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1.
Chinese Journal of Orthopaedic Trauma ; (12): 1063-1068, 2017.
Artigo em Chinês | WPRIM | ID: wpr-707413

RESUMO

Objective To report the clinical effects of a 3D-printed metal drilling template used in surgery for complex upper cervical disorders.Methods Between August 2015 and June 2017,5 patients with upper cervical disorder complicated with complex cranial cervical junction deformity underwent instrumentation and fusion.They were 4 males and one female,aged from 3 to 36 years.All the patients underwent thin slice CT scan before operation.The CT image data were imported into a computer workstation for three dimensional reconstruction of individualized models of the upper cervical spine on which individualized drilling templates were designed.Guided by each of the individualized metal drilling templates manufactured by 3D printing,surgery via the posterior approach was performed in 2 cases and surgery via the combined anterior and posterior approach in 3 cases.After surgery,the screw trajectory was evaluated by CT scan.Results Surgery succeeded in all the 5 patients.A total of 5 pedicle screws and 5 laminar screws were drilled.Postoperative CT scan showed accurate placement of all the 10 screws.The patients recovered with no neurovascular complications.Conclusion Since an individualized 3D-printed metal drilling template can improve the accuracy and safety of screw placement,it can reduce surgical risks and enhance surgical success in the surgery for complex upper cervical disorders.

2.
Chinese Journal of Biotechnology ; (12): 1248-1252, 2008.
Artigo em Chinês | WPRIM | ID: wpr-275395

RESUMO

We found seven tag sequence with high homology in dbEST by using human musclin gene, and got its cDNA sequence, which consists of 651bp and the open reading frame was 54-452 bp detected by RT-PCR, encoding 132 amino acid residue protein. The new gene has high homology with that of human, mouse and rat, the rate is 87.2%, 77.6% and 77.9%, respectively; the gene fragment was cloned into expression vector pGEX-4T-1, and the recombinant was transformed into E. coli BL21. Induced by IPTG, the fusion protein GST-musclin, a 38.59 kD protein was successfully expressed in E. coli BL21 and identified by Western blotting.


Assuntos
Animais , Humanos , Camundongos , Ratos , Sequência de Aminoácidos , Sequência de Bases , Clonagem Molecular , DNA Complementar , Genética , Escherichia coli , Genética , Metabolismo , Dados de Sequência Molecular , Proteínas Musculares , Genética , Músculo Esquelético , Metabolismo , Fases de Leitura Aberta , Genética , Proteínas Recombinantes de Fusão , Genética , Suínos , Genética , Fatores de Transcrição , Genética
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