Výsledky vyhľadávania - "Pair 7/genetics"
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1
Autori: a ďalší
Zdroj: J Hematol Oncol
Journal of Hematology & Oncology, Vol 17, Iss 1, Pp 1-18 (2024)Predmety: Male, Adult, 0301 basic medicine, Cancer Research, Adolescent, DNA Copy Number Variations, Protein Tyrosine Phosphatase, Non-Receptor Type 11, Monosomy 7, Cohort Studies, Young Adult, 03 medical and health sciences, SDG 3 - Good Health and Well-being, AML, del(7q), Exome Sequencing, Humans, Diseases of the blood and blood-forming organs, TP53, RC254-282, Aged, Chromosome Aberrations, Aged, 80 and over, 0303 health sciences, Aged, 80 and over [MeSH], Aged [MeSH], Leukemia, Myeloid, Acute/mortality [MeSH], Cohort Studies [MeSH], Male [MeSH], Leukemia, Myeloid, Acute/genetics [MeSH], Protein Tyrosine Phosphatase, Non-Receptor Type 11/genetics [MeSH], Chromosome Aberrations [MeSH], Adolescent [MeSH], Female [MeSH], Mutation [MeSH], Adult [MeSH], Humans [MeSH], Chromosomes, Human, Pair 7/genetics [MeSH], Genomics/methods [MeSH], Middle Aged [MeSH], Exome Sequencing [MeSH], Tumor Suppressor Protein p53/genetics [MeSH], DNA Copy Number Variations [MeSH], Research, Prognosis [MeSH], Young Adult [MeSH], Leukemia, Myeloid, Acute/drug therapy [MeSH], Complex karyotype, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, KMT2C, Genomics, Middle Aged, Prognosis, 3. Good health, Leukemia, Myeloid, Acute, Mutation, Female, RC633-647.5, Tumor Suppressor Protein p53, Chromosomes, Human, Pair 7
Popis súboru: application/pdf
Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/39160538
https://doaj.org/article/c4bde76aa3284c6f887bca011315517d
https://pure.eur.nl/en/publications/d5d46142-9d53-4b2a-ac4e-22b8a30fb9a7
https://doi.org/10.1186/s13045-024-01590-1
https://edoc.mdc-berlin.de/id/eprint/24622/2/24622suppl.zip
https://ora.ox.ac.uk/objects/uuid:c42613d1-4872-4aa7-880e-e2bbcc3481ae
https://doi.org/10.1186/s13045-024-01590-1
https://repository.publisso.de/resource/frl:6491728 -
2
Autori: a ďalší
Prispievatelia: a ďalší
Zdroj: Acta Neuropathol
Acta Neuropathologica
Suwala, A K, Stichel, D, Schrimpf, D, Maas, S L N, Sill, M, Dohmen, H, Banan, R, Reinhardt, A, Sievers, P, Hinz, F, Blattner-Johnson, M, Hartmann, C, Schweizer, L, Boldt, H B, Kristensen, B W, Schittenhelm, J, Wood, M D, Chotard, G, Bjergvig, R, Das, A, Tabori, U, Hasselblatt, M, Korshunov, A, Abdullaev, Z, Quezado, M, Aldape, K, Harter, P N, Snuderl, M, Hench, J R, Frank, S, Acker, T, Brandner, S, Winkler, F, Wesseling, P, Pfister, S M, Reuss, D E, Wick, W, von Deimling, A, Jones, D T W & Sahm, F 2021, 'Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1', Acta Neuropathologica, vol. 142, no. 1, pp. 179-189. https://doi.org/10.1007/s00401-021-02302-6
Suwala, A K, Stichel, D, Schrimpf, D, Maas, S L N, Sill, M, Dohmen, H, Banan, R, Reinhardt, A, Sievers, P, Hinz, F, Blattner-johnson, M, Hartmann, C, Schweizer, L, Boldt, H B, Kristensen, B W, Schittenhelm, J, Wood, M D, Chotard, G, Bjergvig, R, Das, A, Tabori, U, Hasselblatt, M, Korshunov, A, Abdullaev, Z, Quezado, M, Aldape, K, Harter, P N, Snuderl, M, Hench, J, Frank, S, Acker, T, Brandner, S, Winkler, F, Wesseling, P, Pfister, S M, Reuss, D E, Wick, W, Von Deimling, A, Jones, D T W & Sahm, F 2021, ' Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1 ', Acta Neuropathologica, vol. 142, pp. 179–189 . https://doi.org/10.1007/s00401-021-02302-6
