Proctitis research, articles, guidelines & medical evidence database search.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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Research
Segmented Filamentous Bacteria Prevent and Cure Rotavirus Infection.
Shi Zhenda, Zou Jun, Zhang Zhan, Zhao Xu, Noriega Juan ...
Cell Vol 179(3)
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Date 17 Oct 2019
Research
Adrenergic Signaling in Muscularis Macrophages Limits Infection-Induced Neuronal Loss.
Matheis Fanny, Muller Paul A, Graves Christina L, Gabanyi Ilana, Kerner Zachary J ...
Cell Vol 180(1)
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Date 09 Jan 2020
Research
Pathogenic simian immunodeficiency virus infection is associated with expansion of the enteric virome.
Handley Scott A, Thackray Larissa B, Zhao Guoyan, Presti Rachel, Miller Andrew D ...
Cell Vol 151(2)
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Date 12 Oct 2012
Research
Immunoglobulin A coating identifies colitogenic bacteria in inflammatory bowel disease.
Palm Noah W, de Zoete Marcel R, Cullen Thomas W, Barry Natasha A, Stefanowski Jonathan ...
Cell Vol 158(5)
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Date 28 Aug 2014
Research
A mouse model of Salmonella typhi infection.
Mathur Ramkumar, Oh Hyunju, Zhang Dekai, Park Sung-Gyoo, Seo Jin ...
Cell Vol 151(3)
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Date 26 Oct 2012
Research
Yersinia virulence depends on mimicry of host Rho-family nucleotide dissociation inhibitors.
Prehna Gerd, Ivanov Maya I, Bliska James B, Stebbins C Erec
Cell Vol 126(5)
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Date 08 Sep 2006
Research
Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number.
Lyons Jonathan J, Yu Xiaomin, Hughes Jason D, Le Quang T, Jamil Ali ...
Nature genetics Vol 48(12)
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Date 01 Dec 2016
Research
X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
Wildin R S, Ramsdell F, Peake J, Faravelli F, Casanova J L ...
Nature genetics Vol 27(1)
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Date 01 Jan 2001
Research
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
Bennett C L, Christie J, Ramsdell F, Brunkow M E, Ferguson P J ...
Nature genetics Vol 27(1)
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Date 01 Jan 2001
Research
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
Bitner-Glindzicz M, Lindley K J, Rutland P, Blaydon D, Smith V V ...
Nature genetics Vol 26(1)
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Date 01 Sep 2000
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