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J Gusella

Showing results (11-20 of 32) with videos related to

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Oncogene|September 19, 1996
The merlin tumor suppressor localizes preferentially in membrane rufflesC Gonzalez-Agosti, L Xu, D Pinney, et al.
Journal of Virology|October 1, 1982
DNA methylation affecting the expression of murine leukemia provirusesJ W Hoffmann, D Steffen, J Gusella, et al.
American Journal of Human Genetics|September 1, 1986
Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridizationR E Magenis, J Gusella, K Weliky, et al.
American Journal of Human Genetics|January 1, 1990
Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locusE Ikonen, J Palo, J Ott, et al.
Prenatal Diagnosis|September 1, 1995
Prenatal diagnostic testing for familial dysautonomia using linked genetic markersC Oddoux, E Reich, F Axelrod, et al.
American Journal of Human Genetics|December 18, 1997
Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosisL B Jacoby, D Jones, K Davis, et al.
Annals of Neurology|September 1, 1996
A point mutation associated with a severe phenotype of neurofibromatosis 2M MacCollin, N Braverman, D Viskochil, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 1999
Transglutaminase aggregates huntingtin into nonamyloidogenic polymers, and its enzymatic activity increases in Huntington's disease brain nucleiM V Karpuj, H Garren, H Slunt, et al.
The Journal of Biological Chemistry|January 27, 1998
NHE-RF, a regulatory cofactor for Na(+)-H+ exchange, is a common interactor for merlin and ERM (MERM) proteinsA Murthy, C Gonzalez-Agosti, E Cordero, et al.
Human Molecular Genetics|January 1, 1994
Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease geneH Hummerich, S Baxendale, R Mott, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Oncogene|September 19, 1996
The merlin tumor suppressor localizes preferentially in membrane rufflesC Gonzalez-Agosti, L Xu, D Pinney, et al.
Journal of Virology|October 1, 1982
DNA methylation affecting the expression of murine leukemia provirusesJ W Hoffmann, D Steffen, J Gusella, et al.
American Journal of Human Genetics|September 1, 1986
Huntington disease-linked restriction fragment length polymorphism localized within band p16.1 of chromosome 4 by in situ hybridizationR E Magenis, J Gusella, K Weliky, et al.
American Journal of Human Genetics|January 1, 1990
Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locusE Ikonen, J Palo, J Ott, et al.
Prenatal Diagnosis|September 1, 1995
Prenatal diagnostic testing for familial dysautonomia using linked genetic markersC Oddoux, E Reich, F Axelrod, et al.
American Journal of Human Genetics|December 18, 1997
Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosisL B Jacoby, D Jones, K Davis, et al.
Annals of Neurology|September 1, 1996
A point mutation associated with a severe phenotype of neurofibromatosis 2M MacCollin, N Braverman, D Viskochil, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 1999
Transglutaminase aggregates huntingtin into nonamyloidogenic polymers, and its enzymatic activity increases in Huntington's disease brain nucleiM V Karpuj, H Garren, H Slunt, et al.
The Journal of Biological Chemistry|January 27, 1998
NHE-RF, a regulatory cofactor for Na(+)-H+ exchange, is a common interactor for merlin and ERM (MERM) proteinsA Murthy, C Gonzalez-Agosti, E Cordero, et al.
Human Molecular Genetics|January 1, 1994
Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease geneH Hummerich, S Baxendale, R Mott, et al.
Pageof 4