Showing 88,501 - 88,520 results of 118,788 for search '"defected"', query time: 1.04s Refine Results
  1. 88501

    Age-related decline in function of ON and OFF visual pathways. by Amithavikram R Hathibelagal, Vishal Prajapati, Indrani Jayagopi, Subhadra Jalali, Shonraj Ballae Ganeshrao

    Published 2022-01-01
    “…<h4>Conclusions</h4>This normative database will be useful to quantify disease-specific defects. More importantly, the ON pathway function can potentially serve as a surrogate for rod photoreceptor function.…”
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  2. 88502

    Dilemma of t-tests: Retaining or discarding choice and solutions by WenJun Zhang

    Published 2022-12-01
    “…In terms of significance test, the t-test has the general defects of statistical significance tests, coupled with the inherent fallacies of confidence intervals, and the peculiar uncertainty problems of t-intervals, make the t-test methodology obviously insufficient. …”
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  3. 88503

    Measuring F-actin properties in dendritic spines by Mikko eKoskinen, Pirta eHotulainen

    Published 2014-08-01
    “…Synaptic stimulation rapidly changes the actin dynamics and many actin regulators have been shown to play roles in neuron functionality. Accordingly, defects in the regulation of the actin cytoskeleton in neurons have been implicated in memory disorders. …”
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  4. 88504

    Manifestation of glucose-6-phosphate dehydrogenase deficiency in the wake of new-onset type 1 diabetes mellitus: a case report by Sandhya Govindarajan, Imran Zamir, Sunil Bagewadi, Emily Moore

    Published 2022-08-01
    “…Abstract Background Diabetes mellitus is the most common metabolic disease globally, while glucose-6-phosphate dehydrogenase deficiency, an X-linked inherited disorder, is the most common erythrocyte enzyme defect. The association between the two in children has been infrequently reported. …”
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  5. 88505

    Analysis, Modeling and Simulation of Mechatronic Systems using the Bond Graph Method by A. Alabakhshizadeh, Y. Iskandarani, G. Hovland, O. M. Midtgård

    Published 2011-01-01
    “…The Bond Graph is the proper choice of physical system used for: (i) Modeling which can be applied to systems combining multidisciplinary energy domains, (ii) Analysis to provide a great value proposition for finding the algebraic loops within the system enabling the process of troubleshooting and eliminating the defects by using the proper component(s) to fix the causality conflict even without being acquainted in the proper system, and (iii) Simulation facilitated through derived state space equations from the Bond Graph model is solved using industrial simulation software, such as 20-Sim. …”
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  6. 88506

    36-year Follow-up on Scalp Reconstruction Using Free Latissimus Dorsi Muscle Flap, Skin Grafting, and Scalp Expansion by Nourollah B. Ghorbani, MD

    Published 2024-05-01
    “…Then, scalp tissue surrounding the defect and forehead skin were expanded and used to restore the scalp to its original shape. …”
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  7. 88507

    Do Enamelin, Lactotransferrin, and Amelogenin-X Polymorphisms Predispose Dental Caries Susceptibility in Egyptian Children? A Cross-Sectional Study by Hassan Mossad Hassan Negm

    Published 2023-12-01
    “…These particular polymorphisms exhibited a noteworthy presence or occurrence rate in individuals who were more prone to developing dental caries.Conclusion ENAM rs3796703, AMELX rs946252 were frequently detected in the caries-susceptible group, suggesting the possible correlation between the defect in these proteins and the incidence of developing dental caries. …”
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  8. 88508

    A rare case of dysferlinopathy with paternal isodisomy for chromosome 2 determined by exome sequencing by Huan Li, Liang Wang, Cheng Zhang

    Published 2023-02-01
    “…Abstract Background Dysferlinopathies are autosomal recessive muscular dystrophies resulting from defects in DYSF (MIM: 603009), which is located on chromosome 2p13 and encodes the dysferlin protein. …”
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  9. 88509
  10. 88510

    Seroprevalence of high incidence congenital infections among pregnant women in Coatepeque, Guatemala and surrounding areas, 2017-2018. by Victoria J Hicks, César Sánchez, María Reneé López, Anna Gottschlich, Laura M Grajeda, Amanda Balish, Ana Gómez, Nevis Nuñez, Julio Juárez, Beatriz López, Mariangeli Freitas-Ning, Celia Cordón-Rosales, Manuel Sagastume, John P McCracken, Andrés Espinosa-Bode, Loren Cadena, Terrence Q Lo

