نتائج البحث - "Muhammad-Tanweer Khan"

1

دورية أكاديمية

Induction of farnesoid X receptor signaling in germ-free mice colonized with a human microbiota

المؤلفون: Annika Wahlström, Petia Kovatcheva-Datchary, Marcus Ståhlman, Muhammad-Tanweer Khan, Fredrik Bäckhed, Hanns-Ulrich Marschall

المصدر: Journal of Lipid Research, Vol 58, Iss 2, Pp 412-419 (2017)

مصطلحات موضوعية: bile acids and salts, biosynthesis and metabolism, enzyme mechanisms and regulation, farnesoid X receptor agonist, farnesoid X receptor antagonist, gut microbiota, Biochemistry, QD415-436

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S002222752031422X; https://doaj.org/toc/0022-2275

URL الوصول: https://doaj.org/article/a67b6b21e24b47a494f4720dc7d74bef

2

دورية أكاديمية

Synergy and oxygen adaptation for development of next-generation probiotics

المؤلفون: Muhammad Tanweer Khan, Chinmay Dwibedi, Daniel Sundh, Meenakshi Pradhan, Jamie D. Kraft, Robert Caesar, Valentina Tremaroli, Mattias Lorentzon, Fredrik Bäckhed

المصدر: Nature, Nature. 620(7973):381-385

الإتاحة: https://ideas.repec.org/a/nat/nature/v620y2023i7973d10.1038_s41586-023-06378-w.html

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6α-hydroxylated bile acids mediate TGR5 signalling to improve glucose metabolism upon dietary fiber supplementation in mice

المؤلفون: Kassem Makki, Harald Brolin, Natalia Petersen, Marcus Henricsson, Dan Ploug Christensen, Muhammad Tanweer Khan, Annika Wahlström, Per-Olof Bergh, Valentina Tremaroli, Kristina Schoonjans, Hanns-Ulrich Marschall, Fredrik Bäckhed

المصدر: Gut, 72 (2)
Makki, K, Brolin, H, Petersen, N, Henricsson, M, Christensen, D P, Khan, M T, Wahlström, A, Bergh, P-O, Tremaroli, V, Schoonjans, K, Marschall, H-U & Bäckhed, F 2023, ' 6α-hydroxylated bile acids mediate TGR5 signalling to improve glucose metabolism upon dietary fiber supplementation in mice ', Gut, vol. 72, pp. 314-324 . https://doi.org/10.1136/gutjnl-2021-326541

مصطلحات موضوعية: Gastroenterology

وصف الملف: application/application/pdf; application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0bf96e61639223e36cacfb3ff99cc01
https://hdl.handle.net/20.500.11850/553802

Find this article in full text from ProQuest

4

دورية أكاديمية

Structural characterization of the microbial enzyme urocanate reductase mediating imidazole propionate production

المؤلفون: Raminta Venskutonytė, Ara Koh, Olof Stenström, Muhammad Tanweer Khan, Annika Lundqvist, Mikael Akke, Fredrik Bäckhed, Karin Lindkvist-Petersson

المصدر: Nature, Nature Communications. 12(1):1-11

الإتاحة: https://ideas.repec.org/a/nat/natcom/v12y2021i1d10.1038_s41467-021-21548-y.html

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Donor metabolic characteristics drive effects of faecal microbiota transplantation on recipient insulin sensitivity, energy expenditure and intestinal transit time

المساهمون: Internal medicine, Graduate School, Vascular Medicine, ACS - Atherosclerosis & ischemic syndromes, ACS - Diabetes & metabolism, AGEM - Digestive immunity, AGEM - Endocrinology, metabolism and nutrition, Experimental Vascular Medicine, 01 Internal and external specialisms, Endocrinology Laboratory, Endocrinology, ACS - Amsterdam Cardiovascular Sciences, Gastroenterology and Hepatology, AGEM - Re-generation and cancer of the digestive system, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism

المصدر: Gut, 502-512. BMJ Publishing Group
STARTPAGE=502;ENDPAGE=512;ISSN=0017-5749;TITLE=Gut
Gut, 69, 502-512. BMJ Publishing Group
Gut
de Groot, P, Scheithauer, T, Bakker, G J, Prodan, A, Levin, E, Khan, M T, Herrema, H, Ackermans, M, Serlie, M J M, de Brauw, M, Levels, J H M, Sales, A, Gerdes, V E, Ståhlman, M, Schimmel, A W M, Dallinga-Thie, G, Bergman, J J, Holleman, F, Hoekstra, J B L, Groen, A, Bäckhed, F & Nieuwdorp, M 2019, ' Donor metabolic characteristics drive effects of faecal microbiota transplantation on recipient insulin sensitivity, energy expenditure and intestinal transit time ', Gut, pp. 502-512 . https://doi.org/10.1136/gutjnl-2019-318320

