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Gustavo J. Melen

Researcher at Autonomous University of Madrid

Publications -  41
Citations -  1474

Gustavo J. Melen is an academic researcher from Autonomous University of Madrid. The author has contributed to research in topics: Mesenchymal stem cell & Oncolytic virus. The author has an hindex of 20, co-authored 41 publications receiving 1293 citations. Previous affiliations of Gustavo J. Melen include University of Granada & Menéndez Pelayo International University.

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Embryonic stem cell-specific miR302-367 cluster: human gene structure and functional characterization of its core promoter.

TL;DR: This study represents the first identification, characterization, and functional validation of a human miRNA promoter in stem cells and opens up new avenues to further investigate the upstream transcriptional regulation of the miR302-367 cluster.
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Bone marrow mesenchymal stem cells from infants with MLL-AF4+ acute leukemia harbor and express the MLL-AF4 fusion gene

TL;DR: The absence of monoclonal rearrangements in MLL-AF4+ BM-MSCs precludes the possibility of cellular plasticity or de-differentiation of B-ALL blasts and suggests that MLL -AF4 might arise in a population of prehematopoietic precursors.
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Threshold responses to morphogen gradients by zero‐order ultrasensitivity

TL;DR: It is proposed that a reversible loop of Yan phosphorylation implements a zero‐order ultrasensitivity‐like threshold mechanism, with the capacity to form sharp thresholds that are independent of the level of Yan.
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Coordination between transcription and pre-mRNA processing.

TL;DR: The presence and degree of phosphorylation of the carboxy‐terminal domain of RNA polymerase II large subunit is important for functioning of the capping enzymes, the assembly of spliceosomes and the binding of the cleavage/polyadenylation complex.
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Feeder-free maintenance of hESCs in mesenchymal stem cell-conditioned media: distinct requirements for TGF-beta and IGF-II.

TL;DR: In this article, a paracrine regulation was proposed in human embryonic stem cells (hESCs) grown in MEF-conditioned media (MEF-CM), where hESCs spontaneously differentiate into autologous fibroblast-like cells to maintain culture homeostasis by producing TGF-beta and insulin-like growth factor-II (IGF-II) in response to basic fibroblasts growth factor (bFGF).