神経外科学分野の英文校正サンプル

エナゴは、神経外科学および神経生物学分野でも多くの論文を校正し、高い評価をいただいてきました。生理学、解剖学、分子生物学、発生生物学、細胞学、数学モデリング、心理学などさまざまな領域との関連も踏まえ、神経化学、認知科学、心理学など、各種の専門知識を有する校正者が校閲・校正を行います。こちらが神経科学論文の修正履歴付き校正サンプルです。アドバンス英文校正とノーマル英文校正の2つのサービスプランを比較いただき、各種サンプルをPDF形式でダウンロードすることもできます。

Optic nerves of anesthetized adult Sprague Dawley rats were surgically exposed surgically in anaesthetized adult Sprague Dawley rats through using a supraorbital approach and were crushed using the an aneurysm clip (YASARGIL) aneurysm clip, which was placed 2 mm behind the posterior eye pole, as described in previous lyreports. Using a transscleral approach, Ccultured neural stem cells (NSCs) 1 were transplanted into the subretinal space immediately after crushing the optic nerve crush using a transscleral approach. A 33-gauge G blunt needle attached to a 10-μL syringe (Hamilton, Reno, NV) was introduced tangentially introduced through the sclerotomy site into the subretinal region, causing retinal detachment, which was . The retinal detachment was confirmed microscopically confirmed.  2 The same procedure was then repeated to slowly inject a suspension of pigment epithelium-derived factor (PEDF)- 3 modified NSCs (2 μL of 2.0 × ×4105 cells). In this study, 72 rats withunder going optic nerve injury were randomly assigned to 3 three groups: group with receiving injections of phosphate- buffered saline (PBS) injections (n = 24), receiving , group with weekly injections of PEDF injections (n = 24), and receiving , and group with PEDF- modified NSCs (n = 24). Subsequently, 0.67 nM of PEDF dissolved in 5 μL of sterile PBS was injected immediately after the optic nerve was crushed (day 0 days) and at 1 and 2 1week and 2 weeks thereafter. The All rats (from each group) were examined at each of the time point after s post-injection (2 or and 4 weeks). At each time point, Ssamples were harvested and placed at each time point into a protein extraction buffer. Equal amounts of protein were denatured for 5 minutes at 95 °C in a sample buffer and were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresissodium dodecyl sulfatepolyacrylamide gel electrophoresis (SDSPAGE).

Explanations

Optic nerves were exposed surgically exposed in anaesthetized 1 adult Sprague Dawley rats through using a supraorbital approach and crushed using the an aneurysm clip (YASARGIL) aneurysm clip, which was placed 2 mm behind the posterior eye pole, as described in previous reports. Cultured neural stem cells (NSCs) 2 were transplanted into the subretinal space immediately after the optic nerve crush using a transscleral approach. A 33-gauge G blunt needle attached to a 10-μL syringe (Hamilton, Reno, NV) was introduced tangentially through the sclerotomy site into the subretinal region and , causing caused retinal detachment. The retinal detachment was confirmed microscopically confirmed. The same procedure was then repeated to slowly inject a suspension of pigment epithelium-derived factor (PEDF)- 3modified NSCs (2 μL of 2.0 × ×4105 cells). In this study, 72 rats withunder going optic nerve injury were randomly assigned to 3 three groups: a group with that received injections of phosphate- buffered saline (PBS) (n = 24), a group that received , group with weekly injections of PEDF (n = 24), and a group that received , and group with PEDF- modified NSCs (n = 24). Subsequently, 0.67 nM of PEDF dissolved in 5 μL of sterile PBS was injected immediately after the optic nerve crush (day 0 days) and at 1 and 2 1week and 2 weeks thereafter. The rRats (from each group) were examined at each of the time points post- injection (2 or and 4 weeks). At each time point, Ssamples were harvested and placed at each time point into a protein extraction buffer. Equal amounts of protein were denatured for 5 minutes at 95 °C in a sample buffer and then separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDSPAGE).

Explanations

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