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Cellular and Molecular Life Sciences : CMLS
|
June 19, 2013
Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy
Alessandra Govoni, Francesca Magri, Simona Brajkovic, et al.
Molecular Biology and Evolution
|
March 19, 2010
Polymorphisms in the CPB2 gene are maintained by balancing selection and result in haplotype-preferential splicing of exon 7
Rachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
Genome Research
|
November 11, 2008
Widespread balancing selection and pathogen-driven selection at blood group antigen genes
Matteo Fumagalli, Rachele Cagliani, Uberto Pozzoli, et al.
Human Mutation
|
November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions
Alessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Therapeutic Advances in Neurological Disorders
|
May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies
Daniela Piga, Sabrina Salani, Francesca Magri, et al.
Journal of Cellular Biochemistry
|
August 14, 2001
Oxidative stress signalling in the apoptosis of Jurkat T-lymphocytes
R Chiaramonte, E Bartolini, P Riso, et al.
Nucleic Acids Research
|
March 23, 2004
Silencer elements as possible inhibitors of pseudoexon splicing
Manuela Sironi, Giorgia Menozzi, Laura Riva, et al.
Journal of Neurology
|
October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature
Gauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS
|
April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translation
Irene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
European Journal of Biochemistry
|
January 1, 1983
Delta thalassemia: a non-deletion defect
R Taramelli, B Giglioni, P Comi, et al.
Page
of 35
Search research articles
Search
Showing results (81-90 of 346) with videos related to
Sort By:
Page
of 35
Cellular and Molecular Life Sciences : CMLS
|
June 19, 2013
Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy
Alessandra Govoni, Francesca Magri, Simona Brajkovic, et al.
Molecular Biology and Evolution
|
March 19, 2010
Polymorphisms in the CPB2 gene are maintained by balancing selection and result in haplotype-preferential splicing of exon 7
Rachele Cagliani, Matteo Fumagalli, Stefania Riva, et al.
Genome Research
|
November 11, 2008
Widespread balancing selection and pathogen-driven selection at blood group antigen genes
Matteo Fumagalli, Rachele Cagliani, Uberto Pozzoli, et al.
Human Mutation
|
November 25, 2003
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions
Alessio Di Fonzo, Andreina Bordoni, Marco Crimi, et al.
Therapeutic Advances in Neurological Disorders
|
May 21, 2019
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies
Daniela Piga, Sabrina Salani, Francesca Magri, et al.
Journal of Cellular Biochemistry
|
August 14, 2001
Oxidative stress signalling in the apoptosis of Jurkat T-lymphocytes
R Chiaramonte, E Bartolini, P Riso, et al.
Nucleic Acids Research
|
March 23, 2004
Silencer elements as possible inhibitors of pseudoexon splicing
Manuela Sironi, Giorgia Menozzi, Laura Riva, et al.
Journal of Neurology
|
October 26, 2013
Extended phenotype description and new molecular findings in late onset glycogen storage disease type II: a northern Italy population study and review of the literature
Gauthier Remiche, Dario Ronchi, Francesca Magri, et al.
Cellular and Molecular Life Sciences : CMLS
|
April 5, 2014
Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translation
Irene Faravelli, Giulietta Riboldi, Monica Nizzardo, et al.
European Journal of Biochemistry
|
January 1, 1983
Delta thalassemia: a non-deletion defect
R Taramelli, B Giglioni, P Comi, et al.
Page
of 35