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NR9192

Screening of mutations and polymorphisms in neonatal Fc receptor gene in patients with primary disorders of antibody production

Public support

  • Provider

    Ministry of Health

  • Programme

    Branch programm of research of the Ministry of Health

  • Call for proposals

    VaV pro Ministerstvo zdravotnictví 4 (SMZ02007NR)

  • Main participants

  • Contest type

    VS - Public tender

  • Contract ID

    NR9192-3/2007

Alternative language

  • Project name in Czech

    Screening mutací a polymorfismů v genu pro neonatální Fc receptor u pacientů s primárními poruchami tvorby protilátek

  • Annotation in Czech

    Cílem projektu je zmapovat kompletní spektrum mutací a/nebo polymorfismů v genu pro FcRn v populaci zdravých jedinců a pacientů trpících XLA a CVID. Na základě výsledků genetické analýzy genu pro FcRn a známého klinického projevu pacientů s XLA a CVID bude stanoveno, zda a jak ovlivňuje sekvenční variabilita genu fenotyp těchto onemocnění, zejména pak reakci pacientů na léčbu IVIG.

Scientific branches

  • R&D category

    NV - Nonindustrial research (Applied research excluded Industrial research)

  • CEP classification - main branch

    EB - Genetics and molecular biology

  • CEP - secondary branch

    EC - Immunology

  • CEP - another secondary branch

    FN - Epidemiology, infection diseases and clinical immunology

  • OECD FORD - equivalent branches <br>(according to the <a href="http://www.vyzkum.cz/storage/att/E6EF7938F0E854BAE520AC119FB22E8D/Prevodnik_oboru_Frascati.pdf">converter</a>)

    10603 - Genetics and heredity (medical genetics to be 3)<br>10604 - Reproductive biology (medical aspects to be 3)<br>10605 - Developmental biology<br>10608 - Biochemistry and molecular biology<br>10609 - Biochemical research methods<br>30101 - Human genetics<br>30102 - Immunology<br>30302 - Epidemiology<br>30303 - Infectious Diseases

Completed project evaluation

  • Provider evaluation

    V - Vynikající výsledky projektu (s mezinárodním významem atd.)

  • Project results evaluation

    Three FCRN mutations were detected in CVID patients. The FCRN VNTR promoter polymorphism has no influence on IgG levels in serum, maternofoetal IgG transfer or clinical CVID phenotype. Lower FCRN expression is associated with lung abnormities in CVID.

Solution timeline

  • Realization period - beginning

    Jan 1, 2007

  • Realization period - end

    Dec 31, 2009

  • Project status

    U - Finished project

  • Latest support payment

    Dec 18, 2009

Data delivery to CEP

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

  • Data delivery code

    CEP10-MZ0-NR-U/03:3

  • Data delivery date

    Apr 27, 2011

Finance

  • Total approved costs

    3,526 thou. CZK

  • Public financial support

    3,476 thou. CZK

  • Other public sources

    50 thou. CZK

  • Non public and foreign sources

    0 thou. CZK