Evidence map›Paper›PMID 32917241›Full record

ArticleMolecular brain2020

Altered presynaptic function and number of mitochondria in the medial prefrontal cortex of adult Cyfip2 heterozygous mice.

Gyu Hyun Kim, Yinhua Zhang, Hyae Rim Kang, Seung-Hyun Lee, Jiwon Shin, Chan Hee Lee, Hyojin Kang, Ruiying Ma, Chunmei Jin, Yoonhee Kim and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 1 country.

Gyu Hyun KimNeural Circuits Research Group, Korea Brain Research Institute, 61, Cheomdan-ro, Dong-gu, Daegu, 41062, South Korea.
Yinhua ZhangDepartment of Neuroscience, College of Medicine, Korea University, 73, Goryeodae-ro, Seongbuk-gu, Seoul, 02841, South Korea.
Hyae Rim KangDepartment of Neuroscience, College of Medicine, Korea University, 73, Goryeodae-ro, Seongbuk-gu, Seoul, 02841, South Korea.
Seung-Hyun LeeDepartment of Physiology, Dental Research Institute, Seoul National University School of Dentistry, 101, Daehak-ro, Jongno-gu, Seoul, 03080, South Korea.
Jiwon ShinNeural Circuits Research Group, Korea Brain Research Institute, 61, Cheomdan-ro, Dong-gu, Daegu, 41062, South Korea.
Chan Hee LeeNeural Circuits Research Group, Korea Brain Research Institute, 61, Cheomdan-ro, Dong-gu, Daegu, 41062, South Korea.
Hyojin KangDivision of National Supercomputing, Korea Institute of Science and Technology Information, Daejeon, South Korea.
Ruiying MaDepartment of Neuroscience, College of Medicine, Korea University, 73, Goryeodae-ro, Seongbuk-gu, Seoul, 02841, South Korea.
Chunmei JinDepartment of Neuroscience, College of Medicine, Korea University, 73, Goryeodae-ro, Seongbuk-gu, Seoul, 02841, South Korea.
Yoonhee KimDepartment of Neuroscience, College of Medicine, Korea University, 73, Goryeodae-ro, Seongbuk-gu, Seoul, 02841, South Korea.
Su Yeon KimDepartment of Neuroscience, College of Medicine, Korea University, 73, Goryeodae-ro, Seongbuk-gu, Seoul, 02841, South Korea.
Seok-Kyu KwonKorea Institute of Science and Technology, Center for Functional Connectomics, Brain Science Institute, Seoul, 02792, South Korea.
Se-Young ChoiDepartment of Physiology, Dental Research Institute, Seoul National University School of Dentistry, 101, Daehak-ro, Jongno-gu, Seoul, 03080, South Korea. sychoi@snu.ac.kr.
Kea Joo LeeNeural Circuits Research Group, Korea Brain Research Institute, 61, Cheomdan-ro, Dong-gu, Daegu, 41062, South Korea. relaylee@kbri.re.kr.
Kihoon HanDepartment of Neuroscience, College of Medicine, Korea University, 73, Goryeodae-ro, Seongbuk-gu, Seoul, 02841, South Korea. neurohan@korea.ac.kr.
Korea University · KRKorea Brain Research Institute · KRKorea Institute of Science and Technology · KRSeoul National University · KRDaegu Gyeongbuk Institute of Science and Technology · KRKorea Institute of Science & Technology Information · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Variants of the cytoplasmic FMR1-interacting protein (CYFIP) gene family, CYFIP1 and CYFIP2, are associated with numerous neurodevelopmental and neuropsychiatric disorders. According to several studies, CYFIP1 regulates the development and function of both pre- and post-synapses in neurons. Furthermore, various studies have evaluated CYFIP2 functions in the postsynaptic compartment, such as regulating dendritic spine morphology; however, no study has evaluated whether and how CYFIP2 affects presynaptic functions. To address this issue, in this study, we have focused on the presynapses of layer 5 neurons of the medial prefrontal cortex (mPFC) in adult Cyfip2 heterozygous (Cyfip2

Indexed as

Adaptor Proteins, Signal TransducingAnimalsHeterozygoteMiceMitochondriaPrefrontal CortexPresynaptic TerminalsAdaptor Proteins, Signal TransducingCyfip2 protein, mouseCytoplasmic FMR1-interacting protein 2Medial prefrontal cortexMitochondriaPresynapse

Identifiers

PMID32917241
PMCPMC7488858
OpenAlexW3086977165

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.