Search Results - "CRANE, Ana"

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    Caspase activity mediates the differentiation of embryonic stem cells by Fujita, Jun, Crane, Ana M, Souza, Marlon K, Dejosez, Marion, Kyba, Michael, Flavell, Richard A, Thomson, James A, Zwaka, Thomas P

    Published in Cell stem cell (05-06-2008)
    “…Embryonic stem cells (ESCs) are capable of indefinite self-renewal while retaining the ability to differentiate to any of the three germ layers that give rise…”
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    Journal Article
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    Assembly, Maturation, and Turnover of KATP Channel Subunits by Crane, Ana, Aguilar-Bryan, Lydia

    Published in The Journal of biological chemistry (05-03-2004)
    “…ATP-sensitive K+, or KATP, channels are comprised of KIR6.x and sulfonylurea receptor (SUR) subunits that assemble as octamers, (KIR/SUR)4. The assembly…”
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    Journal Article
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    Homology Requirements for Efficient, Footprintless Gene Editing at the CFTR Locus in Human iPSCs with Helper-dependent Adenoviral Vectors by Palmer, Donna J, Grove, Nathan C, Ing, Jordan, Crane, Ana M, Venken, Koen, Davis, Brian R, Ng, Philip

    Published in Molecular therapy. Nucleic acids (2016)
    “…Helper-dependent adenoviral vectors mediate high efficiency gene editing in induced pluripotent stem cells without needing a designer nuclease thereby avoiding…”
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    Journal Article
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    Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor by THORNTON, Paul S, MACMULLEN, Courtney, GANGULY, Arupa, RUCHELLI, Eduardo, STEINKRAUSS, Linda, CRANE, Ana, AGUILAR-BRYAN, Lydia, STANLEY, Charles A

    Published in Diabetes (New York, N.Y.) (01-09-2003)
    “…Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor Paul…”
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    Journal Article
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    cAMP-Activated Protein Kinase-Independent Potentiation of Insulin Secretion by cAMP Is Impaired in SUR1 Null Islets by NAKAZAKI, Mitsuhiro, CRANE, Ana, MIN HU, SEGHERS, Victor, ULLRICH, Susanne, AGUILAR-BRYAN, Lydia, BRYAN, Joseph

    Published in Diabetes (New York, N.Y.) (01-12-2002)
    “…cAMP-Activated Protein Kinase-Independent Potentiation of Insulin Secretion by cAMP Is Impaired in SUR1 Null Islets Mitsuhiro Nakazaki 1 , Ana Crane 2 , Min Hu…”
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    Journal Article
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    The C Terminus of SUR1 Is Required for Trafficking of KATP Channels by Sharma, N, Crane, A, Clement, 4th, J P, Gonzalez, G, Babenko, A P, Bryan, J, Aguilar-Bryan, L

    Published in The Journal of biological chemistry (16-07-1999)
    “…In beta cells from the pancreas, ATP-sensitive potassium channels, or K ATP channels, are composed of two subunits, SUR1 and K IR 6.2, assembled in a (SUR1/K…”
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    Journal Article
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    Assembly, maturation, and turnover of K(ATP) channel subunits by Crane, Ana, Aguilar-Bryan, Lydia

    Published in The Journal of biological chemistry (05-03-2004)
    “…ATP-sensitive K(+), or K(ATP), channels are comprised of K(IR)6.x and sulfonylurea receptor (SUR) subunits that assemble as octamers, (K(IR)/SUR)(4). The…”
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    Journal Article
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    Familial hyperinsulinism and pancreatic β-cell ATP-sensitive potassium channels by Sharma, Nidhi, Crane, Ana, Gonzalez, Gabriela, Bryan, Joseph, Aguilar-Bryan, Lydia

    Published in Kidney international (01-03-2000)
    “…Familial hyperinsulinism and pancreatic β-cell ATP-sensitive potassium channels. Familial hyperinsulinism, also known as persistent hyperinsulinemic…”
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    Journal Article Conference Proceeding
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    Effective Cryopreservation and Long-Term Storage of Primary Human Hepatocytes with Recovery of Viability, Differentiation, and Replicative Potential by R. Mark Adams, Mary Wang, Ana Maria Crane, Bridgette Brown, Gretchen J. Darlington, Fred D. Ledley

    Published in Cell transplantation (01-11-1995)
    “…Despite reports of successful cryopreservation of primary human hepatocytes, existing methods do not produce sufficient recovery of viable cells to meet the…”
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    Journal Article
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    Overexpression of human methylmalonyl CoA mutase in mice after in vivo gene transfer with asialoglycoprotein/polylysine/DNA complexes by Stankovics, J, Crane, A M, Andrews, E, Wu, C H, Wu, G Y, Ledley, F D

    Published in Human gene therapy (01-09-1994)
    “…Methylmalonic acidemia resulting from genetic deficiency of methylmalonyl CoA mutase (MCM) is an often fatal metabolic disease. Somatic gene therapy for this…”
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    Journal Article