Výsledky vyhledávání - "Olof H. Sundin"

Akademický článek

The human jejunum has an endogenous microbiota that differs from those in the oral cavity and colon

Autor: Olof H. Sundin, Antonio Mendoza-Ladd, Mingtao Zeng, Diana Diaz-Arévalo, Elisa Morales, B. Matthew Fagan, Javier Ordoñez, Philip Velez, Nishaal Antony, Richard W. McCallum

Publikováno v: BMC Microbiology, Vol 17, Iss 1, Pp 1-17 (2017)

Abstract Background The upper half of the human small intestine, known as the jejunum, is the primary site for absorption of nutrient-derived carbohydrates, amino acids, small peptides, and vitamins. In contrast to the colon, which contains 1011–10

Externí odkaz: https://doaj.org/article/32bd564378664e70a9b8e8e138d2955e

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Investigation of Oral, Gastric, and Duodenal Microbiota in Patients with Upper Gastrointestinal Symptoms

Autor: Majd Michael, Mingtao Zeng, Aden Springer, Burgandy Mendoza, Bo-Young Hong, Hua Guo, Jorge Cervantes, Olof H. Sundin, Richard W. McCallum

Publikováno v: Journal of Investigative Medicine. 69:870-877

Disease-associated alterations of the intestinal microbiota composition, known as dysbiosis, have been well described in several functional gastrointestinal (GI) disorders. Several studies have described alterations in the gastric microbiota in funct

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a685c21db6a7e42796eafbb7404ff3b
https://doi.org/10.1136/jim-2020-001642

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Does a glucose-based hydrogen and methane breath test detect bacterial overgrowth in the jejunum?

Autor: Elisa Morales, Barry M. Fagan, Mingtao Zeng, Javier Ordonez, Diana Diaz-Arévalo, Olof H. Sundin, Antonio Mendoza-Ladd, Richard W. McCallum

Publikováno v: Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society. 30(11)

BACKGROUND Direct diagnosis of small intestinal bacterial overgrowth (SIBO) requires the collection and culture of fluid from the jejunal lumen, with a finding of over 105 viable bacteria per mL. More often, SIBO is diagnosed indirectly, using a non-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a55bbb8e7b838f1af366f1f948ee9d92
https://pubmed.ncbi.nlm.nih.gov/29687525

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The human jejunum has an endogenous microbiota that differs from those in the oral cavity and colon

Autor: Richard W. McCallum, Olof H. Sundin, Antonio Mendoza-Ladd, Philip Velez, Diana Diaz-Arévalo, Javier Ordonez, Elisa Morales, Nishaal Antony, B. Matthew Fagan, Mingtao Zeng

Publikováno v: BMC Microbiology, Vol 17, Iss 1, Pp 1-17 (2017)
BMC Microbiology

Background The upper half of the human small intestine, known as the jejunum, is the primary site for absorption of nutrient-derived carbohydrates, amino acids, small peptides, and vitamins. In contrast to the colon, which contains 1011–1012 colony

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c326c380457a6b19df4deb7d97c85309
https://doi.org/10.1186/s12866-017-1059-6

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A Spontaneous Missense Mutation in Branched Chain Keto Acid Dehydrogenase Kinase in the Rat Affects Both the Central and Peripheral Nervous Systems

Autor: J. Samuel Zigler, Karl W. Broman, Cory Brayton, Megan Wright, Colin A. Hodgkinson, Andrew Klise, David Goldman, Olof H. Sundin, Yuri V. Sergeev, Susumu Mori, Debasish Sinha, Bonnie Patek, Jiao Xaiodong, Fielding Hejtmancik, Nicholas J. Maragakis, Stacey Hose, David Vasquez, Ahmet Hoke, Hao Huang

Publikováno v: PLoS ONE, Vol 11, Iss 7, p e0160447 (2016)
PLoS ONE

A novel mutation, causing a phenotype we named frogleg because its most obvious characteristic is a severe splaying of the hind limbs, arose spontaneously in a colony of Sprague-Dawley rats. Frogleg is a complex phenotype that includes abnormalities

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82b20a194cd0940e8d2496688a774ef6
http://europepmc.org/articles/PMC4966912?pdf=render

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A missense mutation inGUCY2Dacts as a genetic modifier inRPE65-related Leber Congenital Amaurosis

Autor: Ana Luisa Pina, Robert K. Koenekoop, George Theodossiadis, Sharola Dharmaraj, Elias I. Traboulsi, Irene H. Maumenee, Yingying Li, Olof H. Sundin, Eduardo D Silva, Robert Colin Carter, Magali Loyer

Publikováno v: Ophthalmic Genetics. 25:205-217

Leber congenital amaurosis (LCA) is a clinically and genetically heterogeneous severe retinal dystrophy presenting in infancy. To explain the phenotypical variability observed in two affected siblings of a consanguineous pedigree diagnosed with LCA a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f19ded24828dc05defef3a199bcef92
https://doi.org/10.1080/13816810490513451

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Novel membrane frizzled-related protein gene mutation as cause of posterior microphthalmia resulting in high hyperopia with macular folds

Autor: Joke B. G. M. Verheij, Jolien S. Klein Wassink-Ruiter, Rosemarie A. Wasmann, Olof H. Sundin, Elisa Morales, Jan Willem R. Pott

Publikováno v: Acta ophthalmologica, 92(3), 276-281. Wiley

Purpose: We present a genetic and clinical analysis of two sisters, 3 and 4 years of age, with nanophthalmos and macular folds.Methods: Ophthalmological examination, general paediatric examination and molecular genetic analysis of the MFRP gene were

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2942c3785c316d796375f493b4be4d11
https://research.rug.nl/en/publications/f3fa7649-25c7-49b1-83cd-238ee14764c9

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