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Garavelli

Showing results (561-570 of 610) with videos related to

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Immunity|May 18, 2021
Signals of pseudo-starvation unveil the amino acid transporter SLC7A11 as key determinant in the control of Treg cell proliferative potentialClaudio Procaccini, Silvia Garavelli, Fortunata Carbone, et al.
Journal of Intellectual Disability Research : JIDR|October 20, 2025
Transition From Children's to Adults' Healthcare for Youth With (Genetic) Intellectual Disabilities: An ERN-ITHACA GuidelineMirthe J Klein Haneveld, Katarzyna Świeczkowska, Tomasz Grybek, et al.
Molecular Cell|November 19, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brainSanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
American Journal of Medical Genetics. Part A|October 12, 2020
Expanding the phenotype of Wiedemann-Steiner syndrome: Craniovertebral junction anomaliesSara Giangiobbe, Stefano Giuseppe Caraffi, Ivan Ivanovski, et al.
Molecular Cell|October 12, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brainSanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
Bioinformatics (Oxford, England)|April 6, 2021
UniRule: a unified rule resource for automatic annotation in the UniProt KnowledgebaseAlistair MacDougall, Vladimir Volynkin, Rabie Saidi, et al.
Clinical Genetics|December 17, 2015
Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk predictionI Parenti, C Gervasini, J Pozojevic, et al.
Bioinformatics (Oxford, England)|May 14, 2020
UniRule: a unified rule resource for automatic annotation in the UniProt KnowledgebaseAlistair MacDougall, Vladimir Volynkin, Rabie Saidi, et al.
Epilepsy & Behavior : E&B|October 7, 2021
Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individualsEmilia Ricci, Anna Fetta, Livia Garavelli, et al.
Kidney International|February 25, 2017
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosisViviana Palazzo, Aldesia Provenzano, Francesca Becherucci, et al.
Pageof 61

Showing results (561-570 of 610) with videos related to

Sort By:
Pageof 61
Immunity|May 18, 2021
Signals of pseudo-starvation unveil the amino acid transporter SLC7A11 as key determinant in the control of Treg cell proliferative potentialClaudio Procaccini, Silvia Garavelli, Fortunata Carbone, et al.
Journal of Intellectual Disability Research : JIDR|October 20, 2025
Transition From Children's to Adults' Healthcare for Youth With (Genetic) Intellectual Disabilities: An ERN-ITHACA GuidelineMirthe J Klein Haneveld, Katarzyna Świeczkowska, Tomasz Grybek, et al.
Molecular Cell|November 19, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brainSanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
American Journal of Medical Genetics. Part A|October 12, 2020
Expanding the phenotype of Wiedemann-Steiner syndrome: Craniovertebral junction anomaliesSara Giangiobbe, Stefano Giuseppe Caraffi, Ivan Ivanovski, et al.
Molecular Cell|October 12, 2021
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brainSanxiong Liu, Kimberly A Aldinger, Chi Vicky Cheng, et al.
Bioinformatics (Oxford, England)|April 6, 2021
UniRule: a unified rule resource for automatic annotation in the UniProt KnowledgebaseAlistair MacDougall, Vladimir Volynkin, Rabie Saidi, et al.
Clinical Genetics|December 17, 2015
Expanding the clinical spectrum of the 'HDAC8-phenotype' - implications for molecular diagnostics, counseling and risk predictionI Parenti, C Gervasini, J Pozojevic, et al.
Bioinformatics (Oxford, England)|May 14, 2020
UniRule: a unified rule resource for automatic annotation in the UniProt KnowledgebaseAlistair MacDougall, Vladimir Volynkin, Rabie Saidi, et al.
Epilepsy & Behavior : E&B|October 7, 2021
Further delineation and long-term evolution of electroclinical phenotype in Mowat Wilson Syndrome. A longitudinal study in 40 individualsEmilia Ricci, Anna Fetta, Livia Garavelli, et al.
Kidney International|February 25, 2017
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosisViviana Palazzo, Aldesia Provenzano, Francesca Becherucci, et al.
Pageof 61