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

Adsorption and anion exchange insight of indigo carmine onto CuAl-LDH/SWCNTs nanocomposite: kinetic, thermodynamic and isotherm analysis

靛蓝胭脂红在CuAl-LDH/SWCNTs纳米复合材料上的吸附和阴离子交换研究:动力学、热力学和等温线分析

Almoisheer, Noha; Alseroury, F A; Kumar, Rajeev; Aslam, M; Barakat, M A

Identification of a novel MKS locus defined by TMEM107 mutation

鉴定由 TMEM107 突变定义的新型 MKS 基因座

Ranad Shaheen, Agaadir Almoisheer, Eissa Faqeih, Zainab Babay, Dorota Monies, Nada Tassan, Mohamed Abouelhoda, Wesam Kurdi, Elham Al Mardawi, Mohamed M I Khalil, Mohammed Zain Seidahmed, Maha Alnemer, Nada Alsahan, Samira Sogaty, Amal Alhashem, Ankur Singh, Manisha Goyal, Seema Kapoor, Rana Alomar, 

A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies

Jeune 窒息性胸廓营养不良症的创始 CEP120 突变扩大了中心粒蛋白在骨骼纤毛病中的作用

Ranad Shaheen, Miriam Schmidts, Eissa Faqeih, Amal Hashem, Ekkehart Lausch, Isabel Holder, Andrea Superti-Furga; UK10K Consortium; Hannah M Mitchison, Agaadir Almoisheer, Rana Alamro, Tarfa Alshiddi, Fatma Alzahrani, Philip L Beales, Fowzan S Alkuraya

Neu-Laxova syndrome, an inborn error of serine metabolism, is caused by mutations in PHGDH

纽-拉索瓦综合征是一种先天性丝氨酸代谢异常,由PHGDH基因突变引起。

Shaheen, Ranad; Rahbeeni, Zuhair; Alhashem, Amal; Faqeih, Eissa; Zhao, Qi; Xiong, Yong; Almoisheer, Agaadir; Al-Qattan, Sarah M; Almadani, Halima A; Al-Onazi, Noufa; Al-Baqawi, Badi S; Saleh, Mohammad Ali; Alkuraya, Fowzan S