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Identification of a Thyroid Hormone Response Element in the Mouse Kruppel-Like Factor 9 Gene to Explain Its Postnatal Expression in the Brain

https://doi.org/10.1210/en.2009-0050
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Two regulatory proteins that bind to the basic transcription element (BTE), a GC box sequence in the promoter region of the rat P‐4501A1 gene.
inferredcites →https://doi.org/10.1007/bf03344003openalex-snapshot
Action of thyroid hormone in brain
inferredcites →https://doi.org/10.1016/0006-8993(90)90884-eopenalex-snapshot
Dendritic spine density of adult hippocampal pyramidal cells is sensitive to thyroid hormone
inferredcites →https://doi.org/10.1016/0092-8674(95)90199-xopenalex-snapshot
The nuclear receptor superfamily: The second decade
inferredcites →https://doi.org/10.1016/0306-4530(91)90071-zopenalex-snapshot
The hippocampal formation: Morphological changes induced by thyroid, gonadal and adrenal hormones
inferredcites →https://doi.org/10.1016/0960-0760(91)90160-7openalex-snapshot
Steroid and thyroid hormones modulate a changing brain
inferredcites →https://doi.org/10.1016/j.ygeno.2005.01.005openalex-snapshot
Mammalian SP/KLF transcription factors: Bring in the family
inferredcites →https://doi.org/10.1016/s0021-9258(17)36839-4openalex-snapshot
Identification of thyroid hormone response elements in rodent Pcp-2, a developmentally regulated gene of cerebellar Purkinje cells.
inferredcites →https://doi.org/10.1016/s0092-8674(02)00641-4openalex-snapshot
Combinatorial Control of Gene Expression by Nuclear Receptors and Coregulators
inferredcites →https://doi.org/10.1016/s0965-1748(00)00035-7openalex-snapshot
Autoinduction of nuclear hormone receptors during metamorphosis and its significance
inferredcites →https://doi.org/10.1016/s1043-2760(00)00263-0openalex-snapshot
Gene Regulation by Thyroid Hormone
inferredcites →https://doi.org/10.1046/j.1440-169x.2002.00650.xopenalex-snapshot
Basic transcription element binding protein is a thyroid hormone‐regulated transcription factor expressed during metamorphosis in Xenopus laevis
inferredcites →https://doi.org/10.1073/pnas.0507519103openalex-snapshot
Leptin ( ob gene) of the South African clawed frog Xenopus laevis
inferredcites →https://doi.org/10.1073/pnas.260141297openalex-snapshot
Targeted chromatin binding and histone acetylation in vivo by thyroid hormone receptor during amphibian development
inferredcites →https://doi.org/10.1073/pnas.91.7.2644openalex-snapshot
Overexpression of the beta 1 thyroid receptor induces differentiation in neuro-2a cells.
inferredcites →https://doi.org/10.1073/pnas.93.5.1924openalex-snapshot
The thyroid hormone-induced tail resorption program during Xenopus laevis metamorphosis.
inferredcites →https://doi.org/10.1073/pnas.94.16.8527openalex-snapshot
The product of a thyroid hormone-responsive gene interacts with thyroid hormone receptors
inferredcites →https://doi.org/10.1074/jbc.272.13.8179openalex-snapshot
Thyroid Hormone-dependent Gene Expression Program for Xenopus Neural Development
inferredcites →https://doi.org/10.1074/jbc.274.33.23128openalex-snapshot
Basic Transcription Element-binding Protein (BTEB) Is a Thyroid Hormone-regulated Gene in the Developing Central Nervous System
inferredcites →https://doi.org/10.1074/jbc.m509593200openalex-snapshot
Gene-specific Changes in Promoter Occupancy by Thyroid Hormone Receptor during Frog Metamorphosis
inferredcites →https://doi.org/10.1074/jbc.m709306200openalex-snapshot
A Role for Basic Transcription Element-binding Protein 1 (BTEB1) in the Autoinduction of Thyroid Hormone Receptor β
inferredcites →https://doi.org/10.1093/bioinformatics/18.2.333openalex-snapshot
PROMO: detection of known transcription regulatory elements using species-tailored searches
inferredcites →https://doi.org/10.1093/nar/gkg605openalex-snapshot
Identification of patterns in biological sequences at the ALGGEN server: PROMO and MALGEN
inferredcites →https://doi.org/10.1101/gad.916701openalex-snapshot
The hairless gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
inferredcites →https://doi.org/10.1111/j.0906-6705.2004.00175.xopenalex-snapshot
The hairless promoter is differentially regulated by thyroid hormone in keratinocytes and neuroblastoma cells
inferredcites →https://doi.org/10.1128/mcb.01230-07openalex-snapshot
Wingless Signaling Induces Widespread Chromatin Remodeling of Target Loci
inferredcites →https://doi.org/10.1128/mcb.22.24.8527-8538.2002openalex-snapshot
Nuclear Receptor Corepressor Recruitment by Unliganded Thyroid Hormone Receptor in Gene Repression during Xenopus laevis Development
inferredcites →https://doi.org/10.1128/mcb.23.7.2489-2500.2003openalex-snapshot
Functional Analysis of Basic Transcription Element Binding Protein by Gene Targeting Technology
inferredcites →https://doi.org/10.1152/physrev.2001.81.3.1097openalex-snapshot
Physiological and Molecular Basis of Thyroid Hormone Action
inferredcites →https://doi.org/10.1186/gb-2003-4-2-206openalex-snapshot
Sp1- and Krüppel-like transcription factors.
