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Showing results 10 to 17 of 17

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Issue Date	Title	Journal Title
2022	In vivo outer hair cell gene editing ameliorates progressive hearing loss in dominant-negative Kcnq4 murine model	THERANOSTICS
2021	Microbiome analysis reveals that Ralstonia is responsible for decreased renal function in patients with ulcerative colitis	CLINICAL AND TRANSLATIONAL MEDICINE
2019	Mutations of ADAMTS9 Cause Nephronophthisis-Related Ciliopathy	AMERICAN JOURNAL OF HUMAN GENETICS
2022	OSBPL2 mutations impair autophagy and lead to hearing loss, potentially remedied by rapamycin	AUTOPHAGY
2020	SGLT2 Inhibition Modulates NLRP3 Inflammasome Activity via Ketones and Insulin in Diabetes With Cardiovascular Disease	NATURE COMMUNICATIONS
2019	Systematic evaluation of gene variants linked to hearing loss based on allele frequency threshold and filtering allele frequency	Scientific Reports
2010	The L441P mutation of cystic fibrosis transmembrane conductance regulator and its molecular pathogenic mechanisms in a Korean patient with cystic fibrosis	JOURNAL OF KOREAN MEDICAL SCIENCE
2019	The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report	BMC MEDICAL GENETICS