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Nature Genetics 2017 Mar;49(3):341-348. doi: 10.1038/ng.3771. Epub 2017 Jan 23. Erratum in: Nat Genet. 2017 Oct 27;49(11):1661.

A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers.

Glodzik D, Morganella S, Davies H, Simpson PT, Li Y, Zou X, Diez-Perez J, Staaf J, Alexandrov LB, Smid M, Brinkman AB, Rye IH, Russnes H, Raine K, Purdie CA, Lakhani SR, Thompson AM, Birney E, Stunnenberg HG, van de Vijver MJ, Martens JW, Børresen-Dale AL, Richardson AL, Kong G, Viari A, Easton D, Evan G, Campbell PJ, Stratton MR, Nik-Zainal S.

Nature Communications 2019 Aug 23;10(1):3835. doi: 10.1038/s41467-019-11680-1.

Genomic landscape and chronological reconstruction of driver events in multiple myeloma.

Maura F, Bolli N, Angelopoulos N, Dawson KJ, Leongamornlert D, Martincorena I, Mitchell TJ, Fullam A, Gonzalez S, Szalat R, Abascal F, Rodriguez-Martin B, Samur MK, Glodzik D, Roncador M, Fulciniti M, Tai YT, Minvielle S, Magrangeas F, Moreau P, Corradini P, Anderson KC, Tubio JMC, Wedge DC, Gerstung M, Avet-Loiseau H, Munshi N, Campbell PJ.

Nature Medicine 2017 Apr;23(4):517-525. doi: 10.1038/nm.4292. Epub 2017 Mar 13.

HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures.

Davies H, Glodzik D, Morganella S, Yates LR, Staaf J, Zou X, Ramakrishna M, Martin S, Boyault S, Sieuwerts AM, Simpson PT, King TA, Raine K, Eyfjord JE, Kong G, Borg Å, Birney E, Stunnenberg HG, van de Vijver MJ, Børresen-Dale AL, Martens JW, Span PN, Lakhani SR, Vincent-Salomon A, Sotiriou C, Tutt A, Thompson AM, Van Laere S, Richardson AL, Viari A, Campbell PJ, Stratton MR, Nik-Zainal S.

Nature. 2016 Jun 2;534(7605):47-54. doi: 10.1038/nature17676. Epub 2016 May 2. Erratum in: Nature. 2019 Feb;566(7742):E1.

Landscape of somatic mutations in 560 breast cancer whole-genome sequences.

Nik-Zainal S, Davies H, Staaf J, Ramakrishna M, Glodzik D, Zou X, Martincorena I, Alexandrov LB, Martin S, Wedge DC, Van Loo P, Ju YS, Smid M, Brinkman AB, Morganella S, Aure MR, Lingjærde OC, Langerød A, Ringnér M, Ahn SM, Boyault S, Brock JE, Broeks A, Butler A, Desmedt C, Dirix L, Dronov S, Fatima A, Foekens JA, Gerstung M, Hooijer GK, Jang SJ, Jones DR, Kim HY, King TA, Krishnamurthy S, Lee HJ, Lee JY, Li Y, McLaren S, Menzies A, Mustonen V, O'Meara S, Pauporté I, Pivot X, Purdie CA, Raine K, Ramakrishnan K, Rodríguez-González FG, Romieu G, Sieuwerts AM, Simpson PT, Shepherd R, Stebbings L, Stefansson OA, Teague J, Tommasi S, Treilleux I, Van den Eynden GG, Vermeulen P, Vincent-Salomon A, Yates L, Caldas C, van't Veer L, Tutt A, Knappskog S, Tan BK, Jonkers J, Borg Å, Ueno NT, Sotiriou C, Viari A, Futreal PA, Campbell PJ, Span PN, Van Laere S, Lakhani SR, Eyfjord JE, Thompson AM, Birney E, Stunnenberg HG, van de Vijver MJ, Martens JW, Børresen-Dale AL, Richardson AL, Kong G, Thomas G, Stratton MR.

Nature Communications 2019 Apr 15;10(1):1749. doi: 10.1038/s41467-019-09828-0.

Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation.

Brinkman AB, Nik-Zainal S, Simmer F, Rodríguez-González FG, Smid M, Alexandrov LB, Butler A, Martin S, Davies H, Glodzik D, Zou X, Ramakrishna M, Staaf J, Ringnér M, Sieuwerts A, Ferrari A, Morganella S, Fleischer T, Kristensen V, Gut M, van de Vijver MJ, Børresen-Dale AL, Richardson AL, Thomas G, Gut IG, Martens JWM, Foekens JA, Stratton MR, Stunnenberg HG.

