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26 results on '"Murthy, Kruthi"'

2. Data from eRapa Restores a Normal Life Span in a FAP Mouse Model

Author

Hasty, Paul, primary, Livi, Carolina B., primary, Dodds, Sherry G., primary, Jones, Diane, primary, Strong, Randy, primary, Javors, Martin, primary, Fischer, Kathleen E., primary, Sloane, Lauren, primary, Murthy, Kruthi, primary, Hubbard, Gene, primary, Sun, Lishi, primary, Hurez, Vincent, primary, Curiel, Tyler J., primary, and Sharp, Zelton Dave, primary

Published
2023
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3. Supplementary Video 1 from eRapa Restores a Normal Life Span in a FAP Mouse Model

Author

Hasty, Paul, primary, Livi, Carolina B., primary, Dodds, Sherry G., primary, Jones, Diane, primary, Strong, Randy, primary, Javors, Martin, primary, Fischer, Kathleen E., primary, Sloane, Lauren, primary, Murthy, Kruthi, primary, Hubbard, Gene, primary, Sun, Lishi, primary, Hurez, Vincent, primary, Curiel, Tyler J., primary, and Sharp, Zelton Dave, primary

Published
2023
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4. Supplementary Video 2 from eRapa Restores a Normal Life Span in a FAP Mouse Model

Author

Hasty, Paul, primary, Livi, Carolina B., primary, Dodds, Sherry G., primary, Jones, Diane, primary, Strong, Randy, primary, Javors, Martin, primary, Fischer, Kathleen E., primary, Sloane, Lauren, primary, Murthy, Kruthi, primary, Hubbard, Gene, primary, Sun, Lishi, primary, Hurez, Vincent, primary, Curiel, Tyler J., primary, and Sharp, Zelton Dave, primary

Published
2023
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5. Data from Tumor-Intrinsic PD-L1 Signals Regulate Cell Growth, Pathogenesis, and Autophagy in Ovarian Cancer and Melanoma

Author

Clark, Curtis A., primary, Gupta, Harshita B., primary, Sareddy, Gangadhara, primary, Pandeswara, Srilakshmi, primary, Lao, Shunhua, primary, Yuan, Bin, primary, Drerup, Justin M., primary, Padron, Alvaro, primary, Conejo-Garcia, José, primary, Murthy, Kruthi, primary, Liu, Yang, primary, Turk, Mary Jo, primary, Thedieck, Kathrin, primary, Hurez, Vincent, primary, Li, Rong, primary, Vadlamudi, Ratna, primary, and Curiel, Tyler J., primary

Published
2023
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6. Combined supplemental figures 1-7 from Tumor-Intrinsic PD-L1 Signals Regulate Cell Growth, Pathogenesis, and Autophagy in Ovarian Cancer and Melanoma

Author

Clark, Curtis A., primary, Gupta, Harshita B., primary, Sareddy, Gangadhara, primary, Pandeswara, Srilakshmi, primary, Lao, Shunhua, primary, Yuan, Bin, primary, Drerup, Justin M., primary, Padron, Alvaro, primary, Conejo-Garcia, José, primary, Murthy, Kruthi, primary, Liu, Yang, primary, Turk, Mary Jo, primary, Thedieck, Kathrin, primary, Hurez, Vincent, primary, Li, Rong, primary, Vadlamudi, Ratna, primary, and Curiel, Tyler J., primary

Published
2023
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7. Supplementary Figures 1-9 from Mitigating Age-Related Immune Dysfunction Heightens the Efficacy of Tumor Immunotherapy in Aged Mice

Author

Hurez, Vincent, primary, Daniel, Benjamin J., primary, Sun, Lishi, primary, Liu, Ai-Jie, primary, Ludwig, Sara M., primary, Kious, Mark J., primary, Thibodeaux, Suzanne R., primary, Pandeswara, Srilakshmi, primary, Murthy, Kruthi, primary, Livi, Carolina B., primary, Wall, Shawna, primary, Brumlik, Michael J., primary, Shin, Tahiro, primary, Zhang, Bin, primary, and Curiel, Tyler J., primary

