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

In vivo functional screens reveal KEAP1 loss as a driver of chemoresistance in small cell lung cancer.

体内功能筛选揭示 KEAP1 缺失是小细胞肺癌化疗耐药性的驱动因素

Brumage Lauren, Best Scott, Hippe Daniel S, Grunblatt Eli, Chanana Pritha, Wu Feinan, Lee Myung Chang, Ying Zhe, Ibrahim Ali, Chung Jae Heun, Vigil Anna, Fatherree Jackson, Beronja Slobodan, Paddison Patrick, Sullivan Lucas, Nabet Barzin, MacPherson David

DNA Damage Sensing and TP53 Function as Modulators of Sensitivity to Calicheamicin-Based Antibody-Drug Conjugates for Acute Leukemia

DNA损伤感知和TP53功能作为急性白血病中基于卡利奇霉素的抗体-药物偶联物敏感性的调节因子

Pettenger-Willey, Camryn M; Laszlo, George S; Gang, Margery; Cole, Frances M; Godwin, Colin D; Erraiss, Sarah; Chanana, Pritha; Kehret, Allie R; Li, Junyang; Barton, Jacob W; Yochim, Meghann M; Rodríguez-Arbolí, Eduardo; Walter, Roland B

Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease

利用外显子组和转录组测序鉴定疑似罕见遗传病患者的X染色体失活偏倚

Fadra, Numrah; Schultz-Rogers, Laura E; Chanana, Pritha; Cousin, Margot A; Macke, Erica L; Ferrer, Alejandro; Pinto E Vairo, Filippo; Olson, Rory J; Oliver, Gavin R; Mulvihill, Lindsay A; Jenkinson, Garrett; Klee, Eric W

Using viral sequence diversity to estimate time of HIV infection in infants

利用病毒序列多样性估算婴儿感染艾滋病毒的时间

Russell, Magdalena L; Fish, Carolyn S; Drescher, Sara; Cassidy, Noah A J; Chanana, Pritha; Benki-Nugent, Sarah; Slyker, Jennifer; Mbori-Ngacha, Dorothy; Bosire, Rose; Richardson, Barbra; Wamalwa, Dalton; Maleche-Obimbo, Elizabeth; Overbaugh, Julie; John-Stewart, Grace; Matsen, Frederick A 4th; Lehman, Dara A

Combined VEGFR and MAPK pathway inhibition in angiosarcoma

血管肉瘤中VEGFR和MAPK通路联合抑制

Wagner, Michael J; Lyons, Yasmin A; Siedel, Jean H; Dood, Robert; Nagaraja, Archana S; Haemmerle, Monika; Mangala, Lingegowda S; Chanana, Pritha; Lazar, Alexander J; Wang, Wei-Lien; Ravi, Vinod; Holland, Eric C; Sood, Anil K

Frequent POLE-driven hypermutation in ovarian endometrioid cancer revealed by mutational signatures in RNA sequencing

RNA测序突变特征揭示卵巢子宫内膜样癌中POLE驱动的频繁超突变

Davila, Jaime I; Chanana, Pritha; Sarangi, Vivekananda; Fogarty, Zachary C; Weroha, S John; Guo, Ruifeng; Goode, Ellen L; Huang, Yajue; Wang, Chen

A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease

针对融合转录本鉴定的定制化方法可提高罕见遗传病的诊断率。

Oliver, Gavin R; Tang, Xiaojia; Schultz-Rogers, Laura E; Vidal-Folch, Noemi; Jenkinson, W Garrett; Schwab, Tanya L; Gaonkar, Krutika; Cousin, Margot A; Nair, Asha; Basu, Shubham; Chanana, Pritha; Oglesbee, Devin; Klee, Eric W

Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome

婴儿猝死综合征的全外显子组罕见变异分析

Tester, David J; Wong, Leonie C H; Chanana, Pritha; Gray, Belinda; Jaye, Amie; Evans, Jared M; Evans, Margaret; Fleming, Peter; Jeffrey, Iona; Cohen, Marta; Tfelt-Hansen, Jacob; Simpson, Michael A; Behr, Elijah R; Ackerman, Michael J

A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression

TREM基因簇上的一个候选调控变异与阿尔茨海默病风险降低以及TREML1和TREM2脑基因表达增加相关。

Carrasquillo, Minerva M; Allen, Mariet; Burgess, Jeremy D; Wang, Xue; Strickland, Samantha L; Aryal, Shivani; Siuda, Joanna; Kachadoorian, Michaela L; Medway, Christopher; Younkin, Curtis S; Nair, Asha; Wang, Chen; Chanana, Pritha; Serie, Daniel; Nguyen, Thuy; Lincoln, Sarah; Malphrus, Kimberly G; Morgan, Kevin; Golde, Todd E; Price, Nathan D; White, Charles C; De Jager, Philip L; Bennett, David A; Asmann, Yan W; Crook, Julia E; Petersen, Ronald C; Graff-Radford, Neill R; Dickson, Dennis W; Younkin, Steven G; Ertekin-Taner, Nilüfer