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

Limiting ER-associated degradation capacity triggers acute and chronic effects on insulin biosynthesis

限制内质网相关降解能力会对胰岛素生物合成产生急性及慢性影响。

Arunagiri, Anoop; Haataja, Leena; Alam, Maroof; Gleason, Noah F; Mastroianni, Emma; Cheng, Chao-Yin; Bazzi, Sami; Knupp, Jeffrey; Metawea, Ibrahim; Hassan, Anis; Larkin, Dennis; Fang, Deyu; Tsai, Billy; Qi, Ling; Arvan, Peter

Aged murine bone marrow myeloid and mesenchymal cells develop unique senescence phenotypes.

老年小鼠骨髓髓系细胞和间充质细胞会发展出独特的衰老表型。

Doolittle Madison L, Froemming Mitchell N, Rowsey Jennifer L, Ruan Ming, Sapra Leena, Farr Joshua N, Monroe David G, Khosla Sundeep

Global trends in clozapine utilisation between 2014 and 2024: a longitudinal epidemiological study with data from 75 countries

2014年至2024年氯氮平使用情况的全球趋势:一项基于75个国家数据的纵向流行病学研究

Fitzgerald, Ita; O'Dwyer, Sarah; Dhubhlaing, Ciara Ní; Gee, Siobhan; Sahm, Laura J; Wheeler, Amanda; Hurley, Eoin; Saastamoinen, Leena; Waksmundzka-Walczuk, Anna; Donohue, Grainne; Shiers, David; Gupta, Veenu; Howe, Jo; Correll, Christoph U; Højlund, Mikkel

The Prevalence of Symptomatic Dermographism: Results of the International UCARE PREVALENCE-D Study

症状性皮肤划痕症的患病率:国际UCARE PREVALENCE-D研究结果

Kulthanan, Kanokvalai; Bernstein, Jonathan A; Rudenko, Michael; Salameh, Pascale; Komoltri, Chulaluk; Adışen, Esra; Al Abri, Salma; Al-Ahmad, Mona; Al-Ahmed, Nasser; Al Hinai, Bushra; Allenova, Anastasiia; Alshareef, Saad; Angkoolpakdeekul, Nattha; Arnaout, Rand; Bartosińska, Joanna; Cherrez-Ojeda, Ivan; Chularojanamontri, Leena; Criado, Paulo Ricardo; Ensina, Luis Felipe; Criado, Roberta Fachini Jardim; Calle, Cesar Alberto Galvan; Giménez-Arnau, Ana Maria; Godse, Kiran; Gotua, Maia; Inomata, Naoko; Jantanapornchai, Nuttagarn; Jung, Chang-Gyu; Kasperska-Zając, Alicja; Khoshkhui, Maryam; Kolkhir, Pavel; Krasowska, Dorota; Laomoleethorn, Jomgriditip; Maiorowa, Antonina; Meshkova, Raisa; Mijakoski, Dragan; Munoz, Melba; Nanchaipruek, Yanisorn; Nasr, Iman; Kara, Rabia Öztaş; Panjapakkul, Waratchaya; Paringkarn, Teerapat; Podder, Indrashis; Robles-Velasco, Karla; Rosmaninho, Isabel; Presa, Ana Rita; Rujitharanawong, Chuda; Saengthong-Aram, Phuwakorn; Tafrishi, Rana; Mitrevska, Natasa Teovska; Tuchinda, Papapit; Wannawittayapa, Teerapat; Wilson, Anushka; Ye, Young-Min; Zalewska-Janowska, Anna; Maurer, Marcus; Zuberbier, Torsten

Dietary intake of vitamins A, B, C, D and E and risk of islet autoimmunity and type 1 diabetes in genetically at-risk children: a prospective study from the DIPP birth cohort

维生素A、B、C、D和E的膳食摄入量与遗传高危儿童胰岛自身免疫和1型糖尿病风险的关系:一项来自DIPP出生队列的前瞻性研究

Mattila, Markus; Haario, Peppi; Hakola, Leena; Takkinen, Hanna-Mari; Peltonen, Essi J; Korhonen, Tuuli E; Ahonen, Suvi; Ilonen, Jorma; Toppari, Jorma; Knip, Mikael; Veijola, Riitta; Niinistö, Sari; Virtanen, Suvi M

GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy

GRIN2A基因的无义突变会增加早发性精神分裂症和其他精神障碍的风险,并有可能实现精准治疗。

Lemke, Johannes R; Eoli, Andrea; Krey, Ilona; Popp, Bernt; Strehlow, Vincent; Wittekind, Dirk A; Vuorinen, Anna-Leena; Aldhalaan, Hesham M; Baer, Sarah; de Saint Martin, Anne; Hammer, Trine B; Herman, Isabella; Hornemann, Frauke; Ingebrigtsen, Trine; Lederer, Damien; Lesca, Gaetan; Marafie, Dana; Mathot, Mikael; Rosenfeld, Jill A; Møller, Rikke S; Schelhaas, Helenius J; Stillman, Chelsey; Orsini, Alessandro; Patel, Anup D; Piard, Juliette; Veggiotti, Pierangelo; Vlaskamp, Danique R M; Weckhuysen, Sarah; Traynelis, Stephen F; Benke, Tim A; Heyne, Henrike O; Syrbe, Steffen

Correction: GRIN2A null variants confer a high risk for early-onset schizophrenia and other mental disorders and potentially enable precision therapy

更正:GRIN2A 基因缺失变异会增加早发性精神分裂症和其他精神障碍的风险,并可能使精准治疗成为可能。

Lemke, Johannes R; Eoli, Andrea; Krey, Ilona; Popp, Bernt; Strehlow, Vincent; Wittekind, Dirk A; Vuorinen, Anna-Leena; Aldhalaan, Hesham M; Baer, Sarah; de Saint Martin, Anne; Hammer, Trine B; Herman, Isabella; Hornemann, Frauke; Ingebrigtsen, Trine; Lederer, Damien; Lesca, Gaetan; Marafie, Dana; Mathot, Mikael; Rosenfeld, Jill A; Møller, Rikke S; Schelhaas, Helenius J; Stillman, Chelsey; Orsini, Alessandro; Patel, Anup D; Piard, Juliette; Veggiotti, Pierangelo; Vlaskamp, Danique R M; Weckhuysen, Sarah; Traynelis, Stephen F; Benke, Tim A; Heyne, Henrike O; Syrbe, Steffen

Subcellular mass spectrometry reveals proteome remodeling in an asymmetrically dividing (frog) embryonic stem cell

亚细胞质谱分析揭示了不对称分裂(蛙)胚胎干细胞中的蛋白质组重塑

Shen, Bowen; Pade, Leena R; Zhou, Fei; Nemes, Peter

Placental histopathology and early childhood neurodevelopment in the Environmental influences on Child Health Outcomes cohort

环境因素对儿童健康结果影响队列研究中胎盘组织病理学和幼儿早期神经发育

Fisher, Stephanie A; Xun, Xiaoshuang; Gemmill, Alison; Yee, Lynn M; Mithal, Leena B; Hamvas, Aaron; Regnier, Raye-Ann de; Aschner, Judy L; Maitre, Nathalie L; O'Connor, Thomas G; Cowell, Whitney; Kahn, Linda G; Newman, Roger B; Miller, Richard K; Salafia, Carolyn; Elliott, Amy J; Singh, Anne M; Baumann-Blackmore, Nicole; Goldstein, Jeffery A

Bi-allelic variants in OLA1 cause a neurodevelopmental disorder with joint hypermobility

OLA1基因的双等位基因变异会导致一种伴有关节过度活动的神经发育障碍。

AlAbdi, Lama; Sezer, Abdullah; Alzahrani, Fatema; Cevik, Sebiha; Demir, Zanyar; Abdullah, Nor Linda; Durukan, Özlem; Dallı, Efe; Hashem, Mais O; Abuyousef, Omar; Aljamal, Bayan; Helaby, Rana; Radwan, Mona; Jaafar, Amal; Alshidi, Tarfa; Salem, Israa; Hamid, Halima; Alhaddad, Bader; Bakur, Khadijah; Taşdelen, Elifcan; Kılıç, Mustafa; Al-Owain, Mohammed; Alhashem, Amal; Bratland, Eirik; Paulsen, Julie; Houge Douzgos, Gunnar; Politi, Anya Revah; Uguen, Kevin; Masson, Emmanuelle; Audebert, Severine; AlAnzi, Talal; Arold, Stefan T; Ergin, Bora; Ibrahim, Leena A; Kaplan, Oktay I; Alkuraya, Fowzan S