    Published 2023-04-01
    “…Maternal infections during pregnancy can potentially cause birth defects and severe adverse effects in infants. From 2017 to 2018, we investigated the seroprevalence of five antibodies among 436 mother-infant pairs enrolled in a pregnancy cohort study in Coatepeque, Guatemala. …”
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  11. 88511

    Whole transcriptome RNA-seq reveals key regulatory factors involved in type 2 diabetes pathology in peripheral fat of Asian Indians by Aditya Saxena, Nitish Mathur, Pradeep Tiwari, Sandeep Kumar Mathur

    Published 2021-05-01
    “…In conclusions, this RNS-Seq study finds that peripheral subcutaneous adipose tissue among Asian Indians show pathology characterized by altered lipid, glucose and protein metabolism, adipogenesis defect and inflammation. A network of regulatory transcription factors, protein kinases and microRNAs have been imputed which converge on the process of adipogenesis. …”
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  12. 88512

    VISUAL EVOKED POTENTIALS OF SICK INFANTS WITH EPILEPSY by V. P. Zykov, I. M. Mosin, D. L. Safronov, E. B. Izumova, I. L. Stepanishev, O. A. Voronenko

    Published 2016-08-01
    “…The first group consisted of 19 sick infants with symptomatic epilepsy, the second – 10 infants with motor defect without epilepsy, the third – 10 healthy infants. …”
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  13. 88513

    The Drosophila melanogaster Y-linked gene, WDY, is required for sperm to swim in the female reproductive tract by Yassi Hafezi, Arsen Omurzakov, Jolie A. Carlisle, Ian V. Caldas, Mariana F. Wolfner, Andrew G. Clark

    Published 2024-01-01
    “…Finally, we show that mutants for another Y-linked gene, PRY, also show a sperm storage defect that may explain their subfertility. Overall, we provide direct evidence for the long-held presumption that protein-coding genes on the Drosophila Y regulate sperm motility.…”
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  14. 88514

    Surgical Repair of Symptomatic Chronic Achilles Tendon Rupture Using Synthetic Graft Augmentation by Ahmed Shoaib MBBS, MRCS, Viren Mishra MS Orth, MSc Orth Engineering, FRCS(Orth)

    Published 2016-08-01
    “…Category: Other Introduction/Purpose: Surgical repair of symptomatic chronic Achilles tendon (TA) rupture is a challenging problem due to the presence of large defect between tendon edges. We report the results of surgical repair of symptomatic chronic TA rupture by synthetic graft augmentation. …”
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  15. 88515

    Chemical-genetic profiling of imidazo[1,2-a]pyridines and -pyrimidines reveals target pathways conserved between yeast and human cells. by Lisa Yu, Andres Lopez, Abderrahmane Anaflous, Brahim El Bali, Abdellah Hamal, Elke Ericson, Lawrence E Heisler, Angus McQuibban, Guri Giaever, Corey Nislow, Charles Boone, Grant W Brown, Mohammed Bellaoui

    Published 2008-11-01
    “…Using validated chemogenomic assays in Saccharomyces cerevisiae, we discovered that two closely related compounds, an imidazo[1,2-a]pyridine and -pyrimidine that differ by a single atom, have distinctly different mechanisms of action in vivo. 2-phenyl-3-nitroso-imidazo[1,2-a]pyridine was toxic to yeast strains with defects in electron transport and mitochondrial functions and caused mitochondrial fragmentation, suggesting that compound 13 acts by disrupting mitochondria. …”
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  16. 88516

    Gene expression in a Drosophila model of mitochondrial disease. by Daniel J M Fernández-Ayala, Shanjun Chen, Esko Kemppainen, Kevin M C O'Dell, Howard T Jacobs

    Published 2010-01-01
    “…<h4>Background</h4>A point mutation in the Drosophila gene technical knockout (tko), encoding mitoribosomal protein S12, was previously shown to cause a phenotype of respiratory chain deficiency, developmental delay, and neurological abnormalities similar to those presented in many human mitochondrial disorders, as well as defective courtship behavior.<h4>Methodology/principal findings</h4>Here, we describe a transcriptome-wide analysis of gene expression in tko(25t) mutant flies that revealed systematic and compensatory changes in the expression of genes connected with metabolism, including up-regulation of lactate dehydrogenase and of many genes involved in the catabolism of fats and proteins, and various anaplerotic pathways. …”
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  17. 88517
  18. 88518
  19. 88519
  20. 88520