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Valérie Gailus‐Durner

helmholtz association

60H指数
279论文数
1.3W被引数
收录论文 109
发表时间
Establishing standardized transthoracic echocardiography reference ranges for mouse models: insights into the impact of anesthesia, sex, and age
err2025-12-19
err0
errOAAI
errOestereicher, Manuela A.; Ward, Christopher S.; Schneltzer, Elida; Marschall, Susan; Fuchs, Helmut; Gailus-Durner, Valerie; Bou About, Ghina; Selloum, Mohammed; Meziane, Hamid; Stewart, Michelle; Teboul, Lydia; Norris, Clare; Pimm, Dale; Kan, Marina; Lopez Gomez, Federico; Wilson, Robert; Monroy, Mayra; Pasha, Sheraz; Zabrodska, Eva; Prochazka, Jan; Pajuelo Reguera, David; Nichtova, Zuzana; Herault, Yann; Wells, Sara; Parkinson, Helen; Heaney, Jason D.; Sedlacek, Radislav; Gao, Xiang; Hrabe de Angelis, Martin; Spielmann, Nadine
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Loss of histone macroH2A1.1 causes kidney abnormalities secondary to a change in nutrient metabolization组蛋白macroH2A1.1的丢失导致肾脏异常,继发于营养代谢的改变。
err2025-10-24
err0
PREAI
errRené Winkler; Gemma Comas-Armangué; David Corujo; Adrián Sanz-Moreno; Julia Calzada-Wack; Shubhra Ashish Bhattacharya; Birgit Rathkolb; Nathalia Romanelli Vicente Dragano; Colina X. Qiao; Valentina Chiodi; Dan Filipescu; Dylan H. Park; Maria Rosaria Domenici; Valentina Kirigin Callaú; Raffaele Gerlini; Jan Rozman; Tanja Klein-Rodewald; Antonio Aguilar-Pimentel; Lore Becker; Claudia Seisenberger; Susan Marschall; Helmut Fuchs; Valérie Gailus-Durner; Emily Bernstein; Manlio Vinciguerra; Philipp Oberdoerffer; Martin Hrabě de Angelis; Raffaele Teperino; Marcus Buschbeck
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Abcb5-deficient mice show a subtle, pleiotropic phenotype indicating a role for this transporter in intermediary metabolismABCB5缺陷小鼠表现出一种细微的、多效性的表型,表明该转运蛋白在中间代谢中发挥作用。
err2025-09-20
err0
errOAAI
errJean-Pierre Gillet; Louise Gerard; Wilfred Vieira; Marie Fourrez; Florence Gaudray; Birgit Rathkolb; Jan Rozman; Tanja Klein-Rodewald; Lore Becker; Antonio Aguilar-Pimentel; Marion Horsch; Nadine Spielmann; Cornelia Prehn; Benoît Bihin; Johannes Beckers; Helmut Fuchs; Valérie Gailus-Durner; Martin Hrabe de Angelis; Eileen Southon; Lino Tessarollo; Di Xia; Michael M. Gottesman
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Therapeutic AASS inhibition by AAV-miRNA rescues glutaric aciduria type I severe phenotype in miceAAV-miRNA介导的治疗性AASS抑制可拯救小鼠中戊二酸尿症I型的严重表型
err2025-07-17
err0
errOAAI
errEulàlia Segur-Bailach; Anna Mateu-Bosch; Xavier Bofill-De Ros; Marta Parés; Patricia da Silva Buttkus; Birgit Rathkolb; Valérie Gailus-Durner; Martin Hrabě de Angelis; Pedram Moeini; Gloria Gonzalez-Aseguinolaza; Frederic Tort; Antonia Ribes; Clara D.M. van Karnebeek; Judit García-Villoria; Cristina Fillat
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Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenitaTen1在小鼠中的缺失诱导端粒缩短,并模拟人类先天性角化不良
err2025-04-11
err0
errOAAI
errSanz-Moreno, Adrian; Becker, Lore; Xie, Kan; da Silva-Buttkus, Patricia; Dragano, Nathalia R. V.; Aguilar-Pimentel, Antonio; Amarie, Oana V.; Calzada-Wack, Julia; Kraiger, Markus; Leuchtenberger, Stefanie; Seisenberger, Claudia; Marschall, Susan; Rathkolb, Birgit; Scifo, Enzo; Liu, Ting; Thanabalasingam, Anoja; Sanchez-Vazquez, Raul; Martinez, Paula; Blasco, Maria A.; Savage, Sharon A.; Fuchs, Helmut; Ehninger, Dan; Gailus-Durner, Valerie
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New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouse由于ALDH7A1缺乏引起的吡哆醇依赖性癫痫的新疗法:小鼠中上游酶抑制的首个原理验证
err2025-01-01
err2
errOAAI
errvan Karnebeek, Clara D. M.; Gailus-Durner, Valerie; Engelke, Udo F.; Seisenberger, Claudia; Marschall, Susan; Dragano, Nathalia R., V; da Silva-Buttkus, Patricia; Leuchtenberger, Stefanie; Fuchs, Helmut; Hrabe de Angelis, Martin; Wevers, Ron A.; Coughlin, Curtis R.; Lefeber, Dirk J.
