SPG7 抗体
(Spastic Paraplegia 7 (SPG7))
This gene encodes a nuclear-encoded mitochondrial metalloprotease protein that is a member of the AAA (ATPases associated with a variety of cellular activities) protein family. Members of this protein family share an ATPase domain and have roles in diverse cellular processes including membrane trafficking, intracellular motility, organelle biogenesis, protein folding, and proteolysis. Two transcript variants encoding distinct isoforms have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 7. [provided by RefSeq, Jul 2008].
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Latest Publications for our SPG7 抗体
: "Loss of Mitochondrial AAA Proteases AFG3L2 and YME1L Impairs Mitochondrial Structure and Respiratory Chain Biogenesis." in: International journal of molecular sciences, Vol. 19, Issue 12, (2019) (PubMed).: "Dopamine D3 receptor-modulated neuroprotective effects of lisuride." in: Neuropharmacology, Vol. 117, pp. 14-20, (2017) (PubMed).
: "Proteomic Analysis of a Rat Cerebral Ischemic Injury Model after Human Cerebral Endothelial Cell Transplantation." in: Journal of Korean Neurosurgical Society, Vol. 59, Issue 6, pp. 544-550, (2016) (PubMed).
Aliases for SPG7 抗体
SPG7, paraplegin matrix AAA peptidase subunit (SPG7) 抗体SPG7, paraplegin matrix AAA peptidase subunit (Spg7) 抗体
AI452278 抗体
AU015315 抗体
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