inferredcites →https://doi.org/10.1210/en.143.6.2242openalex-snapshot
Suppression of the Basic Transcription Element-Binding Protein in Brain Neuronal Cultures Inhibits Thyroid Hormone-Induced Neurite Branching
inferredcites →https://doi.org/10.1210/en.2002-220126openalex-snapshot
The Transcription Factor Basic Transcription Element-Binding Protein 1 Is a Direct Thyroid Hormone Response Gene in the Frog Xenopus laevis
inferredcites →https://doi.org/10.1210/en.2006-1413openalex-snapshot
Structural and Functional Conservation of Vertebrate Corticotropin-Releasing Factor Genes: Evidence for a Critical Role for a Conserved Cyclic AMP Response Element
inferredcites →https://doi.org/10.1210/en.2008-1441openalex-snapshot
Stressor and Glucocorticoid-Dependent Induction of the Immediate Early Gene Kruppel-Like Factor 9: Implications for Neural Development and Plasticity
inferredcites →https://doi.org/10.1210/endo-105-1-80openalex-snapshot
Depletion of L-3,5,3'-Triiodothyronine and L-Thyroxine in Euthyroid Calf Serum for Use in Cell Culture Studies of the Action of Thyroid Hormone*
inferredcites →https://doi.org/10.1210/endo.140.1.6461openalex-snapshot
The Human RC3 Gene Homolog, NRGN Contains a Thyroid Hormone-Responsive Element Located in the First Intron**This work was supported by grants from Fundacion Ramon Areces and DGICYT (PM95–0019).
inferredcites →https://doi.org/10.1210/er.14.1.94openalex-snapshot
The role of thyroid hormones in prenatal and neonatal neurological development--current perspectives
inferredcites →https://doi.org/10.1242/jcs.00247openalex-snapshot
The nuclear receptor superfamily
inferredcites →https://doi.org/10.1523/jneurosci.10-03-00996.1990openalex-snapshot
Sex differences and thyroid hormone sensitivity of hippocampal pyramidal cells
inferredcites →https://doi.org/10.2144/000112014openalex-snapshot
Two-Step Cross-Linking Method for Identification of NF-κB Gene Network by Chromatin Immunoprecipitation

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Multiple transcription factor families regulate axon growth and regeneration
inferred← citeshttps://doi.org/10.1002/dvdy.535openalex-snapshot
Transcriptome analysis of the response to thyroid hormone in Xenopus neural stem and progenitor cells
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Inflammation severely alters thyroid hormone signaling in the central nervous system during experimental allergic encephalomyelitis in rat: Direct impact on OPCs differentiation failure
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Mechanisms for Thyroid Hormone Action in the CNS
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Effect of bexarotene on differentiation of glioblastoma multiforme compared with ATRA
inferred← citeshttps://doi.org/10.1007/s12035-015-9375-zopenalex-snapshot
Thyroid Hormone Potentially Benefits Multiple Sclerosis via Facilitating Remyelination
inferred← citeshttps://doi.org/10.1007/s12035-016-0013-1openalex-snapshot
Thyroid Hormone Signaling in Oligodendrocytes: from Extracellular Transport to Intracellular Signal
inferred← citeshttps://doi.org/10.1007/s12035-020-01971-wopenalex-snapshot
Molecular Mechanisms for Krüppel-Like Factor 13 Actions in Hippocampal Neurons
inferred← citeshttps://doi.org/10.1007/s12311-009-0127-3openalex-snapshot
Animal Models of Human Cerebellar Ataxias: a Cornerstone for the Therapies of the Twenty-First Century
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.04.003openalex-snapshot
Thyroid Hormone and the White Matter of the Central Nervous System: From Development to Repair
inferred← citeshttps://doi.org/10.1016/bs.vh.2021.11.001openalex-snapshot
Synergistic gene regulation by thyroid hormone and glucocorticoid in the hippocampus
