Duodenal Obstruction research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Duodenal Obstruction 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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15253 Abstracts
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
Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.
Sun Lei, Rommens Johanna M, Corvol Harriet, Li Weili, Li Xin ...
Nature genetics Vol 44(5)
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Date 01 May 2012
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
Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13.
Zielenski J, Corey M, Rozmahel R, Markiewicz D, Aznarez I ...
Nature genetics Vol 22(2)
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Date 01 Jun 1999
Research
Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans.
de Pontual Loïc, Yao Evelyn, Callier Patrick, Faivre Laurence, Drouin Valérie ...
Nature genetics Vol 43(10)
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Date 04 Sep 2011
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
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