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M Albus

Showing results (81-90 of 118) with videos related to

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American Journal of Medical Genetics|October 9, 1995
Systematic screening for mutations in the promoter and the coding region of the 5-HT1A geneJ Erdmann, D Shimron-Abarbanell, S Cichon, et al.
Psychiatric Genetics|January 1, 1995
Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor geneS Cichon, M M Nöthen, M Catalano, et al.
Fortschritte Der Neurologie-Psychiatrie|January 1, 1986
[Psychopathologic changes in chronic schizophrenic patients following withdrawal of neuroleptics: relation to therapeutic, neuroendocrine and computer tomography variables]M Albus, D Naber, M Ackenheil, et al.
Nature Genetics|November 1, 1995
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysisS G Schwab, M Albus, J Hallmayer, et al.
Biological Psychiatry|October 1, 1993
Mutation in the beta amyloid precursor protein gene and schizophreniaM M Nöthen, J Erdmann, P Propping, et al.
Pharmacopsychiatry|June 1, 1990
ICD-10 field trial in German-speaking countries--summary, judgement and perspectivesV Dittmann, H J Freyberger, M Albus, et al.
Molecular Psychiatry|March 1, 1997
Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysisS G Schwab, G N Eckstein, J Hallmayer, et al.
Pharmacogenetics|February 24, 2001
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patientsB Niesler, B Weiss, C Fischer, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|January 1, 1996
Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophreniaJ Deckert, M M Nöthen, M Rietschel, et al.
Schizophrenia Research|May 1, 1996
Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial casesM Rietschel, M M Nöthen, M Albus, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|October 9, 1995
Systematic screening for mutations in the promoter and the coding region of the 5-HT1A geneJ Erdmann, D Shimron-Abarbanell, S Cichon, et al.
Psychiatric Genetics|January 1, 1995
Identification of two novel polymorphisms and a rare deletion variant in the human dopamine D4 receptor geneS Cichon, M M Nöthen, M Catalano, et al.
Fortschritte Der Neurologie-Psychiatrie|January 1, 1986
[Psychopathologic changes in chronic schizophrenic patients following withdrawal of neuroleptics: relation to therapeutic, neuroendocrine and computer tomography variables]M Albus, D Naber, M Ackenheil, et al.
Nature Genetics|November 1, 1995
Evaluation of a susceptibility gene for schizophrenia on chromosome 6p by multipoint affected sib-pair linkage analysisS G Schwab, M Albus, J Hallmayer, et al.
Biological Psychiatry|October 1, 1993
Mutation in the beta amyloid precursor protein gene and schizophreniaM M Nöthen, J Erdmann, P Propping, et al.
Pharmacopsychiatry|June 1, 1990
ICD-10 field trial in German-speaking countries--summary, judgement and perspectivesV Dittmann, H J Freyberger, M Albus, et al.
Molecular Psychiatry|March 1, 1997
Evidence suggestive of a locus on chromosome 5q31 contributing to susceptibility for schizophrenia in German and Israeli families by multipoint affected sib-pair linkage analysisS G Schwab, G N Eckstein, J Hallmayer, et al.
Pharmacogenetics|February 24, 2001
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patientsB Niesler, B Weiss, C Fischer, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|January 1, 1996
Human adenosine A2a receptor (A2aAR) gene: systematic mutation screening in patients with schizophreniaJ Deckert, M M Nöthen, M Rietschel, et al.
Schizophrenia Research|May 1, 1996
Dopamine D3 receptor Gly9/Ser9 polymorphism and schizophrenia: no increased frequency of homozygosity in German familial casesM Rietschel, M M Nöthen, M Albus, et al.
Pageof 12