Výsledky vyhledávání - "Carol Vogler"

Disease correction by combined neonatal intracranial AAV and systemic lentiviral gene therapy in Sanfilippo Syndrome type B mice

Autor: Wei Hou, Brett E. Crawford, Elizabeth Y. Qin, Jillian R. Brown, Kevin K. Ohlemiller, Carol Vogler, Erik D. Herzog, Mark S. Sands, John L. Orrock, Coy D. Heldermon

Publikováno v: Gene therapy

Mucopolysaccharidosis type IIIB (MPS IIIB) or Sanfilippo Syndrome type B is a lysosomal storage disease resulting from the deficiency of N-acetyl glucosaminidase (NAGLU) activity. We previously showed that intracranial adeno-associated virus (AAV)-ba

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d94285553395d7c316e9f660ecfc654a
http://europepmc.org/articles/PMC3701029

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Morphology of liver repair following cholestatic liver injury: resolution of ductal hyperplasia, matrix deposition and regression of myofibroblasts Note

Autor: Bruce R. Bacon, Carol Vogler, Lin Li, Sandra C. Carr, Darrell H. G. Crawford, Thomas F. Tracy, Kim R. Bridle, Grant A. Ramm, Robert S. Britton

Publikováno v: Liver. 20:387-396

Background/Aims: Myofibroblasts are the primary cells responsible for increased matrix deposition in hepatic fibrosis. Activation of hepatic stellate cells and portal fibroblasts to myofibroblasts during cholestatic liver injury is accompanied by inc

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::65d035c6aa23bdd872f922530b5a9447
https://doi.org/10.1034/j.1600-0676.2000.020005387.x

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EWS/FLI-1 fusion signal inserted into chromosome 11 in one patient with morphologic features of Ewing sarcoma, but lacking t(11;22)

Autor: Bharti Gadre, Julia A. Bridge, Yufeng Huang, Carol Vogler, Robert S. Wickert, Jacqueline R. Batanian

Publikováno v: Cancer genetics and cytogenetics. 133(1)

A reciprocal t(11;22)(q24;q12) is found in 85% of Ewing sarcomas (ES) cases. We report a case of a child with ES, in whom trisomy 8 was observed as the sole chromosomal abnormality. Fluorescence in situ hybridization—using a set of probes that loca

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d8eeb7c6e7e834725ba2588093b4ff6
https://pubmed.ncbi.nlm.nih.gov/11890993

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Paucifascicular Congenital Sensory Neuropathy in Identical Twins

Autor: Gail Borgatti Croall, Carol Vogler, Stephen R. Bates, Susan T. Iannaccone, Kevin E. Bove

Publikováno v: Archives of Pediatrics & Adolescent Medicine. 140:589

• A male infant had sensory and autonomic dysfunction, and his identical twin had a similar clinical finding. One twin was extensively studied, utilizing sural nerve, skin, and conjunctival biopsy specimens, to evaluate the status of peripheral sen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::719136bb174b5d6faed10fc7db1005b3
https://doi.org/10.1001/archpedi.1986.02140200099037

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