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81por Van der Mieren, Gerry, Nevelsteen, Ines, Vanderper, Annelies, Oosterlinck, Wouter, Flameng, Willem, Herijgers, Paul“…METHODS: C57Bl6/J wild type (WT) mice, leptin deficient ob/ob (model for type II diabetes) and double knock-out (LDLR-/-;ob/ob, further called DKO) mice with combined leptin and LDL-receptor deficiency (model for metabolic syndrome) were used. …”
Publicado 2012
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82por Wu, Tingxin, Li, Fenglei, Chen, Yongyan, Wei, Haiming, Tian, Zhigang, Sun, Cheng, Sun, Rui“…We further tried to find the bacterial species responsible for maintaining anti-HBV immunity, and found that each antibiotic alone could not significantly influence HBV clearance compared to antibiotic combination, suggesting that global commensal microbial load is critical for promoting HBV clearance. We also confirmed that TLRs (e.g., TLR2, 4, 9) are not major players in immune clearance of HBV using their agonists and knock-out mice. …”
Publicado 2019
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83por McGuckin Wuertz, Kathryn, Treuting, Piper M., Hemann, Emily A., Esser-Nobis, Katharina, Snyder, Annelise G., Graham, Jessica B., Daniels, Brian P., Wilkins, Courtney, Snyder, Jessica M., Voss, Kathleen M., Oberst, Andrew, Lund, Jennifer, Gale, Michael“…When challenged with WNV, STING knock out (-/-) mice displayed increased morbidity and mortality compared to wild type (WT) mice. …”
Publicado 2019
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84por Mayuramart, Oraphan, Poomipak, Witthaya, Rattanaburi, Somruthai, Khongnomnan, Kritsada, Anuntakarun, Songtham, Saengchoowong, Suthat, Chavalit, Tanit, Chantaravisoot, Naphat, Payungporn, Sunchai“…Interferon regulating factor 7 (IRF7) is a transcription factor for type-I IFN that plays an important role in regulating the anti-viral mechanism and eliminating viruses. We developed IRF7 knock-out MDCK cells (IRF7(−/ −) MDCK) using CRISPR/Cas9 technology. …”
Publicado 2022
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85por Massé, Priscilla G, Boskey, Adele L, Ziv, Israel, Hauschka, Peter, Donovan, Sharon M, Howell, David S, Cole, David EC“…We also conclude that the hCySH-supplemented chick is a promising model for study of the connective tissue abnormalities associated with homocystinuria and an important alternative model to the CBS knock-out mouse.…”
Publicado 2003
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86“…METHODS: We illustrate this by critically re-examining a specific case of the causal role of insulin in glucose homeostasis using five different approaches (1) Systematic review of tissue specific insulin receptor knock-outs, (2) Systematic review of insulin suppression and insulin enhancement experiments, (3) Differentiating steady state and post-meal state glucose levels in streptozotocin treated rats in primary experiments, (4) Mathematical and theoretical considerations and (5) Glucose-insulin relationship in human epidemiological data. …”
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87por Nico, Dirlei, Feijó, Daniel Ferreira, Maran, Naiara, Morrot, Alexandre, Scharfstein, Julio, Palatnik, Marcos, Palatnik-de-Sousa, Clarisa Beatriz“…FINDINGS: B2R (−/−) C57BL/6 knock-out (KOB2) and B2R(+/+) C57BL/6-wild type control mice (C57) were infected with amastigotes of Leishmania (L.) chagasi. …”
Publicado 2012
