Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Ivy Lin"'
Autor:
Kira Mascho, Svetlana A. Yatsenko, Cecilia W. Lo, Xinxiu Xu, Jennifer Johnson, Lindsey R. Helvaty, Stephanie Burns Wechsler, Chaya N. Murali, Seema R. Lalani, Vidu Garg, Jennelle C. Hodge, Kim L. McBride, Stephanie M. Ware, Jiuann-Huey Ivy Lin
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Introduction5p deletion syndrome, also called Cri-du-chat syndrome 5p is a rare genetic syndrome with reports up to 36% of patients are associated with congenital heart defects. We investigated the association between left outflow tract obstruction a
Externí odkaz:
https://doaj.org/article/2ea28b86dde34d79982956d3247450a9
Autor:
Benjamin J. Landis, Lindsey R. Helvaty, Gabrielle C. Geddes, Jiuann‐Huey Ivy Lin, Svetlana A. Yatsenko, Cecilia W. Lo, William L. Border, Stephanie Burns Wechsler, Chaya N. Murali, Mahshid S. Azamian, Seema R. Lalani, Robert B. Hinton, Vidu Garg, Kim L. McBride, Jennelle C. Hodge, Stephanie M. Ware
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 18 (2023)
Background Chromosomal microarray analysis (CMA) provides an opportunity to understand genetic causes of congenital heart disease (CHD). The methods for describing cardiac phenotypes in patients with CMA abnormalities have been inconsistent, which ma
Externí odkaz:
https://doaj.org/article/3ce4e66e20b2416085e8144a51318ce2
Autor:
Mascho, Kira, Yatsenko, Svetlana A., Lo, Cecilia W., Xinxiu Xu, Johnson, Jennifer, Helvaty, Lindsey R., Wechsler, Stephanie Burns, Murali, Chaya N., Lalani, Seema R., Garg, Vidu, Hodge, Jennelle C., McBride, Kim L., Ware, Stephanie M., Jiuann-Huey Ivy Lin
Publikováno v:
Frontiers in Genetics; 2024, p1-8, 8p
Autor:
Xinxiu Xu, Jiuann-Huey Ivy Lin, Abha S. Bais, Michael John Reynolds, Tuantuan Tan, George C. Gabriel, Zoie Kondos, Xiaoqin Liu, Sruti S. Shiva, Cecilia W. Lo
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Background: Congenital heart disease (CHD) with single-ventricle (SV) physiology is now survivable with a three-stage surgical course ending with Fontan palliation. However, 10-year transplant-free survival remains at 39–50%, with ventricular dysfu
Externí odkaz:
https://doaj.org/article/ae509c34d44f4add901f9f5ae723502c
Autor:
Ashlee Shields, Jiuann-Huey Ivy Lin
Publikováno v:
American Journal of Critical Care. 32:216-220
Background Children with congenital heart disease have unique risk factors associated with the pathophysiology of an abnormal heart; hence, this population is most likely at increased risk of acquiring a pressure injury during hospitalization. Few st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7386f5a195d99893d69b3f2ea1c2f7f1
https://doi.org/10.4037/ajcc2023811
https://doi.org/10.4037/ajcc2023811
Autor:
Luciana Da Fonseca Da Silva, William A. Devine, Tarek Alsaied, Justin Yeh, Jiuann-Huey Ivy Lin, Jose Da Silva
Publikováno v:
Congenital Heart Defects-Recent Advances
Ebstein’s anomaly of the tricuspid valve is a cardiac malformation characterized by downward displacement of the septal and inferior tricuspid valve (TV) leaflets, redundant anterior leaflets with a sail-like morphology, dilation of the true right
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8414e65d85508d842c0df1746f241976
https://mts.intechopen.com/articles/show/title/ebstein-s-anomaly-1
https://mts.intechopen.com/articles/show/title/ebstein-s-anomaly-1
Akademický článek
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Publikováno v:
Genome Biology and Evolution
Comparative genomics of fungal mitochondrial genomes (mitogenomes) have revealed a remarkable pattern of rearrangement between and within major phyla owing to horizontal gene transfer (HGT) and recombination. The role of recombination was exemplified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06ecd23fa11479ac290f5f2437ee3431
http://europepmc.org/articles/PMC6786477
http://europepmc.org/articles/PMC6786477
Autor:
Chih-Yao Hsu, Min Hung Hsu, Lo-Yu Chang, Kun Pin Wu, Yu Ching Liu, Hui Ting Yang, Isheng J. Tsai, Jim Leebens-Mack, Yu Wei Wu, Shu-Miaw Chaw, Huei-Mien Ke, Chung-Shien Wu, Ling Ni Wang, Chan Yi Ivy Lin, Han Yu Wang, Edi Sudianto
Publikováno v:
Nature Plants. 5:63-73
We present reference-quality genome assembly and annotation for the stout camphor tree (Cinnamomum kanehirae (Laurales, Lauraceae)), the first sequenced member of the Magnoliidae comprising four orders (Laurales, Magnoliales, Canellales and Piperales
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c45fb51588d0a5c08496aaffde57b3f2
https://doi.org/10.1038/s41477-018-0337-0
https://doi.org/10.1038/s41477-018-0337-0
Autor:
Catherine K. Kuo, Phillip S. Adams, Xinxiu Xu, Wenjuan Zhu, Timothy N. Feinstein, George A. Porter, Gloria S. Pryhuber, Dennis Kostka, Madhavi K. Ganapathiraju, Nguyen P, Jiuann-Huey Ivy Lin, Sruti Shiva, Hisato Yagi, Gisela Beutner, Cecilia W. Lo, Xiaoqin Liu, Kang Jin, Kalyani B. Karunakaran, Criscione J, Abha S. Bais, Bruce J. Aronow
SummaryHypoplastic left heart syndrome (HLHS) is a severe congenital heart defect with 30% mortality from heart failure (HF) in the first year of life, but why only some patients suffer early-HF and its cause remain unknown. Modeling using induced pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e9712cf17d1ccb76b2643f0882c4b6c
https://doi.org/10.1101/2021.05.09.443165
https://doi.org/10.1101/2021.05.09.443165