Search Results - "phenotyping"

From Phenotype to Molecules: Unveiling the Genetic and Immunological Bridges Between Autoimmune Diseases and Vitiligo by Hu Y, Wang SB, Wang K, He MJ

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QTLs of factors of the metabolic syndrome and echocardiographic phenotypes: the hypertension genetic epidemiology network study by de Simone Giovanni, Devereux Richard B, Lewis Cora E, North Kari E, Hunt Steven C, Tang Weihong, Huang Pinchia, Kraja Aldi T, Arnett Donna K, Rice Treva, Rao DC

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Macrophage-related therapeutic strategies: Regulation of phenotypic switching and construction of drug delivery systems by Xi Wang, Yixuan Li, Xueyu Pu, Guiquan Liu, Honglin Qin, Weimin Wan, Yuying Wang, Yan Zhu, Jian Yang

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Phelan-McDermid Syndrome in Pediatric Patients With Novel Mutations: Genetic and Phenotypic Analyses by Liang Chen, Zhi-ye Yao, Xiangtao Wu, Shao-ru He, Yu-mei Liu, Xue-yan Wang, De-zhi Cao, Xing-kun Yang, Jian-bo Zhao, Zi Ren, Hong Li, Zheng Pei, Hong-ke Ding, Zhi-chun Feng

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The Phenotypic and Transcriptomic Response of the Caenorhabditis elegans Nematode to Background and Below-Background Radiation Levels by Wayne A. Van Voorhies, Hugo A. Castillo, Cung N. Thawng, Geoffrey B. Smith

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Impact of phenotypic rapid diagnostic assay on duration of empiric antibiotics for gram-negative bacteremia by Sana M. Mohayya, Mohammad Arsalan, Navaneeth Narayanan, Purvi Patel, Christin G. Hong, Thomas J. Kirn, Pinki J. Bhatt, Tanaya Bhowmick

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Study of disease phenotype and its association with prognosis of paediatric inflammatory bowel disease in China by Xin-Qiong Wang, Yuan Xiao, Xu Xu, Yi Yu, Cheng-Yan Shan, Yan Guo, Ling Gong, Tong Zhou, Shen-Shen Gao, Yao-Zong Yuan, Xiao-Jin Wang, Chun-Di Xu

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Phenotypic and Functional Changes in Peripheral Blood Natural Killer Cells in Crohn Disease Patients by Suzanne Samarani, Patrick Sagala, Prevost Jantchou, Guy Grimard, Christophe Faure, Colette Deslandres, Devendra K. Amre, Ali Ahmad

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Arsenic Trioxide Compound Modulates Multiple Myeloma Phenotypes: Assessment on Cell Line Models by MR Khorramizadeh, F Saadat, H Allahyary, S Sadeghian, A Sarrafnejad, A Mirshafiey, F Safavifar, K Alimoghaddam, A Ghavamzadeh, M Pezeshki

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Phenotypic Modulation of Macrophages and Vascular Smooth Muscle Cells in Atherosclerosis-Nitro-Redox Interconnections by Justine Bonetti, Alessandro Corti, Lucie Lerouge, Alfonso Pompella, Caroline Gaucher

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Dysregulated Monocyte and Neutrophil Functional Phenotype in Infants With Neonatal Encephalopathy Requiring Therapeutic Hypothermia by Mary Isabel O'Dea, Mary Isabel O'Dea, Mary Isabel O'Dea, Lynne Kelly, Ellen McKenna, Ashanty M. Melo, Megan Ni Bhroin, Tim Hurley, Angela T. Byrne, Gabrielle Colleran, Claudine Vavasseur, Afif El-Khuffash, Jan Miletin, John Murphy, Fionnuala Hickey, Eleanor J. Molloy, Eleanor J. Molloy, Eleanor J. Molloy, Eleanor J. Molloy, Eleanor J. Molloy

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Case Report: A Relatively Mild Phenotype Produced by Novel Mutations in the SEPSECS Gene by Tingyu Rong, Tingyu Rong, Tingyu Rong, Ruen Yao, Yujiao Deng, Yujiao Deng, Yujiao Deng, Qingmin Lin, Qingmin Lin, Qingmin Lin, Guanghai Wang, Guanghai Wang, Guanghai Wang, Jian Wang, Fan Jiang, Fan Jiang, Fan Jiang, Yanrui Jiang, Yanrui Jiang, Yanrui Jiang

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Classical fragile-X phenotype in a female infant disclosed by comprehensive genomic studies by Paula Jorge, Elsa Garcia, Ana Gonçalves, Isabel Marques, Nuno Maia, Bárbara Rodrigues, Helena Santos, Jacinta Fonseca, Gabriela Soares, Cecília Correia, Margarida Reis-Lima, Vincenzo Cirigliano, Rosário Santos

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CYP2D6 phenotypes are associated with adverse outcomes related to opioid medications by St Sauver JL, Olson JE, Roger VL, Nicholson WT, Black III JL, Takahashi PY, Caraballo PJ, Bell EJ, Jacobson DJ, Larson NB, Bielinski SJ

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CNNM2-Related Disorders: Phenotype and Its Severity Were Associated With the Mode of Inheritance by Han Zhang, Ye Wu, Yuwu Jiang

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Genomic and phenotypic analyses suggest moderate fitness differences among Zika virus lineages. by Glenn Oliveira, Chantal B F Vogels, Ashley Zolfaghari, Sharada Saraf, Raphaelle Klitting, James Weger-Lucarelli, Karla P Leon, Carlos O Ontiveros, Rimjhim Agarwal, Konstantin A Tsetsarkin, Eva Harris, Gregory D Ebel, Shirlee Wohl, Nathan D Grubaugh, Kristian G Andersen

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An atypical phenotype of hypokalemic periodic paralysis caused by a mutation in the sodium channel gene by Yang Hee Park, June Bum Kim

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Intractable chronic diarrhea associated with phenotypic diarrhea of infancy (tricho-hepato-enteric syndrome) by José Francisco Cadena-León, Rodolfo Rodríguez-Jurado

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Behavioral and Synaptic Phenotypes of Female <i>Prdx6</i>^−/− Mice by Tanita Pairojana, Sarayut Phasuk, Pavithra Suresh, Ingrid Y. Liu

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Neurochemical phenotype and function of endomorphin 2-immunopositive neurons in the myenteric plexus of the rat colon by Yun-Qing eLi

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