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Articles 137191 - 137220 of 5154623
Full-Text Articles in Entire DC Network
Arendt, Hannah–Ephemera 011
Hannah Arendt Personal Library-Ephemera
011 Found in L’Essence du Prophetisme: Arendt copy contained ephemera consisting of a French publication notice for this edition.
Arendt, Hannah–Ephemera 013
Hannah Arendt Personal Library-Ephemera
013 Galbraith. Found in The Affluent Society: A fragment of a cardboard coupon advertising a hearing aid company was found between pages 278-279. Writing appears on both sides of the coupon, largely illegible.
Arendt, Hannah–Ephemera 014
Hannah Arendt Personal Library-Ephemera
014 Barnet. Found in The Economy of Death: The personal card of a Mrs. Phyllis C. Vescovi was found inside the front page of the book.
Arendt, Hannah–Ephemera 015
Hannah Arendt Personal Library-Ephemera
015 Knutsen. Found in The Human Basis of the Polity: A typed letter of thanks from the author, a former student of Hannah Arendt, was found inside the book.
Arendt, Hannah–Ephemera 016
Hannah Arendt Personal Library-Ephemera
016 Neumann. Found in Die Portieren der Weima Republik: German language publisher notice for the book Der Gescheiterte Frieden : Europa 1933-1939 by Martin Gilbert and Richard Gott.
Arendt, Hannah–Ephemera 017
Hannah Arendt Personal Library-Ephemera
017 Lerner. Found in America as a Civilization: Book reviews torn from a January 6 issue of Time Magazine.
Arendt, Hannah–Ephemera 018
Hannah Arendt Personal Library-Ephemera
018 Solberg. Found in Riding High: America in the Cold War: Typewritten note by the author acknowledging Hannah Arendt's influence and requesting comments on his new book.
Arendt, Hannah–Ephemera 019
Hannah Arendt Personal Library-Ephemera
019 Found in Printzhorn. Leib-Seele- Einheit…: A postcard, handwritten in German, addressed to Hannah Stern in Paris, from Walter Benjamin.
Arendt, Hannah–Ephemera 020
Hannah Arendt Personal Library-Ephemera
020 Found in Verfassung des Deutschen Reiches…: An undated German invoice from a shoe store made out to Herr Dr. Stern. Found on p. 163.
Extraction Of Mesoporous Silica From Local Soil Samples And Using As Sorbent In Dispersive Solid Phase Extraction Application, Zahraa Abdulsahib Qasim, Atheer Al Khudhair, Ahmed Fadhil Khudhair
Extraction Of Mesoporous Silica From Local Soil Samples And Using As Sorbent In Dispersive Solid Phase Extraction Application, Zahraa Abdulsahib Qasim, Atheer Al Khudhair, Ahmed Fadhil Khudhair
Al-Bahir
Mesoporous silica was successfully extracted from selected local soil samples (sandy, clay, and loamy) from Karbala city using sol-gel method. The extraction method was simple and environmentally friendly. Pure silica was characterized using different techniques such as EDX, SEM, BET, XRD, and FTIR. Amorphous silica was used as an adsorbent to extract Fe(III)-salicylicaldehyde oxime complex from aqueous solutions using solid phase extraction method. The optimum conditions of method were 0.10 gm of silica, 0.04 mol.L-1 of salicylaldehyde oxime reagent, pH 7.0 , temperature 35°C, shaking time 15 min, which showed very good extraction percent of Fe(III) - salicyaldehyde oxime …
Fish Oil And Vernonia Amygdalina Leaves-Supplemented Biscuits Increased Insulin Secretion And Suppressed Pro-Inflammatory Cytokines In Type 2 Diabetic Wistar Rats, Omolola Soji-Omoniwa, Uthman Olanrewaju Abdulazeez, Christfavour Oluwaseyi Oloba, Samuel Olajuwon Kolawole, Johnson Opeyemi Olayinka, Emmanuel Olorunleke Oludipe, Anuoluwapo Faith Ajediti, Habib Tajudeen Yusuf
Fish Oil And Vernonia Amygdalina Leaves-Supplemented Biscuits Increased Insulin Secretion And Suppressed Pro-Inflammatory Cytokines In Type 2 Diabetic Wistar Rats, Omolola Soji-Omoniwa, Uthman Olanrewaju Abdulazeez, Christfavour Oluwaseyi Oloba, Samuel Olajuwon Kolawole, Johnson Opeyemi Olayinka, Emmanuel Olorunleke Oludipe, Anuoluwapo Faith Ajediti, Habib Tajudeen Yusuf
Al-Bahir
This research determined the effect of fish oil and Vernonia amygdalina-enriched biscuits (FVSB) on insulin sensitivity and inflammatory cytokines in type 2 diabetic rats. Forty-nine male rats were grouped into seven, i.e. A-G. Type 2 diabetes (T2DM) was induced in groups B-G by administering 230 mg/kg body weight [BW] NAD (ip) and 65 mg/kg BW streptozotocin (ip). Group A represented the control (Non-diabetic + unsupplemented biscuit), B (untreated diabetic), C (diabetic + 120 mg/kg BW metformin), D-F (diabetic + FVSB at 1g, 2g and 3g leaf inclusion respectively), and G (diabetic + conventional biscuit). The experiment lasted 35 days, …
Arendt, Hannah–Ephemera 003
Hannah Arendt Personal Library-Ephemera
003 Found in Dante’s Other World: Postcard written to Heinrich Blucher by Elizabeth Stambler. "Dear Heinrich, I'd like to give you something in thanks for your picture, which I find beautiful. I'd like you to have this book in any case, for it does contain much of my happy life. You might like to give it away some day- if you like it-in as sweet and friendly a moment as when you gave me the picture. Elizabeth."
Arendt, Hannah–Ephemera 004
Hannah Arendt Personal Library-Ephemera
004 Found in The Viking Book of Poetry: Typewritten verses from the old English song "Green Grow the Rushes-Ho."
Arendt, Hannah–Ephemera 005
Hannah Arendt Personal Library-Ephemera
005 Found in Social Contract: 5 x 3 in. notepad page inserted in book with brief notes pertaining to the text.
Arendt, Hannah–Ephemera 006
Hannah Arendt Personal Library-Ephemera
006 Found in Poems of Edgar Allan Poe: Personal note to Hannah Arendt from the author written on a 3.5 x 4.5 in. scrap of paper.
Arendt, Hannah–Ephemera 007
Hannah Arendt Personal Library-Ephemera
007 Found in Selected Poems: Personal note to Hannah Arendt from author on 6x4 in. note paper; dated 01/20/75.
Arendt, Hannah–Ephemera 009
Hannah Arendt Personal Library-Ephemera
009 Found in Aristotle’s Politics: Contained ephemera: seven handwritten notes in English, one typed note in English, and a pink strip of acidic paper.
Arendt, Hannah–Ephemera 010
Hannah Arendt Personal Library-Ephemera
010 Found in Bernanos, Bloy, Clavdel, Peguy…: Ephemera removed from book consists of a French publication notice for this edition.
