Literature DB >> 17318014

FOXE1 polymorphisms: a new piece in the puzzle of thyroid dysgenesis.

P E Macchia.   

Abstract

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Year:  2007        PMID： 17318014     DOI： 10.1007/bf03347387

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN： 0391-4097            Impact factor:   4.256


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  8 in total

1.  Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis.

Authors:  Monica Dentice; Viviana Cordeddu; Annamaria Rosica; Alfonso Massimiliano Ferrara; Libero Santarpia; Domenico Salvatore; Luca Chiovato; Anna Perri; Lidia Moschini; Cristina Fazzini; Antonella Olivieri; Pietro Costa; Vera Stoppioni; Mariangiola Baserga; Mario De Felice; Mariella Sorcini; Gianfranco Fenzi; Roberto Di Lauro; Marco Tartaglia; Paolo Emidio Macchia
Journal:  J Clin Endocrinol Metab       Date:  2006-01-17       Impact factor: 5.958

2.  TTF-2/FOXE1 gene polymorphisms in Sicilian patients with permanent primary congenital hypothyroidism.

Authors:  L Santarpia; M Valenzise; G Di Pasquale; T Arrigo; G San Martino; M P Cicciò; F Trimarchi; F De Luca; S Benvenga
Journal:  J Endocrinol Invest       Date:  2007-01       Impact factor: 4.256

Review 3.  Polyalanine expansions in human.

Authors:  Jeanne Amiel; Delphine Trochet; Mathieu Clément-Ziza; Arnold Munnich; Stanislas Lyonnet
Journal:  Hum Mol Genet       Date:  2004-10-01       Impact factor: 6.150

4.  An investigation into FOXE1 polyalanine tract length in premature ovarian failure.

Authors:  Wendy J Watkins; Sarah E Harris; Megan J Craven; Andrea L Vincent; Ingrid M Winship; Ksenija Gersak; Andrew N Shelling
Journal:  Mol Hum Reprod       Date:  2006-02-15       Impact factor: 4.025

5.  A mouse model demonstrates a multigenic origin of congenital hypothyroidism.

Authors:  Elena Amendola; Pasquale De Luca; Paolo Emidio Macchia; Daniela Terracciano; Annamaria Rosica; Gennaro Chiappetta; Shioko Kimura; Ahmed Mansouri; Andrea Affuso; Claudio Arra; Vincenzo Macchia; Roberto Di Lauro; Mario De Felice
Journal:  Endocrinology       Date:  2005-09-08       Impact factor: 4.736

Review 6.  Thyroid development and its disorders: genetics and molecular mechanisms.

Authors:  Mario De Felice; Roberto Di Lauro
Journal:  Endocr Rev       Date:  2004-10       Impact factor: 19.871

7.  The thyroid transcription factor 2 (TTF-2) is a promoter-specific DNA-binding independent transcriptional repressor.

Authors:  L Perrone; M Pasca di Magliano; M Zannini; R Di Lauro
Journal:  Biochem Biophys Res Commun       Date:  2000-08-18       Impact factor: 3.575

8.  A mouse model for hereditary thyroid dysgenesis and cleft palate.

Authors:  M De Felice; C Ovitt; E Biffali; A Rodriguez-Mallon; C Arra; K Anastassiadis; P E Macchia; M G Mattei; A Mariano; H Schöler; V Macchia; R Di Lauro
Journal:  Nat Genet       Date:  1998-08       Impact factor: 38.330
  8 in total
  1 in total

Review 1.  The molecular causes of thyroid dysgenesis: a systematic review.

Authors:  I C Nettore; V Cacace; C De Fusco; A Colao; P E Macchia
Journal:  J Endocrinol Invest       Date:  2013-05-22       Impact factor: 4.256
  1 in total

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