Research graph
References from Can neurodevelopmental disorders be part of brain-lung-thyroid syndrome? A case report. Local targets link to admitted publications; unresolved targets remain external evidence.
The requirement of Nkx2-1 in the temporal specification of cortical interneuron subtypes.
10.1016/j.neuron.2008.07.031 · 2008 · External reference
Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case.
10.1093/hmg/ddp162 · 2009 · External reference
Evaluation of parent involvement multiple oppositions intervention for children with speech sound disorders: descriptive research.
10.5336/healthsci.2023-98084 · 2024 · External reference
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
10.1136/jnnp-2012-302505 · 2012 · External reference
NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in “Brain-Lung-Thyroid Syndrome”.
10.1002/humu.21183 · 2010 · External reference
The relationship between the phonological loop and receptive language and nonverbal intelligence in speech sound disorders.
10.21565/ozelegitimdergisi.1614314 · 2026 · External reference
Thyroid-specific enhancer-binding protein/NKX2.1 is required for the maintenance of ordered architecture and function of the differentiated thyroid.
10.1210/me.2005-0327 · 2006 · External reference
The transcription factor TTF-1 is expressed at the onset of thyroid and lung morphogenesis and in restricted regions of the foetal brain.
10.1242/dev.113.4.1093 · 1991 · External reference
Transcriptional control of lung morphogenesis.
10.1152/physrev.00028.2006 · 2007 · External reference
Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress.
10.1210/jc.2005-1497 · 2006 · External reference
Postmitotic Nkx2-1 controls the migration of telencephalic interneurons by direct repression of guidance receptors.
10.1016/j.neuron.2008.07.024 · 2008 · External reference
NKX2-1 mutations in brain-lung-thyroid syndrome: a case series of four patients.
10.1515/jpem-2013-0109 · 2014 · External reference
PAX8, TITF1, and FOXE1 gene expression patterns during human development: new insights into human thyroid development and thyroid dysgenesis-associated malformations.
10.1210/jc.2004-1358 · 2005 · External reference
