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

Facilitators and Barriers to Uptake of Genetic and Cascade Testing in Familial Hypercholesterolemia: a Systematic Review

家族性高胆固醇血症基因检测和级联检测普及的促进因素和障碍:系统评价

Lenin, Chaitanyasre; Lim, Phoebe X H; Nastar, Ashna; Subramaniam, Tavintharan; Pek, Sharon; Daccord, Magdalena; Evans, Elsie; Print, Emma; Chan, Frederick H F; Griva, Konstadina

FH Genetic Testing in Preventive Cardiology: Unpacking Challenges and Enablers Beyond Cost

预防心脏病学中的FH基因检测:成本之外的挑战与推动因素

Lenin, Chaitanyasre; Chan, Frederick H F; Lim, Phoebe X H; Ang, Gregory; Nastar, Ashna; Daccord, Magdalena; Print, Emma; Pek, Sharon; Subramaniam, Tavintharan; Griva, Konstadina

Monitoring rapid degradation of NANOG reveals UTP15 maintains pluripotency by regulating nascent transcripts.

监测 NANOG 的快速降解表明 UTP15 通过调节新生转录本来维持多能性。

Deng Mingqiang, He Dongmei, Wang Xiwei, Yuan Yuting, Wang Lishen, Hou Yanlin, Zhu Qiuyue, Zhou Chuanman, Mai Zhibiao, Zhang Yulong, Nie Zhengwen, Song Yuling, Wu Qiongfang, Pan Luyao, Dong Bei, Xiong Zhi, Li Duo, Liu Dongjun, Xu Jinxin, Qin Dajiang, Zheng Hui, Zhao Yu, Tang Peng, Wang Jinkai, Print Cristin, Jauch Ralf, Zhang Wensheng, Wu Guangming, Bao Xichen

Living with Elevated Lipoprotein(a) Levels: The Experiences of Patients and Caregivers

高脂蛋白(a)水平患者的生活:患者和护理人员的经历

Steinhagen-Thiessen, Elisabeth; Daccord, Magdalena; Print, Emma C; Wang, Yujiao; Shipton, Janine; Rijken, India; Shipton, Michael; Perna, Flavia; Schoenberger, Matthias

Rakeiora Genomics Platform: a pathfinder for genomic medicine research in Aotearoa New Zealand

拉凯奥拉基因组学平台:新西兰基因组医学研究的先行者

Rye, Claire E; Puketapu-Watson, Huti; Wihongi, Helen; Aika, Ben Te; Macartney-Coxson, Donia; de Ligt, Joep; Print, Cristin G; Le Quesne Stabej, Polona; Tsai, Peter; Curran, Ben; Jones, Nick; Huh, Jun; Perkins, E Owen; Pestle, Matt; Zhao, Kenny; Halytskyy, Yuriy; Robertson, Stephen P; Halliday, Benjamin J; Goodin, Elizabeth; Markie, David M; Lamont, Alastair; Wilcox, Phillip

Analyzing 6211 unique variants in the upgraded interactive FVIII web database reveals novel insights into hemophilia A

对升级后的交互式FVIII网络数据库中6211个独特变异体的分析,揭示了血友病A的新见解

Print, Emily H T; Simmons, Anna M; Spencer, Holly J; Efthymiou, Christos; Harris, Victoria A; Perkins, Stephen J

Vaginal microbiome dysbiosis and sexually transmitted infections correlate with concentrations of immunoglobulin isotypes in human cervicovaginal mucus: insights into HIV-1 transmission

阴道微生物群失调和性传播感染与人类宫颈阴道粘液中免疫球蛋白同种型的浓度相关:对 HIV-1 传播的启示

Akiso, Matrona M; Abook, Israel; Mureithi, Marianne W; Kombo, Janet; Koi, Print; Musando, Joel; Chirchir, Ruth J; McRaven, Michael D; Carias, Ann M; Joseph, Sarah; Anzala, Omu; Hope, Thomas J

Blending space and time to talk about cancer in extended reality

融合空间和时间,以扩展现实的方式探讨癌症

Robb, Tamsin J; Liu, Yinan; Woodhouse, Braden; Windahl, Charlotta; Hurley, Daniel; McArthur, Grant; Fox, Stephen B; Brown, Lisa; Guilford, Parry; Minhinnick, Alice; Jackson, Christopher; Blenkiron, Cherie; Parker, Kate; Henare, Kimiora; McColl, Rose; Haux, Bianca; Young, Nick; Boyle, Veronica; Cameron, Laird; Deva, Sanjeev; Reeve, Jane; Print, Cristin G; Davis, Michael; Rieger, Uwe; Lawrence, Ben

Biallelic ATP2B1 variants as a likely cause of a novel neurodevelopmental malformation syndrome with primary hypoparathyroidism

双等位基因 ATP2B1 变异可能是导致一种伴有原发性甲状旁腺功能减退的新型神经发育畸形综合征的原因

Yap, Patrick; Riley, Lisa G; Kakadia, Purvi M; Bohlander, Stefan K; Curran, Ben; Rahimi, Meer Jacob; Alburaiky, Salam; Hayes, Ian; Oppermann, Henry; Print, Cristin; Cooper, Sandra T; Le Quesne Stabej, Polona

A validated restriction enzyme ddPCR cg05575921 (AHRR) assay to accurately assess smoking exposure

经验证的限制性内切酶 ddPCR cg05575921 (AHRR) 检测方法可准确评估吸烟暴露

Fitzgerald, Sandra; Bhat, Basharat; Print, Cristin; Jones, Gregory T