Drosophila lacking dfmr1 activity show defects in circadian output and fail to maintain courtship interest (Q47071627)

5 January 2018

title

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

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5 January 2018

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GOA release 2020-03-11

author name string

Thomas C Dockendorff

1

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5 January 2018

Henry S Su

2

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5 January 2018

Sean M J McBride

3

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5 January 2018

Zhaohai Yang

4

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5 January 2018

Catherine H Choi

5

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5 January 2018

Kathleen K Siwicki

6

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5 January 2018

Amita Sehgal

7

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5 January 2018

Thomas A Jongens

8

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5 January 2018

language of work or name

English

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publication date

1 June 2002

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5 January 2018

published in

Neuron

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5 January 2018

volume

34

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5 January 2018

page(s)

973-984

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5 January 2018

issue

6

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5 January 2018

FMR1 protein: conserved RNP family domains and selective RNA binding

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Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse

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Photophobe (Ppb), a Drosophila mutant with a reversed sign of phototaxis; the mutation shows an allele-specific interaction with sevenless

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The Drosophila dCREB2 gene affects the circadian clock.

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Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein.

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Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

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Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits

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Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

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The fragile X syndrome

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Disruption of neurotransmission in Drosophila mushroom body blocks retrieval but not acquisition of memory.

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Molecular bases for circadian clocks

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Clonal analysis of cmp44E, which encodes a conserved putative transmembrane protein, indicates a requirement for cell viability in Drosophila.

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Genetic feminization of brain structures and changed sexual orientation in male Drosophila

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7 January 2021

Courtship in Drosophila

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A neurofibromatosis-1-regulated pathway is required for learning in Drosophila.

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The period clock gene is expressed in central nervous system neurons which also produce a neuropeptide that reveals the projections of circadian pacemaker cells within the brain of Drosophila melanogaster

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Robust circadian rhythmicity of Drosophila melanogaster requires the presence of lateral neurons: a brain-behavioral study of disconnected mutants

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Pigment-dispersing hormone-immunoreactive neurons in the nervous system of wild-type Drosophila melanogaster and of several mutants with altered circadian rhythmicity.

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Ectopic expression of the neuropeptide pigment-dispersing factor alters behavioral rhythms in Drosophila melanogaster.

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7 January 2021

Drosophila Futsch/22C10 is a MAP1B-like protein required for dendritic and axonal development

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Development of neuronal connectivity in Drosophila antennal lobes and mushroom bodies

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7 January 2021

Understanding the molecular basis of fragile X syndrome

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7 January 2021

Clock Mutants of Drosophila melanogaster

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Drosophila melanogaster deficient in protein kinase A manifests behavior-specific arrhythmia but normal clock function

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7 January 2021

Central complex substructures are required for the maintenance of locomotor activity in Drosophila melanogaster

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7 January 2021

Mushroom body ablation impairs short-term memory and long-term memory of courtship conditioning in Drosophila melanogaster.

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The role of Drosophila mushroom body signaling in olfactory memory.

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A pdf neuropeptide gene mutation and ablation of PDF neurons each cause severe abnormalities of behavioral circadian rhythms in Drosophila

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A modular misexpression screen in Drosophila detecting tissue-specific phenotypes

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Loss of circadian behavioral rhythms and per RNA oscillations in the Drosophila mutant timeless

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7 January 2021

SCOP, a novel gene product expressed in a circadian manner in rat suprachiasmatic nucleus

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7 January 2021

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

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7 January 2021

Essential role for KH domains in RNA binding: impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome

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7 January 2021

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

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7 January 2021

Preferential expression in mushroom bodies of the catalytic subunit of protein kinase A and its role in learning and memory

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7 January 2021

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

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7 January 2021

Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation

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7 January 2021

Molecular components of the circadian system in Drosophila

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7 January 2021

A circadian output in Drosophila mediated by neurofibromatosis-1 and Ras/MAPK.

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7 January 2021

Role of molecular oscillations in generating behavioral rhythms in Drosophila.

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7 January 2021

Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila

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7 January 2021

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

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7 January 2021

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Identifiers

DOI

1 reference

5 January 2018

PubMed ID

12086644

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5 January 2018