Gastroesophageal Reflux research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Gastroesophageal Reflux 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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17181 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
An Airway Protection Program Revealed by Sweeping Genetic Control of Vagal Afferents.
Prescott Sara L, Umans Benjamin D, Williams Erika K, Brust Rachael D, Liberles Stephen D
Cell Vol 181(3)
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Date 30 Apr 2020
Research
Residual embryonic cells as precursors of a Barrett's-like metaplasia.
Wang Xia, Ouyang Hong, Yamamoto Yusuke, Kumar Pooja Ashok, Wei Tay Seok ...
Cell Vol 145(7)
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Date 24 Jun 2011
Research
Mutations in MEGF10, a regulator of satellite cell myogenesis, cause early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD).
Logan Clare V, Lucke Barbara, Pottinger Caroline, Abdelhamed Zakia A, Parry David A ...
Nature genetics Vol 43(12)
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Date 20 Nov 2011
Research
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.
Su Zhan, Gay Laura J, Strange Amy, Palles Claire, Band Gavin ...
Nature genetics Vol 44(10)
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Date 01 Oct 2012
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
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
Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22.
Quaderi N A, Schweiger S, Gaudenz K, Franco B, Rugarli E I ...
Nature genetics Vol 17(3)
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Date 01 Nov 1997
Research
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.
Xiao S, Yu C, Chou X, Yuan W, Wang Y ...
Nature genetics Vol 27(2)
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Date 01 Feb 2001
Research
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy.
Brais B, Bouchard J P, Xie Y G, Rochefort D L, Chrétien N ...
Nature genetics Vol 18(2)
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Date 01 Feb 1998
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