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

Foxr1 deletion causes microcephaly and leads to cortical and hippocampal hypoplasia

Foxr1基因缺失会导致小头畸形,并导致皮质和海马发育不全。

Waxman, Hannah; Kankkunen, Marcus; Gupta, Arya; Dowgiewicz, Margo; Beffert, Uwe; Ho, Angela

Beyond Glycolysis: Aldolase A Is a Novel Effector in Reelin-Mediated Dendritic Development.

超越糖酵解:醛缩酶 A 是 Reelin 介导的树突发育中的一种新型效应因子

Lagani Gavin D, Sha Mingqi, Lin Weiwei, Natarajan Sahana, Kankkunen Marcus, Kistler Sabrina A, Lampl Noah, Waxman Hannah, Harper Evelyn R, Emili Andrew, Beffert Uwe, Ho Angela

Morphological comparison of astrocytes in the lamina cribrosa and glial lamina

筛板和胶质板中星形胶质细胞的形态学比较

Susannah Waxman, Hannah Schilpp, Ashley Linton, Tatjana C Jakobs, Ian A Sigal

Genetic variants in the bipolar disorder risk locus SYNE1 that affect CPG2 expression and protein function

双相情感障碍风险基因位点SYNE1的遗传变异会影响CPG2的表达和蛋白质功能。

Rathje, Mette; Waxman, Hannah; Benoit, Marc; Tammineni, Prasad; Leu, Costin; Loebrich, Sven; Nedivi, Elly