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88por Turovsky, Egor A., Braga, Alice, Yu, Yichao, Esteras, Noemi, Korsak, Alla, Theparambil, Shefeeq M., Hadjihambi, Anna, Hosford, Patrick S., Teschemacher, Anja G., Marina, Nephtali, Lythgoe, Mark F., Haydon, Philip G., Gourine, Alexander V.“…In astrocyte-specific Cx43 knock-out mice the magnitude of heart rate responses to acute increases in intracranial pressure was not affected by Cx43 deficiency. …”
Publicado 2020
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89por McCann, Cat, Quinteros, Michael, Adelugba, Ifeoluwa, Morgada, Marcos N., Castelblanco, Aida R., Davis, Emily J., Lanzirotti, Antonio, Hainer, Sarah J., Vila, Alejandro J., Navea, Juan G., Padilla-Benavides, Teresita“…PiC2 deletion using CRISPR/Cas9 showed that the transporter is required for proliferation and differentiation of primary myoblasts, as both processes are delayed upon PiC2 knock-out. The effects of PiC2 deletion were rescued by the addition of Cu to the growth medium, implying the deleterious effects of PiC2 knockout in myoblasts may be in part due to a failure to deliver sufficient Cu to the mitochondria, which can be compensated by other mitochondrial cuproproteins. …”
Publicado 2022
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90por Renieris, Georgios, Droggiti, Dionysia-Eirini, Katrini, Konstantina, Koufargyris, Panagiotis, Gkavogianni, Theologia, Karakike, Eleni, Antonakos, Nikolaos, Damoraki, Georgia, Karageorgos, Athanasios, Sabracos, Labros, Katsouda, Antonia, Jentho, Elisa, Weis, Sebastian, Wang, Rui, Bauer, Michael, Szabo, Csaba, Platoni, Kalliopi, Kouloulias, Vasilios, Papapetropoulos, Andreas, Giamarellos-Bourboulis, Evangelos J.“…Animal experiments using a model of severe systemic multidrug-resistant P. aeruginosa infection were performed using mice with a constitutive knock-out of cystathionine-γ lyase (Cse) gene (Cse(-/-)) and wild-type mice with a physiological expression (Cse(+/+)). …”
Publicado 2021
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91por Deffert, Christine, Schäppi, Michela G., Pache, Jean-Claude, Cachat, Julien, Vesin, Dominique, Bisig, Ruth, Ma Mulone, Xiaojuan, Kelkka, Tiina, Holmdahl, Rikard, Garcia, Irene, Olleros, Maria L., Krause, Karl-Heinz“…We therefore investigated BCG infection in three different mouse models of CGD: Ncf1 mutants in two different genetic backgrounds and Cybb knock-out mice. In addition, we investigated a macrophage-specific rescue (transgenic expression of Ncf1 under the control of the CD68 promoter). …”
Publicado 2014
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92por Rudenko, Olga, Shang, Jin, Munk, Alexander, Ekberg, Jeppe P., Petersen, Natalia, Engelstoft, Maja S., Egerod, Kristoffer L., Hjorth, Siv A., Wu, Margaret, Feng, Yue, Zhou, Yun-Ping, Mokrosinski, Jacek, Thams, Peter, Reimann, Frank, Gribble, Fiona, Rehfeld, Jens F., Holst, Jens J., Treebak, Jonas T., Howard, Andrew D., Schwartz, Thue W.“…METHODS AND RESULTS: We find that GPR142 is expressed not only in β- but also in α-cells of the islets as well as in enteroendocrine cells, and we confirm that GPR142 is a highly selective sensor of essential aromatic amino acids, in particular Trp and oligopeptides with N-terminal Trp. GPR142 knock-out mice displayed a very limited metabolic phenotype but demonstrated that L-Trp induced secretion of pancreatic and gut hormones is mediated through GPR142 but that the receptor is not required for protein-induced hormone secretion. …”
Publicado 2018
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93“…In this report, using murine macrophages generated from a series of knock-out mice, we have demonstrated that M. catarrhalis lipooligosaccharide (LOS) and either heat killed or live bacteria are recognized by one or more TLRs. …”
