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86 Possible Causes for C3H, Inbred, Mouse

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  • Urinary Tract Infection

    […] in an immunocompromised mouse model of UTI.[] Poltorak A, He X, Smirnova I, Liu MY, Huffel CV, Du X, Birdwell D, Alejos E, Silva M, Galanos C et al (1998) Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations[] Flagellin/immunology* Humans Immunization* Immunoglobulin A Immunoglobulin G/blood Immunoglobulin Isotypes Interferon-gamma Interleukin-17 Kidney/microbiology Mice Mice, Inbred[]

  • Malignant Neoplasm

    In this study, the plasma fraction containing AIS is shown to inhibit mouse erythroblast formation in vitro.[] The upper curve is for BALB/3T3 cells and the bottom curve for C3H/10T 1/2 cells.[] First characterized 130 years ago ( Novinski, 1876 ), CTVT was frequently used by cancer researchers to study tumor transplantation until the development of inbred strains[]

  • Venezuelan Equine Encephalitis

    Since TC-83 is exempt as a select agent, this mouse model was used in the evaluation of antiviral therapies.[] , Venezuelan Equine/virology Female Genetic Vectors/administration & dosage Genetic Vectors/genetics Genetic Vectors/immunology* Humans Immunoglobulin G/blood Mice Mice, Inbred[] Venezuelan Equine/immunology Encephalomyelitis, Venezuelan Equine/prevention & control Encephalomyelitis, Venezuelan Equine/virology Humans Immunization, Passive Mice Mice, Inbred[]

  • Lymphocytic Choriomeningitis

    Human cerebrospinal fluid (CSF) samples and mouse specimens were added to Vero cells.[] C57BL/6, BALB, SWR/J, A/J, 129, C3H, and all but one collaborative cross (CC) mouse strain following Cl 13 infection have immunosuppressed T cell responses, high PD-1, and[] Choriomeningitis/immunology* Lymphocytic Choriomeningitis/virology Lymphocytic choriomeningitis virus/genetics* Lymphocytic choriomeningitis virus/pathogenicity* Mice Mice, Inbred[]

  • Laron Syndrome

    In summary, we report the generation and initial data on the dwarf phenotype of a mouse with a GHR/BP gene knockout (the Laron mouse).[] Klotho Tg [161] Klotho 20% 18% C57BL/6 C3H NC ? NC ? Surf1 KO [76] Surf1 18% 18% 129S1/SvJxC57 BL6J DBA2 NC ? ? ? ? P66 shc KO [209] p66 shc 30% 30% C57Bl/6Sv/129 NC ? ?[] It is our conclusion that the findings from the island of Flores, which were attributed to a new species of the genus Homo, may in fact represent a local, highly inbred, Homo[]

  • Human Granulocytic Ehrlichiosis

    This study validates the appropriateness of the mouse as a model of HGE, including its usefulness for the investigation of thrombocytopenia.[] Similarly, the p44 genes were differentially expressed in infected C3H mice, in SCID mice, and in cultured HGE bacteria.[] The white-footed mouse serves as a natural reservoir for AP-ha, and laboratory studies have shown that numerous inbred strains of mice (e.g., Balb/C, C3H, DBA/2) are also[]

  • Toxoplasma Gondii

    Chronic Toxoplasma infections and familiarity-novelty discrimination in the mouse , Ann Trop Med Parasitol , 1980 , vol. 74 (pg. 145 - 150 ) 17.[] We have previously demonstrated that immunization with the serine protease inhibitor-1 (TgPI-1) confers partial protection to C3H/HeN and C57BL/6 mice.[] […] blood Antibodies, Protozoan/immunology* Female Humans Immunity, Cellular/immunology* Immunity, Humoral/immunology* Immunization Injections, Intraperitoneal Male Mice Mice, Inbred[]

  • Toxoplasmosis

    This study begins to address how the mouse p47 GTPases function.[] We have previously demonstrated that immunization with the serine protease inhibitor-1 (TgPI-1) confers partial protection to C3H/HeN and C57BL/6 mice.[] Antigens, Protozoan/immunology* Cell Proliferation Cytokines/blood Disease Models, Animal Female Humans Immunity, Cellular Immunity, Humoral Immunoglobulin G/blood Mice, Inbred[]

  • Renal Coloboma Syndrome

    […] observed in the Krd mouse and the Pax2 1Neu mouse.[] We describe a novel mouse model of PRS due to a missense mutation in a highly-conserved threonine residue in the paired domain of Pax2 (p.T74A) that recapitulates the ocular[] Abstract We describe a new mouse frameshift mutation (Pax2(1Neu)) with a 1-bp insertion in the Pax2 gene.[]

  • Chediak Higashi Syndrome

    Abstract Chediak-Higashi syndrome (CHS) is a rare autosomal recessive disorder of human, mouse (beige) and other mammalian species.[] Chediak-Higashi, and control mice (Li et al. 2004) Chediak-Higashi mouse is Lyst(bg-J) (third row, fourth column) Control mice are C57BL/6J (row 1 counting from the top, column 1), C3H[] Activation/immunology Lymphohistiocytosis, Hemophagocytic/etiology* Lymphohistiocytosis, Hemophagocytic/genetics Lymphohistiocytosis, Hemophagocytic/immunology* Mice Mice, Inbred[]