Search Results - "phenotyping"

circ_TGFBR2 Inhibits Vascular Smooth Muscle Cells Phenotypic Switch and Suppresses Aortic Dissection Progression by Sponging miR-29a by Xu Z, Zhong K, Guo G, Xu C, Song Z, Wang D, Pan J

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∆Np63/p40 correlates with the location and phenotype of basal/mesenchymal cancer stem‐like cells in human ER+ and HER2+ breast cancers by Yajing Liu, Marta Nekulova, Rudolf Nenutil, Iva Horakova, M Virginia Appleyard, Karen Murray, Jitka Holcakova, Michaela Galoczova, Philip Quinlan, Lee B Jordan, Colin A Purdie, Borivoj Vojtesek, Alastair M Thompson, Philip J Coates

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A novel TCN2 mutation with unusual clinical manifestations of hemolytic crisis and unexplained metabolic acidosis: expanding the genotype and phenotype of transcobalamin II deficiency by Pongpak Pongphitcha, Nongnuch Sirachainan, Arthaporn Khongkraparn, Thipwimol Tim-Aroon, Duantida Songdej, Duangrurdee Wattanasirichaigoon

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The Genotypic and Phenotypic Characteristics Contributing to Flomoxef Sensitivity in Clinical Isolates of ESBL-Producing <i>E. coli</i> Strains from Urinary Tract Infections by Kazuma Sakaeda, Takuya Sadahira, Yuki Maruyama, Takehiro Iwata, Masami Watanabe, Koichiro Wada, Motoo Araki

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A rare cause of epileptic encephalopathy: case report of a novel patient with PEHO-like phenotype and CCDC88A gene pathogenic variants by Sorina-Mihaela Papuc, Adelina Glangher, Alina Erbescu, Oana Tarta Arsene, Aurora Arghir, Magdalena Budisteanu

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Epidemiological Prevalence of Phenotypical Resistances and Mobilised Colistin Resistance in Avian Commensal and Pathogenic <i>E. coli</i> from Denmark, France, The Netherlands, and the UK by Andrew Mead, Candice Billon-Lotz, Rikke Olsen, Ben Swift, Pascal Richez, Richard Stabler, Ludovic Pelligand

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Phenotypic and Proteomic Characteristics of Human Dental Pulp Derived Mesenchymal Stem Cells from a Natal, an Exfoliated Deciduous, and an Impacted Third Molar Tooth by Gurler Akpinar, Murat Kasap, Ayca Aksoy, Gokhan Duruksu, Gulcin Gacar, Erdal Karaoz

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Highly Proliferative Immortalized Human Dental Pulp Cells Retain the Odontogenic Phenotype when Combined with a Beta-Tricalcium Phosphate Scaffold and BMP2 by Xiangfen Li, Liu Wang, Qin Su, Ling Ye, Xuedong Zhou, Dongzhe Song, Dingming Huang

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Searching Novel Therapeutic Targets for Scleroderma: P2X7-Receptor Is Up-regulated and Promotes a Fibrogenic Phenotype in Systemic Sclerosis Fibroblasts by Daniela Gentile, Pietro E. Lazzerini, Alessandra Gamberucci, Mariarita Natale, Enrico Selvi, Francesca Vanni, Alessandra Alì, Paolo Taddeucci, Silvia Del-Ry, Manuela Cabiati, Veronica Della-Latta, David J. Abraham, Maria A. Morales, Rosella Fulceri, Franco Laghi-Pasini, Pier L. Capecchi

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A Case of Ankyloblepharon-ectodermal Defects-cleft Lip/Palate-syndrome with Choanal Atresia and Skin Erosions: Phenotypic Variability of TP63-related Disorders by Luana Niculescu, Matias Wagner, Dominik S. Westphal, Marcus Fischer, Walter Mihatsch, Anke Prothmann, Thomas Ruzicka, Andreas Wollenberg, Hans Wolff, Heinrich Schmidt, Kathrin A.

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Phenotypic and Genotypic Characteristics of Antimicrobial Resistance in <i>Citrobacter freundii</i> Isolated from Domestic Ducks (<i>Anas platyrhynchos domesticus</i>) in Bangladesh by Tarana Ahmed, Md. Saiful Islam, Najmul Haider, Linzy Elton, Badrul Hasan, Mohammad Nuruzzaman, Md. Tanvir Rahman, S. M. Lutful Kabir, Md. Shahidur Rahman Khan

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High-fat diet combined with dextran sulfate sodium failed to induce a more serious NASH phenotype than high-fat diet alone by Yan Zhou, Ya Feng, Lili Yang, Peiyong Zheng, Lu Hang, Fengru Jiang, Jianye Yuan, Lixin Zhu

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Ahsa1 and Hsp90 activity confers more severe craniofacial phenotypes in a zebrafish model of hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR) by Kelly Sheehan-Rooney, Mary E. Swartz, Feng Zhao, Dong Liu, Johann K. Eberhart

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Gender-Specific Impact of Metabolic Obesity Phenotypes on the Risk of Hashimoto’s Thyroiditis: A Retrospective Data Analysis Using a Health Check-Up Database by Yang H, Xia Q, Shen Y, Chen TL, Wang J, Lu YY

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Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report by Jinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, Yuping Yu, Wei Liu

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Reduced Proliferative Potential with Conserved Stem/Stromal Phenotype of Human Umbilical Cord Mesenchymal Stem Cells in Placental Syndromes: A Prospective Cohort Study by Luigi Marino, Maria Antonietta Castaldi, Caterina Fulgione, Salvatore Giovanni Castaldi, Paola Manzo, Valentina Giudice, Francesca Picone, Maria Rosaria Campitiello, Mario Polichetti, Maurizio Guida, Carmine Selleri, Bianca Serio

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Down-regulation of DNA key protein-FEN1 inhibits OSCC growth by affecting immunosuppressive phenotypes via IFN-γ/JAK/STAT-1 by Shimeng Wang, Xiangjian Wang, Jun Sun, Jin Yang, Deyang Wu, Fanglong Wu, Hongmei Zhou

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Quantitative proteomic analysis of amastigotes from Leishmania (L.) amazonensis LV79 and PH8 strains reveals molecular traits associated with the virulence phenotype. by Eloiza de Rezende, Rebeca Kawahara, Mauricio S Peña, Giuseppe Palmisano, Beatriz S Stolf

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Screen for abnormal mitochondrial phenotypes in mouse embryonic stem cells identifies a model for succinyl-CoA ligase deficiency and mtDNA depletion by Taraka R. Donti, Carmen Stromberger, Ming Ge, Karen W. Eldin, William J. Craigen, Brett H. Graham

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Successful Control of an Outbreak by Phenotypically Identified Extended-Spectrum Beta-Lactamase-Producing <i>Klebsiella pneumoniae</i> in a Neonatal Intensive Care Unit by Elena Priante, Chiara Minotti, Cristina Contessa, Margherita Boschetto, Paola Stano, Federico Dal Bello, Ettore De Canale, Elisabetta Lolli, Vincenzo Baldo, Eugenio Baraldi, Daniele Donà

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