Výsledky vyhledávání - "Sophie K M, Heinrichs"

First genotype‐phenotype study reveals HLA‐DQβ1 insertion heterogeneity in high‐resolution manometry achalasia subtypes

Autor: Jessica Becker, Timo Hess, Markus M. Nöthen, Stavroula Kanoni, Stefan Niebisch, Ines Gockel, René Thieme, Panos Deloukas, Jan Martinek, Zuzana Vackova, Vitalia Schüller, Nicole Kreuser, Dimitris Theodorou, Johannes Schumacher, Julius Spicak, Sophie K. M. Heinrichs, Michael Knapp, Tania Triantafyllou

Publikováno v: United European Gastroenterology Journal. 7:45-51

BACKGROUND: Achalasia is a primary oesophageal motility disorder. Although aetiology remains mainly unknown, a genetic risk variant, rs28688207 in HLA-DQB1, showed strong achalasia association suggesting involvement of immune-mediated processes in th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d187c6f38654af45fc7c75e49b58a564
https://doi.org/10.1177/2050640618804717

Zobrazit plný text záznamu

Evidence for PTGER4 ,PSCA, and MBOAT7 as risk genes for gastric cancer on the genome and transcriptome level

Autor: Jesús Espinel, Ines Gockel, Daniela Collette, Thomas Schmidt, Gisela Keller, Katja Butterbach, Yogesh K. Vashist, Martin Kruschewski, Michael Knapp, P. Malfertheiner, Anne C. Böhmer, Angel Lanas, Elisabeth Mangold, Rafael Campo, Oliver Pech, Lutz Hamann, Markus Moehler, Jessica Becker, Aksana Höblinger, Jan Gehlen, Concha Thomson, Maria Asuncion Garcia-Gonzalez, Katharina Weise, Peter P. Grimminger, Hakan Alakus, Hermann Brenner, Hans Lippert, Jakob R. Izbicki, Sebastian J. Hofer, Hauke Lang, Evita Gasenko, Philipp Lingohr, Nicole Kreuser, Timo Hess, Fernando Geijo, Markus M. Nöthen, Marino Venerito, Iurii Krasniuk, Florian Lordick, Michael Vieth, Karsten Ridwelski, Claus Schildberg, Alexander F. Hagel, Christiane J. Bruns, Ralf R. Schumann, Katharina Messerle, Lothar Veits, Johannes Schumacher, Katja Ott, Julia Schröder, Marcis Leja, Vitalia Schüller, Limas Kupčinskas, Federico Sopena, Ernst Rodermann, Juozas Kupcinskas, Nikolaos Vassos, Ángeles Pérez-Aisa, Monika Ludwig, Ugne Gyvyte, Luis Bujanda, Sophie K. M. Heinrichs

Publikováno v: Cancer Medicine
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname

Genetic associations between variants on chromosome 5p13 and 8q24 and gastric cancer (GC) have been previously reported in the Asian population. We aimed to replicate these findings and to characterize the associations at the genome and transcriptome

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cec9666338eed5d98bfda531e28ffdd9
https://doi.org/10.1002/cam4.1719

Zobrazit plný text záznamu

The Barrett‐associated variants at GDF 7 and TBX 5 also increase esophageal adenocarcinoma risk

Publikováno v: Cancer Medicine. 5:888-891

Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC) represent two stages within the esophagitis-metaplasia-dysplasia-adenocarcinoma sequence. Previously genetic risk factors have been identified that confer risk to BE and EAC development. Ho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f2913f3d39e3ec190c51e976a9748706
https://doi.org/10.1002/cam4.641

Zobrazit plný text záznamu

Plný text ve formátu HTML

Supportive evidence for FOXP 1 , BARX 1 , and FOXF 1 as genetic risk loci for the development of esophageal adenocarcinoma

