Search Results - "Danesin, C"

Distinct sites of origin of oligodendrocytes and somatic motoneurons in the chick spinal cord: oligodendrocytes arise from Nkx2.2-expressing progenitors by a Shh-dependent mechanism by Soula, C, Danesin, C, Kan, P, Grob, M, Poncet, C, Cochard, P

“…In the vertebrate spinal cord, oligodendrocytes arise from the ventral part of the neuroepithelium, a region also known to generate somatic motoneurons. The…”
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Converse control of oligodendrocyte and astrocyte lineage development by Sonic hedgehog in the chick spinal cord by Agius, Eric, Soukkarieh, Chadi, Danesin, Cathy, Kan, Paulette, Takebayashi, Hirohide, Soula, Cathy, Cochard, Philippe

“…In the developing spinal cord, oligodendrocyte progenitors (OLPs) originate from the ventral neuroepithelium and the specification of this lineage depends on…”
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The PAI-1 gene 4G/5G polymorphism and deep vein thrombosis in patients with inherited thrombophilia by Sartori, Maria Teresa, Danesin, Cristina, Saggiorato, Graziella, Tormene, Daniela, Simioni, Paolo, Spiezia, Luca, Patrassi, Giovanni Maurizio, Girolami, Antonio

“…Genetic and acquired factors may influence phenotypic expression of inherited thrombophilia. Hypofibrinolysis due to excess PAI-1 can be found in patients with…”
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A subtractive approach to characterize genes with regionalized expression in the gliogenic ventral neuroepithelium: identification of chick Sulfatase 1 as a new oligodendrocyte lineage gene by Braquart-Varnier, Christine, Danesin, Cathy, Clouscard-Martinato, Catherine, Agius, Eric, Escalas, Nathalie, Benazeraf, Bertrand, Ai, Xingbin, Emerson, Charles, Cochard, Philippe, Soula, Cathy

“…To address the question of the origin of glial cells and the mechanisms leading to their specification, we have sought to identify novel genes expressed in…”
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Impairment of fibrinolytic potential in long-term steroid treatment after heart transplantation by PATRASSI, G. M, SARTORI, M. T, LIVI, U, CASONATO, A, DANESIN, C, VETTORE, S, GIROLAMI, A

“…Thrombotic complications constitute an important risk in transplant recipients, in whom a hypercoagulable state and hypofibrinolysis have been associated with…”
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Familial association of hypoplasminogenemia and heterozygous factor V deficiency by Sartori, M T, Patrassi, G M, Theodoridis, P, Danesin, C, Abati, C, Girolami, A

“…The coinheritance of hypoplasminogenemia and heterozygous factor V deficiency in a relative with thrombotic disease and no hemorrhagic tendency is described…”
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