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Implication of thyroid hormone signaling in neural crest cells migration: Evidence from thyroid hormone receptor beta knockdown and NH3 antagonist studies
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bdrc.21078openalex-snapshot
Neural crest development in fetal alcohol syndrome
inferredcites →https://doi.org/10.1002/bies.950150404openalex-snapshot
Gene expression during metamorphosis: An ideal model for post‐embryonic development
inferredcites →https://doi.org/10.1002/bies.950180509openalex-snapshot
Tadpole competence and tissue‐specific temporal regulation of amphibian metamorphosis: Roles of thyroid hormone and its receptors
inferredcites →https://doi.org/10.1002/j.1460-2075.1990.tb08185.xopenalex-snapshot
Accumulation of proto‐oncogene c‐erb‐A related transcripts during Xenopus development: association with early acquisition of response to thyroid hormone and estrogen.
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb00664.xopenalex-snapshot
Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: evidence for tissue‐specific modulation of receptor function.
inferredcites →https://doi.org/10.1002/wdev.76openalex-snapshot
Signaling and transcriptional regulation in neural crest specification and migration: lessons from xenopus embryos
inferredcites →https://doi.org/10.1006/dbio.2000.9723openalex-snapshot
Relationship between Gene Expression Domains of Xsnail, Xslug, and Xtwist and Cell Movement in the Prospective Neural Crest of Xenopus
inferredcites →https://doi.org/10.1006/dbio.2000.9945openalex-snapshot
Use of Large-Scale Expression Cloning Screens in the Xenopus laevis Tadpole to Identify Gene Function
inferredcites →https://doi.org/10.1006/dbio.2001.0565openalex-snapshot
Morpholino Oligos: Making Sense of Antisense?
inferredcites →https://doi.org/10.1006/dbio.2002.0621openalex-snapshot
Transcription Factor AP-2 Is an Essential and Direct Regulator of Epidermal Development in Xenopus
inferredcites →https://doi.org/10.1006/gcen.1994.1060openalex-snapshot
Changes in Whole-Body Thyroxine and Triiodothyronine Concentrations and Total Content during Early Development and Metamorphosis of the Toad Bufo marinus
inferredcites →https://doi.org/10.1007/s00427-007-0158-zopenalex-snapshot
The olig family: phylogenetic analysis and early gene expression in Xenopus tropicalis
inferredcites →https://doi.org/10.1007/s100249900162openalex-snapshot
Early Death of Neural Crest Cells is Responsible for Total Enteric Aganglionosis in Sox10Dom/Sox10Dom Mouse Embryos
inferredcites →https://doi.org/10.1007/s10048-009-0200-6openalex-snapshot
Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy
inferredcites →https://doi.org/10.1007/s10653-015-9681-4openalex-snapshot
The importance of iodine in public health
inferredcites →https://doi.org/10.1016/0012-1606(68)90050-xopenalex-snapshot
Early metamorphic competence of Xenopus larvae
inferredcites →https://doi.org/10.1016/0012-1606(83)90255-5openalex-snapshot
Axis determination in eggs of Xenopus laevis: A critical period before first cleavage, identified by the common effects of cold, pressure and ultraviolet irradiation
inferredcites →https://doi.org/10.1016/0012-1606(88)90189-3openalex-snapshot
The entire mesodermal mantle behaves as Spemann's organizer in dorsoanterior enhanced Xenopus laevis embryos
inferredcites →https://doi.org/10.1016/b978-0-12-385979-2.00013-7openalex-snapshot
Is Thyroid Hormone Signaling Relevant for Vertebrate Embryogenesis?
