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Wyszukujesz frazę ""Haribabu, Bodduluri"" wg kryterium: Autor


Tytuł :
Absence of CCR2 reduces spontaneous intestinal tumorigenesis in the Apc mouse model.
Autorzy :
Jala, Venkatakrishna Rao
Bodduluri, Sobha Rani
Ghosh, Sweta
Chheda, Zinal
Singh, Rajbir
Smith, Michelle E.
Chilton, Paula M.
Fleming, Christopher J.
Mathis, Steven Paul
Sharma, Rajesh Kumar
Knight, Rob
Yan, Jun
Haribabu, Bodduluri
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Temat :
NEOPLASTIC cell transformation
CELL analysis
INTESTINAL tumors
T cells
INTESTINES
Źródło :
International Journal of Cancer; May2021, Vol. 148 Issue 10, p2594-2607, 14p
Czasopismo naukowe
Tytuł :
Regulation of Intestinal Barrier Function by Microbial Metabolites.
Autorzy :
Ghosh S; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky.
Whitley CS; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky.
Haribabu B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky.
Jala VR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky. Electronic address: .
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Źródło :
Cellular and molecular gastroenterology and hepatology [Cell Mol Gastroenterol Hepatol] 2021; Vol. 11 (5), pp. 1463-1482. Date of Electronic Publication: 2021 Feb 18.
Typ publikacji :
Journal Article; Review
Czasopismo naukowe
Tytuł :
The role for the metagenome in the pathogenesis of COVID-19.
Autorzy :
Friedland RP; Department of Neurology, University of Louisville School of Medicine, Louisville, KY 40202, United States. Electronic address: .
Haribabu B; Department of Microbiology and Immunology, University of Louisville School of Medicine, Louisville, KY 40202, United States.
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Źródło :
EBioMedicine [EBioMedicine] 2020 Nov; Vol. 61, pp. 103019. Date of Electronic Publication: 2020 Oct 07.
Typ publikacji :
Letter; Review
MeSH Terms :
Metagenome*
COVID-19/*etiology
COVID-19/microbiology ; Humans ; Inflammation ; Metagenomics
Recenzja
Tytuł :
Microbial Metabolite Urolithin B Inhibits Recombinant Human Monoamine Oxidase A Enzyme.
Autorzy :
Singh R; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Chandrashekharappa S; Institute for Stem Cell Science and Regenerative Medicine (inStem), University of Agricultural Sciences-Gandhi Krishi Vignan Kendra (UAS-GKVK) Campus, Bellary Road, Bangalore, Karnataka 560065, India.
Vemula PK; Institute for Stem Cell Science and Regenerative Medicine (inStem), University of Agricultural Sciences-Gandhi Krishi Vignan Kendra (UAS-GKVK) Campus, Bellary Road, Bangalore, Karnataka 560065, India.
Haribabu B; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Jala VR; Department of Microbiology and Immunology, James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
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Źródło :
Metabolites [Metabolites] 2020 Jun 19; Vol. 10 (6). Date of Electronic Publication: 2020 Jun 19.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Zinc Oxide Nanowires Exposure Induces a Distinct Inflammatory Response via CCL11-Mediated Eosinophil Recruitment.
Autorzy :
Alghsham RS; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Satpathy SR; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Bodduluri SR; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Hegde B; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Jala VR; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Twal W; Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC, United States.
Burlison JA; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
Sunkara M; Department of Chemical Engineering, Conn Center for Renewable Energy, University of Louisville, Louisville, KY, United States.
Haribabu B; Department of Microbiology and Immunology, University of Louisville, Louisville, KY, United States.; James Graham Brown Cancer Center, University of Louisville, Louisville, KY, United States.
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Źródło :
Frontiers in immunology [Front Immunol] 2019 Nov 08; Vol. 10, pp. 2604. Date of Electronic Publication: 2019 Nov 08 (Print Publication: 2019).
