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Garavelli

Showing results (521-530 of 610) with videos related to

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Toxicology in Vitro : an International Journal Published in Association with BIBRA|August 5, 2017
[Ru(pipe)(dppb)(bipy)]PF<sub>6</sub>: A novel ruthenium complex that effectively inhibits ERK activation and cyclin D1 expression in A549 cellsGuilherme A Ferreira-Silva, Marina M Ortega, Marco A Banionis, et al.
Genes|January 21, 2022
Clinical and Genetic Findings in a Series of Eight Families with ArthrogryposisMarzia Pollazzon, Stefano Giuseppe Caraffi, Silvia Faccioli, et al.
Haematologica|October 5, 2019
Multiple myeloma exploits Jagged1 and Jagged2 to promote intrinsic and bone marrow-dependent drug resistanceMichela Colombo, Silvia Garavelli, Mara Mazzola, et al.
Journal of Inherited Metabolic Disease|June 18, 2022
ALG8-CDG: Molecular and phenotypic expansion suggests clinical management guidelinesDaniah Albokhari, Bobby G Ng, Alis Guberinic, et al.
European Journal of Human Genetics : EJHG|October 12, 2025
The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disordersKaren J Low, Julia Foreman, Rachel J Hobson, et al.
American Journal of Human Genetics|January 17, 2012
A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndromeViviana Caputo, Luciano Cianetti, Marcello Niceta, et al.
Nucleic Acids Research|January 1, 1997
The Protein Information Resource (PIR) and the PIR-International Protein Sequence DatabaseD G George, R J Dodson, J S Garavelli, et al.
Clinical Genetics|April 10, 2023
Identification of bi-allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3Mauro Lecca, Maria Francesca Bedeschi, Claudia Izzi, et al.
Nature Communications|November 13, 2023
The carbonyl-lock mechanism underlying non-aromatic fluorescence in biological matterGonzalo Díaz Mirón, Jonathan A Semelak, Luca Grisanti, et al.
Frontiers in Genetics|August 28, 2023
Case Report: Sequential postzygotic <i>HRAS</i> mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving <i>HRAS</i> in oncogenic transformationRoberta Zuntini, Chiara Cattani, Lucia Pedace, et al.
Pageof 61

Showing results (521-530 of 610) with videos related to

Sort By:
Pageof 61
Toxicology in Vitro : an International Journal Published in Association with BIBRA|August 5, 2017
[Ru(pipe)(dppb)(bipy)]PF<sub>6</sub>: A novel ruthenium complex that effectively inhibits ERK activation and cyclin D1 expression in A549 cellsGuilherme A Ferreira-Silva, Marina M Ortega, Marco A Banionis, et al.
Genes|January 21, 2022
Clinical and Genetic Findings in a Series of Eight Families with ArthrogryposisMarzia Pollazzon, Stefano Giuseppe Caraffi, Silvia Faccioli, et al.
Haematologica|October 5, 2019
Multiple myeloma exploits Jagged1 and Jagged2 to promote intrinsic and bone marrow-dependent drug resistanceMichela Colombo, Silvia Garavelli, Mara Mazzola, et al.
Journal of Inherited Metabolic Disease|June 18, 2022
ALG8-CDG: Molecular and phenotypic expansion suggests clinical management guidelinesDaniah Albokhari, Bobby G Ng, Alis Guberinic, et al.
European Journal of Human Genetics : EJHG|October 12, 2025
The LMSz method - an automatable scalable approach to constructing gene-specific growth charts in rare disordersKaren J Low, Julia Foreman, Rachel J Hobson, et al.
American Journal of Human Genetics|January 17, 2012
A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndromeViviana Caputo, Luciano Cianetti, Marcello Niceta, et al.
Nucleic Acids Research|January 1, 1997
The Protein Information Resource (PIR) and the PIR-International Protein Sequence DatabaseD G George, R J Dodson, J S Garavelli, et al.
Clinical Genetics|April 10, 2023
Identification of bi-allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3Mauro Lecca, Maria Francesca Bedeschi, Claudia Izzi, et al.
Nature Communications|November 13, 2023
The carbonyl-lock mechanism underlying non-aromatic fluorescence in biological matterGonzalo Díaz Mirón, Jonathan A Semelak, Luca Grisanti, et al.
Frontiers in Genetics|August 28, 2023
Case Report: Sequential postzygotic <i>HRAS</i> mutation and gains of the paternal chromosome 11 carrying the mutated allele in a patient with epidermal nevus and rhabdomyosarcoma: evidence of a multiple-hit mechanism involving <i>HRAS</i> in oncogenic transformationRoberta Zuntini, Chiara Cattani, Lucia Pedace, et al.
Pageof 61