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Journal of Neurosurgical Sciences
|
December 10, 2020
Transpars approach for L5-S1 foraminal and extra-foraminal lumbar disc herniations: technical note
Pasquale De Bonis, Antonio Musio, Lorenzo Mongardi, et al.
Biochemical and Biophysical Research Communications
|
April 1, 2014
Early senescence in heterozygous ABCA1 mutation skin fibroblasts: a gene dosage effect beyond HDL deficiency?
Mariarita Puntoni, Federico Bigazzi, Laura Sabatino, et al.
Journal of Proteome Research
|
October 31, 2012
Proteomic profile identifies dysregulated pathways in Cornelia de Lange syndrome cells with distinct mutations in SMC1A and SMC3 genes
Anna Gimigliano, Linda Mannini, Laura Bianchi, et al.
Journal of Translational Medicine
|
June 27, 2012
Claspin as a biomarker of human papillomavirus-related high grade lesions of uterine cervix
Maria Benevolo, Antonio Musio, Amina Vocaturo, et al.
Epilepsia
|
March 2, 2026
Mutation type-specific transcriptomic signatures and readthrough therapy rescue in SMC1A-related developmental and epileptic encephalopathy
Maddalena Di Nardo, Francesca Sardina, Maria M Pallotta, et al.
Scientific Reports
|
November 20, 2015
Mutant cohesin affects RNA polymerase II regulation in Cornelia de Lange syndrome
Linda Mannini, Fabien C Lamaze, Francesco Cucco, et al.
International Journal of Molecular Sciences
|
March 18, 2020
Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile
Stefano Barone, Patrizia Sarogni, Roberto Valli, et al.
Journal of Neurointerventional Surgery
|
August 26, 2021
Use of the SpineJack direct reduction for treating type A2, A3 and A4 fractures of the thoracolumbar spine: a retrospective case series
Giorgio Lofrese, Luca Ricciardi, Pasquale De Bonis, et al.
Aging Cell
|
November 22, 2012
Cytogenetic analysis of human cells reveals specific patterns of DNA damage in replicative and oncogene-induced senescence
Germana Falcone, Alessia Mazzola, Flavia Michelini, et al.
American Journal of Medical Genetics. Part A
|
June 2, 2020
Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome
Francesco Cucco, Patrizia Sarogni, Sara Rossato, et al.
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of 8
Search research articles
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Showing results (31-40 of 72) with videos related to
Sort By:
Page
of 8
Journal of Neurosurgical Sciences
|
December 10, 2020
Transpars approach for L5-S1 foraminal and extra-foraminal lumbar disc herniations: technical note
Pasquale De Bonis, Antonio Musio, Lorenzo Mongardi, et al.
Biochemical and Biophysical Research Communications
|
April 1, 2014
Early senescence in heterozygous ABCA1 mutation skin fibroblasts: a gene dosage effect beyond HDL deficiency?
Mariarita Puntoni, Federico Bigazzi, Laura Sabatino, et al.
Journal of Proteome Research
|
October 31, 2012
Proteomic profile identifies dysregulated pathways in Cornelia de Lange syndrome cells with distinct mutations in SMC1A and SMC3 genes
Anna Gimigliano, Linda Mannini, Laura Bianchi, et al.
Journal of Translational Medicine
|
June 27, 2012
Claspin as a biomarker of human papillomavirus-related high grade lesions of uterine cervix
Maria Benevolo, Antonio Musio, Amina Vocaturo, et al.
Epilepsia
|
March 2, 2026
Mutation type-specific transcriptomic signatures and readthrough therapy rescue in SMC1A-related developmental and epileptic encephalopathy
Maddalena Di Nardo, Francesca Sardina, Maria M Pallotta, et al.
Scientific Reports
|
November 20, 2015
Mutant cohesin affects RNA polymerase II regulation in Cornelia de Lange syndrome
Linda Mannini, Fabien C Lamaze, Francesco Cucco, et al.
International Journal of Molecular Sciences
|
March 18, 2020
Chromosome Missegregation in Single Human Oocytes Is Related to the Age and Gene Expression Profile
Stefano Barone, Patrizia Sarogni, Roberto Valli, et al.
Journal of Neurointerventional Surgery
|
August 26, 2021
Use of the SpineJack direct reduction for treating type A2, A3 and A4 fractures of the thoracolumbar spine: a retrospective case series
Giorgio Lofrese, Luca Ricciardi, Pasquale De Bonis, et al.
Aging Cell
|
November 22, 2012
Cytogenetic analysis of human cells reveals specific patterns of DNA damage in replicative and oncogene-induced senescence
Germana Falcone, Alessia Mazzola, Flavia Michelini, et al.
American Journal of Medical Genetics. Part A
|
June 2, 2020
Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndrome
Francesco Cucco, Patrizia Sarogni, Sara Rossato, et al.
Page
of 8