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Showing results 41 to 54 of 54.
Article
TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone
April 13, 2015
Article
Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation.
March 01, 2015
Article
Missing genetic risk in neural tube defects: Can exome sequencing yield an insight?
August 01, 2014
Article
Identification of Chiari Type I Malformation subtypes using whole genome expression profiles and cranial base morphometrics
June 01, 2014
Article
Genetic evaluation and application of posterior cranial fossa traits as endophenotypes for Chiari type I malformation
January 01, 2014
Article
Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype
October 01, 2013
Article
Outcome and life satisfaction of adults with myelomeningocele
July 01, 2013
Article
Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates
April 01, 2013
Article
SLITRK1 mutations in trichotillomania
October 01, 2006
Article
Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder
April 01, 2002
Article
No association between the WNT2 gene and autistic disorder
January 08, 2002
Article
Immune modulatory effects of neural cell adhesion molecules on lipopolysaccharide-induced nitric oxide production by cultured glia
September 30, 2000
Article
High concentrations of extracellular potassium enhance bacterial endotoxin lipopolysaccharide-induced neurotoxicity in glia-neuron mixed cultures
May 01, 2000
Article
Reduction by naloxone of lipopolysaccharide-induced neurotoxicity in mouse cortical neuron-glia co-cultures
May 01, 2000