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

Schwann cell deletion of Tumor Susceptibility Gene 101 ( Tsg101 ) in mice results in severe peripheral neuropathy

小鼠雪旺细胞中肿瘤易感基因101 (Tsg101) 的缺失会导致严重的周围神经病变

Silvius, Derek; Hurley, Edward; Poitelon, Yannick; Wagner, Kay-Uwe; Feltri, M Laura; Gunn, Teresa M

Discovery and Synthesis of Hydroxy-l-Proline Blockers of the Neutral Amino Acid Transporters SLC1A4 (ASCT1) and SLC1A5 (ASCT2)

中性氨基酸转运蛋白SLC1A4 (ASCT1) 和 SLC1A5 (ASCT2) 的羟基-L-脯氨酸阻滞剂的发现与合成

Lyda, Brent R; Leary, Gregory P; Farnsworth, Jill; Seaver, Benjamin; Silvius, Derek; Kavanaugh, Michael P; Esslinger, C Sean; Natale, Nicholas R

Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice.

SOX10 功能紊乱会导致灰震颤小鼠出现海绵状神经退行性变

Anderson Sarah R, Lee Inyoul, Ebeling Christine, Stephenson Dennis A, Schweitzer Kelsey M, Baxter David, Moon Tara M, LaPierre Sarah, Jaques Benjamin, Silvius Derek, Wegner Michael, Hood Leroy E, Carlson George, Gunn Teresa M

Levels of the Mahogunin Ring Finger 1 E3 ubiquitin ligase do not influence prion disease

Mahogunin环指1 E3泛素连接酶的水平不影响朊病毒病

Silvius, Derek; Pitstick, Rose; Ahn, Misol; Meishery, Delisha; Oehler, Abby; Barsh, Gregory S; DeArmond, Stephen J; Carlson, George A; Gunn, Teresa M

Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome

转录因子SIX5在鳃耳肾综合征患者中发生突变。

Hoskins, Bethan E; Cramer, Carl H; Silvius, Derek; Zou, Dan; Raymond, Richard M; Orten, Dana J; Kimberling, William J; Smith, Richard J H; Weil, Dominique; Petit, Christine; Otto, Edgar A; Xu, Pin-Xian; Hildebrandt, Friedhelm

Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1

Six 和 Eya1 发现第三咽囊形成胸腺/甲状旁腺。

Zou, Dan; Silvius, Derek; Davenport, Julie; Grifone, Raphaelle; Maire, Pascal; Xu, Pin-Xian

Eya 1 acts as a critical regulator for specifying the metanephric mesenchyme

Eya 1 在后肾间充质的形成中起着关键的调控作用。

Sajithlal, Gangadharan; Zou, Dan; Silvius, Derek; Xu, Pin-Xian

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

SIX1基因突变通过破坏EYA1-SIX1-DNA复合物导致鳃耳肾综合征。

Ruf, Rainer G; Xu, Pin-Xian; Silvius, Derek; Otto, Edgar A; Beekmann, Frank; Muerb, Ulla T; Kumar, Shrawan; Neuhaus, Thomas J; Kemper, Markus J; Raymond, Richard M Jr; Brophy, Patrick D; Berkman, Jennifer; Gattas, Michael; Hyland, Valentine; Ruf, Eva-Maria; Schwartz, Charles; Chang, Eugene H; Smith, Richard J H; Stratakis, Constantine A; Weil, Dominique; Petit, Christine; Hildebrandt, Friedhelm

The role of Six1 in mammalian auditory system development

Six1在哺乳动物听觉系统发育中的作用

Zheng, Weiming; Huang, Li; Wei, Zhu-Bo; Silvius, Derek; Tang, Bihui; Xu, Pin-Xian

Six1 is required for the early organogenesis of mammalian kidney

Six1是哺乳动物肾脏早期器官发生所必需的

Xu, Pin-Xian; Zheng, Weiming; Huang, Li; Maire, Pascal; Laclef, Christine; Silvius, Derek