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P Marynen

Showing results (121-130 of 185) with videos related to

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Kidney International|December 1, 1993
Differential splicing of COL4A5 mRNA in kidney and white blood cells: a complex mutation in the COL4A5 gene of an Alport patient deletes the NC1 domainC Guo, B Van Damme, R Van Damme-Lombaerts, et al.
Cancer Research|June 1, 1996
Biallelic alterations of both ETV6 and CDKN1B genes in a t(12;21) childhood acute lymphoblastic leukemia caseI Wlodarska, M Baens, P Peeters, et al.
Development (Cambridge, England)|November 1, 1993
Spatial and temporal changes in the expression of fibroglycan (syndecan-2) during mouse embryonic developmentG David, X M Bai, B Van der Schueren, et al.
Journal of Medical Genetics|November 1, 1990
A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephewH Cuppens, P Marynen, C De Boeck, et al.
Acta Endocrinologica|April 1, 1993
Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescentsK Devriendt, G Massa, F de Zegher, et al.
American Journal of Medical Genetics|July 12, 1996
Linkage analysis in three families with nonspecific X-linked mental retardationS Claes, X X Gu, E Legius, et al.
Current Biology : CB|September 22, 2001
NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardationL Jun, S Frints, H Duhamel, et al.
Cell Biology International Reports|May 1, 1982
Human osteosarcoma derived clonal variants: stable differences in cell surface compositionD De Martelaere, J J Cassiman, F Van Leuven, et al.
Journal of Neuroimmunology|June 1, 1995
Importance of HLA-DRB1 and DQA1 genes and of the amino acid polymorphisms in the functional domain of DR beta 1 chain in multiple sclerosisM Z Ghabanbasani, X X Gu, M Spaepen, et al.
Clinical Genetics|May 1, 1995
Increased and decreased relative risk for non-insulin-dependent diabetes mellitus conferred by HLA class II and by CD4 allelesM Z Ghabanbasani, M Spaepen, I Buyse, et al.
Pageof 19

Showing results (121-130 of 185) with videos related to

Sort By:
Pageof 19
Kidney International|December 1, 1993
Differential splicing of COL4A5 mRNA in kidney and white blood cells: a complex mutation in the COL4A5 gene of an Alport patient deletes the NC1 domainC Guo, B Van Damme, R Van Damme-Lombaerts, et al.
Cancer Research|June 1, 1996
Biallelic alterations of both ETV6 and CDKN1B genes in a t(12;21) childhood acute lymphoblastic leukemia caseI Wlodarska, M Baens, P Peeters, et al.
Development (Cambridge, England)|November 1, 1993
Spatial and temporal changes in the expression of fibroglycan (syndecan-2) during mouse embryonic developmentG David, X M Bai, B Van der Schueren, et al.
Journal of Medical Genetics|November 1, 1990
A child, homozygous for a stop codon in exon 11, shows milder cystic fibrosis symptoms than her heterozygous nephewH Cuppens, P Marynen, C De Boeck, et al.
Acta Endocrinologica|April 1, 1993
Opposite effects of growth hormone and estrogens on the pregnancy zone protein serum levels in children and adolescentsK Devriendt, G Massa, F de Zegher, et al.
American Journal of Medical Genetics|July 12, 1996
Linkage analysis in three families with nonspecific X-linked mental retardationS Claes, X X Gu, E Legius, et al.
Current Biology : CB|September 22, 2001
NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardationL Jun, S Frints, H Duhamel, et al.
Cell Biology International Reports|May 1, 1982
Human osteosarcoma derived clonal variants: stable differences in cell surface compositionD De Martelaere, J J Cassiman, F Van Leuven, et al.
Journal of Neuroimmunology|June 1, 1995
Importance of HLA-DRB1 and DQA1 genes and of the amino acid polymorphisms in the functional domain of DR beta 1 chain in multiple sclerosisM Z Ghabanbasani, X X Gu, M Spaepen, et al.
Clinical Genetics|May 1, 1995
Increased and decreased relative risk for non-insulin-dependent diabetes mellitus conferred by HLA class II and by CD4 allelesM Z Ghabanbasani, M Spaepen, I Buyse, et al.
Pageof 19