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首页  >  多肽  >  Human PHOX2B Peptide
PHOX2B (基因名), Paired mesoderm homeobox protein 2B (蛋白名), PHX2B_HUMAN.
产品名称:

Human PHOX2B/ Paired mesoderm homeobox protein 2B 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 PHOX2B Peptide
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Human PHOX2B Peptide
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该产品尚未在任何出版物中被引用。

[1].
"PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome."

[2].
"Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma."

[3].
"Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China."

[4].
"Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE."

[5].
"PHOX2B analysis in non-syndromic neuroblastoma cases shows novel mutations and genotype-phenotype associations."

[6].
"The French Congenital Central Hypoventilation Syndrome Registry: general data, phenotype, and genotype."

[7].
"Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease."

[8].
"Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development."

[9].
"Association study of PHOX2B as a candidate gene for Hirschsprung's disease."

[10].
"Molecular analysis of congenital central hypoventilation syndrome."
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