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B Axelrod

Showing results (171-180 of 190) with videos related to

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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.
The Journal of Pediatrics|January 15, 2004
Growth hormone treatment in children with familial dysautonomiaManmohan K Kamboj, Felicia B Axelrod, Raphael David, et al.
Human Molecular Genetics|January 8, 2004
Rescue of a human mRNA splicing defect by the plant cytokinin kinetinSusan A Slaugenhaupt, James Mull, Maire Leyne, et al.
Plos One|December 29, 2010
Olfactory stem cells, a new cellular model for studying molecular mechanisms underlying familial dysautonomiaNathalie Boone, Béatrice Loriod, Aurélie Bergon, et al.
Journal of Autism and Developmental Disorders|November 5, 2025
Practices of Self-Advocacy and Their Implications From the Perspectives of Transition-Age, Young Adults With Intellectual and/or Developmental DisabilitiesK M Schmarder, D B Axelrod, R Agarwal, et al.
American Journal of Human Genetics|February 11, 2003
Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomiaMath P Cuajungco, Maire Leyne, James Mull, et al.
American Journal of Medical Genetics. Part A|April 11, 2003
Identification of the first non-Jewish mutation in familial DysautonomiaMaire Leyne, James Mull, Sandra P Gill, et al.
Genomics|February 10, 1995
The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia geneS A Slaugenhaupt, A Blumenfeld, C B Liebert, et al.
Clinical Journal of the American Society of Nephrology : CJASN|June 19, 2010
Renal transplantation in familial dysautonomia: report of two cases and review of the literatureYelena Rekhtman, Andrew S Bomback, Martin A Nash, et al.
Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.
Pageof 19

Showing results (171-180 of 190) with videos related to

Sort By:
Pageof 19
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.
The Journal of Pediatrics|January 15, 2004
Growth hormone treatment in children with familial dysautonomiaManmohan K Kamboj, Felicia B Axelrod, Raphael David, et al.
Human Molecular Genetics|January 8, 2004
Rescue of a human mRNA splicing defect by the plant cytokinin kinetinSusan A Slaugenhaupt, James Mull, Maire Leyne, et al.
Plos One|December 29, 2010
Olfactory stem cells, a new cellular model for studying molecular mechanisms underlying familial dysautonomiaNathalie Boone, Béatrice Loriod, Aurélie Bergon, et al.
Journal of Autism and Developmental Disorders|November 5, 2025
Practices of Self-Advocacy and Their Implications From the Perspectives of Transition-Age, Young Adults With Intellectual and/or Developmental DisabilitiesK M Schmarder, D B Axelrod, R Agarwal, et al.
American Journal of Human Genetics|February 11, 2003
Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomiaMath P Cuajungco, Maire Leyne, James Mull, et al.
American Journal of Medical Genetics. Part A|April 11, 2003
Identification of the first non-Jewish mutation in familial DysautonomiaMaire Leyne, James Mull, Sandra P Gill, et al.
Genomics|February 10, 1995
The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia geneS A Slaugenhaupt, A Blumenfeld, C B Liebert, et al.
Clinical Journal of the American Society of Nephrology : CJASN|June 19, 2010
Renal transplantation in familial dysautonomia: report of two cases and review of the literatureYelena Rekhtman, Andrew S Bomback, Martin A Nash, et al.
Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.
Pageof 19