Výsledky vyhledávání - "T O Harville"

Nonhomologous end joining and V(D)J recombination require an additional factor

Autor: Kostas G. Manolis, T. O. Harville, Penny A. Jeggo, Yan Dai, L. A. Hanakahi, Boris Kysela, Markus Stumm, Stephen C. West, Enriqueta Riballo, Marjorie A. Oettinger

Publikováno v: Proceedings of the National Academy of Sciences. 100:2462-2467

DNA nonhomologous end-joining (NHEJ) is the major pathway for repairing DNA double-strand breaks in mammalian cells. It also functions to carry out rearrangements at the specialized breaks introduced during V(D)J recombination. Here, we describe a pa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9df5a589476e6af60519169d07007f25
https://doi.org/10.1073/pnas.0437964100

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Arrested rearrangement of TCR V beta genes in thymocytes from children with X-linked severe combined immunodeficiency disease

Autor: J W Sleasman, T O Harville, G B White, J F George, D J Barrett, M M Goodenow

Publikováno v: The Journal of Immunology. 153:442-448

Human X-linked severe combined immunodeficiency disease (SCID) is an immunodeficiency disorder in which T cell development is arrested in the thymic cortex. B lymphocytes in children with X-linked SCID seem to differentiate normally. X-linked SCID is

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::066ed5200bfb390384435ce1e290878c
https://doi.org/10.4049/jimmunol.153.1.442

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Severe laryngomalacia and bronchomalacia in DiGeorge syndrome and CHARGE association

Autor: M L, Markert, M, Majure, T O, Harville, G, Hulka, K, Oldham

Publikováno v: Pediatric pulmonology. 24(5)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d1621258267f18f9f08866921b48f21e
https://pubmed.ncbi.nlm.nih.gov/9407570

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Oligoclonal expansion of CD45RO+ T lymphocytes in Omenn syndrome

Autor: T O, Harville, D M, Adams, T A, Howard, R E, Ware

Publikováno v: Journal of clinical immunology. 17(4)

Omenn syndrome comprises a rare form of combined immunodeficiency with TH2-type features of eosinophilia and elevated IgE. Previous studies have led to reports of restricted heterogeneity in the T lymphocyte repertoire, and in vitro cloned T lymphocy

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::560649f6deb9644624a4ae12403dcacc
https://pubmed.ncbi.nlm.nih.gov/9258771

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Tumor necrosis factor-alpha suppresses hematopoiesis in children with myelodysplasia

Autor: S S, Winter, G A, Hanissian, T O, Harville, R E, Ware

Publikováno v: Medical and pediatric oncology. 28(1)

The term myelodysplasia (MDS) refers to a group of bone marrow failure syndromes which are relatively rare in childhood. The pathogenesis of MDS is unknown, but a variety of chromosomal, molecular, and cytochemical abnormalities have been reported. W

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::28f6d026b8dc89912291e12d9d400830
https://pubmed.ncbi.nlm.nih.gov/8950341

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177 A FAMILY COHORT WITH X-LINKED CHRONIC GRANULOMATOUS DISEASE AND DUCHENE'S MUSCULAR DYSTROPHY AS PART OF A CONTIGUOUS DELETION SYNDROME

Autor: J Jh Bleesing, T O Harville, B L Jones, D Noack, J G Wheeler, Stacie M. Jones

Publikováno v: Journal of Investigative Medicine. 52:S288.5-S288

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d9fcb0bc607a261c3b44ea25f49db599
https://doi.org/10.1136/jim-52-suppl1-730

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