Zobrazeno 1 - 10
of 648
pro vyhledávání: '"diepoxybutane"'
Akademický článek
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Publikováno v:
Environmental Health Perspectives, 2003 Nov 01. 111(14), 1699-1703.
Externí odkaz:
https://www.jstor.org/stable/3435349
Publikováno v:
Biomedical Papers, Vol 161, Iss 2, Pp 158-163 (2017)
Background: Fanconi anemia is a rare autosomal recessive disorder of genetic instability. It is both molecularly and clinically, a heterogeneous disorder. Its incidence is 1 in 129,000 births and relatively high in some ethnic groups. Sixteen genes h
Externí odkaz:
https://doaj.org/article/a1bd360f7c17415fa5255b0f1a864892
Autor:
Joanna Kowalska, Anna Jeżewska
Publikováno v:
Medycyna Pracy, Vol 67, Iss 5, Pp 645-652 (2016)
Background: 1,2:3,4-Diepoxybutane (DEB) is a substance classified to a group of carcinogens. The maximum admissible concentration (MAC) value for this substance in workplace air is not specified in Poland. Due to the fact that DEB has been used in do
Externí odkaz:
https://doaj.org/article/bdfa332328594a8c9d12134d355d75c3
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Smaranda Arghirescu, Mihai Ioana, Nicoleta Andreescu, Razvan Mihail Plesea, Anca-Lelia Riza, Cristina Popa, Adela Chirita-Emandi, Alexandra Mihailescu, Maria Puiu
Publikováno v:
Journal of Medical Genetics. 58:648-652
Pathogenic variants in BRCA1 gene in heterozygous state are known to be associated with breast-ovarian cancer susceptibility; however, biallelic variants cause a phenotype recognised as Fanconi anaemia complementation group S. Due to its rarity, medi
Autor:
Lmb Silva, Lrf Lucena, S C de Lima, T Marques-Salles, Edvane Borges da Silva, Simey de Souza Leão Pereira Magnata, M. M. P. Lemos-Pinto, Ademir Amaral
Publikováno v:
Archives in Biosciences & Health. 1:189-200
Fanconi Anemia (FA) is a syndrome associated with chromosomal fragility. Current laboratory tests to diagnose this disease are based on the scoring of chromosomal aberrations induced in peripheral blood lymphocytes by clastogenic chemical agents, mai
Publikováno v:
Balkan Journal of Medical Genetics, Vol 14, Iss 2, Pp 65-70 (2011)
Externí odkaz:
https://doaj.org/article/11de3b8318da4c9ea5419e3cee3c942b
Autor:
Sevgi Gözdaşoğlu, Mehmet Ertem, Zümrüt Uysal, Emel Babacan, Memnune Yüksel, Işık Bökesoy, Asuman Sunguroğlu, Ayten Arcasoy, Ayhan Çavdar
Publikováno v:
Turkish Journal of Hematology, Vol 26, Iss 03, Pp 118-122 (2009)
Objective: Fanconi’s anemia (FA) is an autosomal recessive disorder characterized by a progressive pancytopenia,variable congenital abnormalities and an increased risk for the development of acute myeloid leukemia (AML). The objective of this study
Externí odkaz:
https://doaj.org/article/2bf35a257e5a47c2931bf39459b7c5cb
Autor:
D.V. Pilonetto, N.F. Pereira, M.A. Bitencourt, N.I.R. Magdalena, E.R. Vieira, L.B.A. Veiga, I.J. Cavalli, R.C. Ribeiro, R. Pasquini
Publikováno v:
Brazilian Journal of Medical and Biological Research, Vol 42, Iss 3, Pp 237-243 (2009)
Fanconi anemia is a rare hereditary disease showing genetic heterogeneity due to a variety of mutations in genes involved in DNA repair pathways, which may lead to different clinical manifestations. Phenotypic variability makes diagnosis difficult ba
Externí odkaz:
https://doaj.org/article/6bae605d42454d27a4378dc76c24c16f