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pro vyhledávání: '"Jeong-A Lim"'
Publikováno v:
Viruses, Vol 16, Iss 7, p 1155 (2024)
Bacteriophages (phages) have gained considerable attention as effective antimicrobial agents that infect and kill pathogenic bacteria. Based on this feature, phages have been increasingly used to achieve food safety. They are stored in a medium or bu
Externí odkaz:
https://doaj.org/article/b5ff18f820634ab8b89f3044c864a9bc
Publikováno v:
Micro and Nano Systems Letters, Vol 10, Iss 1, Pp 1-8 (2022)
Abstract A microarray detection method based on on-chip signal amplification using terminal deoxynucleotidyl transferase (TdT) was developed to visualize pathogenic genes. Cyclic olefin copolymer (COC) substrate for microarrays was treated with oxyge
Externí odkaz:
https://doaj.org/article/ef712eea0f774d43a060df5980a7a80f
Autor:
Rebecca Gibson, Jeong-A Lim, Su Jin Choi, Neha Jumani, Deeksha Bali, Sarah Young, William Jeck, Baodong Sun, Aravind Asokan, Priya Kishnani
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100202- (2023)
Externí odkaz:
https://doaj.org/article/d63af71a953446e8916fffd5b0b011d6
Publikováno v:
JCI Insight, Vol 7, Iss 23 (2022)
Glycogen debranching enzyme deficiency in glycogen storage disease type III (GSD III) results in excessive glycogen accumulation in multiple tissues, primarily the liver, heart, and skeletal muscle. We recently reported that an adeno-associated virus
Externí odkaz:
https://doaj.org/article/a7cb7fa0b4554822bd8d93f4d9a18adb
Publikováno v:
Microorganisms, Vol 11, Iss 6, p 1539 (2023)
Silver nanoparticles (AgNPs) were synthesized using the whole plant of Duchesnea indica (DI) which was extracted in different solvents; the antimicrobial effects of the extract were investigated in this study. The extraction of DI was performed using
Externí odkaz:
https://doaj.org/article/e12c7f47f0d24b44a73a8ba1ddce5b88
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 240-249 (2020)
Glycogen storage disease type III (GSD III) is an inherited disorder caused by a deficiency of glycogen debranching enzyme (GDE), which results in the accumulation of abnormal glycogen (limit dextrin) in the cytoplasm of liver, heart, and skeletal mu
Externí odkaz:
https://doaj.org/article/4560144da7dc471082c8175480e50f1a
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 12, Iss , Pp 233-245 (2019)
Pompe disease, a severe and often fatal neuromuscular disorder, is caused by a deficiency of the lysosomal enzyme acid alpha-glucosidase (GAA). The disease is characterized by the accumulation of excess glycogen in the heart, skeletal muscle, and CNS
Externí odkaz:
https://doaj.org/article/0b297c69d3504cfd9f4e78a0f30a449b
Autor:
Eun Kyung Choi, Jeong-A Lim, Jong Kwang Kim, Moon Sun Jang, Sun Eui Kim, Hye Jung Baek, Eun Jung Park, Tae Hyun Kim, Chu-Xia Deng, Rui-Hong Wang, Sang Soo Kim
Publikováno v:
Experimental and Molecular Medicine, Vol 50, Iss 10, Pp 1-16 (2018)
Breast cancer: A protein link for treatment? The role of disrupted activity of the protein BRCA1 in the progression of breast cancer has been clarified, suggesting that targeting another protein with which it interacts could offer a new route to trea
Externí odkaz:
https://doaj.org/article/b03c389a8efc4cbebc4837f800b6d45a
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 7, Iss C, Pp 11-14 (2017)
Externí odkaz:
https://doaj.org/article/43738e81a5ff4e7cb06f0d3be012553b
Autor:
Aditi Korlimarla, Jeong-A Lim, Paul McIntosh, Kanecia Zimmerman, Baodong D. Sun, Priya S. Kishnani
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 15, p 3395 (2021)
Background: There are new emerging phenotypes in Pompe disease, and studies on smooth muscle pathology are limited. Gastrointestinal (GI) manifestations are poorly understood and underreported in Pompe disease. Methods: To understand the extent and t
Externí odkaz:
https://doaj.org/article/36996edd2da646048fc5190cd13755d7