TRPM7: Difference between revisions

From Magnesium
(Created page with "TRPM7 as member or the Transient Receptor Potential Ion Channel family is a nonselective cation channel which is inhibited by magnesium. It imports toxic cations like Zn2+, Cd2+, Co2+, and its kinase function hase some specific effects. Activity is needed for cellular magnesium import. Essential for Fibrosis (EMT), Calcification processes, Cell viability, it transforms magnesium action into cardiovascular, renal and neurologic diseases. While clinical trial data on magne...")
 
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*'''[[Bone and Implants (TRPM7)]]'''
*'''[[Bone and Implants (TRPM7)]]'''
*'''[[Vascular Calcification (TRPM7)]]'''
*'''[[Vascular Calcification (TRPM7)]]'''
*'''[[Hypertension]]'''
*'''[[Glomus caroticus]]'''
*'''[[Diabetes (TRPM7)]]'''
*'''[[Diabetes (TRPM7)]]'''
*'''[[Nephrology clinical (TRPM7)]]'''
*'''[[Nephrology clinical (TRPM7)]]'''
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*'''[[Neurology (TRPM7)]]'''
*'''[[Neurology (TRPM7)]]'''
*'''[[Cancer (TRPM7)]]'''
*'''[[Structure Signal Transduction]]'''
*'''[[Cell Death (TRPM7)]]'''  
*'''[[Cell Death (TRPM7)]]'''  
*'''[[Toxic cations (TRPM7)]]'''
*'''[[Toxic cations (TRPM7)]]'''
*'''[[Cancer (TRPM7)]]'''
*'''[[Structure]]'''


*'''[[Myalgic encephalitis]]'''
*'''[[Coronaviruses (TRPM7)]]'''
*'''[[Sepsis Coagulation AKI]]'''
*'''[[Immunology (TRPM7)]]'''
*'''[[Immunology (TRPM7)]]'''
*'''[[Coronaviruses (TRPM7)]]'''
*'''[[Pharmacology (TRPM7)]]'''
*'''[[Pharmacology (TRPM7)]]'''
*'''[[RNA]]'''
*'''[[Human genetics (TRPM7)]]'''
*'''[[Human genetics (TRPM7)]]'''
*'''[[Magnesium physiology (TRPM7)]]'''
*'''[[Magnesium physiology (TRPM7)]]'''

Revision as of 14:56, 25 January 2024

TRPM7 as member or the Transient Receptor Potential Ion Channel family is a nonselective cation channel which is inhibited by magnesium. It imports toxic cations like Zn2+, Cd2+, Co2+, and its kinase function hase some specific effects. Activity is needed for cellular magnesium import. Essential for Fibrosis (EMT), Calcification processes, Cell viability, it transforms magnesium action into cardiovascular, renal and neurologic diseases. While clinical trial data on magnesium substitution is lacking, physiological effects of established leads as sacubitril, candesartan, and aldosterone antagonism act as TRPM7 inhibitors.

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