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首页  >  多肽  >  Mouse Pah Peptide
Pah (基因名), Phenylalanine-4-hydroxylase (蛋白名), PH4H_MOUSE.
产品名称:

Mouse Pah/ Phenylalanine-4-hydroxylase 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 Pah Peptide
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Mouse Pah 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].
"High resolution crystal structures of the catalytic domain of human phenylalanine hydroxylase in its catalytically active Fe(II) form and binary complex with tetrahydrobiopterin."

[2].
"Structure of tetrameric human phenylalanine hydroxylase and its implications for phenylketonuria."

[3].
"[Mutation spectrum of phenylalanine hydroxylase gene in patients with phenylketonuria in Tianjin and surrounding areas of Northern China]."

[4].
"A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterin."

[5].
"Genotype-predicted tetrahydrobiopterin (BH4)-responsiveness and molecular genetics in Croatian patients with phenylalanine hydroxylase (PAH) deficiency."

[6].
"Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples."

[7].
"[Spectrum of phenylalanine hydroxylase gene mutations and genotype-phenotype correlation in the patients with phenylketonuria in Beijing area of China]."

[8].
"Predicting a clinical/biochemical phenotype for PKU/MHP patients with PAH gene mutations."

[9].
"Mutation analysis of PAH gene and characterization of a recurrent deletion mutation in Korean patients with phenylketonuria."

[10].
"Loss of function in phenylketonuria is caused by impaired molecular motions and conformational instability."
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