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Giuseppe Merla

Showing results (21-30 of 129) with videos related to

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Journal of Cancer|May 22, 2023
<i>In Vitro</i> Effects of Low-energy Ultrasound Treatment on Healthy CD3/CD8+ Lymphocytes, Red blood cells, Acute Myeloid leukemia cells, and Jurkat cell lineFrancesco De Leonardis, Simona Nicole Barile, Claudia Cianci, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligaseLucia Micale, Carmela Fusco, Bartolomeo Augello, et al.
American Journal of Human Genetics|July 11, 2006
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genesGiuseppe Merla, Cédric Howald, Charlotte N Henrichsen, et al.
Journal of Biomedicine & Biotechnology|February 11, 2010
VHL frameshift mutation as target of nonsense-mediated mRNA decay in Drosophila melanogaster and human HEK293 cell lineLucia Micale, Lucia Anna Muscarella, Marco Marzulli, et al.
Molecular Genetics and Metabolism|October 25, 2011
Chromosomal 17p13.3 microdeletion unmasking recessive Canavan disease mutationMariarosaria Cozzolino, Bartolomeo Augello, Massimo Carella, et al.
Genetic Testing and Molecular Biomarkers|July 17, 2009
GPR143 mutational analysis in two Italian families with X-linked ocular albinismLucia Micale, Bartolomeo Augello, Carmela Fusco, et al.
Epigenetics & Chromatin|April 17, 2026
Loss of maternal PADI6 disrupts DNA methylation and genomic imprinting maintenance in late preimplantation mouse embryosCarlo Giaccari, Francesco Cecere, Angela Pagano, et al.
BMC Medical Genetics|January 30, 2014
Bronchial isomerism in a Kabuki syndrome patient with a novel mutation in MLL2 geneGerarda Cappuccio, Alessandro Rossi, Paolo Fontana, et al.
International Journal of Molecular Sciences|September 21, 2017
Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the LiteraturePaolo Prontera, Daniela Rogaia, Amedea Mencarelli, et al.
Journal of Pediatric Genetics|May 13, 2017
A New Split Hand/Foot Malformation with Long Bone Deficiency Familial CaseCarmela Fusco, Pasquelena De Nittis, Ali Abdullah Alfaiz, et al.
Pageof 13

Showing results (21-30 of 129) with videos related to

Sort By:
Pageof 13
Journal of Cancer|May 22, 2023
<i>In Vitro</i> Effects of Low-energy Ultrasound Treatment on Healthy CD3/CD8+ Lymphocytes, Red blood cells, Acute Myeloid leukemia cells, and Jurkat cell lineFrancesco De Leonardis, Simona Nicole Barile, Claudia Cianci, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligaseLucia Micale, Carmela Fusco, Bartolomeo Augello, et al.
American Journal of Human Genetics|July 11, 2006
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genesGiuseppe Merla, Cédric Howald, Charlotte N Henrichsen, et al.
Journal of Biomedicine & Biotechnology|February 11, 2010
VHL frameshift mutation as target of nonsense-mediated mRNA decay in Drosophila melanogaster and human HEK293 cell lineLucia Micale, Lucia Anna Muscarella, Marco Marzulli, et al.
Molecular Genetics and Metabolism|October 25, 2011
Chromosomal 17p13.3 microdeletion unmasking recessive Canavan disease mutationMariarosaria Cozzolino, Bartolomeo Augello, Massimo Carella, et al.
Genetic Testing and Molecular Biomarkers|July 17, 2009
GPR143 mutational analysis in two Italian families with X-linked ocular albinismLucia Micale, Bartolomeo Augello, Carmela Fusco, et al.
Epigenetics & Chromatin|April 17, 2026
Loss of maternal PADI6 disrupts DNA methylation and genomic imprinting maintenance in late preimplantation mouse embryosCarlo Giaccari, Francesco Cecere, Angela Pagano, et al.
BMC Medical Genetics|January 30, 2014
Bronchial isomerism in a Kabuki syndrome patient with a novel mutation in MLL2 geneGerarda Cappuccio, Alessandro Rossi, Paolo Fontana, et al.
International Journal of Molecular Sciences|September 21, 2017
Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the LiteraturePaolo Prontera, Daniela Rogaia, Amedea Mencarelli, et al.
Journal of Pediatric Genetics|May 13, 2017
A New Split Hand/Foot Malformation with Long Bone Deficiency Familial CaseCarmela Fusco, Pasquelena De Nittis, Ali Abdullah Alfaiz, et al.
Pageof 13