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

Genetically Engineered, Multichromophore Virus-Like Nanoparticles with Ultranarrow Distribution of Emission Intensity

基因工程改造的多色团病毒样纳米颗粒,具有超窄的发射强度分布

Tsvetkova, Irina B; Roos, Nora; Miller, Lohra M; DiNunno, Nadia; Conrady, Marcel; Ebert, Domenic; Lilie, Hauke; Scott, Liam W; Jarrold, Martin F; Wang, Joseph Che-Yen; Simon, Claudia; Dragnea, Bogdan

HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvement

HTRA1/lncRNA HTRA1-AS1 在年龄相关性黄斑变性网状假性玻璃膜疣的遗传风险中占主导地位,且不涉及补体系统。

Farashi, Samaneh; Abbott, Carla J; Ansell, Brendan R E; Wu, Zhichao; Altay, Lebriz; Arnon, Ella; Arnould, Louis; Bagdasarova, Yelena; Balaskas, Konstantinos; Chen, Fred K; Chew, Emily; Chowers, Itay; Clarke, Steven; Cukras, Catherine; Delcourt, Cécile; Delyfer, Marie-Noëlle; den Hollander, Anneke I; Fauser, Sascha; Finger, Robert P; Gabrielle, Pierre-Henry; Han, Jiru; Hodgson, Lauren A B; Hogg, Ruth; Holz, Frank G; Hoyng, Carel; Kumar, Himeesh; Lad, Eleonora M; Lee, Aaron; Luhmann, Ulrich F O; Mauschitz, Matthias M; McKnight, Amy J; McLenachan, Samuel; Mishra, Aniket; Moghul, Ismail; Orozco, Luz D; Sampson, Danuta M; Scott, Liam W; Sitnilska, Vasilena; Song, Scott; Stockwell, Amy; Swaroop, Anand; Terheyden, Jan H; Tiosano, Liran; Tufail, Adnan; Yaspan, Brian L; Pébay, Alice; Fletcher, Erica L; Guymer, Robyn H; Bahlo, Melanie

Quantitative Protein Expression of Antibody-Drug Conjugate Targets in EGFR Mutated and Wild-type Non-Small Cell Lung Cancer.

EGFR突变型和野生型非小细胞肺癌中抗体药物偶联靶点的定量蛋白表达

Trontzas Ioannis P, He Mengni, Wurtz Anna, Robbins Charles J, Robinson Nathaniel, Bates Katherine, Liu Matthew, Aung Thazin N, Scott Liam, Chan Nay, Burela Sneha, Schillo Jacob, Liebler Daniel C, Hill Salisha, Morrison Ryan D, Vathiotis Ioannis, Syrigos Konstantinos N, Goldberg Sarah B, Politi Katerina, Rimm David L

Quantitative Multiplex Immunofluorescence Assay for Trophoblast Cell-Surface Antigen 2 and Human Epidermal Growth Factor Receptor 2 Expression in Breast Cancer: Toward Guiding Patient Selection for Antibody-Drug Conjugate Therapies

乳腺癌滋养层细胞表面抗原2和人表皮生长因子受体2表达的定量多重免疫荧光检测:指导抗体药物偶联疗法的患者选择

Robbins, Charles J; He, Mengni; Chan, Nay; Khaimova, Revekka; Bates, Katherine; Trontzas, Ioannis P; Scott, Liam; Moutafi, Myrto; Coleman, Chandra B; Hill, Salisha; Liebler, Daniel C; Fulton, Regan; Rimm, David L

A prospective trial comparing programmable targeted long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxia

一项前瞻性试验比较了可编程靶向长读长测序和短读长基因组测序在小脑共济失调基因诊断中的应用。

Rafehi, Haloom; Fearnley, Liam G; Read, Justin; Snell, Penny; Davies, Kayli C; Scott, Liam; Gillies, Greta; Thompson, Genevieve C; Field, Tess A; Eldo, Aleena; Bodek, Simon; Butler, Ernest; Chen, Luke; Drago, John; Goel, Himanshu; Hackett, Anna; Halmagyi, G Michael; Hannaford, Andrew; Kotschet, Katya; Kumar, Kishore R; Kumble, Smitha; Lee-Archer, Matthew; Malhotra, Abhishek; Paine, Mark; Poon, Michael; Pope, Kate; Reardon, Katrina; Ring, Steven; Ronan, Anne; Silsby, Matthew; Smyth, Renee; Stutterd, Chloe; Wallis, Mathew; Waterston, John; Wellings, Thomas; West, Kirsty; Wools, Christine; Wu, Kathy H C; Szmulewicz, David J; Delatycki, Martin B; Bahlo, Melanie; Lockhart, Paul J

Validation and Prospective Testing of a High-Sensitivity, Quantitative Analytic Assay for HER2 on Histopathology Slides

