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M Steen

Showing results (151-160 of 312) with videos related to

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Acta Physiologica Scandinavica. Supplementum|January 1, 1990
Molecular analysis of mutation at the human hprt locusB Lambert, B Andersson, S M He, et al.
Psychopharmacology|May 1, 1997
Non-functional CYP2D6 alleles and risk for neuroleptic-induced movement disorders in schizophrenic patientsO A Andreassen, T MacEwan, A K Gulbrandsen, et al.
Genomics|October 27, 1997
Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA)G Sjøholt, A Molven, R Løvlie, et al.
Schizophrenia Research|December 15, 2018
Analysis of differentially methylated regions in great apes and extinct hominids provides support for the evolutionary hypothesis of schizophreniaNiladri Banerjee, Tatiana Polushina, Francesco Bettella, et al.
Molecular Psychiatry|May 24, 2000
A human myo-inositol monophosphatase gene (IMPA2) localized in a putative susceptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patientsG Sjøholt, A K Gulbrandsen, R Løvlie, et al.
The Journal of the American Academy of Orthopaedic Surgeons|December 3, 2013
AAOS appropriate use criteria: optimizing the management of full-thickness rotator cuff tearsIoannis P Pappou, Christopher C Schmidt, Claudius D Jarrett, et al.
The Journal of Clinical Psychiatry|September 16, 2004
Breastfeeding during maternal antidepressant treatment with serotonin reuptake inhibitors: infant exposure, clinical symptoms, and cytochrome p450 genotypesJan Øystein Berle, Vidar M Steen, Trond Oskar Aamo, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 4, 2012
Imaging and cognitive genetics: the Norwegian Cognitive NeuroGenetics sampleThomas Espeseth, Andrea Christoforou, Astri J Lundervold, et al.
Journal of Medical Genetics|November 3, 2004
The ser9gly SNP in the dopamine D3 receptor causes a shift from cAMP related to PGE2 related signal transduction mechanisms in transfected CHO cellsM Hellstrand, E A Danielsen, V M Steen, et al.
BMC Neuroscience|July 13, 2013
LOC689986, a unique gene showing specific expression in restricted areas of the rodent neocortexKari M Ersland, Bjarte Håvik, Johanne Egge Rinholm, et al.
Pageof 32

Showing results (151-160 of 312) with videos related to

Sort By:
Pageof 32
Acta Physiologica Scandinavica. Supplementum|January 1, 1990
Molecular analysis of mutation at the human hprt locusB Lambert, B Andersson, S M He, et al.
Psychopharmacology|May 1, 1997
Non-functional CYP2D6 alleles and risk for neuroleptic-induced movement disorders in schizophrenic patientsO A Andreassen, T MacEwan, A K Gulbrandsen, et al.
Genomics|October 27, 1997
Genomic structure and chromosomal localization of a human myo-inositol monophosphatase gene (IMPA)G Sjøholt, A Molven, R Løvlie, et al.
Schizophrenia Research|December 15, 2018
Analysis of differentially methylated regions in great apes and extinct hominids provides support for the evolutionary hypothesis of schizophreniaNiladri Banerjee, Tatiana Polushina, Francesco Bettella, et al.
Molecular Psychiatry|May 24, 2000
A human myo-inositol monophosphatase gene (IMPA2) localized in a putative susceptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patientsG Sjøholt, A K Gulbrandsen, R Løvlie, et al.
The Journal of the American Academy of Orthopaedic Surgeons|December 3, 2013
AAOS appropriate use criteria: optimizing the management of full-thickness rotator cuff tearsIoannis P Pappou, Christopher C Schmidt, Claudius D Jarrett, et al.
The Journal of Clinical Psychiatry|September 16, 2004
Breastfeeding during maternal antidepressant treatment with serotonin reuptake inhibitors: infant exposure, clinical symptoms, and cytochrome p450 genotypesJan Øystein Berle, Vidar M Steen, Trond Oskar Aamo, et al.
Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies|August 4, 2012
Imaging and cognitive genetics: the Norwegian Cognitive NeuroGenetics sampleThomas Espeseth, Andrea Christoforou, Astri J Lundervold, et al.
Journal of Medical Genetics|November 3, 2004
The ser9gly SNP in the dopamine D3 receptor causes a shift from cAMP related to PGE2 related signal transduction mechanisms in transfected CHO cellsM Hellstrand, E A Danielsen, V M Steen, et al.
BMC Neuroscience|July 13, 2013
LOC689986, a unique gene showing specific expression in restricted areas of the rodent neocortexKari M Ersland, Bjarte Håvik, Johanne Egge Rinholm, et al.
Pageof 32