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

Label-free Brillouin endo-microscopy for the quantitative 3D imaging of sub-micrometre biology

无标记布里渊内窥镜用于亚微米生物学的定量三维成像

Salvatore La Cavera 3rd, Veeren M Chauhan, William Hardiman, Mengting Yao, Rafael Fuentes-Domínguez, Kerry Setchfield, Sidahmed A Abayzeed, Fernando Pérez-Cota, Richard J Smith, Matt Clark

Tropomyosin 1: Multiple roles in the developing heart and in the formation of congenital heart defects

原肌球蛋白 1:在心脏发育和先天性心脏缺陷形成中发挥多种作用

Jennifer England, Javier Granados-Riveron, Luis Polo-Parada, Diji Kuriakose, Christopher Moore, J David Brook, Catrin S Rutland, Kerry Setchfield, Christopher Gell, Tushar K Ghosh, Frances Bu'Lock, Christopher Thornborough, Elisabeth Ehler, Siobhan Loughna

Rare variants in NR2F2 cause congenital heart defects in humans

NR2F2基因的罕见变异会导致人类先天性心脏缺陷。

Saeed Al Turki ,Ashok K Manickaraj ,Catherine L Mercer ,Sebastian S Gerety ,Marc-Phillip Hitz ,Sarah Lindsay ,Lisa C A D'Alessandro ,G Jawahar Swaminathan ,Jamie Bentham ,Anne-Karin Arndt ,Jacoba Louw, Jacoba Low ,Jeroen Breckpot ,Marc Gewillig ,Bernard Thienpont ,Hashim Abdul-Khaliq ,Christine Harnack ,Kirstin Hoff ,Hans-Heiner Kramer ,Stephan Schubert ,Reiner Siebert ,Okan Toka ,Catherine Cosgrove ,Hugh Watkins ,Anneke M Lucassen ,Ita M O'Kelly ,Anthony P Salmon ,Frances A Bu'lock ,Javier Granados-Riveron ,Kerry Setchfield ,Chris Thornborough ,J David Brook ,Barbara Mulder ,Sabine Klaassen ,Shoumo Bhattacharya ,Koen Devriendt ,David F Fitzpatrick ,Seema Mital ,Matthew E Hurles

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

全球罕见拷贝数变异对散发性先天性心脏病风险的贡献

Rachel Soemedi, Ian J Wilson, Jamie Bentham, Rebecca Darlay, Ana Töpf, Diana Zelenika, Catherine Cosgrove, Kerry Setchfield, Chris Thornborough, Javier Granados-Riveron, Gillian M Blue, Jeroen Breckpot, Stephen Hellens, Simon Zwolinkski, Elise Glen, Chrysovalanto Mamasoula, Thahira J Rahman, Darroch