Vande Pol Scott相关文献与解析，生知库 | 链接生命科学的每一步

Multiple regions of E6AP (UBE3A) contribute to interaction with papillomavirus E6 proteins and the activation of ubiquitin ligase activity

E6AP（UBE3A）的多个区域参与与乳头瘤病毒E6蛋白的相互作用，并激活泛素连接酶活性。

期刊:PLoS Pathogens

影响因子:4.9

doi:10.1371/journal.ppat.1008295

Drews, Camille M; Brimer, Nicole; Vande Pol, Scott B

E6 proteins from high-risk HPV, low-risk HPV, and animal papillomaviruses activate the Wnt/β-catenin pathway through E6AP-dependent degradation of NHERF1

来自高危型HPV、低危型HPV和动物乳头瘤病毒的E6蛋白通过E6AP依赖性降解NHERF1激活Wnt/β-catenin通路。

期刊:PLoS Pathogens

影响因子:4.9

doi:10.1371/journal.ppat.1007575

Drews, Camille M; Case, Samuel; Vande Pol, Scott B

Association of papillomavirus E6 proteins with either MAML1 or E6AP clusters E6 proteins by structure, function, and evolutionary relatedness

乳头瘤病毒E6蛋白与MAML1或E6AP簇的关联，以及E6蛋白的结构、功能和进化相关性

期刊:PLoS Pathogens

影响因子:4.9

doi:10.1371/journal.ppat.1006781

Brimer, Nicole; Drews, Camille M; Vande Pol, Scott B

微生物学

发表日期：2017

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Structure of the E6/E6AP/p53 complex required for HPV-mediated degradation of p53.

HPV介导的p53降解所需的E6/E6AP/p53复合物的结构

期刊:Nature

影响因子:48.5

doi:10.1038/nature16481

Martinez-Zapien Denise, Ruiz Francesc Xavier, Poirson Juline, Mitschler AndrÃ©, Ramirez Juan, Forster Anne, Cousido-Siah Alexandra, Masson Murielle, Vande Pol Scott, Podjarny Alberto, TravÃ© Gilles, Zanier Katia

Papillomavirus E6 Oncoproteins Take Common Structural Approaches to Solve Different Biological Problems

乳头瘤病毒E6癌蛋白采用共同的结构方法来解决不同的生物学问题

期刊:PLoS Pathogens

影响因子:4.9

doi:10.1371/journal.ppat.1005138

Interactions between E6, FAK, and GIT1 at paxillin LD4 are necessary for transformation by bovine papillomavirus 1 E6

牛乳头瘤病毒1 E6 转化需要 E6、FAK 和 GIT1 在 paxillin LD4 处的相互作用。

期刊:Journal of Virology

影响因子:3.8

doi:10.1128/JVI.00552-14

Brimer, Nicole; Wade, Ramon; Vande Pol, Scott

Paxillin contracts the osteoclast cytoskeleton

帕克辛蛋白收缩破骨细胞骨架

期刊:Journal of Bone and Mineral Research

影响因子:5.9

doi:10.1002/jbmr.1706

Zou, Wei; Deselm, Carl J; Broekelmann, Thomas J; Mecham, Robert P; Vande Pol, Scott; Choi, Kyunghee; Teitelbaum, Steven L

细胞生物学

发表日期：2012

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Human papillomavirus E6 regulates the cytoskeleton dynamics of keratinocytes through targeted degradation of p53

人乳头瘤病毒E6通过靶向降解p53来调节角质形成细胞的细胞骨架动力学。

期刊:Journal of Virology

影响因子:3.8

doi:10.1128/JVI.01083-07

Cooper, Brooke; Brimer, Nicole; Vande Pol, Scott B

Minimal features of paxillin that are required for the tyrosine phosphorylation of focal adhesion kinase

黏着斑激酶酪氨酸磷酸化所需的paxillin的最小特征

期刊:Biochemical Journal

影响因子:4.3

doi:10.1042/BJ20051241

Wade, Ramon; Vande Pol, Scott

Human papillomavirus type 16 E6 induces cell competition

人乳头瘤病毒16型E6诱导细胞竞争

Multiple regions of E6AP (UBE3A) contribute to interaction with papillomavirus E6 proteins and the activation of ubiquitin ligase activity

E6AP（UBE3A）的多个区域参与与乳头瘤病毒E6蛋白的相互作用，并激活泛素连接酶活性。

E6 proteins from high-risk HPV, low-risk HPV, and animal papillomaviruses activate the Wnt/β-catenin pathway through E6AP-dependent degradation of NHERF1

来自高危型HPV、低危型HPV和动物乳头瘤病毒的E6蛋白通过E6AP依赖性降解NHERF1激活Wnt/β-catenin通路。

Association of papillomavirus E6 proteins with either MAML1 or E6AP clusters E6 proteins by structure, function, and evolutionary relatedness

乳头瘤病毒E6蛋白与MAML1或E6AP簇的关联，以及E6蛋白的结构、功能和进化相关性

Structure of the E6/E6AP/p53 complex required for HPV-mediated degradation of p53.

HPV介导的p53降解所需的E6/E6AP/p53复合物的结构

Papillomavirus E6 Oncoproteins Take Common Structural Approaches to Solve Different Biological Problems

乳头瘤病毒E6癌蛋白采用共同的结构方法来解决不同的生物学问题

Interactions between E6, FAK, and GIT1 at paxillin LD4 are necessary for transformation by bovine papillomavirus 1 E6

牛乳头瘤病毒1 E6 转化需要 E6、FAK 和 GIT1 在 paxillin LD4 处的相互作用。

Paxillin contracts the osteoclast cytoskeleton

帕克辛蛋白收缩破骨细胞骨架

Human papillomavirus E6 regulates the cytoskeleton dynamics of keratinocytes through targeted degradation of p53

人乳头瘤病毒E6通过靶向降解p53来调节角质形成细胞的细胞骨架动力学。

Minimal features of paxillin that are required for the tyrosine phosphorylation of focal adhesion kinase

黏着斑激酶酪氨酸磷酸化所需的paxillin的最小特征