RICERCA ITALIANA     

Programmi di ricerca simili:

• 1 - Genetica, biologia e clinica dei paragangliomi: le mutazioni della succinodeidrogenasi mitocondriale come modello di studio della trasmissione, crescita, variabilità e trattamento dei tumori di derivazione dalla cresta neurale
• 2 - Geni dell'angiogenesi indotti da ipossia: fattori di suscettibilità nella Sclerosi Laterale Amiotrofica ?
• 3 - Meccanismi di controllo dell’eritropoiesi e policitemie congenite e familiari: ruolo delle vie di risposta alla pressione di ossigeno
• 4 - Patogenesi molecolare ed analisi sequenziale di interazioni cellulari e marcatori biologici di progressione di malattia e di resistenza al trattamento nella leucemia linfatica cronica
• 5 - Variabilità e funzione delle mutazioni mitocondriali in condizioni fisiologiche e patologiche
• 6 - Un approccio integrato allo studio della eziopatogenesi delle mitocondriopatie
• 7 - Analisi genomica e funzionale delle cellule emopoietiche nelle malattie mieloproliferative croniche
• 8 - Implicazioni diagnostico-terapeutiche delle nuove conoscenze cliniche e molecolari del carcinoma midollare della tiroide.
• 9 - Paraparesi spastiche ereditarie: studio genetico, funzionale, clinico
• 10 - Meccanismi di leucemogenesi e terapia target nelle sindromi Mielodisplastiche e nelle Leucemie Acute Mieloidi

Classificazione scientifico-disciplinare

• Area scientifico disciplinare: Scienze mediche
  • GENETICA MEDICA
  • ONCOLOGIA MEDICA
  • MALATTIE DEL SANGUE

Classificazione brevettuale

• CHEMISTRY; METALLURGY
  • BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS (immunoassay G01N33/53); COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES

Bibliografia

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Parole Chiave

DISPLASIE/NEOPLASIE MIELOIDI, SINDROME DI SHWACHMAN, MONOSOMIA 7, ANALISI DI MUTAZIONE, REAL-TIME PCR, RIARRANGIAMENTO BCR/ABL, GENE SBDS, GENE PTPN11, GENE RUNX1