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

Neonatal brain MRI to prognosticate neurodevelopmental outcomes in fetal growth restricted infants: a systematic review

新生儿脑部MRI在预测胎儿生长受限婴儿神经发育结局中的应用:系统评价

Ramdial, Randy; MacNamara, Madeline A; Moldrich, Randal; Colditz, Paul B; Wixey, Julie A

Validation of an MRI Brain Injury and Growth Scoring System in Very Preterm Infants Scanned at 29- to 35-Week Postmenstrual Age

对胎龄29至35周的极早产儿进行MRI脑损伤和生长评分系统的验证

George, J M; Fiori, S; Fripp, J; Pannek, K; Bursle, J; Moldrich, R X; Guzzetta, A; Coulthard, A; Ware, R S; Rose, S E; Colditz, P B; Boyd, R N

EMX1 regulates NRP1-mediated wiring of the mouse anterior cingulate cortex

EMX1 调节小鼠前扣带皮层的 NRP1 介导连接

Jonathan W C Lim, Amber-Lee S Donahoo, Jens Bunt, Timothy J Edwards, Laura R Fenlon, Ying Liu, Jing Zhou, Randal X Moldrich, Michael Piper, Ilan Gobius, Timothy L Bailey, Naomi R Wray, Nicoletta Kessaris, Mu-Ming Poo, John L R Rubenstein, Linda J Richards

Formation of functional areas in the cerebral cortex is disrupted in a mouse model of autism spectrum disorder

在自闭症谱系障碍小鼠模型中,大脑皮层功能区的形成受到干扰。

Fenlon, Laura R; Liu, Sha; Gobius, Ilan; Kurniawan, Nyoman D; Murphy, Skyle; Moldrich, Randal X; Richards, Linda J

Loss of neuronal potassium/chloride cotransporter 3 (KCC3) is responsible for the degenerative phenotype in a conditional mouse model of hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum

神经元钾/氯协同转运蛋白 3 (KCC3) 的缺失是导致与胼胝体发育不全相关的遗传性运动和感觉神经病条件小鼠模型出现退化表型的原因

Masoud Shekarabi, Randal X Moldrich, Sarah Rasheed, Adéle Salin-Cantegrel, Janet Laganière, Daniel Rochefort, Pascale Hince, Karine Huot, Rébecca Gaudet, Nyoman Kurniawan, Susana G Sotocinal, Jennifer Ritchie, Patrick A Dion, Jeffrey S Mogil, Linda J Richards, Guy A Rouleau

Comparative mouse brain tractography of diffusion magnetic resonance imaging

小鼠脑扩散磁共振成像的比较研究

Moldrich, Randal X; Pannek, Kerstin; Hoch, Renee; Rubenstein, John L; Kurniawan, Nyoman D; Richards, Linda J

NFIA controls telencephalic progenitor cell differentiation through repression of the Notch effector Hes1

NFIA通过抑制Notch效应因子Hes1来控制端脑祖细胞分化。

Piper, Michael; Barry, Guy; Hawkins, John; Mason, Sharon; Lindwall, Charlotta; Little, Erica; Sarkar, Anindita; Smith, Aaron G; Moldrich, Randal X; Boyle, Glen M; Tole, Shubha; Gronostajski, Richard M; Bailey, Timothy L; Richards, Linda J

Molecular regulation of the developing commissural plate

发育中的连合板的分子调控

Randal X Moldrich ,Ilan Gobius, Thomas Pollak, Jiangyang Zhang, Tianbo Ren, Lucia Brown, Susumu Mori, Camino De Juan Romero, Olga Britanova, Victor Tarabykin, Linda J Richards

Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development

唐氏综合征小鼠模型出生后发育过程中小脑发育不全的基因表达特征

Laffaire, Julien; Rivals, Isabelle; Dauphinot, Luce; Pasteau, Fabien; Wehrle, Rosine; Larrat, Benoit; Vitalis, Tania; Moldrich, Randal X; Rossier, Jean; Sinkus, Ralph; Herault, Yann; Dusart, Isabelle; Potier, Marie-Claude

Multiple non-cell-autonomous defects underlie neocortical callosal dysgenesis in Nfib-deficient mice

Nfib缺陷小鼠新皮质胼胝体发育不全的根本原因在于多种非细胞自主性缺陷。

Piper, Michael; Moldrich, Randal X; Lindwall, Charlotta; Little, Erica; Barry, Guy; Mason, Sharon; Sunn, Nana; Kurniawan, Nyoman Dana; Gronostajski, Richard M; Richards, Linda J