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The molecular basis of congenital afibriogenemia: mutations, phenotypic modifiers and gene therapy

English title The molecular basis of congenital afibriogenemia: mutations, phenotypic modifiers and gene therapy
Applicant Neerman-Arbez Marguerite
Number 66023
Funding scheme SNSF Professorships
Research institution Dépt Microbiologie et Médecine Moléculaire Faculté de Médecine Université de Genève
Institution of higher education University of Geneva - GE
Main discipline Genetics
Start/End 01.03.2002 - 28.02.2006
Approved amount 1'050'114.00
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All Disciplines (2)

Discipline
Genetics
Pathophysiology

Keywords (7)

COAGULATION, FIBRINOGEN; MUTATION IDENTIFICATION; AND EXPRESSION, SPLICING; DIFFERENTIAL GENE EXPRES-; SION, MICROARRAYS; MODIFYING GENES, KNOCK-; OUT MICE, GENE THERAPY

Responsible applicant and co-applicants

Employees

Associated projects

Number Title Start Funding scheme
119845 Molecular exploration of the fibrinogen gene cluster and genomic landscape 01.04.2008 Project funding (Div. I-III)
110429 Molecular basis of fibrinogen disorders: mutations, genetic modifiers and gene therapy 01.03.2006 SNSF Professorships
64987 The molecular basis of congenital afibriogenemia: mutations, phenotypic modifiers and gene therapy 01.10.2001 Project funding (Div. I-III)

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