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Results: 26-38/38
Authors:
Sijbrands, EJ
Hoffer, MJV
Meinders, AE
Havekes, LM
Frants, RR
Smelt, AHM
De Knijff, P
Citation: Ej. Sijbrands et al., Severe hyperlipidemia in apolipoprotein E2 homozygotes due to a combined effect of hyperinsulinemia and an SstI polymorphism, ART THROM V, 19(11), 1999, pp. 2722-2729
Authors:
Stout, K
van der Maarel, S
Frants, RR
Padberg, GW
Ropers, HH
Haaf, T
Citation: K. Stout et al., Somatic pairing between subtelomeric chromosome regions: implications for human genetic disease?, CHROMOS RES, 7(5), 1999, pp. 323-329
Authors:
van Geel, M
Heather, LJ
Lyle, R
Hewitt, JE
Frants, RR
de Jong, PJ
Citation: M. Van Geel et al., The FSHD region on human chromosome 4q35 contains potential coding regionsamong pseudogenes and a high density of repeat elements, GENOMICS, 61(1), 1999, pp. 55-65
Authors:
Grewal, PK
Jones, AM
Maconochie, M
Lemmers, RJF
Frants, RR
Hewitt, JE
Citation: Pk. Grewal et al., Cloning of the murine unconventional myosin gene Myo9b and identification of alternative splicing, GENE, 240(2), 1999, pp. 389-398
Authors:
Gabriels, J
Beckers, MC
Ding, H
De Vriese, A
Plaisance, S
van der Maarel, SM
Padberg, GW
Frants, RR
Hewitt, JE
Collen, D
Belayew, A
Citation: J. Gabriels et al., Nucleotide sequence of the partially deleted D4Z4 locus in a patient with FSHD identifies a putative gene within each 3.3 kb element, GENE, 236(1), 1999, pp. 25-32
Authors:
Grewal, PK
van Geel, M
Frants, RR
de Jong, P
Hewitt, JE
Citation: Pk. Grewal et al., Recent amplification of the human FRG1 gene during primate evolution, GENE, 227(1), 1999, pp. 79-88
Authors:
Vergouwe, MN
Tijssen, MAJ
Peters, ACB
Wielaard, R
Frants, RR
Citation: Mn. Vergouwe et al., Hyperekplexia phenotype due to compound heterozygosity for GLRA1 gene mutations, ANN NEUROL, 46(4), 1999, pp. 634-638
Authors:
Frants, RR
Citation: Rr. Frants, The use of isolates in migraine genetic research, CEPHALALGIA, 19, 1999, pp. 19-24
Authors:
Haan, J
Terwindt, GM
Maassen, JA
't Hart, LM
Frants, RR
Ferrari, MD
Citation: J. Haan et al., Search for mitochondrial DNA mutations in migraine subgroups, CEPHALALGIA, 19(1), 1999, pp. 20-22
Authors:
Oberstein, SAJL
Ferrari, MD
Bakker, E
van Gestel, J
Kneppers, ALJ
Frants, RR
Breuning, MH
Haan, J
Citation: Sajl. Oberstein et al., Diagnostic Notch3 sequence analysis in CADASIL: Three new mutations in Dutch patients, NEUROLOGY, 52(9), 1999, pp. 1913-1915
Authors:
van der Maarel, SM
Deidda, G
Lemmers, RJLF
Bakker, E
van der Wielen, MJR
Sandkuijl, L
Hewitt, JE
Padberg, GW
Frants, RR
Citation: Sm. Van Der Maarel et al., A new dosage test for subtelomeric 4;10 translocations improves conventional diagnosis of facioscapulohumeral muscular dystrophy (FSHD), J MED GENET, 36(11), 1999, pp. 823-828
Authors:
de Winther, MPJ
van Dijk, KW
van Vlijmen, BJM
Gijbels, MJJ
Heus, JJ
Wijers, ER
van den Bos, AC
Breuer, M
Frants, RR
Havekes, LM
Hofker, MH
Citation: Mpj. De Winther et al., Macrophage specific overexpression of the human macrophage scavenger receptor in transgenic mice, using a 180-kb yeast artificial chromosome, leads to enhanced foam cell formation of isolated peritoneal macrophages, ATHEROSCLER, 147(2), 1999, pp. 339-347
Authors:
de Winther, MPJ
Gijbels, MJJ
van Dijk, KW
van Gorp, PJJ
Suzuki, H
Kodama, T
Frants, RR
Havekes, LM
Hofker, MH
Citation: Mpj. De Winther et al., Scavenger receptor deficiency leads to more complex atherosclerotic lesions in APOE3Leiden transgenic mice, ATHEROSCLER, 144(2), 1999, pp. 315-321