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X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes
err2024-12-05
err0
errOAAI
errHasenbein, Tim P.; Hoelzl, Sarah; Smith, Zachary D.; Gerhardinger, Chiara; Gonner, Marion O. C.; Aguilar-Pimentel, Antonio; Amarie, Oana V.; Becker, Lore; Calzada-Wack, Julia; Dragano, Nathalia R. V.; da Silva-Buttkus, Patricia; Garrett, Lillian; Hoelter, Sabine M.; Kraiger, Markus; Oestereicher, Manuela A.; Rathkolb, Birgit; Sanz-Moreno, Adrian; Spielmann, Nadine; Wurst, Wolfgang; Gailus-Durner, Valerie; Fuchs, Helmut; de Angelis, Martin Hrabe; Meissner, Alexander; Engelhardt, Stefan; Rinn, John L.; Andergassen, Daniel
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Comparative Phenotyping of Mice Reveals Canonical and Noncanonical Physiological Functions of TRα and TRβ
err2024-06-13
err2
errOAAI
errHoenes, Georg Sebastian; Geist, Daniela; Wenzek, Christina; Pfluger, Paul Thomas; Mueller, Timo Dirk; Aguilar-Pimentel, Juan Antonio; Amarie, Oana Veronica; Becker, Lore; Dragano, Natalia; Garrett, Lillian; Hoelter, Sabine Maria; Rathkolb, Birgit; Rozman, Jan; Spielmann, Nadine; Treise, Irina; Wolf, Eckhard; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Fuehrer, Dagmar; Moeller, Lars Christian
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Canonical and Noncanonical Contribution of Thyroid Hormone Receptor Isoforms Alpha and Beta to Cardiac Hypertrophy and Heart Rate in Male Mice甲状腺激素受体亚型 α 和 β 对雄性小鼠心脏肥大和心率的规范和非规范贡献
errTHYROID
IF6.7
err2024-06-01
err2
errOAAI
errGeist, Daniela; Hoenes, Georg Sebastian; Grund, Susanne Camilla; Pape, Janina; Siemes, Devon; Spangenberg, Philippa; Tolstik, Elen; Doerr, Stefanie; Spielmann, Nadine; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Mittag, Jens; Engel, Daniel Robert; Fuehrer, Dagmar; Lorenz, Kristina; Moeller, Lars Christian
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TRPS1 maintains luminal progenitors in the mammary gland by repressing SRF/MRTF activity
err2024-05-03
err0
errOAAI
errTollot-Wegner, Marie; Jessen, Marco; Kim, KyungMok; Sanz-Moreno, Adrian; Spielmann, Nadine; Gailus-Durner, Valerie; Fuchs, Helmut; de Angelis, Martin Hrabe; von Eyss, Bjoern
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Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
err2024-04-01
err0
errOAAI
errRiedhammer, Korbinian M.; Nguyen, Thanh-Minh T.; Kosukcu, Can; Calzada-Wack, Julia; Li, Yong; Batzir, Nurit Assia; Saygili, Seha; Wimmers, Vera; Kim, Gwang-Jin; Chrysanthou, Marialena; Bakey, Zeineb; Sofrin-Drucker, Efrat; Kraiger, Markus; Sanz-Moreno, Adrian; Amarie, Oana V.; Rathkolb, Birgit; Klein-Rodewald, Tanja; Garrett, Lillian; Hoelter, Sabine M.; Seisenberger, Claudia; Haug, Stefan; Schlosser, Pascal; Marschall, Susan; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; Wuttke, Matthias; de Angelis, Martin Hrabe; Comic, Jasmina; Dogan, Ozlem Akgun; Ozluk, Yasemin; Tasdemir, Mehmet; Agbas, Ayse; Canpolat, Nur; Orenstein, Naama; Caliskan, Salim; Weber, Ruthild G.; Bergmann, Carsten; Jeanpierre, Cecile; Saunier, Sophie; Lim, Tze Y.; Hildebrandt, Friedhelm; Alhaddad, Bader; Basel-Salmon, Lina; Borovitz, Yael; Wu, Kaman; Antony, Dinu; Matschkal, Julia; Schaaf, Christian W.; Renders, Lutz; Schmaderer, Christoph; Rogg, Manuel; Schell, Christoph; Meitinger, Thomas; Heemann, Uwe; Koettgen, Anna; Arnold, Sebastian J.; Ozaltin, Fatih; Schmidts, Miriam; Hoefele, Julia