inferredcites →https://doi.org/10.1016/j.bbagen.2012.04.009openalex-snapshot
The pathophysiological consequences of thyroid hormone transporter deficiencies: Insights from mouse models
inferredcites →https://doi.org/10.1016/j.bbagen.2012.04.020openalex-snapshot
Mechanisms of thyroid hormone receptor action during development: Lessons from amphibian studies
inferredcites →https://doi.org/10.1016/j.bbagen.2012.08.005openalex-snapshot
The syndromes of reduced sensitivity to thyroid hormone
inferredcites →https://doi.org/10.1016/j.beem.2004.03.012openalex-snapshot
Maternal thyroid hormones early in pregnancy and fetal brain development
inferredcites →https://doi.org/10.1016/j.mce.2008.09.016openalex-snapshot
Complex actions of thyroid hormone receptor antagonist NH-3 on gene promoters in different cell lines
inferredcites →https://doi.org/10.1016/j.mce.2009.09.008openalex-snapshot
Thyroid hormone action during brain development: More questions than answers
inferredcites →https://doi.org/10.1016/j.mce.2011.09.005openalex-snapshot
Thyroid effects of endocrine disrupting chemicals
inferredcites →https://doi.org/10.1016/j.mce.2016.01.020openalex-snapshot
Patterns of thyroid hormone receptor expression in zebrafish and generation of a novel model of resistance to thyroid hormone action
inferredcites →https://doi.org/10.1016/j.neuroscience.2015.09.070openalex-snapshot
Influence of maternal thyroid hormones during gestation on fetal brain development
inferredcites →https://doi.org/10.1016/j.reprotox.2015.04.012openalex-snapshot
Comparative analysis of goitrogenic effects of phenylthiourea and methimazole in zebrafish embryos
inferredcites →https://doi.org/10.1016/j.semcdb.2011.07.009openalex-snapshot
The role of iodine in human growth and development
inferredcites →https://doi.org/10.1016/j.ydbio.2011.12.041openalex-snapshot
Neural crest delamination and migration: From epithelium-to-mesenchyme transition to collective cell migration
inferredcites →https://doi.org/10.1016/j.ydbio.2012.11.005openalex-snapshot
Thyroid hormone and retinoic acid interact to regulate zebrafish craniofacial neural crest development
inferredcites →https://doi.org/10.1016/j.ygcen.2009.12.008openalex-snapshot
Expression and T3 regulation of thyroid hormone- and sex steroid-related genes during Silurana (Xenopus) tropicalis early development
inferredcites →https://doi.org/10.1016/s0012-1606(03)00161-1openalex-snapshot
Sox10 regulates the development of neural crest-derived melanocytes in Xenopus
inferredcites →https://doi.org/10.1016/s0012-1606(03)00247-1openalex-snapshot
Sox10 is required for the early development of the prospective neural crest in Xenopus embryos
inferredcites →https://doi.org/10.1016/s0021-9258(19)51106-1openalex-snapshot
Quantitation of endogenous thyroid hormone receptors alpha and beta during embryogenesis and metamorphosis in Xenopus laevis.
inferredcites →https://doi.org/10.1016/s0046-8177(74)80021-3openalex-snapshot
The neurocristopathiesA unifying concept of disease arising in neural crest maldevelopment
inferredcites →https://doi.org/10.1016/s0083-6729(04)68007-1openalex-snapshot
Corepressor Requirement and Thyroid Hormone Receptor Function During Xenopus Development
inferredcites →https://doi.org/10.1016/s0303-7207(01)00529-9openalex-snapshot
Expression of thyroid hormone receptor βA gene assayed by transgenic Xenopus laevis carrying its promoter sequences
inferredcites →https://doi.org/10.1016/s1043-2760(02)00043-7openalex-snapshot
Thyroid hormone receptors: lessons from knockout and knock-in mutant mice
inferredcites →https://doi.org/10.1016/s1701-2163(16)30420-0openalex-snapshot
The Role of Thyroid Hormone in Trophoblast Function, Early Pregnancy Maintenance, and Fetal Neurodevelopment
inferredcites →https://doi.org/10.1021/jm0201013openalex-snapshot
Rational Design and Synthesis of a Novel Thyroid Hormone Antagonist That Blocks Coactivator Recruitment
inferredcites →https://doi.org/10.1038/311716a0openalex-snapshot
Cell type-specific activation of actin genes in the early amphibian embryo
inferredcites →https://doi.org/10.1038/ncpendmet0590openalex-snapshot
Potential therapeutic applications of thyroid hormone analogs
