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

Novel GLCCI1-BRAF fusion drives kinase signaling in a case of pheochromocytomatosis

新型 GLCCI1-BRAF 融合在嗜铬细胞瘤病中驱动激酶信号传导

Benjamin L Green, Robert R C Grant, Christopher T Richie, Bishwanath Chatterjee, Michelly Sampaio De Melo, Frederic G Barr, Karel Pacak, Sunita K Agarwal, Naris Nilubol

Serine hydroxymethyltransferase 2 expression promotes tumorigenesis in rhabdomyosarcoma with 12q13-q14 amplification

丝氨酸羟甲基转移酶 2 表达促进 12q13-q14 扩增的横纹肌肉瘤发生

Thanh H Nguyen, Prasantha L Vemu, Gregory E Hoy, Salah Boudjadi, Bishwanath Chatterjee, Jack F Shern, Javed Khan, Wenyue Sun, Frederic G Barr

A Fusion Transcription Factor-Driven Cancer Progresses to a Fusion-Independent Relapse via Constitutive Activation of a Downstream Transcriptional Target

融合转录因子驱动的癌症通过下游转录靶标的组成性激活进展为融合独立的复发

Salah Boudjadi, Puspa Raj Pandey, Bishwanath Chatterjee, Thanh Hung Nguyen, Wenyue Sun, Frederic G Barr

The complex genetics of hypoplastic left heart syndrome

左心发育不全综合征的复杂遗传学

Xiaoqin Liu, Hisato Yagi, Shazina Saeed, Abha S Bais, George C Gabriel, Zhaohan Chen, Kevin A Peterson, You Li, Molly C Schwartz, William T Reynolds, Manush Saydmohammed, Brian Gibbs, Yijen Wu, William Devine, Bishwanath Chatterjee, Nikolai T Klena, Dennis Kostka, Karen L de Mesy Bentley, Madhavi K

Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects

Prickle1 突变导致平面细胞极性和定向细胞迁移缺陷,与心脏流出道异常和其他结构性出生缺陷有关

Brian C Gibbs, Rama Rao Damerla, Eszter K Vladar, Bishwanath Chatterjee, Yong Wan, Xiaoqin Liu, Cheng Cui, George C Gabriel, Maliha Zahid, Hisato Yagi, Heather L Szabo-Rogers, Kaye L Suyama, Jeffrey D Axelrod, Cecilia W Lo

Wdpcp, a PCP protein required for ciliogenesis, regulates directional cell migration and cell polarity by direct modulation of the actin cytoskeleton

Wdpcp 是纤毛发生所需的 PCP 蛋白,它通过直接调节肌动蛋白细胞骨架来调节定向细胞迁移和细胞极性

Cheng Cui, Bishwanath Chatterjee, Thomas P Lozito, Zhen Zhang, Richard J Francis, Hisato Yagi, Lisa M Swanhart, Subramaniam Sanker, Deanne Francis, Qing Yu, Jovenal T San Agustin, Chandrakala Puligilla, Tania Chatterjee, Terry Tansey, Xiaoqin Liu, Matthew W Kelley, Elias T Spiliotis, Adam V Kwiatkow

Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing heterotaxy

大规模平行测序鉴定出因 ENU 诱发突变而导致异位的基因 Megf8

Zhen Zhang, Deanne Alpert, Richard Francis, Bishwanath Chatterjee, Qing Yu, Terry Tansey, Steven L Sabol, Cheng Cui, Yongli Bai, Maxim Koriabine, Yuko Yoshinaga, Jan-Fang Cheng, Feng Chen, Joel Martin, Wendy Schackwitz, Teresa M Gunn, Kenneth L Kramer, Pieter J De Jong, Len A Pennacchio, Cecilia W L