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Cisca Wijmenga

Veröffentlichungen von Cisca Wijmenga zu Wijmenga, Cisca ->
weitere Veröffentlichungen von Cisca Wijmenga:
The gene product Murr1 restricts HIV-1 replication in resting CD4+ lymphocytes (2003)
The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus (1993)
Refined genetic and comparative physical mapping of the canine copper toxicosis locus (2000)
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy (1992)
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect (2005)
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC (2006)
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 (2007)
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes (2007)
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes (2007)
Veröffentlichungen zu Wijmenga, Cisca
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1
Ganesh, Lakshmanan, Burstein, Ezra, ... The gene product Murr1 restricts HIV-1 replication in resting CD4<sup>+</sup> lymphocytes
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 426, No. 6968 (2003), p. 853-857
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2003
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2
Wijmenga, Cisca, Winokur, SaraT., ... The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus
in: Human genetics , ISSN 1432-1203, Vol. 92 (2. 1993), p. 198-203
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1993
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3
van de Sluis, Bart, Kole, Susan, ... Refined genetic and comparative physical mapping of the canine copper toxicosis locus
in: Mammalian genome , ISSN 1432-1777, Vol. 11 (6. 2000), p. 455-460
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2000
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4
Wijmenga, Cisca, Hewitt, Jane E., ... Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 2, No. 1 (1992), p. 26-30
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1992
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5
Monsuur, Alienke J, Bakker, Paul I W de, ... Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 37, No. 12 (2005), p. 1341-1344
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2005
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6
de Bakker, Paul I W, McVean, Gil, ... A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 38, No. 10 (2006), p. 1166-1172
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2006
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7
van Heel, David A, Franke, Lude, ... A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 7 (2007), p. 827-829
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2007
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8
Steinthorsdottir, Valgerdur, Thorleifsson, Gudmar, ... A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 6 (2007), p. 770-775
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2007
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9
Gudmundsson, Julius, Sulem, Patrick, ... Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 39, No. 8 (2007), p. 977-983
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2007