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Pnpla1 (基因名), Patatin-like phospholipase domain-containing protein 1 (蛋白名), PLPL1_MOUSE.
产品名称:

Mouse Pnpla1/ Patatin-like phospholipase domain-containing protein 1 Peptide

货号:

-

监管等级:
商标:
EIAab®
种属:
Mouse
形态:
Lyophilized powder
表征:
The peptide is characterized by mass spectroscopy
溶液澄清度:
In DMSO clear solution
Mouse Pnpla1 Peptide
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Mouse Pnpla1 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].
"Characterization of the human patatin-like phospholipase family."

[2].
"PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans."

[3].
"Mammalian patatin domain containing proteins: a family with diverse lipolytic activities involved in multiple biological functions."

[4].
"Genetic variance in the adiponutrin gene family and childhood obesity."

[5].
"Genetic variants associated with arsenic susceptibility: study of purine nucleoside phosphorylase, arsenic (+3) methyltransferase, and glutathione S-transferase omega genes."

[6].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[7].
"Molecular mechanism of the ichthyosis pathology of Chanarin-Dorfman syndrome: Stimulation of PNPLA1-catalyzed ω-O-acylceramide production by ABHD5."

[8].
"PNPLA1 Deficiency in Mice and Humans?Leads to a Defect in the Synthesis?of Omega-O-Acylceramides."

[9].
"Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of Consanguinity."

[10].
"Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier function."
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