FMRP Expression Levels in Mouse Central Nervous System Neurons Determine Behavioral Phenotype. (Q30365865)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27604541%20AND%20SRC:MED&resulttype=core&format=json

22 March 2020

title

FMRP Expression Levels in Mouse Central Nervous System Neurons Determine Behavioral Phenotype (English)

1 reference

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22 March 2020

1 reference

1

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22 March 2020

Ayumu Konno

7

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22 March 2020

Hirokazu Hirai

8

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22 March 2020

author name string

Shervin Gholizadeh

2

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22 March 2020

Yosuke Niibori

3

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22 March 2020

Laura K Pacey

4

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22 March 2020

Sebok K Halder

5

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22 March 2020

Enea Koxhioni

6

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22 March 2020

David R Hampson

9

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22 March 2020

publication date

7 September 2016

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22 March 2020

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22 March 2020

volume

27

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22 March 2020

page(s)

982-996

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issue

12

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AAV-Mediated Gene Therapy for Research and Therapeutic Purposes

22 March 2020

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3 June 2018

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FMRP targets distinct mRNA sequence elements to regulate protein expression

3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation condition

3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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26 November 2018

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Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function.

26 November 2018

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Genetic deletion of regulator of G-protein signaling 4 (RGS4) rescues a subset of fragile X related phenotypes in the FMR1 knockout mouse.

26 November 2018

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The MECP2 duplication syndrome.

26 November 2018

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Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene.

26 November 2018

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Different-sized duplications of Xq28, including MECP2, in three males with mental retardation, absent or delayed speech, and recurrent infections.

26 November 2018

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Suppression of two major Fragile X Syndrome mouse model phenotypes by the mGluR5 antagonist MPEP.

26 November 2018

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26 November 2018

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Duplication of the Xq27.3-q28 region, including the FMR1 gene, in an X-linked hypogonadism, gynecomastia, intellectual disability, short stature, and obesity syndrome

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27604541

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1089/HUM.2016.090

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27604541%20AND%20SRC:MED&resulttype=core&format=json

22 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27604541%20AND%20SRC:MED&resulttype=core&format=json

22 March 2020

1 reference