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Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
August 1, 1994
Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia
E Gagné, J Genest, H Zhang, et al.
Brain Pathology (Zurich, Switzerland)
|
July 1, 1997
Toward understanding the molecular pathology of Huntington's disease
C L Wellington, R R Brinkman, J R O'Kusky, et al.
Clinical Genetics
|
July 22, 2014
Use of genetic technologies to compare medicines
S E Kolitz, F Towfic, I Grossman, et al.
American Journal of Human Genetics
|
April 17, 1999
A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease
E W Almqvist, M Bloch, R Brinkman, et al.
American Journal of Human Genetics
|
October 1, 1992
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa
O Riess, A Noerremoelle, B Weber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 22, 2013
A systematic review and meta-analysis of clinical variables used in Huntington disease research
Sonia Franciosi, Yaein Shim, Margaret Lau, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 6, 1987
Molecular genetics and Huntington's disease. The South African situation
M R Hayden, J Goldblatt, G Wallis, et al.
Trends in Neurosciences
|
October 6, 2014
Autophagy in Huntington disease and huntingtin in autophagy
Dale D O Martin, Safia Ladha, Dagmar E Ehrnhoefer, et al.
Clinical Biochemistry
|
April 1, 1985
Urinary proteins in a patient with Tangier disease
P H Pritchard, M Bergseth, R McLeod, et al.
Brain Research
|
March 20, 1999
Neuronal degeneration in the basal ganglia and loss of pallido-subthalamic synapses in mice with targeted disruption of the Huntington's disease gene
J R O'Kusky, J Nasir, F Cicchetti, et al.
Page
of 104
Search research articles
Search
Showing results (251-260 of 1,032) with videos related to
Sort By:
Page
of 104
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
August 1, 1994
Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia
E Gagné, J Genest, H Zhang, et al.
Brain Pathology (Zurich, Switzerland)
|
July 1, 1997
Toward understanding the molecular pathology of Huntington's disease
C L Wellington, R R Brinkman, J R O'Kusky, et al.
Clinical Genetics
|
July 22, 2014
Use of genetic technologies to compare medicines
S E Kolitz, F Towfic, I Grossman, et al.
American Journal of Human Genetics
|
April 17, 1999
A worldwide assessment of the frequency of suicide, suicide attempts, or psychiatric hospitalization after predictive testing for Huntington disease
E W Almqvist, M Bloch, R Brinkman, et al.
American Journal of Human Genetics
|
October 1, 1992
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa
O Riess, A Noerremoelle, B Weber, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 22, 2013
A systematic review and meta-analysis of clinical variables used in Huntington disease research
Sonia Franciosi, Yaein Shim, Margaret Lau, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 6, 1987
Molecular genetics and Huntington's disease. The South African situation
M R Hayden, J Goldblatt, G Wallis, et al.
Trends in Neurosciences
|
October 6, 2014
Autophagy in Huntington disease and huntingtin in autophagy
Dale D O Martin, Safia Ladha, Dagmar E Ehrnhoefer, et al.
Clinical Biochemistry
|
April 1, 1985
Urinary proteins in a patient with Tangier disease
P H Pritchard, M Bergseth, R McLeod, et al.
Brain Research
|
March 20, 1999
Neuronal degeneration in the basal ganglia and loss of pallido-subthalamic synapses in mice with targeted disruption of the Huntington's disease gene
J R O'Kusky, J Nasir, F Cicchetti, et al.
Page
of 104