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321por Smith, Brittany N., Ghazanfari, Arash M., Bohm, Rudolf A., Welch, William P., Zhang, Bing, Masly, John P.“…In particular, this approach brings together existing GAL4 transgenes, newly developed enhancer-trap flippase transgenes, and GAL80 transgenes flanked by Flippase recognition target sites. …”
Publicado 2015
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322por Kim, Jin Bum, Park, Seung Won, Lee, Young Seok, Nam, Taek Kyun, Park, Yong Sook, Kim, Young Baeg“…Klippel-Feil syndrome (KFS) is a congenital developmental disorder of cervical spine, showing short neck with restricted neck motion, low hairline, and high thoracic cage due to multilevel cervical fusion. …”
Publicado 2015
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323por Yara, Nana, Masamoto, Hitoshi, Iraha, Yuko, Wakayama, Akihiko, Chinen, Yukiko, Nitta, Hayase, Kinjo, Tadatsugu, Aoki, Yoichi“…We experienced a rare case of a pregnant woman with Klippel-Trénaunay syndrome complicated with diffuse venous malformation of the uterus. …”
Publicado 2016
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324“…First time described in 1912, from Maurice Klippel and Andre Feil independently, Klippel-Feil syndrome (synonyms: cervical vertebra fusion syndrome, Klippel-Feil deformity, Klippel-Feil sequence disorder) is a bone disorder characterized by the abnormal joining (fusion) of two or more spinal bones in the neck (cervical vertebrae), which is present from birth. …”
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325“…By reconstructing the relocated positions of the elongation complex as inferred from the sequences inserted or deleted during transcription, we show that continuation of transcription after slippage hinges on the degree of nucleotide complementarity within the RNA:DNA hybrid at the new DNA template location.…”
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327por Sakakura, Kazuki, Fujimoto, Ayataka, Ichikawa, Naoki, Ishikawa, Eiichi, Matsumura, Akira, Enoki, Hideo, Okanishi, Tohru“…BACKGROUND: Although complications have been associated with head clamp systems, few reports have described head slippage. The present study aimed to determine risk factors for head slippage and speculated that the position of head holder pins might be associated. …”
Publicado 2020
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328“…Klippel–Trenaunay–Weber syndrome (KTWS) is a rare congenital disorder characterized by asymmetric limb hypertrophy, usually of the lower limbs, as well as vascular anomalies and capillary malformations under the skin, termed as port-wine stain. …”
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329“…Our hypothesis was that the suture would pull out of the lateral anchor (suture slippage), changing the positions of the medial suture knots during healing. …”
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330“…Klippel-Trénaunay-Weber syndrome (KTWS) is a rare condition characterized by a classic clinical triad. …”
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331por Caydasi, Ayse Koca, Khmelinskii, Anton, Darieva, Zoulfia, Kurtulmus, Bahtiyar, Knop, Michael, Pereira, Gislene“…Cells lacking SWR1-C were able to activate SPOC upon spindle misorientation but underwent mitotic slippage upon prolonged SPOC arrest. This mitotic slippage required the Cdc14-early anaphase release pathway and other factors including the SAGA (Spt-Ada-Gcn5 acetyltransferase) histone acetyltransferase complex, proteasome components and the mitotic cyclin-dependent kinase inhibitor Sic1. …”
Publicado 2023
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333por Chua, Geok-Lin, Tan, Bryan C., Loke, Randy Y. J., He, Menglan, Chin, Cheen-Fei, Wong, Bernice H., Kuk, Alvin C. Y., Ding, Mei, Wenk, Markus R., Guan, Lan, Torta, Federico, Silver, David L.“…These studies provide direct biochemical evidence that Mfsd2a functions as a lysolipid flippase.…”
Publicado 2023
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334por van Dijk, Myrthe, van Oirschot, Brigitte, Harrison, Alexander, Recktenwald, Steffen, Stommen, Amaury, Dey, Kuntal, Bos, Jennifer, Rab, Minke, Bogdanova, Anna, Minetti, Giampaolo, Tyteca, Donatienne, Egée, Stéphane, Kaestner, Lars, Molday, Robert, van Beers, Eduard, Van Wijk, RichardEnlace del recurso
Publicado 2023
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335por Napthine, Sawsan, Vidakovic, Marijana, Girnary, Roseanne, Namy, Olivier, Brierley, Ian“…Conversely, asparaginyl-tRNA promoted a dual slippage event in either system. Thus, the tRNAs themselves are the main determinants in the selection of single- or dual-tRNA slippage mechanisms. …”
Publicado 2003
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336por Tsaridis, Efstathios, Papasoulis, Efthimios, Manidakis, Nikolaos, Koutroumpas, Ioannis, Lykoudis, Savvas, Banos, Athanasios, Sarikloglou, Savvas“…INTRODUCTION: Klippel-Trenaunay-Weber syndrome is a rare congenital disorder of the peripheral vascular system that is characterized by haemangiomas, soft tissue and/or osseous hypertrophy, venous and lymphatic anomalies as well as arterio-venous malformations. …”
Publicado 2009
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337“…For example, the issue of a minimum threshold length for DNA slippage remains contentious. Model-fitting methods have generally concluded that slippage only occurs over a threshold length of about eight nucleotides, in contradiction with some direct observations of tandem duplications at shorter repeated sites. …”
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338“…In this study we experimentally uncoupled these two pathways using zVAD-fmk to block cell death or Cdc20 knockdown to block slippage. We then used time-lapse imaging to score the kinetics of single cells adopting the remaining fate. …”
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339“…The ideal airway management modality in pediatric patients with syndromes like Klippel-Feil syndrome is a great challenge and is technically difficult for an anesthesiologist. …”
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340por Cho, Woojin, Lee, Dong-Ho, Auerbach, Joshua D., Sehn, Jennifer K., Nabb, Colin E., Riew, K. Daniel“…Objectives To confirm the fact that spinal cord dimensions are smaller in adults with Klippel-Feil syndrome (KFS) than in pediatric patients with KFS and to compare the clinical characteristics and outcomes of neurologic complications in patients with KFS with matched controls. …”
Publicado 2014
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