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

IL-17A-producing NKp44(-) group 3 innate lymphoid cells accumulate in Familial Adenomatous Polyposis duodenal tissue.

IL-17A 产生 NKp44(-) 组 3 先天性淋巴细胞在家族性腺瘤性息肉病十二指肠组织中积聚

Kaiser Kim M, Raabe Jan, ToVinh Michael, Hack Gudrun, Ahmad Sarah, Müller Niko, Cassella Julia, Walravens Sofia I, Alfaro Paula, Arias Garcia Lauren, Kaczmarek Dominik J, Marwitz Tim, Goeser Felix, Nischalke Hans Dieter, Lutz Philipp, Sommer Nils, Vilz Tim, Toma Marieta, Steiner Susanne, Hommerding Oliver, Oldenburg Johannes, Hölzel Michael, Kadzik Sebastian, Maas Alexander, Eckrich Jonas, Zumfelde Philipp, Shakeri Farhad, Nesic Svetozar, Buness Andreas, De Caro Emilia, Becker Matthias, Beyer Marc D, Ulas Thomas, Aschenbrenner Anna C, Steinheuer Lisa M, Thurley Kevin, Kroh Sandy, Uecker Ralf, Hauser Anja E, Gohr Florian N, Schmidt Florian I, Wang Danni, Held Kathrin, Baranov Olga, Geldmacher Christof, Strassburg Christian P, Hüneburg Robert, Krämer Benjamin, Nattermann Jacob

Comment on "Effectiveness and safety of oral vancomycin for the treatment of inflammatory bowel disease associated with primary sclerosing cholangitis: a systematic review and pooled analysis"

对“口服万古霉素治疗原发性硬化性胆管炎相关炎症性肠病的有效性和安全性:系统评价和汇总分析”的评论

Kellermayer, Richard; Lewindon, Peter; Buness, Cynthia; Tabibian, James; Johnson, Kevin; Shah, Shamita; Dulai, Parambir; Ali, Ahmad H; Shah, Ayesha; Holtmann, Gerald; Winter, Harland S

Retention of ES cell-derived 129S genome drives NLRP1 hypersensitivity and transcriptional deregulation in Nlrp3tm1Flv mice

ES细胞来源的129S基因组的保留导致Nlrp3tm1Flv小鼠中NLRP1超敏反应和转录失调。

Felix D Weiss ,Yubell Alvarez ,Farhad Shakeri ,Anshupa Sahu ,Petro Leka ,Alesja Dernst ,Jessika Rollheiser ,Matilde Vasconcelos ,Adriana Geraci ,Fraser Duthie ,Rainer Stahl ,Hye Eun Lee ,Anne-Kathrin Gellner ,Andreas Buness ,Eicke Latz ,Felix Meissner

Neuropilin2 in Mesenchymal Stromal Cells as a Potential Novel Therapeutic Target in Myelofibrosis

间充质基质细胞中的神经纤毛蛋白2作为骨髓纤维化的潜在新型治疗靶点

Vosbeck, Karla; Förster, Sarah; Mayr, Thomas; Sahu, Anshupa; Haddouti, El-Mustapha; Al-Adilee, Osamah; Körber, Ruth-Miriam; Bisht, Savita; Muders, Michael H; Nesic, Svetozar; Buness, Andreas; Kristiansen, Glen; Schildberg, Frank A; Gütgemann, Ines

An 'Adaptive Treatment Strategy' for Oral Vancomycin in Patients with the Orphan Disease Primary Sclerosing Cholangitis

针对罕见病原发性硬化性胆管炎患者,采用口服万古霉素的“适应性治疗策略”

Shah, Ayesha; Tabibian, James; Buness, Cynthia; Holtmann, Gerald J

Deficiency for SAMHD1 activates MDA5 in a cGAS/STING-dependent manner

SAMHD1 的缺乏以 cGAS/STING 依赖的方式激活 MDA5。

Tina Schumann ,Santiago Costas Ramon ,Nadja Schubert ,Mohamad Aref Mayo ,Melanie Hega ,Katharina Isabell Maser ,Servi-Remzi Ada ,Lukas Sydow ,Mona Hajikazemi ,Markus Badstübner ,Patrick Müller ,Yan Ge ,Farhad Shakeri ,Andreas Buness ,Benjamin Rupf ,Stefan Lienenklaus ,Barbara Utess ,Lina Muhandes ,Michael Haase ,Luise Rupp ,Marc Schmitz ,Thomas Gramberg ,Nicolas Manel ,Gunther Hartmann ,Thomas Zillinger ,Hiroki Kato ,Stefan Bauer ,Alexander Gerbaulet ,Katrin Paeschke ,Axel Roers ,Rayk Behrendt

Genome-wide identification of disease-causing copy number variations in 450 individuals with anorectal malformations

对450名肛门直肠畸形患者进行全基因组致病拷贝数变异鉴定

Fabian, Julia; Dworschak, Gabriel C; Waffenschmidt, Lea; Schierbaum, Luca; Bendixen, Charlotte; Heilmann-Heimbach, Stefanie; Sivalingam, Sugirthan; Buness, Andreas; Schwarzer, Nicole; Boemers, Thomas M; Schmiedeke, Eberhard; Neser, Jörg; Leonhardt, Johannes; Kosch, Ferdinand; Weih, Sandra; Gielen, Helen Maya; Hosie, Stuart; Kabs, Carmen; Palta, Markus; Märzheuser, Stefanie; Bode, Lena Marie; Lacher, Martin; Schäfer, Frank-Mattias; Stehr, Maximilian; Knorr, Christian; Ure, Benno; Kleine, Katharina; Rolle, Udo; Zaniew, Marcin; Phillip, Grote; Zwink, Nadine; Jenetzky, Ekkehart; Reutter, Heiko; Hilger, Alina C

Gene-based burden scores identify rare variant associations for 28 blood biomarkers

基于基因的负担评分可识别28种血液生物标志物的罕见变异关联

Aldisi, Rana; Hassanin, Emadeldin; Sivalingam, Sugirthan; Buness, Andreas; Klinkhammer, Hannah; Mayr, Andreas; Fröhlich, Holger; Krawitz, Peter; Maj, Carlo

NCBench: providing an open, reproducible, transparent, adaptable, and continuous benchmark approach for DNA-sequencing-based variant calling

NCBench:为基于DNA测序的变异检测提供开放、可重复、透明、可适应且持续的基准测试方法

Hanssen, Friederike; Gabernet, Gisela; Bäuerle, Famke; Stöcker, Bianca; Wiegand, Felix; Smith, Nicholas H; Mertes, Christian; Neogi, Avirup Guha; Brandhoff, Leon; Ossowski, Anna; Altmueller, Janine; Becker, Kerstin; Petzold, Andreas; Sturm, Marc; Stöcker, Tyll; Sivalingam, Sugirthan; Brand, Fabian; Schmidt, Axel; Buness, Andreas; Probst, Alexander J; Motameny, Susanne; Köster, Johannes

Oscillatory rheotaxis of artificial swimmers in microchannels

微通道中人工游泳者的振荡趋流性

Dey, Ranabir; Buness, Carola M; Hokmabad, Babak Vajdi; Jin, Chenyu; Maass, Corinna C