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Thyroid hormone receptors: The challenge of elucidating isotype-specific functions and cell-specific response
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Utilization of temperature-mediated activation of thyroid hormone-induced molecular memory to evaluate early signaling events in the olfactory epithelium of Rana [Lithobates] catesbeiana tadpoles
inferred← citeshttps://doi.org/10.1016/j.envint.2024.108838openalex-snapshot
The pollutant perfluorohexane sulfonate (PFHxS) reduces serum thyroxine but does not alter thyroid action in the postnatal rat brain
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Iodide Intake During Pregnancy and Lactation Stimulates KLF9, BDNF Expression in Offspring Brain with Elevated DHA, EPA Metabolites
inferred← citeshttps://doi.org/10.1016/j.jhep.2019.12.018openalex-snapshot
Thyroid hormone inhibits hepatocellular carcinoma progression via induction of differentiation and metabolic reprogramming
inferred← citeshttps://doi.org/10.1016/j.mce.2009.09.008openalex-snapshot
Thyroid hormone action during brain development: More questions than answers
inferred← citeshttps://doi.org/10.1016/j.mce.2011.05.009openalex-snapshot
Coordination of mitochondrial biogenesis by thyroid hormone
inferred← citeshttps://doi.org/10.1016/j.mce.2013.07.016openalex-snapshot
Retinoic X receptor subtypes exert differential effects on the regulation of Trh transcription
inferred← citeshttps://doi.org/10.1016/j.mce.2017.01.007openalex-snapshot
Neuronal effects of thyroid hormone metabolites
inferred← citeshttps://doi.org/10.1016/j.mcn.2011.05.005openalex-snapshot
Krüppel-like transcription factors in the nervous system: Novel players in neurite outgrowth and axon regeneration
inferred← citeshttps://doi.org/10.1016/j.mcn.2012.03.007openalex-snapshot
The T3-induced gene KLF9 regulates oligodendrocyte differentiation and myelin regeneration
inferred← citeshttps://doi.org/10.1016/j.pbb.2023.173620openalex-snapshot
Postpartum scarcity-adversity inflicts sex-specific cerebellar adaptations and reward behaviors in adolescence
inferred← citeshttps://doi.org/10.1016/j.scr.2013.08.001openalex-snapshot
Molecular and cell biological effects of 3,5,3′-triiodothyronine on progenitor cells of the enteric nervous system in vitro
inferred← citeshttps://doi.org/10.1016/j.tiv.2015.06.018openalex-snapshot
Pituitary specific retinoid-X receptor ligand interactions with thyroid hormone receptor signaling revealed by high throughput reporter and endogenous gene responses
inferred← citeshttps://doi.org/10.1016/j.tox.2026.154542openalex-snapshot
Integrating transcriptomics and molecular AOPs to identify T3-dependent regulation of neuronal development in the human neural progenitor test
inferred← citeshttps://doi.org/10.1016/j.ydbio.2015.02.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ydbio.2017.03.026openalex-snapshot
The heterochronic gene Lin28 regulates amphibian metamorphosis through disturbance of thyroid hormone function
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.03.013openalex-snapshot
DNA methylation dynamics underlie metamorphic gene regulation programs in Xenopus tadpole brain
inferred← citeshttps://doi.org/10.1016/j.ygcen.2010.03.013openalex-snapshot
Mechanisms and significance of nuclear receptor auto- and cross-regulation
inferred← citeshttps://doi.org/10.1016/j.ygcen.2014.03.003openalex-snapshot
Krüppel-like factors are effectors of nuclear receptor signaling
inferred← citeshttps://doi.org/10.1016/j.ygcen.2018.11.007openalex-snapshot
Effects of thyroid hormone disruption on the ontogenetic expression of thyroid hormone signaling genes in developing zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.ygcen.2022.114047openalex-snapshot
