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首页  >  多肽  >  Human PHOX2A Peptide
PHOX2A (基因名), Paired mesoderm homeobox protein 2A (蛋白名), PHX2A_HUMAN.
产品名称:

Human PHOX2A/ Paired mesoderm homeobox protein 2A Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Human
序列:
预估分子量:
30kDa (monomer)
应用:
WB
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Human PHOX2A Peptide
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该产品尚未在任何出版物中被引用。

[1].
"Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development."

[2].
"Molecular analysis of congenital central hypoventilation syndrome."

[3].
"A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2)."

[4].
"Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2."

[5].
"Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13."

[6].
"The Phox2 pathway is differentially expressed in neuroblastoma tumors, but no mutations were found in the candidate tumor suppressor gene PHOX2A."

[7].
"Effects of transcription factors Phox2 on expression of norepinephrine transporter and dopamine beta-hydroxylase in SK-N-BE(2)C cells."

[8].
"Clinical features, ARIX and PHOX2B nucleotide changes in three families with congenital superior oblique muscle palsy."

[9].
"PHOX2A and PHOX2B genes are highly co-expressed in human neuroblastoma."

[10].
"Transcriptional regulation of TLX2 and impaired intestinal innervation: possible role of the PHOX2A and PHOX2B genes."
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