Search Results - "genetically modified"

Positive aspects of the mRNA platform for SARS-CoV-2 vaccines by Khalid Hajissa, Ali Mussa

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A CRISPR New World: Attitudes in the Public toward Innovations in Human Genetic Modification by Steven M. Weisberg, Daniel Badgio, Anjan Chatterjee

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Progress of oncolytic virotherapy for neuroblastoma by Xiao-Tong Chen, Shu-Yang Dai, Yong Zhan, Ran Yang, De-Qian Chen, Yi Li, En-Qing Zhou, Rui Dong

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Generation of primary tumors with Flp recombinase in FRT-flanked p53 mice by Chang-Lung Lee, Everett J. Moding, Xiaofang Huang, Yifan Li, Loretta Z. Woodlief, Rafaela C. Rodrigues, Yan Ma, David G. Kirsch

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Gene Therapy for Regenerative Medicine by Hossein Hosseinkhani, Abraham J. Domb, Ghorbanali Sharifzadeh, Victoria Nahum

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Correlation between large rearrangements and patient phenotypes in NF1 deletion syndrome: an update and review by Laurence Pacot, Milind Girish, Samantha Knight, Gill Spurlock, Vinod Varghese, Manuela Ye, Nick Thomas, Eric Pasmant, Meena Upadhyaya

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Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay by Ji Yoon Han, Hyun Jeong Kim, Ja Hyun Jang, In Goo Lee, Joonhong Park, Joonhong Park

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Current Understanding of Inherited Modifiers of FVIII Pharmacokinetic Variation by Swystun LL, Lillicrap D

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Absence of strong strain effects in behavioral analyses of Shank3-deficient mice by Elodie Drapeau, Nate P. Dorr, Gregory A. Elder, Joseph D. Buxbaum

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Association between <it>CFL1 </it>gene polymorphisms and spina bifida risk in a California population by Lammer Edward J, Shaw Gary M, Ma Chen, Enaw James, Zhu Huiping, Finnell Richard H

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Familial Melanoma Phenotype With Xeroderma Pigmentosum Group C (XP-C) Genotype - The Putative Role of MC1R Polymorphism as Modifier by Franciele Antonieta Bianchi Leidenz, Flavia Vasques Bittencourt, Williana Garcia Braga, Ellio Magno de Sá Araujo, Carolina Cavalieri Gomes, Vanessa de Fatima Bernardes, Eitan Friedman, Luiz De Marco

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Association analysis identifies <it>ZNF750 </it>regulatory variants in psoriasis by Birnbaum Ramon Y, Hayashi Genki, Cohen Idan, Poon Annie, Chen Haoyan, Lam Ernest T, Kwok Pui-Yan, Birk Ohad S, Liao Wilson

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Influence of Oxidative Stress Biomarkers and Genetic Polymorphisms on the Clinical Severity of Hydroxyurea-Free Senegalese Children with Sickle Cell Anemia by Fatou Gueye Tall, Cyril Martin, El hadji Malick Ndour, Camille Faes, Indou Déme Ly, Vincent Pialoux, Philippe Connes, Papa Madieye Gueye, Rokhaya Ndiaye Diallo, Céline Renoux, Ibrahima Diagne, Pape Amadou Diop, Aynina Cissé, Philomène Lopez Sall, Philippe Joly

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The Drosophila junctophilin gene is functionally equivalent to its four mammalian counterparts and is a modifier of a Huntingtin poly-Q expansion and the Notch pathway by Eduardo Calpena, Víctor López del Amo, Mouli Chakraborty, Beatriz Llamusí, Rubén Artero, Carmen Espinós, Máximo I. Galindo

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Two compound heterozygous variants in the CLN8 gene are responsible for neuronal cereidolipofuscinoses disorder in a child: a case report by Federico Baltar, Federico Baltar, Camila Simoes, Camila Simoes, Francisco Garagorry, Martín Graña, Soledad Rodríguez, María Haydée Aunchayna, Alejandra Tapié, Alfredo Cerisola, Gabriel González, Hugo Naya, Hugo Naya, Lucía Spangenberg, Lucía Spangenberg, Víctor Raggio

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In Vitro and In Vivo Studies for the Investigation of γ-Globin Gene Induction by Adhatoda vasica: A Pre-Clinical Study of HbF Inducers for β-Thalassemia by Fizza Iftikhar, Saeedur Rahman, Muhammad Behroz Naeem Khan, Kanwal Khan, Muhammad Noman Khan, Reaz Uddin, Syed Ghulam Musharraf, Syed Ghulam Musharraf

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Co-occurrence of mutations in KIF7 and KIAA0556 in Joubert syndrome with ocular coloboma, pituitary malformation and growth hormone deficiency: a case report and literature review by Marcello Niceta, Maria Lisa Dentici, Andrea Ciolfi, Romana Marini, Sabina Barresi, Francesca Romana Lepri, Antonio Novelli, Enrico Bertini, Marco Cappa, Maria Cristina Digilio, Bruno Dallapiccola, Marco Tartaglia

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Next-Generation Sequencing Advances the Genetic Diagnosis of Cerebral Cavernous Malformation (CCM) by Valerio Benedetti, Rosalia Canzoneri, Andrea Perrelli, Carlo Arduino, Andrea Zonta, Alfredo Brusco, Saverio Francesco Retta

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A novel nonsense ATP2C1 mutation causes Hailey-Hailey disease in a Tunisian family by Marwa Chourabi, Dorra H'mida-Ben Brahim, Carine Bonnard, Amina Aounallah, Alvin Yu Ng, Sumanty Tohari, Byrappa Venkatesh, Ali Saad, Lobna Boussofara, Bruno Reversade, Mohamed Denguezli

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Technical challenges and limitations of current mouse models of ovarian cancer by Garson Kenneth, Gamwell Lisa F, Pitre Elizabeth MG, Vanderhyden Barbara C

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