inferredcites →https://doi.org/10.1038/ng0198-60openalex-snapshot
SOX10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
inferredcites →https://doi.org/10.1038/ng0298-171openalex-snapshot
SOX10 mutations in patients with Waardenburg-Hirschsprung disease
inferredcites →https://doi.org/10.1038/ng0598-87openalex-snapshot
Follicular cells of the thyroid gland require Pax8 gene function
inferredcites →https://doi.org/10.1038/ng0796-354openalex-snapshot
Thyroid hormone receptor β is essential for development of auditory function
inferredcites →https://doi.org/10.1038/nrd2830openalex-snapshot
Thyroid hormone mimetics: potential applications in atherosclerosis, obesity and type 2 diabetes
inferredcites →https://doi.org/10.1038/sj.emboj.7601356openalex-snapshot
Unliganded thyroid hormone receptor is essential for Xenopus laevis eye development
inferredcites →https://doi.org/10.1042/bc20060074openalex-snapshot
Expression of enzymes involved in thyroid hormone metabolism during the early development of Xenopus tropicalis
inferredcites →https://doi.org/10.1046/j.1365-2265.1999.00602.xopenalex-snapshot
Thyroid hormones and neurodevelopment
inferredcites →https://doi.org/10.1046/j.1365-2265.1999.00639.xopenalex-snapshot
Low maternal free thyroxine concentrations during early pregnancy are associated with impaired psychomotor development in infancy
inferredcites →https://doi.org/10.1056/nejm198510033131401openalex-snapshot
Retinoic Acid Embryopathy
inferredcites →https://doi.org/10.1056/nejm199412293312603openalex-snapshot
Timing of Vulnerability of the Brain to Iodine Deficiency in Endemic Cretinism
inferredcites →https://doi.org/10.1073/pnas.0401843101openalex-snapshot
Thyroid hormone receptor α is a molecular switch of cardiac function between fetal and postnatal life
inferredcites →https://doi.org/10.1073/pnas.062413299openalex-snapshot
Deletion of the thyroid hormone receptor α1 prevents the structural alterations of the cerebellum induced by hypothyroidism
inferredcites →https://doi.org/10.1073/pnas.0905190107openalex-snapshot
Thyroid hormone exerts negative feedback on hypothalamic type 4 melanocortin receptor expression
inferredcites →https://doi.org/10.1073/pnas.1219124110openalex-snapshot
Pax3 and Zic1 drive induction and differentiation of multipotent, migratory, and functional neural crest in Xenopus embryos
inferredcites →https://doi.org/10.1073/pnas.87.18.7090openalex-snapshot
Xenopus laevis alpha and beta thyroid hormone receptors.
inferredcites →https://doi.org/10.1073/pnas.95.9.5161openalex-snapshot
Mutation of the Sry-related Sox10 gene in Dominant megacolon , a mouse model for human Hirschsprung disease
inferredcites →https://doi.org/10.1074/jbc.m205608200openalex-snapshot
A Thyroid Hormone Antagonist That Inhibits Thyroid Hormone Action in Vivo
inferredcites →https://doi.org/10.1080/15513819609169308openalex-snapshot
Retinoic Acid Embryopathy: Case Report and Review of Literature
inferredcites →https://doi.org/10.1089/oli.2006.16.26openalex-snapshot
Characterization of Modified Antisense Oligonucleotides in Xenopus laevis Embryos
inferredcites →https://doi.org/10.1089/thy.1996.6.497openalex-snapshot
Nongenomic Actions of Thyroid Hormone
inferredcites →https://doi.org/10.1093/emboj/18.3.623openalex-snapshot
Different functions for the thyroid hormone receptors TRα and TRβ in the control of thyroid hormone production and post‐natal development
inferredcites →https://doi.org/10.1096/fj.10-179234openalex-snapshot
Strain‐specific vulnerability to alcohol exposure in utero via hippocampal parent‐of‐origin expression of deiodinase‐III
inferredcites →https://doi.org/10.1097/aog.0b013e3181996fe5openalex-snapshot
Thyroid Dysfunction in Pregnancy
inferredcites →https://doi.org/10.1101/gad.13.10.1329openalex-snapshot
Mice devoid of all known thyroid hormone receptors are viable but exhibit disorders of the pituitary-thyroid axis, growth, and bone maturation
inferredcites →https://doi.org/10.1101/gad.186601openalex-snapshot
The transcription factor Sox10 is a key regulator of peripheral glial development
inferredcites →https://doi.org/10.1101/gad.4.11.1917openalex-snapshot
A correlation of thyroid hormone receptor gene expression with amphibian metamorphosis.