Nucleic Acids Research 2017 Nov 2;45(19):11213-11221. doi: 10.1093/nar/gkx731.

Short inverted repeats contribute to localized mutability in human somatic cells.

Zou X, Morganella S, Glodzik D, Davies H, Li Y, Stratton MR, Nik-Zainal S.

Nature Communications 2016 May 2;7:11383. doi: 10.1038/ncomms11383.

The topography of mutational processes in breast cancer genomes.

Morganella S, Alexandrov LB, Glodzik D, Zou X, Davies H, Staaf J, Sieuwerts AM, Brinkman AB, Martin S, Ramakrishna M, Butler A, Kim HY, Borg Å, Sotiriou C, Futreal PA, Campbell PJ, Span PN, Van Laere S, Lakhani SR, Eyfjord JE, Thompson AM, Stunnenberg HG, van de Vijver MJ, Martens JW, Børresen-Dale AL, Richardson AL, Kong G, Thomas G, Sale J, Rada C, Stratton MR, Birney E, Nik-Zainal S.

Nature Medicine 2019 Oct;25(10):1526-1533. doi: 10.1038/s41591-019-0582-4. Epub 2019 Sep 30.

Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study.

Staaf J, Glodzik D, Bosch A, Vallon-Christersson J, Reuterswärd C, Häkkinen J, Degasperi A, Amarante TD, Saal LH, Hegardt C, Stobart H, Ehinger A, Larsson C, Rydén L, Loman N, Malmberg M, Kvist A, Ehrencrona H, Davies HR, Borg Å, Nik-Zainal S.

Cancer Research 2017 Sep 15;77(18):4755-4762. doi: 10.1158/0008-5472.CAN-17-1083.

Whole-Genome Sequencing Reveals Breast Cancers with Mismatch Repair Deficiency.

Davies H, Morganella S, Purdie CA, Jang SJ, Borgen E, Russnes H, Glodzik D, Zou X, Viari A, Richardson AL, Børresen-Dale AL, Thompson A, Eyfjord JE, Kong G, Stratton MR, Nik-Zainal S.

Proceedings of the National Academy of Sciences of the United States of America 2012 Dec 18;109(51):20871-6. doi: 10.1073/pnas.1211922109. Epub 2012 Nov 26.

Capturing reaction paths and intermediates in Cre-loxP recombination using single-molecule fluorescence.

Pinkney JN, Zawadzki P, Mazuryk J, Arciszewska LK, Sherratt DJ, Kapanidis AN.

Proceedings of the National Academy of Sciences of the United States of America 2013 Oct 22;110(43):17302-7. doi: 10.1073/pnas.1311065110. Epub 2013 Oct 7.

Conformational transitions during FtsK translocase activation of individual XerCD-dif recombination complexes.

Zawadzki P, May PF, Baker RA, Pinkney JN, Kapanidis AN, Sherratt DJ, Arciszewska LK.

Proceedings of the National Academy of Sciences of the United States of America 2015 Aug 11;112(32):E4390-9. doi: 10.1073/pnas.1507592112. Epub 2015 Jul 29.

Live-cell superresolution microscopy reveals the organization of RNA polymerase in the bacterial nucleoid.

Stracy M, Lesterlin C, Garza de Leon F, Uphoff S, Zawadzki P, Kapanidis AN.

Molecular Cell 2016 Sep 15;63(6):939-50. doi: 10.1016/j.molcel.2016.08.011. Epub 2016 Sep 8.

RNA Polymerase Pausing during Initial Transcription.

Duchi D, Bauer DL, Fernandez L, Evans G, Robb N, Hwang LC, Gryte K, Tomescu A, Zawadzki P, Morichaud Z, Brodolin K, Kapanidis AN.

Nucleic Acids Research 2019 Jan 10;47(1):210-220. doi: 10.1093/nar/gky1143.

Single-molecule imaging of DNA gyrase activity in living Escherichia coli.

Stracy M, Wollman AJM, Kaja E, Gapinski J, Lee JE, Leek VA, McKie SJ, Mitchenall LA, Maxwell A, Sherratt DJ, Leake MC, Zawadzki P.

Nature Communications 2016 Aug 26;7:12568. doi: 10.1038/ncomms12568.

Single-molecule imaging of UvrA and UvrB recruitment to DNA lesions in living Escherichia coli.

Stracy M, Jaciuk M, Uphoff S, Kapanidis AN, Nowotny M, Sherratt DJ, Zawadzki P.

Cell Reports 2015 Dec 22;13(11):2587-2596. doi: 10.1016/j.celrep.2015.11.034. Epub 2015 Dec 10.

The Localization and Action of Topoisomerase IV in Escherichia coli Chromosome Segregation Is Coordinated by the SMC Complex, MukBEF.

Zawadzki P, Stracy M, Ginda K, Zawadzka K, Lesterlin C, Kapanidis AN, Sherratt DJ.

Elife. 2018 Jan 11;7. pii: e31522

MukB ATPases are regulated independently by the N-and C-terminal domains of MukF kleisin

Katarzyna Zawadzka, Pawel Zawadzki, Rachel Baker, Karthik V Rajasekar, Florence Wagner, David J Sherratt, Lidia K Arciszewska

Nucleic Acids Research, Volume 47, Issue 18, 10 October 2019, Pages 9696–9707

Dynamic architecture of the Escherichia coli structural maintenance of chromosomes (SMC) complex, MukBEF

Karthik V Rajasekar, Rachel Baker, Gemma L M Fisher, Jani R Bolla, Jarno Mäkelä, Minzhe Tang, Katarzyna Zawadzka, Oliwia Koczy, Florence Wagner, Carol V Robinson, Lidia K Arciszewska, David J Sherratt

Nature Communications, 2016 Jan 28;7:10466.

MatP regulates the coordinated action of topoisomerase IV and MukBEF in chromosome segregation

Sophie Nolivos, Amy L. Upton, Anjana Badrinarayanan, Julius Müller, Katarzyna Zawadzka, Jakub Wiktor, Amber Gill, Lidia Arciszewska, Emilien Nicolas, David Sherratt

Nature Genetics 2015 May;47(5):518-522.

A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis.

Fjeld K, Weiss FU, Lasher D, Rosendahl J, Chen JM, Johansson BB, Kirsten H, Ruffert C, Masson E, Steine SJ, Bugert P, Cnop M, Grützmann R, Mayerle J, Mössner J, Ringdal M, Schulz HU, Sendler M, Simon P, Sztromwasser P, Torsvik J, Scholz M, Tjora E, Férec C, Witt H, Lerch MM, Njølstad PR, Johansson S, Molven A.

European Journey of Neurology 2016 Jul;23(7):1188-94

ADCK3 mutations with epilepsy, stroke-like episodes and ataxia: a POLG mimic?

Hikmat O, Tzoulis C, Knappskog PM, Johansson S, Boman H, Sztromwasser P, Lien E, Brodtkorb E, Ghezzi D, Bindoff LA.

EMBO Molecular Medicine 2016 Mar 1;8(3):176-90.

Defective PITRM1 mitochondrial peptidase is associated with Aβ amyloidotic neurodegeneration.

Brunetti D, Torsvik J, Dallabona C, Teixeira P, Sztromwasser P, Fernandez-Vizarra E, Cerutti R, Reyes A, Preziuso C, D'Amati G, Baruffini E, Goffrini P, Viscomi C, Ferrero I, Boman H, Telstad W, Johansson S, Glaser E, Knappskog PM, Zeviani M, Bindoff LA.

American Journal of Ophthalmology 2015 May;159(5):973-9.e2.

High myopia-excavated optic disc anomaly associated with a frameshift mutation in the MYC-binding protein 2 gene (MYCBP2).

Bredrup C, Johansson S, Bindoff LA, Sztromwasser P, Kråkenes J, Mellgren AE, Brurås KR, Lind O, Boman H, Knappskog PM, Rødahl E.

PLoS One. 2016 Feb 10;11(2)

Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy.

Flønes I, Sztromwasser P, Haugarvoll K, Dölle C, Lykouri M, Schwarzlmüller T, Jonassen I, Miletic H, Johansson S, Knappskog PM, Bindoff LA, Tzoulis C.

The Cerebellum 2017 Feb;16(1):272-275

PNKP Mutations Identified by Whole-Exome Sequencing in a Norwegian Patient with Sporadic Ataxia and Edema.

Tzoulis C, Sztromwasser P, Johansson S, Gjerde IO, Knappskog P, Bindoff LA.

Movement Disorder 2018 Oct;33(10):1591-1600.

Rare genetic variation in mitochondrial pathways influences the risk for Parkinson’s disease.

Gaare JJ, Nido GS, Sztromwasser P, Knappskog PM, Dahl O, Lund-Johansen M, Maple-Grødem J, Alves G, Tysnes OB, Johansson S, Haugarvoll K, Tzoulis C.

Diabetologia. 2017 Apr;60(4):625-635

Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry.

Johansson BB, Irgens HU, Molnes J, Sztromwasser P, Aukrust I, Juliusson PB, Søvik O, Levy S, Skrivarhaug T, Joner G, Molven A, Johansson S, Njølstad PR.

Bioinformatics. 2016 Jun 10. Volume 32, Issue 19, Pages 3018-3020. doi:10.1093//bioinformatics/btw359

RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.

Stokowy T, Garbulowski M, Fiskerstrand T, Holdhus R, Labun K, Sztromwasser P, Gilissen C, Hoischen A, Houge G, Petersen K, Jonassen I, Steen VM.

European Journal of Human Genetics 2018 Dec 20. doi: 10.1038/s41431-018-0323-z. [Epub ahead of print]

A tyrosine kinase-activating variant Asn666Ser in PDGFRB causes a progeria-like condition in the severe end of Penttinen syndrome.

Bredrup C, Stokowy T, McGaughran J, Lee S, Sapkota D, Cristea I, Xu L, Tveit KS, Høvding G, Steen VM, Rødahl E, Bruland O, Houge G.

Clinical Chemistry 2017 Feb;63(2):503-512. doi: 10.1373/clinchem.2016.263897. Epub 2016 Dec 14.

BRCA Testing by Single-Molecule Molecular Inversion Probes.

Neveling K, Mensenkamp AR, Derks R, Kwint M, Ouchene H, Steehouwer M, van Lier B, Bosgoed E, Rikken A, Tychon M, Zafeiropoulou D, Castelein S, Hehir-Kwa J, Tjwan Thung D, Hofste T, Lelieveld SH, Bertens SM, Adan IB, Eijkelenboom A, Tops BB, Yntema H, Stokowy T, Knappskog PM, Høberg-Vetti H, Steen VM, Boyle E, Martin B, Ligtenberg MJ, Shendure J, Nelen MR, Hoischen A.

American Journal of Human Genetics 2017 May 4;100(5):737-750. doi: 10.1016/j.ajhg.2017.03.012. Epub 2017 Apr 27.

Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian Families.

Ngcungcu T, Oti M, Sitek JC, Haukanes BI, Linghu B, Bruccoleri R, Stokowy T, Oakeley EJ, Yang F, Zhu J, Sultan M, Schalkwijk J, van Vlijmen-Willems IMJJ, von der Lippe C, Brunner HG, Ersland KM, Grayson W, Buechmann-Moller S, Sundnes O, Nirmala N, Morgan TM, van Bokhoven H, Steen VM, Hull PR, Szustakowski J, Staedtler F, Zhou H, Fiskerstrand T, Ramsay M.

Genome Medicine 2019 Jun 17;11(1):38. doi: 10.1186/s13073-019-0649-3.

Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.

Arts P, Simons A, AlZahrani MS, Yilmaz E, AlIdrissi E, van Aerde KJ, Alenezi N, AlGhamdi HA, AlJubab HA, Al-Hussaini AA, AlManjomi F, Alsaad AB, Alsaleem B, Andijani AA, Asery A, Ballourah W, Bleeker-Rovers CP, van Deuren M, van der Flier M, Gerkes EH, Gilissen C, Habazi MK, Hehir-Kwa JY, Henriet SS, Hoppenreijs EP, Hortillosa S, Kerkhofs CH, Keski-Filppula R, Lelieveld SH, Lone K, MacKenzie MA, Mensenkamp AR, Moilanen J, Nelen M, Ten Oever J, Potjewijd J, van Paassen P, Schuurs-Hoeijmakers JHM, Simon A, Stokowy T, van de Vorst M, Vreeburg M, Wagner A, van Well GTJ, Zafeiropoulou D, Zonneveld-Huijssoon E, Veltman JA, van Zelst-Stams WAG, Faqeih EA, van de Veerdonk FL, Netea MG, Hoischen A.

Molecular and Cellular Endocrinology 2016 Sep 15;433:130-7. doi: 10.1016/j.mce.2016.06.007. Epub 2016 Jun 6.