Uncovering early thyroid hormone signalling events through temperature-mediated activation of molecular memory in the cultured bullfrog tadpole tail fin
inferred← citeshttps://doi.org/10.1016/j.ygcen.2024.114579openalex-snapshot
Comparative analysis of Krüppel-like factors expression in the retinas of zebrafish and mice during development and after injury
inferred← citeshttps://doi.org/10.1021/envhealth.5c00167openalex-snapshot
Oral Intake of Plasticizer Di-(2-ethylhexyl) Phthalate Disrupts Cerebellar Myelination via Thyroid Signaling in Aging Mice
inferred← citeshttps://doi.org/10.1038/s41419-024-06690-xopenalex-snapshot
Impact of the thyroid hormone T3 and its nuclear receptor TRα1 on colon cancer stem cell phenotypes and response to chemotherapies
inferred← citeshttps://doi.org/10.1056/nejmoa1110296openalex-snapshot
A Mutation in the Thyroid Hormone Receptor Alpha Gene
inferred← citeshttps://doi.org/10.1073/pnas.1119853109openalex-snapshot
Thyroid hormone triggers the developmental loss of axonal regenerative capacity via thyroid hormone receptor α1 and krüppel-like factor 9 in Purkinje cells
inferred← citeshttps://doi.org/10.1084/jem.20091892openalex-snapshot
Both XPD alleles contribute to the phenotype of compound heterozygote xeroderma pigmentosum patients
inferred← citeshttps://doi.org/10.1089/thy.2022.0373openalex-snapshot
Epigenome-Wide Association Study Reveals CpG Sites Associated with Thyroid Function and Regulatory Effects on KLF9
inferred← citeshttps://doi.org/10.1093/bioinformatics/bts693openalex-snapshot
NURBS: a database of experimental and predicted nuclear receptor binding sites of mouse
inferred← citeshttps://doi.org/10.1093/cercor/bht364openalex-snapshot
Transient Maternal Hypothyroxinemia Potentiates the Transcriptional Response to Exogenous Thyroid Hormone in the Fetal Cerebral Cortex Before the Onset of Fetal Thyroid Function: A Messenger and MicroRNA Profiling Study
inferred← citeshttps://doi.org/10.1093/cercor/bhv273openalex-snapshot
Global Transcriptome Analysis of Primary Cerebrocortical Cells: Identification of Genes Regulated by Triiodothyronine in Specific Cell Types
inferred← citeshttps://doi.org/10.1093/toxsci/kfy190openalex-snapshot
Thyroid Hormone Disruption in the Fetal and Neonatal Rat: Predictive Hormone Measures and Bioindicators of Hormone Action in the Developing Cortex
inferred← citeshttps://doi.org/10.1101/2020.11.03.366468openalex-snapshot
ZIKA virus effects on neuroprogenitors are exacerbated by the main pyriproxyfen metabolite via thyroid hormone signaling disruption
inferred← citeshttps://doi.org/10.1101/2025.02.07.636951openalex-snapshot
Multiplexed CRISPRi Reveals a Transcriptional Switch Between KLF Activators and Repressors in the Maturing Neocortex
inferred← citeshttps://doi.org/10.1111/apha.12648openalex-snapshot
Emerging role of thyroid hormone metabolites
inferred← citeshttps://doi.org/10.1111/j.1365-2826.2012.02329.xopenalex-snapshot
Thyroid Hormone Accelerates the Differentiation of Adult Hippocampal Progenitors
inferred← citeshttps://doi.org/10.1126/sciadv.adi1863openalex-snapshot
Brain hypothyroidism silences the immune response of microglia in Alzheimer’s disease animal model
inferred← citeshttps://doi.org/10.1126/science.abe8244openalex-snapshot
From cohorts to molecules: Adverse impacts of endocrine disrupting mixtures
inferred← citeshttps://doi.org/10.1128/mcb.00363-21openalex-snapshot
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone α
inferred← citeshttps://doi.org/10.1177/0748730420913205openalex-snapshot
The Paralogous Krüppel-like Factors 9 and 13 Regulate the Mammalian Cellular Circadian Clock Output Gene Dbp
inferred← citeshttps://doi.org/10.1177/15473287261440389openalex-snapshot
