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

De Novo Germline L858R EGFR Variants and Generalized Acanthosis Nigricans.

De Novo Germline L858R EGFR 变异与全身性黑棘皮病。

Jiang Xingyuan, Jeng Mark Y, Yang Zhou, Ugwu Nelson, Cheng Yuan, Echeandia-Francis Caroline, Mortlock Ryland D, Mani Mitra V, Rekhtman Natasha, Podolanczuk Anna J, Fiorino Elizabeth, Plodkowski Andrew, Lekwuttikarn Ramrada, Teng Joyce, Walsh Michael F, Yu Helena A, Lin Zhimiao, Choate Keith A

Development of an early prediction model for endometriosis risk: the simplified adolescent factors for endometriosis (SAFE) score

建立子宫内膜异位症风险早期预测模型:简化的青少年子宫内膜异位症因素(SAFE)评分

Mishra, Gita D; Baneshi, Mohammad Reza; Mortlock, Sally; Montgomery, Grant W; Doust, Jenny; Dobson, Annette J; Abbott, Jason

Prenatal Intraportal Delivery of Polymeric Nanoparticles to Fetal Rhesus Monkeys (Macaca mulatta)

向恒河猴胎儿(Macaca mulatta)进行产前门静脉内聚合物纳米颗粒递送

Piotrowski-Daspit, Alexandra S; Lynn, Anna Y; Eaton, David A; Bracaglia, Laura G; Markey, Arianna I; Mortlock, Ryland D; Stitelman, David H; Martinez, Michele L; Lee, Charles C; Kliman, Harvey J; Glazer, Peter M; Tarantal, Alice F; Saltzman, W Mark

Impact of adverse childhood experiences on health-related quality of life in Australian women with endometriosis: a population-based cohort study

童年期不良经历对澳大利亚子宫内膜异位症女性健康相关生活质量的影响:一项基于人群的队列研究

Gete, Dereje G; Doust, Jenny; Mortlock, Sally; Abbott, Jason; Mishra, Gita D

Erythrokeratodermia-Cardiomyopathy Syndrome: Expanding the DSP Mutational Spectrum Beyond Proline Substitutions

红斑角化病-心肌病综合征:DSP突变谱的扩展,超越脯氨酸取代

Hamzehlou, Sepideh; Mortlock, Ryland D; Echeandia-Francis, Caroline; Zhou, Jing; Xing, Chao; Agim, Nnenna G; Choate, Keith A; Glass, Donald A 2nd

Decoding the blueprint of receptor binding by filoviruses through large-scale binding assays and machine learning.

通过大规模结合试验和机器学习解码丝状病毒受体结合的蓝图

Lasso Gorka, Grodus Michael, Valencia Estefania, DeJesus Veronica, Liang Eliza, Delwel Isabel, Bortz Rob H 3rd, Lupyan Dmitry, Ehrlich Hanna Y, Castellanos Adrian A, Gazzo Andrea, Wells Heather L, Wacharapluesadee Supaporn, Tremeau-Bravard Alexandre, Seetahal Janine F R, Hughes Tom, Lee Jimmy, Lee Mei-Ho, Sjodin Anna R, Geldenhuys Marike, Mortlock Marinda, Navarrete-Macias Isamara, Gilardi Kirsten, Willig Michael R, Nava Alessandra F D, Loh Elisabeth H, Asrat Makda, Smiley-Evans Tierra, Magesa Walter S, Zikankuba Sijali, Wolking David, Suzán Gerardo, Ojeda-Flores Rafael, Carrington Christine V F, Islam Ariful, Epstein Jonathan H, Markotter Wanda, Johnson Christine K, Goldstein Tracey, Han Barbara A, Mazet Jonna A K, Jangra Rohit K, Chandran Kartik, Anthony Simon J

Multi-state detection and spatial addressing in a microscope for ultracold molecules

超冷分子显微镜中的多态检测和空间寻址

Mortlock, Jonathan M; Raghuram, Adarsh P; Maddox, Benjamin P; Gregory, Philip D; Cornish, Simon L

M2 Macrophages are Major Mediators of Germline Risk of Endometriosis and Explain Pleiotropy With Comorbid Traits

M2巨噬细胞是子宫内膜异位症生殖系风险的主要介质,并解释了其与合并症特征的多效性。

Ochoa, Soledad; Rasquel-Oliveira, Fernanda S; McKinnon, Brett; Haro, Marcela; Subramaniam, Sugarniya; Yu, Pak; Coetzee, Simon; Anglesio, Michael S; Wright, Kelly N; Meyer, Raanan; Porter, Anne E; Gargett, Caroline E; Mortlock, Sally; Montgomery, Grant W; Rogers, Michael S; Lawrenson, Kate

Autosomal dominant SLURP1 variants cause palmoplantar keratoderma and progressive symmetric erythrokeratoderma

常染色体显性遗传的SLURP1变异会导致掌跖角化症和进行性对称性红斑角化症。

Jiang, Xingyuan; Mortlock, Ryland D; Lomakin, Ivan B; Zhou, Jing; Hu, Ronghua; Cossio, María Laura; Bunick, Christopher G; Choate, Keith A

Linear epidermal naevus associated with a novel mosaic heterozygous PTPN11 variant

与一种新型嵌合杂合PTPN11变异相关的线状表皮痣

Jiang, Xingyuan; Chen, Tiffany X; Hu, Ronghua; Mortlock, Ryland D; Ko, Christine; Choate, Keith A