Suchergebnisse - "DNA, Neoplasm/genetics"

Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin

Autoren: Rouzbeh Banan Christian Hartmann Alisa Förster et al.

Quelle: Acta Neuropathol
Acta Neuropathologica
Acta Neuropathol (2021) 142:191–210

Schlagwörter: Adenoma, 0301 basic medicine, Oligodendroglioma, Rats, Sprague-Dawley, 03 medical and health sciences, Antigens, CD, Animals, Humans, Gene Knock-In Techniques, Protein Kinase Inhibitors, 2. Zero hunger, ddc:610, Original Paper, 0303 health sciences, Aniline Compounds, Whole Genome Sequencing, Brain Neoplasms, Carcinoma, Genetic Variation, DNA, Neoplasm, Cadherins, Neoplasms, Neuroepithelial, Rats, 3. Good health, HEK293 Cells, Purines, Cadherins/genetics [MeSH], Gene Knock-In Techniques [MeSH], Rats, Sprague-Dawley [MeSH], Adenoma/pathology [MeSH], Antibody Diversity [MeSH], β-catenin, Genetic Variation [MeSH], Carcinoma/genetics [MeSH], Aniline Compounds/therapeutic use [MeSH], E-cadherin, Whole Genome Sequencing [MeSH], Brain Neoplasms/genetics [MeSH], Humans [MeSH], Rats [MeSH], Oligodendroglioma/pathology [MeSH], Animals [MeSH], Neoplasms, Neuroepithelial/genetics [MeSH], Protein Kinase Inhibitors/therapeutic use [MeSH], Oligodendroglioma/genetics [MeSH], Antigens, CD/genetics [MeSH], Purines/therapeutic use [MeSH], DNA, Neoplasm/genetics [MeSH], Neoplasms, Neuroepithelial/drug therapy [MeSH], Carcinoma/drug therapy [MeSH], Whole-genome sequencing, HEK293 Cells [MeSH], Adenoma/genetics [MeSH], Brain Neoplasms/drug therapy [MeSH], Familial glioma, Antibody Diversity

Dateibeschreibung: application/pdf

Zugangs-URL: https://link.springer.com/content/pdf/10.1007/s00401-021-02307-1.pdf
https://pubmed.ncbi.nlm.nih.gov/33929593
https://pub.h-brs.de/frontdoor/index/index/docId/5398
https://www.scilit.net/article/09e53110745d7bb98b66772f78ffc377
https://d-nb.info/123699079X/34
https://portal.dnb.de/opac.htm?method=simpleSearch&cqlMode=true&query=idn%3D123699079X
https://pubmed.ncbi.nlm.nih.gov/33929593/
https://link.springer.com/article/10.1007/s00401-021-02307-1
https://nbn-resolving.org/urn:nbn:de:hbz:1044-opus-53988
https://pub.h-brs.de/frontdoor/index/index/docId/5398
https://pub.h-brs.de/files/5398/Foerster2021_Article_Rare_germline_variants.pdf
https://repository.publisso.de/resource/frl:6450710

A practical guide to cancer subclonal reconstruction from DNA sequencing

Autoren: Máire Ni Leathlobhair David C. Wedge Adriana Salcedo et al.

Quelle: Tarabichi, M, Salcedo, A, Deshwar, A G, Ni Leathlobhair, M, Wintersinger, J, Wedge, D C, Van Loo, P, Morris, Q D & Boutros, P C 2021, 'A practical guide to cancer subclonal reconstruction from DNA sequencing', Nature Methods, vol. 18, no. 2, pp. 144-155. https://doi.org/10.1038/s41592-020-01013-2
Nature Methods, vol 18, iss 2

Schlagwörter: 0301 basic medicine, Technology, Bioinformatics and Computational Biology, Medical and Health Sciences, Polymorphism, Single Nucleotide, 03 medical and health sciences, Cancer Genomics, Neoplasms, Genetics, Humans, Polymorphism, DNA, Neoplasm/genetics, Cancer, 0303 health sciences, Neoplasm/genetics, Manchester Cancer Research Centre, Human Genome, DNA, Single Nucleotide, DNA, Neoplasm, Sequence Analysis, DNA, Biological Sciences, Neoplasms/genetics, ResearchInstitutes_Networks_Beacons/mcrc, name=Manchester Cancer Research Centre, 3. Good health, DNA/methods, Biological sciences, Sequence Analysis, DNA/methods, Neoplasm, Sequence Analysis, Algorithms, Developmental Biology

Zugangs-URL: https://europepmc.org/articles/pmc7867630?pdf=render
https://pubmed.ncbi.nlm.nih.gov/33398189
https://www.research.manchester.ac.uk/portal/en/publications/a-practical-guide-to-cancer-subclonal-reconstruction-from-dna-sequencing(500859e1-a1de-452f-b2ca-0db6ec57e65b).html
http://www-nature-com-443.webvpn.bjmu.tsg211.com/articles/s41592-020-01013-2
https://www.nature.com/articles/s41592-020-01013-2
http://europepmc.org/article/MED/33398189
https://escholarship.org/uc/item/0p64n4sf
https://christie.openrepository.com/handle/10541/623745
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867630/pdf/nihms-1663334.pdf
https://doi.org/10.1038/s41592-020-01013-2
https://research.manchester.ac.uk/en/publications/500859e1-a1de-452f-b2ca-0db6ec57e65b
https://escholarship.org/uc/item/0p64n4sf

Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1

Autoren: Stephan Frank Andreas Unterberg Daniel Schrimpf et al.