inferredcites →https://doi.org/10.1101/gr.9.3.215openalex-snapshot
The Sox10Dom Mouse: Modeling the Genetic Variation of Waardenburg-Shah (WS4) Syndrome
inferredcites →https://doi.org/10.1111/j.1365-2265.1976.tb02827.xopenalex-snapshot
MATERNAL THYROID FUNCTION, IODINE DEFICIENCY AND FETAL DEVELOPMENT
inferredcites →https://doi.org/10.1111/j.1365-2265.1984.tb00119.xopenalex-snapshot
MATERNAL HYPERTHYROIDISM AND CONGENITAL MALFORMATION IN THE OFFSPRING
inferredcites →https://doi.org/10.1111/j.1365-2265.2009.03743.xopenalex-snapshot
Abnormalities of maternal thyroid function during pregnancy affect neuropsychological development of their children at 25–30 months
inferredcites →https://doi.org/10.1111/j.1432-0436.2004.07205006.xopenalex-snapshot
Early expression of thyroid hormone receptor β and retinoid X receptor γ in the Xenopus embryo
inferredcites →https://doi.org/10.1111/j.1530-0277.2010.01373.xopenalex-snapshot
Candidate Placental Biomarkers for Intrauterine Alcohol Exposure
inferredcites →https://doi.org/10.1128/mcb.11.10.5079openalex-snapshot
The thyroid hormone receptor gene (c-erbA alpha) is expressed in advance of thyroid gland maturation during the early embryonic development of Xenopus laevis.
inferredcites →https://doi.org/10.1128/mcb.21.14.4748-4760.2001openalex-snapshot
Genetic Analysis Reveals Different Functions for the Products of the Thyroid Hormone Receptor α Locus
inferredcites →https://doi.org/10.1146/annurev-physiol-021909-135917openalex-snapshot
Structural Overview of the Nuclear Receptor Superfamily: Insights into Physiology and Therapeutics
inferredcites →https://doi.org/10.1152/physrev.2001.81.3.1097openalex-snapshot
Physiological and Molecular Basis of Thyroid Hormone Action
inferredcites →https://doi.org/10.1159/000055682openalex-snapshot
Role of Thyroid Hormone in Craniofacial and Eye Development Using a Rat Model
inferredcites →https://doi.org/10.1159/000363153openalex-snapshot
The Role of Thyroid Hormones for Brain Development and Cognitive Function
inferredcites →https://doi.org/10.1172/jci115023openalex-snapshot
Screening of nineteen unrelated families with generalized resistance to thyroid hormone for known point mutations in the thyroid hormone receptor beta gene and the detection of a new mutation.
inferredcites →https://doi.org/10.1172/jci117376openalex-snapshot
Mutations of CpG dinucleotides located in the triiodothyronine (T3)-binding domain of the thyroid hormone receptor (TR) beta gene that appears to be devoid of natural mutations may not be detected because they are unlikely to produce the clinical phenotype of resistance to thyroid hormone.
inferredcites →https://doi.org/10.1186/1471-2164-8-118openalex-snapshot
Exploring nervous system transcriptomes during embryogenesis and metamorphosis in Xenopus tropicalis using EST analysis
inferredcites →https://doi.org/10.1210/en.2006-0609openalex-snapshot
Deiodinase Activity Is Present inXenopus laevisduring Early Embryogenesis
inferredcites →https://doi.org/10.1210/en.2012-1463openalex-snapshot
Thyroid Hormone Signaling in the Xenopus laevis Embryo Is Functional and Susceptible to Endocrine Disruption
inferredcites →https://doi.org/10.1210/en.2013-1660openalex-snapshot
Knockdown of Type 3 Iodothyronine Deiodinase Severely Perturbs Both Embryonic and Early Larval Development in Zebrafish
inferredcites →https://doi.org/10.1210/en.2013-1962openalex-snapshot
Knockdown of Monocarboxylate Transporter 8 (mct8) Disturbs Brain Development and Locomotion in Zebrafish
inferredcites →https://doi.org/10.1210/en.2014-1439openalex-snapshot
Unliganded Thyroid Hormone Receptor α Controls Developmental Timing in Xenopus tropicalis
inferredcites →https://doi.org/10.1210/en.2014-1554openalex-snapshot
Unliganded Thyroid Hormone Receptor α Regulates Developmental Timing via Gene Repression in Xenopus tropicalis
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/10.1210/er.2009-0002openalex-snapshot
Endocrine-Disrupting Chemicals: An Endocrine Society Scientific Statement
inferredcites →https://doi.org/10.1210/er.2009-0007openalex-snapshot
Molecular Aspects of Thyroid Hormone Actions
inferredcites →https://doi.org/10.1210/jc.2010-0415openalex-snapshot
