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

A randomized, double-blinded, phase 2 trial of EDP1815, an oral immunomodulatory preparation of Prevotella histicola, in adults with mild-to-moderate plaque psoriasis

一项针对轻度至中度斑块状银屑病成年患者的随机、双盲、2期临床试验,研究了口服免疫调节剂Prevotella histicola(组织普雷沃氏菌)EDP1815的疗效。

Ehst, Benjamin D; Strober, Bruce; Blauvelt, Andrew; Maslin, Douglas; Macaro, Debbie; Carpenter, Nancy; Bodmer, Mark; McHale, Duncan

Clinical translation of anti-inflammatory effects of Prevotella histicola in Th1, Th2, and Th17 inflammation

普雷沃氏菌(Prevotella histicola)抗炎作用在Th1、Th2和Th17炎症中的临床转化

Itano, Andrea; Maslin, Douglas; Ramani, Kritika; Mehraei, Golbarg; Carpenter, Nancy; Cormack, Taylor; Saghari, Mahdi; Moerland, Matthijs; Troy, Erin; Caffry, Will; Wardwell-Scott, Leslie; Abel, Stuart; McHale, Duncan; Bodmer, Mark

Long-term treatment with romiplostim and treatment-free platelet responses in children with chronic immune thrombocytopenia

罗米司亭长期治疗及慢性免疫性血小板减少症患儿的无治疗血小板反应

Tarantino, Michael D; Bussel, James B; Blanchette, Victor S; Beam, Donald; Roy, John; Despotovic, Jenny; Raj, Ashok; Carpenter, Nancy; Mehta, Bhakti; Eisen, Melissa

Safety and efficacy of romiplostim in splenectomized and nonsplenectomized patients with primary immune thrombocytopenia

罗米司亭在脾切除和未脾切除的原发性免疫性血小板减少症患者中的安全性和有效性

Cines, Douglas B; Wasser, Jeffrey; Rodeghiero, Francesco; Chong, Beng H; Steurer, Michael; Provan, Drew; Lyons, Roger; Garcia-Chavez, Jaime; Carpenter, Nancy; Wang, Xuena; Eisen, Melissa

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Determine the Effect of Romiplostim on Health-Related Quality of Life in Children with Primary Immune Thrombocytopenia and Associated Burden in Their Parents

一项 3 期随机、双盲、安慰剂对照研究,旨在确定罗米司亭对原发性免疫性血小板减少症患儿的健康相关生活质量及其父母负担的影响

Mathias, Susan D; Li, Xiaoyan; Eisen, Melissa; Carpenter, Nancy; Crosby, Ross D; Blanchette, Victor S

The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies

通过对人类节段性三体进行高分辨率分析揭示唐氏综合征表型的遗传结构

Korbel, Jan O; Tirosh-Wagner, Tal; Urban, Alexander Eckehart; Chen, Xiao-Ning; Kasowski, Maya; Dai, Li; Grubert, Fabian; Erdman, Chandra; Gao, Michael C; Lange, Ken; Sobel, Eric M; Barlow, Gillian M; Aylsworth, Arthur S; Carpenter, Nancy J; Clark, Robin Dawn; Cohen, Monika Y; Doran, Eric; Falik-Zaccai, Tzipora; Lewin, Susan O; Lott, Ira T; McGillivray, Barbara C; Moeschler, John B; Pettenati, Mark J; Pueschel, Siegfried M; Rao, Kathleen W; Shaffer, Lisa G; Shohat, Mordechai; Van Riper, Alexander J; Warburton, Dorothy; Weissman, Sherman; Gerstein, Mark B; Snyder, Michael; Korenberg, Julie R

Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.

编码衔接蛋白 1 复合物 Sigma 2 亚基的基因 AP1S2 发生突变,会导致 X 连锁智力低下

Tarpey Patrick S, Stevens Claire, Teague Jon, Edkins Sarah, O'Meara Sarah, Avis Tim, Barthorpe Syd, Buck Gemma, Butler Adam, Cole Jennifer, Dicks Ed, Gray Kristian, Halliday Kelly, Harrison Rachel, Hills Katy, Hinton Jonathon, Jones David, Menzies Andrew, Mironenko Tatiana, Perry Janet, Raine Keiran, Richardson David, Shepherd Rebecca, Small Alexandra, Tofts Calli, Varian Jennifer, West Sofie, Widaa Sara, Yates Andy, Catford Rachael, Butler Julia, Mallya Uma, Moon Jenny, Luo Ying, Dorkins Huw, Thompson Deborah, Easton Douglas F, Wooster Richard, Bobrow Martin, Carpenter Nancy, Simensen Richard J, Schwartz Charles E, Stevenson Roger E, Turner Gillian, Partington Michael, Gecz Jozef, Stratton Michael R, Futreal P Andrew, Raymond F Lucy