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Showing results (191-200 of 270) with videos related to

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Human Molecular Genetics|June 1, 1997
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsyO K Steinlein, A Magnusson, J Stoodt, et al.
Biochemical and Biophysical Research Communications|September 14, 1995
Human adenosine A1 receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 1q31-32.1 using a silent polymorphism in the coding regionJ Deckert, M M Nöthen, S P Bryant, et al.
Human Heredity|November 14, 1997
Investigation of complement C4B deficiency in schizophreniaR Schroers, M M Nöthen, M Rietschel, et al.
Biochemical and Biophysical Research Communications|April 7, 1997
Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated regionD Shimron-Abarbanell, J Erdmann, I R Vogt, et al.
Schizophrenia Research|December 14, 1999
Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophreniaE G Jönsson, M M Nöthen, H Neidt, et al.
Psychological Medicine|September 2, 1998
Lack of association between dopamine D4 receptor gene and personality traitsE G Jönsson, M M Nöthen, J P Gustavsson, et al.
American Journal of Human Genetics|July 6, 2000
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36K Bosse, R C Betz, Y A Lee, et al.
Human Genetics|December 1, 1996
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?R Kruse, C Lamberti, Y Wang, et al.
Addiction Biology|June 26, 2010
Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approachP Franke, T Wang, M M Möthen, et al.
The British Journal of Dermatology|January 4, 2007
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?E Mangold, N Rahner, N Friedrichs, et al.
Pageof 27

Showing results (191-200 of 270) with videos related to

Sort By:
Pageof 27
Human Molecular Genetics|June 1, 1997
An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsyO K Steinlein, A Magnusson, J Stoodt, et al.
Biochemical and Biophysical Research Communications|September 14, 1995
Human adenosine A1 receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 1q31-32.1 using a silent polymorphism in the coding regionJ Deckert, M M Nöthen, S P Bryant, et al.
Human Heredity|November 14, 1997
Investigation of complement C4B deficiency in schizophreniaR Schroers, M M Nöthen, M Rietschel, et al.
Biochemical and Biophysical Research Communications|April 7, 1997
Human 5-HT5A receptor gene: systematic screening for DNA sequence variation and linkage mapping on chromosome 7q34-q36 using a polymorphism in the 5' untranslated regionD Shimron-Abarbanell, J Erdmann, I R Vogt, et al.
Schizophrenia Research|December 14, 1999
Association between a promoter polymorphism in the dopamine D2 receptor gene and schizophreniaE G Jönsson, M M Nöthen, H Neidt, et al.
Psychological Medicine|September 2, 1998
Lack of association between dopamine D4 receptor gene and personality traitsE G Jönsson, M M Nöthen, J P Gustavsson, et al.
American Journal of Human Genetics|July 6, 2000
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36K Bosse, R C Betz, Y A Lee, et al.
Human Genetics|December 1, 1996
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?R Kruse, C Lamberti, Y Wang, et al.
Addiction Biology|June 26, 2010
Susceptibility for alcoholism: DRD4 exon III polymorphism: a case-control and a family-based association approachP Franke, T Wang, M M Möthen, et al.
The British Journal of Dermatology|January 4, 2007
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?E Mangold, N Rahner, N Friedrichs, et al.
Pageof 27