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Chemokine CCL11/*immunology
Eosinophils/*drug effects
Eosinophils/*immunology
Inflammation/*etiology
Nanowires/*adverse effects
Zinc Oxide/*adverse effects
Animals ; Chemokine CCL11/genetics ; Chemokine CCL2/genetics ; Disease Models, Animal ; In Vitro Techniques ; Inflammation/genetics ; Inflammation/immunology ; Inflammation Mediators/metabolism ; Interleukin-6/genetics ; Macrophages/drug effects ; Macrophages/immunology ; Mice ; Mice, Inbred C57BL ; Nanowires/chemistry ; Neutrophils/drug effects ; Neutrophils/immunology ; RAW 264.7 Cells ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Tumor Necrosis Factor-alpha/genetics ; Up-Regulation/drug effects ; Zinc Oxide/chemistry
Czasopismo naukowe
Tytuł :
Co-localization of autophagy-related protein p62 with cancer stem cell marker dclk1 may hamper dclk1's elimination during colon cancer development and progression.
Autorzy :
Roy BC; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Ahmed I; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Ramalingam S; Department of Genetic Engineering, School of Bio-Engineering, SRM Institute of Science and Technology, Kattankulathur, Kanchipuram, Tamil Nadu, India.
Jala V; James Graham Brown Cancer Center and Department of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.
Haribabu B; James Graham Brown Cancer Center and Department of Microbiology and Immunology, University of Louisville, Louisville, KY, USA.
Ramamoorthy P; Department of Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Ashcraft J; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Valentino J; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Anant S; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
Sampath V; Division of Neonatology, Children's Mercy Hospital, Kansas City, MO, USA.
Umar S; Departments of Surgery and Cancer Biology, University of Kansas Medical Center, Kansas City, KS, USA.
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Źródło :
Oncotarget [Oncotarget] 2019 Mar 22; Vol. 10 (24), pp. 2340-2354. Date of Electronic Publication: 2019 Mar 22 (Print Publication: 2019).
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Plant-Derived Exosomal MicroRNAs Shape the Gut Microbiota.
Autorzy :
Teng Y; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA. Electronic address: .
Ren Y; Department of Breast and Thyroid Surgery, The Affiliated Huaian No. 1 People's Hospital of Nanjing Medical University, Huaian, Jiangsu 223300, China.
Sayed M; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Hu X; Department of Genomic Medicine, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Lei C; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Kumar A; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Hutchins E; Translational Genomics Research Institute, Phoenix, AZ 85004, USA.
Mu J; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Deng Z; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Luo C; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Sundaram K; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Sriwastva MK; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Zhang L; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Hsieh M; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Reiman R; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Haribabu B; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Yan J; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Jala VR; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Miller DM; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Van Keuren-Jensen K; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA.
Merchant ML; Kidney Disease Program and Clinical Proteomics Center, University of Louisville, Louisville, KY, USA.
McClain CJ; Robley Rex Veterans Affairs Medical Center, Louisville, KY 40206, USA; Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition, University of Louisville School of Medicine, Louisville, KY 40202, USA.
Park JW; Department of Computer Engineering and Computer Science, University of Louisville, Louisville, KY 40202, USA; KBRIN Bioinformatics Core, University of Louisville, Louisville, KY 40202, USA.
Egilmez NK; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA.
Zhang HG; Robley Rex Veterans Affairs Medical Center, Louisville, KY 40206, USA; James Graham Brown Cancer Center, Department of Microbiology & Immunology, University of Louisville, CTRB 309, 505 Hancock Street, Louisville, KY 40202, USA. Electronic address: .
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Źródło :
Cell host & microbe [Cell Host Microbe] 2018 Nov 14; Vol. 24 (5), pp. 637-652.e8. Date of Electronic Publication: 2018 Oct 25.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.
MeSH Terms :
Exosome Multienzyme Ribonuclease Complex/*pharmacology
Gastrointestinal Microbiome/*drug effects
Intestines/*microbiology
Intestines/*physiology
MicroRNAs/*pharmacology
Plants/*chemistry
Animals ; Bacterial Proteins ; Colitis/therapy ; Disease Models, Animal ; Disease Susceptibility ; Female ; Food ; Gastrointestinal Microbiome/genetics ; Germ-Free Life ; Host-Pathogen Interactions ; Immunity, Mucosal ; Indoles/metabolism ; Interleukins/metabolism ; Lactobacillus rhamnosus/drug effects ; Lactobacillus rhamnosus/genetics ; Male ; Mice ; Mice, Inbred C57BL ; RNA, Ribosomal, 16S/genetics ; Receptors, Aryl Hydrocarbon/metabolism ; Serine Endopeptidases ; Tryptophan/metabolism
Czasopismo naukowe
Tytuł :
Inflammasome-Independent Leukotriene B 4 Production Drives Crystalline Silica-Induced Sterile Inflammation.
