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

Identification of UBA7 expression downregulation in myelodysplastic neoplasm with SF3B1 mutations

SF3B1突变型骨髓增生异常肿瘤中UBA7表达下调的鉴定

Alatawi, Sael; Alzahrani, Othman R; Alatawi, Fuad A; Almazni, Ibrahim A; Almotiri, Alhomidi; Almsned, Fahad M

Clinical exome sequencing identifies novel gene variants associated with ischemic stroke in the Saudi Tabuk population

临床外显子组测序在沙特阿拉伯塔布克人群中发现了与缺血性卒中相关的新基因变异

Hamadi, Abdullah; Mir, Rashid; Al-Amer, Osama M; Alasseiri, Mohammed; AlZamzami, Waseem; Alatawi, Sael; Alanazi, Mohammad A; Moawadh, Mamdoh S; Oyouni, Atif Abdulwahab A; Al Tuwaijri, Abeer; Althenayyan, Saleh; Madkhali, Hassan A; Alserihi, Raed

Exploring the genetic frontier: Unraveling ANRIL, PAI-1, and HNF1α in stroke progression

探索遗传前沿:揭示 ANRIL、PAI-1 和 HNF1α 在卒中进展中的作用

Hamadi, Abdullah; Mir, Rashid; Al-Amer, Osama M; Alasseiri, Mohammed; Dobie, Gasim; Elfaki, Imadeldin; AlZamzami, Waseem; Alatawi, Sael; Oyouni, Atif Abdulwahab A; Alanazi, Mohammad A; Muthupandian, Saravanan

Genetic Variations in BCL3, MDM4, KLF14, and miR-146a and Their Associations with the Predisposition and Progression of Myeloproliferative Disorder and Chronic Myeloid Leukemia Patients

BCL3、MDM4、KLF14 和 miR-146a 的基因变异及其与骨髓增生性疾病和慢性粒细胞白血病患者的易感性和进展的关系

Al-Amer, Osama M; Alasseiri, Mohammed I; Tayeb, Faris J; Alanazi, Mansour A; Hamadi, Abdullah; Jalal, Mohammed M; Altayar, Malik A; Almotairi, Reema M; Niaz, Hanan A; Moawadh, Mamdoh; Alatawi, Sael; AlZamzami, Waseem; Oyouni, Atif Abdulwahab A; Alassiri, Mohammed; Alharthi, Fahad; Althagafi, Hussam A; Alanazi, Mohammad A; Mir, Rashid

Genome-scale clustered regularly interspaced short palindromic repeats screen identifies nucleotide metabolism as an actionable therapeutic vulnerability in diffuse large B-cell lymphoma.

基因组规模的规律成簇间隔短回文重复序列筛选发现核苷酸代谢是弥漫性大B细胞淋巴瘤中可操作的治疗弱点

Davies Nicholas, Francis Tegan, Oldreive Ceri, Azam Maria, Wilson Jordan, Byrd Philip J, Burley Megan, Sharma-Oates Archana, Keane Peter, Alatawi Sael, Higgs Martin R, Rudzki Zbigniew, Ibrahim Maha, Perry Tracey, Agathanggelou Angelo, Hewitt Anne-Marie, Smith Edward, Bonifer Constanze, O'Connor Mark, Forment Josep V, Murray Paul G, Fennell Eanna, Kelly Gemma, Chang Catherine, Stewart Grant S, Stankovic Tatjana, Kwok Marwan, Taylor Alexander Malcolm

New insights into PSAT1 as a therapeutic target for myelodysplastic syndrome (MDS)

PSAT1作为骨髓增生异常综合征(MDS)治疗靶点的新见解

Alatawi, Sael; Alzamzami, Waseem

AIVariant: a deep learning-based somatic variant detector for highly contaminated tumor samples

AIVariant:一种基于深度学习的体细胞变异检测器,适用于高污染肿瘤样本

Jeon, Hyeonseong; Ahn, Junhak; Na, Byunggook; Hong, Soona; Sael, Lee; Kim, Sun; Yoon, Sungroh; Baek, Daehyun

Practices of Cancer Screening for Average-Risk Cancer Patients Among Primary Healthcare Center Physicians in Al-Qassim Region, Saudi Arabia

沙特阿拉伯卡西姆地区基层医疗中心医生对普通风险癌症患者进行癌症筛查的实践

Aljohani, Moath; Alsaykhan, Abdulrahman; Almutairi, Ahmed; Almadhi, Faisal; Alhawshani, Talal; Almishrafi, Sael; Alharbi, Bader

Antiapoptotic Gene Genotype and Allele Variations and the Risk of Lymphoma

抗凋亡基因基因型和等位基因变异与淋巴瘤风险

Osama M Al-Amer, Rashid Mir, Abdullah Hamadi, Mohammed I Alasseiri, Malik A Altayar, Waseem AlZamzami, Mamdoh Moawadh, Sael Alatawi, Hanan A Niaz, Atif Abdulwahab A Oyouni, Othman R Alzahrani, Hanan E Alatwi, Aishah E Albalawi, Khalaf F Alsharif, Ashraf Albrakati, Yousef M Hawsawi

A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages

SHARPIN 错义变体介导阿尔茨海默病特异性脑损伤

Jun Young Park, Dongsoo Lee, Jang Jae Lee, Jungsoo Gim, Tamil Iniyan Gunasekaran, Kyu Yeong Choi, Sarang Kang, Ah Ra Do, Jinyeon Jo, Juhong Park, Kyungtaek Park, Donghe Li, Sanghun Lee, Hoowon Kim, Immanuel Dhanasingh, Suparna Ghosh, Seula Keum, Jee Hye Choi, Gyun Jee Song, Lee Sael, Sangmyung Rhee,