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The Journal of Continuing Education in the Health Professions|June 28, 2023
Design and Implementation of a Leadership Development Program for Early-Stage Investigators: Initial ResultsMiriam A Bredella, Karan A Patel, Maire Leyne, et al.
Molecular and Cellular Biology|November 19, 2008
Loss of mouse Ikbkap, a subunit of elongator, leads to transcriptional deficits and embryonic lethality that can be rescued by human IKBKAPYei-Tsung Chen, Matthew M Hims, Ranjit S Shetty, et al.
Brain Research|August 14, 2003
Of splice and men: what does the distribution of IKAP mRNA in the rat tell us about the pathogenesis of familial dysautonomia?Eva Mezey, Alissa Parmalee, Ildiko Szalayova, et al.
Genomics|July 24, 2007
A humanized IKBKAP transgenic mouse models a tissue-specific human splicing defectMatthew M Hims, Ranjit S Shetty, James Pickel, et al.
American Journal of Human Genetics|April 23, 2003
A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4Lisa A Freed, James S Acierno, Daisy Dai, et al.
Circulation|September 21, 2005
New locus for autosomal dominant mitral valve prolapse on chromosome 13: clinical insights from genetic studiesFrancesca Nesta, Maire Leyne, Chaim Yosefy, et al.
Pediatric Research|December 20, 2007
IKBKAP mRNA in peripheral blood leukocytes: a molecular marker of gene expression and splicing in familial dysautonomiaGabrielle Gold-von Simson, Maire Leyne, James Mull, et al.
Pediatric Research|November 27, 2008
Kinetin in familial dysautonomia carriers: implications for a new therapeutic strategy targeting mRNA splicingGabrielle Gold-von Simson, Judith D Goldberg, Linda M Rolnitzky, et al.
Pediatric Research|July 22, 2011
Kinetin improves IKBKAP mRNA splicing in patients with familial dysautonomiaFelicia B Axelrod, Leonard Liebes, Gabrielle Gold-Von Simson, et al.
Human Molecular Genetics|August 9, 2011
Specific correction of a splice defect in brain by nutritional supplementationRanjit S Shetty, Cary S Gallagher, Yei-Tsung Chen, et al.
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