List of works - Vincenzo Zappavigna

An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function

scientific article (publication date: April 2003)

An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning

scientific article published on 27 February 2012

Cup is a nucleocytoplasmic shuttling protein that interacts with the eukaryotic translation initiation factor 4E to modulate Drosophila ovary development.

scholarly article

Differential and stage-related expression in embryonic tissues of a new human homoeobox gene

scientific article

Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers

scientific article

HOXD13 binds DNA replication origins to promote origin licensing and is inhibited by geminin

scientific article

Hoxd13 and Hoxa13 directly control the expression of the EphA7 Ephrin tyrosine kinase receptor in developing limbs

scientific journal article

Hoxd13 binds in vivo and regulates the expression of genes acting in key pathways for early limb and skeletal patterning.

scientific article

Identification of a conserved 125 base-pair Hb9 enhancer that specifies gene expression to spinal motor neurons.

scientific article published in July 2005

Inhibition of retinoic acid-induced activation of 3' human HOXB genes by antisense oligonucleotides affects sequential activation of genes located upstream in the four HOX clusters.

scientific article

Integration of anteroposterior and dorsoventral regulation of Phox2b transcription in cranial motoneuron progenitors by homeodomain proteins.

scientific article

MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1

scientific article

MafB is a downstream target of the IL-10/STAT3 signaling pathway, involved in the regulation of macrophage de-activation

scientific article published on 25 January 2014

NUP98 fusion oncoproteins promote aneuploidy by attenuating the mitotic spindle checkpoint

scientific article published on 26 December 2013

PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain.

scientific article

Prep1, a novel functional partner of Pbx proteins.

scientific article

Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1.

scientific article

The Orosomucoid 1 protein is involved in the vitamin D - mediated macrophage de-activation process

scientific article

The recruitment of SOX/OCT complexes and the differential activity of HOXA1 and HOXB1 modulate the Hoxb1 auto-regulatory enhancer function

scientific article (publication date: 8 June 2001)

The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH

scientific article

Translational regulation during oogenesis and early development: the cap-poly(A) tail relationship.

scientific article

Two human homeobox genes, c1 and c8: structure analysis and expression in embryonic development

scientific article

Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development

scientific article

List of works by Vincenzo Zappavigna

An I47L substitution in the HOXD13 homeodomain causes a novel human limb malformation by producing a selective loss of function

An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning

Cup is a nucleocytoplasmic shuttling protein that interacts with the eukaryotic translation initiation factor 4E to modulate Drosophila ovary development.

Differential and stage-related expression in embryonic tissues of a new human homoeobox gene

Emx2 is a dose-dependent negative regulator of Sox2 telencephalic enhancers

HOXD13 binds DNA replication origins to promote origin licensing and is inhibited by geminin

Hoxd13 and Hoxa13 directly control the expression of the EphA7 Ephrin tyrosine kinase receptor in developing limbs

Hoxd13 binds in vivo and regulates the expression of genes acting in key pathways for early limb and skeletal patterning.

Identification of a conserved 125 base-pair Hb9 enhancer that specifies gene expression to spinal motor neurons.

Inhibition of retinoic acid-induced activation of 3' human HOXB genes by antisense oligonucleotides affects sequential activation of genes located upstream in the four HOX clusters.

Integration of anteroposterior and dorsoventral regulation of Phox2b transcription in cranial motoneuron progenitors by homeodomain proteins.

MAB21L2, a vertebrate member of the Male-abnormal 21 family, modulates BMP signaling and interacts with SMAD1

MafB is a downstream target of the IL-10/STAT3 signaling pathway, involved in the regulation of macrophage de-activation

NUP98 fusion oncoproteins promote aneuploidy by attenuating the mitotic spindle checkpoint

PBX1 nuclear export is regulated independently of PBX-MEINOX interaction by PKA phosphorylation of the PBC-B domain.

Prep1, a novel functional partner of Pbx proteins.

Scapula development is governed by genetic interactions of Pbx1 with its family members and with Emx2 via their cooperative control of Alx1.

The Orosomucoid 1 protein is involved in the vitamin D - mediated macrophage de-activation process

The recruitment of SOX/OCT complexes and the differential activity of HOXA1 and HOXB1 modulate the Hoxb1 auto-regulatory enhancer function

The subcellular localization of PBX1 and EXD proteins depends on nuclear import and export signals and is modulated by association with PREP1 and HTH

Translational regulation during oogenesis and early development: the cap-poly(A) tail relationship.

Two human homeobox genes, c1 and c8: structure analysis and expression in embryonic development

Two murine and human homologs of mab-21, a cell fate determination gene involved in Caenorhabditis elegans neural development