Search Results - Christensen, Inga B.

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  1. 1
    Cell‐based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations

    Cell‐based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations by Hatt, Lotte, Singh, Ripudaman, Christensen, Rikke, Ravn, Katarina, Christensen, Inga B, Jeppesen, Line Dahl, Nicolaisen, Bolette Hestbek, Kølvraa, Mathias, Schelde, Palle, Andreassen, Lotte, Farlie, Richard, Uldbjerg, Niels, Vogel, Ida

    Published in Clinical case reports
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  2. 2
    Polarization of membrane associated proteins in the choroid plexus epithelium from normal and slc4a10 knockout mice

    Polarization of membrane associated proteins in the choroid plexus epithelium from normal and slc4a10 knockout mice by Christensen, Inga B, Gyldenholm, Tua, Damkier, Helle H, Praetorius, Jeppe

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  3. 3
    The choroid plexus sodium‐bicarbonate cotransporter NBCe2 regulates mouse cerebrospinal fluid pH

    The choroid plexus sodium‐bicarbonate cotransporter NBCe2 regulates mouse cerebrospinal fluid pH by Christensen, Henriette L., Barbuskaite, Dagne, Rojek, Aleksandra, Malte, Hans, Christensen, Inga B., Füchtbauer, Annette C., Füchtbauer, Ernst‐Martin, Wang, Tobias, Praetorius, Jeppe, Damkier, Helle H.

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  4. 4
    The murine choroid plexus epithelium expresses the 2Cl - /H + exchanger ClC-7 and Na + /H + exchanger NHE6 in the luminal membrane domain

    The murine choroid plexus epithelium expresses the 2Cl - /H + exchanger ClC-7 and Na + /H + exchanger NHE6 in the luminal membrane domain by Damkier, Helle H, Christensen, Henriette L, Christensen, Inga B, Wu, Qi, Fenton, Robert A, Praetorius, Jeppe

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  5. 5
    Cell-based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations

    Cell-based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variations by Hatt, Lotte, Singh, Ripudaman, Christensen, Rikke, Ravn, Katarina, Christensen, Inga B, Jeppesen, Line Dahl, Nicolaisen, Bolette Hestbek, Kølvraa, Mathias, Schelde, Palle, Andreassen, Lotte, Farlie, Richard, Uldbjerg, Niels, Vogel, Ida

    Published in Clinical case reports
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  6. 6
    Ancistrocladinium A and B, the First N,C-Coupled Naphthyldihydroisoquinoline Alkaloids, from a Congolese Ancistrocladus Species

    Ancistrocladinium A and B, the First N,C-Coupled Naphthyldihydroisoquinoline Alkaloids, from a Congolese Ancistrocladus Species by Bringmann, Gerhard, Kajahn, Inga, Reichert, Matthias, Pedersen, Sarah E. H, Faber, Johan H, Gulder, Tanja, Brun, Reto, Christensen, Søren B, Ponte-Sucre, Alicia, Moll, Heidrun, Heubl, Günther, Mudogo, Virima

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  7. 7
    NT-proBNP and stem cell factor plasma concentrations are independently associated with cardiovascular outcomes in end-stage renal disease hemodialysis patients

    NT-proBNP and stem cell factor plasma concentrations are independently associated with cardiovascular outcomes in end-stage renal disease hemodialysis patients by Rossignol, P, Duarte, K, Bresso, E, A, Åsberg, Devignes, M D, Eriksson, N, Girerd, N, Glerup, R, Jardine, A G, Holdaas, H, Lamiral, Z, Leroy, C, Massy, Z, März, W, Krämer, B, Wu, P H, Schmieder, R, Soveri, I, Christensen, J H, Svensson, M, Zannad, F, Fellström, B

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  8. 8
    Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping

    Short/branched-chain acyl-CoA dehydrogenase deficiency due to an IVS3+3A>G mutation that causes exon skipping by MADSEN, Pia Pinholt, KIBAEK, Maria, WANDERS, Ronald J. A, RUITER, Jos P. N, GREGERSEN, Niels, ANDRESEN, Brage Storstein, ROCA, Xavier, SACHIDANANDAM, Ravi, KRAINER, Adrian R, CHRISTENSEN, Ernst, STEINER, Robert D, GIBSON, K. Michael, CORYDON, Thomas J, KNUDSEN, Inga

    Published in Human genetics
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  9. 9
    Isolated 2-Methylbutyrylglycinuria Caused by Short/Branched-Chain Acyl-CoA Dehydrogenase Deficiency: Identification of a New Enzyme Defect, Resolution of Its Molecular Basis, and Evidence for Distinct Acyl-CoA Dehydrogenases in Isoleucine And Valine Metabolism

    Isolated 2-Methylbutyrylglycinuria Caused by Short/Branched-Chain Acyl-CoA Dehydrogenase Deficiency: Identification of a New Enzyme Defect, Resolution of Its Molecular Basis, and E... by Andresen, Brage Storstein, Christensen, Ernst, Corydon, Thomas J., Bross, Peter, Pilgaard, Bente, Wanders, Ronald J.A., Ruiter, Jos P.N., Simonsen, Henrik, Winter, Vibeke, Knudsen, Inga, Schroeder, Lisbeth Dahl, Gregersen, Niels, Skovby, Flemming

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  10. 10
    DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiency

    DNA-based prenatal diagnosis for severe and variant forms of multiple acyl-CoA dehydrogenation deficiency by Olsen, Rikke K. J., Andresen, Brage S., Christensen, Ernst, Mandel, Hanna, Skovby, Flemming, Nielsen, Jens Peter, Knudsen, Inga, Vianey-Saban, Christine, Simonsen, Henrik, Gregersen, Niels

    Published in Prenatal diagnosis
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