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Monoallelic variation in DHX9, the gene encoding the DExH-box helicase DHX9, underlies neurodevelopment disorders and Charcot-Marie-Tooth disease
err2023-08-01
err14
errOAAI
errCalame, Daniel G.; Guo, Tianyu; Wang, Chen; Garrett, Lillian; Jolly, Angad; Dawood, Moez; Kurolap, Alina; Henig, Noa Zunz; Fatih, Jawid M.; Herman, Isabella; Du, Haowei; Mitani, Tadahiro; Becker, Lore; Rathkolb, Birgit; Gerlini, Raffaele; Seisenberger, Claudia; Marschall, Susan; Hunter, Jill, V; Gerard, Amanda; Heidlebaugh, Alexis; Challman, Thomas; Spillmann, Rebecca C.; Jhangiani, Shalini N.; Coban-Akdemir, Zeynep; Lalani, Seema; Liu, Lingxiao; Revah-Politi, Anya; Iglesias, Alejandro; Guzman, Edwin; Baugh, Evan; Boddaert, Nathalie; Rondeau, Sophie; Ormieres, Clothide; Barcia, Giulia; Tan, Queenie K. G.; Thiffault, Sophie Isabelle; Pastinen, Tomi; Sheikh, Kazim; Biliciler, Suur; Mei, Davide; Melani, Federico; Shashi, Vandana; Yaron, Yuval; Steele, Mary; Wakeling, Emma; Ostergaard, Elsebet; Nazaryan-Petersen, Lusine; Millan, Francisca; Santiago-Sim, Teresa; Thevenon, Julien; Bruel, Ange-Line; Thauvin-Robinet, Christel; Popp, Denny; Platzer, Konrad; Gawlinski, Pawel; Wiszniewski, Wojciech; Marafi, Dana; Pehlivan, Davut; Posey, Jennifer E.; Gibbs, Richard A.; Gailus-Durner, Valerie; Guerrini, Renzo; Fuchs, Helmut; de Angelis, Martin Hrabe; Hoelter, Sabine M.; Cheung, Hoi-Hung; Gu, Shen; Lupski, James R.
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Insights into energy balance dysregulation from a mouse model of methylmalonic aciduria
err2023-06-27
err1
errOAAI
errLucienne, Marie; Gerlini, Raffaele; Rathkolb, Birgit; Calzada-Wack, Julia; Forny, Patrick; Wueest, Stephan; Kaech, Andres; Traversi, Florian; Forny, Merima; Burer, Celine; Aguilar-Pimentel, Antonio; Irmler, Martin; Beckers, Johannes; Sauer, Sven; Koelker, Stefan; Dewulf, Joseph P.; Bommer, Guido T.; Hoces, Daniel; Gailus-Durner, Valerie; Fuchs, Helmut; Rozman, Jan; Froese, D. Sean; Baumgartner, Matthias R.; de Angelis, Martin Hrabe
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Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain
err2023-05-02
err5
errOAAI
errStroo, Esther; Janssen, Leen; Sin, Olga; Hogewerf, Wytse; Koster, Mirjam; Harkema, Liesbeth; Youssef, Sameh A.; Beschorner, Natalie; Wolters, Anouk H. G.; Bakker, Bjorn; Becker, Lore; Garrett, Lilian; Marschall, Susan; Hoelter, Sabine M.; Wurst, Wolfgang; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Thathiah, Amanth; Foijer, Floris; van de Sluis, Bart; van Deursen, Jan; Jucker, Matthias; de Brun, Alain; Nollen, Ellen A. A.
