Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Matthew Alonzo"'
Autor:
Meghan Hanley, Matthew Alonzo, Shiqiao Ye, Yang Yu, Javier Contreras, Jade Hayden, Vidu Garg, Ming-Tao Zhao
Publikováno v:
Stem Cell Research, Vol 80, Iss , Pp 103526- (2024)
Pulmonary atresia with intact ventricular septum (PA/IVS) is a rare congenital heart defect that causes a significant decrease of blood outflow from the heart and is fatal if left untreated. iPSC line NCHi013-A was produced from peripheral blood mono
Externí odkaz:
https://doaj.org/article/22a007014752402dbd30d64d1729f91e
Publikováno v:
Stem Cell Research, Vol 80, Iss , Pp 103530- (2024)
Pulmonary atresia with intact ventricular septum (PA-IVS) is a rare congenital heart defect characterized by underdeveloped pulmonary valve and right ventricular hypoplasia. Neonates undergoing surgery to open pulmonary valve have a range of post-sur
Externí odkaz:
https://doaj.org/article/6e1c311a2d2e43b8ba3fc568570f49ff
Publikováno v:
Stem Cell Research, Vol 78, Iss , Pp 103457- (2024)
Truncus arteriosus (TA) is a congenital heart defect where one main blood vessel emerges from the heart, instead of individual aorta and pulmonary artreries. Peripheral mononuclear cells (PBMCs) of a male infant with TA were reporogrammed using Senda
Externí odkaz:
https://doaj.org/article/938bb40affa34493b2bd1c2fc07a97b0
Autor:
Isaac Stanberry, David Cunningham, Shiqiao Ye, Matthew Alonzo, Ming-Tao Zhao, Vidu Garg, Brenda Lilly
Publikováno v:
Stem Cell Research, Vol 72, Iss , Pp 103213- (2023)
Alagille syndrome (ALGS) is a multisystem disease with high variability in clinical features. ALGS is predominantly caused by pathogenic variants in the Notch ligand JAG1. An iPSC line, NCHi011-A, was generated from a ALGS patient with complex cardia
Externí odkaz:
https://doaj.org/article/76446d6f621a40738f84a8d0537f9766
Autor:
David Cunningham, Isaac Stanberry, Shiqiao Ye, Matthew Alonzo, Ming-Tao Zhao, Vidu Garg, Brenda Lilly
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103177- (2023)
Alagille syndrome (ALGS) is an autosomal dominant disease affecting the liver, heart and other organs with high variability. About 95% of ALGS cases are associated with pathogenic variants in JAG1, encoding the Jagged1 ligand that binds to Notch rece
Externí odkaz:
https://doaj.org/article/e6ae087feb1f4ef8823214d3d75727ed
Autor:
Yang Yu, Matthew Alonzo, Shiqiao Ye, Anne Fang, Kandamurugu Manickam, Vidu Garg, Ming-Tao Zhao
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103155- (2023)
Down syndrome is a genetic anomaly that manifests when there is a mistake during cell division, resulting in an additional chromosome 21. Down syndrome can impact cognitive capabilities and physical development, giving rise to diverse developmental d
Externí odkaz:
https://doaj.org/article/4cb0fa3b6c3a4067b22408c293877de6
Publikováno v:
Stem Cell Research, Vol 71, Iss , Pp 103156- (2023)
Down syndrome is a congenital disorder resulting from an extra full or partial chromosome 21, which is characterized by a spectrum of systemic developmental abnormalities, including those affecting the cardiovascular system. Here, we generated an iPS
Externí odkaz:
https://doaj.org/article/28af98132eda4b1cbd0daff20a3b3689
Autor:
Ines Bilkic, Diana Sotelo, Stephanie Anujarerat, Nickolas R. Ortiz, Matthew Alonzo, Raven El Khoury, Carla C. Loyola, Binata Joddar
Publikováno v:
Heliyon, Vol 8, Iss 12, Pp e12250- (2022)
3D bioprinting offers a simplified solution for the engineering of complex tissue parts for in-vitro drug discovery or, in-vivo implantation. However, significant amount of challenges exist in 3D bioprinting of neural tissues, as these are sensitive
Externí odkaz:
https://doaj.org/article/e90eac908ddd4ff39519734a9a0076db
Autor:
Matthew Alonzo, Javier Contreras, Shiqiao Ye, Hui Lin, Lumariz Hernandez-Rosario, Kim L. McBride, Karen Texter, Vidu Garg, Ming-Tao Zhao
Publikováno v:
Stem Cell Research, Vol 64, Iss , Pp 102892- (2022)
Hypoplastic left heart syndrome (HLHS) is a severe congenital heart defect characterized by underdeveloped structures on the left side of the heart, including hypoplasia of the left ventricle and stenosis or atresia of the aortic and mitral valves. H
Externí odkaz:
https://doaj.org/article/a6c781f89b944981a8e8940f952c62db
Autor:
Javier Contreras, Matthew Alonzo, Shiqiao Ye, Hui Lin, Lumariz Hernandez-Rosario, Kim L. McBride, Karen Texter, Vidu Garg, Ming-Tao Zhao
Publikováno v:
Stem Cell Research, Vol 64, Iss , Pp 102893- (2022)
Pulmonary atresia with intact ventricular septum (PA-IVS) is a rare congenital heart defect defined by membranous or muscular atresia of the right ventricular outflow tract where patients display varying degrees of hypoplasia of the right ventricle.
Externí odkaz:
https://doaj.org/article/b77aad0d03844fa28007e4d13b0e0514