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

MON-332 Safety and Efficacy of Levoketoconazole in the Treatment of Endogenous Cushing’s Syndrome (LOGICS): A Double-Blind, Placebo-Controlled, Withdrawal Study

MON-332 左酮康唑治疗内源性库欣综合征的安全性和有效性(LOGICS):一项双盲、安慰剂对照、停药研究

Marietta, Cheryl; Thompson, Larry H; Lamerdin, Jane E; Brooks, P J; Kuwayama, Sayaka; Tarraf, Wassim; Gonzalez, Kevin A; Márquez, Freddie; Anita, Natasha Z; Lamar, Melissa; Parada, Humberto Jr; Stickel, Ariana M; Isasi, Carmen R; Filigrana, Paola; Daviglus, Martha L; Gallo, Linda C; González, Hector M; Loureiro, C M; Corsi-Zuelli, F; Fachim, H A; Shuhama, R; Menezes, P R; Dalton, C F; Louzada-Junior, P; Belangero, S I N; Coeli-Lacchini, F B; Reynolds, G P; Lacchini, R; Del-Ben, C M; Yang, Mo; Xiao, Da Wei; Li, Karen Kwai Har; Li, Chi Kong; Chik, Ki Wai; Fok, Tai Fai; Cohen, Adam D; Lee, Hans C; Trudel, Suzanne; Abdallah, Al-Ola; Callander, Natalie; Libby, Edward; Karlin, Lionel; Lonial, Sagar; Womersley, Lynsey; Baron, January; Lewis, Eric; Nungesser, Katlyn; Gupta, Ira; Opalinska, Joanna; Zacharieva, Sabina Z; Pivonello, Rosario; Elenkova, Atanaska; Tóth, Miklós; Shimon, Ilan; Stigliano, Antonio; Badiu, Corin P; Brue, Thierry; Georgescu, Carmen Emanuela; Cohen, Fredric J; Fleseriu, Maria

Newly identified CHO ERCC3/XPB mutations and phenotype characterization

新发现的CHO ERCC3/XPB突变及其表型特征

Rybanská, Ivana; Gursky, Ján; Fasková, Miriam; Salazar, Edmund P; Kimlícková-Polakovicová, Erika; Kleibl, Karol; Thompson, Larry H; Pirsel, Miroslav

RAD51D- and FANCG-dependent base substitution mutagenesis at the ATP1A1 locus in mammalian cells

哺乳动物细胞中 ATP1A1 基因座的 RAD51D 和 FANCG 依赖性碱基替换突变

Hinz, John M; Urbin, Salustra S; Thompson, Larry H

Disparate contributions of the Fanconi anemia pathway and homologous recombination in preventing spontaneous mutagenesis

范可尼贫血通路和同源重组在预防自发突变方面的不同作用

Hinz, John M; Nham, Peter B; Urbin, Salustra S; Jones, Irene M; Thompson, Larry H

Disparate requirements for the Walker A and B ATPase motifs of human RAD51D in homologous recombination

人类 RAD51D 的 Walker A 和 B ATPase 基序在同源重组中具有不同的需求

Wiese, Claudia; Hinz, John M; Tebbs, Robert S; Nham, Peter B; Urbin, Salustra S; Collins, David W; Thompson, Larry H; Schild, David

Repression of mutagenesis by Rad51D-mediated homologous recombination.

Rad51D介导的同源重组抑制诱变作用

Hinz John M, Tebbs Robert S, Wilson Paul F, Nham Peter B, Salazar Edmund P, Nagasawa Hatsumi, Urbin Salustra S, Bedford Joel S, Thompson Larry H

Fanconi anemia protein FANCD2 promotes immunoglobulin gene conversion and DNA repair through a mechanism related to homologous recombination

范可尼贫血蛋白FANCD2通过与同源重组相关的机制促进免疫球蛋白基因转换和DNA修复。

Yamamoto, Kazuhiko; Hirano, Seiki; Ishiai, Masamichi; Morishima, Kenichi; Kitao, Hiroyuki; Namikoshi, Keiko; Kimura, Masayo; Matsushita, Nobuko; Arakawa, Hiroshi; Buerstedde, Jean-Marie; Komatsu, Kenshi; Thompson, Larry H; Takata, Minoru