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47 results for Constriction,+Pathologic+-+genetics

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ArticlesPeer ReviewedFull Text
Integrating next-generation sequencing to endoscopic retrograde cholangiopancreatography (ERCP)-obtained biliary specimens improves the detection and management of patients with malignant bile duct st...
Author / Creator:Singhi, Aatur D ; Nikiforova, Marina N ; Chennat, Jennifer ; Papachristou, Georgios I ; Khalid, Asif ; Rabinovitz, Mordechai ; Das, Rohit ; Sarkaria, Savreet ; Ayasso, M Samir ; Wald, Abigail I ; Monaco, Sara E ; Nalesnik, Michael ; Ohori, N Paul ; Geller, David ; Tsung, Allan ; Zureikat, Amer H ; Zeh, Herbert ; Marsh, J Wallis ; Hogg, Melissa ; Lee, Kenneth ; Bartlett, David L ; Pingpank, James F ; Humar, Abhinav ; Bahary, Nathan ; Dasyam, Anil K ; Brand, Randall ; Fasanella, Kenneth E ; McGrath, Kevin ; Slivka, Adam
Publisher:England: BMJ Publishing Group LTD
Journal title:Gut, 2020-01, Vol.69 (1), p.52-61
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Fibrosis-Related microRNAs in Crohn's Disease with Fibrostenosis and Inflammatory Stenosis
Author / Creator:Jerala, Miha ; Remic, Tinkara ; Hauptman, Nina ; Zidar, Nina
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-08, Vol.25 (16), p.8826
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Diagnostic utility of quantitative analysis of microRNA in bile samples obtained during endoscopic retrograde cholangiopancreatography for malignant biliary strictures
Author / Creator:Kuniyoshi, Noriyuki ; Imazu, Hiroo ; Masuzaki, Ryota ; Yamazaki, Motomi ; Hamana, Suguru ; Nomura, Shuzo ; Hayama, Jo ; Osawa, Rota ; Yamada, Koji ; Fujisawa, Mariko ; Saito, Kei ; Kogure, Hirofumi
Publisher:United States: Public Library of Science
Journal title:PloS one, 2023-08, Vol.18 (8), p.e0289537-e0289537
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The Prognostic Power of the NOD2 Genotype for Complicated Crohn's Disease: A Meta-Analysis
Author / Creator:ADLER, Jeremy ; RANGWALLA, Sujal C ; DWAMENA, Ben A ; HIGGINS, Peter D. R
Publisher:Basingstoke: Nature Publishing Group
Journal title:The American journal of gastroenterology, 2011-04, Vol.106 (4), p.699-712
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Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease
Author / Creator:Preuss, Christoph ; Capredon, Melanie ; Wünnemann, Florian ; Chetaille, Philippe ; Prince, Andrea ; Godard, Beatrice ; Leclerc, Severine ; Sobreira, Nara ; Ling, Hua ; Awadalla, Philip ; Thibeault, Maryse ; Khairy, Paul ; Samuels, Mark E ; Andelfinger, Gregor
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2016-10, Vol.12 (10), p.e1006335
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Implementing Massive Parallel Sequencing into Biliary Samples Obtained through Endoscopic Retrograde Cholangiopancreatography for Diagnosing Malignant Bile Duct Strictures
Author / Creator:Park, Wonsuk ; Gwack, Jin ; Park, Joonhong
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-09, Vol.25 (17), p.9461
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Low Serum Levels of MicroRNA-19 Are Associated with a Stricturing Crohn's Disease Phenotype
Author / Creator:Lewis, Amy ; Mehta, Shameer ; Hanna, Luke N. ; Rogalski, Laura A. ; Jeffery, Rosemary ; Nijhuis, Anke ; Kumagai, Tomoko ; Biancheri, Paolo ; Bundy, Jake G. ; Bishop, Cleo L. ; Feakins, Roger ; Di Sabatino, Antonio ; Lee, James C. ; Lindsay, James O. ; Silver, Andrew
Publisher:Oxford, UK: Oxford University Press
Journal title:Inflammatory bowel diseases, 2015-08, Vol.21 (8), p.1926-1934
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Crohn’s disease–related single nucleotide polymorphisms are associated with ileal pouch afferent limb stenosis
Author / Creator:O’Brien, Stephen J. ; Hallion, Jacob ; Scheurlen, Katharina M. ; Fiechter, Casey ; Burton, James ; Paas, Mason ; Schmidt, Miranda ; Gardner, Sarah ; Eichenberger, Maurice R. ; Pan, Jianmin ; Rai, Shesh ; Galandiuk, Susan
Publisher:New York: Springer US
Journal title:Journal of gastrointestinal surgery, 2021-09, Vol.25 (9), p.2377-2386
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ArticlesPeer ReviewedFull Text
Genome-Wide Association Study of Intracranial Artery Stenosis Followed by Phenome-Wide Association Study
Author / Creator:Dofuku, Shogo ; Sonehara, Kyuto ; Miyawaki, Satoru ; Sakaue, Saori ; Imai, Hideaki ; Shimizu, Masahiro ; Hongo, Hiroki ; Shinya, Yuki ; Ohara, Kenta ; Teranishi, Yu ; Okano, Atsushi ; Ono, Hideaki ; Nakatomi, Hirofumi ; Teraoka, Akira ; Yamamoto, Kenichi ; Maeda, Yuichi ; Nii, Takuro ; Kishikawa, Toshihiro ; Suzuki, Ken ; Hirata, Jun ; Takahashi, Meiko ; Matsuda, Koichi ; Kumanogoh, Atsushi ; Matsuda, Fumihiko ; Okada, Yukinori ; Saito, Nobuhito
Publisher:New York: Springer US
Journal title:Translational stroke research, 2023-06, Vol.14 (3), p.322-333
