نتائج البحث - "Faubion, William A"

المساهمون: Deutsche Krebshilfe, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, AGA Research Foundation, National Center for Advancing Translational Sciences, Deutsche Forschungsgemeinschaft

المصدر: Gastroenterology ; volume 166, issue 4, page 631-644.e17 ; ISSN 0016-5085

مصطلحات موضوعية: Gastroenterology, Hepatology

الإتاحة: https://doi.org/10.1053/j.gastro.2024.01.007Test
https://api.elsevier.com/content/article/PII:S001650852400009X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S001650852400009X?httpAccept=text/plainTest

View record in BASE

5

دورية أكاديمية

Interleukin 21 Drives a Hypermetabolic State and CD4+ T-Cell–Associated Pathogenicity in Chronic Intestinal Inflammation

المساهمون: Kenneth Rainin Foundation, Mayo Clinic Minnesota Center for Cell Signaling in Gastroenterology, National Institute of Allergy and Infectious Diseases, National Institute of Diabetes and Digestive and Kidney Diseases, Mayo Clinic

المصدر: Gastroenterology ; volume 166, issue 5, page 826-841.e19 ; ISSN 0016-5085

مصطلحات موضوعية: Gastroenterology, Hepatology

الإتاحة: https://doi.org/10.1053/j.gastro.2024.01.026Test
https://api.elsevier.com/content/article/PII:S0016508524000635?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0016508524000635?httpAccept=text/plainTest

View record in BASE

6

دورية أكاديمية

Dual targeting of lymphocyte homing and retention through α4β7 and αEβ7 inhibition in inflammatory bowel disease.

المصدر: Cell reports. Medicine. 2(8)

مصطلحات موضوعية: T cell entry and retention, etrolizumab, inflammatory bowel disease, α4β7, αEβ7

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8f92v3tnTest

View record in eScholarship

7

دورية أكاديمية

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 phagocytosis.

المؤلفون: Akhlaghpour, Marzieh, Haritunians, Talin, More, Shyam K, Thomas, Lisa S, Stamps, Dalton T, Dube, Shishir, Li, Dalin, Yang, Shaohong, Landers, Carol J, Mengesha, Emebet, Hamade, Hussein, Murali, Ramachandran, Potdar, Alka A, Wolf, Andrea J, Botwin, Gregory J, Khrom, Michelle, International IBD Genetics Consortium, Ananthakrishnan, Ashwin N, Faubion, William A, Jabri, Bana, Lira, Sergio A, Newberry, Rodney D, Sandler, Robert S, Sartor, R Balfour, Xavier, Ramnik J, Brant, Steven R, Cho, Judy H, Duerr, Richard H, Lazarev, Mark G, Rioux, John D, Schumm, L Philip, Silverberg, Mark S, Zaghiyan, Karen, Fleshner, Phillip, Melmed, Gil Y, Vasiliauskas, Eric A, Ha, Christina, Rabizadeh, Shervin, Syal, Gaurav, Bonthala, Nirupama N, Ziring, David A, Targan, Stephan R, Long, Millie D, McGovern, Dermot P B, Michelsen, Kathrin S

المساهمون: Georges, Michel

المصدر: Gut, gutjnl-2023-329689 (2023-04-20)

مصطلحات موضوعية: IBD - GENETICS, INFLAMMATORY BOWEL DISEASE, META-ANALYSIS, Gastroenterology, Life sciences, Genetics & genetic processes, Sciences du vivant, Génétique & processus génétiques

العلاقة: https://syndication.highwire.org/content/doi/10.1136/gutjnl-2023-329689Test; urn:issn:0017-5749; urn:issn:1468-3288

الوصول الحر: https://orbi.uliege.be/handle/2268/302287Test

View record in ORBi

8

دورية أكاديمية

Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)

المؤلفون: Pinto e Vairo, Filippo, Kemppainen, Jennifer L., Vitek, Carolyn R. Rohrer, Whalen, Denise A., Kolbert, Kayla J., Sikkink, Kaitlin J., Kroc, Sarah A., Kruisselbrink, Teresa, Shupe, Gabrielle F., Knudson, Alyssa K., Burke, Elizabeth M., Loftus, Elle C., Bandel, Lorelei A., Prochnow, Carri A., Mulvihill, Lindsay A., Thomas, Brittany, Gable, Dale M., Graddy, Courtney B., Garzon, Giovanna G. Moreno, Ekpoh, Idara U., Porquera, Eva M. Carmona, Fervenza, Fernando C., Hogan, Marie C., El Ters, Mireille, Warrington, Kenneth J., Davis, John M., Koster, Matthew J., Orandi, Amir B., Basiaga, Matthew L., Vella, Adrian, Kumar, Seema, Creo, Ana L., Lteif, Aida N., Pittock, Siobhan T., Tebben, Peter J., Abate, Ejigayehu G., Joshi, Avni Y., Ristagno, Elizabeth H., Patnaik, Mrinal S., Schimmenti, Lisa A., Dhamija, Radhika, Sabrowsky, Sonia M., Wierenga, Klaas J., Keddis, Mira T., Samadder, Niloy Jewel J., Presutti, Richard J., Robinson, Steven I., Stephens, Michael C., Roberts, Lewis R., Faubion, William A.

المساهمون: Mayo Clinic Center for Individualized Medicine, Investigative and Functional Genomics Program, William O. Lund, Jr. and Natalie C. Lund Charitable Foundation, Everett J. and Jane M. Hauck

المصدر: Journal of Translational Medicine ; volume 21, issue 1 ; ISSN 1479-5876

مصطلحات موضوعية: General Biochemistry, Genetics and Molecular Biology, General Medicine

الإتاحة: https://doi.org/10.1186/s12967-023-04183-7Test

View record in BASE