TAZ/WWTR1 Mediates the Pulmonary Effects of NKX2-1 Mutations in Brain-Lung-Thyroid Syndrome

The Hippo pathway in tissue homeostasis and regeneration

(2017) Yu Wang et al.   Protein & Cell

TAZ contributes to pulmonary fibrosis by activating profibrotic functions of lung fibroblasts

(2017) Satoshi Noguchi et al.   Scientific Reports

The Hippo pathway in cellular reprogramming and regeneration of different organs

(2016) Iván M Moya et al.   CURRENT OPINION IN CELL BIOLOGY

Disease implication of hyper-Hippo signalling

(2016) Shu-Ping Wang et al.   Open Biology

Thyroid transcription factors in development, differentiation and disease

(2014) Lara P. Fernández et al.   Nature Reviews Endocrinology

WNT/β-Catenin Signaling Induces IL-1β Expression by Alveolar Epithelial Cells in Pulmonary Fibrosis

(2013) Verena Aumiller et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1

(2013) Aaron Hamvas et al.   CHEST

Novel NKX2.1 mutation associated with hypothyroidism and lethal respiratory failure in a full-term neonate

(2013) E S Gillett et al.   Journal of Perinatology

Identification and Functional Characterization of a Novel Mutation in the NKX2-1 Gene: Comparison with the Data in the Literature

(2013) Immacolata Cristina Nettore et al.   THYROID

Role of TAZ as Mediator of Wnt Signaling

(2012) Luca Azzolin et al.   CELL

Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in theTITF1/NKX2-1gene

(2012) Domitille Gras et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1

(2011) Daniel Silberschmidt et al.   BMC DEVELOPMENTAL BIOLOGY

Fatal neonatal respiratory failure in an infant with congenital hypothyroidism due to haploinsufficiency of the NKX2-1 gene: alteration of pulmonary surfactant homeostasis

(2010) B. Kleinlein et al.   Archives of Disease in Childhood-Fetal and Neonatal Edition

TAZ as a novel enhancer of MyoD-mediated myogenic differentiation

(2010) Hana Jeong et al.   FASEB JOURNAL

Advanced magnetic resonance imaging in benign hereditary chorea: Study of two familial cases

(2010) Gloria Maccabelli et al.   MOVEMENT DISORDERS

Transcriptional Coactivator with PDZ-binding Motif Is Essential for Normal Alveolarization in Mice

(2009) Akihisa Mitani et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

NLStradamus: a simple Hidden Markov Model for nuclear localization signal prediction

(2009) Alex N Nguyen Ba et al.   BMC BIOINFORMATICS

Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case

(2009) A. Carre et al.   HUMAN MOLECULAR GENETICS

A Germline Mutation (A339V) in Thyroid Transcription Factor-1 (TITF-1/NKX2.1) in Patients With Multinodular Goiter and Papillary Thyroid Carcinoma

(2009) Elly S. W. Ngan et al.   JNCI-Journal of the National Cancer Institute

Foxp2 Inhibits Nkx2.1-Mediated Transcription of SP-C via Interactions with the Nkx2.1 Homeodomain

(2008) Beiyun Zhou et al.   AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

NKX2.1 specifies cortical interneuron fate by activating Lhx6

(2008) T. Du et al.   DEVELOPMENT

TAZ is a coactivator for Pax8 and TTF-1, two transcription factors involved in thyroid differentiation

(2008) Tina Di Palma et al.   EXPERIMENTAL CELL RESEARCH

CAATT/Enhancer-binding Proteins α and δ Interact with NKX2-1 to Synergistically Activate Mouse Secretoglobin 3A2 Gene Expression

(2008) Takeshi Tomita et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with ade NovoHeterozygous Mutation in theTITF1/NKX2.1Gene

(2008) Emilie Maquet et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM