L’enseignement supérieur en Angola face aux inégalités : influences françaises dans les trajectoires politiques by Isabelle de Geuser, Benoît Josset

“…Since 2002, year of the peace accord signature, this system is structuring and on mutation. In 2009, the arrival of a higher education politics became a leitmotif for answering socioeconomic inequality. …”
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Chronic Lymphocytic Leukemia and Myelofibrosis by Fares Darawshy, Arieh Ben-Yehuda, Karine Atlan, Deborah Rund

“…Etiologic and pathogenic associations—the role of t (1; 6) and JAK-2 V617F mutation—are discussed.…”
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Intestinal Type of Lung Adenocarcinoma in Younger Adults by Jelena Stojsic, Milica Kontic, Dragan Subotic, Marko Popovic, Dragana Tomasevic, Jelena Lukic

“…More investigations are needed for further understanding of ILADC in purpose of personalized lung carcinoma therapy particularly introducing detection of mutation status, especially in younger patients.…”
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Spatio-temporal Distribution Characteristics and Future Trend Analysis of Extreme Climate Indices in Nenjiang River Basin over the Past 60 Years by GONG Xiao, DAI Changlei, LI Shuling, XIAO Yue

“…Meanwhile, methods like the linear fitting, Mann-Kendall mutation test, and sliding T-test are adopted to analyze the spatio-temporal variation characteristics of extreme temperature and precipitation in the basin. …”
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Molar Tooth Sign with Deranged Liver Function Tests: An Indian Case with COACH Syndrome by Rama Krishna Sanjeev, Seema Kapoor, Manisha Goyal, Rajiv Kapur, Joseph Gerard Gleeson

“…We report the first genetically proven case of COACH syndrome from the Indian subcontinent in a 6-year-old girl who presented with typical features of Joubert syndrome along with hepatic involvement. Mutation analysis revealed compound heterozygous missense mutation in the known gene TMEM67 (also called MKS3).…”
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The Hereditary Hyperferritinemia-Cataract Syndrome in 2 Italian Families by Katia Perruccio, Francesco Arcioni, Carla Cerri, Roberta La Starza, Donatella Romanelli, Ilaria Capolsini, Maurizio Caniglia

“…Genetic investigation revealed two distinct mutations in iron haemostasis genes; homozygosity for the HFE gene H63D mutation in the younger and heterozygosity in the elder. …”
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Association between P2X7 Receptor Polymorphisms and Bone Status in Mice by Susanne Syberg, Peter Schwarz, Solveig Petersen, Thomas H. Steinberg, Jens-Erik Beck Jensen, Jenni Teilmann, Niklas Rye Jørgensen

“…Macrophages from mouse strains with the naturally occurring mutation P451L in the purinergic receptor P2X7 have impaired responses to agonists (1). …”
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Self-adaptive fuzzing optimization method based on distribution divergence by XU Hang, JI Jiangan, MA Zheyu, ZHANG Chao

“…The selection for the focused mutation block of a seed file was defined as an action, and the distribution divergence of the approximate distributions of the random fields before and after the action was defined as the reward. …”
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An Improved Grasshopper Optimizer for Global Tasks by Hanfeng Zhou, Zewei Ding, Hongxin Peng, Zitao Tang, Guoxi Liang, Huiling Chen, Chao Ma, Mingjing Wang

“…Firstly, a probabilistic mutation mechanism is introduced into the basic GOA, which makes full use of the strong searchability of Cauchy mutation and the diversity of genetic mutation. …”
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A Giant Right Heart Thrombus-in-Transit: The Challenge of Anticoagulation in Factor V Leiden Thrombophilia by Andrew Chu, Thu Thu Aung, Minni Shreya Arumugam, Mauricio Danckers, Mohi Mitiek, Jonathan Leslie

“…FVL mutation associated with right heart thrombus is a rare entity. …”
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Comparison of molecular analysis results determined by next-generation sequencing to immunohistochemical indicators and clinicopathological parameters in prostate adenocarcinomas by Merve Çırak Balta, İbrahim Halil Erdoğdu, Esin Oktay, Nil Çulhac

