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

Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia

CAPN1激活因子CD99L2的功能缺失变异会导致X连锁痉挛性共济失调。

Menden, Benita; Incebacak Eltemur, Rana D; Demidov, German; Sturm, Marc; Park, Joohyun; Huridou, Chrisovalantou; Fath, Florian; Nümann, Astrid; Baumann, Alexander; Diets, Illja J; Dufke, Claudia; Regensburger, Martin; Rönnefarth, Maria; Wilke, Vera; van Os, Nienke; Vielhaber, Stefan; Rattay, Tim W; Kohl, Zacharias; Peralta, Susana; Pereira Sena, Priscila; Kellner, Melanie; Weissert, Nadine; Traschütz, Andreas; Zeltner, Lena; Boelmans, Kai; Deininger, Natalie; Schütz, Leon; Gross, Caspar; Hinojosa Amaya, Ana Beatriz; Raupach, Katrin; Hengel, Holger; Harmuth, Florian; Admard, Jakob; Bader, Ingrid; Baumann, Sarah; Bender, Friedemann; Bevot, Andrea; Bischoff, Almut; Boschann, Felix; Buchert, Rebecca; Buchzik, Daniel; Casadei, Nicolas; Catarino, Claudia B; Cordts, Isabell; Cremer, Kirsten; Doebler-Neumann, Marion; Ehmke, Nadja; Elbracht, Miriam; Falb, Ruth J; Feindt, Thomas; Fleszar, Zofia; Gerstner, Lea; Gläser, Dieter; Grasshoff, Ute; Grosch, Sarah; Grundmann, Kathrin; Gutschalk, Alexander; Haaga, Manja; Hayer, Stefanie; Hehr, Ute; Hellenbroich, Yorck; Henn, Wolfram; Herr, Barbara; Herzog, Rebecca; Horber, Veronka; Deppe, Jonas; Kaiser, Nadja; Kehrer, Christiane; Kehrer, Martin; Kern, Jan; Keßler, Christoph; Khuller, Katharina; Klinkhammer, Hannah; Kotzaeridou, Urania; Krawitz, Peter; Kreiss, Martina; Küpper, Hanna; Kuster, Alice; Laugwitz, Lucia; Lesemann, Anne; Lichey, Nadine; Linden, Tobias; Macek, Boris; Magg, Janine; Mangold, Elisabeth; Manka, Eva; Marquardt, Iris; Mehnert, Karl; Mengel, David; Morlot, Susanne; Oehl-Jaschkowitz, Barbara; Pauly, Martje G; Philipp, Melanie; Radelfahr, Florentine; Rautenberg, Maren; Riess, Angelika; Saft, Carsten; Schlotter-Weigel, Beate; Schmidt, Axel; Schwaibold, Eva M C; Spahlinger, Veronika; Spranger, Stephanie; Steiner, Katharina Marie; Stendel, Claudia; Thieme, Andreas; Tzschach, Andreas; Velic, Ana; Wiethoff, Sarah; Wilke, Carlo; Züchner, Stephan; Zittel, Simone; Husain, Ralf A; Deschauer, Marcus; Distelmaier, Felix; Dufke, Andreas; Graessner, Holm; Hemmer, Bernhard; Jacobi, Heike; Klockgether, Thomas; Klopstock, Thomas; Kobeleva, Xenia; Korenke, Georg-Christoph; Kuechler, Alma; Kuhlenbäumer, Gregor; Kurth, Ingo; Nguyen, Huu Phuc; Wunderlich, Gilbert; Zeuner, Kirsten E; Klebe, Stephan; Auer-Grumbach, Michaela; Butryn, Michaela; Winkler, Jürgen; Timmann, Dagmar; Synofzik, Matthis; van de Warrenburg, Bart; Schüle, Rebecca; Schöls, Ludger; Ossowski, Stephan; Riess, Olaf; Weber, Jonasz J; Haack, Tobias B

Bi-allelic KICS2 mutations impair KICSTOR complex-mediated mTORC1 regulation, causing intellectual disability and epilepsy.

