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Co-Targeting of DTYMK and PARP1 as a Potential Therapeutic Approach in Uveal Melanoma.
- Published in:
- Cells (2073-4409), 2024, v. 13, n. 16, p. 1348, doi. 10.3390/cells13161348
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- Publication type:
- Article
Rekomendacje Polskiego Towarzystwa Ginekologów i Położników oraz Polskiego Towarzystwa Genetyki Człowieka dotyczące badań przesiewowych oraz diagnostycznych badań genetycznych wykonywanych w okresie prenatalnym.
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- Ginekologia i Perinatologia Praktyczna, 2022, v. 7, n. 1, p. 20
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- Publication type:
- Article
CpG Island Methylator Phenotype—A Hope for the Future or a Road to Nowhere?
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- International Journal of Molecular Sciences, 2022, v. 23, n. 2, p. 830, doi. 10.3390/ijms23020830
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- Publication type:
- Article
The Regulation of Collagen Processing by miRNAs in Disease and Possible Implications for Bone Turnover.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 1, p. 91, doi. 10.3390/ijms23010091
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- Publication type:
- Article
Physical Activity and DNA Methylation in Humans.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 23, p. 12989, doi. 10.3390/ijms222312989
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- Publication type:
- Article
Transcriptomic Profiling for the Autophagy Pathway in Colorectal Cancer.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 19, p. 7101, doi. 10.3390/ijms21197101
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- Publication type:
- Article
Interactions Between Variation in Candidate Genes and Environmental Factors in the Etiology of Schizophrenia and Bipolar Disorder: a Systematic Review.
- Published in:
- Molecular Neurobiology, 2018, v. 55, n. 6, p. 5075, doi. 10.1007/s12035-017-0708-y
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- Publication type:
- Article
Fertility preservation during oncological treatment.
- Published in:
- Oncology in Clinical Practice (2450-1654), 2024, v. 20, n. 2, p. 100, doi. 10.5603/OCP.2023.0033
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- Publication type:
- Article
Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1.
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- Journal of Assisted Reproduction & Genetics, 2016, v. 33, n. 2, p. 189, doi. 10.1007/s10815-015-0622-z
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- Publication type:
- Article
Genetic data protection as an indispensable element of genomic medicine development.
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- Polish Archives of Internal Medicine, 2023, v. 133, n. 2, p. 1, doi. 10.20452/pamw.16425
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- Publication type:
- Article
Giant intracerebral schwannoma of the skull base misinterpreted as a macroprolactinoma.
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- Polish Archives of Internal Medicine, 2023, v. 133, n. 1, p. 1, doi. 10.20452/pamw.16345
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- Publication type:
- Article
Determination and interpretation of MTHFR gene mutations in gynecology and internal medicine.
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- Polish Archives of Internal Medicine, 2019, v. 129, n. 10, p. 728, doi. 10.20452/pamw.15039
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- Publication type:
- Article
Microsatellite Instability in Thyroid Papillary Carcinoma and Multinodular Hyperplasia.
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- Oncology, 2000, v. 58, n. 4, p. 305, doi. 10.1159/000012117
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- Publication type:
- Article
Udział czynników genetycznych i środowiskowych w etiologii wrodzonego zarośnięcia przełyku i przetoki tchawiczo-przełykowej.
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- Advances in Hygiene & Experimental Medicine / Postepy Higieny i Medycyny Doswiadczalnej, 2014, v. 68, p. 238
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- Publication type:
- Article
Basal cell carcinoma of the skin: whole genome screening by comparative genome hybridization revisited.
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- Journal of Cutaneous Pathology, 2013, v. 40, n. 1, p. 25, doi. 10.1111/cup.12033
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- Publication type:
- Article
High-Resolution Array Comparative Genomic Hybridization Utility in Polish Newborns with Isolated Cleft Lip and Palate.
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- Neonatology (16617800), 2015, v. 107, n. 3, p. 173, doi. 10.1159/000368878
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- Publication type:
- Article
Major Histocompatibility Complex Genes as Therapeutic Opportunity for Immune Cold Molecular Cancer Subtypes.
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- 2020
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- Publication type:
- journal article
Multiplex ligation-dependent probe amplification as a screening test in children with autism spectrum disorders.
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- Advances in Clinical & Experimental Medicine, 2020, v. 29, n. 1, p. 101, doi. 10.17219/acem/112609
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- Publication type:
- Article
Transposable Elements and Their Epigenetic Regulation in Mental Disorders: Current Evidence in the Field.
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- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00580
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- Publication type:
- Article
The First Evidence of Cryptosporidium meleagridis Infection in a Colon Adenocarcinoma From an Immunocompetent Patient.
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- Frontiers in Cellular & Infection Microbiology, 2019, v. 9, p. N.PAG, doi. 10.3389/fcimb.2019.00035
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- Publication type:
- Article
PERINATALNA OPIEKA PALIATYWNA REALIZOWANA W ODDZIALE POŁOŻNICZYM I NEONATOLOGICZNYM WE WSPÓŁPRACY Z HOSPICJUM DLA DZIECI - DOŚWIADCZENIA WŁASNE.
- Published in:
- Developmental Period Medicine, 2019, v. 23, n. 4, p. 253
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- Publication type:
- Article
ZESPÓŁ FREEMANA-SHELDONA -- FENOTYP I PRZEBIEG CHOROBY NA PODSTAWIE ANALIZY DWÓCH PRZYPADKÓW POTWIERDZONYCH W BADANIU MOLEKULARNYM.
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- Developmental Period Medicine, 2011, v. 15, n. 4, p. 451
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- Publication type:
- Article
Uncommon constellation of multiglandular deficiency with 2 mutations in AIRE gene in an 18-year-old girl -- 12 years of observation.
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- Polish Journal of Endocrinology / Endokrynologia Polska, 2014, v. 65, n. 6, p. 514, doi. 10.5603/EP.2014.0070
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- Publication type:
- Article
ZESPOŁY GENETYCZNE CHARAKTERYZUJACE SIĘ NADMIERNYM WZROSTEM — ASPEKTY KLINICZNE I PORADNICTWO GENETYCZNE.
- Published in:
- Przeglad Pediatryczny, 2008, v. 38, n. 2, p. 121
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- Publication type:
- Article
Personalised medical management of patients with melanoma (part 2).
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- Nowotwory, 2021, v. 71, n. 4, p. 251, doi. 10.5603/NJO.2021.0045
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- Publication type:
- Article
Personalised medical management of patients with melanoma (part 1).
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- Nowotwory, 2021, v. 71, n. 3, p. 169, doi. 10.5603/NJO.2021.0032
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- Publication type:
- Article
Personalised medicine in lung cancer.
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- Nowotwory, 2021, v. 71, n. 2, p. 122, doi. 10.5603/NJO.2021.0026
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- Publication type:
- Article
Genetics and Oncology (part 2.): Fundamentals of personalised medicine in the treatment of breast and ovarian cancer.
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- Nowotwory, 2020, v. 70, n. 5, p. 187, doi. 10.5603/NJO.2020.0040
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- Publication type:
- Article
Genetics and oncology (part 1.): Fundamentals of genetic testing-based personalised medicine in oncology.
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- Nowotwory, 2020, v. 70, n. 4, p. 144, doi. 10.5603/NJO.2020.0029
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- Publication type:
- Article
Rodzinnie występujące aberracje strukturalne chromosomu X i ich implikacje kliniczne - opis 2 przypadków.
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- Pediatric Endocrinology, Diabetes & Metabolism, 2010, v. 16, n. 4, p. 310
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- Publication type:
- Article