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94por Pankiewicz, Joanna E., Diaz, Jenny R., Martá-Ariza, Mitchell, Lizińczyk, Anita M., Franco, Leor A., Sadowski, Martin J.“…METHODS: APPswe/PS1(dE9) AD transgenic mice were once crossed to mice overexpressing wild-type Prdx6 allele or to Prdx6 knock out mice. Aβ pathology and associated neuritic degeneration were assessed in mice aged 10 months. …”
Publicado 2020
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95por Maric-Biresev, Jelena, Hunn, Julia P., Krut, Oleg, Helms, J. Bernd, Martens, Sascha, Howard, Jonathan C.“…In the Irgm1/Irgm3 double knock-out mouse, activated GKS proteins associate with lipid droplets, but not with lysosomes, and the Irgm1/Irgm3(−/−) does not have the generalized immunodeficiency phenotype expected from its Irgm1 deficiency. …”
Publicado 2016
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96por Dong, Qian, Dunkelberger, Jenelle, Lim, Kyu-Sang, Lunney, Joan K, Tuggle, Christopher K, Rowland, Raymond R R, Dekkers, Jack C M“…Pigs with complete resistance to porcine reproductive and respiratory syndrome (PRRS) virus (PRRSV) have been produced by genetically knocking out the CD163 gene that encodes a receptor of the PRRSV for entry into macrophages. …”
Publicado 2021
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97por Saleheen, Danish, Natarajan, Pradeep, Armean, Irina M., Zhao, Wei, Rasheed, Asif, Khetarpal, Sumeet, Won, Hong-Hee, Karczewski, Konrad J., O’Donnell-Luria, Anne H., Samocha, Kaitlin E., Weisburd, Benjamin, Gupta, Namrata, Zaidi, Mozzam, Samuel, Maria, Imran, Atif, Abbas, Shahid, Majeed, Faisal, Ishaq, Madiha, Akhtar, Saba, Trindade, Kevin, Mucksavage, Megan, Qamar, Nadeem, Zaman, Khan Shah, Yaqoob, Zia, Saghir, Tahir, Rizvi, Syed Nadeem Hasan, Memon, Anis, Mallick, Nadeem Hayyat, Ishaq, Mohammad, Rasheed, Syed Zahed, Memon, Fazal-ur-Rehman, Mahmood, Khalid, Ahmed, Naveeduddin, Do, Ron, Krauss, Ronald M., MacArthur, Daniel G., Gabriel, Stacey, Lander, Eric S., Daly, Mark J., Frossard, Philippe, Danesh, John, Rader, Daniel J., Kathiresan, Sekar“…These pLoF mutations are predicted to knock out 1,317 genes in at least one participant. …”
Publicado 2017
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98por Waugh, Charlie M., Mousavizadeh, Rouhollah, Lee, Jenny, Screen, Hazel R. C., Scott, Alexander“…METHODS: The Achilles tendons of 32 young wild-type (SD) and 32 apolipoprotein E knock-out rats (ApoE(−/−)) were harvested at 15.6 ± 2.3 weeks of age. 32 specimens underwent histological examination to assess the distribution of lipids throughout sub-tendons and ISTM. …”
Publicado 2023
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99por Good, Steven S, Moussa, Adel, Zhou, Xiao-Jian, Sommadossi, Jean-Pierre, Pietropaolo, Keith“…AG129 (α-, β- and γ-interferon knock-out) mice received an oral dose of AT‐752 (1000 mg/kg) 4 h before s.c. inoculation with Dengue virus type 2 (strain D2Y98P, 1x10(5) virus particles) followed by b.i.d. doses (500 mg/kg) for 7 days starting 1 h post‐inoculation (p.i.). …”
Publicado 2020
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100por Nagre, Nagaraja, Nicholson, Gregory, Cong, Xiaofei, Lockett, Janette, Pearson, Andrew C., Chan, Vincent, Kim, Woong-Ki, Vinod, K. Yaragudri, Catravas, John D.“…These effects were abrogated by a CB2R antagonist, SR144528, further confirming the specificity of the CB2R-mediated effects. CB2R-knock out (CB2RKO) mice had a significantly higher level of PA-induced inflammation as compared to that in WT mice. …”
Publicado 2022
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