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    P

    Phoenix Seminary

    院校EST. 1988
    93论文总数
    1,857引用总数

    It was founded in 1988 as a branch campus of Western Seminary and became independent in 2004.

    论文量&引用量时间轴

    机构学者

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    Umrao R. Monani
    Umrao R. Monani
    Ctr Motor Neuron Biol & Dis, Columbia Univ
    论文:7引用:0H-index:0
    Peter J. Gurry
    Peter J. Gurry
    Phoenix Seminary
    论文:6引用:0H-index:0
    Saikat Kumar Basu
    Saikat Kumar Basu
    Department of Biological Sciences;University of Lethbridge;Department of Biological Sciences, University of Lethbridge
    论文:4引用:0H-index:0
    Scott Danielson
    Scott Danielson
    Arizona State University
    论文:4引用:0H-index:0
    Sudhir Mehta
    Sudhir Mehta
    North Dakota State University
    论文:4引用:0H-index:0
    Steven J. Duby
    Steven J. Duby
    Coll Theol, Grand Canyon Univ
    论文:4引用:0H-index:0
    Shingo Kariya
    Shingo Kariya
    Center for Motor Neuron Biology and Disease, Columbia University
    论文:3引用:0H-index:0
    Guillermo Guerao
    Guillermo Guerao
    DEPARTAMENT DE BIOLOGIA;FACULTAT DE BIOLOGIA;DEPARTAMENT DE BIOLOGIA|FACULTAT DE BIOLOGIA
    论文:3引用:0H-index:0
    William R. Cetzal-Ix
    William R. Cetzal-Ix
    National Technological Institute of Mexico
    论文:3引用:0H-index:0

    论文(93)

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    1Hypostatic Unity and the Saving Work of Christ
    Steven J. Duby
    2026NOVA ET VETERA-ENGLISH EDITION(2026)
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    2Transgenic Expression of the Human Glucose Transporter1 (GLUT1) Gene Locus Reduces Disease Burden in Glut1 Deficiency Syndrome Model Mice.
    Maoxue Tang, Sasa Teng, Ashley Y Kim,Yueqing Peng,Umrao R Monani

    Proper brain function relies on an adequate supply of energy - mainly glucose - to power neuronal activity. Delivery of this nutrient to the neuropil is mediated by the Glucose Transporter1 (GLUT1) protein. Perturbing glucose supply to the brain is profoundly damaging and exemplified by the neurodevelopmental disorder, GLUT1 deficiency syndrome (GLUT1DS). Resulting from haploinsufficiency of the SLC2A1 (GLUT1) gene, GLUT1DS is characterized by intractable infantile-onset seizures and a disabling movement disorder. Ketogenic diets, which supply the brain with an alternate energy source, ketone bodies, are currently the preferred therapeutic option for Glut1DS patients but do not address the underlying cause - low brain glucose - of the disease. One intuitively appealing therapeutic strategy that does, involves restoring GLUT1 levels to the patient brain. Here, we demonstrate that transgenic expression of the human GLUT1 genomic locus in a mouse model of GLUT1DS raises brain GLUT1 levels and reduces disease burden. Augmenting GLUT1 levels in mutants correspondingly raised cerebrospinal fluid (CSF) glucose levels, improved motor performance and reduced the frequency of seizures characteristically observed in GLUT1DS. Interestingly, the increased GLUT1 in mutants harboring the human GLUT1 locus was at least partly the result of an increase in murine Slc2a1 (Glut1) activity, most likely the effect of a long non-coding RNA (lncRNA) embedded in the human transgene. Collectively, our work has not only shown that repleting human GLUT1 mitigates GLUT1DS but also has yielded transgenic mice that constitute a useful tool to test and optimize clinically promising agents designed to stimulate this gene for therapeutic purposes.

    2025Neurobiology of disease(2025)
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    3The Old Testament, Calvin and the Reformed Tradition. Edited by Yudha Thianto. (studies in the History of Christian Traditions, 208.) Pp. Xvi + 287 Incl. 2 Colour Ills. Leiden–Boston : Brill, 2024. €99. 978 90 04 41524 9; 1573 5664
    Matthew C. Bingham
    2025The Journal of Ecclesiastical History(2025)
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    4Enforcing the Machine Learning Algorithms to Contemplate on Cough Sound Codification
    Sripada V. S. S. Lakshmi, Rama Krishna Bomma, N. Silpa,V. V. R. Maheswara Rao,Padma Jyothi Uppalapati, K. Srinivasa Rao

    In India, millions of people are suffering from different respiratory diseases, and globally, billions of people are suffering. The main issue in identifying and resolving these diseases is a lack of awareness and costly treatment. Cough is the first identification feature in any respiratory disease. The cough sounds give important information about the respiratory system and the bacteria included. In this chapter, we will analyze the different cough sounds to detect the problem at early stages on the basis of various sound signals. Here, we discuss standard signal processing and domain-specific features in different cough patterns. These cough patterns include widened airways, narrow airways, fluid-filled air sacs, and stiff lungs. The main objective is to review and analyze cough attributes and observe how they differ in various diseases using machine learning (ML). As per the observation, the duration, intensity, type of cough, and frequency of cough are different in different diseases.

    2025Applications of Computational Intelligence in Management and Mathematics I(2025)
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    5ELEMENTAL ANALYSIS AND RADIOACTIVITY EVALUATION OF AEROSOLS GENERATED DURING HEATING OF SIMULATED FUEL DEBRIS IN THE URASOL PROJECT
    Youichi Tsubota, Laffolley Hugo, Emmanuel Porcheron, Christophe Journeau, Jules Delacroix, Célia Guévar, Emmanuelle Brackx, Yvan Lallot, Antonin Bouland
    2024Proceedings of the International Topical Workshop on Fukushima Decommissioning Research(2024)
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    合作机构(49)

    哥伦比亚大学合作论文 7
    亚利桑那州立大学合作论文 5
    北达科他州立大学合作论文 4
    巴塞罗那大学合作论文 2
    弗吉尼亚理工大学合作论文 2
    Krishna University合作论文 2
    蒙彼利埃大学合作论文 1
    Naval Academy合作论文 1
    Missio Seminary合作论文 1
    波士顿大学合作论文 1

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