组织病理切片上HER2高灵敏度定量分析检测的验证和前瞻性测试

Chan, Nay N N; Gaule, Patricia; Benanto, Julia; Scott, Liam; Robbins, Charles J; He, Mengni; Bates, Katherine; Khaimova, Revekka; Liebler, Daniel C; Fulton, Regan; Rimm, David L

Autofluorescence Virtual Staining System for H&E Histology and Multiplex Immunofluorescence Applied to Immuno-Oncology Biomarkers in Lung Cancer

用于肺癌免疫肿瘤生物标志物检测的H&E组织学和多重免疫荧光自发荧光虚拟染色系统

Loo, Jessica; Robbins, Marc; McNeil, Carson; Yoshitake, Tadayuki; Santori, Charles; Shan, Chuanhe Jay; Vyawahare, Saurabh; Patel, Hardik; Wang, Tzu Chien; Findlater, Robert; Steiner, David F; Rao, Sudha; Gutierrez, Michael; Wang, Yang; Sanchez, Adrian C; Yin, Raymund; Velez, Vanessa; Sigman, Julia S; Coutinho de Souza, Patricia; Chandrupatla, Hareesh; Scott, Liam; Weaver, Shamira S; Lee, Chung-Wein; Rivlin, Ehud; Goldenberg, Roman; Couto, Suzana S; Cimermancic, Peter; Wong, Pok Fai

Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing alone

基因组和RNA测序将神经肌肉疾病的诊断率从仅使用外显子组测序的34%提高到62%。

Marchant, Rhett G; Bryen, Samantha J; Bahlo, Melanie; Cairns, Anita; Chao, Katherine R; Corbett, Alastair; Davis, Mark R; Ganesh, Vijay S; Ghaoui, Roula; Jones, Kristi J; Kornberg, Andrew J; Lek, Monkol; Liang, Christina; MacArthur, Daniel G; Oates, Emily C; O'Donnell-Luria, Anne; O'Grady, Gina L; Osei-Owusu, Ikeoluwa A; Rafehi, Haloom; Reddel, Stephen W; Roxburgh, Richard H; Ryan, Monique M; Sandaradura, Sarah A; Scott, Liam W; Valkanas, Elise; Weisburd, Ben; Young, Helen; Evesson, Frances J; Waddell, Leigh B; Cooper, Sandra T

Genetic Risk of Reticular Pseudodrusen in Age-Related Macular Degeneration: HTRA1 /lncRNA BX842242.1 dominates, with no evidence for Complement Cascade involvement

年龄相关性黄斑变性中网状假性玻璃膜疣的遗传风险:HTRA1/lncRNA BX842242.1 占主导地位,无证据表明补体级联参与其中

Farashi, Samaneh; Abbott, Carla J; Ansell, Brendan Re; Wu, Zhichao; Altay, Lebriz; Arnon, Ella; Arnould, Louis; Bagdasarova, Yelena; Balaskas, Konstantinos; Chen, Fred K; Chew, Emily; Chowers, Itay; Clarke, Steven; Cukras, Catherine; Delcourt, Cécile; Delyfer, Marie-Noëlle; den Hollander, Anneke I; Fauser, Sascha; Finger, Robert P; Gabrielle, Pierre-Henry; Han, Jiru; Hodgson, Lauren Ab; Hogg, Ruth; Holz, Frank G; Hoyng, Carel; Kumar, Himeesh; Lad, Eleonora M; Lee, Aaron; Luhmann, Ulrich Fo; Mauschitz, Matthias M; McKnight, Amy J; McLenachan, Samuel; Mishra, Aniket; Moghul, Ismail; Orozco, Luz D; Sampson, Danuta M; Scott, Liam W; Sitnilska, Vasilena; Song, Scott; Stockwell, Amy; Swaroop, Anand; Terheyden, Jan H; Tiosano, Liran; Tufail, Adnan; Yaspan, Brian L; Pébay, Alice; Fletcher, Erica L; Guymer, Robyn H; Bahlo, Melanie

An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA27B/ATX-FGF14

FGF14基因内含子GAA重复序列扩增导致常染色体显性遗传的成人发病型共济失调SCA27B/ATX-FGF14

Rafehi, Haloom; Read, Justin; Szmulewicz, David J; Davies, Kayli C; Snell, Penny; Fearnley, Liam G; Scott, Liam; Thomsen, Mirja; Gillies, Greta; Pope, Kate; Bennett, Mark F; Munro, Jacob E; Ngo, Kathie J; Chen, Luke; Wallis, Mathew J; Butler, Ernest G; Kumar, Kishore R; Wu, Kathy Hc; Tomlinson, Susan E; Tisch, Stephen; Malhotra, Abhishek; Lee-Archer, Matthew; Dolzhenko, Egor; Eberle, Michael A; Roberts, Leslie J; Fogel, Brent L; Brüggemann, Norbert; Lohmann, Katja; Delatycki, Martin B; Bahlo, Melanie; Lockhart, Paul J