Somatic mutation profiling of follicular thyroid cancer by next generation sequencing.

Swierniak M, Pfeifer A, Stokowy T, Rusinek D, Chekan M, Lange D, Krajewska J, Oczko-Wojciechowska M, Czarniecka A, Jarzab M, Jarzab B, Wojtas B.

American Journal of Human Genetics 2019 Apr 4;104(4):749-757. doi: 10.1016/j.ajhg.2019.02.021. Epub 2019 Mar 21.

The Discovery of a LEMD2-Associated Nuclear Envelopathy with Early Progeroid Appearance Suggests Advanced Applications for AI-Driven Facial Phenotyping.

Marbach F, Rustad CF, Riess A, Đukić D, Hsieh TC, Jobani I, Prescott T, Bevot A, Erger F, Houge G, Redfors M, Altmueller J, Stokowy T, Gilissen C, Kubisch C, Scarano E, Mazzanti L, Fiskerstrand T, Krawitz PM, Lessel D, Netzer C.

Scientific reports 2018 Dec 14;8(1):17851. doi: 10.1038/s41598-018-36177-7.

Comparison of three variant callers for human whole genome sequencing.

Supernat A, Vidarsson OV, Steen VM, Stokowy T.

Lung Cancer. 2018 Apr;118:111-118. doi: 10.1016/j.lungcan.2018.02.002. Epub 2018 Feb 6. PubMed PMID: 29571988.

MiR-192 and miR-662 enhance chemoresistance and invasiveness of squamous cell lung carcinoma.

Filipska M, Skrzypski M, Czetyrbok K, Stokowy T, Stasiłojć G, Supernat A, Jassem J, Żaczek AJ, Bigda J.

Oncology Reports 2014 Feb;31(2):1003-13. doi: 10.3892/or.2013.2924. Epub 2013 Dec 13. PubMed PMID: 24337234.

A multimarker qPCR platform for the characterisation of endometrial cancer.

Supernat A, Łapińska-Szumczyk S, Majewska H, Gulczyński J, Biernat W, Wydra D, Zaczek AJ.

Applied Immunohistochemistry & Molecular Morphology 2012 Mar;20(2):103-7. PubMed PMID: 22553809.

CD73 expression as a potential marker of good prognosis in breast carcinoma.

Supernat A, Markiewicz A, Welnicka-Jaskiewicz M, Seroczynska B, Skokowski J, Sejda A, Szade J, Czapiewski P, Biernat W, Zaczek A.

Nature Genetics 2018 Sep;50(9):1262-1270. doi: 10.1038/s41588-018-0179-8. Epub 2018 Aug 13. PubMed PMID: 30104763; PubMed Central PMCID: PMC6130818.

Copy number signatures and mutational processes in ovarian carcinoma.

Macintyre G, Goranova TE, De Silva D, Ennis D, Piskorz AM, Eldridge M, Sie D, Lewsley LA, Hanif A, Wilson C, Dowson S, Glasspool RM, Lockley M, Brockbank E,Montes A, Walther A, Sundar S, Edmondson R, Hall GD, Clamp A, Gourley C, Hall M, Fotopoulou C, Gabra H, Paul J, Supernat A, Millan D, Hoyle A, Bryson G, Nourse C, Mincarelli L, Sanchez LN, Ylstra B, Jimenez-Linan M, Moore L, Hofmann O, Markowetz F, McNeish IA, Brenton JD.

Oncology Letters 2012 Oct;4(4):727-732. Epub 2012 Jul 9. PubMed PMID: 23205091; PubMed Central PMCID: PMC3506608.

Deregulation of RAD21 and RUNX1 expression in endometrial cancer.

Supernat A, Lapińska-Szumczyk S, Sawicki S, Wydra D, Biernat W, Zaczek AJ.

Ginekologia Polska 2014 Oct;85(10):754-9. Polish. PubMed PMID: 25546926.

Endometrial cancer in young women–clinical and molecular aspects

Lapińska-Szumczyk S, Supernat A, Żaczek AJ, Majewska H, Gulczyński J, Sawicki S, Biernat W, Wydra D.

Science Translational Medicine 2018 Nov 7;10(466). pii: eaat4921. doi: 10.1126/scitranslmed.aat4921. PubMed PMID: 30404863; PubMed Central PMCID: PMC6483061.

Enhanced detection of circulating tumor DNA by fragment size analysis.

Mouliere F, Chandrananda D, Piskorz AM, Moore EK, Morris J, Ahlborn LB, Mair R, Goranova T, Marass F, Heider K, Wan JCM, Supernat A, Hudecova I, Gounaris I, Ros S, Jimenez-Linan M, Garcia-Corbacho J, Patel K, Østrup O, Murphy S, Eldridge MD, Gale D, Stewart GD, Burge J, Cooper WN, van der Heijden MS, Massie CE, Watts C, Corrie P, Pacey S, Brindle KM, Baird RD, Mau-Sørensen M, Parkinson CA, Smith CG, Brenton JD, Rosenfeld N.

Anticancer Research 2013 Dec;33(12):5461-9. PubMed PMID: 24324082.

Epithelial-mesenchymal transition and cancer stem cells in endometrial cancer.

Supernat A, Lapinska-Szumczyk S, Majewska H, Gulczynski J, Biernat W, Wydra D, Zaczek AJ.

American Society for Clinical Pharmacology & Therapeutics 2014 Dec;7(6):482-8. doi: 10.1111/cts.12207. Epub 2014 Sep 9. PubMed PMID: 25201050; PubMed Central PMCID: PMC5350924

HER2-positive endometrial cancer subtype carries poor prognosis.

Lapińska-Szumczyk S, Supernat A, Majewska H, Gulczyński J, Luczak A, Biernat W, Wydra D, Zaczek AJ.

International Journal of Clinical and Experimental Medicine 2015 Nov 15;8(11):21981-90. eCollection 2015. PubMed PMID: 26885170; PubMed Central PMCID: PMC4724016.

Immunohistochemical characterisation of molecular subtypes in endometrial cancer

Łapińska-Szumczyk SM, Supernat AM, Majewska HI, Gulczyński J, Biernat W, Wydra D, Żaczek AJ.

Tumor Biology 2016 Oct;37(10):13721-13731. Epub 2016 Jul 30. PubMed PMID: 27476168; PubMed Central PMCID: PMC5097089.

Interactions between FGFR2 and RSK2-implications for breast cancer prognosis.

Czaplinska D, Mieczkowski K, Supernat A, Skladanowski AC, Kordek R, Biernat W, Zaczek AJ, Romanska HM, Sadej R.

Pathology & Oncology Research 2012 Oct;18(4):885-94. Epub 2012 Mar 18. PubMed PMID: 22426810.

Prognostic value of TOP2A gene amplification and chromosome 17 polysomy in early breast cancer.

Zaczek A, Markiewicz A, Supernat A, Bednarz-Knoll N, Brandt B, Seroczyńska B, Skokowski J, Szade J, Czapiewski P, Biernat W, Wełnicka-Jaśkiewicz M, Jassem J.

Ginekologia Polska 2016;87(2):88-93. doi: 10.17772/gp/60559. PubMed PMID: 27306283.

Rak błony śluzowej trzonu macicy u chorych po przebytej chorobie nowotworowej – aspekty kliniczne i molekularne.

Łapińska-Szumczyk SM, Supernat AM, Żaczek AJ, Majewska H, Gulczyński J, Sawicki S, Biernat W, Wydra D.

Translational Oncology 2014 Oct;7(5):613-9. doi: 10.1016/j.tranon.2014.06.001. Epub 2014 Jul 19. PubMed PMID: 25048628; PubMed Central PMCID: PMC4225657.

Tumor heterogeneity at protein level as an independent prognostic factor in endometrial cancer.

Supernat A, Lapińska-Szumczyk S, Majewska H, Gulczyński J, Biernat W, Wydra D, Zaczek AJ.

RNA biology 12 (9), 950-958; 2015

Translational readthrough potential of natural termination codons in eucaryotes–The impact of RNA sequence

Z Bukowy-Bieryllo, A Rabiasz, M Dabrowski, A Pogorzelski, A Wojda, ...

Cancer Immunology and Immunotherapy, September 2019

TNFSF4 (OX40L) expression and survival in locally-advanced and metastatic melanoma

Jason Roszik, Ettai Markovits, Adi Layani, Paula Dobosz, Keren Slabodnik-Kaner, Erez N Baruch, Guy Ben-Betzalel, Elizabeth Grimm, Raanan Berger, Yehezkel Sidi, Jacob Schachter, Ronnie Shapira-Frommer, Dror Avni, Gal Markel, Raya Leibowitz-Amit