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Lucia Micale

Showing results (51-60 of 72) with videos related to

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Human Mutation|June 29, 2019
TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasisSilvia Morlino, Annalucia Carbone, Marco Ritelli, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|April 1, 2018
TRIM50 regulates Beclin 1 proautophagic activityCarmela Fusco, Barbara Mandriani, Martina Di Rienzo, et al.
Genes|July 27, 2024
Phenotypic Expansion of Autosomal Dominant <i>LZTR1</i>-Related Disorders with Special Emphasis on Adult-Onset FeaturesVera Uliana, Enrico Ambrosini, Antonietta Taiani, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 28, 2020
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A > G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagyLucia Micale, Silvia Morlino, Tommaso Biagini, et al.
Molecular Genetics and Metabolism|May 27, 2026
A splice-altering intronic variant in two multiplex families refines autosomal recessive COG4-related congenital disorder of glycosylationLucia Micale, Luisa Sturiale, Federica Russo, et al.
Cancer Letters|January 7, 2020
TRIM8 interacts with KIF11 and KIFC1 and controls bipolar spindle formation and chromosomal stabilitySantina Venuto, Laura Monteonofrio, Flora Cozzolino, et al.
Developmental Cell|March 17, 2010
Morgana/chp-1, a ROCK inhibitor involved in centrosome duplication and tumorigenesisRoberta Ferretti, Valeria Palumbo, Augusta Di Savino, et al.
Blood Cells, Molecules & Diseases|September 28, 2011
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?Lucia Micale, Bartolomeo Augello, Giulia Daniele, et al.
BMC Cancer|June 17, 2015
TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survivalLucia Micale, Carmela Fusco, Andrea Fontana, et al.
European Journal of Human Genetics : EJHG|December 12, 2024
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomaliesLucia Micale, Aikaterini Vourlia, Carmela Fusco, et al.
Pageof 8

Showing results (51-60 of 72) with videos related to

Sort By:
Pageof 8
Human Mutation|June 29, 2019
TAB2 c.1398dup variant leads to haploinsufficiency and impairs extracellular matrix homeostasisSilvia Morlino, Annalucia Carbone, Marco Ritelli, et al.
Biochimica Et Biophysica Acta. Molecular Cell Research|April 1, 2018
TRIM50 regulates Beclin 1 proautophagic activityCarmela Fusco, Barbara Mandriani, Martina Di Rienzo, et al.
Genes|July 27, 2024
Phenotypic Expansion of Autosomal Dominant <i>LZTR1</i>-Related Disorders with Special Emphasis on Adult-Onset FeaturesVera Uliana, Enrico Ambrosini, Antonietta Taiani, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 28, 2020
Insights into the molecular pathogenesis of cardiospondylocarpofacial syndrome: MAP3K7 c.737-7A > G variant alters the TGFβ-mediated α-SMA cytoskeleton assembly and autophagyLucia Micale, Silvia Morlino, Tommaso Biagini, et al.
Molecular Genetics and Metabolism|May 27, 2026
A splice-altering intronic variant in two multiplex families refines autosomal recessive COG4-related congenital disorder of glycosylationLucia Micale, Luisa Sturiale, Federica Russo, et al.
Cancer Letters|January 7, 2020
TRIM8 interacts with KIF11 and KIFC1 and controls bipolar spindle formation and chromosomal stabilitySantina Venuto, Laura Monteonofrio, Flora Cozzolino, et al.
Developmental Cell|March 17, 2010
Morgana/chp-1, a ROCK inhibitor involved in centrosome duplication and tumorigenesisRoberta Ferretti, Valeria Palumbo, Augusta Di Savino, et al.
Blood Cells, Molecules & Diseases|September 28, 2011
Amplification of the G allele at SNP rs6983267 in 8q24 amplicons in myeloid malignancies as cause of the lack of MYC overexpression?Lucia Micale, Bartolomeo Augello, Giulia Daniele, et al.
BMC Cancer|June 17, 2015
TRIM8 downregulation in glioma affects cell proliferation and it is associated with patients survivalLucia Micale, Carmela Fusco, Andrea Fontana, et al.
European Journal of Human Genetics : EJHG|December 12, 2024
Heterozygous variants disrupting the interaction of ERF with activated ERK1/2 cause microcephaly, developmental delay, and skeletal anomaliesLucia Micale, Aikaterini Vourlia, Carmela Fusco, et al.
Pageof 8