ASPIRATSION SINDROMDAN NOBUD BOʼLGAN CHAQALOQLAR BUYRAGINING MORFOLOGIK OʼZGARISHLARI
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Keywords

chaqaloq, neonatal davr, buyrak morfologiyasi

How to Cite

Egamov Bunyodbek Jumanazarovich, & Salaeva Zulfiya Shanazarovna. (2023). ASPIRATSION SINDROMDAN NOBUD BOʼLGAN CHAQALOQLAR BUYRAGINING MORFOLOGIK OʼZGARISHLARI. Journal of Universal Science Research, 1(4), 449–451. Retrieved from https://universalpublishings.com/index.php/jusr/article/view/524

Abstract

Erta neonatal davrda aspiratsiya sindromi  neonatologiyada hali ham dolzarb tadqiqot mavzusi bo'lib qolmoqda, klinik ahamiyatiga qaramay, yangi tug'ilgan chaqaloqlarda va chaqaloqlarda tug'ruqdan keyingi aspiratsiyaga hali ham kamroq e'tibor qaratilаdi. Neoanatal davr shartli ravishda ikkita davrni oʼz ichiga oladi. Erta neonatal davr chaqaloq tugʼilganidan 0-7 kungacha boʼlgan va kechki neonatal davr 8-28 kungacha boʼlgan muddat . Neonatal davrda aksariyat ichki aʼzolarning rivojlanishi xar qanday taʼsirlovchi omillarga javoban tizimli javob reaktsiyasi koʼrinishida namoyon boʼladi.

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References

Зеленцова В. Л. Морфологические особенности почек у плодов и новорожденных, перенесших гипоксию / В. Л. Зеленцова, В. И. Шилко, С. Ю. Медведева // Архив патологии. – 2003. – № 6. – С. 40–44.

Попов С. В. Особенности нарушения функции мочевыделительной системы у новорожденных с гипоксическим поражением ЦНС тяжелой степени / С. В. Попов, В. Н. Облазницкий // Вісник СумДУ. Серія Медицина. – 2008. – Т. 2, – С. 88–91.

Estrada JL, Martens G, Li P, et al. Evaluation of human and nonhuman primate antibody binding to pig cells lacking GGTA1/CMAH/beta4GalNT2 genes. Xenotransplantation. 2015;22:194–202.

Konermann S, Brigham MD, Trevino AE, et al. Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex. Nature. 2015;517:583–588.

Liao HK, Hatanaka F, Araoka T, et al. In vivo target gene activation via CRISPR/Cas9-mediated trans-epigenetic modulation. Cell. 2017;171:1495–1507 e1415.

Niu D, Wei HJ, Lin L, et al. Inactivation of porcine endogenous retrovirus in pigs using CRISPR-Cas9. Science. 2017;357:1303–1307.

Qi LS, Larson MH, Gilbert LA, et al. Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression. Cell. 2013;152:1173–1183.

Wang H, Yang H, Shivalila CS, et al. One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering. Cell. 2013;153:910–918.

Wang X, Cao C, Huang J, et al. One-step generation of triple genetargeted pigs using CRISPR/Cas9 system. Sci Rep. 2016;6:20620.

Yang L, Guell M, Niu D, et al. Genome-wide inactivation of porcine endogenous retroviruses (PERVs). Science. 2015;350:1101–1104.

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