مصطلحات موضوعية: Male, 0301 basic medicine, Gene Expression, Adipose tissue, intestinal microbiology, Feces, 0302 clinical medicine, Gut Microbiota, Chemokine CCL2, Metabolic Syndrome, Gastroenterology, Fecal Microbiota Transplantation, Middle Aged, Tissue Donors, 3. Good health, diabetes mellitus, medicine.symptom, Adult, medicine.medical_specialty, Lipolysis, Gastric Bypass, Subcutaneous Fat, 030209 endocrinology & metabolism, Inflammation, Carbohydrate metabolism, Bile Acids and Salts, Young Adult, 03 medical and health sciences, Internal medicine, Diabetes mellitus, medicine, Humans, Metabolomics, Resting energy expenditure, gastrointestinal transit, Aged, business.industry, bile acid metabolism, Fatty Acids, Volatile, medicine.disease, Gastrointestinal Microbiome, Glucose, 030104 developmental biology, Endocrinology, Insulin Resistance, Metabolic syndrome, Energy Metabolism, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f7a1d71e31a9aac7809038f0de00e4b
https://doi.org/10.1136/gutjnl-2019-318320

Find this article in full text from ProQuest

6

Dynamics of the normal gut microbiota: A longitudinal one-year population study in Sweden

المؤلفون: Lisa M Olsson, Fredrik Boulund, Staffan Nilsson, Muhammad Tanweer Khan, Anders Gummesson, Linn Fagerberg, Lars Engstrand, Rosie Perkins, Mathias Uhlén, Göran Bergström, Valentina Tremaroli, Fredrik Bäckhed

المصدر: Olsson, L M, Boulund, F, Nilsson, S, Khan, M T, Gummesson, A, Fagerberg, L, Engstrand, L, Perkins, R, Uhlén, M, Bergström, G, Tremaroli, V & Bäckhed, F 2022, ' Dynamics of the normal gut microbiota : A longitudinal one-year population study in Sweden ', Cell Host and Microbe, vol. 30, no. 5, pp. 726-739.e3 . https://doi.org/10.1016/j.chom.2022.03.002
Olsson, L M, Boulund, F, Nilsson, S, Khan, M T, Gummesson, A, Fagerberg, L, Engstrand, L, Perkins, R, Uhlén, M, Bergström, G, Tremaroli, V & Bäckhed, F 2022, ' Dynamics of the normal gut microbiota: A longitudinal one-year population study in Sweden ', Cell Host and Microbe, vol. 30, no. 5, pp. 726-739.e3 . https://doi.org/10.1016/j.chom.2022.03.002

مصطلحات موضوعية: Sweden, gut microbiota, Bacteria, stability, Microbiology, digestive system, healthy microbiota, Gastrointestinal Microbiome, Feces, Enterobacteriaceae, Virology, RNA, Ribosomal, 16S, Proteobacteria, biomarker, Parasitology, Bifidobacterium

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fc3f24fdecdd8007ad7eafd4883eba9
https://pubmed.ncbi.nlm.nih.gov/35349787

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Structural characterization of the microbial enzyme urocanate reductase mediating imidazole propionate production

المؤلفون: Muhammad Tanweer Khan, Fredrik Bäckhed, Karin Lindkvist-Petersson, Raminta Venskutonytė, Annika Lundqvist, Mikael Akke, Ara Koh, Olof Stenström

المصدر: Nature Communications
Venskutonytė, R, Koh, A, Stenström, O, Khan, M T, Lundqvist, A, Akke, M, Bäckhed, F & Lindkvist-Petersson, K 2021, ' Structural characterization of the microbial enzyme urocanate reductase mediating imidazole propionate production ', Nature Communications, vol. 12, no. 1 . https://doi.org/10.1038/s41467-021-21548-y
Nature Communications 12(1), 1347 (2021). doi:10.1038/s41467-021-21548-y
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)

مصطلحات موضوعية: Models, Molecular, Shewanella, Protein Conformation, Science, Metabolite, General Physics and Astronomy, Reductase, Arginine, Ligands, Article, General Biochemistry, Genetics and Molecular Biology, Substrate Specificity, Impaired glucose tolerance, chemistry.chemical_compound, Protein Domains, Catalytic Domain, polycyclic compounds, medicine, Histidine, X-ray crystallography, chemistry.chemical_classification, Bacterial structural biology, Multidisciplinary, biology, Urocanic Acid, Imidazoles, Human microbiome, General Chemistry, biochemical phenomena, metabolism, and nutrition, medicine.disease, enzymes and coenzymes (carbohydrates), Kinetics, Insulin receptor, Enzyme, Biochemistry, chemistry, Mechanism of action, Enzyme mechanisms, Flavin-Adenine Dinucleotide, biology.protein, bacteria, Thermodynamics, ddc:500, medicine.symptom, Oxidoreductases