Results 1 -
10
of
200
for
CALCIUM
- ... family of genes that provide instructions for making calcium channels. These channels, which transport positively charged calcium atoms (calcium ions) across cell membranes, play a ...
- ... gene provides instructions for making one of several calcium channels. Calcium channels, which transport positively charged calcium atoms (calcium ions) into cells, play a key ...
- ... family of genes that provide instructions for making calcium channels. These channels transport positively charged calcium atoms (calcium ions) across cell membranes. The CACNA1D ...
- ... main piece (subunit) of a structure called a calcium channel. Channels containing the CACNA1S protein are found ... used for movement (skeletal muscles). These skeletal muscle calcium channels play a key role in a process ...
- ... provides instructions for making a protein called the calcium-sensing receptor (CaSR). Calcium molecules attach (bind) to CaSR, which allows this protein to monitor and regulate the amount of calcium in the blood. The receptor is turned on ( ...
- ... instructions for making a protein called secreted modular calcium-binding protein 1 (SMOC-1). This protein is ... Coloboma More About This Health Condition secreted modular calcium-binding protein 1 SMOC1_HUMAN SPARC-related modular ...
- ... making an enzyme called sarco(endo)plasmic reticulum calcium-ATPase 2 (SERCA2). This enzyme belongs to a ... that helps control the level of positively charged calcium atoms (calcium ions) inside cells. SERCA2 is found ...
- ... making an enzyme called sarco(endo)plasmic reticulum calcium-ATPase 1 (SERCA1). This enzyme belongs to a ... that help control the level of positively charged calcium atoms (calcium ions) inside cells. The SERCA1 enzyme ...
- ... gene provides instructions for making a protein called calcium/calmodulin-dependent serine protein kinase (CASK). The CASK ... about FG syndrome More About This Health Condition calcium/calmodulin-dependent serine protein kinase (MAGUK family) CAMGUK ...
- ... mutations that cause infantile neuroaxonal dystrophy. CaI-PLA2 calcium-independent phospholipase A2 cytosolic, calcium-independent phospholipase A2 GVI INAD1 iPLA2 iPLA2beta NBIA2 ...