Evidence map›Paper›PMID 26148970›Full record

ReviewFASEB journal : official publication of the Federation of American Societies for Experimental Biology2015

Lhx6 and Lhx8: cell fate regulators and beyond.

Chen Zhou, Guodong Yang, Mo Chen, Ling He, Lusai Xiang, Christopher Ricupero, Jeremy J Mao, Junqi Ling

Open access · bronzeAbstract readReview
In one paragraph

Review in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  5. Observational
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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 3 institutions in 2 countries.

Chen Zhou*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.
Guodong Yang*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.
Mo Chen*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.
Ling He*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.
Lusai Xiang*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.
Christopher Ricupero*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China.
Jeremy J Mao*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China jmao@columbia.edu lingjq@mail.sysu.edu.cn.
Junqi Ling*Center for Craniofacial Regeneration, Columbia University Medical Center, New York, New York, USA; Guanghua School of Stomatology, Hospital of Stomatology, and Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China jmao@columbia.edu lingjq@mail.sysu.edu.cn.
Columbia University Irving Medical Center · USStomatology Hospital · CNSun Yat-sen University · CN

Funding

Meniscus Regeneration by Endogenous Stem/Progenitor CellsR01AR065023 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FORTIER, LISA A, LEE, CHANG HUN · 2014 to 2018
$4.6M
Pre-clinical Models of Odontic Analogs by Endogenous Stem CellsR01DE023112 · NIDCR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAO, JEREMY J · 2013 to 2016
$2.9M
Multidisciplinary Training in TMJ Disorders/Pain: Integrating Basic, TranslationK12DE023583 · NIDCR · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAO, JEREMY J, WADHWA, SUNIL · 2013 to 2017
$1.5M
NIAMS NIH HHS R01 AR065023NIAMS NIH HHS R01AR065023NIDCR NIH HHS K12 DE023583NIDCR NIH HHS K12DE023583NIDCR NIH HHS R01 DE023112NIDCR NIH HHS R01DE023112
6 · The paper itself

Abstract

As transcription factors of the lines (LIN)-11/Islet (Isl)-1/mitosis entry checkpoint (MEC)-3 (LIM)-homeobox subfamily, LIM homeobox (Lhx)6 and -8 are remarkably conserved and involved in the morphogenesis of multiple organ systems. Lhx6 and -8 play overlapping and distinctive roles, but in general act as cell fate mediators and in turn are regulated by several transcriptional factors, such as sonic hedgehog, fibroblast growth factors, and wingless-int (Wnt)/β-catenin. In this review, we first summarize Lhx6 and -8 distributions in development and then explore how Lhx6 and -8 act as transcription factors and coregulators of cell lineage specification. Known Lhx6 and -8 functions and targets are outlined in neurogenesis, craniofacial development, and germ cell differentiation. The underlying mechanisms of Lhx6 and -8 in regulating cell fate remain elusive. Whether Lhx6 and -8 affect functions in tissues and organs other than neural, craniofacial, oocytes, and germ cells is largely unexplored. Taken together, Lhx6 and -8 are important regulators of cell lineage specification and may act as one of the pivotal mediators of stem cell fate. Undoubtedly, future investigations of Lhx6 and -8 biology will continue to yield fascinating insights into tissue development and homeostasis, in addition to their putative roles in tissue regeneration and ageing.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DifferentiationHumansLIM-Homeodomain ProteinsMiceModels, GeneticNerve Tissue ProteinsNeurogenesisToothTranscription FactorsLHX6 protein, mouseLIM homeobox protein 8LIM-Homeodomain ProteinsNerve Tissue ProteinsTranscription FactorsLIM homeobox genesneurogenesispalatogenesistooth developmenttranscriptional regulation

Identifiers

PMID26148970
PMCPMC4566936
OpenAlexW2098677700

What OpenQuestion holds

Textmetadata
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.