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

MAPK14 converges on key transcriptional machinery to promote vascular smooth muscle cell degeneration in abdominal aortic aneurysm.

MAPK14 作用于关键转录机制,促进腹主动脉瘤血管平滑肌细胞退化。

Wu Xiaoliang, Wang Chunhui, Ishimwe Nestor, Zhang Wei, Doja Jaser, Shan Shengshuai, Ge Chunyu, Sun Yong, Zhao Jinjing, Castillo Micah, Sotonyi Peter, Gyurok Gergo, Csanyi Gabor, Bryant W Bart, Dong Kunzhe, Chen Yabing, Vazquez-Padron Roberto, Miano Joseph M, Long Xiaochun

Application of machine learning in the diagnostic work-up of telomere biology disorders

机器学习在端粒生物学疾病诊断中的应用

Massaccesi, Erika; Arcuri, Luca; Cavalca, Giacomo; Beier, Fabian; Vankann, Lucia; Lupia, Michela; Cangelosi, Davide; Grossi, Alice; Lanciotti, Marina; Pierri, Filomena; Fioredda, Francesca; Miano, Maurizio; Dell'Orso, Gianluca; Giarratana, Maria Carla; Guardo, Daniela; Bagnasco, Francesca; Pestarino, Sara; Binelli, Maria; Tometten, Mareike; Meyer, Robert; Frenzel, Fanny; Coviello, Domenico; Mariani, Eugenia; Palmisani, Elena; Kainat, Saba; Ceccherini, Isabella; Uva, Paolo; Brümmendorf, Tim Henrik; Dufour, Carlo

Carriage of rare APOB variants predisposes to severe steatotic liver disease and hepatocellular carcinoma

携带罕见APOB变异基因会增加罹患严重脂肪肝和肝细胞癌的风险。

Mureddu, Matteo; Pelusi, Serena; Jamialahmadi, Oveis; Vujkovic, Marijana; Miano, Lorenzo; Eidgah Torghabehei, Hadi; Ronzoni, Luisa; Malvestiti, Francesco; Saracino, Marco; Periti, Giulia; Moretti, Vittoria; Teerlink, Craig C; Lynch, Julie A; Tsao, Philip S; Johnson, Josephine P; La Mura, Vincenzo; Dilena, Robertino; Alqahtani, Saleh A; Cherubini, Alessandro; Russo, Francesco Paolo; D'Ambrosio, Roberta; Fraquelli, Mirella; Petta, Salvatore; Miele, Luca; Vespasiani-Gentilucci, Umberto; Bugianesi, Elisabetta; Mancina, Rosellina M; Parini, Paolo; Prati, Daniele; Chang, Kyong-Mi; Schneider, Carolin V; Romeo, Stefano; Valenti, Luca Vc

The lysine methyltransferase KMT5a and p53 regulate the expression of the key autophagy adaptor p62/SQSTM1 in glioblastoma

赖氨酸甲基转移酶KMT5a和p53调控胶质母细胞瘤中关键自噬衔接蛋白p62/SQSTM1的表达

Della Monica, Rosa; Buonaiuto, Michela; Cuomo, Mariella; Drongitis, Denise; Miano, Maria Giuseppina; Costabile, Davide; de Riso, Giulia; Trio, Federica; Sabbarese, Marta; Ferraro, Sara; Oliva, Lorenza; Piacentino, Nives; Cappiello, Rosaria; Scotti, Gianluca; Lasorsa, Vito Alessandro; Capasso, Mario; De Bellis, Alberto; Del Basso De Caro, Marialaura; Chiariotti, Lorenzo; Visconti, Roberta

Perspective: Taxonomy of Kidney Diseases and Disorders Related to Nephrotoxic Drug Exposure in Hospitalized Patients

视角:住院患者肾毒性药物暴露相关肾脏疾病和病症的分类

Kane-Gill, Sandra L; Barreto, Erin F; Flannery, Alexander H; Miano, Todd A; Murugan, Raghavan; Ozrazgat-Baslanti, Tezcan; Bihorac, Azra; Kellum, John A

Loss of the Coronary Artery Disease Risk Gene Leiomodin1 in Vascular Smooth Muscle Cells Triggers Rapid Onset Coronary Atherosclerosis

血管平滑肌细胞中冠状动脉疾病风险基因Leiomodin1的缺失会引发冠状动脉粥样硬化的快速发生

Salem, Amr R; Doja, Jaser; Ge, Chunyu; Wally, Alshimaa; Slivano, Orazio J; Griffin, Susan H; Marshall, Brendan; Perry, Elizabeth; Seeley, Erin H; Dong, Kunzhe; Singla, Bhupesh; Boczkowska, Malgorzata; Csanyi, Gabor; Vazquez-Padron, Roberto I; Nanda, Vivek; Kumar, Ajay; Bryant, William B; Dominguez, Roberto; Long, Xiaochun; Miano, Joseph M

