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Garavelli

Showing results (491-500 of 609) with videos related to

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Neurobiology of Disease|December 1, 2025
Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitorsIlaria Musante, Giulia Gorrieri, Serena Tamburro, et al.
Frontiers in Endocrinology|July 24, 2019
Type 2 Diabetes: How Much of an Autoimmune Disease?Paola de Candia, Francesco Prattichizzo, Silvia Garavelli, et al.
Cytogenetic and Genome Research|December 10, 2015
Cryptic 13q34 and 4q35.2 Deletions in an Italian FamilyFederica Riccardi, Gianna F Rivolta, Vera Uliana, et al.
Oncotarget|July 28, 2016
Multiple myeloma-derived Jagged ligands increases autocrine and paracrine interleukin-6 expression in bone marrow nicheMichela Colombo, Serena Galletti, Gaetano Bulfamante, et al.
Journal of the American Chemical Society|December 17, 2008
Multistate photo-induced relaxation and photoisomerization ability of fumaramide threads: a computational and experimental studyPiero Altoè, Natalia Haraszkiewicz, Francesco G Gatti, et al.
Journal of Clinical Medicine|January 10, 2026
Feeding-Triggered Seizures in a Newborn with <i>AP1S1</i>-Related MEDNIK Syndrome: Expanding the Phenotype of a Hyper-Rare DiseaseAnna Cavalli, Francesca Peluso, Daniele Frattini, et al.
Nucleic Acids Research|February 21, 1998
The PIR-International Protein Sequence DatabaseW C Barker, J S Garavelli, D H Haft, et al.
Genes|October 17, 2019
Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-<i>B4GALT7</i> and Spondylodysplastic-EDS-<i>B3GALT6</i>Stefano Giuseppe Caraffi, Ilenia Maini, Ivan Ivanovski, et al.
Clinical Genetics|January 7, 2026
White-Sutton Syndrome: Insight of an Italian Cohort of 19 SubjectsAnna Facchini, Maria Pina Concas, Stefania Zampieri, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing lossPaola Primignani, Luca Trotta, Pierangela Castorina, et al.
Pageof 61

Showing results (491-500 of 609) with videos related to

Sort By:
Pageof 61
Neurobiology of Disease|December 1, 2025
Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitorsIlaria Musante, Giulia Gorrieri, Serena Tamburro, et al.
Frontiers in Endocrinology|July 24, 2019
Type 2 Diabetes: How Much of an Autoimmune Disease?Paola de Candia, Francesco Prattichizzo, Silvia Garavelli, et al.
Cytogenetic and Genome Research|December 10, 2015
Cryptic 13q34 and 4q35.2 Deletions in an Italian FamilyFederica Riccardi, Gianna F Rivolta, Vera Uliana, et al.
Oncotarget|July 28, 2016
Multiple myeloma-derived Jagged ligands increases autocrine and paracrine interleukin-6 expression in bone marrow nicheMichela Colombo, Serena Galletti, Gaetano Bulfamante, et al.
Journal of the American Chemical Society|December 17, 2008
Multistate photo-induced relaxation and photoisomerization ability of fumaramide threads: a computational and experimental studyPiero Altoè, Natalia Haraszkiewicz, Francesco G Gatti, et al.
Journal of Clinical Medicine|January 10, 2026
Feeding-Triggered Seizures in a Newborn with <i>AP1S1</i>-Related MEDNIK Syndrome: Expanding the Phenotype of a Hyper-Rare DiseaseAnna Cavalli, Francesca Peluso, Daniele Frattini, et al.
Nucleic Acids Research|February 21, 1998
The PIR-International Protein Sequence DatabaseW C Barker, J S Garavelli, D H Haft, et al.
Genes|October 17, 2019
Severe Peripheral Joint Laxity is a Distinctive Clinical Feature of Spondylodysplastic-Ehlers-Danlos Syndrome (EDS)-<i>B4GALT7</i> and Spondylodysplastic-EDS-<i>B3GALT6</i>Stefano Giuseppe Caraffi, Ilenia Maini, Ivan Ivanovski, et al.
Clinical Genetics|January 7, 2026
White-Sutton Syndrome: Insight of an Italian Cohort of 19 SubjectsAnna Facchini, Maria Pina Concas, Stefania Zampieri, et al.
Genetic Testing and Molecular Biomarkers|April 18, 2009
Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing lossPaola Primignani, Luca Trotta, Pierangela Castorina, et al.
Pageof 61