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

Plasma proteomic profile reveals persistent immune activation in post-acute sequelae of SARS-CoV-2 infection

血浆蛋白质组学分析揭示了SARS-CoV-2感染急性后遗症中持续存在的免疫激活。

Fineschi, Serena; Klar, Joakim; Schuster, Jens; Bergquist, Jonas; Dahl, Niklas

Comprehensive transcriptome assessment in PBMCs of post-COVID patients at a median follow-up of 28 months after a mild COVID infection reveals upregulation of JAK/STAT signaling and a prolonged immune response.

对 COVID 后患者在轻度 COVID 感染后平均随访 28 个月时进行 PBMC 的全面转录组评估显示,JAK/STAT 信号上调和免疫反应延长

Fineschi Serena, Klar Joakim, Lopez Egido Juan Ramon, Schuster Jens, Bergquist Jonas, Kaden René, Dahl Niklas

Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy

NCDN基因的单等位基因和双等位基因变异会导致神经发育迟缓、智力障碍和癫痫。

Fatima, Ambrin; Hoeber, Jan; Schuster, Jens; Koshimizu, Eriko; Maya-Gonzalez, Carolina; Keren, Boris; Mignot, Cyril; Akram, Talia; Ali, Zafar; Miyatake, Satoko; Tanigawa, Junpei; Koike, Takayoshi; Kato, Mitsuhiro; Murakami, Yoshiko; Abdullah, Uzma; Ali, Muhammad Akhtar; Fadoul, Rein; Laan, Loora; Castillejo-López, Casimiro; Liik, Maarika; Jin, Zhe; Birnir, Bryndis; Matsumoto, Naomichi; Baig, Shahid M; Klar, Joakim; Dahl, Niklas

ZEB2 haploinsufficient Mowat-Wilson syndrome induced pluripotent stem cells show disrupted GABAergic transcriptional regulation and function

ZEB2单倍体不足的Mowat-Wilson综合征诱导多能干细胞表现出GABA能转录调控和功能紊乱

Schuster, Jens; Klar, Joakim; Khalfallah, Ayda; Laan, Loora; Hoeber, Jan; Fatima, Ambrin; Sequeira, Velin Marita; Jin, Zhe; Korol, Sergiy V; Huss, Mikael; Nordgren, Ann; Anderlid, Britt Marie; Gallant, Caroline; Birnir, Bryndis; Dahl, Niklas

DNA methylation profiling allows for characterization of atrial and ventricular cardiac tissues and hiPSC-CMs

DNA 甲基化分析可用于表征心房和心室心脏组织以及 hiPSC-CM

Kirstin Hoff, Marta Lemme, Anne-Karin Kahlert, Kerstin Runde, Enrique Audain, Dorit Schuster, Jens Scheewe, Tim Attmann, Thomas Pickardt, Almuth Caliebe, Reiner Siebert, Hans-Heiner Kramer, Hendrik Milting, Arne Hansen, Ole Ammerpohl, Marc-Phillip Hitz3

Altered paracellular cation permeability due to a rare CLDN10B variant causes anhidrosis and kidney damage

一种罕见的CLDN10B变异导致细胞旁阳离子通透性改变,进而引起无汗症和肾损伤。

Klar, Joakim; Piontek, Jörg; Milatz, Susanne; Tariq, Muhammad; Jameel, Muhammad; Breiderhoff, Tilman; Schuster, Jens; Fatima, Ambrin; Asif, Maria; Sher, Muhammad; Mäbert, Katrin; Fromm, Anja; Baig, Shahid M; Günzel, Dorothee; Dahl, Niklas

5'UTR variants of ribosomal protein S19 transcript determine translational efficiency: implications for Diamond-Blackfan anemia and tissue variability

核糖体蛋白S19转录本的5'UTR变体决定翻译效率:对Diamond-Blackfan贫血和组织变异性的影响

Badhai, Jitendra; Schuster, Jens; Gidlöf, Olof; Dahl, Niklas

Strong Maternal Khoisan Contribution to the South African Coloured Population: A Case of Gender-Biased Admixture

