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Francesca Avemaria

Showing results (1-10 of 14) with videos related to

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Bio-Protocol|August 30, 2021
VLA-4 Affinity Assay for Murine Bone Marrow-derived Hematopoietic Stem CellsFrancesca Avemaria, Shiri Gur-Cohen, Seymen Avci, et al.
Bio-Protocol|August 30, 2021
Adhesion Assay for Murine Bone Marrow Hematopoietic Stem CellsSeymen Avci, Shiri Gur-Cohen, Francesca Avemaria, et al.
Neurobiology of Aging|March 9, 2012
Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subjectLorena Mosca, Christian Lunetta, Claudia Tarlarini, et al.
BMJ Open Diabetes Research & Care|May 30, 2020
Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DMGiovanni Sartore, Eugenio Ragazzi, Silvia Burlina, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 29, 2011
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progressionFrancesca Avemaria, Christian Lunetta, Claudia Tarlarini, et al.
Journal of Molecular Neuroscience : MN|December 2, 2010
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex diseaseSilvana Penco, Christian Lunetta, Lorena Mosca, et al.
Clinical Chemistry and Laboratory Medicine|September 10, 2015
Possible role of fructosamine 3-kinase genotyping for the management of diabetic patientsFrancesca Avemaria, Paola Carrera, Annunziata Lapolla, et al.
Journal of Molecular Neuroscience : MN|March 15, 2012
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformationsLorena Mosca, Silvana Pileggi, Francesca Avemaria, et al.
Hemasphere|January 17, 2020
PAR1 Expression Predicts Clinical G-CSF CD34<sup>+</sup> HSPC Mobilization and Repopulation Potential in Transplanted PatientsNeta Nevo, Tsila Zuckerman, Shiri Gur-Cohen, et al.
Leukemia|March 3, 2021
Enhanced thrombin/PAR1 activity promotes G-CSF- and AMD3100-induced mobilization of hematopoietic stem and progenitor cells via NO upregulationNeta Nevo, Lizeth-Alejandra Ordonez-Moreno, Shiri Gur-Cohen, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Bio-Protocol|August 30, 2021
VLA-4 Affinity Assay for Murine Bone Marrow-derived Hematopoietic Stem CellsFrancesca Avemaria, Shiri Gur-Cohen, Seymen Avci, et al.
Bio-Protocol|August 30, 2021
Adhesion Assay for Murine Bone Marrow Hematopoietic Stem CellsSeymen Avci, Shiri Gur-Cohen, Francesca Avemaria, et al.
Neurobiology of Aging|March 9, 2012
Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subjectLorena Mosca, Christian Lunetta, Claudia Tarlarini, et al.
BMJ Open Diabetes Research & Care|May 30, 2020
Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DMGiovanni Sartore, Eugenio Ragazzi, Silvia Burlina, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|March 29, 2011
Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progressionFrancesca Avemaria, Christian Lunetta, Claudia Tarlarini, et al.
Journal of Molecular Neuroscience : MN|December 2, 2010
Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex diseaseSilvana Penco, Christian Lunetta, Lorena Mosca, et al.
Clinical Chemistry and Laboratory Medicine|September 10, 2015
Possible role of fructosamine 3-kinase genotyping for the management of diabetic patientsFrancesca Avemaria, Paola Carrera, Annunziata Lapolla, et al.
Journal of Molecular Neuroscience : MN|March 15, 2012
De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformationsLorena Mosca, Silvana Pileggi, Francesca Avemaria, et al.
Hemasphere|January 17, 2020
PAR1 Expression Predicts Clinical G-CSF CD34<sup>+</sup> HSPC Mobilization and Repopulation Potential in Transplanted PatientsNeta Nevo, Tsila Zuckerman, Shiri Gur-Cohen, et al.
Leukemia|March 3, 2021
Enhanced thrombin/PAR1 activity promotes G-CSF- and AMD3100-induced mobilization of hematopoietic stem and progenitor cells via NO upregulationNeta Nevo, Lizeth-Alejandra Ordonez-Moreno, Shiri Gur-Cohen, et al.
Pageof 2