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

Specialised super-enhancer networks in stem cells and neurons

干细胞和神经元中特化的超级增强子网络

Harabula, Izabela; Speakman, Liam; Musella, Francesco; Forillo, Luca; Zea-Redondo, Luna; Kukalev, Alexander; Beagrie, Robert A; Morris, Kelly J; Fernandes, Lucas; Irastorza-Azcarate, Ibai; Fernandes, Ana M; Carvalho, Silvia; Szabó, Dominik; Ferrai, Carmelo; Nicodemi, Mario; Welch, Lonnie; Pombo, Ana

Induction of kidney-related gene programs through co-option of SALL1 in mole ovotestes

通过在鼹鼠卵睾丸中共同选择SALL1来诱导肾脏相关基因程序

Magdalena Schindler, Marco Osterwalder, Izabela Harabula, Lars Wittler, Athanasia C Tzika, Dina K N Dechmann, Martin Vingron, Axel Visel, Stefan A Haas, Francisca M Real

Cell-type specialization is encoded by specific chromatin topologies

细胞类型特化由特定的染色质拓扑结构编码

Warren Winick-Ng #, Alexander Kukalev #, Izabela Harabula #, Luna Zea-Redondo #, Dominik Szabó #, Mandy Meijer, Leonid Serebreni, Yingnan Zhang, Simona Bianco, Andrea M Chiariello, Ibai Irastorza-Azcarate, Christoph J Thieme, Thomas M Sparks, Sílvia Carvalho, Luca Fiorillo, Francesco Musella, Ehsan

The mole genome reveals regulatory rearrangements associated with adaptive intersexuality

鼹鼠基因组揭示了与适应性雌雄同体相关的调控重排

M Real, Francisca; Haas, Stefan A; Franchini, Paolo; Xiong, Peiwen; Simakov, Oleg; Kuhl, Heiner; Schöpflin, Robert; Heller, David; Moeinzadeh, M-Hossein; Heinrich, Verena; Krannich, Thomas; Bressin, Annkatrin; Hartmann, Michaela F; Wudy, Stefan A; Dechmann, Dina K N; Hurtado, Alicia; Barrionuevo, Francisco J; Schindler, Magdalena; Harabula, Izabela; Osterwalder, Marco; Hiller, Michael; Wittler, Lars; Visel, Axel; Timmermann, Bernd; Meyer, Axel; Vingron, Martin; Jiménez, Rafael; Mundlos, Stefan; Lupiáñez, Darío G

Evolving methodologies and concepts in 4D nucleome research

4D核组研究中不断发展的方法和概念

Sparks, Thomas M; Harabula, Izabela; Pombo, Ana

Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesis

动态三维染色质结构有助于增强子特异性和肢体形态发生。

Kragesteen, Bjørt K; Spielmann, Malte; Paliou, Christina; Heinrich, Verena; Schöpflin, Robert; Esposito, Andrea; Annunziatella, Carlo; Bianco, Simona; Chiariello, Andrea M; Jerković, Ivana; Harabula, Izabela; Guckelberger, Philine; Pechstein, Michael; Wittler, Lars; Chan, Wing-Lee; Franke, Martin; Lupiáñez, Darío G; Kraft, Katerina; Timmermann, Bernd; Vingron, Martin; Visel, Axel; Nicodemi, Mario; Mundlos, Stefan; Andrey, Guillaume

Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome

TGDS基因的纯合突变和复合杂合突变会导致卡特尔-曼兹克综合征。

Ehmke, Nadja; Caliebe, Almuth; Koenig, Rainer; Kant, Sarina G; Stark, Zornitza; Cormier-Daire, Valérie; Wieczorek, Dagmar; Gillessen-Kaesbach, Gabriele; Hoff, Kirstin; Kawalia, Amit; Thiele, Holger; Altmüller, Janine; Fischer-Zirnsak, Björn; Knaus, Alexej; Zhu, Na; Heinrich, Verena; Huber, Celine; Harabula, Izabela; Spielmann, Malte; Horn, Denise; Kornak, Uwe; Hecht, Jochen; Krawitz, Peter M; Nürnberg, Peter; Siebert, Reiner; Manzke, Hermann; Mundlos, Stefan