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

Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing

通过全基因组测序在Diamond-Blackfan贫血综合征患者中鉴定出2个新的非编码变异

Wen, Ting; Boyden, Steven E; Hocutt, Caleb M; Lewis, Robert G; Baldwin, Erin E; Vagher, Jennie; Andrews, Ashley; Nicholas, Thomas J; Chapin, Alexander; Fan, Elaine M; Botto, Lorenzo D; Bayrak-Toydemir, Pinar; Mao, Rong; Meznarich, Jessica A

Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR)

先天性红细胞生成障碍性贫血 I 型:来自北美先天性红细胞生成障碍性贫血登记处 (CDAR) 的首份报告

Niss, Omar; Lorsbach, Robert B; Berger, Mikaela; Chonat, Satheesh; McLemore, Morgan; Buchbinder, David; McCavit, Timothy; Shaffer, Linda G; Simpson, Jessica; Schwartz, Jeffrey H; Meznarich, Jessica; Emberesh, Myesa; Seu, Katie G; Zhang, Wenying; Kalfa, Theodosia A

VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects

人类 VPS4A 突变因胞质分裂和运输缺陷而导致综合征性先天性红细胞生成性贫血

Katie G Seu, Lisa R Trump, Sana Emberesh, Robert B Lorsbach, Clarissa Johnson, Jessica Meznarich, Hunter R Underhill, Stella T Chou, Haripriya Sakthivel, Nicolas N Nassar, Kalani J Seu, Lionel Blanc, Wenying Zhang, Carolyn M Lutzko, Theodosia A Kalfa4

Infantile Pyknocytosis: End-Tidal CO, %Micro-R Measurements, Next-Generation Sequencing, and Transfusion Avoidance with Darbepoetin

婴儿红细胞固缩症:呼气末二氧化碳、微量红细胞百分比测量、下一代测序以及达贝泊汀治疗避免输血

Bahr, Timothy M; Knudsen, Mari C; Lozano-Chinga, Michell; Agarwal, Archana M; Meznarich, Jessica A; Ohls, Robin K; Christensen, Robert D

Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations

胎儿期先天性红细胞生成障碍性贫血1型伴新型复合杂合CDAN1突变

Meznarich, Jessica A; Draper, Lauren; Christensen, Robert D; Yaish, Hassan M; Luem, Nick D; Pysher, Theodore J; Jung, Grace; Nemeth, Elizabeta; Ganz, Tomas; Ward, Diane M

GFI1 functions in transcriptional control and cell fate determination require SNAG domain methylation to recruit LSD1

GFI1 在转录调控和细胞命运决定中发挥作用,这需要 SNAG 结构域甲基化来募集 LSD1。

Velinder, Matthew; Singer, Jason; Bareyan, Diana; Meznarich, Jessica; Tracy, Christopher M; Fulcher, James M; McClellan, David; Lucente, Helena; Franklin, Sarah; Sharma, Sunil; Engel, Michael E

Urokinase plasminogen activator induces pro-fibrotic/m2 phenotype in murine cardiac macrophages

尿激酶型纤溶酶原激活剂诱导小鼠心脏巨噬细胞产生促纤维化/M2表型

Meznarich, Jessica; Malchodi, Laura; Helterline, Deri; Ramsey, Stephen A; Bertko, Kate; Plummer, Tabitha; Plawman, Abigail; Gold, Elizabeth; Stempien-Otero, April

The role of macrophage-derived urokinase plasminogen activator in myocardial infarct repair: urokinase attenuates ventricular remodeling

巨噬细胞来源的尿激酶型纤溶酶原激活剂在心肌梗死修复中的作用:尿激酶可减轻心室重构

Minami, Elina; Castellani, Chiara; Malchodi, Laura; Deem, Jennifer; Bertko, Kate; Meznarich, Jessica; Dishmon, Monja; Murry, Charles E; Stempien-Otero, April

Macrophage fusion, giant cell formation, and the foreign body response require matrix metalloproteinase 9

巨噬细胞融合、巨细胞形成和异物反应都需要基质金属蛋白酶9。

MacLauchlan, Susan; Skokos, Eleni A; Meznarich, Norman; Zhu, Dana H; Raoof, Sana; Shipley, J Michael; Senior, Robert M; Bornstein, Paul; Kyriakides, Themis R