Talk:2009 Lecture 17

Reviews

Werner LA. Issues in human auditory development. J Commun Disord. 2007 Mar 13;

Barald KF, Kelley MW. From placode to polarization: new tunes in inner ear development. Development. 2004 Sep;131(17):4119-30. Review.

Morsli H, Choo D, Ryan A, Johnson R, Wu DK. Development of the mouse inner ear and origin of its sensory organs. J Neurosci. 1998 May 1;18(9):3327-35. J Neuroscience Link

Articles

Villa-Cuesta E, Modolell J. Mutual repression between msh and Iro-C is an essential component of the boundary between body wall and wing in Drosophila. Development. 2005 Aug 10

Goto M, Piper Hanley K, Marcos J, Wood PJ, Wright S, Postle AD, Cameron IT, Mason JI, Wilson DI, Hanley NA. In humans, early cortisol biosynthesis provides a mechanism to safeguard female sexual development. J Clin Invest. 2006 Apr;116(4):953-60.

Jones JM, Montcouquiol M, Dabdoub A, Woods C, Kelley MW. Inhibitors of differentiation and DNA binding (Ids) regulate Math1 and hair cell formation during the development of the organ of Corti. J Neurosci. 2006 Jan 11;26(2):550-8.

"Basic helix-loop-helix (bHLH) transcription factor Math1 (Mouse homolog of ATH1, also called Atoh1) is both necessary and sufficient for hair cell development in the mammalian cochlea. The bHLH-related inhibitors of differentiation and DNA binding (Id) proteins negatively regulate many bHLH transcription factors including Math1. Progenitor cells expressing Ids during the time of hair cell differentiation were inhibited from developing as hair cells. Role for Ids in the regulation of expression of Math1 and hair cell differentiation in the developing cochlea." (text edited from abstract) (More? OMIM ATONAL)

Rodriguez-Vazquez JF. Development of the stapes and associated structures in human embryos. J Anat. 2005 Aug;207(2):165-73.

"The stapedial anlage is a unique formation with two distinct parts: the superior part that will comprise the base and the inferior part that will be crossed by the stapedial artery during embryonic development and will constitute the limbs and the head of the stapes. According to the results, the otic capsule is not involved in formation of the base of the stapes."

Kiernan AE, Pelling AL, Leung KK, Tang AS, Bell DM, Tease C, Lovell-Badge R, Steel KP, Cheah KS. Sox2 is required for sensory organ development in the mammalian inner ear. Nature. 2005 Apr 21;434(7036):1031-5.

"Sensory hair cells and their associated non-sensory supporting cells in the inner ear are fundamental for hearing and balance. They arise from a common progenitor, but little is known about the molecular events specifying this cell lineage."

Molecular Normal Development

Jones JM, Montcouquiol M, Dabdoub A, Woods C, Kelley MW. [See Related Articles ] Inhibitors of differentiation and DNA binding (Ids) regulate Math1 and hair cell formation during the development of the organ of Corti. J Neurosci. 2006 Jan 11;26(2):550-8.

Kawamoto K, Ishimoto S, Minoda R, Brough DE, Raphael Y. [See Related Articles ] Math1 gene transfer generates new cochlear hair cells in mature guinea pigs in vivo. J Neurosci. 2003 Jun 1;23(11):4395-400.

Zine A, de Ribaupierre F. [See Related Articles ] Notch/Notch ligands and Math1 expression patterns in the organ of Corti of wild-type and Hes1 and Hes5 mutant mice. Hear Res. 2002 Aug;170(1-2):22-31.

List of [../Refer/senses/ear_rev.htm Ear Development Reviews (1998)]

Reviews Abnormal Development (1998)

Webster WS. [See Related Articles ] Teratogen update: congenital rubella. Teratology. 1998 Jul;58(1):13-23. Review.

Yates JA, et al. [See Related Articles] Isolated congenital internal auditory canal atresia with normal facial nerve function. Int J Pediatr Otorhinolaryngol. 1997 Jul 18;41(1):1-8. Review.

Lambert PR, et al. [See Related Articles] Congenital malformations of the external auditory canal. Otolaryngol Clin North Am. 1996 Oct;29(5):741-60. Review.

Lin AE, et al. [See Related Articles] Further delineation of the branchio-oculo-facial syndrome. Am J Med Genet. 1995 Mar 13;56(1):42-59. Review.

Strasnick B, et al [See Related Articles] Teratogenic hearing loss. J Am Acad Audiol. 1995 Jan;6(1):28-38. Review.

Kossowska E, et al. [See Related Articles] Prenatal and neonatal prophylaxis in otorhinolaryngology. Int J Pediatr Otorhinolaryngol. 1980 Jun;2(2):85-98. Review.

Gottlieb G. [See Related Articles] Conceptions of prenatal development: behavioral embryology. Psychol Rev. 1976 May;83(3):215-34. Review.

Holme RH, Steel KP Genes involved in deafness. Curr Opin Genet Dev 1999 Jun;9(3):309-314

"Remarkable progress has been made over the past few years in the field of hereditary deafness. To date, mutations in at least 35 genes are known to cause hearing loss. We are now beginning to understand the function of many of these genes, which affect diverse aspects of ear development and function.

Books

Note: books are listed for educational and information purposes only and does not suggest a commercial product endorsement.

Molecular and Cellular Approaches to Neural Development

The Embryonic Human Brain: An Atlas Of Developmental Stages, 3rd Edition

Search PubMed

Search Mar2007 "hearing development" 7,453 reference articles of which 900 were reviews.