Published
2023
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8. Data from Mitigating Age-Related Immune Dysfunction Heightens the Efficacy of Tumor Immunotherapy in Aged Mice

Author

Hurez, Vincent, primary, Daniel, Benjamin J., primary, Sun, Lishi, primary, Liu, Ai-Jie, primary, Ludwig, Sara M., primary, Kious, Mark J., primary, Thibodeaux, Suzanne R., primary, Pandeswara, Srilakshmi, primary, Murthy, Kruthi, primary, Livi, Carolina B., primary, Wall, Shawna, primary, Brumlik, Michael J., primary, Shin, Tahiro, primary, Zhang, Bin, primary, and Curiel, Tyler J., primary

Published
2023
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9. Supplementary Figure Legends 1-9 from Mitigating Age-Related Immune Dysfunction Heightens the Efficacy of Tumor Immunotherapy in Aged Mice

Author

Hurez, Vincent, primary, Daniel, Benjamin J., primary, Sun, Lishi, primary, Liu, Ai-Jie, primary, Ludwig, Sara M., primary, Kious, Mark J., primary, Thibodeaux, Suzanne R., primary, Pandeswara, Srilakshmi, primary, Murthy, Kruthi, primary, Livi, Carolina B., primary, Wall, Shawna, primary, Brumlik, Michael J., primary, Shin, Tahiro, primary, Zhang, Bin, primary, and Curiel, Tyler J., primary

Published
2023
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12. Tumor-Intrinsic PD-L1 Signals Regulate Cell Growth, Pathogenesis, and Autophagy in Ovarian Cancer and Melanoma

Author

Clark, Curtis A., primary, Gupta, Harshita B., additional, Sareddy, Gangadhara, additional, Pandeswara, Srilakshmi, additional, Lao, Shunhua, additional, Yuan, Bin, additional, Drerup, Justin M., additional, Padron, Alvaro, additional, Conejo-Garcia, José, additional, Murthy, Kruthi, additional, Liu, Yang, additional, Turk, Mary Jo, additional, Thedieck, Kathrin, additional, Hurez, Vincent, additional, Li, Rong, additional, Vadlamudi, Ratna, additional, and Curiel, Tyler J., additional

Published
2016
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14. Parasite Mitogen-Activated Protein Kinases as Drug Discovery Targets to Treat Human Protozoan Pathogens

Author

Brumlik, Michael J., Pandeswara, Srilakshmi, Ludwig, Sara M., Murthy, Kruthi, and Curiel, Tyler J.

Subjects
Article Subject, parasitic diseases
Abstract

Protozoan pathogens are a highly diverse group of unicellular organisms, several of which are significant human pathogens. One group of protozoan pathogens includes obligate intracellular parasites such as agents of malaria, leishmaniasis, babesiosis, and toxoplasmosis. The other group includes extracellular pathogens such as agents of giardiasis and amebiasis. An unfortunate unifying theme for most human protozoan pathogens is that highly effective treatments for them are generally lacking. We will review targeting protozoan mitogen-activated protein kinases (MAPKs) as a novel drug discovery approach towards developing better therapies, focusing on Plasmodia, Leishmania, and Toxoplasma, about which the most is known.

Published
2011
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19. eRapa Restores a Normal Life Span in a FAP Mouse Model

Author

Hasty, Paul, primary, Livi, Carolina B., additional, Dodds, Sherry G., additional, Jones, Diane, additional, Strong, Randy, additional, Javors, Martin, additional, Fischer, Kathleen E., additional, Sloane, Lauren, additional, Murthy, Kruthi, additional, Hubbard, Gene, additional, Sun, Lishi, additional, Hurez, Vincent, additional, Curiel, Tyler J., additional, and Sharp, Zelton Dave, additional

Published
2014
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20. TgMAPK1 is a Toxoplasma gondii MAP kinase that hijacks host MKK3 signals to regulate virulence and interferon-γ-mediated nitric oxide production