南非有色人种中科伊桑族母系血统的显著贡献:一个性别偏向性混血案例

Morange, Pierre-Emmanuel; Bezemer, Irene; Saut, Noémie; Bare, Lance; Burgos, Gwenaelle; Brocheton, Jessy; Durand, Hervé; Biron-Andreani, Christine; Schved, Jean-Francois; Pernod, Gilles; Galan, Pilar; Drouet, Ludovic; Zelenika, Diana; Germain, Marine; Nicaud, Viviane; Heath, Simon; Ninio, Ewa; Delluc, Aurélien; Münzel, Thomas; Zeller, Tanja; Brand-Herrmann, Stefan-Martin; Alessi, Marie-Christine; Tiret, Laurence; Lathrop, Mark; Cambien, François; Blankenberg, Stefan; Emmerich, Joseph; Trégouët, David-Alexandre; Rosendaal, Frits R; Bungartz, Kathryn D; Williamson, Robin E; Doherty, Leana; Sheen, Mee Rie; Vlachos, Adrianna; Choesmel, Valerie; O'Donohue, Marie-Françoise; Clinton, Catherine; Schneider, Hal E; Sieff, Colin A; Newburger, Peter E; Ball, Sarah E; Niewiadomska, Edyta; Matysiak, Michal; Glader, Bertil; Arceci, Robert J; Farrar, Jason E; Atsidaftos, Eva; Lipton, Jeffrey M; Gleizes, Pierre-Emmanuel; Gazda, Hanna T; Morange, Pierre-Emmanuel; Bezemer, Irene; Saut, Noémie; Bare, Lance; Burgos, Gwenaelle; Brocheton, Jessy; Durand, Hervé; Biron-Andreani, Christine; Schved, Jean-Francois; Pernod, Gilles; Galan, Pilar; Drouet, Ludovic; Zelenika, Diana; Germain, Marine; Nicaud, Viviane; Heath, Simon; Ninio, Ewa; Delluc, Aurélien; Münzel, Thomas; Zeller, Tanja; Brand-Herrmann, Stefan-Martin; Alessi, Marie-Christine; Tiret, Laurence; Lathrop, Mark; Cambien, François; Blankenberg, Stefan; Emmerich, Joseph; Trégouët, David-Alexandre; Rosendaal, Frits R; Dahlqvist, Johanna; Klar, Joakim; Tiwari, Neha; Schuster, Jens; Törmä, Hans; Badhai, Jitendra; Pujol, Ramon; van Steensel, Maurice AM; Brinkhuizen, Tjinta; Gijezen, Lieke; Chaves, Antonio; Tadini, Gianluca; Vahlquist, Anders; Dahl, Niklas; Garber, Kathryn B; Froyen, Guy; Quintana-Murci, Lluis; Harmant, Christine; Quach, Hélène; Balanovsky, Oleg; Zaporozhchenko, Valery; Bormans, Connie; van Helden, Paul D; Hoal, Eileen G; Behar, Doron M

A single-nucleotide deletion in the POMP 5' UTR causes a transcriptional switch and altered epidermal proteasome distribution in KLICK genodermatosis

在KLICK基因皮肤病中,POMP 5' UTR中的单核苷酸缺失导致转录转换和表皮蛋白酶体分布改变。

Dahlqvist, Johanna; Klar, Joakim; Tiwari, Neha; Schuster, Jens; Törmä, Hans; Badhai, Jitendra; Pujol, Ramon; van Steensel, Maurice A M; Brinkhuizen, Tjinta; Gijezen, Lieke; Chaves, Antonio; Tadini, Gianluca; Vahlquist, Anders; Dahl, Niklas

Down-regulation of progesterone receptor membrane component 1 (PGRMC1) in peripheral nucleated blood cells associated with premature ovarian failure (POF) and polycystic ovary syndrome (PCOS)

外周血有核细胞中孕酮受体膜成分 1 (PGRMC1) 的下调与卵巢早衰 (POF) 和多囊卵巢综合征 (PCOS) 相关

Schuster, Jens; Karlsson, Teresia; Karlström, Per-Olof; Poromaa, Inger Sundström; Dahl, Niklas