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American Journal of Human Genetics
|
March 1, 1997
CAG repeat expansions in bipolar and unipolar disorders
L Oruc, K Lindblad, G R Verheyen, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
November 13, 2001
Genetics of affective disorders
C Johansson, M Jansson, L Linnér, et al.
Experientia
|
July 15, 1987
Coexistence of peptides with classical neurotransmitters
T Hökfelt, D Millhorn, K Seroogy, et al.
Clinical Genetics
|
January 1, 1997
Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred
B 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 immunocytochemistry
K 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 loci
F 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 mesothelioma
S 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 therapy
Q Yao, L Nordfors, J Axelsson, et al.
Progress in Brain Research
|
January 1, 1986
Coexistence of neuronal messengers--an overview
T 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 family
B T Teh, K Linblad, B Nord, et al.
Page
of 17
Search research articles
Search
Showing results (111-120 of 162) with videos related to
Sort By:
Page
of 17
American Journal of Human Genetics
|
March 1, 1997
CAG repeat expansions in bipolar and unipolar disorders
L Oruc, K Lindblad, G R Verheyen, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology
|
November 13, 2001
Genetics of affective disorders
C Johansson, M Jansson, L Linnér, et al.
Experientia
|
July 15, 1987
Coexistence of peptides with classical neurotransmitters
T Hökfelt, D Millhorn, K Seroogy, et al.
Clinical Genetics
|
January 1, 1997
Oculopharyngeal muscular dystrophy (OPMD)--report and genetic studies of an Australian kindred
B 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 immunocytochemistry
K 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 loci
F 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 mesothelioma
S 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 therapy
Q Yao, L Nordfors, J Axelsson, et al.
Progress in Brain Research
|
January 1, 1986
Coexistence of neuronal messengers--an overview
T 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 family
B T Teh, K Linblad, B Nord, et al.
Page
of 17