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Molecular Medicine (Cambridge, Mass.)
|
March 5, 2010
Galectin-1 and its involvement in hepatocellular carcinoma aggressiveness
Daniela Spano, Roberta Russo, Vittorio Di Maso, et al.
Analytical Chemistry
|
May 25, 2018
Label-Free Optical Marker for Red-Blood-Cell Phenotyping of Inherited Anemias
Martina Mugnano, Pasquale Memmolo, Lisa Miccio, et al.
Clinical Chemistry and Laboratory Medicine
|
October 7, 2009
SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cells
Marcello Persico, Roberta Russo, Eliana Persico, et al.
Frontiers in Genetics
|
November 28, 2022
Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participants
Stefania Martone, Autilia Tommasina Buonagura, Roberta Marra, et al.
Journal of the American Heart Association
|
June 18, 2013
Relationship between platelet and urinary 8-Iso-PGF2α levels in subjects with different degrees of NOX2 regulation
Roberto Carnevale, Luigi Iuliano, Cristina Nocella, et al.
Environmental Research
|
April 5, 2026
Antarctic threats: anthropogenic microfibers and plasticizers in the scallop Adamussium colbecki from the Ross Sea
Emma Ferrari, Maria Vittoria Barbieri, Roberta Russo, et al.
Frontiers in Physiology
|
August 28, 2020
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein
Roberta Russo, Roberta Marra, Immacolata Andolfo, et al.
Frontiers in Physiology
|
June 14, 2019
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein
Roberta Russo, Roberta Marra, Immacolata Andolfo, et al.
American Journal of Hematology
|
November 18, 2024
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosis
Barbara Eleni Rosato, Vanessa D'Onofrio, Roberta Marra, et al.
American Journal of Hematology
|
August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population
Roberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
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of 17
Search research articles
Search
Showing results (101-110 of 169) with videos related to
Sort By:
Page
of 17
Molecular Medicine (Cambridge, Mass.)
|
March 5, 2010
Galectin-1 and its involvement in hepatocellular carcinoma aggressiveness
Daniela Spano, Roberta Russo, Vittorio Di Maso, et al.
Analytical Chemistry
|
May 25, 2018
Label-Free Optical Marker for Red-Blood-Cell Phenotyping of Inherited Anemias
Martina Mugnano, Pasquale Memmolo, Lisa Miccio, et al.
Clinical Chemistry and Laboratory Medicine
|
October 7, 2009
SOCS3 and IRS-1 gene expression differs between genotype 1 and genotype 2 hepatitis C virus-infected HepG2 cells
Marcello Persico, Roberta Russo, Eliana Persico, et al.
Frontiers in Genetics
|
November 28, 2022
Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participants
Stefania Martone, Autilia Tommasina Buonagura, Roberta Marra, et al.
Journal of the American Heart Association
|
June 18, 2013
Relationship between platelet and urinary 8-Iso-PGF2α levels in subjects with different degrees of NOX2 regulation
Roberto Carnevale, Luigi Iuliano, Cristina Nocella, et al.
Environmental Research
|
April 5, 2026
Antarctic threats: anthropogenic microfibers and plasticizers in the scallop Adamussium colbecki from the Ross Sea
Emma Ferrari, Maria Vittoria Barbieri, Roberta Russo, et al.
Frontiers in Physiology
|
August 28, 2020
Corrigendum: Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein
Roberta Russo, Roberta Marra, Immacolata Andolfo, et al.
Frontiers in Physiology
|
June 14, 2019
Characterization of Two Cases of Congenital Dyserythropoietic Anemia Type I Shed Light on the Uncharacterized C15orf41 Protein
Roberta Russo, Roberta Marra, Immacolata Andolfo, et al.
American Journal of Hematology
|
November 18, 2024
RAS signaling pathway is essential in regulating PIEZO1-mediated hepatic iron overload in dehydrated hereditary stomatocytosis
Barbara Eleni Rosato, Vanessa D'Onofrio, Roberta Marra, et al.
American Journal of Hematology
|
August 19, 2011
Two founder mutations in the SEC23B gene account for the relatively high frequency of CDA II in the Italian population
Roberta Russo, Antonella Gambale, Maria Rosaria Esposito, et al.
Page
of 17