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TRPM6 gene

Known as: TRANSIENT RECEPTOR POTENTIAL CATION CHANNEL, SUBFAMILY M, MEMBER 6, CHANNEL KINASE 2, TRPM6 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
A comparative study of ammonia transport across ruminal epithelia from Bos indicus crossbreds versus Bos taurus.
Absorption of ammonia from the rumen of cattle decreases nitrogen availability for fermentational protein synthesis, leading to… 
2017
2017
A Nonredundant Role for the TRPM6 Channel in Neural Tube Closure
In humans, germline mutations in Trpm6 cause autosomal dominant hypomagnesemia with secondary hypocalcemia disorder. Loss of… 
2015
2015
Flavaglines Stimulate Transient Receptor Potential Melastatin Type 6 (TRPM6) Channel Activity
Magnesium (Mg2+) is essential for enzymatic activity, brain function and muscle contraction. Blood Mg2+ concentrations are… 
2015
2015
Effects of laser irradiation at different wavelengths (660, 810, 980, and 1064 nm) on transient receptor potential melastatin channels in an animal model of wound healing
The aim of the present study was to compare the effectiveness of four different laser wavelengths used for low-level laser… 
2015
2015
Hypomagnesemia due to two novel TRPM6 mutations
Abstract Background: Although most hypocalcemia with hypomagenesemia in the neonatal period is due to transient neonatal… 
2014
2014
Expressions of TRPM6 and TRPM7 and histopathological evaluation of tissues in ischemia reperfusion performed rats
Abstract There is very little work on the expression of TRPM6/7 in ischemia reperfusion models. In previous studies, after… 
2011
2011
Dietary Mg2+ regulates the epithelial Mg2+ channel TRPM6 in rat mammary tissue.
The epithelial Mg(2+) channel TRPM6 is considered a pivotal component in active Mg(2+)absorption and re-absorption in the… 
Review
2009
Review
2009
Epithelial Mg2+ channel TRPM6: insight into the molecular regulation.
Our understanding of the molecular mechanisms of renal magnesium (Mg2+) handling has greatly enhanced over recent years. This… 
2009
2009
Mice defective in Trpm 6 show embryonic mortality and neural tube defects
The syndrome of hypomagnesemia with secondary hypocalcemia is caused by defective TRPM6. This protein is an ion channel that also… 
2006
2006
Genetic background of HSH in three Polish families and a patient with an X;9 translocation
Hypomagnesemia with secondary hypocalcemia (HSH) is a rare inherited disease, characterised by neurological symptoms, such as… 
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