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Creation and characterization of novel rat model for recessive dystrophic epidermolysis bullosa: Frameshift mutation of the Col7a1 gene leads to severe blistered phenotype.
Stone W, Strege C, Miller W, Geurts AM, Grzybowski M, Riddle M, Lees C, Eide C, Keene DR, Tufa SF, Seelig D, McGrath J, Tolar J. Stone W, et al. Among authors: tolar j. PLoS One. 2024 May 9;19(5):e0302991. doi: 10.1371/journal.pone.0302991. eCollection 2024. PLoS One. 2024. PMID: 38722855 Free PMC article.
Cardiac functional and histopathologic findings in humans and mice with mucopolysaccharidosis type I: implications for assessment of therapeutic interventions in hurler syndrome.
Braunlin E, Mackey-Bojack S, Panoskaltsis-Mortari A, Berry JM, McElmurry RT, Riddle M, Sun LY, Clarke LA, Tolar J, Blazar BR. Braunlin E, et al. Among authors: tolar j. Pediatr Res. 2006 Jan;59(1):27-32. doi: 10.1203/01.pdr.0000190579.24054.39. Epub 2005 Dec 2. Pediatr Res. 2006. PMID: 16326988
Bone marrow transplantation for recessive dystrophic epidermolysis bullosa.
Wagner JE, Ishida-Yamamoto A, McGrath JA, Hordinsky M, Keene DR, Woodley DT, Chen M, Riddle MJ, Osborn MJ, Lund T, Dolan M, Blazar BR, Tolar J. Wagner JE, et al. Among authors: tolar j. N Engl J Med. 2010 Aug 12;363(7):629-39. doi: 10.1056/NEJMoa0910501. N Engl J Med. 2010. PMID: 20818854 Free PMC article. Clinical Trial.
272 results