Search Results - "Silhanova, E"

CCND1 and ZNF217 gene amplification is equally frequent in BRCA1 and BRCA2 associated and non-BRCA breast cancer by Plevova, P, Cerna, D, Balcar, A, Foretova, L, Zapletalova, J, Silhanova, E, Curik, R, Dvorackova, J

“…Breast cancer associated with BRCA1 and BRCA2 gene mutations differs from non-BRCA tumors in several respects. We determined whether there was any difference…”
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Germline variants of the promyelocytic leukemia tumor suppressor gene in patients with familial cancer by Plevova, P, Walczyskova, S, Jeziskova, I, Jurckova, N, Krepelova, A, Puchmajerova, A, Pavlikova, K, Foretova, L, Zapletalova, J, Silhanova, E

“…The promyelocytic leukemia (PML) gene is an important tumor suppressor gene. We tested the hypothesis that germline disruption of the PML gene may be…”
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THE PROMYELOCYTIC LEUKEMIA PROTEIN: FROM ANTIVIRAL RESPONSE TO CANCER by Plevova, P, Jeziskova, I, Walczyskova, S, Krepelova, A, Pavlikova, K, Puchmajerova, A, Zapletalova, J, Silhanova, E

“…The PML (promyelocytic leukemia) gene encodes a multifunctional protein involved in antiviral response, transcription control, induction of apoptosis, growth…”
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Single nucleotide c.645+32c>T substitution in the APC gene is a non-pathogenic polymorphism appearing in about 16% of the Czech population by Plevová, P, Drobcinská, L, Stekrová, J, Silhánová, E

“…Familial adenomatous polyposis is an autosomal dominant disease characterised by predisposition to colon polyposis and colorectal cancer and caused by germline…”
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