die Notwendigkeit, weitere ätiologische und aufrechterhaltende Faktoren zu identifiziere...
متن کاملImmunochemistry of lysosomal storage disorders.
BACKGROUND Lysosomal storage disorders are a group of genetic diseases, each with a broad spectrum of clinical presentation that ranges from attenuated to severe. The immunochemical analysis of patient samples is aimed at several key aspects of patient management, including early detection of the disorder, prediction of clinical severity, determining the most appropriate therapeutic regimen, an...
متن کاملLysosomal Storage Disorders and Malignancy
Lysosomal storage disorders (LSDs) are infrequent to rare conditions caused by mutations that lead to a disruption in the usual sequential degradation of macromolecules or their transit within the cell. Gaucher disease (GD), a lipidosis, is among the most common LSD, with an estimated incidence of 1 in 40,000 among the Caucasian, non-Jewish population. Studies have indicated an increased freque...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Autophagy
سال: 2009
ISSN: 1554-8627,1554-8635
DOI: 10.4161/auto.5.2.7390