WebApr 2, 2024 · In the present study, using newly developed exophilin-5–knockout ( Exph5 -KO) mice and mouse models of asthma, we uncovered a role of exophilin-5 as a regulator of IL-33 signaling in antigen-induced allergic immune responses. Results. Lack of exophilin-5 exacerbates OVA-induced allergic inflammation. WebPigors et al. (2014) sequenced the EXPH5 gene in a cohort of 35 patients with clinically suspected epidermolysis bullosa simplex (EBS) who were negative for mutation in the …
Mutations in EXPH5 result in autosomal recessive inherited skin ...
WebEntrez Gene Summary for EXPH5 Gene. The protein encoded by this gene is a member of the synaptotagmin-like protein (Slp) family lacking a C2 domain. It contains an N-terminal … WebSeveral different genes have been implicated in the pathophysiology of inherited blistering skin diseases. Recently, autosomal recessive loss-of-function mutations in EXPH5 … hide clock in windows 11
320051 - Gene ResultExph5 exophilin 5 [ (house mouse)]
WebEXPH5, also named as KIAA0624 or SLAC2B, is a 1989 amino acid protein, which contains one RabBD (Rab-binding) domain. EXPH5 is expressed in keratinocytes. EXPH5 may act as Rab effector protein and play a role in vesicle trafficking. EXPH5 plays a role in maintaining keratinocyte integrity, and in inherited skin fragility. Web首页 / 抗体 / Mouse monoclonal [B302 (323/A3)] to EpCAM 手机验证. 我的询价. 询价列表 点击加载更多. 暂时没有已询价产品. 发送产品. 快捷询价 发送名片. 让更多商家联系我. 当你希望让更多商家联系你时,可以勾选后发送询价,平台会将你的询价消息推荐给更多商家。 ... WebEpidermolysis bullosa (EB) is a heterogeneous group of heritable blistering diseases. We developed a next generation sequencing (NGS) panel covering 21 genes associated with skin fragility disorders, and it was applied to DNA from 91 probands with the diagnosis of EB. In one patient, novel homozygou … hide chicken