scispace - formally typeset
M

Maurilio Sampaolesi

Researcher at Katholieke Universiteit Leuven

Publications -  207
Citations -  11644

Maurilio Sampaolesi is an academic researcher from Katholieke Universiteit Leuven. The author has contributed to research in topics: Stem cell & Skeletal muscle. The author has an hindex of 44, co-authored 186 publications receiving 10533 citations. Previous affiliations of Maurilio Sampaolesi include University of Rome Tor Vergata & Seattle Children's Research Institute.

Papers
More filters
Journal ArticleDOI

Tie2 identifies a hematopoietic lineage of proangiogenic monocytes required for tumor vessel formation and a mesenchymal population of pericyte progenitors.

TL;DR: It is demonstrated that monocytes expressing the Tie2 receptor (Tie2-expressing monocytes [TEMs]) are a distinct hematopoietic lineage of proangiogenic cells that are selectively recruited to spontaneous and orthotopic tumors and promote angiogenesis in a paracrine manner.
Journal ArticleDOI

Mesoangioblast stem cells ameliorate muscle function in dystrophic dogs.

TL;DR: It is reported that intra-arterial delivery of wild-type canine mesoangioblasts (vessel-associated stem cells) results in an extensive recovery of dystrophin expression, normal muscle morphology and function, and a remarkable clinical amelioration and preservation of active motility.
Journal ArticleDOI

Cell Therapy of α-Sarcoglycan Null Dystrophic Mice Through Intra-Arterial Delivery of Mesoangioblasts

TL;DR: In this paper, the authors used wild-type mesoangioblasts, a class of vessel-associated stem cells, to correct morphologically and functionally the dystrophic phenotype of virtually all downstream muscles in adult immunocompetent α-sarcoglycan null mice.
Journal ArticleDOI

Human postnatal dental pulp cells co-differentiate into osteoblasts and endotheliocytes: a pivotal synergy leading to adult bone tissue formation.

TL;DR: This study provides direct evidence to suggest that osteogenesis and angiogenesis mediated by human SBP-DPSCs may be regulated by distinct mechanisms, leading to the organization of adult bone tissue after stem cell transplantion.