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

Enhancer adoption by an LTR retrotransposon generates viral-like particles, causing developmental limb phenotypes.

LTR逆转录转座子对增强子的利用会产生病毒样颗粒,导致肢体发育表型异常

Glaser Juliane, Cova Giulia, Fauler Beatrix, Prada-Medina Cesar A, Stanislas Virginie, Phan Mai H Q, Schöpflin Robert, Aktas Yasmin, Franke Martin, Andrey Guillaume, Bartzoka Natalia, Paliou Christina, Laupert Verena, Chan Wing-Lee, Wittler Lars, Mielke Thorsten, Mundlos Stefan

Publisher Correction: Combinatorial effects on gene expression at the Lbx1/Fgf8 locus resolve split-hand/foot malformation type 3

出版商更正:Lbx1/Fgf8基因座基因表达的组合效应可解决裂手/裂足畸形3型

Cova, Giulia; Glaser, Juliane; Schöpflin, Robert; Prada-Medina, Cesar Augusto; Ali, Salaheddine; Franke, Martin; Falcone, Rita; Federer, Miriam; Ponzi, Emanuela; Ficarella, Romina; Novara, Francesca; Wittler, Lars; Timmermann, Bernd; Gentile, Mattia; Zuffardi, Orsetta; Spielmann, Malte; Mundlos, Stefan

A 37 kb region upstream of brachyury comprising a notochord enhancer is essential for notochord and tail development

短尾基因上游37 kb区域包含一个脊索增强子,对脊索和尾部的发育至关重要。

Dennis Schifferl ,Manuela Scholze-Wittler ,Lars Wittler ,Jesse V Veenvliet ,Frederic Koch ,Bernhard G Herrmann

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

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder

全基因组关联研究和鼠类表达数据表明,WNT3 和 WNT9b 之间高度保守的 32 kb 基因间区可能是孤立性经典膀胱外翻的易感基因位点。

Reutter, Heiko; Draaken, Markus; Pennimpede, Tracie; Wittler, Lars; Brockschmidt, Felix F; Ebert, Anne-Karolin; Bartels, Enrika; Rösch, Wolfgang; Boemers, Thomas M; Hirsch, Karin; Schmiedeke, Eberhard; Meesters, Christian; Becker, Tim; Stein, Raimund; Utsch, Boris; Mangold, Elisabeth; Nordenskjöld, Agneta; Barker, Gillian; Kockum, Christina Clementsson; Zwink, Nadine; Holmdahl, Gundula; Läckgren, Göran; Jenetzky, Ekkehart; Feitz, Wouter F J; Marcelis, Carlo; Wijers, Charlotte H W; Van Rooij, Iris A L M; Gearhart, John P; Herrmann, Bernhard G; Ludwig, Michael; Boyadjiev, Simeon A; Nöthen, Markus M; Mattheisen, Manuel

De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association

VATER/VACTERL综合征患者中1q41、2q37.3和8q24.3位点的新生微重复

Hilger, Alina; Schramm, Charlotte; Pennimpede, Tracie; Wittler, Lars; Dworschak, Gabriel C; Bartels, Enrika; Engels, Hartmut; Zink, Alexander M; Degenhardt, Franziska; Müller, Annette M; Schmiedeke, Eberhard; Grasshoff-Derr, Sabine; Märzheuser, Stefanie; Hosie, Stuart; Holland-Cunz, Stefan; Wijers, Charlotte H W; Marcelis, Carlo L M; van Rooij, Iris A L M; Hildebrandt, Friedhelm; Herrmann, Bernhard G; Nöthen, Markus M; Ludwig, Michael; Reutter, Heiko; Draaken, Markus

Homeotic arm-to-leg transformation associated with genomic rearrangements at the PITX1 locus

与PITX1基因座基因组重排相关的同源异型手臂到腿部的转化

Spielmann, Malte; Brancati, Francesco; Krawitz, Peter M; Robinson, Peter N; Ibrahim, Daniel M; Franke, Martin; Hecht, Jochen; Lohan, Silke; Dathe, Katarina; Nardone, Anna Maria; Ferrari, Paola; Landi, Antonio; Wittler, Lars; Timmermann, Bernd; Chan, Danny; Mennen, Ulrich; Klopocki, Eva; Mundlos, Stefan

Expression of Msgn1 in the presomitic mesoderm is controlled by synergism of WNT signalling and Tbx6

前体节中胚层中 Msgn1 的表达受 WNT 信号通路和 Tbx6 的协同作用调控。

Wittler, Lars; Shin, Eun-ha; Grote, Phillip; Kispert, Andreas; Beckers, Anja; Gossler, Achim; Werber, Martin; Herrmann, Bernhard G