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Showing results (81-90 of 138) with videos related to

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Human Genetics|June 1, 1987
The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1pM H Brown, P A Gorman, W A Sewell, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Ordering of probes surrounding the Ewing's sarcoma breakpoint on chromosome 22 using fluorescent in situ hybridization to interphase nucleiJ M Shipley, T A Jones, K Patel, et al.
Genomics|July 1, 1991
Isolation of probes specific to human chromosomal region 6p21 from immunoselected irradiation-fusion gene transfer hybridsJ Ragoussis, T A Jones, D Sheer, et al.
Nucleic Acids Research|August 25, 1991
A novel and rapid method for isolating sequences adjacent to rare cutting sites and their use in physical mappingK Patel, R Cox, J Shipley, et al.
Somatic Cell and Molecular Genetics|September 1, 1985
Transformation associated p53 protein is encoded by a gene on human chromosome 17S Benchimol, P Lamb, L V Crawford, et al.
The EMBO Journal|July 1, 1987
The human homologue of the mouse t-complex gene, TCP1, is located on chromosome 6 but is not near the HLA regionK Willison, A Kelly, K Dudley, et al.
British Journal of Cancer|December 1, 1989
Characterisation of human thyroid epithelial cells immortalised in vitro by simian virus 40 DNA transfectionN R Lemoine, E S Mayall, T Jones, et al.
The Journal of Cell Biology|August 29, 1998
The human polycomb group complex associates with pericentromeric heterochromatin to form a novel nuclear domainA J Saurin, C Shiels, J Williamson, et al.
Journal of Medical Genetics|March 1, 1997
Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193R H Flomen, P A Gorman, R Vatcheva, et al.
Genomics|February 1, 1989
Multiple tandem 18-kb sequences clustered in the region of the acute promyelocytic leukemia breakpoint on chromosome 17G Moore, P J Hedge, S H Rider, et al.
Pageof 14

Showing results (81-90 of 138) with videos related to

Sort By:
Pageof 14
Human Genetics|June 1, 1987
The gene coding for the human T-lymphocyte CD2 antigen is located on chromosome 1pM H Brown, P A Gorman, W A Sewell, et al.
Cytogenetics and Cell Genetics|January 1, 1993
Ordering of probes surrounding the Ewing's sarcoma breakpoint on chromosome 22 using fluorescent in situ hybridization to interphase nucleiJ M Shipley, T A Jones, K Patel, et al.
Genomics|July 1, 1991
Isolation of probes specific to human chromosomal region 6p21 from immunoselected irradiation-fusion gene transfer hybridsJ Ragoussis, T A Jones, D Sheer, et al.
Nucleic Acids Research|August 25, 1991
A novel and rapid method for isolating sequences adjacent to rare cutting sites and their use in physical mappingK Patel, R Cox, J Shipley, et al.
Somatic Cell and Molecular Genetics|September 1, 1985
Transformation associated p53 protein is encoded by a gene on human chromosome 17S Benchimol, P Lamb, L V Crawford, et al.
The EMBO Journal|July 1, 1987
The human homologue of the mouse t-complex gene, TCP1, is located on chromosome 6 but is not near the HLA regionK Willison, A Kelly, K Dudley, et al.
British Journal of Cancer|December 1, 1989
Characterisation of human thyroid epithelial cells immortalised in vitro by simian virus 40 DNA transfectionN R Lemoine, E S Mayall, T Jones, et al.
The Journal of Cell Biology|August 29, 1998
The human polycomb group complex associates with pericentromeric heterochromatin to form a novel nuclear domainA J Saurin, C Shiels, J Williamson, et al.
Journal of Medical Genetics|March 1, 1997
Rieger syndrome locus: a new reciprocal translocation t(4;12)(q25;q15) and a deletion del(4)(q25q27) both break between markers D4S2945 and D4S193R H Flomen, P A Gorman, R Vatcheva, et al.
Genomics|February 1, 1989
Multiple tandem 18-kb sequences clustered in the region of the acute promyelocytic leukemia breakpoint on chromosome 17G Moore, P J Hedge, S H Rider, et al.
Pageof 14