Maternal Thyroid Function during Early Pregnancy and Cognitive Functioning in Early Childhood: The Generation R Study
inferredcites →https://doi.org/10.1210/jc.2011-0274openalex-snapshot
Maternal Thyroid Function in the First Twenty Weeks of Pregnancy and Subsequent Fetal and Infant Development: A Prospective Population-Based Cohort Study in China
inferredcites →https://doi.org/10.1210/jc.2011-2642openalex-snapshot
Homozygous Thyroid Hormone Receptor β-Gene Mutations in Resistance to Thyroid Hormone: Three New Cases and Review of the Literature
inferredcites →https://doi.org/10.1210/jc.74.1.49openalex-snapshot
Recessive inheritance of thyroid hormone resistance caused by complete deletion of the protein-coding region of the thyroid hormone receptor- beta gene
inferredcites →https://doi.org/10.1210/jc.87.2.557openalex-snapshot
A Population-Based Study on the Frequency of Additional Congenital Malformations in Infants with Congenital Hypothyroidism: Data from the Italian Registry for Congenital Hypothyroidism (1991-1998)
inferredcites →https://doi.org/10.1210/me.14.7.947openalex-snapshot
Thyroid Hormone Regulation of Hepatic Genes in Vivo Detected by Complementary DNA Microarray
inferredcites →https://doi.org/10.1210/me.2006-0035openalex-snapshot
Thyroid Hormones Signaling Is Getting More Complex: STORMs Are Coming
inferredcites →https://doi.org/10.1210/me.2014-1032openalex-snapshot
Maternal Thyroid Hormones Are Essential for Neural Development in Zebrafish
inferredcites →https://doi.org/10.1210/me.6.11.1797openalex-snapshot
Assignment of the beta-thyroid hormone receptor to 3,5,3'- triiodothyronine-dependent inhibition of transcription from the thyrotropin-releasing hormone promoter in chick hypothalamic neurons
inferredcites →https://doi.org/10.1210/mend.16.1.0766openalex-snapshot
Congenital Hypothyroid Pax8−/− Mutant Mice Can Be Rescued by Inactivating the TRα Gene
inferredcites →https://doi.org/10.1242/dev.105445openalex-snapshot
Establishing neural crest identity: a gene regulatory recipe
inferredcites →https://doi.org/10.1242/dev.111.4.1179openalex-snapshot
Progressively restricted expression of a new homeobox-containing gene during Xenopus laevis embryogenesis
inferredcites →https://doi.org/10.1242/dev.112.4.933openalex-snapshot
Developmental and regional expression of thyroid hormone receptor genes during Xenopus metamorphosis
inferredcites →https://doi.org/10.1242/dev.113.supplement_1.95openalex-snapshot
Gene activation in the amphibian mesoderm
inferredcites →https://doi.org/10.1242/dev.125.4.579openalex-snapshot
Xenopus Zic-related-1 and Sox-2, two factors induced by chordin, have distinct activities in the initiation of neural induction
inferredcites →https://doi.org/10.1242/dev.128.13.2525openalex-snapshot
Requirement ofFoxD3-class signaling for neural crest determination inXenopus
inferredcites →https://doi.org/10.1242/dev.22.2.253openalex-snapshot
The formation of somites in Xenopus
inferredcites →https://doi.org/10.1242/dev.64.1.295openalex-snapshot
The formation of somites and early myotomal myogenesis in Xenopus laevis, Bombina variegata and Pelobates fuscus*
inferredcites →https://doi.org/10.1289/ehp.11058openalex-snapshot
The Relationship between Prenatal PCB Exposure and Intelligence (IQ) in 9-Year-Old Children
inferredcites →https://doi.org/10.1371/journal.pone.0123285openalex-snapshot
Deiodinase Knockdown during Early Zebrafish Development Affects Growth, Development, Energy Metabolism, Motility and Phototransduction
inferredcites →https://doi.org/10.1530/jme-13-0108openalex-snapshot
Analysis of the roles of mutations in thyroid hormone receptor-β by a bacterial biosensor system
inferredcites →https://doi.org/10.1590/s0041-87811999000300007openalex-snapshot
Congenital hyperthyroidism: autopsy report
inferredcites →https://doi.org/10.1597/1545-1569(1995)032<0328:cdawjh>2.3.co;2openalex-snapshot
Craniofacial Deformities Associated with Juvenile Hyperthyroidism
inferredcites →https://doi.org/10.1677/jme-08-0023openalex-snapshot
The role of thyroid hormone receptor DNA binding in negative thyroid hormone-mediated gene transcription
inferredcites →https://doi.org/10.1677/jme.0.0310009openalex-snapshot
Do unliganded thyroid hormone receptors have physiological functions?