Suwala, A K, Stichel, D, Schrimpf, D, Maas, S L N, Sill, M, Dohmen, H, Banan, R, Reinhardt, A, Sievers, P, Hinz, F, Blattner-Johnson, M, Hartmann, C, Schweizer, L, Boldt, H B, Kristensen, B W, Schittenhelm, J, Wood, M D, Chotard, G, Bjergvig, R, Das, A, Tabori, U, Hasselblatt, M, Korshunov, A, Abdullaev, Z, Quezado, M, Aldape, K, Harter, P N, Snuderl, M, Hench, J, Frank, S, Acker, T, Brandner, S, Winkler, F, Wesseling, P, Pfister, S M, Reuss, D E, Wick, W, von Deimling, A, Jones, D T W & Sahm, F 2021, ' Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1 ', Acta Neuropathologica, vol. 142, no. 1, pp. 179-189 . https://doi.org/10.1007/s00401-021-02302-6
Acta Neuropathologica, vol 142, iss 1Predmety: Male, 0301 basic medicine, PNET, Neuroectodermal Tumors, Cohort Studies, Primitive, 2.1 Biological and endogenous factors, Neuroectodermal Tumors, Primitive, Aetiology, 10. No inequality, Cancer, 2. Zero hunger, 0303 health sciences, DNA methylation, Brain Neoplasms, Research Support, Non-U.S. Gov't, Ubiquitin-Protein Ligases/genetics [MeSH], Glial Fibrillary Acidic Protein/biosynthesis [MeSH], Glioblastoma/pathology [MeSH], Cohort Studies [MeSH], Neuroectodermal Tumors, Primitive/genetics [MeSH], Male [MeSH], Retinoblastoma Binding Proteins/genetics [MeSH], Glioblastoma/genetics [MeSH], Gene Deletion [MeSH], Female [MeSH], Neuroectodermal Tumors, Primitive/pathology [MeSH], Phenotype, Brain Neoplasms/genetics [MeSH], GBM, Classification, Humans [MeSH], PTEN Phosphohydrolase/genetics [MeSH], Chromosomes, Human, Pair 7/genetics [MeSH], Middle Aged [MeSH], Glial Fibrillary Acidic Protein/genetics [MeSH], Tumor Suppressor Protein p53/genetics [MeSH], Cyclin-Dependent Kinase Inhibitor p16/genetics [MeSH], DNA Copy Number Variations [MeSH], DNA Methylation [MeSH], Plasticity, Original Paper, Chromosomes, Human, Pair 1/genetics [MeSH], Brain Neoplasms/pathology [MeSH], Middle Aged, Retinoblastoma Binding Proteins, Chromosomes, Human, Pair 1, Pair 1, Pair 7, Female, Chromosomes, Human, Pair 7, Human, DNA Copy Number Variations, Ubiquitin-Protein Ligases, Clinical Sciences, Oncology and Carcinogenesis, Clinical Neurology, Chromosomes, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience, 03 medical and health sciences, Rare Diseases, Glial Fibrillary Acidic Protein, Genetics, Journal Article, Humans, Cyclin-Dependent Kinase Inhibitor p16, Neurology & Neurosurgery, Biomedical and Clinical Sciences, Human Genome, Neurosciences, PTEN Phosphohydrolase, DNA Methylation, Brain Disorders, Brain Cancer, Tumor Suppressor Protein p53, Glioblastoma, Gene Deletion
Popis súboru: application/pdf
Prístupová URL adresa: https://link.springer.com/content/pdf/10.1007/s00401-021-02302-6.pdf
https://pubmed.ncbi.nlm.nih.gov/33876327
https://pubmed.ncbi.nlm.nih.gov/33876327/
http://europepmc.org/article/MED/33876327
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217054
https://link.springer.com/content/pdf/10.1007/s00401-021-02302-6.pdf
https://portal.findresearcher.sdu.dk/en/publications/glioblastomas-with-primitive-neuronal-component-harbor-a-distinct
https://research.vumc.nl/en/publications/glioblastomas-with-primitive-neuronal-component-harbor-a-distinct
https://hdl.handle.net/11250/2838416
https://research.vumc.nl/en/publications/b19cce4f-5688-4146-bc50-f67a1dcb96da
https://dspace.library.uu.nl/handle/1874/443255
https://curis.ku.dk/ws/files/275993976/Suwala2021_Article_GlioblastomasWithPrimitiveNeur.pdf
https://portal.findresearcher.sdu.dk/da/publications/790ecb5e-6834-457e-ab0c-54e543e63689
https://doi.org/10.1007/s00401-021-02302-6
https://findresearcher.sdu.dk:8443/ws/files/184340978/Suwala2021_Article_GlioblastomasWithPrimitiveNeur.pdf
https://repository.publisso.de/resource/frl:6450722