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ArticlesPeer ReviewedFull Text
Heterozygous variant in FGFR3 underlying severe phenotypes in the second trimester: a case report
Author / Creator:Chen, Shujun ; Dong, Hongmei ; Luo, Yong ; Zhang, Yingpin ; Li, Pan
Publisher:England: BioMed Central Ltd
Journal title:BMC medical genomics, 2023-04, Vol.16 (1), p.80-80, Article 80
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ArticlesPeer ReviewedFull Text
β-elemene alleviates airway stenosis via the ILK/Akt pathway modulated by MIR143HG sponging miR-1275
Author / Creator:Zhang, Guoying ; Xue, Cheng ; Zeng, Yiming
Publisher:England: BioMed Central
Journal title:Cellular & molecular biology letters, 2021-06, Vol.26 (1), p.28-28, Article 28
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ArticlesPeer ReviewedFull Text
Chronic enteropathy associated with SLCO2A1 from North India: a rare monogenic condition mimicking Crohn’s disease
Author / Creator:Prasad, Gaurav ; Kulkarni, Kaushal ; Dhua, Anjan Kumar ; Malik, Rohan
Publisher:England: BMJ Publishing Group Ltd
Journal title:BMJ case reports, 2025-01, Vol.18 (1), p.e263684
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ArticlesPeer ReviewedFull Text
Prevalence of RNF213 variants in symptomatic intracranial arterial stenosis/occlusion in China
Author / Creator:Sun, Xunsha ; Luo, Man ; Li, Jiaoxing ; Lai, Rong ; Lin, Jing ; Wang, Yufang ; Xu, Xiaowei ; Wu, Shaoqing ; Sheng, Wenli
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Molecular genetics and genomics : MGG, 2020-05, Vol.295 (3), p.635-643
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The direct and sustained consequences of severe placental hypoxia on vascular contractility
Author / Creator:Vangrieken, Philippe ; Al-Nasiry, Salwan ; Janssen, Ger M J ; Weseler, Antje R ; Spaanderman, Marc E ; Bast, Aalt ; Schiffers, Paul M H
Publisher:United States: Public Library of Science
Journal title:PloS one, 2018-08, Vol.13 (8), p.e0202648-e0202648
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Transcriptional Profiling of Normal, Stenotic, and Regurgitant Human Aortic Valves
Author / Creator:Greene, Christina L ; Jaatinen, Kevin J ; Wang, Hanjay ; Koyano, Tiffany K ; Bilbao, Mary S ; Woo, Y Joseph
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2020-07, Vol.11 (7), p.789
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Detailed phenotype of RNF213 p.R4810K variant identified by the Chinese patients with acute ischaemic stroke or transient ischaemic attack
Author / Creator:Zhou, Hongyu ; Jing, Jing ; Pu, Yuehua ; Li, Wei ; Meng, Xia ; Wang, Anxin ; Zuo, Yingting ; Xu, Zhe ; Xu, Qin ; Suo, Yue ; Li, Hao ; Wang, Yongjun
Publisher:England: BMJ Publishing Group Ltd
Journal title:Stroke and vascular neurology, 2023-12, Vol.8 (6), p.503-510
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The double face of miR-320: cardiomyocytes-derived miR-320 deteriorated while fibroblasts-derived miR-320 protected against heart failure induced by transverse aortic constriction
Author / Creator:Zhang, Xudong ; Yuan, Shuai ; Li, Huaping ; Zhan, Jiabing ; Wang, Feng ; Fan, Jiahui ; Nie, Xiang ; Wang, Yan ; Wen, Zheng ; Chen, Yanghui ; Chen, Chen ; Wang, Dao Wen
Publisher:London: Nature Publishing Group UK
Journal title:Signal transduction and targeted therapy, 2021-02, Vol.6 (1), p.69-69, Article 69
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Hypoxic Gene Expression of Donor Bronchi Linked to Airway Complications after Lung Transplantation
Author / Creator:Kraft, Bryan D ; Suliman, Hagir B ; Colman, Eli C ; Mahmood, Kamran ; Hartwig, Matthew G ; Piantadosi, Claude A ; Shofer, Scott L
Publisher:United States: American Thoracic Society
Journal title:American journal of respiratory and critical care medicine, 2016-03, Vol.193 (5), p.552-560
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Global microRNA profiles and signaling pathways in the development of cardiac hypertrophy
Author / Creator:Feng, H J ; Ouyang, W ; Liu, J H ; Sun, Y G ; Hu, R ; Huang, L H ; Xian, J L ; Jing, C F ; Zhou, M J
Publisher:Brazil: Associacao Brasileira de Divulgacao Cientifica (ABDC)
Journal title:Brazilian journal of medical and biological research, 2014-05, Vol.47 (5), p.361-368
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Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review
Author / Creator:Liao, Xin ; Deng, Jing ; Dai, Wenjie ; Zhang, Tong ; Yan, Junxia
Publisher:England: Komiyama Printing Co., Ltd
Journal title:Environmental health and preventive medicine, 2017-11, Vol.22 (1), p.75-75, Article 75
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Integrating next-generation sequencing to endoscopic retrograde cholangiopancreatography (ERCP)-obtained biliary specimens improves the detection and management of patients with malignant bile duct st...

