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Plekhg5 (基因名), Pleckstrin homology domain-containing family G member 5 (蛋白名), PKHG5_MOUSE.
产品名称:

Mouse Plekhg5/ Pleckstrin homology domain-containing family G member 5 Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Mouse
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Mouse Plekhg5 Peptide
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Mouse Plekhg5 Peptide
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R&D 技术数据
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该产品尚未在任何出版物中被引用。

[1].
"The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset."

[2].
"PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot-Marie-Tooth disease."

[3].
"Mutations in the PLEKHG5 gene is relevant with autosomal recessive intermediate Charcot-Marie-Tooth disease."

[4].
"Common variants at ten loci influence QT interval duration in the QTGEN Study."

[5].
"Association between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicity."

[6].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[7].
"Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways."

[8].
"Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro."

[9].
"Architecture of the human interactome defines protein communities and disease networks."

[10].
"Phosphorylation-mediated 14-3-3 protein binding regulates the function of the rho-specific guanine nucleotide exchange factor (RhoGEF) Syx."
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