Michaela B C Kilander相关文献与解析，生知库 | 链接生命科学的每一步

日期影响因子

Transcriptomic analysis of isolated and pooled human postmortem cerebellar Purkinje cells in autism spectrum disorders

自闭症谱系障碍患者尸检小脑浦肯野细胞分离和汇集的转录组分析

期刊:Frontiers in Genetics

影响因子:2.8

doi:10.3389/fgene.2022.944837

Cheryl Brandenburg, Anthony J Griswold, Derek J Van Booven, Michaela B C Kilander, Jeannine A Frei, Michael W Nestor, Derek M Dykxhoorn, Margaret A Pericak-Vance, Gene J Blatt

发表日期：2022

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Abl2:Cortactin Interactions Regulate Dendritic Spine Stability via Control of a Stable Filamentous Actin Pool

Abl2:Cortactin相互作用通过控制稳定的丝状肌动蛋白池来调节树突棘的稳定性

期刊:Journal of Neuroscience

影响因子:4.4

doi:10.1523/JNEUROSCI.2472-20.2021

Juliana E Shaw ,Michaela B C Kilander ,Yu-Chih Lin ,Anthony J Koleske

发表日期：2021

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Regulation of Neural Circuit Development by Cadherin-11 Provides Implications for Autism

钙粘蛋白-11 对神经回路发育的调节为自闭症提供了启示

影响因子:2.7

doi:10.1523/ENEURO.0066-21.2021

Jeannine A Frei, Robert F Niescier, Morgan S Bridi, Madel Durens, Jonathan E Nestor, Michaela B C Kilander, Xiaobing Yuan, Derek M Dykxhoorn, Michael W Nestor, Shiyong Huang, Gene J Blatt, Yu-Chih Lin

发表日期：2021

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Tomosyn regulates the small RhoA GTPase to control the dendritic stability of neurons and the surface expression of AMPA receptors

Tomosyn 调节小 RhoA GTPase 来控制神经元的树突稳定性和 AMPA 受体的表面表达

期刊:Journal of Neuroscience Research

影响因子:2.9

doi:10.1002/jnr.24608

Wenjuan Shen, Michaela B C Kilander, Morgan S Bridi, Jeannine A Frei, Robert F Niescier, Shiyong Huang, Yu-Chih Lin

发表日期：2020

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A rare human CEP290 variant disrupts the molecular integrity of the primary cilium and impairs Sonic Hedgehog machinery

一种罕见的人类 CEP290 变体破坏了初级纤毛的分子完整性并损害了 Sonic Hedgehog 机制

期刊:Scientific Reports

影响因子:3.8

doi:10.1038/s41598-018-35614-x

Michaela B C Kilander, Chun-Hung Wang, Chia-Hsiang Chang, Jonathan E Nestor, Kevin Herold, Jin-Wu Tsai, Michael W Nestor, Yu-Chih Lin

发表日期：2018

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Assessment of Frizzled 6 membrane mobility by FRAP supports G protein coupling and reveals WNT-Frizzled selectivity

通过 FRAP 评估 Frizzled 6 膜迁移率支持 G 蛋白偶联并揭示 WNT-Frizzled 选择性

期刊:Cellular Signalling

影响因子:4.4

doi:10.1016/j.cellsig.2014.05.012

Michaela B C Kilander, Jenny Dahlström, Gunnar Schulte

发表日期：2014

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Mutations in Frizzled 6 cause isolated autosomal-recessive nail dysplasia

Frizzled 6 基因突变导致孤立性常染色体隐性指甲发育不良

期刊:American Journal of Human Genetics

影响因子:8.1

doi:10.1016/j.ajhg.2011.05.013

Anne-Sophie Fröjmark, Jens Schuster, Maria Sobol, Miriam Entesarian, Michaela B C Kilander, Dana Gabrikova, Sadia Nawaz, Shahid M Baig, Gunnar Schulte, Joakim Klar, Niklas Dahl

发表日期：2011

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