M R Hayden|M M Nelson - JoVE Visualize

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The Journal of Clinical Investigation|May 1, 1993

Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172-->Cys mutation in the lipoprotein lipase geneY Ma, M S Liu, D Ginzinger, et al.

American Journal of Human Genetics|May 1, 1987

DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasM R Hayden, H Kirk, C Clark, et al.

Neurology|September 1, 1987

The combined use of positron emission tomography and DNA polymorphisms for preclinical detection of Huntington's diseaseM R Hayden, J Hewitt, A J Stoessl, et al.

American Journal of Human Genetics|February 1, 1992

Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.

Clinical Genetics|May 20, 1999

Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standardO Bruland, E W Almqvist, Y P Goldberg, et al.

American Journal of Human Genetics|August 1, 1995

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomesB Kremer, E Almqvist, J Theilmann, et al.

Journal of Neurochemistry|April 27, 1999

Subtype-specific enhancement of NMDA receptor currents by mutant huntingtinN Chen, T Luo, C Wellington, et al.

Current Opinion in Lipidology|April 29, 2000

Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiencyM R Hayden, S M Clee, A Brooks-Wilson, et al.

The Journal of Biological Chemistry|February 28, 1997

Segments in the C-terminal folding domain of lipoprotein lipase important for binding to the low density lipoprotein receptor-related protein and to heparan sulfate proteoglycansM S Nielsen, J Brejning, R García, et al.

Human Genetics|March 1, 1994

Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.

Pageof 34

Showing results (121-130 of 333) with videos related to

Sort By:

Pageof 34

The Journal of Clinical Investigation|May 1, 1993

Gene-environment interaction in the conversion of a mild-to-severe phenotype in a patient homozygous for a Ser172-->Cys mutation in the lipoprotein lipase geneY Ma, M S Liu, D Ginzinger, et al.

American Journal of Human Genetics|May 1, 1987

DNA polymorphisms in and around the Apo-A1-CIII genes and genetic hyperlipidemiasM R Hayden, H Kirk, C Clark, et al.

Neurology|September 1, 1987

The combined use of positron emission tomography and DNA polymorphisms for preclinical detection of Huntington's diseaseM R Hayden, J Hewitt, A J Stoessl, et al.

American Journal of Human Genetics|February 1, 1992

Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease regionB Weber, A Hedrick, S Andrew, et al.

Clinical Genetics|May 20, 1999

Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standardO Bruland, E W Almqvist, Y P Goldberg, et al.

American Journal of Human Genetics|August 1, 1995

Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomesB Kremer, E Almqvist, J Theilmann, et al.

Journal of Neurochemistry|April 27, 1999

Subtype-specific enhancement of NMDA receptor currents by mutant huntingtinN Chen, T Luo, C Wellington, et al.

Current Opinion in Lipidology|April 29, 2000

Cholesterol efflux regulatory protein, Tangier disease and familial high-density lipoprotein deficiencyM R Hayden, S M Clee, A Brooks-Wilson, et al.

The Journal of Biological Chemistry|February 28, 1997

Segments in the C-terminal folding domain of lipoprotein lipase important for binding to the low density lipoprotein receptor-related protein and to heparan sulfate proteoglycansM S Nielsen, J Brejning, R García, et al.

Human Genetics|March 1, 1994

Homozygosity for a mutation in the lipoprotein lipase gene (Gly139-->Ser) causes chylomicronaemia in a boy of Spanish descentS M Bijvoet, T Bruin, S Tuzgöl, et al.

Pageof 34