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J P Cheadle

Showing results (21-30 of 27) with videos related to

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Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
Oncogene|February 15, 2001
The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitinationG Benvenuto, S Li, S J Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 1997
Cloning and characterization of a functional human homolog of Escherichia coli endonuclease IIIR Aspinwall, D G Rothwell, T Roldan-Arjona, et al.
Nature Genetics|August 1, 1993
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseR G Snell, J C MacMillan, J P Cheadle, et al.
Human Molecular Genetics|April 18, 2000
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and locationJ P Cheadle, H Gill, N Fleming, et al.
Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
Science (New York, N.Y.)|August 8, 1997
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34M van Slegtenhorst, R de Hoogt, C Hermans, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Lancet (London, England)|October 16, 1993
Molecular analysis and clinical correlations of the Huntington's disease mutationJ C MacMillan, R G Snell, A Tyler, et al.
Oncogene|February 15, 2001
The tuberous sclerosis-1 (TSC1) gene product hamartin suppresses cell growth and augments the expression of the TSC2 product tuberin by inhibiting its ubiquitinationG Benvenuto, S Li, S J Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 1997
Cloning and characterization of a functional human homolog of Escherichia coli endonuclease IIIR Aspinwall, D G Rothwell, T Roldan-Arjona, et al.
Nature Genetics|August 1, 1993
Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's diseaseR G Snell, J C MacMillan, J P Cheadle, et al.
Human Molecular Genetics|April 18, 2000
Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and locationJ P Cheadle, H Gill, N Fleming, et al.
Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
Science (New York, N.Y.)|August 8, 1997
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34M van Slegtenhorst, R de Hoogt, C Hermans, et al.
Pageof 3