Search Results - "phenotype"

Phenotype Profiling and Allergy in Otitis-Prone Children by Sara Torretta, Sara Torretta, Lorenzo Pignataro, Lorenzo Pignataro, Daniela Carioli, Daniela Carioli, Tullio Ibba, Francesco Folino, Francesco Folino, Chiara Rosazza, Chiara Rosazza, Miriam Fattizzo, Paola Marchisio, Paola Marchisio

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Catalase Overexpression Drives an Aggressive Phenotype in Glioblastoma by Susanne Flor, Claudia R. Oliva, Md Yousuf Ali, Kristen L. Coleman, Jeremy D. Greenlee, Karra A. Jones, Varun Monga, Corinne E. Griguer

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Genotype and Phenotype Analysis in X-Linked Hypophosphatemia by Peong Gang Park, Seon Hee Lim, HyunKyung Lee, Yo Han Ahn, Yo Han Ahn, Yo Han Ahn, Hae Il Cheong, Hae Il Cheong, Hee Gyung Kang, Hee Gyung Kang, Hee Gyung Kang, Hee Gyung Kang

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Wheezing in infants and preschoolers: phenotypes and treatment options by Jung Yeon Shim

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PERIODONTAL PHENOTYPE: A CLINICAL AND CURRENT VIEW by Lucas Mendes Gabri, Victor Gila Gomes de Mattos, Luis Paulo Diniz Barreto, Marcela Melo dos Santos

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Genomic Predictors of Asthma Phenotypes and Treatment Response by Natalia Hernandez-Pacheco, Natalia Hernandez-Pacheco, Maria Pino-Yanes, Maria Pino-Yanes, Maria Pino-Yanes, Carlos Flores, Carlos Flores, Carlos Flores

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Turner Syndrome: Phenotypic Variability of Chromosomal Polymorphism by M.O. Ryznychuk, V.P. Pishak

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Deep phenotyping for precision medicine in Parkinson's disease by Ann-Kathrin Schalkamp, Nabila Rahman, Jimena Monzón-Sandoval, Cynthia Sandor

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Relationships between the ABO blood group SNP rs505922 and breast cancer phenotypes: a genotype-phenotype correlation study by Rummel Seth, Shriver Craig D, Ellsworth Rachel E

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Comprehensive phenotypic analysis of the Dp1Tyb mouse strain reveals a broad range of Down syndrome-related phenotypes by Eva Lana-Elola, Heather Cater, Sheona Watson-Scales, Simon Greenaway, Jennifer Müller-Winkler, Dorota Gibbins, Mihaela Nemes, Amy Slender, Tertius Hough, Piia Keskivali-Bond, Cheryl L. Scudamore, Eleanor Herbert, Gareth T. Banks, Helene Mobbs, Tara Canonica, Justin Tosh, Suzanna Noy, Miriam Llorian, Patrick M. Nolan, Julian L. Griffin, Mark Good, Michelle Simon, Ann-Marie Mallon, Sara Wells, Elizabeth M. C. Fisher, Victor L. J. Tybulewicz

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Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study by Li, Jianqiao, Hojlo, Margaret A, Chennuri, Sampath, Gujral, Nitin, Paterson, Heather L, Shefchek, Kent A, Genetti, Casie A, Cohn, Emily L, Sewalk, Kara C, Garvey, Emily A, Buttermore, Elizabeth D, Anderson, Nickesha C, Beggs, Alan H, Agrawal, Pankaj B, Brownstein, John S, Haendel, Melissa A, Holm, Ingrid A, Gonzalez-Heydrich, Joseph, Brownstein, Catherine A

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Linking Neuroinflammation and Glial Phenotypic Changes in Neurological Diseases

Subjects: “…glial phenotype…”
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Modulating Glial Cells Phenotype: New Findings and Therapies

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Phenotypic and Functional Properties of Tumor-Infiltrating Regulatory T Cells by Gap Ryol Lee

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Oligodontia and Facial Phenotype Associated with a Rare Syndrome by Fatima Ezzahra Zidane, Mustapha El Alloussi

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Cell and small animal models for phenotypic drug discovery by Szabo M, Svensson Akusjärvi S, Saxena A, Liu J, Chandrasekar G, Kitambi SS

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The role of phenotypic factors in predicting the effectiveness of chemoprophylaxis in children by K.I. Bodnia, A.M. Zosimov, A.V. Rogozhyn, І.M. Asoyan, V.V. Kondratyuk

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A Phenotypic-Driven Approach for the Diagnosis of WOREE Syndrome by Antonella Riva, Antonella Riva, Giulia Nobile, Thea Giacomini, Thea Giacomini, Marzia Ognibene, Marcello Scala, Marcello Scala, Ganna Balagura, Francesca Madia, Andrea Accogli, Andrea Accogli, Ferruccio Romano, Domenico Tortora, Mariasavina Severino, Paolo Scudieri, Paolo Scudieri, Simona Baldassari, Ilaria Musante, Paolo Uva, Vincenzo Salpietro, Vincenzo Salpietro, Annalaura Torella, Annalaura Torella, Vincenzo Nigro, Vincenzo Nigro, Valeria Capra, Lino Nobili, Lino Nobili, Pasquale Striano, Pasquale Striano, Maria Margherita Mancardi, Maria Margherita Mancardi, Federico Zara, Federico Zara, Michele Iacomino, Michele Iacomino

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The secondary loss of gyrencephaly as an example of evolutionary phenotypical reversal by Iva eKelava, Eric eLewitus, Wieland B eHuttner

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Broadening the phenotype of the TWNK gene associated Perrault syndrome by Bálint Fekete, Klára Pentelényi, Gabor Rudas, Anikó Gál, Zoltán Grosz, Anett Illés, Jimoh Idris, Gabor Csukly, Andor Domonkos, Maria Judit Molnar

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