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R W Hendriks

Showing results (1-10 of 61) with videos related to

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Developmental Immunology|January 12, 2002
Role of Bruton's tyrosine kinase in B cell developmentA Maas, R W Hendriks
Clinical Genetics|September 1, 1992
X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locusR W Hendriks, M E Kraakman, R K Schuurman
Immunodeficiency|January 1, 1993
Patterns of X chromosome inactivation in haematopoietic cells of female carriers of X linked severe combined immunodeficiencyR W Hendriks, M E Kraakman, R K Schuurman
Journal of Immunology (Baltimore, Md. : 1950)|June 3, 1999
Early arrest in B cell development in transgenic mice that express the E41K Bruton's tyrosine kinase mutant under the control of the CD19 promoter regionA Maas, G M Dingjan, F Grosveld, et al.
European Journal of Immunology|January 1, 1995
Immunoglobulin heavy chain germ-line JH-C mu transcription in human precursor B lymphocytes initiates in a unique region upstream of DQ52A Thompson, E Timmers, R K Schuurman, et al.
Genomics|November 1, 1992
The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosomeR W Hendriks, H Hinds, Z Y Chen, et al.
Human Genetics|November 1, 1991
Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locusR W Hendriks, M E Kraakman, R G Mensink, et al.
Journal of Neurochemistry|June 1, 1989
Properties of a Leu-Phe-cleaving endopeptidase activity putatively involved in beta-endorphin metabolism in rat brainJ L Lebouille, R W Hendriks, N M Soeter, et al.
Genomics|July 1, 1992
Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motifH L Hinds, R W Hendriks, I W Craig, et al.
Clinical Genetics|July 1, 1995
Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia MM E Kraakman, M de Weers, T Español, et al.
Pageof 7

Showing results (1-10 of 61) with videos related to

Sort By:
Pageof 7
Developmental Immunology|January 12, 2002
Role of Bruton's tyrosine kinase in B cell developmentA Maas, R W Hendriks
Clinical Genetics|September 1, 1992
X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locusR W Hendriks, M E Kraakman, R K Schuurman
Immunodeficiency|January 1, 1993
Patterns of X chromosome inactivation in haematopoietic cells of female carriers of X linked severe combined immunodeficiencyR W Hendriks, M E Kraakman, R K Schuurman
Journal of Immunology (Baltimore, Md. : 1950)|June 3, 1999
Early arrest in B cell development in transgenic mice that express the E41K Bruton's tyrosine kinase mutant under the control of the CD19 promoter regionA Maas, G M Dingjan, F Grosveld, et al.
European Journal of Immunology|January 1, 1995
Immunoglobulin heavy chain germ-line JH-C mu transcription in human precursor B lymphocytes initiates in a unique region upstream of DQ52A Thompson, E Timmers, R K Schuurman, et al.
Genomics|November 1, 1992
The hypervariable DXS255 locus contains a LINE-1 repetitive element with a CpG island that is extensively methylated only on the active X chromosomeR W Hendriks, H Hinds, Z Y Chen, et al.
Human Genetics|November 1, 1991
Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locusR W Hendriks, M E Kraakman, R G Mensink, et al.
Journal of Neurochemistry|June 1, 1989
Properties of a Leu-Phe-cleaving endopeptidase activity putatively involved in beta-endorphin metabolism in rat brainJ L Lebouille, R W Hendriks, N M Soeter, et al.
Genomics|July 1, 1992
Characterization of a highly polymorphic region near the first exon of the human MAOA gene containing a GT dinucleotide and a novel VNTR motifH L Hinds, R W Hendriks, I W Craig, et al.
Clinical Genetics|July 1, 1995
Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia MM E Kraakman, M de Weers, T Español, et al.
Pageof 7