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The Habtezion lab aims to understand immune mechanisms and identify potential immune-based therapeutic targets for pancreatitis and inflammatory bowel disease. Researchers in the lab study leukocyte trafficking and immune responses pertaining to the intestinal tract in states of both health and disease.
The lab demonstrated a beneficial role and mechanism for heme-oxygenase 1 (HO-1) and its downstream effectors in acute pancreatitis. In chronic pancreatitis the lab characterized macrophage-pancreas stellate cell crosstalk that contributes to disease progression and fibrosis. The significance of this crosstalk is further demonstrated by targeting macrophage polarization and function, as well as altering disease course in established experimental disease. The lab is currently working to elucidate targetable immune pathways that alter and/or reverse the course of disease progression.
A second major project in the lab pertains to understanding immune responses in the intestine and in inflammatory bowel disease (IBD). Multiple projects on intestinal inflammation pertain to understanding the heterogeneity and immune profiles of IBD patients, host immune-microbiome interaction, immune-enteric nervous system interaction, as well as intestine-specific leukocyte recruitment and therapeutic targets using experimental models of inflammation.
The Habtezion lab aims to understand immune mechanisms and identify potential immune-based therapeutic targets for pancreatitis and inflammatory bowel disease. Researchers in the lab study leukocyte trafficking and immune responses pertaining to the intestinal tract in states of both health and disease.
The lab demonstrated a beneficial role and mechanism for heme-oxygenase 1 (HO-1) and its downstream effectors in acute pancreatitis. In chronic pancreatitis the lab characterized macrophage-pancreas stellate cell crosstalk that contributes to disease progression and fibrosis. The significance of this crosstalk is further demonstrated by targeting macrophage polarization and function, as well as altering disease course in established experimental disease. The lab is currently working to elucidate targetable immune pathways that alter and/or reverse the course of disease progression.
A second major project in the lab pertains to understanding immune responses in the intestine and in inflammatory bowel disease (IBD). Multiple projects on intestinal inflammation pertain to understanding the heterogeneity and immune profiles of IBD patients, host immune-microbiome interaction, immune-enteric nervous system interaction, as well as intestine-specific leukocyte recruitment and therapeutic targets using experimental models of inflammation.
Research Interests
Papers共 213 篇Author StatisticsCo-AuthorSimilar Experts
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C. Kulkarni,T. Fardeen,J. Gubatan, K. Jarr, E. Dickson, H. Jang,M. Temby,A. Patel,G. Singh,J. Ye,K. Keyashian,S. Streett,E. Ho,G. Barber,S. Singh,D. Limsui,N. Anaizi,L. Becker,S. Spencer, D. Mehrish,D. Perelman,A. Habtezion,J. Sonnenburg,C. Gardner,S. Sinha
JOURNAL OF CROHNS & COLITIS (2025): i1909-i1910
Gastroenterologyno. 5 (2024): S-263
Gastroenterologyno. 5 (2024): S-1418
Hong Namkoong,Bomi Lee,Gayathri Swaminathan,Seong-Joon Koh,Stephan Rogalla, Maria D. Paraskevopoulou, Jay Tang,David Mikhail,Laren S. Becker,Aida Habtezion
Bomi Lee,Elaina Jones,Murli Manohar,Liang Li,Dhiraj Yadav,Darwin L. Conwell,Phil A. Hart,Santhi Swaroop Vege,Evan L. Fogel,Jose Serrano,Dana K. Andersen,Melena Bellin,Mark Topazian,Stephen K. Van Den Eeden,Stephen J. Pandol,Chris Forsmark,William E. Fisher,Walter G. Park,Sohail Z. Husain,Aida Habtezion
Gastroenterologyno. 6 (2023): S-1005
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY (2023): 38-39
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Gastro Hep Advancesno. 2 (2023): 261-276
Weizhi He,Jinghua Wu,Juanjuan Shi,Yan-Miao Huo, Wentao Dai,Jing Geng,Ping Lu,Min-Wei Yang,Yuan Fang,Wei Wang,Zhi-Gang Zhang,Aida Habtezion,Yong-Wei Sun,Jing Xue
crossref(2023)
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Author Statistics
#Papers: 213
#Citation: 7801
H-Index: 47
G-Index: 87
Sociability: 7
Diversity: 3
Activity: 42
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