Gene alterations associated with closure of the cerebral aqueduct in hydrocephalic H-Tx rats

doi:10.1186/1743-8454-2-S1-S4

Cerebrospinal Fluid Research

Volume 2
Suppl 1

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This article is part of the supplement: 49th Annual Meeting of the Society for Research into Hydrocephalus and Spina Bifida .

Oral presentation

Gene alterations associated with closure of the cerebral aqueduct in hydrocephalic H-Tx rats

Janet M Miller¹^,3 , James P McAllister¹^,3 and Gary S Krause²

¹Departments of Neurosurgery and Physiology, Wayne State University School of Medicine

²Department of Emergency Medicine; Wayne State University School of Medicine

³Department of Pediatric Neurosurgery, Children's Hospital of Michigan. Detroit, Michigan 48201

author email corresponding author email

from 49th Annual Meeting of the Society for Research into Hydrocephalus and Spina Bifida
Barcelona, Spain. 29 June – 2 July 2005

Cerebrospinal Fluid Research 2005, 2(Suppl 1):S4doi:10.1186/1743-8454-2-S1-S4


Published:	30 December 2005

First paragraph (this article has no abstract)

To elucidate the pathogenesis of congenital hydrocephalus we utilized gene array technology as well as quantitative real-time PCR, to identify specific genetic components which act to influence the closure of the cerebral aqueduct in the H-Tx rat.