Author Search Results

1

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

Published 1984

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2

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

Published 1981

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3

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

Published 1990

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4

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

Published 1984

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

Published 1993

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6

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

Published 1993

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7

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

Published 1990

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8

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

Published 1988

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9

$Reduced very-low-density lipoprotein fractional catabolic rate in apolipoprotein C1-deficient mice.$

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

Published 1997

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10

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

Published 1996

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11

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... by Koivisto, U M, Turtola, H, Aalto-Setälä, K, Top, B, Frants, R R, Kovanen, P T, Syvänen, A C, Kontula, K

Published 1992

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12

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

Published 1988

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13

Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree. by 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

Published 1991

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14

Increased response to cholesterol feeding in apolipoprotein C1-deficient mice. by 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

Published 1995

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15

Diet-induced hyperlipoproteinemia and atherosclerosis in apolipoprotein E3-Leiden transgenic mice. by 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

Published 1994

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16

Modulation of very low density lipoprotein production and clearance contributes to age- and gender- dependent hyperlipoproteinemia in apolipoprotein E3-Leiden transgenic mice. by 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

Published 1996

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17

Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers. by 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

Published 1994

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18

Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. by 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.

Published 1996

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19

Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development by 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

Published 2003

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20

Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. by 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.

Published 1996

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Search Results - Frants, R. R.

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

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

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

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

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

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

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

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

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

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

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... by Koivisto, U M, Turtola, H, Aalto-Setälä, K, Top, B, Frants, R R, Kovanen, P T, Syvänen, A C, Kontula, K

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

Familial dysbetalipoproteinemia associated with apolipoprotein E3-Leiden in an extended multigeneration pedigree. by 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

Increased response to cholesterol feeding in apolipoprotein C1-deficient mice. by 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

Diet-induced hyperlipoproteinemia and atherosclerosis in apolipoprotein E3-Leiden transgenic mice. by 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

Modulation of very low density lipoprotein production and clearance contributes to age- and gender- dependent hyperlipoproteinemia in apolipoprotein E3-Leiden transgenic mice. by 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

Variable expression of familial dysbetalipoproteinemia in apolipoprotein E*2 (Lys146-->Gln) Allele carriers. by 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

Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. by 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.

Gene expression profiling identifies tumour markers potentially playing a role in uveal melanoma development by 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

Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. by 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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