https://discovery-pp.ucl.ac.uk/id/eprint/10130401/
https://escholarship.org/content/qt2kz927r8/qt2kz927r8.pdf
https://escholarship.org/uc/item/2kz927r8 -
3
Autori: a ďalší
Predmety: Cell Line, Transformed, Cells, Cultured, Chromosomes, Human, Pair 7/genetics, Gene Deletion, Gene Expression, Humans, Williams Syndrome/genetics
Relation: American Journal of Human Genetics; 0002-9297[print], 0002-9297[linking]; https://iris.unil.ch/handle/iris/196488; serval:BIB_A78B3DE949B3; 000239040400014
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4
Autori: a ďalší
Predmety: Amino Acid Motifs/genetics, Animals, COS Cells, Cell Line, Tumor, Cercopithecus aethiops, Chromosomes, Human, Pair 7/enzymology, Pair 7/genetics, Hela Cells, Humans, Mice, Phenotype, Proteasome Endopeptidase Complex/physiology, Signal Transduction/genetics, Synteny/genetics, Ubiquitin/physiology, Ubiquitin-Protein Ligases/genetics, Williams Syndrome/enzymology, Williams Syndrome/genetics
Popis súboru: application/pdf
Relation: European Journal of Human Genetics; https://iris.unil.ch/handle/iris/172074; serval:BIB_C1B799B255F6; 000258929800003
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5
Autori: a ďalší
Zdroj: Nature Medicine, 22, 8, pp. 952-60
Nature MedicinePredmety: Male, Candida albicans/immunology, Individuality, Bacteroides fragilis, Candida albicans, Leukocytes, European Continental Ancestry Group/genetics, Immunogenetic Phenomena, Radboudumc 4: lnfectious Diseases and Global Health RIMLS: Radboud Institute for Molecular Life Sciences, Single Nucleotide, Middle Aged, 3. Good health, Phenotype, Chromosomes, Human, Pair 1, Cytokines, Aspergillus fumigatus/immunology, Female, N-Terminal Acetyltransferase C/genetics, Staphylococcus aureus/immunology, Chromosomes, Human, Pair 7, Human, Adult, Genotype, Quantitative Trait Loci, Bacteria/immunology, Chromosomes, Innate/immunology, Young Adult, Cytokines/immunology, Pair 1/genetics, Escherichia coli, Humans, Candidemia/immunology, Membrane Proteins/genetics, Polymorphism, Aged, Mononuclear/immunology, Escherichia coli/immunology, Bacteria, Aspergillus fumigatus, Gene Expression Profiling, Fungi/immunology, Immunity, Fungi, Candidemia, Genetic Variation, Radboudumc 9: Rare cancers RIMLS: Radboud Institute for Molecular Life Sciences, Bacteroides fragilis/immunology, Immunity, Innate, Pair 7/genetics, 13. Climate action, Interleukin-6/immunology, Mycobacterium tuberculosis/immunology
Prístupová URL adresa: https://europepmc.org/articles/pmc5084084?pdf=render
https://pubmed.ncbi.nlm.nih.gov/27376574
https://hdl.handle.net/https://repository.ubn.ru.nl/handle/2066/165682
https://doi.org/10.1038/nm.4139
https://core.ac.uk/display/92558650
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5084084
https://www.nature.com/articles/nm.4139.pdf
https://www.narcis.nl/publication/RecordID/oai%3Arepository.ubn.ru.nl%3A2066%2F165682
https://research.rug.nl/en/publications/inter-individual-variability-and-genetic-influences-on-cytokine-r
https://www.nature.com/articles/nm.4139
https://hdl.handle.net/2066/165682
https://repository.ubn.ru.nl//bitstream/handle/2066/165682/165682.pdf -
6
Autori:
Prispievatelia:
Predmety: AML, acute monoblastic leukemia, isochromosome 5p, clonal evolution, Leukaemia Section, Adult, Aged, Antineoplastic Agents, Alkylating/*adverse effects, Chromosome Aberrations, Chromosomes, Human, Pair 5/genetics, Pair 7/genetics, Cyclophosphamide/adverse effects/therapeutic use, Drug Therapy, Combination, Female, Follow-Up Studies, Humans, In Situ Hybridization, Fluorescence, Leukemia, Myeloid, Acute/*etiology/genetics/mortality/pathology, Male, Melphalan/adverse effects/therapeutic use, Middle Aged, Multiple Myeloma/*drug therapy/genetics, Myelodysplastic Syndromes/*etiology/genetics/mortality/pathology
