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A Suomalainen

Showing results (31-40 of 76) with videos related to

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Scandinavian Journal of Immunology|January 1, 1980
Mouse/human T-cell hybrids rosetting with sheep erythrocytesH A Suomalainen, R A Goldsby, B A Osborne, et al.
Oncogene|January 20, 2009
Downregulation of SRF-FOS-JUNB pathway in fumarate hydratase deficiency and in uterine leiomyomasN Raimundo, S Vanharanta, L A Aaltonen, et al.
American Journal of Human Genetics|May 1, 1995
Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locusK Nikali, A Suomalainen, J Terwilliger, et al.
Lancet (London, England)|November 28, 1992
Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNAA Suomalainen, A Paetau, H Leinonen, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Quantification of mitochondrial DNA carrying the tRNA(8344Lys) point mutation in myoclonus epilepsy and ragged-red-fiber diseaseA Suomalainen, P Kollmann, J N Octave, et al.
Journal of the Neurological Sciences|December 1, 1995
Diagnosis of fatal infantile defects of the mitochondrial respiratory chain: age dependence and postmortem analysis of enzyme activitiesA Majander, J Rapola, H Sariola, et al.
Journal of the Neurological Sciences|September 1, 1992
Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNAA Suomalainen, E Ciafaloni, Y Koga, et al.
Medical Biology|October 1, 1982
Specificity of monoclonal antibodies to an EBV transformed B-cell lineJ Schröder, H A Suomalainen, E Parkkinen, et al.
Somatic Cell and Molecular Genetics|May 1, 1986
Genetic assignment of GP90, leukocyte adhesion glycoprotein to human chromosome 21H A Suomalainen, C G Gahmberg, M Patarroyo, et al.
Neurology|January 6, 2011
Dominant encephalopathy mimicking mitochondrial diseaseT Lönnqvist, P Isohanni, L Valanne, et al.
Pageof 8

Showing results (31-40 of 76) with videos related to

Sort By:
Pageof 8
Scandinavian Journal of Immunology|January 1, 1980
Mouse/human T-cell hybrids rosetting with sheep erythrocytesH A Suomalainen, R A Goldsby, B A Osborne, et al.
Oncogene|January 20, 2009
Downregulation of SRF-FOS-JUNB pathway in fumarate hydratase deficiency and in uterine leiomyomasN Raimundo, S Vanharanta, L A Aaltonen, et al.
American Journal of Human Genetics|May 1, 1995
Random search for shared chromosomal regions in four affected individuals: the assignment of a new hereditary ataxia locusK Nikali, A Suomalainen, J Terwilliger, et al.
Lancet (London, England)|November 28, 1992
Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNAA Suomalainen, A Paetau, H Leinonen, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
Quantification of mitochondrial DNA carrying the tRNA(8344Lys) point mutation in myoclonus epilepsy and ragged-red-fiber diseaseA Suomalainen, P Kollmann, J N Octave, et al.
Journal of the Neurological Sciences|December 1, 1995
Diagnosis of fatal infantile defects of the mitochondrial respiratory chain: age dependence and postmortem analysis of enzyme activitiesA Majander, J Rapola, H Sariola, et al.
Journal of the Neurological Sciences|September 1, 1992
Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNAA Suomalainen, E Ciafaloni, Y Koga, et al.
Medical Biology|October 1, 1982
Specificity of monoclonal antibodies to an EBV transformed B-cell lineJ Schröder, H A Suomalainen, E Parkkinen, et al.
Somatic Cell and Molecular Genetics|May 1, 1986
Genetic assignment of GP90, leukocyte adhesion glycoprotein to human chromosome 21H A Suomalainen, C G Gahmberg, M Patarroyo, et al.
Neurology|January 6, 2011
Dominant encephalopathy mimicking mitochondrial diseaseT Lönnqvist, P Isohanni, L Valanne, et al.
Pageof 8