Resultados de procura - Frants, R. R.

Distribution of genetic variants of transcobalamin II in Nigerian black populations. por Porck, H J, Fleming, A F, Frants, R R

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M2 alpha-1-antitrypsin phenotype and primary liver cancer. por Sizaret, P., Clerc, M., Estève, J., Frants, R. R., Pillot, J.

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The human gene for plasminogen activator inhibitor 2 (PAI2) exhibits an EcoRI RFLP por Van Den Berg, E.A., Le Clercq, E., Kooistra, T., Frants, R.R., Bakker, E.

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Pepsinogen synthesis and secretion in isolated gastric glands. por Défize, J, Pals, G, Frants, R R, Westerveld, B D, Meuwissen, S G, Erkisson, A W

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Low-density lipoproteins are degraded in HepG2 cells with low efficiency. por Lombardi, P, Mulder, M, de Wit, E, van Berkel, T J, Frants, R R, Havekes, L M

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PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue. por Gruis, N. A., Abeln, E. C., Bardoel, A. F., Devilee, P., Frants, R. R., Cornelisse, C. J.

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An additional MspI RFLP at the human hepatic lipase (HL) gene locus por Van Eyk, R., Chan, L., Top, B., Stalenhoef, A.F.H., Havekes, L.M., Frants, R.R.

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Linkage relationships and gene order around the locus for X-linked retinoschisis. por Alitalo, T, Forsius, H, Kärnä, J, Frants, R R, Eriksson, A W, Wood, S, Kruse, T A, de la Chapelle, A

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Reduced very-low-density lipoprotein fractional catabolic rate in apolipoprotein C1-deficient mice. por Jong, M C, van Ree, J H, Dahlmans, V E, Frants, R R, Hofker, M H, Havekes, L M

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Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases. por Bakker, E, Van der Wielen, M J, Voorhoeve, E, Ippel, P F, Padberg, G W, Frants, R R, Wijmenga, C

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The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finlan... por Koivisto, U M, Turtola, H, Aalto-Setälä, K, Top, B, Frants, R R, Kovanen, P T, Syvänen, A C, Kontula, K

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Human pancreatic amylase is encoded by two different genes. por Groot, P C, Bleeker, M J, Pronk, J C, Arwert, F, Mager, W H, Planta, R J, Eriksson, A W, Frants, R R

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Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree. por de Knijff, P, van den Maagdenberg, A M, Stalenhoef, A F, Leuven, J A, Demacker, P N, Kuyt, L P, Frants, R R, Havekes, L M

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Increased response to cholesterol feeding in apolipoprotein C1-deficient mice. por van Ree, J H, Hofker, M H, van den Broek, W J, van Deursen, J M, van der Boom, H, Frants, R R, Wieringa, B, Havekes, L M

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Diet-induced hyperlipoproteinemia and atherosclerosis in apolipoprotein E3-Leiden transgenic mice. por van Vlijmen, B J, van den Maagdenberg, A M, Gijbels, M J, van der Boom, H, HogenEsch, H, Frants, R R, Hofker, M H, Havekes, L M

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Modulation of very low density lipoprotein production and clearance contributes to age- and gender- dependent hyperlipoproteinemia in apolipoprotein E3-Leiden transgenic mice. por van Vlijmen, B J, van 't Hof, H B, Mol, M J, van der Boom, H, van der Zee, A, Frants, R R, Hofker, M H, Havekes, L M

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Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers. por de Knijff, P, van den Maagdenberg, A M, Boomsma, D I, Stalenhoef, A F, Smelt, A H, Kastelein, J J, Marais, A D, Frants, R R, Havekes, L M

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Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. por Datson, N. A., Semina, E., van Staalduinen, A. A., Dauwerse, H. G., Meershoek, E. J., Heus, J. J., Frants, R. R., den Dunnen, J. T., Murray, J. C., van Ommen, G. J.

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Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development por Zuidervaart, W, van der Velden, P A, Hurks, M H, van Nieuwpoort, F A, Out-Luiting, C J J, Singh, A D, Frants, R R, Jager, M J, Gruis, N A

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Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. por Semina, E. V., Datson, N. A., Leysens, N. J., Zabel, B. U., Carey, J. C., Bell, G. I., Bitoun, P., Lindgren, C., Stevenson, T., Frants, R. R., van Ommen, G., Murray, J. C.

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