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PEX1 (基因名), Peroxisome biogenesis factor 1 (蛋白名), PEX1_HUMAN.
产品名称:

Human PEX1/ Peroxisome biogenesis factor 1 Peptide

货号:

SR15495h

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 PEX1 Peptide
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Human PEX1 Peptide
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该产品尚未在任何出版物中被引用。

[1].
"Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders."

[2].
"Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders."

[3].
"Novel PEX1 coding mutations and 5' UTR regulatory polymorphisms."

[4].
"Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction."

[5].
"Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I."

[6].
"Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders."

[7].
"Spectrum of PEX1 and PEX6 variants in Heimler syndrome."

[8].
"Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6."

[9].
"The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature."

[10].
"Many sequence variants affecting diversity of adult human height."
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