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Jeongeun Lee

Showing results (71-80 of 75) with videos related to

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Breast Cancer Research : BCR|March 15, 2014
A BRCA1 deficient-like signature is enriched in breast cancer brain metastases and predicts DNA damage-induced poly (ADP-ribose) polymerase inhibitor sensitivityRyan P McMullin, Ben S Wittner, Chuanwei Yang, et al.
Journal of Nanobiotechnology|March 29, 2025
Scalable ion concentration polarization dialyzer for peritoneal dialysate regenerationWonseok Kim, Seongjun Hong, Kihong Kim, et al.
Experimental & Molecular Medicine|November 3, 2022
A database of 5305 healthy Korean individuals reveals genetic and clinical implications for an East Asian populationJeongeun Lee, Jean Lee, Sungwon Jeon, et al.
Frontiers in Genetics|October 10, 2022
Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseasesSoojin Park, Se Song Jang, Seungbok Lee, et al.
Scientific Reports|January 31, 2020
Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred populationYoungha Lee, Soojin Park, Jin Sook Lee, et al.
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Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
Breast Cancer Research : BCR|March 15, 2014
A BRCA1 deficient-like signature is enriched in breast cancer brain metastases and predicts DNA damage-induced poly (ADP-ribose) polymerase inhibitor sensitivityRyan P McMullin, Ben S Wittner, Chuanwei Yang, et al.
Journal of Nanobiotechnology|March 29, 2025
Scalable ion concentration polarization dialyzer for peritoneal dialysate regenerationWonseok Kim, Seongjun Hong, Kihong Kim, et al.
Experimental & Molecular Medicine|November 3, 2022
A database of 5305 healthy Korean individuals reveals genetic and clinical implications for an East Asian populationJeongeun Lee, Jean Lee, Sungwon Jeon, et al.
Frontiers in Genetics|October 10, 2022
Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseasesSoojin Park, Se Song Jang, Seungbok Lee, et al.
Scientific Reports|January 31, 2020
Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred populationYoungha Lee, Soojin Park, Jin Sook Lee, et al.
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