Mostrando 121 - 140 Resultados de 2,550 Para Buscar 'Klippan~', tiempo de consulta: 2.74s Limitar resultados
  1. 121
    por Ohashi, Akihiro
    Publicado 2015
    “…The molecular mechanism responsible for cell fate after mitotic slippage remains unclear. We investigated the different postmitotic effects of aneuploidy versus polyploidy using chemical inhibitors of centromere-associated protein-E (CENP-E) and kinesin family member 11 (KIF11, also known as Eg5). …”
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  2. 122
  3. 123
    “…CONCLUSIONS: “flippant” allows for quick, reproducible data analysis of scramblase activity assays and provides a platform for review, dissemination and extension of the strategies it employs. …”
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  4. 124
    “…We have discovered that the CRL2(ZYG11A/B) ubiquitin ligase promotes mitotic slippage. The combination of antimicrotubule drugs and a CRL2(ZYG11A/B) inhibitor prevents mitotic slippage to increase antimitotic efficacy.…”
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  5. 125
    “…Klippel–Trenaunay syndrome (KTS) is a vascular lymphatic malformation underlying with bony and soft tissue hypertrophy. …”
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  6. 126
    “…In this study, we show a novel ecological approach relying on a wearable robotic device (the Active Pelvis Orthosis, APO) aimed at facilitating balance recovery after unexpected slippages. Specifically, if the APO detects signs of balance loss, then it supplies counteracting torques at the hips to assist balance recovery. …”
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  7. 127
    “…Due to their excellent properties and two-dimensional geometry, graphenes (Grs) have been widely used as reinforced fillers in graphene/aluminum nanolaminated composite (GANC). The separation and slippage behavior of the GANC is highly dependent on the interfacial properties between Gr and aluminum (Al). …”
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  8. 128
    “…BACKGROUND: Klippel-Trenaunay syndrome (KTS) is a rare congenital syndrome characterized by the triad of venous varicosities, capillary malformations and limb hypertrophy. …”
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  9. 129
    “…Klippel-Trenaunay syndrome is a rare disorder consisting of the triad of vascular and/or lymphatic malformations, capillary malformations, and soft tissue or bony hypertrophy. …”
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  10. 130
    “…Anorectal malformations (ARMs) are a complex group of malformations associated with various congenital anomalies. Klippel–Feil syndrome (KFS) is characterized by fusion of cervical vertebrae, short neck, torticollis, and/or facial asymmetry and very rarely associated with ARM. …”
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  11. 131
    “…Here, we report for the first time on the demonstration of a slippage boosted spectral cleaning technique to mitigate the impact of seed laser induced phase errors and to significantly improve the temporal coherence of a seeded FEL with large phase errors in the seed laser. …”
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  12. 132
    “…Klippel-Trénaunay-Weber syndrome (KTWS), also known as angioosteohypertrophy syndrome, is a rare congenital malformation with unknown etiology characterized by the combination of capillary malformations (port-wine strain), venous varicosities, and a soft tissue or bony hypertrophy of the affected limb. …”
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  13. 133
    “…Mitotic slippage (MS), the incomplete mitosis that results in a doubled genome in interphase, is a typical response of TP53-mutant tumors resistant to genotoxic therapy. …”
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  14. 134
  15. 135
    “…Klippel-Trenaunay Syndrome (KTS) is a rare and sporadic congenital disorder, characterized by the classical triad of port-wine stains, varicosities along with bone and soft tissue hypertrophy. …”
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  16. 136
    “…Patients with combined phenotypes of Sturge–Weber syndrome and Klippel–Trenaunay syndrome have been reported, though the underlying genetic spectrum in these individuals remains to be elucidated. …”
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  17. 137
  18. 138
    “…Klippel-Trenaunay syndrome (KTS) is a rare vascular malformation characterized by capillary malformation, venous malformations, and soft tissue or bone hypertrophy that affect the extremities in most cases. …”
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  19. 139
    “…Klippel-Trenaunay syndrome (KTS) is a congenital vascular disorder characterized by the triad of cutaneous capillary malformation, lymphatic and venous anomalies, and soft tissue and bone overgrowth. …”
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  20. 140
    “…P4 ATPases are lipid flippases that are phylogenetically grouped into P4A, P4B and P4C clades. …”
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