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

The mutational spectrum of NRAS gene discovers a novel frameshift mutation (E49R) in Saudi colorectal cancer patients

NRAS基因突变谱在沙特阿拉伯结直肠癌患者中发现了一种新的移码突变(E49R)。

Rasool, Mahmood; Haque, Absarul; Alharthi, Mohammed; Sibiany, Abdulrahman; Alamri, Mohammed Saad; Alqarni, Samer Mohammed Hassan; Rather, Irfan A; Chaudhary, Adeel G; Karim, Sajjad; Pushparaj, Peter Natesan

Pairing 3D-Printing with Nanotechnology to Manage Metabolic Syndrome

3D 打印与纳米技术相结合治疗代谢综合征

Khalid M El-Say, Raed I Felimban, Hossam H Tayeb, Adeel G Chaudhary, Abdelsattar M Omar, Waleed Y Rizg, Fuad H Alnadwi, Fathy I Abd-Allah, Tarek A Ahmed

The Effects of Prenatal Exposure to Pregabalin on the Development of Ventral Midbrain Dopaminergic Neurons

产前接触普瑞巴林对中脑腹侧多巴胺能神经元发育的影响

Walaa F Alsanie, Majid Alhomrani, Ahmed Gaber, Hamza Habeeballah, Heba A Alkhatabi, Raed I Felimban, Sherin Abdelrahman, Charlotte A E Hauser, Adeel G Chaudhary, Abdulhakeem S Alamri, Bassem M Raafat, Abdulwahab Alamri, Sirajudheen Anwar, Khaled A Alswat, Yusuf S Althobaiti, Yousif A Asiri

Association between vitamin D and glycaemic parameters in a multi-ethnic cohort of postmenopausal women with type 2 diabetes in Saudi Arabia

沙特阿拉伯多民族2型糖尿病绝经后妇女队列中维生素D与血糖参数之间的关联

Alharazy, Shatha; Alissa, Eman; Lanham-New, Susan; Naseer, Muhammad Imran; Chaudhary, Adeel G; Robertson, M Denise

Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia

全外显子组测序用于鉴定沙特阿拉伯维生素 D 缺乏症家庭中与维生素 D 代谢途径有关的遗传变异

Shatha Alharazy, Muhammad Imran Naseer, Eman Alissa, Margaret Denise Robertson, Susan Lanham-New, Adeel G Chaudhary

Directly measured free and total 25-hydroxyvitamin D levels in relation to metabolic health in multi-ethnic postmenopausal females in Saudi Arabia

直接测量沙特阿拉伯多民族绝经后女性体内游离和总25-羟基维生素D水平与代谢健康的关系

Alharazy, Shatha; Robertson, M Denise; Lanham-New, Susan; Naseer, Muhammad Imran; Chaudhary, Adeel G; Alissa, Eman

Association of SNPs in GC and CYP2R1 with total and directly measured free 25-hydroxyvitamin D in multi-ethnic postmenopausal women in Saudi Arabia

沙特阿拉伯多民族绝经后妇女中 GC 和 CYP2R1 中的 SNP 与总量和直接测量的游离 25-羟基维生素 D 的关联

Shatha Alharazy, Muhammad Imran Naseer, Eman Alissa, M Denise Robertson, Susan Lanham-New, Mohammad H Alqahtani, Adeel G Chaudhary

Novel Missense Variant in Heterozygous State in the BRPF1 Gene Leading to Intellectual Developmental Disorder With Dysmorphic Facies and Ptosis

BRPF1基因中一种新的杂合状态错义变异导致智力发育障碍,伴有面部畸形和眼睑下垂

Naseer, Muhammad Imran; Abdulkareem, Angham Abdulrahman; Guzmán-Vega, Francisco J; Arold, Stefan T; Pushparaj, Peter Natesan; Chaudhary, Adeel G; AlQahtani, Mohammad H

Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family

全外显子组测序揭示沙特阿拉伯一个家族中HEXA基因的纯合无义突变导致泰-萨克斯病。

Naseer, Muhammad Imran; Abdulkareem, Angham Abdulrahman; Jan, Mohammed Mohammed; Chaudhary, Adeel G; Al-Qahtani, Mohammad H

Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly

新一代测序揭示了PUS7基因中新的纯合移码突变和AASS基因中的剪接受体变异,导致智力障碍、发育迟缓、面部畸形和小头畸形

Naseer, Muhammad Imran; Abdulkareem, Angham Abdulrahman; Jan, Mohammed M; Chaudhary, Adeel G; Alharazy, Shatha; AlQahtani, Mohammad H