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

Depletion of Fibrinogen Suppresses Growth of Primary Tumors and Metastasis of Pancreatic Ductal Adenocarcinoma

纤维蛋白原耗竭抑制原发肿瘤生长和胰腺导管腺癌转移

Chowdhury, Nayela N; Mitchell, Dana K; Kangro, Kadri; Eldridge, Kierra; Abrahams, Sara; Ferraresso, Francesca; Juang, Lih J; Gampala, Silpa; Brewster, Kylee; Revenko, Alexey; Kastrup, Christian; Territo, Paul R; Clapp, D Wade; Wang, Jia; Belgodere, Jorge A; Saeed, Omer; Choi, Sae Rome; Han, Bumsoo; Wolberg, Alisa S; Cao, Sha; Zhang, Chi; Flick, Matthew J; Fishel, Melissa L

A haploinsufficiency restoration strategy corrects neurobehavioral deficits in Nf1+/- mice.

单倍体功能不全恢复策略可纠正 Nf1+/- 小鼠的神经行为缺陷

Park Su Jung, Lukkes Jodi L, Chan Ka-Kui, Drozd Hayley P, Burgin Callie B, Qian Shaomin, Sullivan Morgan McKenzie, Guevara Cesar Gabriel, Cunningham Nolen, Arenas Stephanie, Collins Makenna A, Zucker Jacob, Won JinHee, Smith Abbi, Jiang Li, Mitchell Dana K, Rhodes Steven D, Angus Steven P, Clapp D Wade

TGFβ-dependent signaling drives tumor growth and aberrant extracellular matrix dynamics in NF1-associated plexiform neurofibroma.

TGFβ依赖性信号传导驱动NF1相关丛状神经纤维瘤的肿瘤生长和异常的细胞外基质动力学

Abu-Sultanah Mohannad, Zhou Zhuan, Jiang Chunhui, Mitchell Dana K, Bessler Waylan K, Jiang Li, Li Xiaohong, Qian Shaomin, Smith Abbi E, Mang Henry E, White Emily E, Ciesielski Marisa D, Hickey Brooke E, Brewster Kylee M, Sandusky George E, Masters Andi, Angus Steven P, Clapp D Wade, Le Lu Q, Rhodes Steven D

The absence of Peroxiredoxin-1 in human pancreatic ductal adenocarcinoma (PDAC) markedly reduces cell survival and tumor growth when coupled with the inhibition of Ref-1 redox signaling.

人类胰腺导管腺癌 (PDAC) 中过氧化物酶-1 的缺失,与 Ref-1 氧化还原信号的抑制相结合,会显著降低细胞存活率和肿瘤生长。

Kiran Sonia, Wireman Randall S, Peil Jacqueline, Mitchell Dana K, Potchanant Elizabeth Sierra, Rai Ratan, Vilseck Jonah Z, Cao Sha, Haiaty Sanya, Georgiadis Millie M, Fishel Melissa L, Kelley Mark R

DLK1 Distinguishes Subsets of NF1-Associated Malignant Peripheral Nerve Sheath Tumors with Divergent Molecular Signatures.

DLK1 可区分具有不同分子特征的 NF1 相关恶性周围神经鞘瘤亚型

Mitchell Dana K, Brewster Kylee, Makri Stavriani C, Khan Jaffar, Albright Eric A, Horvai Andrew, Mang Henry, Lu Qingbo, Dixon Shelley A H, White Emily, Saadatzadeh Mohammad Reza, Bijangi-Vishehsaraei Khadijeh, Gampala Silpa, Hickey Brooke E, Leffew Hannah, Li Xiaohong, Jiang Li, Ciesielski Marisa D, Bessler Waylan K, Collier Christopher D, Cohen-Gadol Aaron, Fishel Melissa L, Pratilas Christine A, Pollok Karen E, Angus Steven P, Rhodes Steven, Clapp Wade

PLK1 Inhibition Induces Synthetic Lethality in Fanconi Anemia Pathway-Deficient Acute Myeloid Leukemia.

PLK1 抑制可导致范可尼贫血通路缺陷型急性髓系白血病发生合成致死

Sheth Aditya S, Chan Ka-Kui, Liu Sheng, Wan Jun, Angus Steve P, Rhodes Steven D, Mitchell Dana K, Davis Christopher, Ridinger Maya, Croucher Peter J, Zeidan Amer M, Wijeratne Aruna, Qian Shaomin, Tran Ngoc Tung, Sierra Potchanant Elizabeth A

Targeting APE1 endonuclease activity impairs metastasis and enhances genotoxic therapy response in pancreatic cancer

靶向APE1核酸内切酶活性可抑制胰腺癌转移并增强基因毒性疗法的疗效

Kpenu, Eyram K; Mijiti, Mahmut; Gampala, Silpa; Wan, Jun; Liu, Sheng; Wireman, Randall S; Peil, Jacqueline; Mitchell, Dana K; Haiaty, Sanya; Sardar, Rajesh; Sharma, Akanksha; Georgiadis, Millie M; Fishel, Melissa L; Kelley, Mark R

Rapid Genome Sequencing Shows Diagnostic Utility In Infants With Congenital Heart Defects

快速基因组测序在先天性心脏病患儿的诊断中显示出应用价值

Durbin, Matthew D; Helvaty, Lindsey R; Posorske, Alyx; Zhang, Samuel; Huang, Manyan; Li, Ming; Abreu, Daniel; Fairman, Korre; Geddes, Gabrielle C; Helm, Benjamin M; Landis, Benjamin J; McEntire, Alexis; Mitchell, Dana K; Ware, Stephanie M

Genetic Testing Guidelines Impact Care in Newborns with Congenital Heart Defects

基因检测指南对先天性心脏病新生儿的护理产生影响

Durbin, Matthew D; Fairman, Korre; Helvaty, Lindsey R; Huang, Manyan; Li, Ming; Abreu, Daniel; Geddes, Gabrielle C; Helm, Benjamin M; Landis, Benjamin J; McEntire, Alexis; Mitchell, Dana K; Ware, Stephanie M

A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices

一项针对先天性心脏病患儿的多中心横断面研究表明,基因检测的诊断率很高,但评估方法各不相同。

Durbin, Matthew D; Helvaty, Lindsey R; Li, Ming; Border, William; Fitzgerald-Butt, Sara; Garg, Vidu; Geddes, Gabrielle C; Helm, Benjamin M; Lalani, Seema R; McBride, Kim L; McEntire, Alexis; Mitchell, Dana K; Murali, Chaya N; Wechsler, Stephanie B; Landis, Benjamin J; Ware, Stephanie M