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J P Cheadle

Showing results (1-10 of 27) with videos related to

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Human Molecular Genetics|October 1, 1993
Direct sequencing of the complete CFTR gene: the molecular characterisation of 99.5% of CF chromosomes in WalesJ P Cheadle, M C Goodchild, A L Meredith
Biochemical Society Transactions|July 27, 2005
MutYH (MYH) and colorectal cancerJ R Sampson, S Jones, S Dolwani, et al.
Human Genetics|October 13, 2000
Molecular genetic advances in tuberous sclerosisJ P Cheadle, M P Reeve, J R Sampson, et al.
Journal of Biochemical and Biophysical Methods|February 17, 2001
LD-PCR coupled to long-read direct sequencing: an approach for mutation detection in genes with compact genomic structuresN Fleming, J Maynard, L Tzitzis, et al.
Human Genetics|August 15, 2000
Application and evaluation of denaturing HPLC for molecular genetic analysis in tuberous sclerosisA C Jones, J R Sampson, B Hoogendoorn, et al.
Age and Ageing|November 1, 1994
Late-onset Huntington's disease: a clinical and molecular studyC M James, G D Houlihan, R G Snell, et al.
British Journal of Cancer|April 15, 2004
Increased frequency of the k-ras G12C mutation in MYH polyposis colorectal adenomasS Jones, S Lambert, G T Williams, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1997
Identification of a leader exon and a core promoter for the rat tuberous sclerosis 2 (Tsc2) gene and structural comparison with the human homologT Kobayashi, S Urakami, J P Cheadle, et al.
Oncogene|August 25, 2001
Tuberous sclerosis causing mutants of the TSC2 gene product affect proliferation and p27 expressionT Soucek, M Rosner, A Miloloza, et al.
Human Molecular Genetics|January 1, 1996
Comparative analysis and genomic structure of the tuberous sclerosis 2 (TSC2) gene in human and pufferfishM M Maheshwar, R Sandford, M Nellist, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|October 1, 1993
Direct sequencing of the complete CFTR gene: the molecular characterisation of 99.5% of CF chromosomes in WalesJ P Cheadle, M C Goodchild, A L Meredith
Biochemical Society Transactions|July 27, 2005
MutYH (MYH) and colorectal cancerJ R Sampson, S Jones, S Dolwani, et al.
Human Genetics|October 13, 2000
Molecular genetic advances in tuberous sclerosisJ P Cheadle, M P Reeve, J R Sampson, et al.
Journal of Biochemical and Biophysical Methods|February 17, 2001
LD-PCR coupled to long-read direct sequencing: an approach for mutation detection in genes with compact genomic structuresN Fleming, J Maynard, L Tzitzis, et al.
Human Genetics|August 15, 2000
Application and evaluation of denaturing HPLC for molecular genetic analysis in tuberous sclerosisA C Jones, J R Sampson, B Hoogendoorn, et al.
Age and Ageing|November 1, 1994
Late-onset Huntington's disease: a clinical and molecular studyC M James, G D Houlihan, R G Snell, et al.
British Journal of Cancer|April 15, 2004
Increased frequency of the k-ras G12C mutation in MYH polyposis colorectal adenomasS Jones, S Lambert, G T Williams, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|August 1, 1997
Identification of a leader exon and a core promoter for the rat tuberous sclerosis 2 (Tsc2) gene and structural comparison with the human homologT Kobayashi, S Urakami, J P Cheadle, et al.
Oncogene|August 25, 2001
Tuberous sclerosis causing mutants of the TSC2 gene product affect proliferation and p27 expressionT Soucek, M Rosner, A Miloloza, et al.
Human Molecular Genetics|January 1, 1996
Comparative analysis and genomic structure of the tuberous sclerosis 2 (TSC2) gene in human and pufferfishM M Maheshwar, R Sandford, M Nellist, et al.
Pageof 3