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M Schalling

Showing results (111-120 of 162) with videos related to

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American Journal of Human Genetics|March 1, 1997
CAG repeat expansions in bipolar and unipolar disordersL Oruc, K Lindblad, G R Verheyen, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|November 13, 2001
Genetics of affective disordersC Johansson, M Jansson, L Linnér, et al.
Experientia|July 15, 1987
Coexistence of peptides with classical neurotransmittersT Hökfelt, D Millhorn, K Seroogy, et al.
Clinical Genetics|January 1, 1997
Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindredB T Teh, A A Sullivan, F Farnebo, et al.
Experimental Brain Research|January 1, 1989
Cholecystokinin and tyrosine hydroxylase messenger RNAs in neurons of rat mesencephalon: peptide/monoamine coexistence studies using in situ hybridization combined with immunocytochemistryK Seroogy, M Schalling, S Brené, et al.
International Journal of Molecular Medicine|February 17, 2001
Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene lociF Li, A Szobor, R Croxen, et al.
Nature Genetics|August 1, 1993
The Wilms tumour gene WT1 is expressed in murine mesoderm-derived tissues and mutated in a human mesotheliomaS Park, M Schalling, A Bernard, et al.
Atherosclerosis|August 24, 2005
Peroxisome proliferator-activated receptor gamma polymorphisms affect systemic inflammation and survival in end-stage renal disease patients starting renal replacement therapyQ Yao, L Nordfors, J Axelsson, et al.
Progress in Brain Research|January 1, 1986
Coexistence of neuronal messengers--an overviewT Hökfelt, V R Holets, W Staines, et al.
Journal of Medical Genetics|May 5, 1999
Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one familyB T Teh, K Linblad, B Nord, et al.
Pageof 17

Showing results (111-120 of 162) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|March 1, 1997
CAG repeat expansions in bipolar and unipolar disordersL Oruc, K Lindblad, G R Verheyen, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|November 13, 2001
Genetics of affective disordersC Johansson, M Jansson, L Linnér, et al.
Experientia|July 15, 1987
Coexistence of peptides with classical neurotransmittersT Hökfelt, D Millhorn, K Seroogy, et al.
Clinical Genetics|January 1, 1997
Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindredB T Teh, A A Sullivan, F Farnebo, et al.
Experimental Brain Research|January 1, 1989
Cholecystokinin and tyrosine hydroxylase messenger RNAs in neurons of rat mesencephalon: peptide/monoamine coexistence studies using in situ hybridization combined with immunocytochemistryK Seroogy, M Schalling, S Brené, et al.
International Journal of Molecular Medicine|February 17, 2001
Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene lociF Li, A Szobor, R Croxen, et al.
Nature Genetics|August 1, 1993
The Wilms tumour gene WT1 is expressed in murine mesoderm-derived tissues and mutated in a human mesotheliomaS Park, M Schalling, A Bernard, et al.
Atherosclerosis|August 24, 2005
Peroxisome proliferator-activated receptor gamma polymorphisms affect systemic inflammation and survival in end-stage renal disease patients starting renal replacement therapyQ Yao, L Nordfors, J Axelsson, et al.
Progress in Brain Research|January 1, 1986
Coexistence of neuronal messengers--an overviewT Hökfelt, V R Holets, W Staines, et al.
Journal of Medical Genetics|May 5, 1999
Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one familyB T Teh, K Linblad, B Nord, et al.
Pageof 17