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Tissue Engineering. Part A
|
March 21, 2009
Culture conditions allow selection of different mesenchymal progenitors from adult mouse bone marrow
Maria Teresa Esposito, Rosa Di Noto, Peppino Mirabelli, et al.
Genes
|
August 26, 2023
The Potential Usefulness of the Expanded Carrier Screening to Identify Hereditary Genetic Diseases: A Case Report from Real-World Data
Iolanda Veneruso, Annaluisa Ranieri, Noemi Falcone, et al.
Current Gene Therapy
|
January 16, 2013
Thymidine kinase-mediated shut down of bone morphogenetic protein-4 expression allows regulated bone production
Barbara Lombardo, Teresa Rocco, Maria T Esposito, et al.
Blood Reviews
|
August 28, 2022
Progress, and prospects in the therapeutic armamentarium of persons with congenital hemophilia. Defining the place for liver-directed gene therapy
Giovanni Di Minno, Giancarlo Castaman, Raimondo De Cristofaro, et al.
Cancer Research
|
February 11, 2010
A placental growth factor variant unable to recognize vascular endothelial growth factor (VEGF) receptor-1 inhibits VEGF-dependent tumor angiogenesis via heterodimerization
Valeria Tarallo, Loredana Vesci, Onofrio Capasso, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 15, 2026
Helper-dependent adenoviral vector-mediated expression of an LDL receptor/transferrin chimeric protein in muscle safely reduces atherosclerosis in LDLR-deficient mice
Maria Vitale, Filippo Scialò, Ludovica Coluccino, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 25, 2017
Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing
Gabriella Esposito, Maria Roberta Tremolaterra, Maria Savarese, et al.
Life (Basel, Switzerland)
|
August 26, 2022
Exploring the Role of Krebs von den Lungen-6 in Severe to Critical COVID-19 Patients
Vito D'Agnano, Filippo Scialò, Francesco Perna, et al.
Molecular Genetics & Genomic Medicine
|
May 13, 2020
Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome
Barbara Lombardo, Valeria D'Argenio, Emanuele Monda, et al.
Cellular Signalling
|
July 17, 2007
Endothelial beta2 adrenergic signaling to AKT: role of Gi and SRC
Michele Ciccarelli, Ersilia Cipolletta, Gaetano Santulli, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 87) with videos related to
Sort By:
Page
of 9
Tissue Engineering. Part A
|
March 21, 2009
Culture conditions allow selection of different mesenchymal progenitors from adult mouse bone marrow
Maria Teresa Esposito, Rosa Di Noto, Peppino Mirabelli, et al.
Genes
|
August 26, 2023
The Potential Usefulness of the Expanded Carrier Screening to Identify Hereditary Genetic Diseases: A Case Report from Real-World Data
Iolanda Veneruso, Annaluisa Ranieri, Noemi Falcone, et al.
Current Gene Therapy
|
January 16, 2013
Thymidine kinase-mediated shut down of bone morphogenetic protein-4 expression allows regulated bone production
Barbara Lombardo, Teresa Rocco, Maria T Esposito, et al.
Blood Reviews
|
August 28, 2022
Progress, and prospects in the therapeutic armamentarium of persons with congenital hemophilia. Defining the place for liver-directed gene therapy
Giovanni Di Minno, Giancarlo Castaman, Raimondo De Cristofaro, et al.
Cancer Research
|
February 11, 2010
A placental growth factor variant unable to recognize vascular endothelial growth factor (VEGF) receptor-1 inhibits VEGF-dependent tumor angiogenesis via heterodimerization
Valeria Tarallo, Loredana Vesci, Onofrio Capasso, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 15, 2026
Helper-dependent adenoviral vector-mediated expression of an LDL receptor/transferrin chimeric protein in muscle safely reduces atherosclerosis in LDLR-deficient mice
Maria Vitale, Filippo Scialò, Ludovica Coluccino, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 25, 2017
Unraveling unusual X-chromosome patterns during fragile-X syndrome genetic testing
Gabriella Esposito, Maria Roberta Tremolaterra, Maria Savarese, et al.
Life (Basel, Switzerland)
|
August 26, 2022
Exploring the Role of Krebs von den Lungen-6 in Severe to Critical COVID-19 Patients
Vito D'Agnano, Filippo Scialò, Francesco Perna, et al.
Molecular Genetics & Genomic Medicine
|
May 13, 2020
Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome
Barbara Lombardo, Valeria D'Argenio, Emanuele Monda, et al.
Cellular Signalling
|
July 17, 2007
Endothelial beta2 adrenergic signaling to AKT: role of Gi and SRC
Michele Ciccarelli, Ersilia Cipolletta, Gaetano Santulli, et al.
Page
of 9