Literature DB >> 10669096

The Twirler mouse, a model for the study of cleft lip and palate.

S G Gong1, N J White, A Y Sakasegawa.   

Abstract

Twirler (Tw) is a semidominant mutation in the mouse affecting the embryonic development of the midfacial region. Most heterozygous Tw mice, +/-, become obese at adulthood with a concomitant decrease in fertility. Homozygous mice have clefts of the midfacial region and a disrupted nasal cavity. Midfacial clefts included clefts of the palate combined with either unilateral or bilateral clefts of the lip. The clefts of the lip were either complete or incomplete. The palatal shelves in Tw/Tw were very much reduced. Apart from these defects, homozygous Tw looked normal, and were born alive, although they reportedly die within 24 h after birth. It is proposed that the Twirler model can be used to improve understanding of the genetic mechanisms involved in the normal development of the midfacial region.

Entities:  

Mesh:

Year:  2000        PMID: 10669096     DOI: 10.1016/s0003-9969(99)00101-6

Source DB:  PubMed          Journal:  Arch Oral Biol        ISSN: 0003-9969            Impact factor:   2.633


  12 in total

Review 1.  Development of the upper lip: morphogenetic and molecular mechanisms.

Authors:  Rulang Jiang; Jeffrey O Bush; Andrew C Lidral
Journal:  Dev Dyn       Date:  2006-05       Impact factor: 3.780

2.  The molecular anatomy of mammalian upper lip and primary palate fusion at single cell resolution.

Authors:  Hong Li; Kenneth L Jones; Joan E Hooper; Trevor Williams
Journal:  Development       Date:  2019-06-17       Impact factor: 6.868

3.  Identification and developmental expression analysis of a novel homeobox gene closely linked to the mouse Twirler mutation.

Authors:  Han Liu; Wenjin Liu; Kathleen M Maltby; Yu Lan; Rulang Jiang
Journal:  Gene Expr Patterns       Date:  2006-01-19       Impact factor: 1.224

4.  The atypical homeodomain transcription factor Mohawk controls tendon morphogenesis.

Authors:  Wenjin Liu; Spencer S Watson; Yu Lan; Douglas R Keene; Catherine E Ovitt; Han Liu; Ronen Schweitzer; Rulang Jiang
Journal:  Mol Cell Biol       Date:  2010-08-09       Impact factor: 4.272

5.  Suppression of microRNA 124-3p and microRNA 340-5p ameliorates retinoic acid-induced cleft palate in mice.

Authors:  Hiroki Yoshioka; Akiko Suzuki; Chihiro Iwaya; Junichi Iwata
Journal:  Development       Date:  2022-05-03       Impact factor: 6.862

6.  The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene.

Authors:  Jeffrey O Bush; Yu Lan; Rulang Jiang
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-26       Impact factor: 11.205

7.  Signaling through Tgf-beta type I receptor Alk5 is required for upper lip fusion.

Authors:  Wai-Yee Li; Marek Dudas; Vesa Kaartinen
Journal:  Mech Dev       Date:  2008-06-11       Impact factor: 1.882

Review 8.  Molecular mechanisms of midfacial developmental defects.

Authors:  Akiko Suzuki; Dhruvee R Sangani; Afreen Ansari; Junichi Iwata
Journal:  Dev Dyn       Date:  2015-12-11       Impact factor: 3.780

9.  Gene datasets associated with mouse cleft palate.

Authors:  Akiko Suzuki; Goo Jun; Nada Abdallah; Mona Gajera; Junichi Iwata
Journal:  Data Brief       Date:  2018-03-14

10.  Inactivation of Zeb1 in GRHL2-deficient mouse embryos rescues mid-gestation viability and secondary palate closure.

Authors:  Marina R Carpinelli; Michael E de Vries; Alana Auden; Tariq Butt; Zihao Deng; Darren D Partridge; Lee B Miles; Smitha R Georgy; Jody J Haigh; Charbel Darido; Simone Brabletz; Thomas Brabletz; Marc P Stemmler; Sebastian Dworkin; Stephen M Jane
Journal:  Dis Model Mech       Date:  2020-03-25       Impact factor: 5.758

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