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

Isn't it ironic? Functional iron deficiency at the core of Parkinson's disease pathobiology

这不是很讽刺吗?帕金森病病理生物学的核心竟然是功能性缺铁。

Peikon, Ian; Andrews, Nancy C

Funding FAIRly: A New Model for Biomedical Research

公平资助:生物医学研究的新模式

Agarwal, Anupam; Marek, Kurt; Andrews, Nancy C; Vazquez, Diego R; Incalcaterra, James; Lei, Ming; Fox, Howard; Gordon-Larsen, Penny; Lodge, Jennifer K; Wigginton, Nick; Droegemeier, Kelvin

David Baltimore: Scientist, leader, and mentor

大卫·巴尔的摩:科学家、领导者和导师

Andrews, Nancy C; Daley, George Q

International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease

国际精准儿童健康伙伴关系(IPCHiP):一项旨在加速罕见儿科疾病发现并改善治疗效果的倡议

Howell, Katherine B; White, Susan M; McTague, Amy; D'Gama, Alissa M; Costain, Gregory; Poduri, Annapurna; Scheffer, Ingrid E; Chau, Vann; Smith, Lindsay D; Stephenson, Sarah E M; Wojcik, Monica; Davidson, Andrew; Sebire, Neil; Sliz, Piotr; Beggs, Alan H; Chitty, Lyn S; Cohn, Ronald D; Marshall, Christian R; Andrews, Nancy C; North, Kathryn N; Cross, J Helen; Christodoulou, John; Scherer, Stephen W

Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes

全院范围内获取基因组数据促进了儿科罕见病研究和临床疗效。

French, Courtney E; Andrews, Nancy C; Beggs, Alan H; Boone, Philip M; Brownstein, Catherine A; Chopra, Maya; Chou, Janet; Chung, Wendy K; D'Gama, Alissa M; Doan, Ryan N; Ebrahimi-Fakhari, Darius; Goldstein, Richard D; Irons, Mira; Jacobsen, Christina; Kenna, Margaret; Lee, Ted; Madden, Jill A; Majmundar, Amar J; Mann, Nina; Morton, Sarah U; Poduri, Annapurna; Randolph, Adrienne G; Roberts, Amy E; Roberts, Stephanie; Sampson, Matthew G; Shao, Diane D; Shao, Wanqing; Sharma, Aditi; Shearer, Eliot; Shimamura, Akiko; Snapper, Scott B; Srivastava, Siddharth; Thiagarajah, Jay R; Whitman, Mary C; Wojcik, Monica H; Rockowitz, Shira; Sliz, Piotr

Evidence generation and reproducibility in cell and gene therapy research: A call to action

细胞和基因治疗研究中的证据生成和可重复性:行动呼吁

Abou-El-Enein, Mohamed; Angelis, Aris; Appelbaum, Frederick R; Andrews, Nancy C; Bates, Susan E; Bierman, Arlene S; Brenner, Malcolm K; Cavazzana, Marina; Caligiuri, Michael A; Clevers, Hans; Cooke, Emer; Daley, George Q; Dzau, Victor J; Ellis, Lee M; Fineberg, Harvey V; Goldstein, Lawrence S B; Gottschalk, Stephen; Hamburg, Margaret A; Ingber, Donald E; Kohn, Donald B; Krainer, Adrian R; Maus, Marcela V; Marks, Peter; Mummery, Christine L; Pettigrew, Roderic I; Rutter, Joni L; Teichmann, Sarah A; Terzic, Andre; Urnov, Fyodor D; Williams, David A; Wolchok, Jedd D; Lawler, Mark; Turtle, Cameron J; Bauer, Gerhard; Ioannidis, John P A

Control of Systemic Iron Homeostasis by the 3' Iron-Responsive Element of Divalent Metal Transporter 1 in Mice

小鼠体内二价金属转运蛋白1的3'铁反应元件对系统性铁稳态的控制

Tybl, Elisabeth; Gunshin, Hiromi; Gupta, Sanjay; Barrientos, Tomasa; Bonadonna, Michael; Celma Nos, Ferran; Palais, Gael; Karim, Zoubida; Sanchez, Mayka; Andrews, Nancy C; Galy, Bruno

A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency

TFRC基因(编码转铁蛋白受体1)的错义突变会导致联合免疫缺陷。

Jabara, Haifa H; Boyden, Steven E; Chou, Janet; Ramesh, Narayanaswamy; Massaad, Michel J; Benson, Halli; Bainter, Wayne; Fraulino, David; Rahimov, Fedik; Sieff, Colin; Liu, Zhi-Jian; Alshemmari, Salem H; Al-Ramadi, Basel K; Al-Dhekri, Hasan; Arnaout, Rand; Abu-Shukair, Mohammad; Vatsayan, Anant; Silver, Eli; Ahuja, Sanjay; Davies, E Graham; Sola-Visner, Martha; Ohsumi, Toshiro K; Andrews, Nancy C; Notarangelo, Luigi D; Fleming, Mark D; Al-Herz, Waleed; Kunkel, Louis M; Geha, Raif S

Metabolic Catastrophe in Mice Lacking Transferrin Receptor in Muscle

肌肉中缺乏转铁蛋白受体的小鼠发生代谢灾难

Barrientos, Tomasa; Laothamatas, Indira; Koves, Timothy R; Soderblom, Erik J; Bryan, Miles; Moseley, M Arthur; Muoio, Deborah M; Andrews, Nancy C

Lethal Cardiomyopathy in Mice Lacking Transferrin Receptor in the Heart

缺乏转铁蛋白受体的小鼠心脏发生致命性心肌病

Xu, Wenjing; Barrientos, Tomasa; Mao, Lan; Rockman, Howard A; Sauve, Anthony A; Andrews, Nancy C