Genome-wide association study of long COVID

针对新冠长期症状的全基因组关联研究

Lammi, Vilma; Nakanishi, Tomoko; Jones, Samuel E; Andrews, Shea J; Karjalainen, Juha; Cortés, Beatriz; O'Brien, Heath E; Ochoa-Guzman, Ana; Fulton-Howard, Brian E; Broberg, Martin; Haapaniemi, Hele H; Kanai, Masahiro; Pirinen, Matti; Schmidt, Axel; Mitchell, Ruth E; Mousas, Abdou; Mangino, Massimo; Huerta-Chagoya, Alicia; Sinnott-Armstrong, Nasa; Cirulli, Elizabeth T; Vaudel, Marc; Kwong, Alex S F; Maiti, Amit K; Marttila, Minttu M; Posner, Daniel C; Rodriguez, Alexis A; Batini, Chiara; Minnai, Francesca; Dearman, Anna R; Warmerdam, C A Robert; Sequeros, Celia B; Winkler, Thomas W; Jordan, Daniel M; Rešcenko, Raimonds; Miano, Lorenzo; Lane, Jacqueline M; Chung, Ryan K; Guillen-Guio, Beatriz; Leavy, Olivia C; Carvajal-Silva, Laura; Aguilar-Valdés, Kevin; Frangione, Erika; Guare, Lindsay; Vergasova, Ekaterina; Marouli, Eirini; Striano, Pasquale; Zainulabid, Ummu Afeera; Kumar, Ashutosh; Ahmad, Hajar Fauzan; Edahiro, Ryuya; Azekawa, Shuhei; Luoh, Shiuh-Wen; Erikstrup, Christian; Pedersen, Ole B V; Lerner-Ellis, Jordan; Colombo, Alicia; Grzymski, Joseph J; Ishii, Makoto; Okada, Yukinori; Beckmann, Noam D; Kumari, Meena; Wagner, Ralf; Heid, Iris M; John, Catherine; Short, Patrick J; Magnus, Per; Ansone, Laura; Valenti, Luca V C; Lee, Sulggi A; Wain, Louise V; Verdugo, Ricardo A; Banasik, Karina; Geller, Frank; Franke, Lude H; Rakitko, Alexander; Duncan, Emma L; Renieri, Alessandra; Tsilidis, Konstantinos K; de Cid, Rafael; Niavarani, Ahmadreza; Abner, Erik; Tusié-Luna, Teresa; Verma, Shefali S; Smith, George Davey; Timpson, Nicholas J; Madduri, Ravi K; Cho, Kelly; Daly, Mark J; Ganna, Andrea; Schulte, Eva C; Richards, J Brent; Ludwig, Kerstin U; Marks-Hultström, Michael; Zeberg, Hugo; Ollila, Hanna M

MaTableGPT: GPT-Based Table Data Extractor from Materials Science Literature

MaTableGPT:基于GPT的材料科学文献表格数据提取器

Yi, Gyeong Hoon; Choi, Jiwoo; Song, Hyeongyun; Miano, Olivia; Choi, Jaewoong; Bang, Kihoon; Lee, Byungju; Sohn, Seok Su; Buttler, David; Hiszpanski, Anna; Han, Sang Soo; Kim, Donghun

Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities

腺苷脱氨酶2缺乏症患者早期骨髓改变与疾病表型和严重程度的关系

Dimitri Bulté ,Federica Barzaghi ,Cristina Mesa-Nuñez ,Chiara Rigamonti ,Luca Basso-Ricci ,Camilla Visconti ,Stefania Crippa ,Emanuela Pettinato ,Diego Gilioli ,Raffaella Milani ,Pamela Quaranta ,Roberta Caorsi ,Alessia Cafaro ,Giuliana Cangemi ,Michela Lupia ,Francesca Schena ,Alice Grossi ,Giulia Di Colo ,Silvia Federici ,Antonella Insalaco ,Fabrizio De Benedetti ,Sarah Marktel ,Raffaella Di Micco ,Maria Ester Bernardo ,Serena Scala ,Maria Pia Cicalese ,Francesca Conti ,Maurizio Miano ,Marco Gattorno ,Carlo Dufour ,Alessandro Aiuti ,Alessandra Mortellaro

Early bone marrow alterations in patients with adenosine deaminase 2 deficiency across disease phenotypes and severities

腺苷脱氨酶2缺乏症患者早期骨髓改变与疾病表型和严重程度的关系

Dimitri Bulté,Federica Barzaghi,Cristina Mesa-Nuñez,Chiara Rigamonti,Luca Basso-Ricci,Camilla Visconti,Stefania Crippa,Emanuela Pettinato,Diego Gilioli,Raffaella Milani,Pamela Quaranta,Roberta Caorsi,Alessia Cafaro,Giuliana Cangemi,Michela Lupia,Francesca Schena,Alice Grossi,Giulia Di Colo,Silvia Federici,Antonella Insalaco,Fabrizio De Benedetti,Sarah Marktel,Raffaella Di Micco,Maria Ester Bernardo,Serena Scala,Maria Pia Cicalese,Francesca Conti,Maurizio Miano,Marco Gattorno,Carlo Dufour,Alessandro Aiuti,Alessandra Mortellaro