Experimental Study Of Energy Conversion Efficiency Improvement Of Photovoltaic (Pv) Module Using Hybrid Cooling System, Olufisayo O. Babalola, Olatunji W. Olademeji, Joseph B. Samson
Experimental Study Of Energy Conversion Efficiency Improvement Of Photovoltaic (Pv) Module Using Hybrid Cooling System, Olufisayo O. Babalola, Olatunji W. Olademeji, Joseph B. Samson
Al-Bahir
The elevation of the photovoltaic module operating temperature resulting in diminution of its energy conversion efficiency is one of the key limitations to its application. A decrease of power delivered performance by 0.4-0.5% per 1 rise over its Standard Test Condition (STC) accounted for the overheating of the PV module. This study evaluates the energy conversion efficiency improvement of a PV module using hybrid cooling system. An hourly segmented hybrid cooling system made up of aluminum fins as passive cooling segment and helical structured copper tubules for water conduction as active cooling segment helps to improve the energy conversion efficiency …
A Case Of Extra-Arterial Vascular Anomalies In A Patient With Williams Syndrome, Meredith Barrientez, Katherine Forrester, Margaret Rozier-Chen
A Case Of Extra-Arterial Vascular Anomalies In A Patient With Williams Syndrome, Meredith Barrientez, Katherine Forrester, Margaret Rozier-Chen
Journal of Pediatric Genetics
Williams-Beuren syndrome (WBS), commonly abbreviated to Williams syndrome, is well described in the literature regarding its typical clinical presentation, which is the result of a heterozygous deletion within the genetic sequence located on chromosome 7q11.23. The gene for elastin (ELN) is located within this DNA sequence. Patients with WBS exhibit multi-organ involvement including cardiac abnormalities such as supravalvular aortic stenosis and connective tissue disorders due to the disruption of ELN.1 In this case, we present an infant born with extensive infantile hemangiomas, including cutaneous and organ involvement, verified by skin biopsy, and abnormal hepatic vessels. Our patient received an extensive …
Unresponsiveness To Vitamin Therapy In Twins With Early Onset Biotin-Thiamine Responsive Encephalopathy Type 2 Caused By Biallelic Truncating Variant In Slc19a3 Gene, Siddaramappa J. Patil, Minal Kekatpure, Venkatraman Bhat, Harini Sreedaran, Rajiv Aggarwal
Unresponsiveness To Vitamin Therapy In Twins With Early Onset Biotin-Thiamine Responsive Encephalopathy Type 2 Caused By Biallelic Truncating Variant In Slc19a3 Gene, Siddaramappa J. Patil, Minal Kekatpure, Venkatraman Bhat, Harini Sreedaran, Rajiv Aggarwal
Journal of Pediatric Genetics
Biotin-thiamine responsive encephalopathy type 2 (BTBGD) is caused by biallelic pathogenic variants in SLC19A3 (solute carrier family 19). Among three clinical phenotypes of BTBGD (early infantile onset, classical and adult onset) early infantile form of BTBGD is associated with poor prognosis. Here in we report twins with BTBGD early onset infantile Leigh syndrome phenotype unresponsive to thiamine and biotin therapy, progressive neuroimaging changes and early death. Both twins carried biallelic truncating novel c.307dupG / p.Val103fs*121 variant in SLC19A3 gene and we discuss reasons of unresponsiveness.
Novel Insights Into Wdfy3 Pathogenicity: A Case Report Of Microcephaly And Epilepsy, Pietra Spinardi, Gabriel Bordignon, Gustavo Moura Da Mata Machado Ferreira Pinto, Monica Alexandra De Conto, Daniel Almeida Do Valle
Novel Insights Into Wdfy3 Pathogenicity: A Case Report Of Microcephaly And Epilepsy, Pietra Spinardi, Gabriel Bordignon, Gustavo Moura Da Mata Machado Ferreira Pinto, Monica Alexandra De Conto, Daniel Almeida Do Valle
Journal of Pediatric Genetics
WDFY3 is a critical gene involved in neuronal migration, autophagy, and vesicular transport during brain development. Pathogenic variants in WDFY3 gene are associated with a range of neurodevelopmental disorders, including autism spectrum disorder ASD, epilepsy, and intellectual disability. We present here a case of a female child with a de novo heterozygous WDFY3 variant (c.10189A>T; p.Thr3397Ser), identified through whole exome sequencing. The patient presented with microcephaly, global developmental delay, and epilepsy. Despite the presence of microcephaly, neuroimaging (MRI) revealed no significant abnormalities, a finding consistent with previous reports. Previous studies suggests that WDFY3 haploinsufficiency alters synaptic density and mitochondrial …
