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

Ttc21b is required for proper proliferation of neural progenitor cells.

Ttc21b 是神经祖细胞正常增殖所必需的。

Niewoehner Rebekah, Paulding David, Leal Jesus M, Rushforth Rebekah, Stottmann Rolf W

Cranial neural crest shortage leads to extensive craniofacial anomalies in mice mutant for the NR2F1/2 nuclear receptors.

NR2F1/2 核受体突变小鼠的颅神经嵴不足会导致广泛的颅面畸形。

Paulding David, Han Simon J Y, Timmons Jonathan, Caye Michelle, Riedel Alexa, Brugmann Samantha A, Barske Lindsey

Towards Caring Technologies in Older Adult Care Through the Co-Creation of an Ethical Process Guide

通过共同创建伦理流程指南,迈向老年人护理中的关怀技术

Honinx, Elisabeth; van Schyndel, Cato; Roos, Arend; Paulding, Emily; Wright, Toni; Galvin, Kathleen; Fotis, Theofanis; Huber, Jorg; Laes, Erik; Lambrechts, Nathalie

Effect of PCSK9 Inhibition With Alirocumab in Patients With Probable Familial Hypercholesterolemia or Type III Hyperlipoproteinemia: Results From the ODYSSEY OUTCOMES Trial

使用阿利西尤单抗抑制PCSK9对可能患有家族性高胆固醇血症或III型高脂蛋白血症患者的影响:ODYSSEY OUTCOMES试验的结果

Geba, Gregory P; Mohammadi, Kusha A; Damask, Amy; Paulding, Charles; Lotta, Luca A; Hindy, George; Pordy, Robert; Manvelian, Garen; Shapiro, Michael D; Bittner, Vera A; Bhatt, Deepak L; Szarek, Michael; Schwartz, Gregory G; Steg, Ph Gabriel; Fazio, Sergio

Sox10 is required for systemic initiation of bone mineralization

Sox10 是系统性骨矿化启动所必需的

Stefani Gjorcheska, Sandhya Paudel, Sarah McLeod, David Paulding, Louisa Snape, Karen Camargo Sosa, Cunming Duan, Robert Kelsh, Lindsey Barske

Perdurant TTC21B protein in the early mouse embryo is required for proper forebrain neural progenitor proliferation

在小鼠早期胚胎中,持久存在的TTC21B蛋白是前脑神经祖细胞正常增殖所必需的。

Niewoehner, Rebekah; Paulding, David; Leal, Jesus; Stottmann, Rolf W

Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City

作者更正:对墨西哥城14万名成年人进行基因分型、测序和分析

Ziyatdinov, Andrey; Torres, Jason; Alegre-Díaz, Jesús; Backman, Joshua; Mbatchou, Joelle; Turner, Michael; Gaynor, Sheila M; Joseph, Tyler; Zou, Yuxin; Liu, Daren; Wade, Rachel; Staples, Jeffrey; Panea, Razvan; Popov, Alex; Bai, Xiaodong; Balasubramanian, Suganthi; Habegger, Lukas; Lanche, Rouel; Lopez, Alex; Maxwell, Evan; Jones, Marcus; García-Ortiz, Humberto; Ramirez-Reyes, Raul; Santacruz-Benítez, Rogelio; Nag, Abhishek; Smith, Katherine R; Damask, Amy; Lin, Nan; Paulding, Charles; Reppell, Mark; Zöllner, Sebastian; Jorgenson, Eric; Salerno, William; Petrovski, Slavé; Overton, John; Reid, Jeffrey; Thornton, Timothy A; Abecasis, Gonçalo; Berumen, Jaime; Orozco-Orozco, Lorena; Collins, Rory; Baras, Aris; Hill, Michael R; Emberson, Jonathan R; Marchini, Jonathan; Kuri-Morales, Pablo; Tapia-Conyer, Roberto

Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes

作者更正:常见和罕见变异与克隆性造血表型的关联

Kessler, Michael D; Damask, Amy; O'Keeffe, Sean; Banerjee, Nilanjana; Li, Dadong; Watanabe, Kyoko; Marketta, Anthony; Van Meter, Michael; Semrau, Stefan; Horowitz, Julie; Tang, Jing; Kosmicki, Jack A; Rajagopal, Veera M; Zou, Yuxin; Houvras, Yariv; Ghosh, Arkopravo; Gillies, Christopher; Mbatchou, Joelle; White, Ryan R; Verweij, Niek; Bovijn, Jonas; Parikshak, Neelroop N; LeBlanc, Michelle G; Jones, Marcus; Glass, David J; Lotta, Luca A; Cantor, Michael N; Atwal, Gurinder S; Locke, Adam E; Ferreira, Manuel A R; Deering, Raquel; Paulding, Charles; Shuldiner, Alan R; Thurston, Gavin; Ferrando, Adolfo A; Salerno, Will; Reid, Jeffrey G; Overton, John D; Marchini, Jonathan; Kang, Hyun M; Baras, Aris; Abecasis, Gonçalo R; Jorgenson, Eric

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

药物和基因手段下调前蛋白转化酶枯草杆菌蛋白酶/Kexin 9型与脓毒症生存率

Lawler, Patrick R; Manvelian, Garen; Coppi, Alida; Damask, Amy; Cantor, Michael N; Ferreira, Manuel A R; Paulding, Charles; Banerjee, Nilanjana; Li, Dadong; Jorgensen, Susan; Attre, Richa; Carey, David J; Krebs, Kristi; Milani, Lili; Hveem, Kristian; Damås, Jan K; Solligård, Erik; Stender, Stefan; Tybjærg-Hansen, Anne; Nordestgaard, Børge G; Hernandez-Beeftink, Tamara; Rogne, Tormod; Flores, Carlos; Villar, Jesús; Walley, Keith R; Liu, Vincent X; Fohner, Alison E; Lotta, Luca A; Kyratsous, Christos A; Sleeman, Mark W; Scemama, Michel; DelGizzi, Richard; Pordy, Robert; Horowitz, Julie E; Baras, Aris; Martin, Greg S; Steg, Philippe Gabriel; Schwartz, Gregory G; Szarek, Michael; Goodman, Shaun G

Common and rare variant associations with clonal haematopoiesis phenotypes

常见和罕见变异与克隆性造血表型的关联

Kessler, Michael D; Damask, Amy; O'Keeffe, Sean; Banerjee, Nilanjana; Li, Dadong; Watanabe, Kyoko; Marketta, Anthony; Van Meter, Michael; Semrau, Stefan; Horowitz, Julie; Tang, Jing; Kosmicki, Jack A; Rajagopal, Veera M; Zou, Yuxin; Houvras, Yariv; Ghosh, Arkopravo; Gillies, Christopher; Mbatchou, Joelle; White, Ryan R; Verweij, Niek; Bovijn, Jonas; Parikshak, Neelroop N; LeBlanc, Michelle G; Jones, Marcus; Glass, David J; Lotta, Luca A; Cantor, Michael N; Atwal, Gurinder S; Locke, Adam E; Ferreira, Manuel A R; Deering, Raquel; Paulding, Charles; Shuldiner, Alan R; Thurston, Gavin; Ferrando, Adolfo A; Salerno, Will; Reid, Jeffrey G; Overton, John D; Marchini, Jonathan; Kang, Hyun M; Baras, Aris; Abecasis, Gonçalo R; Jorgenson, Eric