双等位基因 KICS2 突变会损害 KICSTOR 复合物介导的 mTORC1 调节,导致智力障碍和癫痫

Buchert Rebecca, Burkhalter Martin D, Huridou Chrisovalantou, Sofan Linda, Roser Timo, Cremer Kirsten, Alvi Javeria Raza, Efthymiou Stephanie, Froukh Tawfiq, Gulieva Sughra, Guliyeva Ulviyya, Hamdallah Moath, Holder-Espinasse Muriel, Kaiyrzhanov Rauan, Klingler Doreen, Koko Mahmoud, Matthies Lars, Park Joohyun, Sturm Marc, Velic Ana, Spranger Stephanie, Sultan Tipu, Engels Hartmut, Lerche Holger, Houlden Henry, Pagnamenta Alistair T, Borggraefe Ingo, Weber Yvonne, Bonnen Penelope E, Maroofian Reza, Riess Olaf, Weber Jonasz J, Philipp Melanie, Haack Tobias B

CDKL1 variants affecting ciliary formation predispose to thoracic aortic aneurysm and dissection

影响纤毛形成的CDKL1变异体易导致胸主动脉瘤和夹层。

Nauth, Theresa; Philipp, Melanie; Renner, Sina; Burkhalter, Martin D; Schüler, Helke; Saygi, Ceren; Händler, Kristian; Siebels, Bente; Busch, Alice; Mair, Thomas; Rickassel, Verena; Deden, Sophia; Hoffer, Konstantin; Olfe, Jakob; Mir, Thomas S; von Kodolitsch, Yskert; Girdauskas, Evaldas; Rybczynski, Meike; Kriegs, Malte; Voß, Hannah; Sauvigny, Thomas; Spielmann, Malte; Alawi, Malik; Krasemann, Susanne; Kubisch, Christian; Demal, Till J; Rosenberger, Georg

Elevated Hedgehog activity contributes to attenuated DNA damage responses in aged hematopoietic cells

老年造血细胞中 Hedgehog 信号通路活性升高会导致 DNA 损伤反应减弱。

Scheffold, Annika; Baig, Ali H; Chen, Zhiyang; von Löhneysen, Sarah E; Becker, Friedrich; Morita, Yohei; Avila, Alush I; Groth, Marco; Lechel, André; Schmid, Florian; Kraus, Johann M; Kestler, Hans A; Stilgenbauer, Stephan; Philipp, Melanie; Burkhalter, Martin D

Analysis of cilia dysfunction phenotypes in zebrafish embryos depleted of Origin recognition complex factors

对缺乏起始识别复合物因子的斑马鱼胚胎纤毛功能障碍表型进行分析

Maerz, Lars D; Casar Tena, Teresa; Gerhards, Julian; Donow, Cornelia; Jeggo, Penelope A; Philipp, Melanie

The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5

对异位症患者的分析揭示了GRK5基因新的功能缺失变异

Lessel, Davor; Muhammad, Tariq; Casar Tena, Teresa; Moepps, Barbara; Burkhalter, Martin D; Hitz, Marc-Phillip; Toka, Okan; Rentzsch, Axel; Schubert, Stephan; Schalinski, Adelheid; Bauer, Ulrike M M; Kubisch, Christian; Ware, Stephanie M; Philipp, Melanie

ATR promotes cilia signalling: links to developmental impacts

ATR促进纤毛信号传导:与发育影响相关

Stiff, Tom; Casar Tena, Teresa; O'Driscoll, Mark; Jeggo, Penny A; Philipp, Melanie

Left-right asymmetry in the light of TOR: An update on what we know so far

从TOR视角看左右不对称性:我们目前所了解的最新进展

Casar Tena, Teresa; Burkhalter, Martin D; Philipp, Melanie

Overlapping and opposing functions of G protein-coupled receptor kinase 2 (GRK2) and GRK5 during heart development

G蛋白偶联受体激酶2 (GRK2) 和GRK5在心脏发育过程中的重叠和拮抗功能

Philipp, Melanie; Berger, Ina M; Just, Steffen; Caron, Marc G

Grk5l controls heart development by limiting mTOR signaling during symmetry breaking

Grk5l通过在对称性破缺期间限制mTOR信号传导来控制心脏发育。

Burkhalter, Martin D; Fralish, Gregory B; Premont, Richard T; Caron, Marc G; Philipp, Melanie