Diagnosis And Initial Tratment Of Gorham-Stout’S Disease, Jesús González Cayón, Maria Del Carmen San Basilio Berenguer, Julio César Moreno Alfonso, Santiago De La Puente Pérez, Paloma Triana Junco, Juan Carlos López Gutiérrez
Diagnosis And Initial Tratment Of Gorham-Stout’S Disease, Jesús González Cayón, Maria Del Carmen San Basilio Berenguer, Julio César Moreno Alfonso, Santiago De La Puente Pérez, Paloma Triana Junco, Juan Carlos López Gutiérrez
Journal of Pediatric Genetics
The Gorham-Stout’s disease, also known as massive osteolysis or evanescent bone disease; is an extremely rare disease characterized by a proliferation of intraosseous lymphatic channels causing progressive osteolysis. Usually, surgery, sclerotherapy and radiotherapy have been reserved for local and symptomatic control of the disease, while medical treatments have presented variable results that are not entirely satisfactory according to literature. The recent identification of germline-activating somatic mutations in the PIK3CA gene has opened the way to treatment with mTOR inhibitors, being Sirolimus an effective option with a low incidence of serious adverse effects. We present a patient diagnosed with GSD and …
Infantile Hypertriglyceridemia Secondary To Gpd1 Defects: An Underdiagnosed Differential Of Infantile Hepatomegaly And Hepatic Steatosis, Snigdha Verma, Vikrant Sood, Bikrant Bihari Lal, Rajeev Khanna, Chhagan Bihari, Seema Alam
Infantile Hypertriglyceridemia Secondary To Gpd1 Defects: An Underdiagnosed Differential Of Infantile Hepatomegaly And Hepatic Steatosis, Snigdha Verma, Vikrant Sood, Bikrant Bihari Lal, Rajeev Khanna, Chhagan Bihari, Seema Alam
Journal of Pediatric Genetics
Disorders of carbohydrate and lipid metabolism are the leading underlying etiologies of hepatomegaly and hepatic steatosis in young children. With ever increasing access to genetic analysis methods, previously hitherto unknown and under-diagnosed entities like transient infantile hypertriglyceridemia, have been recently added as one of the differential diagnosis for the same. As per the available literature, this entity has been reported to have a benign course, however with increasing number of reported cases, there is yet much more to explore. We hereby present two such pediatric cases presenting with infantile onset hepatomegaly and hepatic steatosis along with a review of literature …
Phenotyping And Provisional Diagnosis Of Mucopolysaccharidoses Based On Machine Learning, Srilatha Kadali, Shaik Mohammad Naushad, Vijaya Lakshmi Bodiga
Phenotyping And Provisional Diagnosis Of Mucopolysaccharidoses Based On Machine Learning, Srilatha Kadali, Shaik Mohammad Naushad, Vijaya Lakshmi Bodiga
Journal of Pediatric Genetics
In view of significant overlapping clinical features in mucopolysaccharidoses (MPS) subtypes, clinicians face difficulty in differential diagnosis, thus requiring the need for a machine learning-based clinical tool for the provisional diagnosis of MPS subtypes. Out of 520 patients with suspicion of MPS, 296 patients were identified with MPS types. To develop the model, we took 53 clinical symptoms of MPS patients (n=255) into account for differential diagnosis. The diagnosis was based on enzyme testing. Among mucopolysaccharidoses, MPS I was the most prevalent. Different machine learning tools were examined, and classification and regression tree (CART) emerged as the most promising. The …
Unraveling The Etiology Of Childhood Hypotonia Using Exome Sequencing, Arya Shambhavi, Amita Moirangthem, Rajesh Kumar Maurya, Varunvenkat M. Srinivasan, Haseena Sait, Somya Srivastava, Renu Suthar, Shubha R. Phadke
Unraveling The Etiology Of Childhood Hypotonia Using Exome Sequencing, Arya Shambhavi, Amita Moirangthem, Rajesh Kumar Maurya, Varunvenkat M. Srinivasan, Haseena Sait, Somya Srivastava, Renu Suthar, Shubha R. Phadke