Quelle: Acta Neuropathol
Sievers, P, Sill, M, Blume, C, Tauziede-Espariat, A, Schrimpf, D, Stichel, D, Reuss, D E, Dogan, H, Hartmann, C, Mawrin, C, Hasselblatt, M, Stummer, W, Schick, U, Hench, J, Frank, S, Ketter, R, Schweizer, L, Schittenhelm, J, Puget, S, Brandner, S, Jaunmuktane, Z, Küsters, B, Abdullaev, Z, Pekmezci, M, Snuderl, M, Ratliff, M, Herold-Mende, C, Unterberg, A, Aldape, K, Ellison, D W, Wesseling, P, Reifenberger, G, Wick, W, Perry, A, Varlet, P, Pfister, S M, Jones, D T W, von Deimling, A, Sahm, F & The German Consortium “Aggressive Meningiomas” 2021, 'Clear cell meningiomas are defined by a highly distinct DNA methylation profile and mutations in SMARCE1', Acta Neuropathologica, vol. 141, no. 2, pp. 281-290. https://doi.org/10.1007/s00401-020-02247-2
Acta Neuropathologica, 141, 2, pp. 281-290
Acta Neuropathologica, vol 141, iss 2

Schlagwörter: Male, 0301 basic medicine, Chromosomal Proteins, Non-Histone, DNA Mutational Analysis, DNA methylation profile, Epigenesis, Genetic, Cohort Studies, 2.1 Biological and endogenous factors, Aetiology, Child, 10. No inequality, Cancer, Pediatric, 0303 health sciences, Brain Neoplasms, DNA, Neoplasm, SMARCE1, Immunohistochemistry, 3. Good health, Chromosomal Proteins, DNA-Binding Proteins, Treatment Outcome, Local, Disease Progression, Female, Meningioma, DNA Methylation/genetics [MeSH], Disease Progression [MeSH], Meningioma/genetics [MeSH], DNA-Binding Proteins/genetics [MeSH], DNA Mutational Analysis [MeSH], Cohort Studies [MeSH], Male [MeSH], Meningioma/pathology [MeSH], Neoplasm Recurrence, Local [MeSH], Child [MeSH], Mutation/genetics [MeSH], Female [MeSH], Brain Neoplasms/genetics [MeSH], Humans [MeSH], Treatment Outcome [MeSH], Genome-Wide Association Study [MeSH], DNA, Neoplasm/genetics [MeSH], Epigenesis, Genetic [MeSH], Immunohistochemistry [MeSH], Chromosomal Proteins, Non-Histone/genetics [MeSH], Brain tumor, Original Paper, Young Adult [MeSH], Clear cell, Brain Neoplasms/pathology [MeSH], German Consortium 'Aggressive Meningiomas', Clinical Sciences, Young Adult, 03 medical and health sciences, Rare Diseases, Genetic, Genetics, Humans, Neurology & Neurosurgery, Human Genome, Neurosciences, Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical Neuroscience, Non-Histone, DNA, DNA Methylation, Brain Disorders, Brain Cancer, Neoplasm Recurrence, Mutation, Neoplasm, Neoplasm Recurrence, Local, Epigenesis, Genome-Wide Association Study

Zugangs-URL: https://link.springer.com/content/pdf/10.1007/s00401-020-02247-2.pdf
https://pubmed.ncbi.nlm.nih.gov/33319313
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/232881
https://europepmc.org/article/PMC/PMC7847462
https://discovery.ucl.ac.uk/id/eprint/10118339/
https://pubmed.ncbi.nlm.nih.gov/33319313/
https://escholarship.org/uc/item/9371c7rn
https://research.vumc.nl/en/publications/clear-cell-meningiomas-are-defined-by-a-highly-distinct-dna-methy
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7847462
https://research.vumc.nl/en/publications/68651bb7-70f0-4935-a40c-263c52b76b37
https://repository.ubn.ru.nl/handle/2066/232881
https://repository.ubn.ru.nl//bitstream/handle/2066/232881/232881.pdf
https://repository.publisso.de/resource/frl:6466520
https://escholarship.org/uc/item/9371c7rn

A non-diploid DNA status is linked to poor prognosis in renal cell cancer

Autoren: Büscheck, Franziska Fraune, Christoph Kluth, Martina et al.

Quelle: World J Urol

Schlagwörter: Aged, 80 and over, Ploidies, DNA, Neoplasm, Middle Aged, Prognosis, Kidney Neoplasms, 3. Good health, DNA, Neoplasm/analysis [MeSH], Ploidies [MeSH], Aged, 80 and over [MeSH], Aged [MeSH], Humans [MeSH], Kidney Neoplasms/chemistry [MeSH], Retrospective Studies [MeSH], Carcinoma, Renal Cell/chemistry [MeSH], Middle Aged [MeSH], DNA, Neoplasm/genetics [MeSH], Original Article, Survival Rate [MeSH], Carcinoma, Renal Cell/mortality [MeSH], Kidney Neoplasms/genetics [MeSH], Kidney Neoplasms/mortality [MeSH], Prognosis [MeSH], DNA ploidy, Renal cell cancer, Flow cytometry, Carcinoma, Renal Cell/genetics [MeSH], Survival Rate, 03 medical and health sciences, 0302 clinical medicine, Humans, Carcinoma, Renal Cell, Aged, Retrospective Studies

Zugangs-URL: https://link.springer.com/content/pdf/10.1007/s00345-020-03226-8.pdf
https://pubmed.ncbi.nlm.nih.gov/32361874
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7969487
https://link.springer.com/article/10.1007/s00345-020-03226-8
https://europepmc.org/articles/PMC7969487/
https://www.ncbi.nlm.nih.gov/pubmed/32361874
https://link.springer.com/content/pdf/10.1007/s00345-020-03226-8.pdf
https://repository.publisso.de/resource/frl:6466828

TRIM28 haploinsufficiency predisposes to Wilms tumor

Autoren: Jenny Wegert Christian Thiel Roland P. Kuiper et al.

Weitere Verfasser: Jenny Wegert Christian Thiel Roland P. Kuiper et al.

