Literature DB >> 4073528

Development of rib-vertebrae: a new mutation in the house mouse with accessory caudal duplications.

K Theiler, D S Varnum.   

Abstract

The new recessive mutation rib-vertebrae (rv) causes fusions of lower ribs and malformations of vertebrae, which results from disturbed somite arrangement. In addition, duplications of the caudal neural tube and sometimes unilateral suppression of kidney formation can be observed. The new mutation is compared with the six already known mutations in mice with "Wirbel-Rippen-Syndrome" and with a similar syndrome in man. From the various effects of the rv-gene observed, it is suggested that the gene causes abnormal inner and outer surface formation, producing manifold secondary effects.

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Year:  1985        PMID: 4073528     DOI: 10.1007/BF00707309

Source DB:  PubMed          Journal:  Anat Embryol (Berl)        ISSN: 0340-2061


  7 in total

1.  Anatomy and development of the "truncate" (boneless) mutation in the mouse.

Authors:  K THEILER
Journal:  Am J Anat       Date:  1959-05

2.  The development of rib fusions, a mutation in the house mouse.

Authors:  K THEILER; L C STEVENS
Journal:  Am J Anat       Date:  1960-03

3.  The morphological effects and the development of the fused mutation in the mouse.

Authors:  K THEILER; S GLUECKSOHN-WAELSCH
Journal:  Anat Rec       Date:  1956-05

4.  Development of rachiterata, a mutation in the house mouse with 6 cervical vertebrae.

Authors:  K Theiler; D Varnum; L C Stevens
Journal:  Z Anat Entwicklungsgesch       Date:  1974

5.  [Vertebra-rib syndrome].

Authors:  K Theiler
Journal:  Schweiz Med Wochenschr       Date:  1968-06-15

6.  [Costovertebral dysplasia. A receptor defect of sclerotome development?].

Authors:  M Gassner
Journal:  Schweiz Med Wochenschr       Date:  1982-05-29

7.  Malformed vertebrae: a new mutant with the "wirbel-rippen syndrom" in the mouse.

Authors:  K Theiler; D S Varnum; J L Southard; L C Stevens
Journal:  Anat Embryol (Berl)       Date:  1975-08-09
  7 in total
  3 in total

1.  tbx6l and tbx16 are redundantly required for posterior paraxial mesoderm formation during zebrafish embryogenesis.

Authors:  Zachary T Morrow; Adrienne M Maxwell; Kazuyuki Hoshijima; Jared C Talbot; David J Grunwald; Sharon L Amacher
Journal:  Dev Dyn       Date:  2017-08-30       Impact factor: 3.780

2.  TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia.

Authors:  Maria Sandbacka; Hannele Laivuori; Érika Freitas; Mervi Halttunen; Varpu Jokimaa; Laure Morin-Papunen; Carla Rosenberg; Kristiina Aittomäki
Journal:  Orphanet J Rare Dis       Date:  2013-08-16       Impact factor: 4.123

3.  A study of vertebra number in pigs confirms the association of vertnin and reveals additional QTL.

Authors:  Gary A Rohrer; Dan J Nonneman; Ralph T Wiedmann; James F Schneider
Journal:  BMC Genet       Date:  2015-10-30       Impact factor: 2.797

  3 in total

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