Canlyniadau Chwilio - Frants, R. R.

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

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M2 alpha-1-antitrypsin phenotype and primary liver cancer. gan 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 gan 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. gan 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. gan 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. gan 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 gan 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. gan 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. gan 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. gan 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... gan 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. gan 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. gan 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. gan 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. gan 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. gan 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. gan 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. gan 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 gan 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. gan 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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