Search Results - "Mosor, M."

Semi-automation of process analytics reduces operator effect by Christler, A., Felföldi, E., Mosor, M., Sauer, D., Walch, N., Dürauer, A., Jungbauer, A.

“…The aim of this study was to semi-automate process analytics for the quantification of common impurities in downstream processing such as host cell DNA, host…”
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Correction to: Semi-automation of process analytics reduces operator effect by Christler, A., Felföldi, E., Mosor, M., Sauer, D., Walch, N., Dürauer, A., Jungbauer, A.

“…In the original publication, open access funding institution was incorrectly mentioned in the acknowledgement section…”
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Uric acid and obesity-related phenotypes in postmenopausal women by Grygiel-Górniak, B., Mosor, M., Marcinkowska, J., Przysławski, J., Nowak, J.

“…The aim of this study was to find the genetic, metabolic, and nutritional risk factors, which can be associated with uric acid (UA) level. The risk factors…”
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The gene-diet associations in postmenopausal women with newly diagnosed dyslipidemia by Grygiel-Górniak, Bogna, Kaczmarek, E., Mosor, M., Przysławski, J., Nowak, J.

“…Objectives The aim of this study was to determine the relationship between polymorphisms of peroxisome proliferator activated receptor - PPAR gamma-2…”
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Association of the heterozygous germline I171V mutation of the NBS1 gene with childhood acute lymphoblastic leukemia by Mosor, M, Ziółkowska, I, Pernak-Schwarz, M, Januszkiewicz-Lewandowska, D, Nowak, J

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PPARgamma-2 and ADRB3 polymorphisms in connective tissue diseases and lipid disorders by Grygiel-Górniak, Bogna, Ziółkowska-Suchanek, Iwona, Kaczmarek, Elżbieta, Mosor, Maria, Nowak, Jerzy, Puszczewicz, Mariusz

“…The aim of the research genetic study was to investigate the association between variants (C1431T and Pro12Ala) of the peroxisome proliferator-activated…”
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419 Nbn Gene Mutation I171V as a Potential Risk Factor for Children Malignancies by Nowak, J, Mosor, M, Nowicka, K, Rembowska, J, Januszkiewicz, D

“…NBN (former NBS1 ) gene is considered as one of the low to moderate cancer susceptibility gene. At least four germinal NBN mutations have been found in several…”
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Impact of heterozygous c.657-661del, p.I171V and p.R215W mutations in NBN on nibrin functions by DZIKIEWICZ-KRAWCZYK, Agnieszka, MOSOR, Maria, JANUSZKIEWICZ, Danuta, NOWAK, Jerzy

“…Nibrin, product of the NBN gene, together with MRE11 and RAD50 is involved in DNA double-strand breaks (DSBs) sensing and repair, induction of apoptosis and…”
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Increased cancer risk of heterozygotes with NBS1 germline mutations in poland by Steffen, Jan, Varon, Raymonda, Mosor, Maria, Maneva, Galina, Maurer, Martin, Stumm, Markus, Nowakowska, Dorota, Rubach, Maryna, Kosakowska, Ewa, Ruka, Włodzimierz, Nowecki, Zbigniew, Rutkowski, Piotr, Demkow, Tomasz, Sadowska, Małgorzata, Bidziński, Mariusz, Gawrychowski, Krzysztof, Sperling, Karl

“…It has been suggested based on familial data that Nijmegen breakage syndrome (NBS) heterozygotes have an increased risk of malignant tumors. We found 15…”
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Polymorphisms and haplotypes of the NBS1 gene in childhood acute leukaemia by Mosor, Maria, Ziółkowska, Iwona, Januszkiewicz-Lewandowska, Danuta, Nowak, Jerzy

“…Abstract DNA repair gene polymorphisms and mutations may influence cancer risk. The product of the NBS1 gene, nibrin, is functionally involved in the…”
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Heterozygous carriers of the I171V mutation of the NBS1 gene have a significantly increased risk of solid malignant tumours by Nowak, Jerzy, Mosor, Maria, Ziółkowska, Iwona, Wierzbicka, Malgorzta, Pernak-Schwarz, Monika, Przyborska, Marta, Rożnowski, Krzysztof, Pławski, Andrzej, Słomski, Ryszard, Januszkiewicz, Danuta

“…Abstract Homozygous mutation 657del5 within the NBS1 gene is responsible for the majority of Nijmegen breakage syndrome (NBS) cases. NBS patients are…”
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NBS1 GENE MUTATIONS AS A CANCER RISK FACTOR by Nowak, J, Mosor, M, Ziolkowska, I, Dzikiewicz-Krawczyk, A, Januszkiewicz, D

“…MRE11, RAD50 and NBS1 (MRN) complex is involved in DNA repair and cell cycle checking signaling. NBS1 being a part of MRN complex plays an important role in…”
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Regional distribution of heterozygous 657del5 mutation carriers of the NBS1 gene in Wielkopolska province (Poland) by Ziółkowska, Iwona, Mosor, Maria, Nowak, Jerzy

“…The homozygous 657del5 mutation, called Slavic mutation, of the NBS1 gene, causes the Nijmegen Breakage Syndrome (NBS). This syndrome is connected with a high…”
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