In Vitro Study of Triiodothyronine Effects on C57B6J Mesenchymal Stem Cells Isolated from Bone Marrow and Adipose Tissue
inferred← citeshttps://doi.org/10.1182/blood-2017-05-783043openalex-snapshot
Thyroid hormone regulates hematopoiesis via the TR-KLF9 axis
inferred← citeshttps://doi.org/10.1186/1471-2164-12-634openalex-snapshot
Thyroid hormone-regulated gene expression in juvenile mouse liver: identification of thyroid response elements using microarray profiling and in silico analyses
inferred← citeshttps://doi.org/10.1186/s12864-017-3640-7openalex-snapshot
The Krüppel-like factor 9 cistrome in mouse hippocampal neurons reveals predominant transcriptional repression via proximal promoter binding
inferred← citeshttps://doi.org/10.1210/en.2012-1303openalex-snapshot
Molecular Basis for Glucocorticoid Induction of the Krüppel-Like Factor 9 Gene in Hippocampal Neurons
inferred← citeshttps://doi.org/10.1210/en.2012-1463openalex-snapshot
Thyroid Hormone Signaling in the Xenopus laevis Embryo Is Functional and Susceptible to Endocrine Disruption
inferred← citeshttps://doi.org/10.1210/en.2012-2189openalex-snapshot
Role of Thyroid Hormone Receptor Subtypes α and β on Gene Expression in the Cerebral Cortex and Striatum of Postnatal Mice
inferred← citeshttps://doi.org/10.1210/en.2015-1529openalex-snapshot
Liganded Thyroid Hormone Receptors Transactivate the DNA Methyltransferase 3a Gene in Mouse Neuronal Cells
inferred← citeshttps://doi.org/10.1210/en.2015-1643openalex-snapshot
Mild Thyroid Hormone Insufficiency During Development Compromises Activity-Dependent Neuroplasticity in the Hippocampus of Adult Male Rats
inferred← citeshttps://doi.org/10.1210/en.2016-1465openalex-snapshot
Developmental and Thyroid Hormone Regulation of the DNA Methyltransferase 3a Gene in Xenopus Tadpoles
inferred← citeshttps://doi.org/10.1210/en.2019-00125openalex-snapshot
Thyroid Hormone Protects Primary Cortical Neurons Exposed to Hypoxia by Reducing DNA Methylation and Apoptosis
inferred← citeshttps://doi.org/10.1210/endocr/bqaa155openalex-snapshot
Thyroid Hormone Induces DNA Demethylation in Xenopus Tadpole Brain
inferred← citeshttps://doi.org/10.1210/jc.2013-2215openalex-snapshot
An Adult Female With Resistance to Thyroid Hormone Mediated by Defective Thyroid Hormone Receptor α
inferred← citeshttps://doi.org/10.1210/me.2014-1349openalex-snapshot
Deciphering the Regulatory Logic of an Ancient, Ultraconserved Nuclear Receptor Enhancer Module
inferred← citeshttps://doi.org/10.1242/dev.194357openalex-snapshot
Murine intestinal stem cells are highly sensitive to modulation of the T3/TRα1-dependent pathway
inferred← citeshttps://doi.org/10.1371/journal.pone.0030703openalex-snapshot
Genome-Wide Search Reveals the Existence of a Limited Number of Thyroid Hormone Receptor Alpha Target Genes in Cerebellar Neurons
inferred← citeshttps://doi.org/10.1371/journal.pone.0083358openalex-snapshot
A Coregulatory Network of NR2F1 and microRNA-140
inferred← citeshttps://doi.org/10.1371/journal.pone.0091692openalex-snapshot
Thyroid Hormone Regulation of Gene Expression in Primary Cerebrocortical Cells: Role of Thyroid Hormone Receptor Subtypes and Interactions with Retinoic Acid and Glucocorticoids
inferred← citeshttps://doi.org/10.1371/journal.pone.0101155openalex-snapshot
Thyroid Hormone Response Element Half-Site Organization and Its Effect on Thyroid Hormone Mediated Transcription
inferred← citeshttps://doi.org/10.1371/journal.pone.0220378openalex-snapshot
Coordinated transcriptional regulation by thyroid hormone and glucocorticoid interaction in adult mouse hippocampus-derived neuronal cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0221230openalex-snapshot
Ontogenetic expression of thyroid hormone signaling genes: An in vitro and in vivo species comparison
