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Red cell distribution width is a prognostic factor in severe sepsis and septic shock

The American journal of emergency medicine, 2013-03, Vol.31 (3), p.545-548

2013

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Optimized detection of insertions/deletions (INDELs) in whole-exome sequencing data

PloS one, 2017-08, Vol.12 (8), p.e0182272-e0182272

2017

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Mimulone-induced autophagy through p53-mediated AMPK/mTOR pathway increases caspase-mediated apoptotic cell death in A549 human lung cancer cells

PloS one, 2014-12, Vol.9 (12), p.e114607-e114607

2014

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Socio-economic factors of high trash generation in the city of Los Angeles

Water science and technology, 2019-08, Vol.80 (3), p.408

2019

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Assessment of nutrient distributions in Lake Champlain using satellite remote sensing

Journal of environmental sciences (China), 2014-09, Vol.26 (9), p.1831-1836

2014

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Development of genetic quality tests for good manufacturing practice-compliant induced pluripotent stem cells and their derivatives

Scientific reports, 2020-03, Vol.10 (1), p.3939, Article 3939

2020

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Functional in vivo and in vitro effects of 20q11.21 genetic aberrations on hPSC differentiation

Scientific reports, 2020-10, Vol.10 (1), p.18582, Article 18582

2020

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Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans

PloS one, 2016-10, Vol.11 (10), p.e0165680-e0165680

2016

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Exome sequencing is an efficient tool for genetic screening of Charcot-Marie-Tooth Disease

Human mutation, 2012-11, Vol.33 (11), p.1610-1615

2012

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Evaluation of Watershed Susceptibility to Contaminants of Emerging Concern

Journal - American Water Works Association, 2015-04, Vol.107 (4), p.E174-E186

2015

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Partitioning of Mercury into Several Size Fractions in Highway Runoff

Journal of environmental engineering (New York, N.Y.), 2021-02, Vol.147 (2)

2021

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Drug Discovery Platform Targeting M. tuberculosis with Human Embryonic Stem Cell-Derived Macrophages

Stem cell reports, 2019-12, Vol.13 (6), p.980-991

2019

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Conditional deletion of pten leads to defects in nerve innervation and neuronal survival in inner ear development

PloS one, 2013-02, Vol.8 (2), p.e55609-e55609

2013

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Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing

BMC medical genetics, 2017-10, Vol.18 (1), p.106-106, Article 106

2017

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Comprehensive analysis to improve the validation rate for single nucleotide variants detected by next-generation sequencing

PloS one, 2014-01, Vol.9 (1), p.e86664-e86664

2014

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Patterns of gene expression associated with Pten deficiency in the developing inner ear

PloS one, 2014-06, Vol.9 (6), p.e97544-e97544

2014

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Generation of a patient-specific induced pluripotent stem cell line, KSCBi006-A, for osteogenesis imperfecta type I with the COL1A1, c.3162delT mutation

Stem cell research, 2019-12, Vol.41, p.101622-101622, Article 101622

2019

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Spectrum of CT findings after radiofrequency ablation of hepatic tumors

Radiographics, 2008-03, Vol.28 (2), p.379

2008

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The complete mitochondrial genome of Gruberia lanceolata (Gruber, 1884) Kahl, 1932 (Ciliophora: Heterotrichea)

Mitochondrial DNA. Part B. Resources, 2019-10, Vol.4 (2), p.3443-3445

2019

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Trends in tributary water quality in a water supply reservoir

Journal - American Water Works Association, 2014-04, Vol.106 (4), p.E212-E224

2014

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Coagulant dosage determination using deep learning-based graph attention multivariate time series forecasting model

Water research (Oxford), 2023-04, Vol.232, p.119665-119665, Article 119665

2023

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Multidetector CT diagnosis of non-traumatic gastroduodenal perforation

Journal of medical imaging and radiation oncology, 2016-04, Vol.60 (2), p.182-186

2016

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Generation of a PDX1–EGFP reporter human induced pluripotent stem cell line, KSCBi005-A-3, using the CRISPR/Cas9 system

Stem cell research, 2019-12, Vol.41, p.101632-101632, Article 101632

2019

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Multispectral Remote Sensing of Harmful Algal Blooms in Lake Champlain, USA

Water environment research, 2014-12, Vol.86 (12), p.2271-2278

2014

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Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families

BMC medical genetics, 2013-07, Vol.14 (1), p.72-72, Article 72

2013

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