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

A multimodal dataset for human robot collaborative systems: Experimental data

用于人机协作系统的多模态数据集:实验数据

Mehak, Shakra; Jain, Aayush; Kelleher, John D; Guilfoyle, Michael; Long, Philip; Leva, Maria Chiara

Heterogeneous nuclear ribonucleoprotein E1 binds polycytosine DNA and monitors genome integrity

异质性核糖核蛋白 E1 结合多胞嘧啶 DNA 并监测基因组完整性

Bidyut K Mohanty, Joseph Aq Karam, Breege V Howley, Annamarie C Dalton, Simon Grelet, Toros Dincman, William S Streitfeld, Je-Hyun Yoon, Lata Balakrishnan, Walter J Chazin, David T Long, Philip H Howe

A Holistic Approach to Human-Supervised Humanoid Robot Operations in Extreme Environments

极端环境下人机协作类人机器人操作的整体方法

Wonsick, Murphy; Long, Philip; Önol, Aykut Özgün; Wang, Maozhen; Padır, Taşkın

Benign overfitting in linear regression

线性回归中的良性过拟合

Bartlett, Peter L; Long, Philip M; Lugosi, Gábor; Tsigler, Alexander

Machiavellian Ways to Academic Cheating: A Mediational and Interactional Model

马基雅维利式的学术作弊方式:一种中介和互动模型

Barbaranelli, Claudio; Farnese, Maria L; Tramontano, Carlo; Fida, Roberta; Ghezzi, Valerio; Paciello, Marinella; Long, Philip

Structural and Chemical Modification to Improve Adhesive and Material Properties of Fibrin-Genipin for Repair of Annulus Fibrosus Defects in Intervertebral Disks

结构和化学改性以提高纤维蛋白-京尼平的粘合性和材料性能,用于修复椎间盘纤维环缺损

Michelle A Cruz, Steven McAnany, Nikita Gupta, Rose G Long, Philip Nasser, David Eglin, Andrew C Hecht, Svenja Illien-Junger, James C Iatridis

Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures.

SLC12A5 基因突变与婴儿期游走性局灶性癫痫发作相关

Stödberg Tommy, McTague Amy, Ruiz Arnaud J, Hirata Hiromi, Zhen Juan, Long Philip, Farabella Irene, Meyer Esther, Kawahara Atsuo, Vassallo Grace, Stivaros Stavros M, Bjursell Magnus K, Stranneheim Henrik, Tigerschiöld Stephanie, Persson Bengt, Bangash Iftikhar, Das Krishna, Hughes Deborah, Lesko Nicole, Lundeberg Joakim, Scott Rod C, Poduri Annapurna, Scheffer Ingrid E, Smith Holly, Gissen Paul, Schorge Stephanie, Reith Maarten E A, Topf Maya, Kullmann Dimitri M, Harvey Robert J, Wedell Anna, Kurian Manju A

Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family

MRX78家族中IQSEC2基因的新型错义突变A789V是X连锁智力障碍的根本原因。

Kalscheuer, Vera M; James, Victoria M; Himelright, Miranda L; Long, Philip; Oegema, Renske; Jensen, Corinna; Bienek, Melanie; Hu, Hao; Haas, Stefan A; Topf, Maya; Hoogeboom, A Jeannette M; Harvey, Kirsten; Walikonis, Randall; Harvey, Robert J

Missense Mutation R338W in ARHGEF9 in a Family with X-linked Intellectual Disability with Variable Macrocephaly and Macro-Orchidism

一例X连锁智力障碍家族中,ARHGEF9基因R338W错义突变伴有不同程度的巨头畸形和睾丸增大。

Long, Philip; May, Melanie M; James, Victoria M; Grannò, Simone; Johnson, John P; Tarpey, Patrick; Stevenson, Roger E; Harvey, Kirsten; Schwartz, Charles E; Harvey, Robert J

Spatial distribution of an uranium-respiring betaproteobacterium at the Rifle, CO field research site

科罗拉多州莱福野外研究点铀呼吸β-变形菌的空间分布

Koribanics, Nicole M; Tuorto, Steven J; Lopez-Chiaffarelli, Nora; McGuinness, Lora R; Häggblom, Max M; Williams, Kenneth H; Long, Philip E; Kerkhof, Lee J