ADA 抗体
(Adenosine Deaminase (ADA))
This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for this gene and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia. [provided by RefSeq, Jul 2008].
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Latest Publications for our ADA 抗体
: "Integrative Analysis of Renal Ischemia/Reperfusion Injury and Remote Ischemic Preconditioning in Mice." in: Journal of proteome research, Vol. 16, Issue 8, pp. 2877-2886, (2017) (PubMed).: "Affinity proteomics reveals elevated muscle proteins in plasma of children with cerebral malaria." in: PLoS pathogens, Vol. 10, Issue 4, pp. e1004038, (2014) (PubMed).
: "CD39 and CD161 modulate Th17 responses in Crohn's disease." in: Journal of immunology (Baltimore, Md. : 1950), Vol. 193, Issue 7, pp. 3366-77, (2014) (PubMed).
: "Expression, pharmacology and functional activity of adenosine A1 receptors in genetic models of Huntington's disease." in: Neurobiology of disease, Vol. 71, pp. 193-204, (2014) (PubMed).
Aliases for ADA 抗体
adenosine deaminase (ADA) 抗体adenosine deaminase (Ada) 抗体
adenosine deaminase S homeolog (ada.S) 抗体
Adenosine deaminase (Ada) 抗体
adenosine deaminase (ada) 抗体
ADA 抗体
ADA-like 抗体
CG11994 抗体
dADA 抗体
Dmel\\CG11994 抗体
DrosADA 抗体
xada 抗体
zgc:92028 抗体
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