The Effect of HuR Depletion in the Airway Epithelium in COPD

Autor: A.J. Dabo, O. Evgrafov, T. Feng, M.A. Salathe, N. Baumlin, P. Geraghty, R.F. Foronjy

Publikováno v: C108. IMMUNITY AND INFLAMMATION IN COPD: NOVEL FINDINGS.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f3ecefc67bbc5ad2bc7e813a9b1ae4b5
https://doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a6155

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The Effect of Cigarette Smoke on HuR Expression on Chronic Rhinosinusitis

Autor: Patrick Geraghty, O. Evgrafov, G. Clerger, Marina Boruk, Abdoulaye J. Dabo, Robert F. Foronjy

Publikováno v: C31. COPD BASIC MECHANISMS.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e42ac3abbca855fda3bbaeb2ba5b1917
https://doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a4737

On the origin and frequency of the 35delG allele in GJB2-linked deafness in Europe

Autor: A, Anichkina, T, Kulenich, S, Zinchenko, I, Shagina, A, Polyakov, E, Ginter, O, Evgrafov, T, Viktorova, E, Khusnitdonova

Publikováno v: European journal of human genetics : EJHG. 9(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a68aff00be68c25de1e0a404a086078c
https://pubmed.ncbi.nlm.nih.gov/10713883

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Autor: R.E. Tanzi, K. Petrukhin, I. Chernov, J.L. Pellequer, W. Wasco, B. Ross, D.M. Romano, E. Parano, L. Pavone, L.M. Brzustowicz, M. Devoto, J. Peppercorn, A.I. Bush, I. Sternlieb, M. Pirastu, J.F. Gusella, O. Evgrafov, G.K. Penchaszadeh, B. Honig, I.S. Edelman, M.B. Soares, I.H. Scheinberg, T.C. Gilliam

Publikováno v: Nature Genetics
Nature Genetics, Nature Publishing Group, 1993, 5 (4), pp.344-350. ⟨10.1038/ng1293-344⟩
Nature genetics
5 (1993): 344–350. doi:10.1038/ng1293-344
info:cnr-pdr/source/autori:Tanzi R.E.; Petrukhin K.; Chernov I.; Pellequer J.L.; Wasco W.; Ross B.; Romano D.M.; Parano E.; Pavone L.; Brzustowicz L.M.; Devoto M.; Peppercorn J.; Bush A.I.; Sternlieb I.; Pirastu M.; Gusella J.F.; Evgrafov O.; Penchaszadeh G.K.; Gilliam T.C./titolo:The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene/doi:10.1038%2Fng1293-344/rivista:Nature genetics (Print)/anno:1993/pagina_da:344/pagina_a:350/intervallo_pagine:344–350/volume:5

Wilson disease (WD) is an autosomal recessive disorder characterized by the toxic accumulation of copper in a number of organs, particularly the liver and brain. As shown in the accompanying paper, linkage disequilibrium and haplotype analysis confir

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::403bdaac8bcabdd4c3c152ef6c89b86d
http://hdl.handle.net/11573/497083