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    • 5. 发明申请
    • Revolving door control system
    • 旋转门控制系统
    • US20080028682A1
    • 2008-02-07
    • US11823470
    • 2007-06-27
    • Zachary CasellaMichael StadlerThomas Schluep
    • Zachary CasellaMichael StadlerThomas Schluep
    • E05F15/20
    • E05G5/003E05F15/608E05F15/74E05F2015/767E05Y2400/334E05Y2600/458E05Y2900/132
    • In a method and system for controlling a revolving door that has a plurality of chambers defined by wings of a revolver, at least one imaging sensor is provided for acquiring images of a first area where the plurality of chambers rotatably pass by or through. A drive causes the revolver to rotate in a first direction from a first position where a user can enter a first chamber via the first opening. Images are acquired by the one imaging sensor and signals are acquired from a position sensor that is operative for outputting signals indicative of the angular position of the revolver. Based on the signals acquired from the position sensor, each imaging sensor or its output is disabled and/or each image acquired by each imaging sensor is ignored when each door wing is in field-of-view of the imaging sensor.
    • 在用于控制旋转门的方法和系统中,旋转门具有由左轮手臂的翼限定的多个腔室,提供至少一个成像传感器,用于获取多个腔室可转动地穿过或穿过的第一区域的图像。 驱动器使得左轮手枪从第一位置沿第一方向旋转,在第一位置,用户可以经由第一开口进入第一腔室。 图像由一个成像传感器获取,并且信号从位置传感器获取,位置传感器用于输出指示左轮手枪的角位置的信号。 基于从位置传感器获取的信号,当每个门翼处于成像传感器的视野中时,每个成像传感器或其输出被禁用和/或每个成像传感器获取的每个图像被忽略。
    • 6. 发明申请
    • PROTEIN TYROSINE PHOSPHATASE, NON-RECEPTOR TYPE 11 (PTPN11) AND TRIPLE-NEGATIVE BREAST CANCER
    • US20140134184A1
    • 2014-05-15
    • US14124441
    • 2012-06-05
    • Mohamed Bentires-AljNicola AcetoMichael Stadler
    • Mohamed Bentires-AljNicola AcetoMichael Stadler
    • C12N15/113C12Q1/68C07K16/40
    • C12N15/1137C07K16/40C12N2310/14C12N2310/141C12N2310/531C12Q1/6886C12Q2600/112C12Q2600/158C12Y301/03048
    • The present invention relates to a method for treating breast cancer in a subject having a breast cancer of the triple-negative type, which method comprises the step of administering to said subject a therapeutically effective amount of a modulator of the protein tyrosine phosphatase, non-receptor type 11 (PTPN11) gene or of its gene product (Shp2). The present invention also relates to a method for treating breast cancer in a subject having a breast cancer over-expressing the “SHP2 signature” genes, as compared to normal breast tissue samples, which method comprises the step of administering to said subject a therapeutically effective amount of a modulator of the protein tyrosine phosphatase, non-receptor type 11 (PTPN11) gene or of its gene product (Shp2), wherein said “SHP2 signature” genes consist of the genes