27 research outputs found

    Artificial chordae: A simple clip and tie technique

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    The Student Movement Volume 106 Issue 8: Cardinals Cheer, Thanksgiving is Here!

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    HUMANS Meet Your 2021-2022 AU Cardinals Men\u27s Basketball Team, Interviewed by: Timmy Duado What Are You Thankful For?, Interviewed by: Grace No Meet Your 2021-2022 AU Cardinals Women\u27s Basketball Team, Interviewed by: Taylor Uphus ARTS & ENTERTAINMENT Thanksgiving Film Recommendations!, Megan Napod The Harder They Fall , Hannah Cruse What is CATHARSIS?, Solana Campbell NEWS Andrews Autumn Conference on Science & Religion, Abigail Lee AUSA Hosts Open Gym, Karenna Lee Campus Concert Crawl, Abigail Lee IDEAS Hidden out of Season, Evin-Nazya Musgrove Risk and Reward in Squid Game , Yoel Kim The Necessity of Firearm Safety Education, Nathan Cheng PULSE Honors Testimony: Worship in the Church, Honors Student Productivity... (and Pronouns ), T Bruggemann Thanksgiving Traditions of Your Student Movement Editors, Alannah Tjhatra THE LAST WORD Thanksgiving Dinner and Communion, Alyssa Henriquezhttps://digitalcommons.andrews.edu/sm-106/1007/thumbnail.jp

    Robust estimation of bacterial cell count from optical density

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    Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressing E. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data

    Unusual cardiac paraganglioma mimicking an atypical carcinoid tumor of the lung

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    We present a case of unusual cardiac paraganglioma (PG) initially misdiagnosed as atypical carcinoid tumor of the lung and discuss key clinical and pathologic characteristics that guide surgical management of these rare chromaffin cell tumors. A 64-year-old female with persistent cough and back pain was found to have a 4 cm × 3 cm mass abutting multiple cardiopulmonary structures. A biopsy was performed at an outside institution and pathology reported "atypical neuroendocrine carcinoma, consistent with carcinoid". The patient was transferred to our institution and pericardial resection with right pneumonectomy was performed to excise the tumor. Histology of the mass was that of PG with multiple ethanol embolizations. Immunohistochemical examination revealed that type I (chief) cells were positive for neuroendocrine markers (chromogranin A and synaptophysin), while type II (sustentacular) cells were positive for S100. There was no evidence of atypical carcinoid tumor in the lung. PG is an entity of chromaffin cell tumors that often affects the adrenal glands and carotid body. PG rarely occurs in the thoracic region, accounting for just 1-2% of all PG. Proper diagnosis of cardiac PG is challenging owing to its rare prevalence, subtle symptoms of presentation, and the neuroendocrine histopathological features it shares with atypical carcinoids. These tumors are typically benign and are best treated by surgical resection. Our report examines the approach to appropriate diagnosis of cardiac PG vs. atypical carcinoid, preoperative management, and surgical treatment by describing successful resection through thoracotomy without the use of cardiopulmonary bypass

    Optogenetics

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    Gene insertion of opsin, light-activated cell-membrane channels, into neurons of interest allows researchers to manipulate light to either excite or inhibit neuronal activity to gain a better understanding of brain function and dysfunction, and explore therapeutic applications

    Cocaine Addiction Effects of the Brain: Binge and Craving

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    Cocaine afflicts many individuals and is potently addictive. Originally hailed as a wonder-drug in the late 19th century, cocaine is now considered an illegal substance. Cocaine’s addictive properties can be attributed to changes in the dopamine reward pathway of the Ventral Tegmental Area and Substantia Nigra, Prefrontal Cortex, Dorsal Striatum, Nucleus Accumbens, Amygdala, Globus Pallidus, and Hippocampus. This drug affects the brain in two processes: binge and crave. The binge process highlights cocaine’s ability to block dopamine reuptake from the synapse resulting in hyperstimulation of the postsynaptic neuron in the dopamine reward pathway. The crave process promotes drug-seeking behavior through conditional and contextual cues. Understanding the effects of cocaine in the brain may grant insight in creating future medication and therapies to treat individuals addicted to this drug
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