Autorzy :
Hegde B; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Bodduluri SR; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Satpathy SR; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Alghsham RS; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Jala VR; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
Uriarte SM; Department of Medicine, University of Louisville Health Sciences Center, Louisville, KY 40202.
Chung DH; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.
Lawrenz MB; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202.
Haribabu B; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, KY 40202; .; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, KY 40202; and.
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Źródło :
Journal of immunology (Baltimore, Md. : 1950) [J Immunol] 2018 May 15; Vol. 200 (10), pp. 3556-3567. Date of Electronic Publication: 2018 Apr 02.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Inflammasomes/*metabolism
Inflammation/*chemically induced
Inflammation/*metabolism
Leukotriene B4/*metabolism
Silicon Dioxide/*pharmacology
Animals ; Cell Line ; Humans ; Interleukin-1beta/metabolism ; Macrophages/drug effects ; Macrophages/metabolism ; Mast Cells/drug effects ; Mast Cells/metabolism ; Mice ; Mice, Inbred C57BL ; Mitogen-Activated Protein Kinase 8/metabolism ; NLR Family, Pyrin Domain-Containing 3 Protein/metabolism ; Neutrophils/drug effects ; Neutrophils/metabolism ; Phagosomes/drug effects ; Phagosomes/metabolism ; RAW 264.7 Cells ; Silicosis/metabolism ; rab GTP-Binding Proteins/metabolism ; rab5 GTP-Binding Proteins/metabolism
Czasopismo naukowe
Tytuł :
Mast Cell-Dependent CD8 Mice.
Autorzy :
Bodduluri SR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Mathis S; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Maturu P; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Krishnan E; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Satpathy SR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky.; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Chilton PM; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.; Institute for Cellular Therapeutics, University of Louisville Health Sciences Center, Louisville, Kentucky.
Mitchell TC; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.; Institute for Cellular Therapeutics, University of Louisville Health Sciences Center, Louisville, Kentucky.
Lira S; Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, New York.
Locati M; Humanitas Clinical and Research Center, University of Milan, Milan, Italy.; University of Milan, Milan, Italy.
Mantovani A; Humanitas Clinical and Research Center, University of Milan, Milan, Italy.; Humanitas University, Rozzano, Italy.
Jala VR; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky. .; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
Haribabu B; James Graham Brown Cancer Center, University of Louisville Health Sciences Center, Louisville, Kentucky. .; Department of Microbiology and Immunology, University of Louisville Health Sciences Center, Louisville, Kentucky.
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Źródło :
Cancer immunology research [Cancer Immunol Res] 2018 Mar; Vol. 6 (3), pp. 332-347. Date of Electronic Publication: 2018 Jan 30.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
CD8-Positive T-Lymphocytes/*immunology
Intestinal Neoplasms/*immunology
Mast Cells/*immunology
Adenomatous Polyposis Coli Protein/genetics ; Adenomatous Polyposis Coli Protein/immunology ; Animals ; Female ; Immunologic Surveillance ; Leukotriene B4/immunology ; Male ; Mice, Transgenic ; Receptors, Chemokine/genetics ; Receptors, Chemokine/immunology ; Receptors, Leukotriene B4/genetics ; Receptors, Leukotriene B4/immunology
Czasopismo naukowe
Tytuł :
Leukotriene B 4 -receptor-1 mediated host response shapes gut microbiota and controls colon tumor progression.
Autorzy :
Jala, Venkatakrishna R.
Maturu, Paramahamsa
Bodduluri, Sobha R.
Krishnan, Elangovan
Mathis, Steven
Subbarao, Krishnaprasad
Wang, Min
Jenson, Alfred B.
Proctor, Mary L.
Rouchka, Eric C.
Knight, Rob
Haribabu, Bodduluri
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Temat :
COLON cancer
LEUKOTRIENES
IMMUNE response
Źródło :
OncoImmunology; 2017, Vol. 6 Issue 12, pN.PAG-N.PAG, 1p
Czasopismo naukowe

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