Common mitochondrial polymorphisms as risk factor for endometrial cancer
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* Corresponding author: Anna M Czarnecka anna.czarnecka@gmail.com
- Equal contributors
1 Institute of Genetics and Biotechnology, Faculty of Biology, University of Warsaw, Pawinskiego 5a, 02-106, Warsaw, Poland
2 School of Molecular Medicine, Medical University of Warsaw, Zwirki i Wigury 61, 02-091 Warsaw, Poland
3 II Clinic and Ward of Gynecology, Medical University of Lublin, Lublin, Poland
4 Department of Human Genetics, Lublin University School of Medicine, Lublin, Poland
5 Clinical Pathology Laboratory, Monument Institute of Polish Mothers Health Center, Lodz, Poland
6 Department of Pediatrics, University Hospital Salzburg, Paracelsus Medical University, Müllner Hauptstr 48, A-5020 Salzburg, Austria
7 Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5a, 02-106 Warsaw, Poland
International Archives of Medicine 2009, 2:33 doi:10.1186/1755-7682-2-33
Published: 28 October 2009Additional files
Additional file 1:
Table S1. Germ-line polymorphisms in the D-loop region of mtDNA of the endometrial adenocarcinoma patients.
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Additional file 2:
Table S2. Germ-line polymorphisms in the coding region of mtDNA of the endometrial adenocarcinoma patients.
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Additional file 3:
Table S3. Statistical analysis of haplogroup distribution in endometrial carcinoma vs. general Polish population.
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Additional file 4:
Table S4. Summary of mtDNA polymorphisms relevant to establish European haplogroups and its relation to clinical medicine.
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Additional file 5:
Table S5. Clinical and pathological features of EC patients enrolled in the study.
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Additional file 6:
Table S6. RLFP analysis data for haplogroup assignment; restriction enzymes and primers used in the study are indicated.
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Additional file 7:
Table S7. Sequences of primers used for D-loop sequencing (listed according to start position in mtDNA).
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Additional file 8:
Table S8. Sequences of the primers used for haplogroup analysis (listed according to start position in mtDNA).
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