Search Results - "phenotyping"

Phenotypic miRNA Screen Identifies miR-26b to Promote the Growth and Survival of Endothelial Cells by Andrea Martello, David Mellis, Marco Meloni, Alison Howarth, Daniel Ebner, Andrea Caporali, Ayman Al Haj Zen

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Clinical and life style factors related to the nighttime blood pressure, nighttime dipping and their phenotypes in Korean hypertensive patients by Byung Sik Kim, Ju Han Kim, Wan Kim, Woo Shik Kim, Sungha Park, Sang Jae Lee, Jang Young Kim, Eun Mi Lee, Sang Hyun Ihm, Wook Bum Pyun, Jeong-Hun Shin, Jinho Shin

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Identification of a Novel Frameshift variant of the ATRX gene: a Case Report and Review of the genotype-phenotype relationship by Yishan Wang, Qizhou Ma, Jing Chen, Shaoxin Li, Feifei Zheng, Lei Shi, Xiaoshun Li, Sinan Li, Guanglei Tong, Hong Li

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A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome by Gabriella Lania, Monica Franzese, Noritaka Adachi, Marchesa Bilio, Gemma Flore, Annalaura Russo, Erika D'Agostino, Claudia Angelini, Robert G. Kelly, Antonio Baldini

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Microglia Polarization with M1/M2 Phenotype Changes in rd1 Mouse Model of Retinal Degeneration by Tian Zhou, Zijing Huang, Xiaowei Sun, Xiaowei Zhu, Lingli Zhou, Mei Li, Bing Cheng, Xialin Liu, Chang He

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Comparison of Socio-demographic Characteristics, Tumour Features, and Surgical Treatment Outcomes in Phenotypic Variants of Basal Cell Carcinoma by Yıldız Gürsel Ürün, Mustafa Ürün

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Association of Circulating Heme Oxygenase-1, Lipid Profile and Coronary Disease Phenotype in Patients with Chronic Coronary Syndrome by Chiara Caselli, Raffaele De Caterina, Rosetta Ragusa, Riccardo Liga, Alessia Gimelli, Arthur J. H. A. Scholte, Aldo Clerico, Juhani Knuuti, Danilo Neglia

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Inhibition of CXXC5 function rescues Alzheimer's disease phenotypes by restoring Wnt/β-catenin signaling pathway by Minguen Yoon, Heejene Kim, Heewon Shin, HeeYang Lee, Min-Jeong Kang, Sung-Hye Park, Gyoonhee Han, YoungSoo Kim, Kang-Yell Choi

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Corrigendum: Novel TTC37 Mutations in a Patient with Immunodeficiency without Diarrhea: Extending the Phenotype of Trichohepatoenteric Syndrome. by Nicholas L Rider, Nicholas L Rider

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Gingival phenotype determination: Cutoff values, relationship between gingival and alveolar crest bone thickness at different landmarks by Haiyan Zhao, Lei Zhang, Heng Li, Ahmed Hieawy, Ya Shen, He Liu

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An unexpected, mild phenotype of glucocorticoid resistance associated with glucocorticoid receptor gene mutation case report and review of the literature by Ágnes Molnár, Attila Patócs, István Likó, Gábor Nyírő, Károly Rácz, Miklós Tóth, Beatrix Sármán

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Hypertensive phenotype signs in men with different genetic polymorphisms of aldosterone synthase and angiotensin II type 1 receptors by Susanna A. Tykhonova, Veronika P. Piskovatska

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Cadherin 13: Human cis-Regulation and Selectively Altered Addiction Phenotypes and Cerebral Cortical Dopamine in Knockout Mice by Jana Drgonova, Donna Walther, G. Luke Hartstein, Mohammad O. Bukhari, Michael H. Baumann, Jonathan Katz, F. Scott Hall, Elizabeth R. Arnold, Shaun Flax, Anthony Riley, Olga Rivero, Klaus-Peter Lesch, Juan Troncoso, Barbara Ranscht, George R. Uhl

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Relationship of Clinical Picture, Phenotype of Oxidative Metabolism, Accentuation of Temperament Properties and Compliance in Patients with Gastroesophageal Reflux Disease by A. A. Kalugin, A. A. Stepchenko, M. A. Stepchenko

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Hypertensive phenotype signs in men with different genetic polymorphisms of aldosterone synthase and angiotensin II type 1 receptors by Susanna A. Tykhonova, Veronika P. Piskovatska

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Visualization and identification of health space, based on personalized molecular phenotype and treatment response to relevant underlying biological processes by Bouwman Jildau, Vogels Jack TWE, Wopereis Suzan, Rubingh Carina M, Bijlsma Sabina, van Ommen Ben

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Gastric mucin phenotype indicates aggressive biological behaviour in early differentiated gastric adenocarcinomas following endoscopic treatment by Kai Song, Qi Yang, Yu Yan, Xiaoyan Yu, Kanlun Xu, Jinghong Xu

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Further corroboration of distinct functional features in SCN2A variants causing intellectual disability or epileptic phenotypes by Anaïs Begemann, Mario A. Acuña, Markus Zweier, Marie Vincent, Katharina Steindl, Ruxandra Bachmann-Gagescu, Annette Hackenberg, Lucia Abela, Barbara Plecko, Judith Kroell-Seger, Alessandra Baumer, Kazuhiro Yamakawa, Yushi Inoue, Reza Asadollahi, Heinrich Sticht, Hanns Ulrich Zeilhofer, Anita Rauch

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Case Report: Adenosine kinase deficiency diagnosed 10 years after liver transplantation: Novel phenotypic insights by Patryk Lipiński, Elżbieta Ciara, Dorota Jurkiewicz, Maciej Pronicki, Elżbieta Jurkiewicz, Anna Bogdańska, Rafał Płoski, Irena Jankowska

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Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndrome by Stefanie M. Percival, Holly R. Thomas, Adam Amsterdam, Andrew J. Carroll, Jacqueline A. Lees, H. Joseph Yost, John M. Parant

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