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BMC Medical Genetics
|
May 8, 2007
MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions
Carmela Laperuta, Letizia Spizzichino, Pio D'Adamo, et al.
Journal of Medical Genetics
|
September 15, 2010
Salbutamol increases survival motor neuron (SMN) transcript levels in leucocytes of spinal muscular atrophy (SMA) patients: relevance for clinical trial design
Francesco Danilo Tiziano, Rosa Lomastro, Anna Maria Pinto, et al.
Journal of Biomedicine & Biotechnology
|
October 26, 2012
Lim mineralization protein 3 induces the osteogenic differentiation of human amniotic fluid stromal cells through Kruppel-like factor-4 downregulation and further bone-specific gene expression
Marta Barba, Filomena Pirozzi, Nathalie Saulnier, et al.
European Journal of Human Genetics : EJHG
|
April 8, 2004
Three Rett patients with both MECP2 mutation and 15q11-13 rearrangements
Ilaria Longo, Luisa Russo, Ilaria Meloni, et al.
Investigative Ophthalmology & Visual Science
|
January 24, 2017
HTRA1 and TGF-β1 Concentrations in the Aqueous Humor of Patients With Neovascular Age-Related Macular Degeneration
Gian Marco Tosi, Elena Caldi, Giovanni Neri, et al.
International Journal of Molecular Sciences
|
March 28, 2024
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders
Martina Grandi, Chiara Galber, Cristina Gatto, et al.
Nature Neuroscience
|
April 10, 2007
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability
Francesca Zalfa, Boris Eleuteri, Kirsten S Dickson, et al.
Journal of Cellular Physiology
|
November 19, 2016
CD93 as a Potential Target in Neovascular Age-Related Macular Degeneration
Gian Marco Tosi, Elena Caldi, Barbara Parolini, et al.
Plos One
|
January 4, 2013
Enhancer chip: detecting human copy number variations in regulatory elements
Marco Savarese, Giulio Piluso, Daniela Orteschi, et al.
Scientific Reports
|
January 14, 2018
A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome
Roser Urreizti, Sarah Damanti, Carla Esteve, et al.
Page
of 28
Search research articles
Search
Showing results (201-210 of 273) with videos related to
Sort By:
Page
of 28
BMC Medical Genetics
|
May 8, 2007
MRX87 family with Aristaless X dup24bp mutation and implication for polyAlanine expansions
Carmela Laperuta, Letizia Spizzichino, Pio D'Adamo, et al.
Journal of Medical Genetics
|
September 15, 2010
Salbutamol increases survival motor neuron (SMN) transcript levels in leucocytes of spinal muscular atrophy (SMA) patients: relevance for clinical trial design
Francesco Danilo Tiziano, Rosa Lomastro, Anna Maria Pinto, et al.
Journal of Biomedicine & Biotechnology
|
October 26, 2012
Lim mineralization protein 3 induces the osteogenic differentiation of human amniotic fluid stromal cells through Kruppel-like factor-4 downregulation and further bone-specific gene expression
Marta Barba, Filomena Pirozzi, Nathalie Saulnier, et al.
European Journal of Human Genetics : EJHG
|
April 8, 2004
Three Rett patients with both MECP2 mutation and 15q11-13 rearrangements
Ilaria Longo, Luisa Russo, Ilaria Meloni, et al.
Investigative Ophthalmology & Visual Science
|
January 24, 2017
HTRA1 and TGF-β1 Concentrations in the Aqueous Humor of Patients With Neovascular Age-Related Macular Degeneration
Gian Marco Tosi, Elena Caldi, Giovanni Neri, et al.
International Journal of Molecular Sciences
|
March 28, 2024
Mitochondrial Dysfunction Causes Cell Death in Patients Affected by Fragile-X-Associated Disorders
Martina Grandi, Chiara Galber, Cristina Gatto, et al.
Nature Neuroscience
|
April 10, 2007
A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability
Francesca Zalfa, Boris Eleuteri, Kirsten S Dickson, et al.
Journal of Cellular Physiology
|
November 19, 2016
CD93 as a Potential Target in Neovascular Age-Related Macular Degeneration
Gian Marco Tosi, Elena Caldi, Barbara Parolini, et al.
Plos One
|
January 4, 2013
Enhancer chip: detecting human copy number variations in regulatory elements
Marco Savarese, Giulio Piluso, Daniela Orteschi, et al.
Scientific Reports
|
January 14, 2018
A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome
Roser Urreizti, Sarah Damanti, Carla Esteve, et al.
Page
of 28