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

Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.

Por Tupler, R, Berardinelli, A, Barbierato, L, Frants, R, Hewitt, J E, Lanzi, G, Maraschio, P, Tiepolo, L
Publicado em 1996

Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype

Por Tonini, M, Pavanello, R, Gurgel-Giannetti, J, Lemmers, R, van der Maarel, S M, Frants, R, Zatz, M
Publicado em 2004

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

FRG1P is localised in the nucleolus, Cajal bodies, and speckles

Por van Koningsbrugge..., S, Dirks, R, Mommaas, A, Onderwater, J, Deidda, G, Padberg, G, Frants, R, van der Maarel, S M
Publicado em 2004

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

High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families.

Por Zatz, M, Marie, S K, Passos-Bueno, M R, Vainzof, M, Campiotto, S, Cerqueira, A, Wijmenga, C, Padberg, G, Frants, R
Publicado em 1995

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

A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD)

Por van der Maarel, S. M, Deidda, G., Lemmers, R., Bakker, E., van der Wielen, M. J R, Sandkuijl, L., Hewitt, J., Padberg, G., Frants, R.
Publicado em 1999

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

FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients

Por Rijkers, T, Deidda, G, van Koningsbrugge..., S, van Geel, M, Lemmers, R, van Deutekom, J C T, Figlewicz, D, Hewitt, J, Padberg, G, Frants, R, van der Maarel, S M
Publicado em 2004

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