Literature DB >> 5912439

Influence of the neural tube on the differentiation of the inner ear in the mammalian embryo.

M S Deol.   

Abstract

Entities:  

Mesh：

Year:  1966        PMID： 5912439     DOI： 10.1038/209219a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


× No keyword cloud information.
  11 in total

Review 1.  Genetic deafness.

Authors:  W Reardon
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  Dual embryonic origin of the mammalian otic vesicle forming the inner ear.

Authors:  Laina Freyer; Vimla Aggarwal; Bernice E Morrow
Journal:  Development       Date:  2011-12       Impact factor: 6.868

3.  The interfrontal bone and mutant genes in the mouse.

Authors:  D R Johnson
Journal:  J Anat       Date:  1976-07       Impact factor: 2.610

Review 4.  Splotch locus mouse mutants: models for neural tube defects and Waardenburg syndrome type I in humans.

Authors:  C E Moase; D G Trasler
Journal:  J Med Genet       Date:  1992-03       Impact factor: 6.318

5.  A comparison between trisomy 12 and vitamin A induced exencephaly and associated malformations in the mouse embryo.

Authors:  B Putz; G Krause; T Garde; A Gropp
Journal:  Virchows Arch A Pathol Anat Histol       Date:  1980

6.  Patterning of the mammalian cochlea.

Authors:  R Cantos; L K Cole; D Acampora; A Simeone; D K Wu
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

7.  Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.

Authors:  D Phippard; L Lu; D Lee; J C Saunders; E B Crenshaw
Journal:  J Neurosci       Date:  1999-07-15       Impact factor: 6.167

8.  An ultrastructural analysis of abnormal otic development in exencephalic mutant mice.

Authors:  D B Wilson
Journal:  Arch Otorhinolaryngol       Date:  1985

9.  Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.

Authors:  C Foy; V Newton; D Wellesley; R Harris; A P Read
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

10.  Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new mutations of Lmx1a causing severe cochlear and vestibular defects.

Authors:  Georg Steffes; Beatriz Lorente-Cánovas; Selina Pearson; Rachael H Brooker; Sarah Spiden; Amy E Kiernan; Jean-Louis Guénet; Karen P Steel
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.