inferred← citeshttps://doi.org/10.1530/joe-19-0339openalex-snapshot
Hematopoiesis in aged female mice devoid of thyroid hormone receptors
inferred← citeshttps://doi.org/10.1787/ea5aa069-enopenalex-snapshot
Adverse Outcome Pathway on inhibition of Thyroperoxidase and subsequent adverse neurodevelopmental outcomes in mammals
inferred← citeshttps://doi.org/10.2217/fnl-2019-0014openalex-snapshot
Chronic Stress, Physiological Adaptation and Developmental Programming of the Neuroendocrine Stress System
inferred← citeshttps://doi.org/10.22215/etd/2010-09220openalex-snapshot
Computational identification of thyroid response elements in genomic DNA
inferred← citeshttps://doi.org/10.22215/etd/2014-10122openalex-snapshot
Characterizing Thyroid Hormone Mediated Action on Gene Expression in Mice: Mechanistic Insight into Thyroid Hormone Response Elements, Thyroid Hormone Receptor-binding Sites, and MicroRNAs
inferred← citeshttps://doi.org/10.3389/fendo.2019.00287openalex-snapshot
Insufficiency of Thyroid Hormone in Frog Metamorphosis and the Role of Glucocorticoids
inferred← citeshttps://doi.org/10.3389/fnmol.2020.602638openalex-snapshot
Krüppel-Like Factors 9 and 13 Block Axon Growth by Transcriptional Repression of Key Components of the cAMP Signaling Pathway
inferred← citeshttps://doi.org/10.3390/ijms231911938openalex-snapshot
A Fine Regulation of the Hippocampal Thyroid Signalling Protects Hypothyroid Mice against Glial Cell Activation
inferred← citeshttps://doi.org/10.3390/ijms241311187openalex-snapshot
KLF13 Regulates the Activity of the GH-Induced JAK/STAT Signaling by Targeting Genes Involved in the Pathway
inferred← citeshttps://doi.org/10.3390/ijms27177607openalex-snapshot
Deiodinase 3 Deficiency Impairs Hippocampal and Lateral Ventricle Neurogenesis in Middle-Aged Female Mice
inferred← citeshttps://doi.org/10.3390/toxics10020092openalex-snapshot
Triiodothyronine or Antioxidants Block the Inhibitory Effects of BDE-47 and BDE-49 on Axonal Growth in Rat Hippocampal Neuron-Glia Co-Cultures
inferred← citeshttps://doi.org/10.4061/2011/145762openalex-snapshot
Thyroid Hormone Action in Cerebellum and Cerebral Cortex Development
inferred← citeshttps://doi.org/10.62347/mihm9413openalex-snapshot
Implications of Krüppel-like factor signaling in neuroinflammation for neurodegenerative diseases
inferred← citeshttps://doi.org/10.64898/2026.02.03.703562openalex-snapshot
Whole-body single-cell atlas of an adult vertebrate in homeostasis and regeneration
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Évolution des gènes de la pigmentation chez les Vertébrés et développement pigmentaire chez un modèle émergent de poisson corallien, le poisson-clown Amphiprion ocellaris
inferred← citeshttps://doi.org/10.70675/ebf642e5z6231z45cdzad93zaaa4498bf39dopenalex-snapshot
Importance of metamorphosis in coral-reef fish larval recruitment facing anthropogenic pressures
inferred← citeshttps://doi.org/10.7554/elife.106510openalex-snapshot
Multiplexed CRISPRi Reveals a Transcriptional Switch Between KLF Activators and Repressors in the Maturing Neocortex
inferred← citeshttps://doi.org/10.7554/elife.106510.1openalex-snapshot
Multiplexed CRISPRi Reveals a Transcriptional Switch Between KLF Activators and Repressors in the Maturing Neocortex
inferred← citeshttps://doi.org/10.7554/elife.106510.2openalex-snapshot
Multiplexed CRISPRi Reveals a Transcriptional Switch Between KLF Activators and Repressors in the Maturing Neocortex
inferred← citeshttps://doi.org/10.7554/elife.27595openalex-snapshot
Fish larval recruitment to reefs is a thyroid hormone-mediated metamorphosis sensitive to the pesticide chlorpyrifos
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