Distribution of genetic variants of transcobalamin II in Nigerian black populations.

Por Porck, H J, Fleming, A F, Frants, R R
Publicado em 1984

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

Por Sizaret, P., Clerc, M., Estève, J., Frants, R. R., Pillot, J.
Publicado em 1981

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.
Publicado em 1990

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
Publicado em 1984

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
Publicado em 1993

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.
Publicado em 1990

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.
Publicado em 1993

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
Publicado em 1988

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
Publicado em 1997

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
Publicado em 1992

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
Publicado em 1996

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
Publicado em 1988

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
Publicado em 1991

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
Publicado em 1994

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
Publicado em 1996

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
Publicado em 1995

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
Publicado em 1994

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.
Publicado em 1996

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
Publicado em 2003

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.
Publicado em 1996