about
Cytogenetic and molecular characterization of a de-novo t(2p;7p) translocation involving TNS3 and EXOC6B genes in a boy with a complex syndromic phenotype.SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement.De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay.Potential neoplastic evolution of Vero cells: in vivo and in vitro characterization.Gemcitabine-releasing mesenchymal stromal cells inhibit in vitro proliferation of human pancreatic carcinoma cells.Role of Dopamine D2/D3 Receptors in Development, Plasticity, and Neuroprotection in Human iPSC-Derived Midbrain Dopaminergic Neurons.Molecular and cytogenetic characterization of extra-structurally abnormal chromosomes (ESACs) found prenatally: outcome and follow-up.Cultured human amniocytes express hTERT, which is distributed between nucleus and cytoplasm and is secreted in extracellular vesicles.Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.Biological and chemical selection of Ph-negative clones.ITGB2 mutation combined with deleted ring 21 chromosome in a child with leukocyte adhesion deficiencyFractionation of chronic myelogenous leukemia marrow cells by stroma adherence: implications for marrow purging
P50
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P50
description
researcher ORCID ID = 0000-0003-0001-6435
@en
wetenschapper
@nl
name
Giovanna Piovani
@ast
Giovanna Piovani
@en
Giovanna Piovani
@es
Giovanna Piovani
@nl
type
label
Giovanna Piovani
@ast
Giovanna Piovani
@en
Giovanna Piovani
@es
Giovanna Piovani
@nl
prefLabel
Giovanna Piovani
@ast
Giovanna Piovani
@en
Giovanna Piovani
@es
Giovanna Piovani
@nl
P106
P1153
57190028386
6603043758
P21
P31
P496
0000-0003-0001-6435