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Dalin Li

Showing results (131-140 of 140) with videos related to

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Inflammatory Bowel Diseases|January 27, 2021
Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel DiseaseKaoru Suzuki, Yoichi Kakuta, Takeo Naito, et al.
Gastroenterology|August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome CompositionDalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
BMJ Open|February 13, 2021
Seroprevalence of antibodies to SARS-CoV-2 in healthcare workers: a cross-sectional studyJoseph E Ebinger, Gregory J Botwin, Christine M Albert, et al.
Gastroenterology|June 23, 2026
BIRC3 (Encoding Cellular Inhibitor of Apoptosis Protein 2) Variants Result in Dysregulated Receptor-Interacting Protein Kinase 1 Signaling Leading to Increased Epithelial Cell Death and Are Associated With Monogenic Crohn's DiseaseQi Li, Ryusuke Nambu, Hu Yaqiang, et al.
Gut|April 20, 2023
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosisMarzieh Akhlaghpour, Talin Haritunians, Shyam K More, et al.
Journal of Crohn'S & Colitis|April 23, 2021
Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune DysregulationJodie Ouahed, Judith R Kelsen, Waldo A Spessott, et al.
Science Translational Medicine|January 12, 2018
Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.
Gastroenterology|July 6, 2016
A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSFLing-Shiang Chuang, Nicole Villaverde, Ken Y Hui, et al.
Nature Communications|August 10, 2016
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitisManuel A Rivas, Daniel Graham, Patrick Sulem, et al.
Leukemia|October 23, 2022
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypesSonja I Berndt, Joseph Vijai, Yolanda Benavente, et al.
Pageof 14

Showing results (131-140 of 140) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 140 results.
Inflammatory Bowel Diseases|January 27, 2021
Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel DiseaseKaoru Suzuki, Yoichi Kakuta, Takeo Naito, et al.
Gastroenterology|August 6, 2016
A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome CompositionDalin Li, Jean-Paul Achkar, Talin Haritunians, et al.
BMJ Open|February 13, 2021
Seroprevalence of antibodies to SARS-CoV-2 in healthcare workers: a cross-sectional studyJoseph E Ebinger, Gregory J Botwin, Christine M Albert, et al.
Gastroenterology|June 23, 2026
BIRC3 (Encoding Cellular Inhibitor of Apoptosis Protein 2) Variants Result in Dysregulated Receptor-Interacting Protein Kinase 1 Signaling Leading to Increased Epithelial Cell Death and Are Associated With Monogenic Crohn's DiseaseQi Li, Ryusuke Nambu, Hu Yaqiang, et al.
Gut|April 20, 2023
Genetic coding variant in complement factor B (CFB) is associated with increased risk for perianal Crohn's disease and leads to impaired CFB cleavage and phagocytosisMarzieh Akhlaghpour, Talin Haritunians, Shyam K More, et al.
Journal of Crohn'S & Colitis|April 23, 2021
Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune DysregulationJodie Ouahed, Judith R Kelsen, Waldo A Spessott, et al.
Science Translational Medicine|January 12, 2018
Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn's disease and Parkinson's diseaseKen Y Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu, et al.
Gastroenterology|July 6, 2016
A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSFLing-Shiang Chuang, Nicole Villaverde, Ken Y Hui, et al.
Nature Communications|August 10, 2016
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitisManuel A Rivas, Daniel Graham, Patrick Sulem, et al.
Leukemia|October 23, 2022
Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypesSonja I Berndt, Joseph Vijai, Yolanda Benavente, et al.
Pageof 14