Search Results - "Crnić, I."

Involvement of PTCH gene in various noninflammatory cysts by Levanat, S, Pavelić, B, Crnić, I, Oresković, S, Manojlović, S

“…Constitutional hemizygous inactivation of PTCH, the Shh signaling pathway gene that moderates the signal, manifests itself as nevoid basal cell carcinoma…”
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Aberration of FHIT gene is associated with increased tumor proliferation and decreased apoptosis-clinical evidence in lung and head and neck carcinomas by Pavelić, K, Krizanac, S, Cacev, T, Hadzija, M P, Radosević, S, Crnić, I, Levanat, S, Kapitanović, S

“…Human FHIT (fragile histidine triad) gene is highly conserved gene homologous to a group of genes identified in prokaryotes and eukaryotes. Loss of FHIT…”
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Involvement of PTCH gene in various noninflammatory cysts by Levanat, S., Pavelić, B., Crnić, I., Orešković, S., Manojlović, S.

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PTCH gene altered in dentigerous cysts by Pavelić, B., Levanat, S., Crnić, I., Kobler, P., Anić, I., Manojlović, S., Šutalo, J.

“…: Motivated by the evidence that odontogenic keratocysts are associated with genetic alterations, we examined the possibility that development of other…”
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Variable expression of Gorlin syndrome may reflect complexity of the signalling pathway by Levanat, S, Mubrin, M K, Crnić, I, Situm, M, Basta-Juzbasić, A

“…Nevoid Basal Cell Carcinoma Syndrome (NBCCS) or Gorlin syndrome is an autosomal dominant disorder characterized by cancer predisposition and multiple…”
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Involvement of patched (PTCH) gene in Gorlin syndrome and related disorders: three family cases by Situm, M, Levanat, S, Crnic, I, Pavelic, B, Macan, D, Grgurević, J, Mubrin-Koncar, M, Lipozencić, J

“…To find genetic alterations in PTC or other genes of the Shh/PTCH pathway in tumorous and non- tumorous samples from three families and to correlate them with…”
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