Epsin Endocytic Adaptor Proteins in Angiogenic and Lymphangiogenic Signaling
Cowan, Douglas B, Hao Wu, and Hong Chen. 2023. “Epsin Endocytic Adaptor Proteins in Angiogenic and Lymphangiogenic Signaling”. Cold Spring Harbor Perspectives in Medicine.
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Mauris felis ante montes rhoncus semper, iaculis nisl facilisis malesuada maecenas
Fames, Pulvinar, Hasellus Dignissim, Imperdiet Sociosqu, and Dictum Gravida. 2019. “Mauris Felis ante Montes Rhoncus Semper, Iaculis Nisl Facilisis Malesuada Maecenas”. Journal of Iaculis Nisl Facilisis Malesuada Maecenas.
A Drug Screen using Human iPSC-Derived Hepatocyte-like Cells Reveals Cardiac Glycosides as a Potential Treatment for Hypercholesterolemia
Cayo, M. A., S. K. Mallanna, F. Di Furio, R. Jing, L. B. Tolliver, M. Bures, A. Urick, et al. 2017. “A Drug Screen Using Human IPSC-Derived Hepatocyte-Like Cells Reveals Cardiac Glycosides As a Potential Treatment for Hypercholesterolemia”. Cell Stem Cell 20: 478-489 e5.
Development of functional resident macrophages in human pluripotent stem cell-derived colonic organoids and human fetal colon
Munera, J. O., D. O. Kechele, C. Bouffi, N. Qu, R. Jing, P. Maity, J. R. Enriquez, et al. 2023. “Development of Functional Resident Macrophages in Human Pluripotent Stem Cell-Derived Colonic Organoids and Human Fetal Colon”. Cell Stem Cell 30: 1434-1451 e9.
FGF2 mediates hepatic progenitor cell formation during human pluripotent stem cell differentiation by inducing the WNT antagonist NKD1
Twaroski, K., S. K. Mallanna, R. Jing, F. DiFurio, A. Urick, and S. A. Duncan. 2015. “FGF2 Mediates Hepatic Progenitor Cell Formation During Human Pluripotent Stem Cell Differentiation by Inducing the WNT Antagonist NKD1”. Genes Dev 29: 2463-74.
Association of genetic and sulcal traits with executive function in congenital heart disease.
Maleyeff, Lara, Jane W Newburger, David Wypij, Nina H Thomas, Evdokia Anagnoustou, Martina Brueckner, Wendy K Chung, et al. 2024. “Association of Genetic and Sulcal Traits With Executive Function in Congenital Heart Disease.”. Annals of Clinical and Translational Neurology 11 (2): 278-90.
Multiple serotonergic brainstem abnormalities in sudden infant death syndrome.
Paterson, David, Felicia Trachtenberg, Eric Thompson, Richard Belliveau, Alan Beggs, Ryan Darnall, Amy Chadwick, Henry Krous, and Hannah Kinney. 2006. “Multiple Serotonergic Brainstem Abnormalities in Sudden Infant Death Syndrome.”. JAMA 296 (17): 2124-32.
X-linked myotubular and centronuclear myopathies.
Pierson, Christopher, Kinga Tomczak, Pankaj Agrawal, Behzad Moghadaszadeh, and Alan Beggs. 2005. “X-Linked Myotubular and Centronuclear Myopathies.”. J Neuropathol Exp Neurol 64 (7): 555-64.
Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations.
Agrawal, Pankaj, Corinne Strickland, Charles Midgett, Ana Morales, Daniel Newburger, Melisa Poulos, Kinga Tomczak, et al. 2004. “Heterogeneity of Nemaline Myopathy Cases With Skeletal Muscle Alpha-Actin Gene Mutations.”. Ann Neurol 56 (1): 86-96.
Tryptophan biosynthesis protects mycobacteria from CD4 T cell-mediated killing
Zhang, Yanjia, Manchi Reddy, Thomas Ioerger, Alissa Rothchild, Veronique Dartois, Brian Schuster, Andrej Trauner, et al. 2013. “Tryptophan Biosynthesis Protects Mycobacteria from CD4 T Cell-Mediated Killing”. Cell 155 (6): 1296-308.