Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Min-Young Jang"'
Autor:
Jin Geun Kwon, Yeongsong Kim, Min Young Jang, Hyunsuk Peter Suh, Changsik John Pak, Vaughan Keeley, Jae Yong Jeon, Joon Pio Hong
Publikováno v:
Archives of Plastic Surgery, Vol 50, Iss 05, Pp 514-522 (2023)
Background This is a prospective study on 118 patients who underwent lymphaticovenous anastomosis (LVA) due to secondary lower limb lymphedema between January 2018 and October 2020 to evaluate patients' quality of life (QOL) using the Quality of Life
Externí odkaz:
https://doaj.org/article/6ce51ce4df31490995451baa22301b3a
Publikováno v:
The transactions of The Korean Institute of Electrical Engineers. 72:413-418
GATA6 mutations in hiPSCs inform mechanisms for maldevelopment of the heart, pancreas, and diaphragm
Autor:
Arun Sharma, Lauren K Wasson, Jon AL Willcox, Sarah U Morton, Joshua M Gorham, Daniel M DeLaughter, Meraj Neyazi, Manuel Schmid, Radhika Agarwal, Min Young Jang, Christopher N Toepfer, Tarsha Ward, Yuri Kim, Alexandre C Pereira, Steven R DePalma, Angela Tai, Seongwon Kim, David Conner, Daniel Bernstein, Bruce D Gelb, Wendy K Chung, Elizabeth Goldmuntz, George Porter, Martin Tristani-Firouzi, Deepak Srivastava, Jonathan G Seidman, Christine E Seidman, Pediatric Cardiac Genomics Consortium
Publikováno v:
eLife, Vol 9 (2020)
Damaging GATA6 variants cause cardiac outflow tract defects, sometimes with pancreatic and diaphragmic malformations. To define molecular mechanisms for these diverse developmental defects, we studied transcriptional and epigenetic responses to GATA6
Externí odkaz:
https://doaj.org/article/de48ca73426c4e9e8cd88b2b87f1b9e5
Autor:
Min Young Jang, Parth N. Patel, Alexandre C. Pereira, Jon A.L. Willcox, Alireza Haghighi, Angela C. Tai, Kaoru Ito, Sarah U. Morton, Joshua M. Gorham, David M. McKean, Steven R. DePalma, Daniel Bernstein, Martina Brueckner, Wendy K. Chung, Alessandro Giardini, Elizabeth Goldmuntz, Jonathan R. Kaltman, Richard Kim, Jane W. Newburger, Yufeng Shen, Deepak Srivastava, Martin Tristani-Firouzi, Bruce D. Gelb, George A. Porter, Christine E. Seidman, Jonathan G. Seidman
Publikováno v:
Circulation: Genomic and Precision Medicine.
BACKGROUND: Known genetic causes of congenital heart disease (CHD) explain METHODS: We tested de novo variants from trio studies of 2649 CHD probands and their parents, as well as rare (allele frequency, − 6 ) variants from 4472 CHD probands in the
Autor:
Min-Young Jang
Publikováno v:
Public Law Journal. 22:27-55
Autor:
Moo-Sik Lee, Kwan Lee, Ji-Hyuk Park, Jee-Young Hong, Min Young Jang, Byoung-Hak Jeon, Sang Yun Cho, Sun Ja Choi, Jeong Ik Hong
Publikováno v:
Epidemiology and Health, Vol 39 (2017)
We used a survey about the need for an educational training of infectious disease response staff in Korea Centers for Disease Control and Prevention (KCDC) and officer in metropolitan cities and provincial government to conduct field epidemiological
Externí odkaz:
https://doaj.org/article/5a19ea71ad1d4880b26a59d4153e584f
Autor:
Jordan S. Leyton-Mange, Robert W. Mills, Vincenzo S. Macri, Min Young Jang, Faraz N. Butte, Patrick T. Ellinor, David J. Milan
Publikováno v:
Stem Cell Reports, Vol 2, Iss 2, Pp 163-170 (2014)
In addition to their promise in regenerative medicine, pluripotent stem cells have proved to be faithful models of many human diseases. In particular, patient-specific stem cell-derived cardiomyocytes recapitulate key features of several life-threate
Externí odkaz:
https://doaj.org/article/279e7a5e797148158615c7e16a830fbd
Publikováno v:
Journal of Korea Planning Association. 55:110-124
Autor:
John Donlan, Vicki A. Jackson, Nneka N. Ufere, Jennifer L. Halford, Areej El-Jawahri, Min Young Jang, Joshua Caldwell, Raymond T. Chung, Janet Ho, Sunil Bhatt
Publikováno v:
J Pain Symptom Manage
Context Patients with decompensated cirrhosis have high rates of health care utilization at end of life (EOL). However, the impact of transplant candidacy on intensity of EOL care is currently unknown. Objectives To assess the relationship between tr
Autor:
Barbara McDonough, Alireza Haghighi, Joshua M. Gorham, Christine E. Seidman, Min Young Jang, Diane Fatkin, Neal K. Lakdawala, Parth N Patel, Amy E. Roberts, Kaoru Ito, Lien Lam, Steven R. DePalma, Jon G. Seidman, Renee Johnson, Stuart A. Cook, Jon A. L. Willcox, Paul J.R. Barton
Publikováno v:
Circulation: Genomic and Precision Medicine. 14
Background:HeterozygousTTNtruncating variants cause 10% to 20% of idiopathic dilated cardiomyopathy (DCM). Although variants which disrupt canonical splice signals (ie, invariant dinucleotide of the splice donor site, invariant dinucleotide of the sp