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

Redirecting the route: Monocyte-mediated delivery of oHSV-1 across a human BBB-on-chip model

改变传播途径:单核细胞介导的oHSV-1跨越人血脑屏障芯片模型的递送

Micheli, Sara; Reale, Alberto; Rossetto, Alessandra; Parolin, Cristina; Mammano, Fabio; Calistri, Arianna; Cimetta, Elisa

Connexin hemichannel blockade by abEC1.1 disrupts glioblastoma progression, suppresses invasiveness, and reduces hyperexcitability in preclinical models.

abEC1.1 阻断连接蛋白半通道可破坏胶质母细胞瘤的进展,抑制其侵袭性,并降低临床前模型中的过度兴奋性

Donati Viola, Di Pietro Chiara, Persano Luca, Rampazzo Elena, Panarelli Mariateresa, Cambria Clara, Selimi Anna, Manfreda Lorenzo, de Oliveira do Rêgo Ana Gabriela, La Sala Gina, Sprega Camilla, Calistri Arianna, Ciubotaru Catalin Dacian, Yang Guang, Zonta Francesco, Antonucci Flavia, Marazziti Daniela, Mammano Fabio

Correction: A fully human IgG1 antibody targeting connexin 32 extracellular domain blocks CMTX1 hemichannel dysfunction in an in vitro model

更正:一种靶向连接蛋白32胞外结构域的全人源IgG1抗体可在体外模型中阻断CMTX1半通道功能障碍。

Tettey-Matey, Abraham; Donati, Viola; Cimmino, Chiara; Pietro, Chiara Di; Buratto, Damiano; Panarelli, Mariateresa; Reale, Alberto; Calistri, Arianna; Fornaini, Maria Vittoria; Zhou, Ruhong; Yang, Guang; Zonta, Francesco; Marazziti, Daniela; Mammano, Fabio

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development

全基因组筛选揭示哺乳动物胚胎眼发育的遗传基础

Chee, Justine M; Lanoue, Louise; Clary, Dave; Higgins, Kendall; Bower, Lynette; Flenniken, Ann; Guo, Ruolin; Adams, David J; Bosch, Fatima; Braun, Robert E; Brown, Steve D M; Chin, H-J Genie; Dickinson, Mary E; Hsu, Chih-Wei; Dobbie, Michael; Gao, Xiang; Galande, Sanjeev; Grobler, Anne; Heaney, Jason D; Herault, Yann; de Angelis, Martin Hrabe; Mammano, Fabio; Nutter, Lauryl M J; Parkinson, Helen; Qin, Chuan; Shiroishi, Toshi; Sedlacek, Radislav; Seong, J-K; Xu, Ying; Brooks, Brian; McKerlie, Colin; Lloyd, K C Kent; Westerberg, Henrik; Moshiri, Ala

Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

广泛鉴定与先天性和结构性心脏疾病以及心肌病相关的基因

Spielmann, Nadine; Miller, Gregor; Oprea, Tudor I; Hsu, Chih-Wei; Fobo, Gisela; Frishman, Goar; Montrone, Corinna; Haseli Mashhadi, Hamed; Mason, Jeremy; Munoz Fuentes, Violeta; Leuchtenberger, Stefanie; Ruepp, Andreas; Wagner, Matias; Westphal, Dominik S; Wolf, Cordula; Görlach, Agnes; Sanz-Moreno, Adrián; Cho, Yi-Li; Teperino, Raffaele; Brandmaier, Stefan; Sharma, Sapna; Galter, Isabella Rikarda; Östereicher, Manuela A; Zapf, Lilly; Mayer-Kuckuk, Philipp; Rozman, Jan; Teboul, Lydia; Bunton-Stasyshyn, Rosie K A; Cater, Heather; Stewart, Michelle; Christou, Skevoulla; Westerberg, Henrik; Willett, Amelia M; Wotton, Janine M; Roper, Willson B; Christiansen, Audrey E; Ward, Christopher S; Heaney, Jason D; Reynolds, Corey L; Prochazka, Jan; Bower, Lynette; Clary, David; Selloum, Mohammed; Bou About, Ghina; Wendling, Olivia; Jacobs, Hugues; Leblanc, Sophie; Meziane, Hamid; Sorg, Tania; Audain, Enrique; Gilly, Arthur; Rayner, Nigel W; Hitz, Marc-Phillip; Zeggini, Eleftheria; Wolf, Eckhard; Sedlacek, Radislav; Murray, Steven A; Svenson, Karen L; Braun, Robert E; White, Jaqueline K; Kelsey, Lois; Gao, Xiang; Shiroishi, Toshihiko; Xu, Ying; Seong, Je Kyung; Mammano, Fabio; Tocchini-Valentini, Glauco P; Beaudet, Arthur L; Meehan, Terrence F; Parkinson, Helen; Smedley, Damian; Mallon, Ann-Marie; Wells, Sara E; Grallert, Harald; Wurst, Wolfgang; Marschall, Susan; Fuchs, Helmut; Brown, Steve D M; Flenniken, Ann M; Nutter, Lauryl M J; McKerlie, Colin; Herault, Yann; Lloyd, K C Kent; Dickinson, Mary E; Gailus-Durner, Valerie; Hrabe de Angelis, Martin

Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and cardiomyopathy

出版商更正:广泛鉴定与先天性和结构性心脏疾病及心肌病相关的基因

Spielmann, Nadine; Miller, Gregor; Oprea, Tudor I; Hsu, Chih-Wei; Fobo, Gisela; Frishman, Goar; Montrone, Corinna; Haseli Mashhadi, Hamed; Mason, Jeremy; Munoz Fuentes, Violeta; Leuchtenberger, Stefanie; Ruepp, Andreas; Wagner, Matias; Westphal, Dominik S; Wolf, Cordula; Görlach, Agnes; Sanz-Moreno, Adrián; Cho, Yi-Li; Teperino, Raffaele; Brandmaier, Stefan; Sharma, Sapna; Galter, Isabella Rikarda; Östereicher, Manuela A; Zapf, Lilly; Mayer-Kuckuk, Philipp; Rozman, Jan; Teboul, Lydia; Bunton-Stasyshyn, Rosie K A; Cater, Heather; Stewart, Michelle; Christou, Skevoulla; Westerberg, Henrik; Willett, Amelia M; Wotton, Janine M; Roper, Willson B; Christiansen, Audrey E; Ward, Christopher S; Heaney, Jason D; Reynolds, Corey L; Prochazka, Jan; Bower, Lynette; Clary, David; Selloum, Mohammed; Bou About, Ghina; Wendling, Olivia; Jacobs, Hugues; Leblanc, Sophie; Meziane, Hamid; Sorg, Tania; Audain, Enrique; Gilly, Arthur; Rayner, Nigel W; Hitz, Marc-Phillip; Zeggini, Eleftheria; Wolf, Eckhard; Sedlacek, Radislav; Murray, Steven A; Svenson, Karen L; Braun, Robert E; White, Jaqueline K; Kelsey, Lois; Gao, Xiang; Shiroishi, Toshihiko; Xu, Ying; Seong, Je Kyung; Mammano, Fabio; Tocchini-Valentini, Glauco P; Beaudet, Arthur L; Meehan, Terrence F; Parkinson, Helen; Smedley, Damian; Mallon, Ann-Marie; Wells, Sara E; Grallert, Harald; Wurst, Wolfgang; Marschall, Susan; Fuchs, Helmut; Brown, Steve D M; Flenniken, Ann M; Nutter, Lauryl M J; McKerlie, Colin; Herault, Yann; Lloyd, K C Kent; Dickinson, Mary E; Gailus-Durner, Valerie; Hrabe de Angelis, Martin

Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes

对全基因组敲除小鼠数据库的分析鉴定出纤毛病候选基因

Higgins, Kendall; Moore, Bret A; Berberovic, Zorana; Adissu, Hibret A; Eskandarian, Mohammad; Flenniken, Ann M; Shao, Andy; Imai, Denise M; Clary, Dave; Lanoue, Louise; Newbigging, Susan; Nutter, Lauryl M J; Adams, David J; Bosch, Fatima; Braun, Robert E; Brown, Steve D M; Dickinson, Mary E; Dobbie, Michael; Flicek, Paul; Gao, Xiang; Galande, Sanjeev; Grobler, Anne; Heaney, Jason D; Herault, Yann; de Angelis, Martin Hrabe; Chin, Hsian-Jean Genie; Mammano, Fabio; Qin, Chuan; Shiroishi, Toshihiko; Sedlacek, Radislav; Seong, J-K; Xu, Ying; Lloyd, K C Kent; McKerlie, Colin; Moshiri, Ala

Single-Cell RNA Sequencing Analysis Reveals Greater Epithelial Ridge Cells Degeneration During Postnatal Development of Cochlea in Rats

单细胞RNA测序分析揭示大鼠耳蜗出生后发育过程中上皮脊细胞退化加剧

Chen, Jianyong; Gao, Dekun; Chen, Junmin; Hou, Shule; He, Baihui; Li, Yue; Li, Shuna; Zhang, Fan; Sun, Xiayu; Mammano, Fabio; Sun, Lianhua; Yang, Jun; Zheng, Guiliang

Human and mouse essentiality screens as a resource for disease gene discovery

人类和小鼠必需基因筛选作为疾病基因发现的资源

Cacheiro, Pilar; Muñoz-Fuentes, Violeta; Murray, Stephen A; Dickinson, Mary E; Bucan, Maja; Nutter, Lauryl M J; Peterson, Kevin A; Haselimashhadi, Hamed; Flenniken, Ann M; Morgan, Hugh; Westerberg, Henrik; Konopka, Tomasz; Hsu, Chih-Wei; Christiansen, Audrey; Lanza, Denise G; Beaudet, Arthur L; Heaney, Jason D; Fuchs, Helmut; Gailus-Durner, Valerie; Sorg, Tania; Prochazka, Jan; Novosadova, Vendula; Lelliott, Christopher J; Wardle-Jones, Hannah; Wells, Sara; Teboul, Lydia; Cater, Heather; Stewart, Michelle; Hough, Tertius; Wurst, Wolfgang; Sedlacek, Radislav; Adams, David J; Seavitt, John R; Tocchini-Valentini, Glauco; Mammano, Fabio; Braun, Robert E; McKerlie, Colin; Herault, Yann; de Angelis, Martin Hrabě; Mallon, Ann-Marie; Lloyd, K C Kent; Brown, Steve D M; Parkinson, Helen; Meehan, Terrence F; Smedley, Damian

The Deep Genome Project

深度基因组计划

Lloyd, K C Kent; Adams, David J; Baynam, Gareth; Beaudet, Arthur L; Bosch, Fatima; Boycott, Kym M; Braun, Robert E; Caulfield, Mark; Cohn, Ronald; Dickinson, Mary E; Dobbie, Michael S; Flenniken, Ann M; Flicek, Paul; Galande, Sanjeev; Gao, Xiang; Grobler, Anne; Heaney, Jason D; Herault, Yann; de Angelis, Martin Hrabě; Lupski, James R; Lyonnet, Stanislas; Mallon, Ann-Marie; Mammano, Fabio; MacRae, Calum A; McInnes, Roderick; McKerlie, Colin; Meehan, Terrence F; Murray, Stephen A; Nutter, Lauryl M J; Obata, Yuichi; Parkinson, Helen; Pepper, Michael S; Sedlacek, Radislav; Seong, Je Kyung; Shiroishi, Toshihiko; Smedley, Damian; Tocchini-Valentini, Glauco; Valle, David; Wang, Chi-Kuang Leo; Wells, Sara; White, Jacqueline; Wurst, Wolfgang; Xu, Ying; Brown, Steve D M