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/i05p10ID1825.html; Adriana, Zamecnikova. i(5)(p10) in hematological malignancies. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 10, p. 304-306; http://hdl.handle.net/2042/70576; https://doi.org/10.4267/2042/70576
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7
Autori: a ďalší
Prispievatelia: a ďalší
Predmety: Reports Section, Adult, Aged, 80 and over, Chromosome Aberrations, Chromosomes, Human, Pair 3/genetics, Pair 7/genetics, Cohort Studies, Cytogenetics, DNA-Binding Proteins/*genetics/metabolism, Female, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Leukemia, Myeloid, Acute/*genetics/metabolism/pathology, MDS1 and EVI1 Complex Locus Protein, Male, Middle Aged, Prognosis, Proto-Oncogenes/*genetics, Transcription Factors/*genetics/metabolism, Translocation, Genetic
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Reports/t0120q21p13MitevID100090.html; Lubomir, Mitev; Liliya, Grahlyova; Aselina, Asenova; Verginia, Uzunova; Julian, Raynov. Isolated 1q21 rearrangement der(20)t(1;20)(q21;p13) with telomere involvement of 20p in a case of longstanding myelodysplastic syndrome. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2019, 07, p. 200-203; http://hdl.handle.net/2042/70472; https://doi.org/10.4267/2042/70472
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8
Autori: a ďalší
Prispievatelia: a ďalší
Zdroj: Nat Genet
Predmety: endometriosis, 0301 basic medicine, Carrier Proteins/genetics, Pair 6/genetics, Pair 9/genetics, Genetic Loci, Severity of Illness Index, Cohort Studies, 0302 clinical medicine, Neoplasm Proteins/genetics, Genome-Wide Association Study, European Continental Ancestry Group/genetics, Cancer, Single Nucleotide, European women, Neoplasm Proteins, 3. Good health, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 2, Chromosomes, Human, Pair 6, Female, Chromosomes, Human, Pair 9, Chromosomes, Human, Pair 7, Human, Risk, Endometriosis, genome-wide association meta-analysis, Polymorphism, Single Nucleotide, Chromosomes, Article, White People, Hmlh1, 03 medical and health sciences, Endometriosis/*genetics, 1311 Genetics, Asian People, Pair 1/genetics, Humans, Asian Continental Ancestry Group/genetics, Genetic Predisposition to Disease, Membrane Proteins/genetics, Polymorphism, Japanese women, genetic variants, Membrane Proteins, Pair 7/genetics, Japanese, Pair 2/genetics, Wnt4 Protein/genetics, Carrier Proteins
Popis súboru: application/pdf
Prístupová URL adresa: https://europepmc.org/articles/pmc3527416?pdf=render
https://pubmed.ncbi.nlm.nih.gov/23104006
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527416/
https://www.ncbi.nlm.nih.gov/pubmed/23104006
http://europepmc.org/abstract/MED/23104006
https://www.obs-gyn.ox.ac.uk/publications/358308
https://genepi.qimr.edu.au/contents/p/staff/Nyholt_2012_NatGenet_Endometriosis_Study.pdf
https://espace.library.uq.edu.au/view/UQ:287935
https://ora.ox.ac.uk/objects/uuid:1a2c8697-b67d-411c-a10a-0031743b45cb
https://doi.org/10.1038/ng.2445
https://ora.ox.ac.uk/objects/uuid:cc287175-977c-4cd2-9bb7-0d7c8def441f
https://doi.org/10.1038/ng.2445 -
9
Autori: a ďalší
Prispievatelia: a ďalší
Zdroj: International Journal of Cancer. 128:857-868
