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Oncology Reports
|
December 15, 2010
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells
Cinzia Puppin, Nadia Passon, Alessandra Franzoni, et al.
Biochemical and Biophysical Research Communications
|
December 27, 2011
Histone post-translational modifications associated to BAALC expression in leukemic cells
Alessandra Franzoni, Nadia Passon, Dora Fabbro, et al.
Haematologica
|
October 16, 2012
Q141K polymorphism of ABCG2 protein is associated with poor prognosis in adult acute myeloid leukemia treated with idarubicin-based chemotherapy
Mario Tiribelli, Dora Fabbro, Alessandra Franzoni, et al.
Molecular Syndromology
|
June 15, 2017
Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy
Chiara Gnan, Alessandra Franzoni, Federica Baldan, et al.
Neuropediatrics
|
August 14, 2023
Long-Term Visual and Neurodevelopmental Outcomes in Two Children with Congenital Nystagmus Secondary to Methadone Exposure In utero
Jessica Galli, Erika Loi, Alessandra Franzoni, et al.
Cytogenetic and Genome Research
|
May 23, 2018
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder
Federica Baldan, Chiara Gnan, Alessandra Franzoni, et al.
Le Infezioni in Medicina
|
June 24, 2014
Chlamydia trachomatis conjunctivitis in a male teenager: a case report
Giorgia Sulis, Lucia Urbinati, Alessandra Franzoni, et al.
Molecular and Cellular Probes
|
December 7, 2016
A CGH array procedure to detect PAX6 gene structural defects
Alessandra Franzoni, Patrizia Dello Russo, Federica Baldan, et al.
Molecular Cytogenetics
|
June 29, 2018
Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability
Luca Lovrecic, Chiara Gnan, Federica Baldan, et al.
American Journal of Medical Genetics. Part A
|
November 11, 2022
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC gene
Jessica Galli, Enza Maria Valente, Joseph Dewulf, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
Oncology Reports
|
December 15, 2010
Histone deacetylase inhibitors control the transcription and alternative splicing of prohibitin in thyroid tumor cells
Cinzia Puppin, Nadia Passon, Alessandra Franzoni, et al.
Biochemical and Biophysical Research Communications
|
December 27, 2011
Histone post-translational modifications associated to BAALC expression in leukemic cells
Alessandra Franzoni, Nadia Passon, Dora Fabbro, et al.
Haematologica
|
October 16, 2012
Q141K polymorphism of ABCG2 protein is associated with poor prognosis in adult acute myeloid leukemia treated with idarubicin-based chemotherapy
Mario Tiribelli, Dora Fabbro, Alessandra Franzoni, et al.
Molecular Syndromology
|
June 15, 2017
Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy
Chiara Gnan, Alessandra Franzoni, Federica Baldan, et al.
Neuropediatrics
|
August 14, 2023
Long-Term Visual and Neurodevelopmental Outcomes in Two Children with Congenital Nystagmus Secondary to Methadone Exposure In utero
Jessica Galli, Erika Loi, Alessandra Franzoni, et al.
Cytogenetic and Genome Research
|
May 23, 2018
Genomic Deletion Involving the IMMP2L Gene in Two Cases of Autism Spectrum Disorder
Federica Baldan, Chiara Gnan, Alessandra Franzoni, et al.
Le Infezioni in Medicina
|
June 24, 2014
Chlamydia trachomatis conjunctivitis in a male teenager: a case report
Giorgia Sulis, Lucia Urbinati, Alessandra Franzoni, et al.
Molecular and Cellular Probes
|
December 7, 2016
A CGH array procedure to detect PAX6 gene structural defects
Alessandra Franzoni, Patrizia Dello Russo, Federica Baldan, et al.
Molecular Cytogenetics
|
June 29, 2018
Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability
Luca Lovrecic, Chiara Gnan, Federica Baldan, et al.
American Journal of Medical Genetics. Part A
|
November 11, 2022
Expanding the spectrum of clinical severity of AICA-ribosiduria: Report of two siblings with mild phenotype caused by a novel pathogenic variant in ATIC gene
Jessica Galli, Enza Maria Valente, Joseph Dewulf, et al.
Page
of 4