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cs
- Protein C deficiency is a disorder that increases the risk of developing abnormal blood clots; the condition can be ...
- Cytochrome c oxidase deficiency is a genetic condition that can affect several parts of the body, including the muscles used for movement (skeletal muscles), the ...
- MN1 C-terminal truncation (MCTT) syndrome is a condition characterized by intellectual disability, developmental delay, distinctive facial features, and ... mutations are reflected in the condition name, MN1 C-terminal truncation syndrome.Research shows that a shortened ...
- ... instructions for making a protein called surfactant protein-C (SP-C). This protein is one of four proteins (each ...
- ... beta 4 isoform) of a protein called phospholipase C. This protein is involved in a signaling pathway ... outside the cell to inside the cell. Phospholipase C carries out one particular step in the phosphoinositide ...
- ... Condition AC40 DNA-directed RNA polymerase I subunit C DNA-directed RNA polymerases I and III 40 ... and III subunit RPAC1 polymerase (RNA) I polypeptide C polymerase (RNA) I polypeptide C, 30kDa polymerase (RNA) ...
- ... called inositol 1,4,5-trisphosphate 3-kinase C (ITPKC). It is involved in a mechanism called ... Condition inositol 1,4,5-trisphosphate 3-kinase C InsP 3 kinase C insP 3-kinase C ...
- ... ABCC9_HUMAN ATFB12 ATP-binding cassette sub-family C member 9 ATP-binding cassette sub-family C member 9 isoform SUR2A ATP-binding cassette sub-family C member 9 isoform SUR2B ATP-binding cassette transporter ...
- ... to the recurrent infections common in WHIM syndrome. C-X-C chemokine receptor type 4 CD184 CD184 antigen chemokine (C-X-C motif) receptor 4 CXCR4_HUMAN D2S201E ...
- ... characteristic features of the KRAS mutation-associated phenotype. C-K-RAS c-K-ras protein c-K-ras2 protein c-Kirsten-ras protein cellular c-Ki-ras2 proto- ...