Author

Brumlik, Michael J., primary, Pandeswara, Srilakshmi, additional, Ludwig, Sara M., additional, Jeansonne, Duane P., additional, Lacey, Michelle R., additional, Murthy, Kruthi, additional, Daniel, Benjamin J., additional, Wang, Rong-Fu, additional, Thibodeaux, Suzanne R., additional, Church, Kristina M., additional, Hurez, Vincent, additional, Kious, Mark J., additional, Zhang, Bin, additional, Alagbala, Adebusola, additional, Xia, Xiaojun, additional, and Curiel, Tyler J., additional

Published
2013
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23. Mitigating Age-Related Immune Dysfunction Heightens the Efficacy of Tumor Immunotherapy in Aged Mice

Author

Hurez, Vincent, primary, Daniel, Benjamin J., additional, Sun, Lishi, additional, Liu, Ai-Jie, additional, Ludwig, Sara M., additional, Kious, Mark J., additional, Thibodeaux, Suzanne R., additional, Pandeswara, Srilakshmi, additional, Murthy, Kruthi, additional, Livi, Carolina B., additional, Wall, Shawna, additional, Brumlik, Michael J., additional, Shin, Tahiro, additional, Zhang, Bin, additional, and Curiel, Tyler J., additional

Published
2012
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25. The Mechanism To Redress Grievances.

Author

PRAKASH, ANSHUL, PAL, ABHIMANYU, and MURTHY, KRUTHI N.

Subjects
WAGES & labor productivity, PRODUCTIVITY incentives, MECHANISM (Philosophy), FRUSTRATION-aggression theory, EMPLOYEES
Published
2018

26. Phenotypic Characterization of Escherichia coli strains taken from human Intestinal and Urinary Tracts

Author

Murthy, Kruthi

Subjects
Biology, Microbiology, minimal media, STRAINS, OPE002, motile, coli, uropathogenic, OPE013
Abstract

Escherichia coli (E. coli) is a gram negative bacterium commonly found as a commensal in the intestinal tract of humans and other warm blooded animals. The commensal strains of E. coli are non-pathogenic and do not cause an infection in the host. However, some strains of E. coli are pathogenic and can cause several diseases in humans that include neonatal meningitis, intestinal infections and urinary tract infections. Almost 80-85% of the uncomplicated urinary tract infections are caused by uropathogenic E. coli. Our project involved the characterization of 12 strains of E. coli, isolated from humans in health and disease. These strains were characterized since no studies had been conducted on them previously. The E. coli strains were isolated from patients with urinary tract infections and from the intestinal tracts of partners of these patients. Laboratory E. coli strain K12 served as a control. Phenotypic studies were carried out by studying the bacterial physiology in three different conditions. Motility tests were done to identify phenotypes that were similar to and different in behavior with respect to the wild type. Since antimicrobial resistance was a growing problem in urinary tract infections, susceptibility tests were done for these novel strains of E. coli, with the most commonly used antibiotics to treat these infections. Additionally phenotypic profiles were generated for the wild type strain as well as one uropathogenic strain using Phenotype Microarrays manufactured by Biolog., Inc which was a novel technique especially for uropathogenic strains. These plates were unique in helping us identify different phenotypes within a limited time period. The results of our tests showed, some isolates whose phenotypic behavior differed, in terms of growth and motility when compared to the wild type. Antibiotic susceptibility tests enhanced our understanding of determinants of resistance which was crucial for the management of urinary tract infections. Phenotype micro array profiles generated for 2 strains, the wild type E. coli strain and one uropathogenic strain showed a total of 37 differences in carbon, nitrogen, sulfur and phosphorus metabolism in these strains. These differences indicated the likely genome variations between two strains, a fact that was shown for recently sequenced UTI strain CFT073. Therefore phenotypic characterization was useful in establishing genetic variability of the isolates and more specifically of E. coli strains causing urinary tract infections.

Published
2006

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