Literature DB >> 21322126

Morphogenetics of early thyroid development.

Henrik Fagman1, Mikael Nilsson.   

Abstract

The thyroid develops from the foregut endoderm. Yet uncharacterized inductive signals specify endoderm progenitors to a thyroid cell fate that assembles in the pharyngeal floor from which the primordium buds and migrates to the final position of the gland. The morphogenetic process is regulated by both cell-autonomous (e.g. activated by NKX2-1, FOXE1, PAX8, and HHEX) and mesoderm-derived (e.g. mediated by TBX1 and fibroblast growth factors) mechanisms acting in concert to promote growth and survival of progenitor cells. The developmental role of TSH is limited to thyroid differentiation set to work after the gross anatomy of the gland is already sculptured. This review summarizes recent advances on the molecular genetics of thyroid morphogenesis put into context of endoderm developmental traits and highlights established and novel mechanisms of thyroid dysgenesis of potential relevance to congenital hypothyroidism in man.

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Year:  2011        PMID: 21322126     DOI: 10.1677/jme-10-0084

Source DB:  PubMed          Journal:  J Mol Endocrinol        ISSN: 0952-5041            Impact factor:   5.098


  36 in total

Review 1.  Selenium, selenoproteins and the thyroid gland: interactions in health and disease.

Authors:  Lutz Schomburg
Journal:  Nat Rev Endocrinol       Date:  2011-10-18       Impact factor: 43.330

2.  Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.

Authors:  Peter Gergics; Michelle L Brinkmeier; Sally A Camper
Journal:  Mol Endocrinol       Date:  2015-02-10

3.  The transcription factor NKX1-2 promotes adipogenesis and may contribute to a balance between adipocyte and osteoblast differentiation.

Authors:  Noah Chen; Rebecca L Schill; Michael O'Donnell; Kevin Xu; Devika P Bagchi; Ormond A MacDougald; Ronald J Koenig; Bin Xu
Journal:  J Biol Chem       Date:  2019-10-15       Impact factor: 5.157

4.  Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.

Authors:  Joshua C Denny; Dana C Crawford; Marylyn D Ritchie; Suzette J Bielinski; Melissa A Basford; Yuki Bradford; High Seng Chai; Lisa Bastarache; Rebecca Zuvich; Peggy Peissig; David Carrell; Andrea H Ramirez; Jyotishman Pathak; Russell A Wilke; Luke Rasmussen; Xiaoming Wang; Jennifer A Pacheco; Abel N Kho; M Geoffrey Hayes; Noah Weston; Martha Matsumoto; Peter A Kopp; Katherine M Newton; Gail P Jarvik; Rongling Li; Teri A Manolio; Iftikhar J Kullo; Christopher G Chute; Rex L Chisholm; Eric B Larson; Catherine A McCarty; Daniel R Masys; Dan M Roden; Mariza de Andrade
Journal:  Am J Hum Genet       Date:  2011-10-07       Impact factor: 11.025

5.  An ex vivo culture system to study thyroid development.

Authors:  Anne-Sophie Delmarcelle; Mylah Villacorte; Anne-Christine Hick; Christophe E Pierreux
Journal:  J Vis Exp       Date:  2014-06-06       Impact factor: 1.355

6.  Human embryonic stem cells form functional thyroid follicles.

Authors:  Risheng Ma; Rauf Latif; Terry F Davies
Journal:  Thyroid       Date:  2015-02-06       Impact factor: 6.568

Review 7.  New model systems to illuminate thyroid organogenesis. Part I: an update on the zebrafish toolbox.

Authors:  Robert Opitz; Francesco Antonica; Sabine Costagliola
Journal:  Eur Thyroid J       Date:  2013-12-03

Review 8.  Normal vs cancer thyroid stem cells: the road to transformation.

Authors:  M Zane; E Scavo; V Catalano; M Bonanno; M Todaro; R De Maria; G Stassi
Journal:  Oncogene       Date:  2015-05-11       Impact factor: 9.867

9.  Follicular epithelial dysplasia of the thyroid: morphological and immunohistochemical characterization of a putative preneoplastic lesion to papillary thyroid carcinoma in chronic lymphocytic thyroiditis.

Authors:  Michael Herman Chui; Clarissa A Cassol; Sylvia L Asa; Ozgur Mete
Journal:  Virchows Arch       Date:  2013-03-27       Impact factor: 4.064

10.  A Novel Mutation (S54C) of the PAX8 Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affected Individuals.

Authors:  Panudda Srichomkwun; Osnat Admoni; Samuel Refetoff; Liat de Vries
Journal:  Horm Res Paediatr       Date:  2016-05-21       Impact factor: 2.852

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