Quelle: International Journal of Cancer, 145, 4, pp. 941-951

Schlagwörter: Male, 0301 basic medicine, Haploinsufficiency/genetics, Cancer Research, Heterozygote, Genes, Wilms Tumor, Genotype, Whole Exome Sequencing/methods, Carcinogenesis, Loss of Heterozygosity, Haploinsufficiency, Tripartite Motif-Containing Protein 28, Germ-Line Mutation/genetics, Wilms Tumor, Kidney Neoplasms/genetics, Loss of Function Mutation/genetics, 03 medical and health sciences, Loss of Function Mutation, Exome Sequencing, Journal Article, Humans, Genetic Predisposition to Disease, DNA, Neoplasm/genetics, Genes, Wilms Tumor/physiology, Germ-Line Mutation, Radboudumc 4: lnfectious Diseases and Global Health RIMLS: Radboud Institute for Molecular Life Sciences, 0303 health sciences, Loss of Heterozygosity/genetics, Genetic Predisposition to Disease/genetics, Research Support, Non-U.S. Gov't, TRIM28, Infant, Wilms tumor, DNA, Neoplasm, Kidney Neoplasms, haploinsufficiency, 3. Good health, Wilms Tumor/genetics, Radboudumc 14: Tumours of the digestive tract RIMLS: Radboud Institute for Molecular Life Sciences, Oncology, Child, Preschool, Tripartite Motif-Containing Protein 28/genetics, Human Genetics - Radboud University Medical Center, Female, Carcinogenesis/genetics, genetic predisposition, Radboudumc 10: Reconstructive and regenerative medicine RIHS: Radboud Institute for Health Sciences, Health Evidence - Radboud University Medical Center

Dateibeschreibung: application/pdf; image/pdf

Zugangs-URL: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.32167
https://pubmed.ncbi.nlm.nih.gov/30694527
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/205528
https://doi.org/10.1002/ijc.32167
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ijc.32167
https://onlinelibrary.wiley.com/doi/10.1002/ijc.32167
https://repository.ubn.ru.nl/handle/2066/205528
https://www.narcis.nl/publication/RecordID/oai%3Adspace.library.uu.nl%3A1874%2F391353
https://www.ncbi.nlm.nih.gov/pubmed/30694527
https://pubmed.ncbi.nlm.nih.gov/30694527/
https://hdl.handle.net/20.500.12831/1122
https://doi.org/10.1002/ijc.32167
https://dspace.library.uu.nl/handle/1874/391353
https://repository.ubn.ru.nl//bitstream/handle/2066/205528/205528.pdf
https://hdl.handle.net/2066/205528

G-quadruplexes: a promising target for cancer therapy

Autoren: Nils Kosiol Stefan Juranek Peter Brossart et al.

Quelle: Mol Cancer
Molecular Cancer, Vol 20, Iss 1, Pp 1-18 (2021)

Schlagwörter: 0301 basic medicine, 0303 health sciences, acute myeloid leukemia, Mutation [MeSH], malignant melanoma, G-quadruplex, Humans [MeSH], cancer progression, Structure-Activity Relationship [MeSH], Antineoplastic Agents/pharmacology [MeSH], Genomic Instability [MeSH], Neoplasms/genetics [MeSH], pancreatic cancer, DNA, Neoplasm/drug effects [MeSH], G-Quadruplexes/drug effects [MeSH], DNA, Neoplasm/genetics [MeSH], Ligands [MeSH], Neoplasms/drug therapy [MeSH], Antineoplastic Agents/therapeutic use [MeSH], Review, cancer therapy, genome instability, DNA, Neoplasm/chemistry [MeSH], Promoter Regions, Genetic [MeSH], Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Antineoplastic Agents, DNA, Neoplasm, Ligands, Genomic Instability, 3. Good health, G-Quadruplexes, Structure-Activity Relationship, 03 medical and health sciences, Neoplasms, Mutation, Humans, Promoter Regions, Genetic, RC254-282

Zugangs-URL: https://molecular-cancer.biomedcentral.com/track/pdf/10.1186/s12943-021-01328-4
https://pubmed.ncbi.nlm.nih.gov/33632214
https://doaj.org/article/647ef10326ef4a228aa7bfc2157bdad1
https://molecular-cancer.biomedcentral.com/articles/10.1186/s12943-021-01328-4
https://link.springer.com/content/pdf/10.1186/s12943-021-01328-4.pdf
https://www.scilit.net/article/c420807642993b284513465ac97ecf90?action=show-references
https://pubmed.ncbi.nlm.nih.gov/33632214/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7905668
https://link.springer.com/article/10.1186/s12943-021-01328-4
https://repository.publisso.de/resource/frl:6463331

Ethical considerations for modern molecular pathology

Autoren: Shoko Vos Paul J van Diest Margreet GEM Ausems et al.

Weitere Verfasser: Shoko Vos Paul J van Diest Margreet GEM Ausems et al.

Quelle: The Journal of Pathology. 246:405-414

Schlagwörter: 0301 basic medicine, Genetic Privacy/ethics, Genetic Counseling, Sequence Analysis, DNA/ethics, Pathology and Forensic Medicine, 03 medical and health sciences, 0302 clinical medicine, molecular pathology, Predictive Value of Tests, Neoplasms, Journal Article, Biomarkers, Tumor, cancer, Humans, genetics, Genetic Predisposition to Disease, Pathology, Molecular, Practice Patterns, Physicians', Genetic Privacy, DNA, Neoplasm/genetics, Genetic Counseling/ethics, Pathologists/ethics, 0303 health sciences, Informed Consent, Reproducibility of Results, personalized medicine, DNA, Neoplasm, Sequence Analysis, DNA, Informed Consent/ethics, Pathology, Molecular/ethics, ethics, Neoplasms/genetics, 3. Good health, Pathologists, Guideline Adherence/ethics, Phenotype, Practice Guidelines as Topic, Practice Patterns, Physicians'/ethics, pathology, next-generation sequencing, Guideline Adherence, Biomarkers, Tumor/genetics

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/30125358
https://dspace.library.uu.nl/handle/1874/388470
https://europepmc.org/article/MED/30125358
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=201802258422339550
https://www.ncbi.nlm.nih.gov/pubmed/30125358
https://www.narcis.nl/publication/RecordID/oai%3Adspace.library.uu.nl%3A1874%2F388470
https://onlinelibrary.wiley.com/doi/abs/10.1002/path.5157
https://dspace.library.uu.nl/handle/1874/388470

Hypermethylation of Secreted Frizzled Related Protein 1 gene promoter in different astrocytoma grades

Autoren: Kafka, Anja Karin-Kujundžić, Valentina Šerman, Ljiljana et al.

