about
Jaw transformation with gain of symmetry after Dlx5/Dlx6 inactivation: mirror of the past?Activation of the Wnt-beta catenin pathway in a cell population on the surface of the forebrain is essential for the establishment of olfactory axon connectionsRegulation of Dlx5 and Dlx6 gene expression by p63 is involved in EEC and SHFM congenital limb defectsThe Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathwayDefective bone formation in Krox-20 mutant miceSpatio-temporal dynamics of gene expression of the Edn1-Dlx5/6 pathway during development of the lower jawTargeted Gene Correction in Osteopetrotic-Induced Pluripotent Stem Cells for the Generation of Functional OsteoclastsPolyethylenimine-based intravenous delivery of transgenes to mouse lung.Role of Krox-20 in endochondral bone formation.BMP-mediated functional cooperation between Dlx5;Dlx6 and Msx1;Msx2 during mammalian limb developmentRole of Toll interleukin-1 receptor (IL-1R) 8, a negative regulator of IL-1R/Toll-like receptor signaling, in resistance to acute Pseudomonas aeruginosa lung infection.Intestinal microbiota sustains inflammation and autoimmunity induced by hypomorphic RAG defects.The apical ectodermal ridge of the mouse model of ectrodactyly Dlx5;Dlx6-/- shows altered stratification and cell polarity, which are restored by exogenous Wnt5a ligandFusion between cancer cells and macrophages occurs in a murine model of spontaneous neu+ breast cancer without increasing its metastatic potential.Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5.The Dlx5 homeodomain gene is essential for olfactory development and connectivity in the mouse.Hypomorphic mutation in the RAG2 gene affects dendritic cell distribution and migration.Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implications.CTLA-4 is constitutively expressed on tumor cells and can trigger apoptosis upon ligand interaction.The human antibody repertoire: heavy and light chain variable region gene usage in six alloantibodies specific for human HLA class I and class II alloantigens.Impairment of PMP22 transgenic Schwann cells differentiation in culture: implications for Charcot-Marie-Tooth type 1A disease.HLA-DR expression in conjunctival cells after latanoprost.The medico-legal observation of an aggressive urogenital fibromatosis with isolated development not related to any traumatic event.The role of Dlx homeogenes in early development of the olfactory pathway.B lymphocytes limit senescence-driven fibrosis resolution and favor hepatocarcinogenesis in mouse liver injury.Autonomous role of Wiskott-Aldrich Syndrome platelet deficiency in inducing autoimmunity and inflammation.Differential regulation of the zinc finger genes Krox-20 and Krox-24 (Egr-1) suggests antagonistic roles in Schwann cells.UHRF1 epigenetically orchestrates smooth muscle cell plasticity in arterial disease.Hyperplasia and impaired involution in the mammary gland of transgenic mice expressing human FGF4.Osteopetrosis rescue upon RANKL administration to Rankl(-/-) mice: a new therapy for human RANKL-dependent ARO.The Therapeutic Potential of the Humoral Pattern Recognition Molecule PTX3 in Chronic Lung Infection Caused by Pseudomonas aeruginosaCorrection: The Therapeutic Potential of the Humoral Pattern Recognition Molecule PTX3 in Chronic Lung Infection Caused by Pseudomonas aeruginosaEffects of cooling micrografts in hair transplantation surgeryThe role of Dlx homeogenes in early development of the olfactory pathwayMutations in the Neuroblastoma Amplified Sequence gene in a family affected by Acrofrontofacionasal Dysostosis type 1
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
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հետազոտող
@hy
name
Stefano Mantero
@ast
Stefano Mantero
@en
Stefano Mantero
@es
Stefano Mantero
@nl
Stefano Mantero
@sl
type
label
Stefano Mantero
@ast
Stefano Mantero
@en
Stefano Mantero
@es
Stefano Mantero
@nl
Stefano Mantero
@sl
prefLabel
Stefano Mantero
@ast
Stefano Mantero
@en
Stefano Mantero
@es
Stefano Mantero
@nl
Stefano Mantero
@sl
P106
P1153
7003693037
P21
P31
P496
0000-0003-0608-2724