Journal of Pediatric Genetics
This cohort study of 48 unrelated probands with rare monogenic childhood hypotonia was designed to assess the clinical presentations, spectrum of disorders, and utility of exome sequencing in selected cases where preliminary genetic tests did not sufficiently explain the etiology. Clinically 56.3% of the cases appeared to be of peripheral hypotonia, 33.3% cases were of central hypotonia, and remaining 10.4% were mixed hypotonia cases. Exome sequencing was able to provide a diagnosis in 52.1% cases in the entire cohort of rare monogenic childhood hypotonia. Majority (41.6%) of the probands had a clinical diagnosis of congenital myopathy/muscular dystrophy in the cohort …
Systematic Exploration Of Trpv6 Variants In Pancreatitis: Unraveling Genetic Associations And Pathophysiological Insights Through Comprehensive Systematic Review And In-Silico Analysis, Omar Alomari, Rumeysa Yegin, Muhammed Edib Mokresh, Ghazaleh Kokabi Ghahremanpour, Nurullah Komurcu, Elif Nur Ari, Magda Wojtara, Ali Karaman, Abdulqadir J. Nashwan
Systematic Exploration Of Trpv6 Variants In Pancreatitis: Unraveling Genetic Associations And Pathophysiological Insights Through Comprehensive Systematic Review And In-Silico Analysis, Omar Alomari, Rumeysa Yegin, Muhammed Edib Mokresh, Ghazaleh Kokabi Ghahremanpour, Nurullah Komurcu, Elif Nur Ari, Magda Wojtara, Ali Karaman, Abdulqadir J. Nashwan
Journal of Pediatric Genetics
Background and Aims: The transient receptor potential vanilloid subfamily member 6 (TRPV6), a calcium-selective channel, is crucial for intracellular calcium (Ca2+) transport, impacting the maintenance of Ca2+ homeostasis in the pancreas. Variants in the TRPV6 gene have been associated with disruptions in calcium balance, potentially contributing to chronic pancreatitis (CP). This systematic review aims to unravel the connections between TRPV6 gene variants and pancreatitis, with a particular focus on CP. Additionally, we conducted an in-silico co-expression analysis to explore the interrelationships among validated genetic variants associated with pancreatitis pathophysiology and TRPV6 gene variants . Methods: A comprehensive literature search was …
Long-Term Survival In Lung Cancer With Brain Metastases And Coronary Artery Stenosis: A Case Report, Raghad O. Alharbi, Shahad J. Alshammary, Nasser E. Alotaibi, Ruba M. Aljohani, Bader A. Alotaibi, Ihab F. Suliman
Long-Term Survival In Lung Cancer With Brain Metastases And Coronary Artery Stenosis: A Case Report, Raghad O. Alharbi, Shahad J. Alshammary, Nasser E. Alotaibi, Ruba M. Aljohani, Bader A. Alotaibi, Ihab F. Suliman
Journal of the Saudi Heart Association
Lung cancer is among the most diagnosed cancers worldwide, and its co-occurrence with coronary heart disease is life-threatening. Osimertinib is the standard treatment for epidermal growth factor receptor (EGFR) mutations in advanced non-small cell lung cancer (NSCLC). The addition of pemetrexed and carboplatin increases not only the efficacy but also the cardiotoxicity risk. We report a 59-year-old woman with NSCLC alongside brain, liver, and spleen metastases, who developed cardiovascular events following cancer therapy. With advanced imaging and multidisciplinary intervention, remarkable remission was achieved over two years. Reporting this case contributes to the understanding of its presentation and diagnostic challenges.
Goals And Achievements, Catherine Stemmans Paterson
Goals And Achievements, Catherine Stemmans Paterson
Journal of Community Engagement and Higher Education
This article reflects on the goals and recent achievements of The Journal of Community Engagement and Higher Education(JCEHE). It also describes the articles published in the JCEHE’s fourth issue of volume fourteen.
Journal Of Community Engagement And Higher Education: Changes In Perspective, Catherine S. Paterson
Journal Of Community Engagement And Higher Education: Changes In Perspective, Catherine S. Paterson
Journal of Community Engagement and Higher Education
This article reflects on recent changes that have and will continue to affect the Journal of Community Engagement and Higher Education.