Abstract A tremendous effort has been expended to elucidate the role of apoptotic molecules in ischemia. However, many agents that target apoptosis, despite their proven efficacy in animal models, have failed to translate that efficacy and spec-ificity in clinical settings. Therefore, comprehensive knowledge of apoptotic mechanisms involving key apoptotic regulatory molecules and the temporal expression profiles of various apoptotic molecules after cerebral ischemiamay provide insight for the development of better therapeutic strategies aimed at cerebral ischemia. The present study investigates the extent of apoptosis and the regulation of apoptotic molecules both at mRNA and protein levels at various time points after focal cerebral ischem...
The present study was designed to determine a dose-response relationship between apocynin and infarc...
AIM: Apoptosis after cerebral ischemia/reperfusion (I/R) injury leads to the process of cell death. ...
The online version of this article, along with updated information and services, is located on th
Accumulating biochemical and morphological evidence suggests that apoptosis contributes to neuronal ...
To improve understanding of the molecular mechanisms that underlie ischemic stroke, we analyzed earl...
Apoptosis may contribute to a significant proportion of neuron death following acute brain ischemia ...
Ischaemic stroke is a leading cause of death and disability worldwide. Usually it results from a tra...
Purpose: To investigate the expression and tyrosine 705 phosphorylation of STAT3 in focal cerebral i...
International audienceIn experimental models of cerebral ischemia, cells within the damaged territor...
Ischemic stroke is an important cause of mortality and invalidity. Focal cerebral ischemia induces m...
TNF-related apoptosis inducing ligand (TRAIL), a member of the TNF superfamily released by microglia...
Recovery from the debilitating effects of ischaemic stroke is variable and unpredictable. To maximiz...
International audienceCerebral ischemia is a leading cause of disability worldwide and no other effe...
It has previously been demonstrated that ischemic stroke activates autophagy pathways; however, the ...
Background and Purpose—To clarify the relationship between apurinic/apyrimidinic endonuclease (APE/R...
The present study was designed to determine a dose-response relationship between apocynin and infarc...
AIM: Apoptosis after cerebral ischemia/reperfusion (I/R) injury leads to the process of cell death. ...
The online version of this article, along with updated information and services, is located on th
Accumulating biochemical and morphological evidence suggests that apoptosis contributes to neuronal ...
To improve understanding of the molecular mechanisms that underlie ischemic stroke, we analyzed earl...
Apoptosis may contribute to a significant proportion of neuron death following acute brain ischemia ...
Ischaemic stroke is a leading cause of death and disability worldwide. Usually it results from a tra...
Purpose: To investigate the expression and tyrosine 705 phosphorylation of STAT3 in focal cerebral i...
International audienceIn experimental models of cerebral ischemia, cells within the damaged territor...
Ischemic stroke is an important cause of mortality and invalidity. Focal cerebral ischemia induces m...
TNF-related apoptosis inducing ligand (TRAIL), a member of the TNF superfamily released by microglia...
Recovery from the debilitating effects of ischaemic stroke is variable and unpredictable. To maximiz...
International audienceCerebral ischemia is a leading cause of disability worldwide and no other effe...
It has previously been demonstrated that ischemic stroke activates autophagy pathways; however, the ...
Background and Purpose—To clarify the relationship between apurinic/apyrimidinic endonuclease (APE/R...
The present study was designed to determine a dose-response relationship between apocynin and infarc...
AIM: Apoptosis after cerebral ischemia/reperfusion (I/R) injury leads to the process of cell death. ...
The online version of this article, along with updated information and services, is located on th