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

Distinctive T-cell receptor repertoire in paediatric inflammatory multisystem syndrome temporally associated with coronavirus disease 2019/multisystem inflammatory syndrome in children patients: possible thymus involvement

儿童多系统炎症综合征患者中存在与2019冠状病毒病/儿童多系统炎症综合征暂时相关的独特T细胞受体库:可能与胸腺有关

Yanez, Diana C; Rowell, Jasmine; Woodall, Maximillian; Adams, Stuart; O'Neill, Lauran; Mengrelis, Konstantinos; Lau, Ching-In; Ross, Susan; Benkenstein, Sarah; Plant, Kate; Smith, Claire M; Chain, Benny; Peters, Mark J; Crompton, Tessa

IL-6 inhibition prevents costimulation blockade-resistant allograft rejection in T cell-depleted recipients by promoting intragraft immune regulation in mice

IL-6 抑制可通过促进小鼠移植内免疫调节来预防 T 细胞耗竭受体的共刺激阻断抗性同种异体移植排斥

Moritz Muckenhuber, Konstantinos Mengrelis, Anna Marianne Weijler, Romy Steiner, Verena Kainz, Marlena Buresch, Heinz Regele, Sophia Derdak, Anna Kubetz, Thomas Wekerle

Coupling of a Major Allergen to the Surface of Immune Cells for Use in Prophylactic Cell Therapy for the Prevention of IgE-Mediated Allergy

将主要过敏原结合到免疫细胞表面,用于预防 IgE 介导的过敏症的预防性细胞疗法

Konstantinos Mengrelis, Gerhard Niederacher, Lisa Prickler, Verena Kainz, Anna Marianne Weijler, Elisa Rudolph, Victoria Stanek, Julia Eckl-Dorna, Ulrike Baranyi, Andreas Spittler, Margarete Focke-Tejkl, Barbara Bohle, Rudolf Valenta, Christian Friedrich Wilhelm Becker, Thomas Wekerle, Birgit Linhar

Optimum timing of antithymocyte globulin in relation to adoptive regulatory T cell therapy

抗胸腺球蛋白的最佳给药时机与过继调节性 T 细胞治疗的关系

Moritz Muckenhuber, Jasmin Mucha, Konstantinos Mengrelis, Christopher How, Roman Reindl-Schwaighofer, Andreas Heinzel, Verena Kainz, Nina Worel, Gabriela Berlakovich, Matthias Edinger, Rainer Oberbauer, Thomas Wekerle

Adoptive transfer of allergen-expressing B cells prevents IgE-mediated allergy

表达过敏原的 B 细胞的过继转移可预防 IgE 介导的过敏

Lisa Prickler, Ulrike Baranyi, Konstantinos Mengrelis, Anna Marianne Weijler, Verena Kainz, Bernhard Kratzer, Romy Steiner, Jasmin Mucha, Elisa Rudoph, Nina Pilat, Barbara Bohle, Herbert Strobl, Winfried Franz Pickl, Rudolf Valenta, Birgit Linhart, Thomas Wekerle

T cell phenotype in paediatric heart transplant recipients

儿童心脏移植接受者的 T 细胞表型

Konstantinos Mengrelis, Filip Kucera, Nadia Shahid, Eleanor Watt, Susan Ross, Ching-In Lau, Stuart Adams, Kimberly Gilmour, Dietmar Pils, Tessa Crompton, Michael Burch, E Graham Davies

Sonic Hedgehog Is a Determinant of γδ T-Cell Differentiation in the Thymus

音猬因子是胸腺中γδ T细胞分化的决定因素

Mengrelis, Konstantinos; Lau, Ching-In; Rowell, Jasmine; Solanki, Anisha; Norris, Sonia; Ross, Susan; Ono, Masahiro; Outram, Susan; Crompton, Tessa

Thymus transplantation for complete DiGeorge syndrome: European experience

胸腺移植治疗完全性 DiGeorge 综合征:欧洲经验

E Graham Davies, Melissa Cheung, Kimberly Gilmour, Jesmeen Maimaris, Joe Curry, Anna Furmanski, Neil Sebire, Neil Halliday, Konstantinos Mengrelis, Stuart Adams, Jolanta Bernatoniene, Ronald Bremner, Michael Browning, Blythe Devlin, Hans Christian Erichsen, H Bobby Gaspar, Lizzie Hutchison, Winnie I

Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

SNX14基因突变会导致一种独特的常染色体隐性遗传性小脑共济失调和智力障碍综合征

Zhu, Xiaofeng; Feng, Tao; Tayo, Bamidele O; Liang, Jingjing; Young, J Hunter; Franceschini, Nora; Smith, Jennifer A; Yanek, Lisa R; Sun, Yan V; Edwards, Todd L; Chen, Wei; Nalls, Mike; Fox, Ervin; Sale, Michele; Bottinger, Erwin; Rotimi, Charles; Liu, Yongmei; McKnight, Barbara; Liu, Kiang; Arnett, Donna K; Chakravati, Aravinda; Cooper, Richard S; Redline, Susan; Garber, Kathryn B; Ratzel, Sarah; Cullinan, Sara B; Hansen, Jeanne; Snow, Chelsi; Tuttle, Emily; Ghoneim, Dalia H; Yang, Chun-Song; Spencer, Adam; Gunter, Sonya A; Smyser, Christopher D; Gurnett, Christina A; Shinawi, Marwan; Dobyns, William B; Wheless, James; Halterman, Marc W; Jansen, Laura A; Paschal, Bryce M; Paciorkowski, Alex R; Thomas, Anna C; Williams, Hywel; Setó-Salvia, Núria; Bacchelli, Chiara; Jenkins, Dagan; O’Sullivan, Mary; Mengrelis, Konstantinos; Ishida, Miho; Ocaka, Louise; Chanudet, Estelle; James, Chela; Lescai, Francesco; Anderson, Glenn; Morrogh, Deborah; Ryten, Mina; Duncan, Andrew J; Pai, Yun Jin; Saraiva, Jorge M; Ramos, Fabiana; Farren, Bernadette; Saunders, Dawn; Vernay, Bertrand; Gissen, Paul; Straatmaan-Iwanowska, Anna; Baas, Frank; Wood, Nicholas W; Hersheson, Joshua; Houlden, Henry; Hurst, Jane; Scott, Richard; Bitner-Glindzicz, Maria; Moore, Gudrun E; Sousa, Sérgio B; Stanier, Philip

Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome

SNX14基因突变会导致一种独特的常染色体隐性遗传性小脑共济失调和智力障碍综合征。

Thomas, Anna C; Williams, Hywel; Setó-Salvia, Núria; Bacchelli, Chiara; Jenkins, Dagan; O'Sullivan, Mary; Mengrelis, Konstantinos; Ishida, Miho; Ocaka, Louise; Chanudet, Estelle; James, Chela; Lescai, Francesco; Anderson, Glenn; Morrogh, Deborah; Ryten, Mina; Duncan, Andrew J; Pai, Yun Jin; Saraiva, Jorge M; Ramos, Fabiana; Farren, Bernadette; Saunders, Dawn; Vernay, Bertrand; Gissen, Paul; Straatmaan-Iwanowska, Anna; Baas, Frank; Wood, Nicholas W; Hersheson, Joshua; Houlden, Henry; Hurst, Jane; Scott, Richard; Bitner-Glindzicz, Maria; Moore, Gudrun E; Sousa, Sérgio B; Stanier, Philip