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Journal of Neuroimmunology
|
February 12, 2015
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene
S Nischwitz, C Wolf, T F M Andlauer, et al.
Biochemical and Biophysical Research Communications
|
October 15, 2008
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy
M Elstner, C Schmidt, V C Zingler, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
July 9, 2008
The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders
C K Thoeringer, S Ripke, P G Unschuld, et al.
Human Genetics
|
August 1, 1997
A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype
M Hergersberg, J Balakrishnan, T Bettecken, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
November 10, 2006
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample
P Heiser, A Dempfle, S Friedel, et al.
Acta Neurologica Scandinavica
|
September 21, 2010
More CLEC16A gene variants associated with multiple sclerosis
S Nischwitz, S Cepok, A Kroner, et al.
Molecular Psychiatry
|
January 14, 2009
Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways
C Ditzen, J Varadarajulu, L Czibere, et al.
Genes and Immunity
|
March 21, 2008
IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations
F Weber, B Fontaine, I Cournu-Rebeix, et al.
Molecular Psychiatry
|
April 7, 2010
TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
A Erhardt, L Czibere, D Roeske, et al.
American Journal of Human Genetics
|
October 1, 1989
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
M Koenig, A H Beggs, M Moyer, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 30) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 30 results.
Journal of Neuroimmunology
|
February 12, 2015
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene
S Nischwitz, C Wolf, T F M Andlauer, et al.
Biochemical and Biophysical Research Communications
|
October 15, 2008
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy
M Elstner, C Schmidt, V C Zingler, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
July 9, 2008
The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders
C K Thoeringer, S Ripke, P G Unschuld, et al.
Human Genetics
|
August 1, 1997
A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype
M Hergersberg, J Balakrishnan, T Bettecken, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)
|
November 10, 2006
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample
P Heiser, A Dempfle, S Friedel, et al.
Acta Neurologica Scandinavica
|
September 21, 2010
More CLEC16A gene variants associated with multiple sclerosis
S Nischwitz, S Cepok, A Kroner, et al.
Molecular Psychiatry
|
January 14, 2009
Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways
C Ditzen, J Varadarajulu, L Czibere, et al.
Genes and Immunity
|
March 21, 2008
IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations
F Weber, B Fontaine, I Cournu-Rebeix, et al.
Molecular Psychiatry
|
April 7, 2010
TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
A Erhardt, L Czibere, D Roeske, et al.
American Journal of Human Genetics
|
October 1, 1989
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
M Koenig, A H Beggs, M Moyer, et al.
Page
of 3