Predmety: 0301 basic medicine, Carcinoma, Hepatocellular, Chromosomes, Human, Pair 21, Cell Transformation, Polymerase Chain Reaction, Chromosomes, 03 medical and health sciences, Humans, Neoplastic/pathology, Hepatocellular/genetics, Pair 18/genetics, DNA Methylation, telomere, 0303 health sciences, DNA methylation, Neoplasm/genetics, Hepatocellular/pathology, Carcinoma, hepatocarcinogenesis, Liver Neoplasms, Liver Neoplasms/pathology, Pair 21/genetics, DNA, DNA, Neoplasm, Telomere, Prognosis, hepatocellular,carcinoma, Cell Transformation, Neoplastic, Pair 7/genetics, subtelomere, Liver Neoplasms/genetics, Chromosomes, Human, Pair 18, Chromosomes, Human, Pair 7, Human, Telomere/genetics
Popis súboru: 857~868
Prístupová URL adresa: https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/ijc.25398
https://pubmed.ncbi.nlm.nih.gov/20473888
https://pubmed.ncbi.nlm.nih.gov/20473888/
https://www.ncbi.nlm.nih.gov/pubmed/20473888
http://onlinelibrary.wiley.com/doi/10.1002/ijc.25398/abstract
https://onlinelibrary.wiley.com/doi/10.1002/ijc.25398/full -
10
Autori: a ďalší
Zdroj: J Med Genet
Wakeling, E L, Amero, S A, Alders, M, Bliek, J, Forsythe, E, Kumar, S, Lim, D H, MacDonald, F, Mackay, D J, Maher, E R, Moore, G E, Poole, R L, Price, S M, Tangeraas, T, Turner, C L S, Van Haelst, M M, Willoughby, C, Temple, I K & Cobben, J M 2010, 'Epigenotype-phenotype correlations in Silver-Russell syndrome', Journal of Medical Genetics, vol. 47, no. 11, pp. 760-8. https://doi.org/10.1136/jmg.2010.079111Predmety: Male, 0301 basic medicine, Potassium Channels, RNA, Untranslated, HYPOMETHYLATION, Untranslated/genetics, PHENOTYPE, Epigenesis, Genetic, Prospective Studies, Child, 0303 health sciences, CHROMOSOME 11P15, METHYLATION, Silver-Russell Syndrome/genetics, Potassium Channels, Voltage-Gated, Child, Preschool, IMPRINTING CENTER REGION, Long Noncoding, Original Article, Female, RNA, Long Noncoding, MATERNAL UNIPARENTAL DISOMY, Chromosomes, Human, Pair 7, Human, Adult, Adolescent, DYSTONIA, Chromosomes, Pair 11/genetics, Young Adult, Genomic Imprinting, 03 medical and health sciences, Genetic, ASSISTED REPRODUCTIVE TECHNOLOGY, Humans, Preschool, Genetic Association Studies, SPECTRUM, Chromosomes, Human, Pair 11, Infant, DNA Methylation, Uniparental Disomy, Voltage-Gated/genetics, Genetic Association Studies/methods, Silver-Russell Syndrome, Pair 7/genetics, RNA, Epigenesis, GROWTH-RETARDATION
Prístupová URL adresa: https://jmg.bmj.com/content/47/11/760.full.pdf
https://pubmed.ncbi.nlm.nih.gov/20685669
https://research.rug.nl/en/publications/3cef70e5-4d91-46ce-af98-731ae0ed4185
https://doi.org/10.1136/jmg.2010.079111
https://hdl.handle.net/11370/3cef70e5-4d91-46ce-af98-731ae0ed4185
https://eprints.soton.ac.uk/162267/
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2976034
https://www.rug.nl/research/portal/en/publications/epigenotypephenotype-correlations-in-silverrussell-syndrome(3cef70e5-4d91-46ce-af98-731ae0ed4185).html
https://pubmed.ncbi.nlm.nih.gov/20685669/
https://jmg.bmj.com/content/47/11/760.full.pdf
https://research.birmingham.ac.uk/portal/en/publications/epigenotypephenotype-correlations-in-silverrussell-syndrome(7b6af115-4777-4465-bd2f-512bdbc1de9d).html
https://research.vumc.nl/en/publications/dc255f33-c306-49c7-996a-d1ffb85d61d6 -
11
Autori: a ďalší
Zdroj: Kouwenhoven, M C M, Gorlia, T, Kros, J M, Ibdaih, A, Brandes, A A, Bromberg, J E C, Mokhtari, K, van Duinen, S G, Teepen, J L, Wesseling, P, Vandenbos, F, Grisold, W, Sipos, L, Mirimanoff, R, Vecht, C J, Allgeier, A, Lacombe, D & van den Bent, M J 2009, 'Molecular analysis of anaplastic oligodendroglial tumors in a prospective randomized study : A report from EORTC study 26951', Neuro-Oncology, vol. 11, no. 6, pp. 737-46. https://doi.org/10.1215/15228517-2009-011
