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  1. 301
    por Zhou, Kang, Lei, Shuaishuai, Du, Xiongzi
    Publicado 2022
    “…Combining this velocity, the slippage levels of the four wheels can be quantitatively measured. …”
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    Modelling and dynamic analysis of slippage level for large-scale skid-steered unmanned ground vehicle
  2. 302
    “…CONCLUSION: For patients with C1 occipitalization and a Klippel-Feil syndrome, ROPT may occur due to loading of C1-2 complex. …”
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    A case of nonrheumatoid retro-odontoid pseudotumor in Klippel-Feil syndrome with C1 occipitalization
  3. 303
    “…Our results reveal that, despite strong selection for resistance in a natural host population, genetic slippage after sexual reproduction can be a strong factor for the maintenance of genetic diversity of host resistance.…”
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    Genetic slippage after sex maintains diversity for parasite resistance in a natural host population
  4. 304
    “…Klippel–Trenaunay–Weber syndrome (KTWS) is a rare congenital disorder characterized by cutaneous capillary malformations, bone hypertrophy, and multiple venous or lymphatic malformations. …”
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    Balloon pulmonary angioplasty for chronic thromboembolic pulmonary hypertension concomitant with Klippel–Trenaunay–Weber syndrome
  5. 305
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    Fiber Bragg Grating Sensors for Reinforcing Bar Slippage Detection and Bond-Slip Gradient Characterization
  6. 306
    por Lippman, Edward
    Publicado 1992
    Libro
    A history of Western musical aesthetics /
  7. 307
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    Effect of Dietary and Lifestyle Interventions on the Amelioration of NAFLD in Patients with Metabolic Syndrome: The FLIPAN Study
  8. 308
    “…Cells release extracellular vesicles (EVs) from their surface, but the mechanisms that govern EV release by plasma membrane budding are poorly understood. The lipid flippase TAT-5 inhibits EV release from the plasma membrane in C. elegans , but how the level of flippase activity regulates EV release was unknown. …”
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    The ATPase activity of the phosphatidylethanolamine flippase TAT-5 inhibits extracellular vesicle budding from the plasma membrane
  9. 309
    “…INTRODUCTION: Klippel-Trenaunay Syndrome (KTS) is a rare genetic disorder which is characterised by vascular nevi, venous varicosity, and hyperplasia of soft tissue or bone. …”
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    A case report of multiple renal aneurysms due to Klippel-Trenaunay syndrome requiring laparoscopic nephrectomy
  10. 310
    por Li, Jingyi, Zhao, Yue, Wang, Na
    Publicado 2023
    “…The function of P4-ATPases is to maintain the abundance of phosphatidylserine (PS) and phosphatidylethanolamine (PE) in the inner leaflet as lipid flippases. Transmembrane protein 30A (TMEM30A, also named CDC50A), as an essential β subunit of most P4-ATPases, facilitates their transport and functions. …”
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    Physiological and Pathological Functions of TMEM30A: An Essential Subunit of P4-ATPase Phospholipid Flippases
  11. 311
    “…We report a case of Klippel Trenaunay Syndrome that was monitored both clinically and molecularly over a period of 9 years. …”
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    Case report: PIK3CA somatic mutation leading to Klippel Trenaunay Syndrome and multiple tumors
  12. 312
    “…We show that lack of the AMINOPHOSPHOLIPID ATPASE3 (ALA3) flippase activity caused defects at the plasma membrane and trans-Golgi network, resulting in altered endocytosis and secretion, processes relying on vesicle formation and movement. …”
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    Arabidopsis flippase ALA3 is required for adjustment of early subcellular trafficking in plant response to osmotic stress
  13. 313
    “…We report an exceedingly rare case of Klippel-Feil syndrome (KFS), compounded by ipsilateral absence of the vas deferens, renal agenesis, and diaphragmatic hernia. …”
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    Unilateral renal agenesis and ipsilateral absence of the vas deferens in a cryptorchid infant with Klippel-Feil syndrome
  14. 314
    “…Purpose: We discuss the coexistence of Klippel–Trénaunay–Weber syndrome with various malignancies, the possible histogenetic pathways and therapeutic implications. …”
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    Angiosarcoma With Malignant Peripheral Nerve Sheath Tumour Developing in a Patient With Klippel–Trénaunay–Weber Syndrome
  15. 315
    “…Klippel-Trenaunay syndrome (KTS) is a rare congenital syndrome of vascular malformations and soft tissue and bone hypertrophy. …”
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    Klippel-Trenaunay Syndrome Causing Life-Threatening GI Bleeding: A Case Report and Review of the Literature
  16. 316
    “…KEY WORDS: Congenital spinal malformation, Klippel-Feil syndrome, dermal sinus, dermoid cysts…”
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    Concurrent Klippel-Feil Anomaly, Tethering and Dermoid Cyst Misinterpreted as Pott disease: A Case Report
  17. 317
    por Bae, Youngsook
    Publicado 2014
    “…[Conclusion] CDS exercises were effective interventions for reducing neck pain in a patient with Klippel-Feil syndrome.…”
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    Effects of Cervical Deep Muscle Strengthening in a Neck Pain: A Patient with Klippel-Feil Syndrome
  18. 318
    “…The class 4 P-type ATPases (“flippases”) maintain membrane asymmetry by translocating phosphatidylethanolamine and phosphatidylserine from the outer leaflet to the cytosolic leaflet of the plasma membrane. …”
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    Plasma membrane aminoglycerolipid flippase function is required for signaling competence in the yeast mating pheromone response pathway
  19. 319
    “…Even though phospholipid flippases have been proposed to exist in bacteria, only one such protein, MprF, has been described. …”
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    The Lipid-Modifying Multiple Peptide Resistance Factor Is an Oligomer Consisting of Distinct Interacting Synthase and Flippase Subunits
  20. 320
    “…The Sturge-Weber syndrome, Klippel-Trenaunay syndrome, and the phakomatosis pigmentovascularis have the facial port-wine stain in common. …”
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    Ophthalmic Alterations in the Sturge-Weber Syndrome, Klippel-Trenaunay Syndrome, and the Phakomatosis Pigmentovascularis: An Independent Group of Conditions?
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