至今,GenScript的服务及产品已被Cell, Nature, Science, PNAS等1300多家生物医药类杂志引用近万次,处于行业领先水平。NIH、哈佛、耶鲁、斯坦福、普林斯顿、杜克大学等约400家全球著名机构使用GenScript的基因合成、多肽服务、抗体服务和蛋白服务等成功地发表科研成果,再次证明GenScript 有能力帮助业内科学家Make research easy.

A de novo Ser111Thr variant in aquaporin-4 in a patient with intellectual disability, transient signs of brain ischemia, transient cardiac hypertrophy, and progressive gait disturbance.

Cold Spring Harb Mol Case Stud. 2018; 
Berland S, Toft-Bertelsen TL, Aukrust I, Byska J, Vaudel M,, Bindoff LA,, MacAulay N, Houge G.
Products/Services Used Details Operation
Custom Vector Construction … cDNA encoding the M23 isoform of human AQP4-wt and AQP4-S111T mutant subcloned into the oocyte expression vector pXOOM was purchased from GenScript, and 10 ng of AQP4 cRNA was microinjected into defolliculated Xenopus laevis oocytes … Get A Quote

摘要

Aquaporin-4, encoded by AQP4, is the major water channel in the central nervous system and plays an important role in the brain's water balance, including edema formation and clearance. Using genomic copy-number analysis and trio-exome sequencing, we investigated a male patient with intellectual disability, hearing loss, and progressive gait dysfunction and found a de novo missense change Ser111Thr in AQP4 as the only suspicious finding. Perinatally, signs of brain ischemia were detected in relation to acute collapse 2 h after birth that resolved a few days later. At the age of 3 mo, cardiac hypertrophy was detected that persisted through childhood but was completely resolved by age 16. In theory, this neurodev... More

关键词

brain atrophy; cerebral ischemia; concentric hypertrophic cardiomyopathy; congenital sensorineural hearing impairment; gait imbalance; intellectual disability, mild; macrocephaly at birth; relative macrocephaly; spastic gait