Name of Resource

    Drosophila models for Huntington's and Parkinson's disease (University of Lisbon)

    Name of Principal Investigator - Title

    Dr

    Name of Principal Investigator - First name

    Pedro

    Name of Principal Investigator - Last name

    Domingos

    Address of institution -Institution

    ITQB - Universidade Nova de Lisboa

    Address of institution - Street address

    Av. da República

    Address of institution - City

    Oeiras

    Address of institution - Postcode

    2780-157

    Country

    Portugal

    Website

    Summary

    Drosophila transgenic strain for overexpression of Htt (Huntington disease causing protein) and alpha synuclein (Parkinson's disease)

    Q1a. Please indicate below if your cohort includes or expects to include, incidence of the following conditions? (1)

    Huntington's disease| Parkinson's disease & PD related disorders| Neurodegenerative disease in general

    Q1b. Does your resource hold

    Animals

    Q2a. Does the resource act as a centre for access and distribution to external groups (who are not the Principal Investigators (PI) for the resource)?

    Yes

    Q2b. If Yes, what procedures and rules apply for access?

    Apply to PI or co-ordinator at resource| Access through collaboration with PI only| Access independent of collaboration with PI| Local/ regional access| National access| International access

    Q3a. Does your resource develop experimental models (animal/cell) for external groups?

    No

    Q3b. If YES and your resource is related to an ANIMAL model, what types of models are provided?

    Q3c. If YES and your resource is related to a CELL model, what types of models are provided?

    Q4a. Is this activity supported as:

    Not applicable

    Q4b. Do you deposit what you supply in any kind of central repository?

    Yes

    Disease

    HD| PD

    Species

    Drosophila| Drosophila

    Available to external user

    Yes| Yes

    Full phenotypic character

    No| No

    Please indicate the phenotypes

    Neurodegeneration upon overexpression| Neurodegeneration upon overexpression

    List of genotypes or other subtypes

    UAS-Htt| UAS-alpha-synuclein

    Q5b. Cognitive function, No of models

    2

    Q5b. Cognitive function, Available to external users

    Yes

    Q5b. Cognitive function, Full phenotypic characterisation

    Partial

    Q5b. Cognitive function, Nature of phenotype

    Q5b. Motor function, No of models

    2

    Q5b. Motor function, Available to external users

    Yes

    Q5b. Motor function, Full phenotypic characterisation

    Partial

    Q5b. Motor function, Nature of phenotype

    Q5b. Physiological function, no of models

    2

    Q5b. Physiological function, Available to external users

    Yes

    Q5b. Physiological function, Full phenotypic characterisation

    Partial

    Q5b. Physiological function, Nature of phenotype

    Q5b. Other function (please specify), no of models

    Please specify other function

    Q5b. Other function (please specify), Available to external users

    Q5b. Other function (please specify), Full phenotypic characterisation

    Q5b. Other function (please specify), Nature of phenotype

    Q6. Please indicate if your resource is already linked into European or international consortia or networks?

    Q7a. Is maintenance of this resource dependent on continued funding?

    Yes

    Q7b. If yes, when does the current funding period end?

    2019

    Q7c. What is the expected lifespan of the resource (in years)?

    20

    Q7d. Are there other plans affecting future use that it may be useful to know?

Types: Experimental Models
Member States: Portugal
Diseases: N/A
Years: 2016
Database Categories: N/A
Database Tags: N/A

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