Search Results - "Human genetics"

Small molecule targeting NaV1.7 via inhibition of the CRMP2-Ubc9 interaction reduces pain in chronic constriction injury (CCI) rats by Jiahe Li, Harrison J. Stratton, Sabina A. Lorca, Peter M. Grace, Rajesh Khanna

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Immunogenicity of an adjuvanted broadly active influenza vaccine in immunocompromised and diverse populations by Dylan A. Hendy, Erik S. Pena, Luis Ontiveros‐Padilla, Timothy A. Dixon, Denzel D. Middleton, Grace L. Williamson, Nicole Rose Lukesh, Sean R. Simpson, Rebeca T. Stiepel, Md Jahirul Islam, Michael A. Carlock, Ted M. Ross, Eric M. Bachelder, Kristy M. Ainslie

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Deletion of the App-Runx1 region in mice models human partial monosomy 21 by Thomas Arbogast, Matthieu Raveau, Claire Chevalier, Valérie Nalesso, Doulaye Dembele, Hugues Jacobs, Olivia Wendling, Michel Roux, Arnaud Duchon, Yann Herault

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COVID-19: Aspects of genetic susceptibility and congenital defects by Estela Morales Peralta, Miguel Alfonso Alvarez Fornaris

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NODAL/TGFβ signalling mediates the self-sustained stemness induced by PIK3CAH1047R homozygosity in pluripotent stem cells by Ralitsa R. Madsen, James Longden, Rachel G. Knox, Xavier Robin, Franziska Völlmy, Kenneth G. Macleod, Larissa S. Moniz, Neil O. Carragher, Rune Linding, Bart Vanhaesebroeck, Robert K. Semple

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A recombinant vesicular stomatitis virus-based Lassa fever vaccine protects guinea pigs and macaques against challenge with geographically and genetically distinct Lassa viruses. by David Safronetz, Chad Mire, Kyle Rosenke, Friederike Feldmann, Elaine Haddock, Thomas Geisbert, Heinz Feldmann

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Genetic polymorphisms of 20 autosomal STR loci in the Han population of Putian City, Southeastern China by Xiao-Na Li, Ahmad Al-Sabri, Faud Ameen, Noura Al-Dayan, Atif Adnan, Jun Yao

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Development of a Drosophila melanogaster spliceosensor system for in vivo high-throughput screening in myotonic dystrophy type 1 by Irma García-Alcover, Jordi Colonques-Bellmunt, Raquel Garijo, José R. Tormo, Rubén Artero, Mari Carmen Álvarez-Abril, Arturo López Castel, Manuel Pérez-Alonso

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Regenerative Medicine, Disease Modelling, and Drug Discovery in Human Pluripotent Stem Cell-Derived Kidney Tissue by Navin Gupta, Koichiro Susa, Ryuji Morizane

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Genetic predisposition to metabolic dysfunction-associated fatty liver disease by O.E. Abaturov, A.O. Nikulina

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Montelukast Use Decreases Cardiovascular Events in Asthmatics by Malvina Hoxha, Malvina Hoxha, Calogero C. Tedesco, Silvana Quaglin, Visar Malaj, Linda Pustina, Valerie Capra, Jilly F. Evans, Angelo Sala, Angelo Sala, G. Enrico Rovati

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Race, Ethnicity, and Pharmacogenomic Variation in the United States and the United Kingdom by Shivam Sharma, Leonardo Mariño-Ramírez, I. King Jordan

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Human source identification by using a human-associated Escherichia coli genetic marker in the Mae Klong River, Thailand by Pimchanok Nopprapun, Suwanna Kitpati Boontanon, Pitchaya Piyaviriyakul, Rawiwan Sweattatut, Shigeo Fujii, Hidenori Harada

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Functional testing of a human PBX3 variant in zebrafish reveals a potential modifier role in congenital heart defects by Gist H. Farr, Kimia Imani, Darren Pouv, Lisa Maves

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Manipulation of dipeptidylpeptidase 10 in mouse and human in vivo and in vitro models indicates a protective role in asthma by Youming Zhang, Thanushiyan Poobalasingam, Laura L. Yates, Simone A. Walker, Martin S. Taylor, Lauren Chessum, Jackie Harrison, Loukia Tsaprouni, Ian M. Adcock, Clare M. Lloyd, William O. Cookson, Miriam F. Moffatt, Charlotte H. Dean

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CYP2D6 Genetic Variation and Its Implication for Vivax Malaria Treatment in Madagascar by Rajeev K. Mehlotra, Andrea Gaedigk, Rosalind E. Howes, Rosalind E. Howes, Tovonahary A. Rakotomanga, Tovonahary A. Rakotomanga, Arsene C. Ratsimbasoa, Arsene C. Ratsimbasoa, Peter A. Zimmerman

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Polymorphisms in IL-1β, vitamin D receptor <it>Fok</it>1, and Toll-like receptor 2 are associated with extrapulmonary tuberculosis by Holland Steven M, Levy Shawn, Oki Noffisat O, Antas Paulo RZ, Motsinger-Reif Alison A, Sterling Timothy R

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Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model by Jian-Hua Chen, Kim Jee Goh, Nuno Rocha, Matthijs P. Groeneveld, Marina Minic, Timothy G. Barrett, David Savage, Robert K. Semple

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Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future by Whiteman DAH, Kimura A

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Allelic and haplotypic polymorphisms and paternal genetic analysis of Chinese Shaanxi Han population utilizing a multiplex Y-STR set by Hui Xu, Ming Zhao, Shuyan Mei, Yunying Zhang, Meiming Cai, Fanzhang Lei, Bofeng Zhu

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