SGCB, ZSCAN12, ID4, ZIC3, CPVL, HLA-A, MCOLN3, SPATA18, TMEM45A, GNAL, CYBRD1, TSPAN7, ZEB1, CNTLN, NEFL, CENPV, ARL6, HPRT1, LRRC34, PDPN, BEND7, SLC16A10, FAM27E1, PLEKHA1, HERC5, CHIC1, PHF6, ELOVL4, ANTXR1, PRAME, SCML1, CLIP4, CECR2, CNOT10, IGF2BP3, NAP1L3, GPC3, KIAA1804, DGKE, FAS, EPHA6, KDELC1, CRISPLD1, DOCK3, ACSL4, CNTNAP3, PLEKHM3, RDX, TBX18, RRAGD, HOXB5, SNCA, FUNDC2, ITGA8, HFM1, IGF2BP2, CCND2, SGTB, MKX, CRYBG3, WBP5, LPHN3, BEX4, CPNE8, GLDC, SLC35F1, HOXA13, SERPINF1, NEFM, SYCP2L, FHL1, APOBEC3C, CALD1, FKBP10, HOXD11, DENND2C, LRRC49, FAM55C, KIAA0408, HOXB9, C160RF62, ACN9, TUSC3, ELOVL2, SPOCK3, HOXB6, WDR35, MPP1, FBX038, PRKAA2, SLAIN1, NPHP3, KIAA1524, PRPS1, GJC1, AMOT, SLC9A6, KCTD12, NUP62CL, DZIP3, JAM3, HOXA9, ANKRD19, CDKN2A, BCAT1, OAT, LPHN2, CCDC82, HSD17B11, SAMHD1, WDR17, STK33, GSTP1, TRPC1, CKB, LIN28B, ALDH1L2, SACS, CLGN, MY03A, EPB41L3, SLC25A27, VCAN, GPX8, GALNT13, PVRL3, MOXD1, HEY1, MAP7D3, ESD, MPP6, EYA4, SPG20, ZDBF2, ZNF204, IFT57, AKR1B1, ADAT2, ZNF717, CCDC88A, ZNF215, MIDI, FBN2, LOC100130876, TCEAL8, IGF2BP1, ANKRD18B, PLAGL1, PM20D2, LDHB, C150RF51, PTPN11, EPB41L2, TLE4, GOLM1, C60RF192, HOXD13, SLIT2, UCHL1, DYNC2H1, CPS1, GPR180, PYGL, NRN1, PRTFDC1, SLC16A1, DSC3, TMC01, LRCH2, SLC6A15, DZIP1, HOXA5, HSPA4L, CDR1, PLS3, ECHDC1, SMARCA1, CXORF57, HOXD10, and IRS4.
    • 7. 发明申请
    • METHOD FOR THE PRODUCTION OF CHIRAL AMINOCARBONYL COMPOUNDS
    • 生产磺酰胺化合物的方法
    • US20090281346A1
    • 2009-11-12
    • US12373955
    • 2007-07-17
    • Benjamin ListMichael StadlerJung Woon Yang
    • Benjamin ListMichael StadlerJung Woon Yang
    • C07C271/18
    • C07C269/06C07C271/18
    • Disclosed is a method for producing aminocarbonyl compounds of the general formula (I) wherein R1 and R2 can be identical or different and represents hydrogen, alkyl, alkenyl, alkynyl, or aryl, X represents hydrogen, alkyl, alkenyl, alkynyl, aryl, or OR3, R3 representing hydrogen, alkyl, alkenyl, alkynyl, or aryl. According to said method, an aldehyde of the general formula (II) R1CO  (II) wherein R1 has the meaning indicated above, is reacted with an imine of the general formula (III) wherein R2 and X have the meaning indicated above, in the presence of a catalyst.Aminocarbonyles are obtained by means of catalyzed Mannich reactions with aldehydes. For example, if α-unbranched aldehydes are reacted with previously formed N-Boc imines in the presence of (S)-proline as a catalyst, the desired β-amino aldehydes are obtained at excellent yields, diastereoselectivities and enantioselectivities.
    • 公开了一种制备通式(I)的氨基羰基化合物的方法,其中R 1和R 2可以相同或不同,表示氢,烷基,烯基,炔基或芳基,X表示氢,烷基,烯基,炔基,芳基或 OR3,R3代表氢,烷基,烯基,炔基或芳基。 根据所述方法,通式(II)的化合物R1CO(II)的醛,其中R1具有上述含义,与通式(Ⅲ)的亚胺反应,其中R2和X具有上述含义,在 存在催化剂。 氨基羰基通过与醛的催化曼尼希反应获得。 例如,如果在(S) - 脯氨酸作为催化剂的存在下使α-未分支的醛与先前形成的N-Boc亚胺反应,则获得所需的β-氨基醛,其产率优异,非对映选择性和对映选择性。