Quelle: Croat Med J
Croatian Medical Journal
CODEN CMEJEN
Volume 59
Issue 5

Schlagwörter: Adult, Epigenomics, Male, 0301 basic medicine, Intercellular Signaling Peptides and Proteins/genetics, beta Catenin/genetics, SFRP1, DNA methylation, Wnt signaling, astrocytic brain tumors, LEF1, TCF1, beta-catenin, Lymphoid Enhancer-Binding Factor 1, DNA Mutational Analysis, Astrocytoma, Lymphoid Enhancer-Binding Factor 1/genetics, Polymerase Chain Reaction, Young Adult, 03 medical and health sciences, Basic Science, Humans, Astrocytoma/pathology, Gene Silencing, Membrane Proteins/genetics, Promoter Regions, Genetic, DNA, Neoplasm/genetics, Aged, Brain Neoplasms/genetics, 0303 health sciences, Brain Neoplasms, Membrane Proteins, DNA, Neoplasm, Exons, DNA Methylation, Middle Aged, Immunohistochemistry, 3. Good health, Astrocytoma/genetics, Brain Neoplasms/pathology, Intercellular Signaling Peptides and Proteins, Female, T Cell Transcription Factor 1/genetics

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240821/pdf/CroatMedJ_59_0213.pdf
https://pubmed.ncbi.nlm.nih.gov/30394013
https://www.bib.irb.hr/974357
https://doi.org/10.3325/cmj.2018.59.213
https://hrcak.srce.hr/file/347166
https://pubmed.ncbi.nlm.nih.gov/30394013/
http://www.ncbi.nlm.nih.gov/pubmed/30394013
http://europepmc.org/articles/PMC6240821
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240821/
https://urn.nsk.hr/urn:nbn:hr:105:300029
https://doi.org/10.3325/cmj.2018.59.213

Positioning Europe for the EPITRANSCRIPTOMICS challenge

Autoren: Jantsch, Michael Quattrone, Alessandro O'Connell, Mary et al.

Weitere Verfasser: Jantsch, Michael Quattrone, Alessandro O'Connell, Mary et al.

Quelle: RNA Biol
RISalud-ANDALUCIA. Repositorio Institucional de Salud de Andalucía
instname
RNA Biology
Jantsch, M F, Quattrone, A, O'Connell, M, Helm, M, Frye, M, Macias-Gonzales, M, Ohman, M, Ameres, S, Willems, L, Fuks, F, Oulas, A, Vanacova, S, Nielsen, H, Bousquet-Antonelli, C, Motorin, Y, Roignant, J-Y, Balatsos, N, Dinnyes, A, Baranov, P, Kelly, V, Lamm, A, Rechavi, G, Pelizzola, M, Liepins, J, Holodnuka Kholodnyuk, I, Zammit, V, Ayers, D, Drablos, F, Dahl, J A, Bujnicki, J, Jeronimo, C, Almeida, R, Neagu, M, Costache, M, Bankovic, J, Banovic, B, Kyselovic, J, Valor, L M, Selbert, S, Pir, P, Demircan, T, Cowling, V, Schäfer, M, Rossmanith, W, Lafontaine, D, David, A, Carre, C, Lyko, F, Schaffrath, R, Schwartz, S, Verdel, A, Klungland, A, Purta, E, Timotijevic, G, Cardona, F, Davalos, A, Ballana, E, O Carroll, D, Ule, J & Fray, R 2018, ' Positioning Europe for the EPITRANSCRIPTOMICS challenge ', RNA Biology, vol. 15, no. 6, pp. 829-831 . https://doi.org/10.1080/15476286.2018.1460996

Schlagwörter: Epigenomics, 0301 basic medicine, Gene Expression, Detection of RNA Modification, [SDV.GEN] Life Sciences [q-bio]/Genetics, Epigenesis, Genetic, model systems, 106023 Molekularbiologie, Ecology,Evolution & Ethology, Neoplasms, RNA, Neoplasm, European Funding, Epitranscriptomics, RNA, Neoplasm/genetics, 0303 health sciences, Stem Cells, DNA, Neoplasm, Sciences bio-médicales et agricoles, 106023 Molecular biology, Life sciences, Neoplasms/genetics, 3. Good health, [SDV] Life Sciences [q-bio], Europe, Gene Expression Regulation, Neoplastic, SDG 3 – Gesundheit und Wohlergehen, Detection of RNA modification, Sciences du vivant, Genetics & Genomics, Biochimie, biophysique & biologie moléculaire, Biochemistry & Proteomics, name=Cell Biology, 03 medical and health sciences, Epigenomics/standards, Genetic, SDG 3 - Good Health and Well-being, Model systems, Humans, Database of Modification, detection of RNA modification, DNA, Neoplasm/genetics, database of Modification, epitranscriptomics, European funding, Computational & Systems Biology, [SDV.GEN]Life Sciences [q-bio]/Genetics, Neoplastic, Neoplasm/genetics, Gene Expression Profiling, FOS: Clinical medicine, Neurosciences, Model Systems, name=Molecular Biology, DNA, Gene Expression Regulation, Commentary, RNA, Gene Expression Profiling/methods, Transcriptome, Biochemistry, biophysics & molecular biology, Epigenesis

