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Roberta Russo

Showing results (81-90 of 169) with videos related to

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Journal of Human Genetics|June 11, 2010
MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thicknessMario Capasso, Fabrizio Ayala, Rosa Anna Avvisati, et al.
Advances in Microbial Physiology|September 24, 2013
The globins of cold-adapted Pseudoalteromonas haloplanktis TAC125: from the structure to the physiological functionsDaniela Giordano, Daniela Coppola, Roberta Russo, et al.
American Journal of Hematology|August 11, 2019
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variantImmacolata Andolfo, Barbara Eleni Rosato, Roberta Marra, et al.
International Journal of Molecular Sciences|February 15, 2022
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic CellsBarbara Eleni Rosato, Roberta Marra, Vanessa D'Onofrio, et al.
Genes|January 26, 2024
First Case of a Dominant De Novo <i>SEC23A</i> Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature ReviewElia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, et al.
Blood Cells, Molecules & Diseases|March 5, 2013
Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type IIRoberta Russo, Concetta Langella, Maria Rosaria Esposito, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 27, 2018
Stuttering as a matter of delay in neural activation: A combined TMS/EEG studyPierpaolo Busan, Giovanni Del Ben, Lucia Roberta Russo, et al.
American Journal of Hematology|November 19, 2019
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathwayImmacolata Andolfo, Barbara Eleni Rosato, Francesco Manna, et al.
Hemoglobin|November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chainLoïc Garçon, Achille Iolascon, Serge Pissard, et al.
Frontiers in Physiology|October 2, 2019
CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic AnemiaCristian Tornador, Edgar Sánchez-Prados, Beatriz Cadenas, et al.
Pageof 17

Showing results (81-90 of 169) with videos related to

Sort By:
Pageof 17
Journal of Human Genetics|June 11, 2010
MDM2 SNP309 and p53 Arg72Pro in cutaneous melanoma: association between SNP309 GG genotype and tumor Breslow thicknessMario Capasso, Fabrizio Ayala, Rosa Anna Avvisati, et al.
Advances in Microbial Physiology|September 24, 2013
The globins of cold-adapted Pseudoalteromonas haloplanktis TAC125: from the structure to the physiological functionsDaniela Giordano, Daniela Coppola, Roberta Russo, et al.
American Journal of Hematology|August 11, 2019
The BMP-SMAD pathway mediates the impaired hepatic iron metabolism associated with the ERFE-A260S variantImmacolata Andolfo, Barbara Eleni Rosato, Roberta Marra, et al.
International Journal of Molecular Sciences|February 15, 2022
SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic CellsBarbara Eleni Rosato, Roberta Marra, Vanessa D'Onofrio, et al.
Genes|January 26, 2024
First Case of a Dominant De Novo <i>SEC23A</i> Mutation with Neurological and Psychiatric Features: New Insights into Cranio-Lenticulo-Sutural Dysplasia with Literature ReviewElia Marco Paolo Minale, Alessandro De Falco, Emanuele Agolini, et al.
Blood Cells, Molecules & Diseases|March 5, 2013
Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type IIRoberta Russo, Concetta Langella, Maria Rosaria Esposito, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 27, 2018
Stuttering as a matter of delay in neural activation: A combined TMS/EEG studyPierpaolo Busan, Giovanni Del Ben, Lucia Roberta Russo, et al.
American Journal of Hematology|November 19, 2019
Gain-of-function mutations in PIEZO1 directly impair hepatic iron metabolism via the inhibition of the BMP/SMADs pathwayImmacolata Andolfo, Barbara Eleni Rosato, Francesco Manna, et al.
Hemoglobin|November 17, 2010
A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chainLoïc Garçon, Achille Iolascon, Serge Pissard, et al.
Frontiers in Physiology|October 2, 2019
CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic AnemiaCristian Tornador, Edgar Sánchez-Prados, Beatriz Cadenas, et al.
Pageof 17