“…In all cases with a pathogenic mutation in the androgen receptor gene, a pathogenic mutation in the Protein Tyrosine Phosphatase and Tensin Homolog gene was also observed and a significant relationship was found between them. …”
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Generation and propagation of high fecundity gene edited fine wool sheep by CRISPR/Cas9 by Xuemei Zhang, Meiyu Qiu, Bing Han, Li Liao, Xinrong Peng, Jiapeng Lin, Ning Zhang, Lati Hai, Long Liang, Yila Ma, Wenrong Li, Mingjun Liu

“…The FecB allele in sheep is a mutation in the BMPRIB gene, recognized as the first major gene responsible for the high fecundity trait in sheep, leading to an increased ovulation rate in ewe. …”
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Impact of Bone-Modifying Agents on Post-Bone Metastasis Survival Across Cancer Types by Hironari Tamiya, Kazumi Nishino, Yuji Kato, Reina Nakahashi-Kato, Yurika Kosuga-Tsujimoto, Shota Kinoshita, Rie Suzuki, Makiyo Watanabe, Toru Wakamatsu, Shigeki Kakunaga, Satoshi Takenaka

“…In non-small cell lung cancer (NSCLC), the log-rank test demonstrated that the epidermal growth factor receptor (EGFR) mutation was a significant factor for post-bone metastasis survival: EGFR mutation (−) <i>n</i> = 67, median post-bone metastasis survival 11.5 months (95% CI: 6.0–15.2); EGFR mutation (+) <i>n</i> = 39, median post-bone metastasis survival 28.8 months (95% CI: 18.1–35.7) (<i>p</i> < 0.05). …”
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BRAF V600E-Negative Hairy Cell Leukaemia by Stephen E. Langabeer, David O'Brien, Anthony M. McElligott, Michelle Lavin, Paul V. Browne

“…Since the initial report of the BRAF V600E mutation in hairy cell leukemia, numerous investigators have demonstrated the presence of this activating mutation in nearly all cases of this disease. …”
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Management of asynchronous multifocal adult glioblastoma with loss of BRAFV600E -mutant clonality: a case report by Hannah Haile, Pavan S. Upadhyayula, Esma Karlovich, Michael B. Sisti, Brian J. A. Gill, Laura E. Donovan

“…Abstract Glioblastoma (GBM) classification involves a combination of histological and molecular signatures including IDH1/2 mutation, TERT promoter mutation, and EGFR amplification. …”
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Biofilm-associated metabolism via ERG251 in Candida albicans. by Liping Xiong, Nivea Pereira De Sa, Robert Zarnowski, Manning Y Huang, Caroline Mota Fernandes, Frederick Lanni, David R Andes, Maurizio Del Poeta, Aaron P Mitchell

“…Under those conditions, the erg251Δ/Δ mutation causes defects in growth and hyphal extension. …”
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Primary Hyperoxaluria Type 1 in 18 Children: Genotyping and Outcome by Mohamed S. Al Riyami, Badria Al Ghaithi, Nadia Al Hashmi, Naifain Al Kalbani

“…It results from genetic mutations of the AGXT gene, which is more common due to higher consanguinity rates in the developing countries. …”
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Giant Prolactinoma of Young Onset: A Clue to Diagnosis of MEN-1 Syndrome by Chandrika Jayakanthi Subasinghe, Noel Somasundaram, Pathmanathan Sivatharshya, Lalana Devi Ranasinghe, Márta Korbonits

“…Genetic analysis revealed that one was heterozygous for a nonsense mutation and other for missense mutation in MEN1 gene. …”
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The southern house mosquito Culex quinquefasciatus in Abu Dhabi, UAE, is developing resistance to deltamethrin insecticide by Amgd sayed Ali, Asim Iqbal, Tamilarasan Kamalanathan, Antony Raj Gnanaprakasam, Sabu Shajahan, Mohammad Hamad Alsadeq, Mohamed Mahmood Al Marzooqi, Mohamad Hamdan, Mohammad Ali Al-Deeb

“…We detected the mutation and found the kdr allele in all the sampled locations. …”
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Characterization of a novel covS SNP identified in Australian group A Streptococcus isolates derived from the M1UK lineage by Johanna Richter, Amanda J. Cork, Yvette Ong, Nadia Keller, Andrew J. Hayes, Mark A. Schembri, Amy V. Jennison, Mark R. Davies, Kate Schroder, Mark J. Walker, Stephan Brouwer

“…Such mutations have not been fully characterized in the M1UK lineage. …”
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