Search research articles
Contact Us
Filters
Showing results (101-110 of 124) with videos related to
Page
of 13
Sort By:
Current Pharmaceutical Biotechnology
|
January 31, 2012
DTNBP1 (dysbindin) gene variants: in vivo evidence for effects on hippocampal glutamate status
C Wirth, F Schubert, M Lautenschlager, et al.
Pharmacopsychiatry
|
July 9, 2009
COMT Val 158 Met polymorphism is associated with cognitive flexibility in a signal discrimination task in schizophrenia
A H Neuhaus, C Opgen-Rhein, C Urbanek, et al.
Physics in Medicine and Biology
|
February 2, 2023
Alanine response to low energy synchrotron x-ray radiation
P van den Elzen, T Sander, H Palmans, et al.
Molecular and Cellular Probes
|
September 6, 2000
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy
K Haug, J Kremerskothen, K Hallmann, et al.
Neurology
|
July 16, 2008
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
B A Neubauer, S Waldegger, J Heinzinger, et al.
American Journal of Medical Genetics
|
April 9, 1996
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia
D Shimron-Abarbanell, H Harms, J Erdmann, et al.
Addiction Biology
|
June 26, 2010
Association analysis of a PAX-6 gene promoter-associated polymorphic repeat with alcohol dependence
J Samochowiec, M Rottmann, O Okladnova, et al.
Radiation Protection Dosimetry
|
February 21, 2004
Calibration of dosemeters used in mammography with different X ray qualities: EUROMET project no. 526
J Witzani, H Bjerke, F Bochud, et al.
Neurology
|
September 26, 1997
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6
T Sander, B Bockenkamp, T Hildmann, et al.
Clinical Genetics
|
September 12, 2013
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I
S Assereto, A Robbiano, M Di Rocco, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 124) with videos related to
Sort By:
Page
of 13
Current Pharmaceutical Biotechnology
|
January 31, 2012
DTNBP1 (dysbindin) gene variants: in vivo evidence for effects on hippocampal glutamate status
C Wirth, F Schubert, M Lautenschlager, et al.
Pharmacopsychiatry
|
July 9, 2009
COMT Val 158 Met polymorphism is associated with cognitive flexibility in a signal discrimination task in schizophrenia
A H Neuhaus, C Opgen-Rhein, C Urbanek, et al.
Physics in Medicine and Biology
|
February 2, 2023
Alanine response to low energy synchrotron x-ray radiation
P van den Elzen, T Sander, H Palmans, et al.
Molecular and Cellular Probes
|
September 6, 2000
Mutation screening of the chromosome 8q24.3-human activity-regulated cytoskeleton-associated gene (ARC) in idiopathic generalized epilepsy
K Haug, J Kremerskothen, K Hallmann, et al.
Neurology
|
July 16, 2008
KCNQ2 and KCNQ3 mutations contribute to different idiopathic epilepsy syndromes
B A Neubauer, S Waldegger, J Heinzinger, et al.
American Journal of Medical Genetics
|
April 9, 1996
Systematic screening for mutations in the human serotonin 1F receptor gene in patients with bipolar affective disorder and schizophrenia
D Shimron-Abarbanell, H Harms, J Erdmann, et al.
Addiction Biology
|
June 26, 2010
Association analysis of a PAX-6 gene promoter-associated polymorphic repeat with alcohol dependence
J Samochowiec, M Rottmann, O Okladnova, et al.
Radiation Protection Dosimetry
|
February 21, 2004
Calibration of dosemeters used in mammography with different X ray qualities: EUROMET project no. 526
J Witzani, H Bjerke, F Bochud, et al.
Neurology
|
September 26, 1997
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6
T Sander, B Bockenkamp, T Hildmann, et al.
Clinical Genetics
|
September 12, 2013
Functional characterization of the c.462delA mutation in the NDUFS4 subunit gene of mitochondrial complex I
S Assereto, A Robbiano, M Di Rocco, et al.
Page
of 13