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

Spatially confined sub-tumor microenvironments in pancreatic cancer

胰腺癌中空间受限的肿瘤亚微环境

Barbara T Grünwald, Antoine Devisme, Geoffroy Andrieux, Foram Vyas, Kazeera Aliar, Curtis W McCloskey, Andrew Macklin, Gun Ho Jang, Robert Denroche, Joan Miguel Romero, Prashant Bavi, Peter Bronsert, Faiyaz Notta, Grainne O'Kane, Julie Wilson, Jennifer Knox, Laura Tamblyn, Molly Udaskin, Nikolina Ra

Integration of Genomic and Transcriptional Features in Pancreatic Cancer Reveals Increased Cell Cycle Progression in Metastases

胰腺癌基因组和转录特征的整合揭示转移灶中细胞周期进程加快

Ashton A Connor ,Robert E Denroche ,Gun Ho Jang ,Mathieu Lemire ,Amy Zhang ,Michelle Chan-Seng-Yue ,Gavin Wilson ,Robert C Grant ,Daniele Merico ,Ilinca Lungu ,John M S Bartlett ,Dianne Chadwick ,Sheng-Ben Liang ,Jenna Eagles ,Faridah Mbabaali ,Jessica K Miller ,Paul Krzyzanowski ,Heather Armstrong ,Xuemei Luo ,Lars G T Jorgensen ,Joan M Romero ,Prashant Bavi ,Sandra E Fischer ,Stefano Serra ,Sara Hafezi-Bakhtiari ,Derin Caglar ,Michael H A Roehrl ,Sean Cleary ,Michael A Hollingsworth ,Gloria M Petersen ,Sarah Thayer ,Calvin H L Law ,Sulaiman Nanji ,Talia Golan ,Alyssa L Smith ,Ayelet Borgida ,Anna Dodd ,David Hedley ,Bradly G Wouters ,Grainne M O'Kane ,Julie M Wilson ,George Zogopoulos ,Faiyaz Notta ,Jennifer J Knox ,Steven Gallinger

High prevalence of mTOR complex activity can be targeted using Torin2 in papillary thyroid carcinoma

可以利用 Torin2 靶向治疗乳头状甲状腺癌中高流行的 mTOR 复合物活性

Maqbool Ahmed, Azhar R Hussain, Prashant Bavi, Saeeda O Ahmed, Saif S Al Sobhi, Fouad Al-Dayel, Shahab Uddin, Khawla S Al-Kuraya

Overexpression of leptin receptor predicts an unfavorable outcome in Middle Eastern ovarian cancer

瘦素受体的过度表达预示中东卵巢癌的不良预后

Shahab Uddin, Rong Bu, Maqbool Ahmed, Jehad Abubaker, Fouad Al-Dayel, Prashant Bavi, Khawla S Al-Kuraya

PIK3CA alterations in Middle Eastern ovarian cancers

中东卵巢癌中的 PIK3CA 变异

Jehad Abubaker, Prashant Bavi, Wael Al-Haqawi, Zeenath Jehan, Adnan Munkarah, Shahab Uddin, Khawla S Al-Kuraya

Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature

ADAMTS10 和 ADAMTS17 的纯合突变会导致晶状体近视、晶状体异位、青光眼、球形晶状体症和身材矮小

Jose Morales, Latifa Al-Sharif, Dania S Khalil, Jameela M A Shinwari, Prashant Bavi, Rahima A Al-Mahrouqi, Ali Al-Rajhi, Fowzan S Alkuraya, Brian F Meyer, Nada Al Tassan

Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome

C2orf37 基因突变(编码核仁蛋白)可导致性腺功能低下、脱发、糖尿病、智力低下和锥体外系综合征

Anas M Alazami, Amr Al-Saif, Abdulaziz Al-Semari, Saeed Bohlega, Soumaya Zlitni, Fatema Alzahrani, Prashant Bavi, Namik Kaya, Dilek Colak, Hanif Khalak, Andy Baltus, Borut Peterlin, Sumita Danda, Kailash P Bhatia, Susanne A Schneider, Nadia Sakati, Christopher A Walsh, Futwan Al-Mohanna, Brian Meyer