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Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 30, 2010
A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patients
Lucy Costantino, Laura Claut, Valentina Paracchini, et al.
The Journal of Comparative Neurology
|
April 6, 2019
The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration
Monika Gostic, Angela Martinelli, Carl Tucker, et al.
Mutation Research
|
April 4, 2007
Effects of metabolic genotypes on intermediary biomarkers in subjects exposed to PAHS: results from the EXPAH study
Seymour Garte, Emanuela Taioli, Sara Raimondi, et al.
Molecular and Cellular Endocrinology
|
March 7, 2006
A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity
Mara Giordano, Michela Godi, Francesca Giacopelli, et al.
Journal of Biomedicine & Biotechnology
|
February 9, 2012
Amniotic mesenchymal stem cells: a new source for hepatocyte-like cells and induction of CFTR expression by coculture with cystic fibrosis airway epithelial cells
Valentina Paracchini, Annalucia Carbone, Federico Colombo, et al.
Scientific Reports
|
July 15, 2022
Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix
Elisabetta Versace, Paola Sgadò, Julia George, et al.
The Pharmacogenomics Journal
|
December 14, 2016
A systems biology approach to investigate the mechanism of action of trabectedin in a model of myelomonocytic leukemia
L Mannarino, L Paracchini, I Craparotta, et al.
Biological Psychiatry
|
April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
Tom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Clinical Genetics
|
February 19, 2008
Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions
V Paracchini, M Seia, D Coviello, et al.
Human Molecular Genetics
|
November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexia
Thomas S Scerri, William M Brandler, Silvia Paracchini, et al.
Page
of 24
Search research articles
Search
Showing results (141-150 of 235) with videos related to
Sort By:
Page
of 24
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
September 30, 2010
A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patients
Lucy Costantino, Laura Claut, Valentina Paracchini, et al.
The Journal of Comparative Neurology
|
April 6, 2019
The dyslexia susceptibility KIAA0319 gene shows a specific expression pattern during zebrafish development supporting a role beyond neuronal migration
Monika Gostic, Angela Martinelli, Carl Tucker, et al.
Mutation Research
|
April 4, 2007
Effects of metabolic genotypes on intermediary biomarkers in subjects exposed to PAHS: results from the EXPAH study
Seymour Garte, Emanuela Taioli, Sara Raimondi, et al.
Molecular and Cellular Endocrinology
|
March 7, 2006
A variation in a Pit-1 site in the growth hormone gene (GH1) promoter induces a differential transcriptional activity
Mara Giordano, Michela Godi, Francesca Giacopelli, et al.
Journal of Biomedicine & Biotechnology
|
February 9, 2012
Amniotic mesenchymal stem cells: a new source for hepatocyte-like cells and induction of CFTR expression by coculture with cystic fibrosis airway epithelial cells
Valentina Paracchini, Annalucia Carbone, Federico Colombo, et al.
Scientific Reports
|
July 15, 2022
Light-induced asymmetries in embryonic retinal gene expression are mediated by the vascular system and extracellular matrix
Elisabetta Versace, Paola Sgadò, Julia George, et al.
The Pharmacogenomics Journal
|
December 14, 2016
A systems biology approach to investigate the mechanism of action of trabectedin in a model of myelomonocytic leukemia
L Mannarino, L Paracchini, I Craparotta, et al.
Biological Psychiatry
|
April 5, 2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traits
Tom S Scerri, Andrew P Morris, Lyn-Louise Buckingham, et al.
Clinical Genetics
|
February 19, 2008
Molecular and clinical features associated with CFTR gene rearrangements in Italian population: identification of a new duplication and recurrent deletions
V Paracchini, M Seia, D Coviello, et al.
Human Molecular Genetics
|
November 6, 2010
PCSK6 is associated with handedness in individuals with dyslexia
Thomas S Scerri, William M Brandler, Silvia Paracchini, et al.
Page
of 24