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                             14 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 ABCG2 in peptic ulcer: gene expression and mutation analysis Salagacka-Kubiak, Aleksandra
2015
57 3 p. 335-342
artikel
2 Age-related methylation profiles of equine blood leukocytes in the RNASEL locus Ząbek, T.
2015
57 3 p. 383-388
artikel
3 A simple modification of PCR thermal profile applied to evade persisting contamination Banasik, Michał
2016
57 3 p. 409-415
artikel
4 Difference in resistance to Salmonella enteritidis infection among allelic variants of TLR4 (903, 1832) in SPF chickens Liu, L.
2015
57 3 p. 389-396
artikel
5 eQTL analysis links inflammatory bowel disease associated 1q21 locus to ECM1 gene Repnik, Katja
2016
57 3 p. 363-372
artikel
6 Exposure to volatile anaesthetics is not followed by a massive induction of single-strand DNA breaks in operation theatre personnel Szyfter, Krzysztof
2015
57 3 p. 343-348
artikel
7 Friedreich ataxia is not only a GAA repeats expansion disorder: implications for molecular testing and counselling Hoffman-Zacharska, Dorota
2016
57 3 p. 349-355
artikel
8 Interstitial 11q24 deletion: a new case and review of the literature Tassano, Elisa
2016
57 3 p. 357-362
artikel
9 Molecular characterization and evolutionary origins of farinin genes in Brachypodium distachyon L. Subburaj, Saminathan
2015
57 3 p. 287-303
artikel
10 RNA processing-associated molecular mechanisms of neurodegenerative diseases Tang, Anna Y.
2015
57 3 p. 323-333
artikel
11 The fa2 gene and molecular markers mapping in the gp segment of the Pisum linkage group V Gawłowska, M.
2016
57 3 p. 317-322
artikel
12 Transmission of the Aegilops ovata chromosomes carrying gametocidal factors in hexaploid triticale (×Triticosecale Wittm.) hybrids Kwiatek, M.
2015
57 3 p. 305-315
artikel
13 Trichoderma species occurring on wood with decay symptoms in mountain forests in Central Europe: genetic and enzymatic characterization Błaszczyk, Lidia
2015
57 3 p. 397-407
artikel
14 Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency Ziemnicka, K.
2015
57 3 p. 373-381
artikel
                             14 gevonden resultaten
 
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