Intestinal Volvulus 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 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
Generation of superhelical torsion by ATP-dependent chromatin remodeling activities.
Havas K, Flaus A, Phelan M, Kingston R, Wade P A ...
Cell Vol 103(7)
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Date 22 Dec 2000
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
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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
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
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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
Production of a severe cystic fibrosis mutation in mice by gene targeting.
Ratcliff R, Evans M J, Cuthbert A W, MacVinish L J, Foster D ...
Nature genetics Vol 4(1)
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Date 01 May 1993
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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