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Knockout mice are an important tool for human monogenic heart disease studies
err2023-03-21
err6
errOAAI
errCacheiro, Pilar; Spielmann, Nadine; Mashhadi, Hamed Haseli; Fuchs, Helmut; Gailus-Durner, Valerie; Smedley, Damian; de Angelis, Martin Hrabe
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Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome
err2022-12-01
err4
errOAAI
errMaity-Kumar, Gandhari; Staender, Lisa; DeAngelis, Meri; Lee, Sooyeon; Molenaar, Anna; Becker, Lore; Garrett, Lillian; Amerie, Oana, V; Hoelter, Sabine M.; Wurst, Wolfgang; Fuchs, Helmut; Feuchtinger, Annette; Gailus-Durner, Valerie; Garcia-Caceres, Cristina; Othman, Ahmed E.; Brockmann, Caroline; Schoeffling, Vanessa, I; Beiser, Katja; Krude, Heiko; Mroz, Piotr A.; Hofmann, Susanna; Tuckermann, Jan; DiMarchi, Richard D.; de Angelis, Martin Hrabe; Tschoep, Matthias H.; Pfluger, Paul T.; Mueller, Timo D.
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New C3H KitN824K/WT cancer mouse model develops late-onset malignant mammary tumors with high penetrance
err2022-11-17
err1
errOAAI
errKlein-Rodewald, Tanja; Micklich, Kateryna; Sanz-Moreno, Adrian; Tost, Monica; Calzada-Wack, Julia; Adler, Thure; Klaften, Matthias; Sabrautzki, Sibylle; Aigner, Bernhard; Kraiger, Markus; Gailus-Durner, Valerie; Fuchs, Helmut; Gruender, Albert; Pahl, Heike; Wolf, Eckhard; de Angelis, Martin Hrabe; Rathkolb, Birgit
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Deep phenotyping and lifetime trajectories reveal limited effects of longevity regulators on the aging process in C57BL/6J mice
err2022-11-11
err21
errOAAI
errXie, Kan; Fuchs, Helmut; Scifo, Enzo; Liu, Dan; Aziz, Ahmad; Aguilar-Pimentel, Juan Antonio; Amarie, Oana Veronica; Becker, Lore; da Silva-Buttkus, Patricia; Calzada-Wack, Julia; Cho, Yi-Li; Deng, Yushuang; Edwards, A. Cole; Garrett, Lillian; Georgopoulou, Christina; Gerlini, Raffaele; Hoelter, Sabine M.; Klein-Rodewald, Tanja; Kramer, Michael; Leuchtenberger, Stefanie; Lountzi, Dimitra; Mayer-Kuckuk, Phillip; Nover, Lena L.; Oestereicher, Manuela A.; Overkott, Clemens; Pearson, Brandon L.; Rathkolb, Birgit; Rozman, Jan; Russ, Jenny; Schaaf, Kristina; Spielmann, Nadine; Sanz-Moreno, Adrian; Stoeger, Claudia; Treise, Irina; Bano, Daniele; Busch, Dirk H.; Graw, Jochen; Klingenspor, Martin; Klopstock, Thomas; Mock, Beverly A.; Salomoni, Paolo; Schmidt-Weber, Carsten; Weiergraber, Marco; Wolf, Eckhard; Wurst, Wolfgang; Gailus-Durner, Valerie; Breteler, Monique M. B.; Hrabe de Angelis, Martin; Ehninger, Dan
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Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing
err2022-11-09
err7
errOAAI
errPng, Grace; Gerlini, Raffaele; Hatzikotoulas, Konstantinos; Barysenka, Andrei; Rayner, N. William; Klaric, Lucija; Rathkolb, Birgit; Aguilar-Pimentel, Juan A.; Rozman, Jan; Fuchs, Helmut; Gailus-Durner, Valerie; Tsafantakis, Emmanouil; Karaleftheri, Maria; Dedoussis, George; Pietrzik, Claus; Wilson, James F.; Angelis, Martin Hrabe; Becker-Pauly, Christoph; Gilly, Arthur; Zeggini, Eleftheria
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Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndromeRABGAP1中的双等位基因功能丧失变体导致一种新的神经发育综合征
err2022-11-01
err4
errOAAI
errOh, Rachel Youjin; Deshwar, Ashish R.; Marwaha, Ashish; Sabha, Nesrin; Tropak, Michael; Hou, Huayun; Yuki, Kyoko E.; Wilson, Michael D.; Rump, Patrick; Lunsing, Roelineke; Elserafy, Noha; Chung, Clara W. T.; Hewson, Stacy; Klein-Rodewald, Tanja; Calzada-Wack, Julia; Sanz-Moreno, Adrian; Kraiger, Markus; Marschall, Susan; Fuchs, Helmut; Gailus-Durner, Valerie; de Angelis, Martin Hrabe; Dowling, James; Schulze, Andreas
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