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

NF-κB and STAT3 signaling uniquely stratify survival in female glioblastoma patients.

NF-κB 和 STAT3 信号传导对女性胶质母细胞瘤患者的生存率有独特的分层作用。

Wong Jason P, Llaci Lorida, Tripp Lloyd, Jeon Myung Sik, Yang Lihua, Reinhold Nicholas, Warrington Nicole M, Luo Jingqin, Mitra Robi D, Rubin Joshua B

Clinical and histopathological investigation of the possible occurrence of tracheobronchial disease in cats with chronic gingivostomatitis

对患有慢性龈口炎的猫可能发生气管支气管疾病的临床和组织病理学研究

Lorida, Olga; Konstantinidis, Alexandros; Brellou, Georgia D; Koutouzidou, Georgia; Papadopoulou, Paraskevi; Matiakis, Apostolos; Adamama-Moraitou, Katerina K; Papadimitriou, Serafeim

EGR1 drives sex-differences in glioblastoma tumorigenicity

EGR1驱动胶质母细胞瘤致瘤性的性别差异

Abou-Antoun, Tamara J; Llaci, Lorida; Wong, Jason P; Yang, Lihua; Warrington, Nicole M; Tripp, Lloyd; Luo, Jingqin; Muegge, Brian; Rubin, Joshua B; Mitra, Robi D

Epigenetic developmental mechanisms underlying sex differences in cancer

癌症性别差异的表观遗传发育机制

Rubin, Joshua B; Abou-Antoun, Tamara; Ippolito, Joseph E; Llaci, Lorida; Marquez, Camryn T; Wong, Jason P; Yang, Lihua

Genetic and Protein Network Underlying the Convergence of Rett-Syndrome-like (RTT-L) Phenotype in Neurodevelopmental Disorders

神经发育障碍中雷特综合征样(RTT-L)表型趋同的遗传和蛋白质网络

Frankel, Eric; Podder, Avijit; Sharifi, Megan; Pillai, Roshan; Belnap, Newell; Ramsey, Keri; Dodson, Julius; Venugopal, Pooja; Brzezinski, Molly; Llaci, Lorida; Gerald, Brittany; Mills, Gabrielle; Sanchez-Castillo, Meredith; Balak, Chris D; Szelinger, Szabolcs; Jepsen, Wayne M; Siniard, Ashley L; Richholt, Ryan; Naymik, Marcus; Schrauwen, Isabelle; Craig, David W; Piras, Ignazio S; Huentelman, Matthew J; Schork, Nicholas J; Narayanan, Vinodh; Rangasamy, Sampathkumar

Loss of Quaking RNA binding protein disrupts the expression of genes associated with astrocyte maturation in mouse brain

Quaking RNA 结合蛋白的缺失会破坏小鼠大脑中星形胶质细胞成熟相关基因的表达

Kristina Sakers, Yating Liu, Lorida Llaci, Scott M Lee, Michael J Vasek, Michael A Rieger, Sean Brophy, Eric Tycksen, Renate Lewis, Susan E Maloney, Joseph D Dougherty

Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland

芬兰创始人群体中智力障碍(ID)疾病的外显子组测序结果显示,这些疾病主要由新生突变引起。

Järvelä, Irma; Määttä, Tuomo; Acharya, Anushree; Leppälä, Juha; Jhangiani, Shalini N; Arvio, Maria; Siren, Auli; Kankuri-Tammilehto, Minna; Kokkonen, Hannaleena; Palomäki, Maarit; Varilo, Teppo; Fang, Mary; Hadley, Trevor D; Jolly, Angad; Linnankivi, Tarja; Paetau, Ritva; Saarela, Anni; Kälviäinen, Reetta; Olme, Jan; Nouel-Saied, Liz M; Cornejo-Sanchez, Diana M; Llaci, Lorida; Lupski, James R; Posey, Jennifer E; Leal, Suzanne M; Schrauwen, Isabelle

Transcriptional profiling of multiple system atrophy cerebellar tissue highlights differences between the parkinsonian and cerebellar sub-types of the disease

多系统萎缩症小脑组织的转录组分析突显了该疾病帕金森亚型和小脑亚型之间的差异。

Piras, Ignazio S; Bleul, Christiane; Schrauwen, Isabelle; Talboom, Joshua; Llaci, Lorida; De Both, Matthew D; Naymik, Marcus A; Halliday, Glenda; Bettencourt, Conceicao; Holton, Janice L; Serrano, Geidy E; Sue, Lucia I; Beach, Thomas G; Stefanova, Nadia; Huentelman, Matthew J

Genes Implicated in Rare Congenital Inner Ear and Cochleovestibular Nerve Malformations

与罕见先天性内耳和耳蜗前庭神经畸形相关的基因

Kari, Elina; Llaci, Lorida; Go, John L; Naymik, Marcus; Knowles, James A; Leal, Suzanne M; Rangasamy, Sampath; Huentelman, Matthew J; Liang, Winnie; Friedman, Rick A; Schrauwen, Isabelle

Transcriptomics analysis of pericytes from retinas of diabetic animals reveals novel genes and molecular pathways relevant to blood-retinal barrier alterations in diabetic retinopathy

对糖尿病动物视网膜周细胞的转录组学分析揭示了与糖尿病视网膜病变中血视网膜屏障改变相关的新基因和分子通路

Rangasamy, Sampathkumar; Monickaraj, Finny; Legendre, Christophe; Cabrera, Andrea P; Llaci, Lorida; Bilagody, Cherae; McGuire, Paul; Das, Arup