E-LIB Suche - Ergebnisse für: Hinton, Robert B

1

A Multicenter Analysis of Abnormal Chromosomal Microarray F..:

Landis, Benjamin J. ; Helvaty, Lindsey R. ; Geddes, Gabrielle C....
Journal of the American Heart Association. 12 (2023) 18 - p. , 2023

Link: https://doi.org/10.1161/..

2

Identification of a common polymorphism in COQ8B acting as ..:

Landis, Benjamin J. ; Lai, Dongbing ; Guo, Dong-Chuan...
Human Genetics and Genomics Advances. 3 (2022) 1 - p. 100057 , 2022

Link: https://doi.org/10.1016/..

3

Early Aberrant Angiogenesis Due to Elastic Fiber Fragmentat..:

Hinton, Robert B. ; Juraszek, Amy L. ; Opoka, Amy M....
Journal of Cardiovascular Development and Disease. 8 (2021) 7 - p. 75 , 2021

Link: https://doi.org/10.3390/..

4

Abnormalities of placental development and function are ass..:

Courtney, Jennifer ; Troja, Weston ; Owens, Kathryn J....
Placenta. 101 (2020) - p. 57-65 , 2020

Link: https://doi.org/10.1016/..

5

A Comprehensive Clinical Genetics Approach to Critical Cong..:

Shikany, Amy R. ; Landis, Benjamin J. ; Parrott, Ashley...
The Journal of Pediatrics. 227 (2020) - p. 231-238.e14 , 2020

Link: https://doi.org/10.1016/..

6

Loss of flow responsive Tie1 results in ImpairedAortic valv..:

Qu, Xianghu ; Violette, Kate ; Sewell-Loftin, M.K....
Developmental Biology. 455 (2019) 1 - p. 73-84 , 2019

Link: https://doi.org/10.1016/..

7

Fetal origins of adult cardiac disease: a novel approach to..:

Alsaied, Tarek ; Omar, Khaled ; James, Jeanne F....
Pediatric Research. 81 (2017) 6 - p. 919-925 , 2017

Link: https://doi.org/10.1038/..

8

Molecular Characterization of Pediatric Restrictive Cardiom..:

Rindler, Tara N. ; Hinton, Robert B. ; Salomonis, Nathan.
Scientific Reports. 7 (2017) 1 - p. , 2017

Link: https://doi.org/10.1038/..

9

Proteomic Alterations Associated with Biomechanical Dysfunc..:

Angel, P. M. ; Narmoneva, D. A. ; Sewell-Loftin, M. K....
Annals of Biomedical Engineering. 45 (2017) 11 - p. 2548-2562 , 2017

Link: https://doi.org/10.1007/..

10

Exome Sequencing Identifies Candidate Genetic Modifiers of ..:

Landis, Benjamin J. ; Schubert, Jeffrey A. ; Lai, Dongbing...
Journal of Cardiovascular Translational Research. 10 (2017) 4 - p. 423-432 , 2017

Link: https://doi.org/10.1007/..

11

Familial co-occurrence of congenital heart defects follows ..:

Ellesøe, Sabrina G ; Workman, Christopher T ; Bouvagnet, Patrice...
European Heart Journal. 39 (2017) 12 - p. 1015-1022 , 2017

Link: https://doi.org/10.1093/..

12

Inhibition of MAPK-Erk pathway in vivo attenuates aortic va..:

Munjal, Charu ; Jegga, Anil G. ; Opoka, Amy M....
Physiological Reports. 5 (2017) 5 - p. e13152 , 2017

Link: https://doi.org/10.14814..

13

Clinically relevant variants identified in thoracic aortic ..:

Schubert, Jeffrey A. ; Landis, Benjamin J. ; Shikany, Amy R...
American Journal of Medical Genetics Part A. 170 (2016) 5 - p. 1288-1294 , 2016

Link: https://doi.org/10.1002/..

14

Molecular Mechanisms of Heart Valve Development and Disease:

, In: Etiology and Morphogenesis of Congenital Heart Disease,

Gomez Stallons, M. Victoria ; Wirrig-Schwendeman, Elaine E. ; Fang, Ming... - p. 145-151 , 2016

Link: https://doi.org/10.1007/..

15

Analysis of TGFBR1*6A variant in individuals evaluated for ..:

Somers, Allyson E. ; Hinton, Robert B. ; Pilipenko, Valentina..
American Journal of Medical Genetics Part A. 170 (2016) 7 - p. 1786-1790 , 2016

Link: https://doi.org/10.1002/..