会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明申请
    • Genes from chromosomes 3, 5 and 11 involved in premature canities
    • 来自染色体3,5和11的基因涉及早衰
    • US20070065389A1
    • 2007-03-22
    • US11583512
    • 2006-10-18
    • Olivier De LacharriereJean-Louis BlouinClaire DelocheStylianos Antonarakis
    • Olivier De LacharriereJean-Louis BlouinClaire DelocheStylianos Antonarakis
    • A61K8/73C12Q1/68A61K48/00
    • A61Q5/10A61K8/35A61K48/00A61Q19/04C12Q1/6883C12Q2600/148C12Q2600/156C12Q2600/172
    • The disclosure provides a cosmetic or therapeutic method for combating canities and/or stimulating natural pigmentation and/or treating a pigmentation disorder comprising administering at least one polynucleotide fragment comprising 18 consecutive nucleotides, the sequence of which corresponds to all or part of a gene on human chromosome 3 selected from KIAA1042, CCK, CACNA1D, ARHGEF3 and AL133097 genes, or the sequence of which corresponds to all or part of a gene on human chromosome 5 selected from the KLHL3, HNRPA0, CDC25C, EGR1, C5orf7, LOC51308, ETF1, HSPA9B, PDCHA1 to PDCHA13, CSF1R, RPL7, PDGFRB, TCOF1, AL133039, CD74, RPS14, NDST1, G3BP, GLRA1, C5orf3, MFAP3, GALNT10 and FLJ117151 genes, or the sequence of which corresponds to all or part of a gene or human chromosome 11 selected from the GUCY1A2, CUL5, ACAT1, NPAT, ATM, AF035326, AF035327m A0035328m BC029536, FLJ20535, DRD2, ENS303941, IGSF4, LOC1092, BC010946, TAGLN, PCSK7 and ENS300650 genes, and diagnostic methods employing same.
    • 本公开提供了一种用于对抗癌症和/或刺激天然色素沉着和/或治疗色素沉着病症的化妆品或治疗方法,其包括施用至少一种包含18个连续核苷酸的多核苷酸片段,其中所述多核苷酸片段的序列对应于人的全部或部分基因 染色体3选自KIAA1042,CCK,CACNA1D,ARHGEF3和AL133097基因,或其序列对应于选自KLHL3,HNRPA0,CDC25C,EGR1,C5orf7,LOC51308,ETF1,HSPA9B的人染色体5上的全部或部分基因 ,PDCHA1至PDCHA13,CSF1R,RPL7,PDGFRB,TCOF1,AL133039,CD74,RPS14,NDST1,G3BP,GLRA1,C5orf3,MFAP3,GALNT10和FLJ117151基因,或其序列对应于全部或部分基因或人染色体 11选自GUCY1A2,CUL5,ACAT1,NPAT,ATM,AF035326,AF035327m A0035328m BC029536,FLJ20535,DRD2,ENS303941,IGSF4,LOC1092,BC010946,TAGLN,PCSK7和ENS300650基因,以及采用 相同