2025年3月30日 · PCDH15 (Protocadherin Related 15) is a Protein Coding gene. Diseases associated with PCDH15 include Usher Syndrome, Type If and Deafness, Autosomal …

Family members encode integral membrane proteins that mediate calcium -dependent cell-cell adhesion. The protein product of this gene consists of a signal peptide, 11 extracellular …

2025年2月8日 · Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways. Whole-exome sequencing for ocular …

2023年4月26日 · Usher syndrome type 1 F (USH1F), caused by mutations in the protocadherin-15 gene (PCDH15), is characterized by congenital deafness, lack of balance, and progressive …

Protocadherin 15 (PCDH15) is expressed in hair cells of the inner ear and in photoreceptors of the retina. Mutations in PCDH15 cause Usher Syndrome (deaf-blindness) and recessive …

2022年5月30日 · Herein, we show that Pcdh15 knockdown significantly increases extracellular signal-related kinase (ERK) phosphorylation and activation to enhance OPC proliferation in …

Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and cochlear function. …

2024年12月10日 · Family members encode integral membrane proteins that mediate calcium-dependent cell-cell adhesion. It plays an essential role in maintenance of normal retinal and …

Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene. Anorectal malformations with sacral bony abnormalities. Autosomal dominant sacral agenesis: Currarino …

Small proline-rich protein 2A is a gut bactericidal protein deployed during helminth infection. 预测能激活钙离子结合活性。 在几个过程的上游或内部发挥作用，包括成年行走行为；参与感觉 …