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首页  >  多肽  >  Human PNPT1 Peptide
PNPT1 (基因名), Polyribonucleotide nucleotidyltransferase 1, mitochondrial (蛋白名), PNPT1_HUMAN.
产品名称:

Human PNPT1/ Polyribonucleotide nucleotidyltransferase 1, mitochondrial Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Human
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Human PNPT1 Peptide
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Human PNPT1 Peptide
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该产品尚未在任何出版物中被引用。

[1].
"Human mitochondrial SUV3 and polynucleotide phosphorylase form a 330-kDa heteropentamer to cooperatively degrade double-stranded RNA with a 3'-to-5' directionality."

[2].
"Analysis of the human polynucleotide phosphorylase (PNPase) reveals differences in RNA binding and response to phosphate compared to its bacterial and chloroplast counterparts."

[3].
"Stable PNPase RNAi silencing: its effect on the processing and adenylation of human mitochondrial RNA."

[4].
"Mammalian polynucleotide phosphorylase is an intermembrane space RNase that maintains mitochondrial homeostasis."

[5].
"Defining the domains of human polynucleotide phosphorylase (hPNPaseOLD-35) mediating cellular senescence."

[6].
"Protein-protein interactions between human exosome components support the assembly of RNase PH-type subunits into a six-membered PNPase-like ring."

[7].
"A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss."

[8].
"Mutation in PNPT1, which encodes a polyribonucleotide nucleotidyltransferase, impairs RNA import into mitochondria and causes respiratory-chain deficiency."

[9].
"Human mitochondrial RNA turnover caught in flagranti: involvement of hSuv3p helicase in RNA surveillance."

[10].
"The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature."
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