inferredcites →https://doi.org/10.3389/fendo.2016.00016openalex-snapshot
Preliminary Findings Show Maternal Hypothyroidism May Contribute to Abnormal Cortical Morphology in Offspring
inferredcites →https://doi.org/10.3791/51118openalex-snapshot
Dissection of Xenopus laevis Neural Crest for in vitro Explant Culture or in vivo Transplantation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/bdr2.1644openalex-snapshot
The role of teratogens in neural crest development
inferred← citeshttps://doi.org/10.1002/dvg.23000openalex-snapshot
Frogs model man: In vivo thyroid hormone signaling during development
inferred← citeshttps://doi.org/10.1002/evan.21777openalex-snapshot
Evaluating the self‐domestication hypothesis of human evolution
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.04.004openalex-snapshot
Thyroid Hormone Receptor Antagonists: From Environmental Pollution to Novel Small Molecules
inferred← citeshttps://doi.org/10.1016/j.envint.2025.109381openalex-snapshot
Fetal exposure to perfluoroalkyl substances (PFAS) in drinking water and congenital malformations: A nation-wide register-based study on PFAS in drinking water
inferred← citeshttps://doi.org/10.1016/j.materresbull.2024.112774openalex-snapshot
Room-temperature NH3 sensor based on CoFe2O4/PANI composite with porous structure
inferred← citeshttps://doi.org/10.1016/j.mce.2017.01.045openalex-snapshot
Dissecting the role of regulators of thyroid hormone availability in early brain development: Merits and potential of the chicken embryo model
inferred← citeshttps://doi.org/10.1016/j.mce.2017.05.020openalex-snapshot
Comparative approaches to understanding thyroid hormone regulation of neurogenesis
inferred← citeshttps://doi.org/10.1016/j.neuro.2021.03.003openalex-snapshot
Investigation of NH3 as a selective thyroid hormone receptor modulator in larval zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.04.113openalex-snapshot
Agricultural expansion as risk to endangered wildlife: Pesticide exposure in wild chimpanzees and baboons displaying facial dysplasia
inferred← citeshttps://doi.org/10.1016/j.snb.2017.08.117openalex-snapshot
A novel coral-shaped Dy2O3 gas sensor for high sensitivity NH3 detection at room temperature
inferred← citeshttps://doi.org/10.1080/15287394.2024.2311828openalex-snapshot
How do different concentrations of aluminum and zinc affect the survival, body size, morphology and immune system of Physalaemus cuvieri (Fitzinger, 1826) tadpole?
inferred← citeshttps://doi.org/10.1093/toxsci/kfad063openalex-snapshot
Cross-species applicability of an adverse outcome pathway network for thyroid hormone system disruption
inferred← citeshttps://doi.org/10.1101/2021.03.30.437624openalex-snapshot
Epigenome erosion drives neural crest-like phenotypic mimicry in triple-negative breast cancer and other SOX10+ malignancies
inferred← citeshttps://doi.org/10.1210/en.2016-1953openalex-snapshot
Thyroid Hormone Receptor α Controls Developmental Timing and Regulates the Rate and Coordination of Tissue-Specific Metamorphosis in Xenopus tropicalis
inferred← citeshttps://doi.org/10.1210/en.2017-00108openalex-snapshot
Functional Characterization of Xenopus Thyroid Hormone Transporters mct8 and oatp1c1
inferred← citeshttps://doi.org/10.1289/ehp9478openalex-snapshot
Prenatal Exposure to Per- and Polyfluoroalkyl Substances and Facial Features at 5 Years of Age: A Study from the Danish National Birth Cohort
inferred← citeshttps://doi.org/10.14739/2310-1237.2021.1.216292openalex-snapshot
The morphofunctional state of the fetal thyroid gland in maternal-fetal infections caused by Escherichia coli, Staphylococcus aureus and Klebsiella pneumoniae
inferred← citeshttps://doi.org/10.18699/vj17.262openalex-snapshot
Revisiting two hypotheses on the “domestication syndrome” in light of genomic data
inferred← citeshttps://doi.org/10.3389/fendo.2019.00066openalex-snapshot
The Role of Maternal Thyroid Hormones in Avian Embryonic Development
inferred← citeshttps://doi.org/10.3389/fphys.2019.00154openalex-snapshot
Xenbase: Facilitating the Use of Xenopus to Model Human Disease
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Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
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