Search Results - "Hickey, Raymond D."

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    Concise Review: Liver Regenerative Medicine: From Hepatocyte Transplantation to Bioartificial Livers and Bioengineered Grafts by Nicolas, Clara T., Hickey, Raymond D., Chen, Harvey S., Mao, Shennen A., Lopera Higuita, Manuela, Wang, Yujia, Nyberg, Scott L.

    Published in Stem cells (Dayton, Ohio) (01-01-2017)
    “…Donor organ shortage is the main limitation to liver transplantation as a treatment for end‐stage liver disease and acute liver failure. Liver regenerative…”
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    Journal Article
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    The ploidy conveyor of mature hepatocytes as a source of genetic variation by Duncan, Andrew W, Taylor, Matthew H, Hickey, Raymond D, Hanlon Newell, Amy E, Lenzi, Michelle L, Olson, Susan B, Finegold, Milton J, Grompe, Markus

    Published in Nature (London) (07-10-2010)
    “…Mononucleated and binucleated polyploid hepatocytes (4n, 8n, 16n and higher) are found in all mammalian species, but the functional significance of this…”
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    An siRNA Screen Identifies the U2 snRNP Spliceosome as a Host Restriction Factor for Recombinant Adeno-associated Viruses by Schreiber, Claire A, Sakuma, Toshie, Izumiya, Yoshihiro, Holditch, Sara J, Hickey, Raymond D, Bressin, Robert K, Basu, Upamanyu, Koide, Kazunori, Asokan, Aravind, Ikeda, Yasuhiro

    Published in PLoS pathogens (01-08-2015)
    “…Adeno-associated viruses (AAV) have evolved to exploit the dynamic reorganization of host cell machinery during co-infection by adenoviruses and other helper…”
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    Ploidy reductions in murine fusion-derived hepatocytes by Duncan, Andrew W, Hickey, Raymond D, Paulk, Nicole K, Culberson, Andrew J, Olson, Susan B, Finegold, Milton J, Grompe, Markus

    Published in PLoS genetics (01-02-2009)
    “…We previously showed that fusion between hepatocytes lacking a crucial liver enzyme, fumarylacetoacetate hydrolase (FAH), and wild-type blood cells resulted in…”
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    Effect of amine content and chemistry on long‐term, three‐dimensional hepatocyte spheroid culture atop aminated elastin‐like polypeptide coatings by Weeks, C. Andrew, Aden, Bethany, Zhang, Junlin, Singh, Anisha, Hickey, Raymond D., Kilbey, S. Michael, Nyberg, Scott L., Janorkar, Amol V.

    “…Culture conditions that induce hepatic spheroidal aggregates sustain liver cells with metabolism that mimics in vivo hepatocytes. Here we present an array of…”
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    Fumarylacetoacetate hydrolase deficient pigs are a novel large animal model of metabolic liver disease by Hickey, Raymond D., Mao, Shennen A., Glorioso, Jaime, Lillegard, Joseph B., Fisher, James E., Amiot, Bruce, Rinaldo, Piero, Harding, Cary O., Marler, Ronald, Finegold, Milton J., Grompe, Markus, Nyberg, Scott L.

    Published in Stem cell research (01-07-2014)
    “…Hereditary tyrosinemia type I (HT1) is caused by deficiency in fumarylacetoacetate hydrolase (FAH), an enzyme that catalyzes the last step of tyrosine…”
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    Suspension culture of hepatocyte-derived reporter cells in presence of albumin to form stable three-dimensional spheroids by Weeks, C. Andrew, Newman, Kristen, Turner, Paul A., Rodysill, Brian, Hickey, Raymond D., Nyberg, Scott L., Janorkar, Amol V.

    Published in Biotechnology and bioengineering (01-09-2013)
    “…Several studies in the past have formed 3‐dimensional (3D) spheroids of primary hepatocytes in suspension culture. Unfortunately, primary hepatocytes in a…”
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    Efficient production of Fah‐null heterozygote pigs by chimeric adeno‐associated virus‐mediated gene knockout and somatic cell nuclear transfer by Hickey, Raymond D., Lillegard, Joseph B., Fisher, James E., McKenzie, Travis J., Hofherr, Sean E., Finegold, Milton J., Nyberg, Scott L., Grompe, Markus

    Published in Hepatology (Baltimore, Md.) (01-10-2011)
    “…Hereditary tyrosinemia type I (HT1) results in hepatic failure, cirrhosis, and hepatocellular carcinoma (HCC) early in childhood and is caused by a deficiency…”
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    Chronic Phenotype Characterization of a Large-Animal Model of Hereditary Tyrosinemia Type 1 by Elgilani, Faysal, Mao, Shennen A, Glorioso, Jaime M, Yin, Meng, Iankov, Ianko D, Singh, Anisha, Amiot, Bruce, Rinaldo, Piero, Marler, Ronald J, Ehman, Richard L, Grompe, Markus, Lillegard, Joseph B, Hickey, Raymond D, Nyberg, Scott L

    Published in The American journal of pathology (01-01-2017)
    “…Hereditary tyrosinemia type 1 (HT1) is an autosomal recessive disease caused by deficiency in fumarylacetoacetate hydrolase, the last enzyme in the tyrosine…”
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