Literature DB >> 9388186

Multistep control of pituitary organogenesis.

H Z Sheng1, K Moriyama, T Yamashita, H Li, S S Potter, K A Mahon, H Westphal.   

Abstract

Lhx3 and Lhx4 (Gsh4), two closely related LIM homeobox genes, determine formation of the pituitary gland in mice. Rathke's pouch is formed in two steps-first as a rudiment and later as a definitive pouch. Lhx3 and Lhx4 have redundant control over formation of the definitive pouch. Lhx3 controls a subsequent step of pituitary fate commitment. Thereafter, Lhx3 and Lhx4 together regulate proliferation and differentiation of pituitary-specific cell lineages. Thus, Lhx3 and Lhx4 dictate pituitary organ identity by controlling developmental decisions at multiple stages of organogenesis.

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Year:  1997        PMID: 9388186     DOI: 10.1126/science.278.5344.1809

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  87 in total

Review 1.  HESX1 and Septo-Optic Dysplasia.

Authors:  Mehul Tulsidas Dattani; Iain Caf Robinson
Journal:  Rev Endocr Metab Disord       Date:  2002-12       Impact factor: 6.514

Review 2.  Other transcription factors and hypopituitarism.

Authors:  Laurie E Cohen; Sally Radovick
Journal:  Rev Endocr Metab Disord       Date:  2002-12       Impact factor: 6.514

Review 3.  From panhypopituitarism to combined pituitary deficiencies: do we need the anterior pituitary?

Authors:  Catherine Carrière; Anatoli Gleiberman; Chijen R Lin; Michael G Rosenfeld
Journal:  Rev Endocr Metab Disord       Date:  2004-03       Impact factor: 6.514

4.  Tbx19, a tissue-selective regulator of POMC gene expression.

Authors:  J Liu; C Lin; A Gleiberman; K A Ohgi; T Herman; H P Huang; M J Tsai; M G Rosenfeld
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

5.  Novel Lethal Form of Congenital Hypopituitarism Associated With the First Recessive LHX4 Mutation.

Authors:  L C Gregory; K N Humayun; J P G Turton; M J McCabe; S J Rhodes; M T Dattani
Journal:  J Clin Endocrinol Metab       Date:  2015-04-14       Impact factor: 5.958

6.  A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency.

Authors:  Susanne Bechtold-Dalla Pozza; Stefan Hiedl; Julia Roeb; Peter Lohse; Raleigh E Malik; Soyoung Park; Mario Durán-Prado; Simon J Rhodes
Journal:  Horm Res Paediatr       Date:  2012-01-26       Impact factor: 2.852

7.  Three novel single-nucleotide polymorphisms of the bovine LHX3 gene.

Authors:  Y J Jing; X Y Lan; H Chen; L Z Zhang; C L Zhang; C Y Pan; M J Li; G Ren; T B Wei; M Zhao
Journal:  J Biosci       Date:  2008-12       Impact factor: 1.826

8.  Authentic cell-specific and developmentally regulated expression of pro-opiomelanocortin genomic fragments in hypothalamic and hindbrain neurons of transgenic mice.

Authors:  J I Young; V Otero; M G Cerdán; T L Falzone; E C Chan; M J Low; M Rubinstein
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

9.  A role of the LIM-homeobox gene Lhx2 in the regulation of pituitary development.

Authors:  Yangu Zhao; Christina M Mailloux; Edit Hermesz; Miklos Palkóvits; Heiner Westphal
Journal:  Dev Biol       Date:  2009-11-06       Impact factor: 3.582

10.  Premature differentiation and aberrant movement of pituitary cells lacking both Hes1 and Prop1.

Authors:  Ashley D Himes; Lori T Raetzman
Journal:  Dev Biol       Date:  2008-11-01       Impact factor: 3.582

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