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Biochimica Et Biophysica Acta. General Subjects
|
December 12, 2018
TRIM8-driven transcriptomic profile of neural stem cells identified glioma-related nodal genes and pathways
Santina Venuto, Stefano Castellana, Maria Monti, et al.
Human Mutation
|
February 12, 2014
TBC1D7 mutations are associated with intellectual disability, macrocrania, patellar dislocation, and celiac disease
Ali Abdullah Alfaiz, Lucia Micale, Barbara Mandriani, et al.
European Journal of Human Genetics : EJHG
|
July 2, 2009
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient
Giovanni Battista Ferrero, Cédric Howald, Lucia Micale, et al.
Journal of Autism and Developmental Disorders
|
April 12, 2014
Brief report: functional MRI of a patient with 7q11.23 duplication syndrome and autism spectrum disorder
Paolo Prontera, Domenico Serino, Bernardo Caldini, et al.
Molecular Cancer
|
September 4, 2010
Identification of tumor-associated cassette exons in human cancer through EST-based computational prediction and experimental validation
Alessio Valletti, Anna Anselmo, Marina Mangiulli, et al.
Blood
|
March 22, 2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome
Samuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, et al.
Plos One
|
November 3, 2012
A fish-specific transposable element shapes the repertoire of p53 target genes in zebrafish
Lucia Micale, Maria Nicla Loviglio, Marta Manzoni, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2016
A novel MED12 mutation: Evidence for a fourth phenotype
Paolo Prontera, Valentina Ottaviani, Daniela Rogaia, et al.
Cancer Research
|
March 17, 2019
AQP4 Aggregation State Is a Determinant for Glioma Cell Fate
Laura Simone, Francesco Pisani, Maria G Mola, et al.
European Journal of Human Genetics : EJHG
|
April 3, 2019
Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene
Paolo Prontera, Daniela Rogaia, Ester Sallicandro, et al.
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of 13
Search research articles
Search
Showing results (31-40 of 129) with videos related to
Sort By:
Page
of 13
Biochimica Et Biophysica Acta. General Subjects
|
December 12, 2018
TRIM8-driven transcriptomic profile of neural stem cells identified glioma-related nodal genes and pathways
Santina Venuto, Stefano Castellana, Maria Monti, et al.
Human Mutation
|
February 12, 2014
TBC1D7 mutations are associated with intellectual disability, macrocrania, patellar dislocation, and celiac disease
Ali Abdullah Alfaiz, Lucia Micale, Barbara Mandriani, et al.
European Journal of Human Genetics : EJHG
|
July 2, 2009
An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient
Giovanni Battista Ferrero, Cédric Howald, Lucia Micale, et al.
Journal of Autism and Developmental Disorders
|
April 12, 2014
Brief report: functional MRI of a patient with 7q11.23 duplication syndrome and autism spectrum disorder
Paolo Prontera, Domenico Serino, Bernardo Caldini, et al.
Molecular Cancer
|
September 4, 2010
Identification of tumor-associated cassette exons in human cancer through EST-based computational prediction and experimental validation
Alessio Valletti, Anna Anselmo, Marina Mangiulli, et al.
Blood
|
March 22, 2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome
Samuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, et al.
Plos One
|
November 3, 2012
A fish-specific transposable element shapes the repertoire of p53 target genes in zebrafish
Lucia Micale, Maria Nicla Loviglio, Marta Manzoni, et al.
American Journal of Medical Genetics. Part A
|
June 18, 2016
A novel MED12 mutation: Evidence for a fourth phenotype
Paolo Prontera, Valentina Ottaviani, Daniela Rogaia, et al.
Cancer Research
|
March 17, 2019
AQP4 Aggregation State Is a Determinant for Glioma Cell Fate
Laura Simone, Francesco Pisani, Maria G Mola, et al.
European Journal of Human Genetics : EJHG
|
April 3, 2019
Schilbach-Rott syndrome associated with 9q22.32q22.33 duplication, involving the PTCH1 gene
Paolo Prontera, Daniela Rogaia, Ester Sallicandro, et al.
Page
of 13