Dateibeschreibung: application/pdf; No full-text files

Zugangs-URL: https://www.tandfonline.com/doi/pdf/10.1080/15476286.2018.1460996?needAccess=true
https://pubmed.ncbi.nlm.nih.gov/29671387
http://hdl.handle.net/10668/12369
https://ucrisportal.univie.ac.at/de/publications/7a872f9f-8467-4b43-8b2b-36ed7ac737e2
https://doi.org/10.1080/15476286.2018.1460996
http://www.ncbi.nlm.nih.gov/pubmed/29671387
https://core.ac.uk/display/159111164
https://discovery.ucl.ac.uk/id/eprint/10047787/
https://orbi.uliege.be/handle/2268/232539
https://www.muni.cz/vyzkum/publikace/1474618
https://difusion.ulb.ac.be/vufind/Record/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/272929/Details
https://imagine.imgge.bg.ac.rs/handle/123456789/1100
https://imagine.imgge.bg.ac.rs/bitstream/id/2674/RNABiol_2018.pdf
https://hdl.handle.net/10281/446721
https://doi.org/10.1080/15476286.2018.1460996
https://hdl.handle.net/10668/12369
https://curis.ku.dk/ws/files/217115445/Positioning_Europe_for_the_EPITRANSCRIPTOMICS_challenge.pdf
https://discovery-pp.ucl.ac.uk/id/eprint/10047787/
https://radar.ibiss.bg.ac.rs/handle/123456789/3063
https://radar.ibiss.bg.ac.rs//bitstream/id/4261/RNABiol_2018.pdf
https://www.tandfonline.com/doi/full/10.1080/15476286.2018.1460996

Possible Role of GADD45γ Methylation in Diffuse Large B-Cell Lymphoma: Does It Affect the Progression and Tissue Involvement?

Autoren: Barış İC Caner V Şen Türk N et al.

Quelle: Turk J Haematol

Schlagwörter: Male, 0301 basic medicine, very elderly, Adolescent, Adult, Aged, Aged, 80 and over, Child, Child, Preschool, DNA Methylation, DNA, Neoplasm/genetics, Disease Progression, Female, Gene Expression Regulation, Neoplastic, Humans, Infant, Intracellular Signaling Peptides and Proteins/biosynthesis/genetics/*physiology, Lymphoma, Large B-Cell, Diffuse/genetics/metabolism/*pathology, Middle Aged, Neoplasm Proteins/biosynthesis/genetics/*physiology, Nucleic Acid Denaturation, Organ Specificity, Promoter Regions, Genetic/genetics, Pseud, preschool child, Pseudolymphoma, middle aged, 80 and over, DNA denaturation, genetics, Genetik ve Kalıtım, Hücre Biyolojisi, Hematoloji, Onkoloji, Patoloji, high resolution melting analysis, Promoter Regions, Genetic, comparative study, clinical article, large cell lymphoma, larynx squamous cell carcinoma, child, DNA methylation, adult, disease course, Intracellular Signaling Peptides and Proteins, Diffuse large B-cell lymphoma, gene expression regulation, DNA, Neoplasm, GADD45?, 3. Good health, unclassified drug, Neoplasm Proteins, aged, female, immunohistochemistry, young adult, GADD45γ, Lymphoma, Large B-Cell, Diffuse, cancer tissue, Research Article, pseudolymphoma, Article, cancer growth, GADD45G protein, human, Young Adult, 03 medical and health sciences, growth arrest and DNA damage inducible protein 45 gamma, promoter region, tumor protein, male, signal peptide, controlled study, human, Preschool, lymphoid tissue, protein methylation, protein expression, growth arrest and DNA damage inducible protein 45, cancer staging, disease association, antibody specificity, lymphoid hyperplasia, DNA, DNA isolation, infant, human tissue, diffuse large B cell lymphoma, GADD45G protein, adolescent, physiology, pathology, biosynthesis, metabolism

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/25912017
https://core.ac.uk/display/90584315
http://europepmc.org/articles/PMC4805329
https://www.ncbi.nlm.nih.gov/pubmed/25912017
https://app.trdizin.gov.tr/makale/TVRrME9UWTBOQT09/possible-role-of-gadd45-methylation-in-diffuse-large-b-cell-lymphoma-does-it-affect-the-progression-and-tissue-involvement-
https://www.journalagent.com/tjh/pdfs/TJH_32_SUP_4_295_303.pdf
https://pubmed.ncbi.nlm.nih.gov/25912017/
https://avesis.yyu.edu.tr/publication/details/50bdab50-63b7-4772-aa35-b5ff5063a674/oai
https://hdl.handle.net/11499/42797
https://hdl.handle.net/11499/10201
https://doi.org/10.4274/tjh.2014.0174
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/10201

Multimodal Image Analysis of Chronic Leukemic Lymphoproliferative Disorders and the Hypothesis of 'Single' and 'Multiple' Programmed Stops in the Development of Typical and Atypical Forms of Leukaemias and Lymphomas

Autoren: Kardum-Skelin, Ika Jelić Puškarić, Biljana Radić-Krišto, Delfa et al.

Weitere Verfasser: Kardum-Skelin, Ika Jelić Puškarić, Biljana Radić-Krišto, Delfa et al.

Quelle: Collegium antropologicum
CODEN COANDS
Volume 34
Issue 2

Schlagwörter: Lymphoproliferative Disorders / pathology, Leukemia, Lymphocytic, Chronic, B-Cell / pathology, Leukemia, B-Cell / pathology, subacute and subchronic leukemias, Lymphoproliferative Disorders / immunology, multimodal image analysis, Antigens, Nuclear / analysis, DNA, Neoplasm / genetics, DNA / genetics, Humans, Leukemia / pathology, Leukemia, B-Cell / immunology, Leukocytes / pathology, Neoplasm Staging, Multimodal image analysis, Leukemia / immunology, Lymphoproliferative Disorders / classification, Lymph Nodes / pathology, chronic leukemic lymphoproliferative disorders, single and multiple programmed stops, Leukemia / classification, Leukemia, Lymphocytic, Chronic, B-Cell / immunology, Bone Marrow / pathology, Cell Division

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.bib.irb.hr/459599
https://www.bib.irb.hr/527707
http://hrcak.srce.hr/index.php?show=clanak&id_clanak_jezik=85707
https://urn.nsk.hr/urn:nbn:hr:105:502620
https://hrcak.srce.hr/56434
https://hrcak.srce.hr/file/85707
https://hrcak.srce.hr/56434

Aberrant methylation of cyclooxygenase-2 in breast cancer patients

Autoren: Loo, WTY Lui, ELH Chow, LWC et al.

Quelle: Biomedicine & Pharmacotherapy. 59:S264-S267

Schlagwörter: DNA, Neoplasm - genetics, Adult, Aged, 80 and over, 0301 basic medicine, 0303 health sciences, Reverse Transcriptase Polymerase Chain Reaction, Breast Neoplasms, DNA, Neoplasm, Cyclooxygenase 2 - metabolism, Middle Aged, Immunohistochemistry, Methylation, 3. Good health, 03 medical and health sciences, Cyclooxygenase 2, Humans, CpG Islands, Female, Gene Silencing, CpG Islands - genetics, Breast Neoplasms - enzymology, Aged

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/16507389
https://www.ncbi.nlm.nih.gov/pubmed/16507389
https://pubmed.ncbi.nlm.nih.gov/16507389/
https://hub.hku.hk/handle/10722/211380
https://www.sciencedirect.com/science/article/abs/pii/S0753332205800423
http://hdl.handle.net/10722/211380

Clinicopathologic and Molecular Analysis of a Choroidal Pigmented Schwannoma in the Context of a PTEN Hamartoma Tumor Syndrome

Autoren: Venturini, Giulia Moulin, Alexandre P. Deprez, Manuel et al.

Quelle: Ophthalmology

Schlagwörter: RNA, Messenger/genetics, 0301 basic medicine, Ophtalmologie, DNA Mutational Analysis, Visual Acuity, Sciences de la santé humaine, Eye Enucleation, Neurilemmoma/genetics/pathology/ultrasonography, 03 medical and health sciences, 0302 clinical medicine, Choroid Neoplasms/genetics/pathology/ultrasonography, Neurofibromin 2/genetics, Humans, RNA, Messenger, Human health sciences, Child, DNA, Neoplasm/genetics, Ultrasonography, Neurofibromin 2, Reverse Transcriptase Polymerase Chain Reaction, Choroid Neoplasms, PTEN Phosphohydrolase, PTEN Phosphohydrolase/genetics, DNA, Neoplasm, DNA Methylation, Hamartoma Syndrome, Multiple/genetics/pathology/ultrasonography, Immunohistochemistry, 3. Good health, Ophthalmology, Female, Hamartoma Syndrome, Multiple, Neurilemmoma

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/22281088
https://orbi.uliege.be/handle/2268/144191
https://www.ncbi.nlm.nih.gov/pubmed/?term=22281088
https://core.ac.uk/display/18154378
https://www.sciencedirect.com/science/article/pii/S0161642011009444
http://www.sciencedirect.com/science/article/pii/S0161642011009444
https://hdl.handle.net/2268/113683
https://doi.org/10.1016/j.ophtha.2011.09.057

Microsatellite instability, Epstein–Barr virus, mutation of type II transforming growth factor β receptor and BAX in gastric carcinomas in Hong Kong Chinese

Autoren: Chung, LP Yuen, ST Branicki, FJ et al.

Quelle: Br J Cancer

Schlagwörter: Male, 0301 basic medicine, Hong Kong Chinese, Herpesvirus 4, Human, DNA Mutational Analysis, Cell Transformation, 0302 clinical medicine, Receptors, TβRII, Genes, Tumor Suppressor, Cell Transformation, Neoplastic - Genetics, Herpesviridae Infections - Complications, Regular Article, DNA, Neoplasm, Herpesviridae Infections, Middle Aged, 3. Good health, Dna Mutational Analysis, Proto-Oncogene Proteins - Genetics, Carcinoma - Genetics - Pathology - Virology, Cell Transformation, Neoplastic, Proto-Oncogene Proteins c-bcl-2, Hong Kong, Female, Genes, Tumor Suppressor - Genetics, Adult, Receptors, Transforming Growth Factor Beta - Genetics, Neoplasm - Genetics, Bcl-2-Associated X Protein, Herpesvirus 4, Human - Pathogenicity, Medical sciences, 03 medical and health sciences, Stomach Neoplasms, Proto-Oncogene Proteins, Epstein-Barr virus, Humans, Aged, Carcinoma, Transforming Growth Factor Beta - Genetics, Herpesvirus 4, Gastric carcinoma, Human - Pathogenicity, Dna, Microsatellite Repeats - Genetics, Dna, Neoplasm - Genetics, Tumor Virus Infections - Complications, Neoplastic - Genetics, Tumor Virus Infections, Genes, BAX, Microsatellite instability, Stomach Neoplasms - Genetics - Pathology - Virology, Proto-Oncogene Proteins C-Bcl-2, Receptors, Transforming Growth Factor beta, Tumor Suppressor - Genetics, Microsatellite Repeats

Dateibeschreibung: 225 bytes; 99363 bytes; text/plain; application/pdf

Zugangs-URL: https://www.nature.com/articles/6690092.pdf
https://pubmed.ncbi.nlm.nih.gov/10027334
http://hub.hku.hk/handle/10722/48479
https://core.ac.uk/display/37969312
http://europepmc.org/articles/PMC2362448
https://www.nature.com/bjc/journal/v79/n3/abs/6690092a.html
https://www.nature.com/articles/6690092.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362448/
http://hdl.handle.net/10722/148158
http://hdl.handle.net/10722/48479

Prevalence of double pituitary adenomas in a surgical series: Clinical, histological and genetic features

Autoren: Magri, F Villa, C Locatelli, D et al.

Weitere Verfasser: Magri, F Villa, C Locatelli, D et al.

Quelle: Journal of Endocrinological Investigation. 33:325-331

Schlagwörter: Adenoma, Adult, Male, Lactotrophs, DNA Mutational Analysis, Transcription Factors/genetics, Adenoma/epidemiology/genetics/surgery, pituitary, Sciences de la santé humaine, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, metabolism & nutrition, Carrier Proteins, DNA, Neoplasm, Humans, Immunohistochemistry, Magnetic Resonance Imaging, Middle Aged, Pituitary Neoplasms, Prolactinoma, Proto-Oncogene Proteins, Reverse Transcriptase Polymerase Chain Reaction, Transcription Factors, Treatment Outcome, AIP, Human health sciences, DNA, Neoplasm/genetics, Adaptor Proteins, Signal Transducing, Lactotrophs/pathology, Carrier Proteins/biosynthesis/genetics, 3. Good health, Proto-Oncogene Proteins/genetics, AIP gene, double pituitary adenoma, menin gene, pituitary transcription factor, double adenoma, Pituitary Neoplasms/epidemiology/genetics/surgery, Prolactinoma/genetics/pathology/surgery, Guanylate Kinases, Endocrinologie, métabolisme & nutrition

Dateibeschreibung: STAMPA

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/19955848
https://pubmed.ncbi.nlm.nih.gov/19955848/
https://link.springer.com/article/10.1007/BF03346594
https://orbi.uliege.be/handle/2268/155131
http://orbi.ulg.ac.be/handle/2268/155131
https://www.ncbi.nlm.nih.gov/pubmed/19955848
https://moh-it.pure.elsevier.com/en/publications/prevalence-of-double-pituitary-adenomas-in-a-surgical-series-clin
https://hdl.handle.net/2268/155131
https://doi.org/10.3275/6716
https://hdl.handle.net/11383/2061271
https://doi.org/10.3275/6716
https://hdl.handle.net/11379/569578
https://doi.org/10.1007/BF03346594

Interlaboratory Diagnostic Validation of Conformation-Sensitive Capillary Electrophoresis for Mutation Scanning

Autoren: Mattocks, C.J. Watkins, G. Ward, D. et al.

Weitere Verfasser: Mattocks, C.J. Watkins, G. Ward, D. et al.

Quelle: Clinical Chemistry, 56, 4, pp. 593-602

Schlagwörter: 0301 basic medicine, DNA Mutational Analysis, DNA Mutational Analysis/methods, Breast Neoplasms, Breast Neoplasms/genetics, Sensitivity and Specificity, Automation, 03 medical and health sciences, IGMD 3: Genomic disorders and inherited multi-system disorders, ONCOL 1: Hereditary cancer and cancer-related syndromes, Humans, DNA, Neoplasm/genetics, automation, BRCA2 Protein, 0303 health sciences, Base Sequence, BRCA1 Protein, Electrophoresis, Capillary, Genetic Variation, Reproducibility of Results, DNA, Neoplasm, BRCA2 Protein/genetics, 3. Good health, Genetic Variation/genetics, Mutation, BRCA1 Protein/genetics, Nucleic Acid Conformation, reproducibility of results, mutation, Apoptosis Regulatory Proteins, Laboratories

Zugangs-URL: http://clinchem.aaccjnls.org/content/56/4/593.full.pdf
https://pubmed.ncbi.nlm.nih.gov/20167696
https://eprints.soton.ac.uk/72745/
https://core.ac.uk/display/1480551
http://clinchem.aaccjnls.org/content/56/4/593
http://www.ncbi.nlm.nih.gov/pubmed/20167696
https://researchportal.vub.be/en/publications/interlaboratory-diagnostic-validation-of-conformation-sensitive-c
https://academic.oup.com/clinchem/article/56/4/593/5622408
https://repository.ubn.ru.nl//bitstream/handle/2066/87980/87980.pdf
https://hdl.handle.net/2066/87980
https://biblio.vub.ac.be/vubir/interlaboratory-diagnostic-validation-of-conformationsensitive-capillary-electrophoresis-for-mutation-scanning(9b1c57e3-a42f-4f23-a252-c3542fbad4c1).html
https://doi.org/10.1373/clinchem.2009.135426
https://hdl.handle.net/20.500.14017/9b1c57e3-a42f-4f23-a252-c3542fbad4c1

The prolyl‐hydroxylase EGLN3 and not EGLN1 is inactivated by methylation in plasma cell neoplasia

Autoren: Hatzimichael, E Dasoula, A Shah, R et al.

Weitere Verfasser: Hatzimichael, E Dasoula, A Shah, R et al.

Quelle: European Journal of Haematology. 84:47-51

Schlagwörter: Male, 0301 basic medicine, Lymphoma, B-Cell, Multiple Myeloma/complications/enzymology/genetics/mortality, Paraproteinemias, Procollagen-Proline Dioxygenase, DNA Methylation, Dioxygenases/biosynthesis/*genetics, Monoclonal Gammopathy of Undetermined Significance, Gene Expression Regulation, Enzymologic, Dioxygenases, Hypoxia-Inducible Factor-Proline Dioxygenases, 03 medical and health sciences, 0302 clinical medicine, CpG Islands/*genetics, Procollagen-Proline Dioxygenase/biosynthesis/*genetics, Cell Line, Tumor, Waldenstrom Macroglobulinemia/enzymology/genetics, Humans, Gene Silencing, Cell Line, Tumor/enzymology, DNA, Neoplasm/genetics, Aged, Monoclonal Gammopathy of Undetermined Significance/enzymology/genetics, DNA, Neoplasm, Middle Aged, Paraproteinemias/enzymology/*genetics, Gene Expression Regulation, Neoplastic, Lymphoma, B-Cell/classification/enzymology/genetics, CpG Islands, Female, Waldenstrom Macroglobulinemia, Multiple Myeloma

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/19737309
https://pubmed.ncbi.nlm.nih.gov/19737309/
http://onlinelibrary.wiley.com/doi/10.1111/j.1600-0609.2009.01344.x/abstract
https://core.ac.uk/display/82933525
https://www.ncbi.nlm.nih.gov/pubmed/19737309
https://onlinelibrary.wiley.com/doi/10.1111/j.1600-0609.2009.01344.x
http://olympias.lib.uoi.gr/jspui/handle/123456789/23587

Prognostic relevance of DNA copy number changes in colorectal cancer

Autoren: Harrison, DJ Poulogiannis, G Ichimura, K et al.

Quelle: The Journal of Pathology. 220:338-347

Schlagwörter: DNA, Neoplasm - genetics, 0301 basic medicine, Adult, Male, Neoplasm - genetics, Survival, DNA Copy Number Variations, CELF4, 03 medical and health sciences, 0302 clinical medicine, Recurrence, Array-comparative genomic hybridization, Humans, Aged, Neoplasm Staging, Aged, 80 and over, 0303 health sciences, Comparative Genomic Hybridization, BRUNOL4, DNA, DNA, Neoplasm, Middle Aged, Prognosis, Colorectal cancer, 3. Good health, Colorectal Neoplasms - genetics - pathology, Lymphatic Metastasis, Microsatellite instability, Female, Microsatellite Instability, Colorectal Neoplasms, Epidemiologic Methods

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/19911421
http://hub.hku.hk/handle/10722/65485
https://www.research.ed.ac.uk/portal/en/publications/prognostic-relevance-of-dna-copy-number-changes-in-colorectal-cancer(a00b64b6-f69f-4b97-9ab9-8c69e6c280ec)/export.html
http://www.research.ed.ac.uk/portal/en/publications/prognostic-relevance-of-dna-copy-number-changes-in-colorectal-cancer(a00b64b6-f69f-4b97-9ab9-8c69e6c280ec)/export.html
https://onlinelibrary.wiley.com/doi/abs/10.1002/path.2640
https://www.ncbi.nlm.nih.gov/pubmed/19911421
http://hdl.handle.net/10722/65485

Overexpression of prostate stem cell antigen is associated with gestational trophoblastic neoplasia

Autoren: Wong, E Liao, XY Kwan, HS et al.

Quelle: Histopathology. 52:167-174

Schlagwörter: DNA, Neoplasm - genetics, Adult, Male, 0301 basic medicine, Membrane Glycoproteins - genetics - metabolism, Neoplasm - genetics, Prostate stem cell antigen, Hydatidiform Mole - genetics - metabolism - pathology, Adolescent, Gestational Trophoblastic Disease - genetics - metabolism - pathology, GPI-Linked Proteins, 03 medical and health sciences, 0302 clinical medicine, Tumor Suppressor Protein p53 - genetics - metabolism, Antigens, Neoplasm, Pregnancy, Biomarkers, Tumor, Humans, Antigens, Gestational Trophoblastic Disease, Tumor Markers, Gestational trophoblastic neoplasia, Cell Proliferation, Oligonucleotide Array Sequence Analysis, cDNA microarray, Neoplastic, Membrane Glycoproteins, Neoplasm Proteins - genetics - metabolism, Prostatic Neoplasms, DNA, DNA, Neoplasm, Hydatidiform Mole, Middle Aged, Prostatic Neoplasms - genetics - metabolism - pathology, 3. Good health, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, Gene Expression Regulation, Biological - metabolism, Neoplasm, Female, Signal Transduction - genetics, Tumor Markers, Biological - metabolism, Signal Transduction

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/18184265
https://europepmc.org/abstract/MED/18184265
https://hub.hku.hk/handle/10722/67402
http://www.ncbi.nlm.nih.gov/pubmed/18184265
https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2559.2007.02925.x
http://hdl.handle.net/10722/67402

Mutations in theAryl Hydrocarbon Receptor Interacting ProteinGene Are Not Highly Prevalent among Subjects with Sporadic Pituitary Adenomas

Autoren: Barlier, Anne Vanbellinghem, Jean-François Daly, Adrian F. et al.

Weitere Verfasser: Barlier, Anne Vanbellinghem, Jean-François Daly, Adrian F. et al.

Quelle: The Journal of Clinical Endocrinology & Metabolism. 92:1952-1955

Schlagwörter: Adenoma, Adult, Male, Genotype, [SHS.ANTHRO-BIO]Humanities and Social Sciences/Biological anthropology, Sciences de la santé humaine, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, metabolism & nutrition, Gene Frequency, Multiple Endocrine Neoplasia Type 1, Humans, Pituitary Neoplasms, Human health sciences, Polymorphism, Genetic/genetics, DNA, Neoplasm/genetics, Aryl Hydrocarbon Receptor Interacting Protein, Polymorphism, Genetic, Multiple Endocrine Neoplasia Type 1/genetics, Intracellular Signaling Peptides and Proteins, Proteins, DNA, Neoplasm, Middle Aged, Adenoma/genetics, Pituitary Neoplasms/genetics, [SHS.ANTHRO-BIO] Humanities and Social Sciences/Biological anthropology, 3. Good health, Proteins/genetics, Mutation, Mutation/genetics/physiology, Female, Endocrinologie, métabolisme & nutrition

Zugangs-URL: https://academic.oup.com/jcem/article-pdf/92/5/1952/9056000/jcem1952.pdf
https://pubmed.ncbi.nlm.nih.gov/17299063
https://hal.science/hal-00141378v1
https://moh-it.pure.elsevier.com/en/publications/mutations-in-the-aryl-hydrocarbon-receptor-interacting-protein-ge
https://europepmc.org/abstract/MED/17299063
http://press.endocrine.org/doi/pdf/10.1210/jc.2006-2702
https://academic.oup.com/jcem/article/92/5/1952/2598952
https://hal-amu.archives-ouvertes.fr/hal-01076905v1
https://hal.archives-ouvertes.fr/hal-01076905
https://hdl.handle.net/2268/12090
https://doi.org/10.1210/jc.2006-2702
https://hal.science/hal-01076905v1
https://doi.org/10.1210/jc.2006-2702
https://hdl.handle.net/11697/2932
https://doi.org/10.1210/jc.2006-2702