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J P Cheadle

Showing results (11-20 of 27) with videos related to

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Clinical Chemistry|August 3, 1999
Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysisA C Jones, J Austin, N Hansen, et al.
Human Genetics|December 29, 2000
Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumoursL Parry, J H Maynard, A Patel, et al.
Human Molecular Genetics|December 14, 2001
Pathological mutations in TSC1 and TSC2 disrupt the interaction between hamartin and tuberinA K Hodges, S Li, J Maynard, et al.
Human Molecular Genetics|September 25, 1997
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosisM M Maheshwar, J P Cheadle, A C Jones, et al.
British Journal of Cancer|November 17, 2001
Analysis of the TSC1 and TSC2 genes in sporadic renal cell carcinomasL Parry, J H Maynard, A Patel, et al.
American Journal of Human Genetics|April 17, 1999
Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosisA C Jones, M M Shyamsundar, M W Thomas, et al.
Human Molecular Genetics|November 5, 1997
Molecular genetic and phenotypic analysis reveals differences between TSC1 and TSC2 associated familial and sporadic tuberous sclerosisA C Jones, C E Daniells, R G Snell, et al.
Journal of Medical Genetics|December 1, 1992
Severity of chest disease in cystic fibrosis patients in relation to their genotypesL N al-Jader, A L Meredith, H C Ryley, et al.
American Journal of Human Genetics|October 23, 1997
Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 geneJ R Sampson, M M Maheshwar, R Aspinwall, et al.
Human Mutation|January 1, 1995
Cystic fibrosis mutation analysis: report from 22 U.K. regional genetics laboratoriesM J Schwarz, G M Malone, A Haworth, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Clinical Chemistry|August 3, 1999
Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysisA C Jones, J Austin, N Hansen, et al.
Human Genetics|December 29, 2000
Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumoursL Parry, J H Maynard, A Patel, et al.
Human Molecular Genetics|December 14, 2001
Pathological mutations in TSC1 and TSC2 disrupt the interaction between hamartin and tuberinA K Hodges, S Li, J Maynard, et al.
Human Molecular Genetics|September 25, 1997
The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosisM M Maheshwar, J P Cheadle, A C Jones, et al.
British Journal of Cancer|November 17, 2001
Analysis of the TSC1 and TSC2 genes in sporadic renal cell carcinomasL Parry, J H Maynard, A Patel, et al.
American Journal of Human Genetics|April 17, 1999
Comprehensive mutation analysis of TSC1 and TSC2-and phenotypic correlations in 150 families with tuberous sclerosisA C Jones, M M Shyamsundar, M W Thomas, et al.
Human Molecular Genetics|November 5, 1997
Molecular genetic and phenotypic analysis reveals differences between TSC1 and TSC2 associated familial and sporadic tuberous sclerosisA C Jones, C E Daniells, R G Snell, et al.
Journal of Medical Genetics|December 1, 1992
Severity of chest disease in cystic fibrosis patients in relation to their genotypesL N al-Jader, A L Meredith, H C Ryley, et al.
American Journal of Human Genetics|October 23, 1997
Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 geneJ R Sampson, M M Maheshwar, R Aspinwall, et al.
Human Mutation|January 1, 1995
Cystic fibrosis mutation analysis: report from 22 U.K. regional genetics laboratoriesM J Schwarz, G M Malone, A Haworth, et al.
Pageof 3