Expression of human PQBP-1 in Drosophila impairs long-term memory and induces abnormal courtship. (Q48592641)

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19 January 2020

title

Expression of human PQBP-1 in Drosophila impairs long-term memory and induces abnormal courtship (English)

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19 January 2020

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1

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19 January 2020

Minoru Saitoe

4

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19 January 2020

author name string

Daisuke Horiuchi

2

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19 January 2020

Masao Shibata

3

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19 January 2020

Mei-Ling Qi

5

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19 January 2020

Hitoshi Okazawa

6

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19 January 2020

language of work or name

English

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publication date

31 March 2006

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19 January 2020

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19 January 2020

volume

580

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19 January 2020

issue

9

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19 January 2020

page(s)

2335-2340

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PQBP-1, a novel polyglutamine tract-binding protein, inhibits transcription activation by Brn-2 and affects cell survival

19 January 2020

cites work

1 reference

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Interaction between mutant ataxin-1 and PQBP-1 affects transcription and cell death

21 January 2018

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Mutant huntingtin promotes the fibrillogenesis of wild-type huntingtin: a potential mechanism for loss of huntingtin function in Huntington's disease

21 January 2018

1 reference

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PQBP-1 (Np/PQ): a polyglutamine tract-binding and nuclear inclusion-forming protein

21 January 2018

1 reference

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NeW wrinkles for an old domain

21 January 2018

1 reference

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PQBP-1/Npw38, a nuclear protein binding to the polyglutamine tract, interacts with U5-15kD/dim1p via the carboxyl-terminal domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2006.03.056

Evidence that dim1 associates with proteins involved in pre-mRNA splicing, and delineation of residues essential for dim1 interactions with hnRNP F and Npw38/PQBP-1

21 January 2018

1 reference

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Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

21 January 2018

1 reference

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Genotype-phenotype studies in three families with mutations in the polyglutamine-binding protein 1 gene (PQBP1)

21 January 2018

1 reference

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Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly

21 January 2018

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Renpenning syndrome comes into focus

21 January 2018

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Classical conditioning and retention in normal and mutantDrosophila melanogaster

21 January 2018

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Transcriptional repression induces a slowly progressive atypical neuronal death associated with changes of YAP isoforms and p73

21 January 2018

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Temporally manipulated rescue of visual and courtship abnormalities caused by a nonA mutation in Drosophila.

21 January 2018

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Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

21 January 2018

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Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function

21 January 2018

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Fathoming fragile X in fruit flies

21 January 2018

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Drosophila lacking dfmr1 activity show defects in circadian output and fail to maintain courtship interest

21 January 2018

1 reference

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