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Fibrosis-Related microRNAs in Crohn's Disease with Fibrostenosis and Inflammatory Stenosis

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Diagnostic utility of quantitative analysis of microRNA in bile samples obtained during endoscopic retrograde cholangiopancreatography for malignant biliary strictures

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The Prognostic Power of the NOD2 Genotype for Complicated Crohn's Disease: A Meta-Analysis

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Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease

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Implementing Massive Parallel Sequencing into Biliary Samples Obtained through Endoscopic Retrograde Cholangiopancreatography for Diagnosing Malignant Bile Duct Strictures

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Low Serum Levels of MicroRNA-19 Are Associated with a Stricturing Crohn's Disease Phenotype

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Crohn’s disease–related single nucleotide polymorphisms are associated with ileal pouch afferent limb stenosis

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Genome-Wide Association Study of Intracranial Artery Stenosis Followed by Phenome-Wide Association Study

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Heterozygous variant in FGFR3 underlying severe phenotypes in the second trimester: a case report

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β-elemene alleviates airway stenosis via the ILK/Akt pathway modulated by MIR143HG sponging miR-1275

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Chronic enteropathy associated with SLCO2A1 from North India: a rare monogenic condition mimicking Crohn’s disease

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Prevalence of RNF213 variants in symptomatic intracranial arterial stenosis/occlusion in China

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The direct and sustained consequences of severe placental hypoxia on vascular contractility

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Transcriptional Profiling of Normal, Stenotic, and Regurgitant Human Aortic Valves

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Detailed phenotype of RNF213 p.R4810K variant identified by the Chinese patients with acute ischaemic stroke or transient ischaemic attack

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The double face of miR-320: cardiomyocytes-derived miR-320 deteriorated while fibroblasts-derived miR-320 protected against heart failure induced by transverse aortic constriction

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Hypoxic Gene Expression of Donor Bronchi Linked to Airway Complications after Lung Transplantation

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Global microRNA profiles and signaling pathways in the development of cardiac hypertrophy

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Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review

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