Esophageal Achalasia research, articles, guidelines & medical evidence database search.
Access the latest scientific research and medical evidence related to Esophageal Achalasia 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 20 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
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
Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.
Gockel Ines, Becker Jessica, Wouters Mira M, Niebisch Stefan, Gockel Henning R ...
Nature genetics Vol 46(8)
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Date 01 Aug 2014
Research
Mutant WD-repeat protein in triple-A syndrome.
Tullio-Pelet A, Salomon R, Hadj-Rabia S, Mugnier C, de Laet M H ...
Nature genetics Vol 26(3)
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Date 01 Nov 2000
Research
Mutations in NNT encoding nicotinamide nucleotide transhydrogenase cause familial glucocorticoid deficiency.
Meimaridou Eirini, Kowalczyk Julia, Guasti Leonardo, Hughes Claire R, Wagner Florian ...
Nature genetics Vol 44(7)
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Date 27 May 2012
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
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
Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases.
Lenz Tobias L, Deutsch Aaron J, Han Buhm, Hu Xinli, Okada Yukinori ...
Nature genetics Vol 47(9)
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Date 01 Sep 2015
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