Evidence map›Paper›PMID 24647753›Full record

ArticleBrain structure & function2015

The Lhx9 homeobox gene controls pineal gland development and prevents postnatal hydrocephalus.

Fumiyoshi Yamazaki, Morten Møller, Cong Fu, Samuel J Clokie, Artem Zykovich, Steven L Coon, David C Klein, Martin F Rath

Open access · greenAbstract read
In one paragraph

Article in Brain structure & function, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

24 citing papers in PubMed, 37 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

8 authors at 4 institutions in 3 countries.

Fumiyoshi YamazakiSection on Neuroendocrinology, Program in Developmental Endocrinology and Genetics, The Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, 49 Convent Drive, Room 6A82, Bethesda, MD, 20892-4510, USA.
Morten Møller
Cong Fu
Samuel J Clokie
Artem Zykovich
Steven L Coon
David C Klein
Martin F Rath
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USUniversity of Copenhagen · DKJilin University · CNNational Institutes of Health · US

Funding

Pineal Regulation: Developmental and Circadian Changes in the Transcriptome ZIAHD008836 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KLEIN, DAVID · 2009 to 2015
$2.4M
Pineal Regulation: Neural, transsynaptic and intracellular control mechanismsZIAHD008838 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KLEIN, DAVID · 2009 to 2015
$2.1M
Pineal Regulation: Molecular basis of developmentZIAHD008837 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI KLEIN, DAVID · 2009 to 2015
$1.8M
Intramural NIH HHS ZIA HD008836Intramural NIH HHS ZIA HD008837Intramural NIH HHS ZIA HD008838
6 · The paper itself

Abstract

Lhx9 is a member of the LIM homeobox gene family. It is expressed during mammalian embryogenesis in the brain including the pineal gland. Deletion of Lhx9 results in sterility due to failure of gonadal development. The current study was initiated to investigate Lhx9 biology in the pineal gland. Lhx9 is highly expressed in the developing pineal gland of the rat with transcript abundance peaking early in development; transcript levels decrease postnatally to nearly undetectable levels in the adult, a temporal pattern that is generally similar to that reported for Lhx9 expression in other brain regions. Studies with C57BL/6J Lhx9(-/-) mutant mice revealed marked alterations in brain and pineal development. Specifically, the superficial pineal gland is hypoplastic, being reduced to a small cluster of pinealocytes surrounded by meningeal and vascular tissue. The deep pineal gland and the pineal stalk are also reduced in size. Although the brains of neonatal Lhx9(-/-) mutant mice appear normal, severe hydrocephalus develops in about 70% of the Lhx9(-/-) mice at 5-8 weeks of age; these observations are the first to document that deletion of Lhx9 results in hydrocephalus and as such indicate that Lhx9 contributes to the maintenance of normal brain structure. Whereas hydrocephalus is absent in neonatal Lhx9(-/-)mutant mice, the neonatal pineal gland in these animals is hypoplastic. Accordingly, it appears that Lhx9 is essential for early development of the mammalian pineal gland and that this effect is not secondary to hydrocephalus.

Indexed as

AnimalsHydrocephalusLIM-Homeodomain ProteinsMiceMice, Inbred C57BLMice, KnockoutPineal GlandRatsRats, Sprague-DawleyTranscription FactorsLhx9 protein, mouseLhx9 protein, ratLIM-Homeodomain ProteinsTranscription Factors

Identifiers

PMID24647753
PMCPMC4197116
OpenAlexW2007985135

What OpenQuestion holds

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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.