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

DPP6 Loss Causes Age-Dependent Sleep Dysregulation and Depression-like Phenotypes Linked to Neurodegeneration

DPP6 缺失导致与年龄相关的睡眠紊乱和抑郁样表型,这些表型与神经退行性疾病有关。

Lin, Lin; Pratt, Ashley E; Hoffman, Dax A

Neuronal Roles of the Multifunctional Protein Dipeptidyl Peptidase-like 6 (DPP6)

多功能蛋白二肽基肽酶样蛋白6 (DPP6) 的神经元作用

Malloy, Cole; Ahern, Maisie; Lin, Lin; Hoffman, Dax A

DPP6 Loss Impacts Hippocampal Synaptic Development and Induces Behavioral Impairments in Recognition, Learning and Memory

DPP6 缺失影响海马突触发育,并导致识别、学习和记忆方面的行为障碍

Lin, Lin; Murphy, Jonathan G; Karlsson, Rose-Marie; Petralia, Ronald S; Gutzmann, Jakob J; Abebe, Daniel; Wang, Ya-Xian; Cameron, Heather A; Hoffman, Dax A

FRMPD4 mutations cause X-linked intellectual disability and disrupt dendritic spine morphogenesis

FRMPD4基因突变会导致X连锁智力障碍,并破坏树突棘形态发生。

Piard, Juliette; Hu, Jia-Hua; Campeau, Philippe M; Rzonca, Sylwia; Van Esch, Hilde; Vincent, Elizabeth; Han, Mei; Rossignol, Elsa; Castaneda, Jennifer; Chelly, Jamel; Skinner, Cindy; Kalscheuer, Vera M; Wang, Ruihua; Lemyre, Emmanuelle; Kosinska, Joanna; Stawinski, Piotr; Bal, Jerzy; Hoffman, Dax A; Schwartz, Charles E; Van Maldergem, Lionel; Wang, Tao; Worley, Paul F

Matrix Metalloproteinase-9 Regulates Neuronal Circuit Development and Excitability

基质金属蛋白酶-9调节神经元回路发育和兴奋性

Murase, Sachiko; Lantz, Crystal L; Kim, Eunyoung; Gupta, Nitin; Higgins, Richard; Stopfer, Mark; Hoffman, Dax A; Quinlan, Elizabeth M

Functional characterization of two novel germline mutations of the KCNJ5 gene in hypertensive patients without primary aldosteronism but with ACTH-dependent aldosterone hypersecretion

对两种新的KCNJ5基因种系突变在无原发性醛固酮增多症但伴有ACTH依赖性醛固酮分泌过多的高血压患者中的功能表征

Sertedaki, Amalia; Markou, Athina; Vlachakis, Dimitrios; Kossida, Sophia; Campanac, Emilie; Hoffman, Dax A; Sierra, Maria De La Luz; Xekouki, Paraskevi; Stratakis, Constantine A; Kaltsas, Gregory; Piaditis, George P; Chrousos, George P; Charmandari, Evangelia

Human endogenous retrovirus-K contributes to motor neuron disease

人类内源性逆转录病毒-K与运动神经元疾病有关

Li, Wenxue; Lee, Myoung-Hwa; Henderson, Lisa; Tyagi, Richa; Bachani, Muzna; Steiner, Joseph; Campanac, Emilie; Hoffman, Dax A; von Geldern, Gloria; Johnson, Kory; Maric, Dragan; Morris, H Douglas; Lentz, Margaret; Pak, Katherine; Mammen, Andrew; Ostrow, Lyle; Rothstein, Jeffrey; Nath, Avindra

Repeated cocaine exposure increases fast-spiking interneuron excitability in the rat medial prefrontal cortex.

反复接触可卡因会增加大鼠内侧前额叶皮层快速放电中间神经元的兴奋性

Campanac Emilie, Hoffman Dax A

A novel point mutation in the KCNJ5 gene causing primary hyperaldosteronism and early-onset autosomal dominant hypertension

KCNJ5基因中的一种新型点突变导致原发性醛固酮增多症和早发性常染色体显性高血压

Charmandari, Evangelia; Sertedaki, Amalia; Kino, Tomoshige; Merakou, Christina; Hoffman, Dax A; Hatch, Michael M; Hurt, Darrell E; Lin, Lin; Xekouki, Paraskevi; Stratakis, Constantine A; Chrousos, George P

KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome

美国国立卫生研究院原发性醛固酮增多症患者队列中的KCNJ5基因突变:康恩综合征的一种罕见遗传病因

Xekouki, Paraskevi; Hatch, Michael M; Lin, Lin; Rodrigo, De Alexandre; Azevedo, Monalisa; de la Luz Sierra, Maria; Levy, Isaac; Saloustros, Emmanouil; Moraitis, Andreas; Horvath, Anelia; Kebebew, E; Hoffman, Dax A; Stratakis, Constantine A