Peptic Ulcer research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Peptic Ulcer treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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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
A tyrosine-based signal targets H/K-ATPase to a regulated compartment and is required for the cessation of gastric acid secretion.
Courtois-Coutry N, Roush D, Rajendran V, McCarthy J B, Geibel J ...
Cell Vol 90(3)
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Date 08 Aug 1997
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
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
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
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
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
Research
Diet and the evolution of human amylase gene copy number variation.
Perry George H, Dominy Nathaniel J, Claw Katrina G, Lee Arthur S, Fiegler Heike ...
Nature genetics Vol 39(10)
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Date 01 Oct 2007
Research
Keap1-null mutation leads to postnatal lethality due to constitutive Nrf2 activation.
Wakabayashi Nobunao, Itoh Ken, Wakabayashi Junko, Motohashi Hozumi, Noda Shuhei ...
Nature genetics Vol 35(3)
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Date 01 Nov 2003
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