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V van Heyningen

Showing results (81-90 of 148) with videos related to

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Human Molecular Genetics|October 9, 2001
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6D A Kleinjan, A Seawright, A Schedl, et al.
Psychiatric Genetics|July 21, 1999
Psychiatric disorder and cognitive function in a family with an inherited novel mutation of the developmental control gene PAX6I Heyman, I Frampton, V van Heyningen, et al.
Clinical Chemistry|August 1, 1987
Development and utility of a monoclonal-antibody-based, highly sensitive immunoradiometric assay of thyrotropinV van Heyningen, S R Abbott, S G Daniel, et al.
Molecular and Cellular Probes|August 1, 1997
Combined SSCP/heteroduplex analysis in the screening for PAX6 mutationsR A Axton, I M Hanson, J Love, et al.
Birth Defects Original Article Series|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
Human Molecular Genetics|July 1, 1993
PAX6 mutations in aniridiaI M Hanson, A Seawright, K Hardman, et al.
Cell|July 12, 1996
Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalitiesA Schedl, A Ross, M Lee, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
Annals of Human Genetics|January 1, 1975
Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13V van Heyningen, M Bobrow, W F Bodmer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1992
Zinc finger point mutations within the WT1 gene in Wilms tumor patientsM H Little, J Prosser, A Condie, et al.
Pageof 15

Showing results (81-90 of 148) with videos related to

Sort By:
Pageof 15
Human Molecular Genetics|October 9, 2001
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6D A Kleinjan, A Seawright, A Schedl, et al.
Psychiatric Genetics|July 21, 1999
Psychiatric disorder and cognitive function in a family with an inherited novel mutation of the developmental control gene PAX6I Heyman, I Frampton, V van Heyningen, et al.
Clinical Chemistry|August 1, 1987
Development and utility of a monoclonal-antibody-based, highly sensitive immunoradiometric assay of thyrotropinV van Heyningen, S R Abbott, S G Daniel, et al.
Molecular and Cellular Probes|August 1, 1997
Combined SSCP/heteroduplex analysis in the screening for PAX6 mutationsR A Axton, I M Hanson, J Love, et al.
Birth Defects Original Article Series|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
Human Molecular Genetics|July 1, 1993
PAX6 mutations in aniridiaI M Hanson, A Seawright, K Hardman, et al.
Cell|July 12, 1996
Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalitiesA Schedl, A Ross, M Lee, et al.
Cytogenetics and Cell Genetics|January 1, 1975
Assignment of the genes for human mitochondrial malate dehydrogenase to chromosome 7, for mannose phosphate isomerase and pyruvate kinase to chromosome 15, and, probably, for human esterase-D to chromosome 13 using man-mouse hybridsV van Heyningen, M Bobrow, W F Bodmer, et al.
Annals of Human Genetics|January 1, 1975
Chromosome assignment of some human enzyme loci: mitochondrial malate dehydrogenase to 7, mannosephosphate isomerase and pyruvate kinase to 15 and probably, esterase D to 13V van Heyningen, M Bobrow, W F Bodmer, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1992
Zinc finger point mutations within the WT1 gene in Wilms tumor patientsM H Little, J Prosser, A Condie, et al.
Pageof 15