日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Serotonin type 3 receptor subunit gene polymorphisms associated with psychosomatic symptoms in irritable bowel syndrome: A multicenter retrospective study

血清素3型受体亚基基因多态性与肠易激综合征的心身症状相关:一项多中心回顾性研究

Berens, Sabrina; Dong, Yuanjun; Fritz, Nikola; Walstab, Jutta; D'Amato, Mauro; Zheng, Tenghao; Wahl, Verena; Boekstegers, Felix; Bermejo, Justo Lorenzo; Martinez, Cristina; Schmitteckert, Stefanie; Clevers, Egbert; Engel, Felicitas; Gauss, Annika; Herzog, Wolfgang; Spiller, Robin; Goebel-Stengel, Miriam; Mönnikes, Hubert; Andresen, Viola; Thomas, Frieling; Keller, Jutta; Pehl, Christian; Stein-Thöringer, Christoph; Clarke, Gerard; Dinan, Timothy G; Quigley, Eamonn M; Sayuk, Gregory; Simrén, Magnus; Tesarz, Jonas; Rappold, Gudrun; van Oudenhove, Lukas; Schaefert, Rainer; Niesler, Beate

The serotonin receptor 3E variant is a risk factor for female IBS-D

血清素受体3E变异体是女性腹泻型肠易激综合征(IBS-D)的风险因素。

Fritz, Nikola; Berens, Sabrina; Dong, Yuanjun; Martínez, Cristina; Schmitteckert, Stefanie; Houghton, Lesley A; Goebel-Stengel, Miriam; Wahl, Verena; Kabisch, Maria; Götze, Dorothea; D'Amato, Mauro; Zheng, Tenghao; Röth, Ralph; Mönnikes, Hubert; Tesarz, Jonas; Engel, Felicitas; Gauss, Annika; Raithel, Martin; Andresen, Viola; Keller, Jutta; Frieling, Thomas; Pehl, Christian; Stein-Thöringer, Christoph; Clarke, Gerard; Kennedy, Paul J; Cryan, John F; Dinan, Timothy G; Quigley, Eamonn M M; Spiller, Robin; Beltrán, Caroll; Madrid, Ana María; Torres, Verónica; Mayer, Emeran A; Sayuk, Gregory; Gazouli, Maria; Karamanolis, George; Bustamante, Mariona; Estivil, Xavier; Rabionet, Raquel; Hoffmann, Per; Nöthen, Markus M; Heilmann-Heimbach, Stefanie; Schmidt, Börge; Franke, André; Lieb, Wolfgang; Herzog, Wolfgang; Boeckxstaens, Guy; Wouters, Mira M; Simrén, Magnus; Rappold, Gudrun A; Vicario, Maria; Santos, Javier; Schaefert, Rainer; Lorenzo-Bermejo, Justo; Niesler, Beate

Parkinson mice show functional and molecular changes in the gut long before motoric disease onset

帕金森病小鼠在运动障碍发作前很久,肠道就表现出功能和分子水平的变化。

Gries, Manuela; Christmann, Anne; Schulte, Steven; Weyland, Maximilian; Rommel, Stephanie; Martin, Monika; Baller, Marko; Röth, Ralph; Schmitteckert, Stefanie; Unger, Marcus; Liu, Yang; Sommer, Frederik; Mühlhaus, Timo; Schroda, Michael; Timmermans, Jean-Pierre; Pintelon, Isabel; Rappold, Gudrun A; Britschgi, Markus; Lashuel, Hilal; Menger, Michael D; Laschke, Matthias W; Niesler, Beate; Schäfer, Karl-Herbert

Emerging evidence for gene mutations driving both brain and gut dysfunction in autism spectrum disorder

越来越多的证据表明,基因突变会导致自闭症谱系障碍患者的大脑和肠道功能障碍。

Niesler, Beate; Rappold, Gudrun A

The alternative serotonin transporter promoter P2 impacts gene function in females with irritable bowel syndrome

