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Showing results (101-110 of 346) with videos related to

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Neurology|October 15, 2003
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domainR Del Bo, A Bordoni, M Sciacco, et al.
American Journal of Human Genetics|April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathyO Musumeci, A L Andreu, S Shanske, et al.
Leukemia Research|January 1, 1982
Preferential induction of fetal versus embryonic globin chains in human leukemic cell linesA M Gianni, M Presta, E Polli, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|September 24, 2004
Improvement of combined FISH and immunofluorescence to trace the fate of somatic stem cells after transplantationChiara Donadoni, Stefania Corti, Federica Locatelli, et al.
American Journal of Human Genetics|July 7, 2009
Diverse evolutionary histories for beta-adrenoreceptor genes in humansRachele Cagliani, Matteo Fumagalli, Uberto Pozzoli, et al.
Cellular and Molecular Life Sciences : CMLS|November 19, 2011
Research advances in gene therapy approaches for the treatment of amyotrophic lateral sclerosisMonica Nizzardo, Chiara Simone, Marianna Falcone, et al.
American Journal of Medical Genetics|April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean areaS Lucchiari, I Fogh, A Prelle, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinA Prelle, M Moggio, G P Comi, et al.
Journal of the Neurological Sciences|January 1, 1997
The apolipoprotein E epsilon4 allele causes a faster decline of cognitive performances in Down's syndrome subjectsR Del Bo, G P Comi, N Bresolin, et al.
BMC Evolutionary Biology|June 3, 2009
A complex selection signature at the human AVPR1B geneRachele Cagliani, Matteo Fumagalli, Uberto Pozzoli, et al.
Pageof 35

Showing results (101-110 of 346) with videos related to

Sort By:
Pageof 35
Neurology|October 15, 2003
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domainR Del Bo, A Bordoni, M Sciacco, et al.
American Journal of Human Genetics|April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathyO Musumeci, A L Andreu, S Shanske, et al.
Leukemia Research|January 1, 1982
Preferential induction of fetal versus embryonic globin chains in human leukemic cell linesA M Gianni, M Presta, E Polli, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|September 24, 2004
Improvement of combined FISH and immunofluorescence to trace the fate of somatic stem cells after transplantationChiara Donadoni, Stefania Corti, Federica Locatelli, et al.
American Journal of Human Genetics|July 7, 2009
Diverse evolutionary histories for beta-adrenoreceptor genes in humansRachele Cagliani, Matteo Fumagalli, Uberto Pozzoli, et al.
Cellular and Molecular Life Sciences : CMLS|November 19, 2011
Research advances in gene therapy approaches for the treatment of amyotrophic lateral sclerosisMonica Nizzardo, Chiara Simone, Marianna Falcone, et al.
American Journal of Medical Genetics|April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean areaS Lucchiari, I Fogh, A Prelle, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinA Prelle, M Moggio, G P Comi, et al.
Journal of the Neurological Sciences|January 1, 1997
The apolipoprotein E epsilon4 allele causes a faster decline of cognitive performances in Down's syndrome subjectsR Del Bo, G P Comi, N Bresolin, et al.
BMC Evolutionary Biology|June 3, 2009
A complex selection signature at the human AVPR1B geneRachele Cagliani, Matteo Fumagalli, Uberto Pozzoli, et al.
Pageof 35