Access the latest scientific research and medical evidence related to Esophageal Fistula 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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29208 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
A spatially-organized multicellular innate immune response in lymph nodes limits systemic pathogen spread.
Kastenmüller Wolfgang, Torabi-Parizi Parizad, Subramanian Naeha, Lämmermann Tim, Germain Ronald N
Cell Vol 150(6)
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Date 14 Sep 2012
Research
A rare variant in MYH6 is associated with high risk of sick sinus syndrome.
Holm Hilma, Gudbjartsson Daniel F, Sulem Patrick, Masson Gisli, Helgadottir Hafdis Th ...
Nature genetics Vol 43(4)
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Date 06 Mar 2011
Research
Essential function of Gli2 and Gli3 in the formation of lung, trachea and oesophagus.
Motoyama J, Liu J, Mo R, Ding Q, Post M ...
Nature genetics Vol 20(1)
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Date 01 Sep 1998
Research
Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs.
Salmon Hillbertz Nicolette H C, Isaksson Magnus, Karlsson Elinor K, Hellmén Eva, Pielberg Gerli Rosengren ...
Nature genetics Vol 39(11)
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Date 01 Nov 2007
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
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
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis.
Kristjansson Ragnar P, Benonisdottir Stefania, Davidsson Olafur B, Oddsson Asmundur, Tragante Vinicius ...
Nature genetics Vol 51(2)
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Date 01 Feb 2019
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
An allelic series of miR-17 ∼ 92-mutant mice uncovers functional specialization and cooperation among members of a microRNA polycistron.
Han Yoon-Chi, Vidigal Joana A, Mu Ping, Yao Evelyn, Singh Irtisha ...
Nature genetics Vol 47(7)
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Date 01 Jul 2015
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