替代血清素转运体启动子P2影响患有肠易激综合征女性的基因功能

Mohr, Sandra; Fritz, Nikola; Hammer, Christian; Martínez, Cristina; Berens, Sabrina; Schmitteckert, Stefanie; Wahl, Verena; Schmidt, Malin; Houghton, Lesley A; Goebel-Stengel, Miriam; Kabisch, Maria; Götze, Dorothea; Milovač, Irina; D'Amato, Mauro; Zheng, Tenghao; Röth, Ralph; Mönnikes, Hubert; Engel, Felicitas; Gauss, Annika; Tesarz, Jonas; Raithel, Martin; Andresen, Viola; Frieling, Thomas; Keller, Jutta; Pehl, Christian; Stein-Thöringer, Christoph; Clarke, Gerard; Kennedy, Paul J; Cryan, John F; Dinan, Timothy G; Quigley, Eamonn M M; Spiller, Robin; Beltrán, Caroll; Madrid, Ana María; Torres, Verónica; Pérez de Arce, Edith; Herzog, Wolfgang; Mayer, Emeran A; Sayuk, Gregory; Gazouli, Maria; Karamanolis, George; Kapur-Pojskič, Lejla; Bustamante, Mariona; Rabionet, Raquel; Estivil, Xavier; Franke, André; Lieb, Wolfgang; Boeckxstaens, Guy; Wouters, Mira M; Simrén, Magnus; Rappold, Gudrun A; Vicario, Maria; Santos, Javier; Schaefert, Rainer; Lorenzo-Bermejo, Justo; Niesler, Beate

A complementary study approach unravels novel players in the pathoetiology of Hirschsprung disease

一项补充性研究方法揭示了先天性巨结肠症发病机制中的新因素。

Mederer, Tanja; Schmitteckert, Stefanie; Volz, Julia; Martínez, Cristina; Röth, Ralph; Thumberger, Thomas; Eckstein, Volker; Scheuerer, Jutta; Thöni, Cornelia; Lasitschka, Felix; Carstensen, Leonie; Günther, Patrick; Holland-Cunz, Stefan; Hofstra, Robert; Brosens, Erwin; Rosenfeld, Jill A; Schaaf, Christian P; Schriemer, Duco; Ceccherini, Isabella; Rusmini, Marta; Tilghman, Joseph; Luzón-Toro, Berta; Torroglosa, Ana; Borrego, Salud; Sze-Man Tang, Clara; Garcia-Barceló, Mercè; Tam, Paul; Paramasivam, Nagarajan; Bewerunge-Hudler, Melanie; De La Torre, Carolina; Gretz, Norbert; Rappold, Gudrun A; Romero, Philipp; Niesler, Beate

Molecular Characterization of Embryonic Stem Cell-Derived Cardiac Neural Crest-Like Cells Revealed a Spatiotemporal Expression of an Mlc-3 Isoform

对胚胎干细胞来源的心脏神经嵴样细胞的分子表征揭示了Mlc-3亚型的时空表达

Schmitteckert, Stefanie; Ziegler, Cornelia; Rappold, Gudrun A; Niesler, Beate; Rolletschek, Alexandra

Patients with Multiple Functional Gastrointestinal Disorders (FGIDs) Show Increased Illness Severity: A Cross-Sectional Study in a Tertiary Care FGID Specialty Clinic

一项在三级功能性胃肠疾病专科诊所开展的横断面研究表明,患有多种功能性胃肠疾病(FGID)的患者病情更为严重。

Berens, Sabrina; Engel, Felicitas; Gauss, Annika; Tesarz, Jonas; Herzog, Wolfgang; Niesler, Beate; Stroe-Kunold, Esther; Schaefert, Rainer

Gastrointestinal dysfunction in autism displayed by altered motility and achalasia in Foxp1(+/-) mice

Foxp1(+/-)小鼠表现出自闭症患者的胃肠功能障碍,包括运动异常和贲门失弛症。

Fröhlich, Henning; Kollmeyer, Marie Luise; Linz, Valerie Catherine; Stuhlinger, Manuel; Groneberg, Dieter; Reigl, Amelie; Zizer, Eugen; Friebe, Andreas; Niesler, Beate; Rappold, Gudrun

Abnormalities of mucosal serotonin metabolism and 5-HT(3) receptor subunit 3C polymorphism in irritable bowel syndrome with diarrhoea predict responsiveness to ondansetron

肠易激综合征伴腹泻患者的黏膜血清素代谢异常和5-HT(3)受体亚基3C多态性可预测其对昂丹司琼的反应性

Gunn, David; Garsed, Klara; Lam, Ching; Singh, Gulzar; Lingaya, Melanie; Wahl, Verena; Niesler, Beate; Henry, Amanda; Hall, Ian P; Whorwell, Peter; Spiller, Robin