Defects in autophagy have implications for melanocyte survival and manifestations of skin pigmentary disorders. Zhang et al. (2015) show that mouse melanocytes lacking the autophagy protein Atg7 undergo premature senescence in vitro and accumulate products of oxidative damage, despite activation of the redox response. Interestingly, contrary to previous findings, the melanocyte-specific deficiency in autophagy did not cause major defects in melanosome biogenesis, nor did it produce visually striking changes in mouse coat color
Autophagy is a controlled mechanism of intracellular self-digestion with functions in metabolic adap...
Autophagy is a primary catabolic process in eukaryotes which is responsible for degrading dysfunctio...
The skin is exposed to environmental insults such as UV light that cause oxidative damage to macromo...
Autophagy is the central cellular mechanism for delivering organelles and cytoplasm to lysosomes for...
YesAutophagy is the central cellular mechanism for delivering organelles and cytoplasm to lysosomes ...
Defects in autophagy have implications for melanocyte survival and manifestations of skin pigmentary...
Vitiligo is a common chronic acquired pigmentation disorder characterized by loss of functional mela...
Melanosomes are melanocyte-specific organelles that protect cells from ultraviolet (UV)-induced deox...
Autophagy is a process that regulates cellular turnover by recycling or disassembling unnecessary or...
Melanin in the epidermis determines the wide variation in skin color associated with ethnic skin div...
Autophagy allows cells fundamental adaptations to metabolic needs and to stress. Using autophagic bu...
We have reported recently that inactivation of the essential autophagyrelated gene 7 (Atg7) in kerat...
Senescence is a state of growth arrest resulting mainly from telomere attrition and oxidative stress...
As the principle lysosomal mediated mechanism for the degradation of aged or damaged organelles and ...
Purpose: To examine the effects of autophagy deficiency induced by RPE-specific deletion of Atg5 or ...
Autophagy is a controlled mechanism of intracellular self-digestion with functions in metabolic adap...
Autophagy is a primary catabolic process in eukaryotes which is responsible for degrading dysfunctio...
The skin is exposed to environmental insults such as UV light that cause oxidative damage to macromo...
Autophagy is the central cellular mechanism for delivering organelles and cytoplasm to lysosomes for...
YesAutophagy is the central cellular mechanism for delivering organelles and cytoplasm to lysosomes ...
Defects in autophagy have implications for melanocyte survival and manifestations of skin pigmentary...
Vitiligo is a common chronic acquired pigmentation disorder characterized by loss of functional mela...
Melanosomes are melanocyte-specific organelles that protect cells from ultraviolet (UV)-induced deox...
Autophagy is a process that regulates cellular turnover by recycling or disassembling unnecessary or...
Melanin in the epidermis determines the wide variation in skin color associated with ethnic skin div...
Autophagy allows cells fundamental adaptations to metabolic needs and to stress. Using autophagic bu...
We have reported recently that inactivation of the essential autophagyrelated gene 7 (Atg7) in kerat...
Senescence is a state of growth arrest resulting mainly from telomere attrition and oxidative stress...
As the principle lysosomal mediated mechanism for the degradation of aged or damaged organelles and ...
Purpose: To examine the effects of autophagy deficiency induced by RPE-specific deletion of Atg5 or ...
Autophagy is a controlled mechanism of intracellular self-digestion with functions in metabolic adap...
Autophagy is a primary catabolic process in eukaryotes which is responsible for degrading dysfunctio...
The skin is exposed to environmental insults such as UV light that cause oxidative damage to macromo...