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Prenatal diagnosis of hemophlia in Serbia - twenty years experience
(Wiley-Blackwell, Malden, 2008)
Early communication in Serbian speaking children with 22q11.2 deletion syndrome
(Springer, New York, 2015)
Adverse prognostic impact of IDH mutations on outcome in acute myeloid leukemia with normal karyotype
(Ferrata Storti Foundation, Pavia, 2014)
Association of high-level expression of bcl2l12 gene with adverse outcome in patients with acute myeloid leukemia
(Ferrata Storti Foundation, Pavia, 2010)
Screening for CFTR gene mutations and polymorphisms in patients with chronic pancreatitis
(Springernature, London, 2002)
Galectin-3 deficiency reduces immune-mediated beta cell destruction in vitro
(Springer, New York, 2010)
Genetic analysis of SMAD4 C-terminal domain in patients with microsatellite stable early- age onset colorectal cancer
(Fight Colorectal Cancer (Fight CRC), 2021)
SMAD4 protein loss is a relatively common feature of sporadic
colorectal cancers (CRC), and it was observed to be even more frequent in early-age onset CRC
patients and microsatellite stable (MSS) tumors. Pathogenic ...
Risk factors for thrombosis in acute promyelocytic leukemia
(Pergamon-Elsevier Science Ltd, Oxford, 2014)
Antimicrobial and cytotoxic activity of pigmented Streptomyces spp. culture extracts
(FEMS Conference on Microbiology, 2022)
BACKGROUND
Pigments from microbial origin have promising applications in food, cosmetics, textiles and therapeutics.
Compared to other natural sources pigments from bacteria are more stable, safer, and could be cheaper ...
Three novel 3 ' end prothrombin gene polymorphisms and their association with thrombophilia
(Wiley-Blackwell, Hoboken, 2011)