Autor: Hans‐Werner Karch, Orestis Lyros, Yogesh K. Vashist, Katja Ott, Grischa Terheggen, Thomas Rösch, Mario Anders, Constantin J. Ahlbrand, Brigitte Schumacher, Dietmar Lorenz, Oliver Pech, Arnulf H. Hölscher, Hendrik Manner, Katharina Weise, Jessica Becker, Lothar Veits, Jan‐Hinnerk Hofer, Ines Gockel, Horst Neuhaus, Markus M. Nöthen, Ralf Kiesslich, Markus Moehler, Bertram Müller-Myhsok, Thomas Schmidt, Michael Vieth, Andreas Hackelsberger, Michael Arras, Sebastian J. Hofer, Elisabeth Mangold, Christian Gerges, Johannes Schumacher, Darina Czamara, Josef Weismüller, Tania Noder, Jakob R. Izbicki, Andrea May, Hauke Lang, Stefanie Heilmann-Heimbach, Timo Hess, Thomas L. Vaughan, Marino Venerito, David C. Whiteman, Elfriede Bollschweiler, Sophie K. M. Heinrichs, Christian Ell, Peter Malfertheiner, Rupert Mayershofer

Publikováno v: Cancer Medicine. 4:1700-1704

The Barrett's and Esophageal Adenocarcinoma Consortium (BEACON) recently performed a genome-wide association study (GWAS) on esophageal adenocarcinoma (EAC) and Barrett's esophagus. They identified genome-wide significant association for variants at

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eec85112ae756697ac40deeaf5dabb96
https://doi.org/10.1002/cam4.500

Zobrazit plný text záznamu

Plný text ve formátu HTML

Evidence for PTGER4, PSCA and MBOAT7 as risk genes for gastric cancer on the genome and transcriptome level

Publikováno v: 72. Jahrestagung der Deutschen Gesellschaft für Gastroenterologie, Verdauungs- und Stoffwechselkrankheiten mit Sektion Endoskopie – 11. Herbsttagung der Deutschen Gesellschaft für Allgemein- und Viszeralchirurgie gemeinsam mit den Arbeitsgemeinschaften der DGAV.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::375c129953ee4e554b0e8fec1f908b19
https://doi.org/10.1055/s-0037-1604759

Zobrazit plný text záznamu

Erste Genotyp – Phänotyp Analyse bei Achalasiepatienten zur Korrelation der HLA-DQB1-Inseration mit den 3 Subtypen der Chicaogo-Klassifikation

Autor: René Thieme, D Theodorou, Sophie K. M. Heinrichs, Timo Hess, Z Vackova, Vitalia Schüller, Nicole Kreuser, J Spicak, J Scheuermann, K Kosiol, T Triantafilou, Stefan Niebisch, J Martinek, Michael Knapp, Ines Gockel, J Becker, M. M. Nöthen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d2365ceff24ea1ae604c9f2caedbba46
https://doi.org/10.1055/s-0037-1604735

Zobrazit plný text záznamu

The Barrett-associated variants at GDF7 and TBX5 also increase esophageal adenocarcinoma risk

Publikováno v: Cancer Medicine

Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC) represent two stages within the esophagitis‐metaplasia‐dysplasia‐adenocarcinoma sequence. Previously genetic risk factors have been identified that confer risk to BE and EAC developme

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::504a2c655fca18a8500d5fc58d54dd3f
https://pubmed.ncbi.nlm.nih.gov/26783083

Zobrazit plný text záznamu

First Genotype-Phenotype Study in Achalasia Implies that the HLA-DQB1-Insertion Affects Different High-Resolution Manometry (HRM) Manifestation of the Disease

Autor: Jessica Becker, Michael Knapp, Timo Hess, Jan Martinek, Markus M. Nöthen, Nicole Kreuser, Dimitris Theodorou, Ines Gockel, Tania Triantafilou, Johannes Schumacher, Sophie K. M. Heinrichs, Zuzana Vackova, Vitalia Schüller, Stefan Niebisch, Julius Spicak, Nils Kosiol

Publikováno v: Gastroenterology. 152:S175

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7f436a78774bf5d753837640f86ead38
https://doi.org/10.1016/s0016-5085(17)30901-0

Zobrazit plný text záznamu

241 Association of the HLA-DQB1-insertion in Idiopathic Achalasia and First Genotype-Phenotype (GxP) Study Using High-Resolution Manometry Data

Autor: Ines Gockel, Johannes Schumacher, Zuzana Vackova, Stefan Niebisch, Sophie K. M. Heinrichs, Nicole Kreuser, Julius Spicak, Nils Kosiol, Markus M. Nöthen, Jan Martinek, Vitalia Schüller, Timo Hess, Jessica Becker

Publikováno v: Gastroenterology. 150:S58

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::203c7e1653945fac767b5f90bf248b81
https://doi.org/10.1016/s0016-5085(16)30315-8

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání