檢索結果 - Frants, R. R.

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

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