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Showing results (451-460 of 566) with videos related to

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Cardiovascular Research|September 11, 2019
Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1Giovanni Cimmino, Plinio Cirillo, Stefano Conte, et al.
Nature Plants|June 12, 2019
A chloroplast-localized mitochondrial calcium uniporter transduces osmotic stress in ArabidopsisEnrico Teardo, Luca Carraretto, Roberto Moscatiello, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 26, 2018
Risk factors for abnormally invasive placenta: a systematic review and meta-analysisAntonia Iacovelli, Marco Liberati, Asma Khalil, et al.
Human Genetics|September 1, 1997
The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samplesF Calì, I Dianzani, L R Desviat, et al.
Nature Communications|March 29, 2023
Real-time insight into the multistage mechanism of nanoparticle exsolution from a perovskite host surfaceEleonora Calì, Melonie P Thomas, Rama Vasudevan, et al.
American Journal of Medical Genetics. Part A|November 16, 2019
Delayed appearance of 3-methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosisAnwar Baban, Rachele Adorisio, Bernadette Corica, et al.
Genes|January 21, 2023
Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature ReviewFlaminia Pugnaloni, Roberta Onesimo, Rita Blandino, et al.
Biomolecules|November 27, 2024
Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic DiagnosticsMaria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, et al.
Genes|December 23, 2023
The Cardiofaciocutaneous Syndrome: From Genetics to Prognostic-Therapeutic ImplicationsGiovanna Scorrano, Emanuele David, Elisa Calì, et al.
Journal of Molecular Neuroscience : MN|June 11, 2026
A de novo Loss-of-function Variant in RAPGEF6 Supports its Role in Neuropsychiatric DisordersSimone Treccarichi, Mirella Vinci, Maria Grazia Figura, et al.
Pageof 57

Showing results (451-460 of 566) with videos related to

Sort By:
Pageof 57
Cardiovascular Research|September 11, 2019
Oxidized low-density lipoproteins induce tissue factor expression in T-lymphocytes via activation of lectin-like oxidized low-density lipoprotein receptor-1Giovanni Cimmino, Plinio Cirillo, Stefano Conte, et al.
Nature Plants|June 12, 2019
A chloroplast-localized mitochondrial calcium uniporter transduces osmotic stress in ArabidopsisEnrico Teardo, Luca Carraretto, Roberto Moscatiello, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 26, 2018
Risk factors for abnormally invasive placenta: a systematic review and meta-analysisAntonia Iacovelli, Marco Liberati, Asma Khalil, et al.
Human Genetics|September 1, 1997
The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samplesF Calì, I Dianzani, L R Desviat, et al.
Nature Communications|March 29, 2023
Real-time insight into the multistage mechanism of nanoparticle exsolution from a perovskite host surfaceEleonora Calì, Melonie P Thomas, Rama Vasudevan, et al.
American Journal of Medical Genetics. Part A|November 16, 2019
Delayed appearance of 3-methylglutaconic aciduria in neonates with early onset metabolic cardiomyopathies: A potential pitfall for the diagnosisAnwar Baban, Rachele Adorisio, Bernadette Corica, et al.
Genes|January 21, 2023
Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature ReviewFlaminia Pugnaloni, Roberta Onesimo, Rita Blandino, et al.
Biomolecules|November 27, 2024
Copy Number Variants in Cardiac Channelopathies: Still a Missed Part in Routine Arrhythmic DiagnosticsMaria Gnazzo, Giovanni Parlapiano, Francesca Di Lorenzo, et al.
Genes|December 23, 2023
The Cardiofaciocutaneous Syndrome: From Genetics to Prognostic-Therapeutic ImplicationsGiovanna Scorrano, Emanuele David, Elisa Calì, et al.
Journal of Molecular Neuroscience : MN|June 11, 2026
A de novo Loss-of-function Variant in RAPGEF6 Supports its Role in Neuropsychiatric DisordersSimone Treccarichi, Mirella Vinci, Maria Grazia Figura, et al.
Pageof 57