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首页  >  多肽  >  Rat Pou4f3 Peptide
Pou4f3 (基因名), POU domain, class 4, transcription factor 3 (蛋白名), PO4F3_RAT.
产品名称:

Rat Pou4f3/ POU domain, class 4, transcription factor 3 Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Rat
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Rat Pou4f3 Peptide
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Rat Pou4f3 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].
"Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding."

[2].
"Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans."

[3].
"Exome sequencing identifies POU4F3 as the causative gene for a large Chinese family with non-syndromic hearing loss."

[4].
"POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss."

[5].
"A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss."

[6].
"SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15)."

[7].
"Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3."

[8].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[9].
"The DFNA15 deafness mutation affects POU4F3 protein stability, localization, and transcriptional activity."

[10].
"Proneural and proneuroendocrine transcription factor expression in cutaneous mechanoreceptor (Merkel) cells and Merkel cell carcinoma."
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