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首页  >  多肽  >  Human PEX7 Peptide
PEX7 (基因名), Peroxisomal targeting signal 2 receptor (蛋白名), PEX7_HUMAN.
产品名称:

Human PEX7/ Peroxisomal targeting signal 2 receptor 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 PEX7 Peptide
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Human PEX7 Peptide
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该产品尚未在任何出版物中被引用。

[1].
"PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter."

[2].
"Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata."

[3].
"Identification of PEX7 as the second gene involved in Refsum disease."

[4].
"Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor."

[5].
"A newly isolated Pex7-binding, atypical PTS2 protein P7BP2 is a novel dynein-type AAA+ protein."

[6].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[7].
"Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia."

[8].
"Rhizomelic chondrodysplasia punctata type 1: report of mutations in 3 children from India."

[9].
"ASK1 and MAP2K6 as modifiers of age at onset in Huntington's disease."

[10].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
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