Neuro-Oncology, 11, 6, pp. 737-46Predmety: NCMLS 3: Tissue engineering and pathology, Pair 19/genetics, Lomustine/administration & dosage, Astrocytoma/drug therapy, 0302 clinical medicine, Lomustine, Pair 10/genetics, Antineoplastic Combined Chemotherapy Protocols, Vincristine/administration & dosage, Prospective Studies, Adjuvant, In Situ Hybridization, In Situ Hybridization, Fluorescence, Oligodendroglioma/drug therapy, Brain Neoplasms, Vascular/cytology, Prognosis, 3. Good health, Phase III as Topic, Survival Rate, Chemotherapy, Adjuvant, Chromosomes, Human, Pair 1, Chromosome Deletion, Chromosomes, Human, Pair 7, Human, Oligodendroglioma, Brain Neoplasms/drug therapy, Astrocytoma, Chromosomes, Fluorescence, EMC MM-03-44-06, Necrosis, 03 medical and health sciences, SDG 3 - Good Health and Well-being, Pair 1/genetics, Chemotherapy, Humans, Clinical Trials, Endothelium, Cell Proliferation, Neoplasm Staging, Chromosomes, Human, Pair 10, Procarbazine/administration & dosage, EMC MM-03-24-01, ONCOL 3: Translational research, Clinical Trials, Phase III as Topic, Pair 7/genetics, Procarbazine, Antineoplastic Combined Chemotherapy Protocols/therapeutic use, Endothelium, Vascular, Chromosomes, Human, Pair 19
Prístupová URL adresa: https://academic.oup.com/neuro-oncology/article-pdf/11/6/737/13065685/04_NO08-00260_Bent_FF.pdf
https://pubmed.ncbi.nlm.nih.gov/19224764
https://pure.eur.nl/en/publications/03864281-5aeb-43cb-b4a3-e6495566a745
https://doi.org/10.1215/15228517-2009-011
http://neuro-oncology.oxfordjournals.org/content/11/6/737.full
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2802394/table/t2-neu-11-6-737/
https://repub.eur.nl/pub/25381
https://academic.oup.com/neuro-oncology/article/11/6/737/1454789
https://paperity.org/p/38550997/molecular-analysis-of-anaplastic-oligodendroglial-tumors-in-a-prospective-randomized
https://core.ac.uk/display/16164107
https://research.vumc.nl/en/publications/c3bf9349-f546-427a-9c78-03428e02d79b
https://pure.amsterdamumc.nl/en/publications/f34a63da-83e6-451f-ad4f-0fffbc456a91
https://doi.org/10.1215/15228517-2009-011
http://hdl.handle.net/2066/79642 -
12
Autori: a ďalší
Zdroj: Nature communications, vol. 8, no. 1, pp. 744
Predmety: Anthropometry, Body Height/genetics, Body Mass Index, Body Size/genetics, Body Weight/genetics, Chromosomes, Human, Pair 1/genetics, Pair 11/genetics, Pair 16/genetics, Pair 18/genetics, Pair 22/genetics, Pair 3/genetics, Pair 7/genetics, DNA Copy Number Variations, European Continental Ancestry Group/genetics, Genome-Wide Association Study, Genotype, Humans, Phenotype, Waist-Hip Ratio
Popis súboru: application/pdf
Relation: info:eu-repo/semantics/altIdentifier/pmid/28963451; info:eu-repo/semantics/altIdentifier/eissn/2041-1723; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_220FBAC01D966; https://serval.unil.ch/notice/serval:BIB_220FBAC01D96; https://serval.unil.ch/resource/serval:BIB_220FBAC01D96.P001/REF.pdf
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13
Autori:
Prispievatelia:
Predmety: Renal cell carcinoma, chromosome X, chromosome 1, SFPQ, TFE3, MiT family, Leukaemia Section, Acute Disease, Amino Acid Sequence, Base Sequence, Chromosomes, Human, Pair 11/genetics, Pair 7/genetics, Homeodomain Proteins/*genetics, Humans, Leukemia, Myeloid/*genetics, Molecular Sequence Data, Multigene Family/genetics, Neoplasm Proteins/genetics, Nuclear Pore Complex Proteins/*genetics, Oncogene Proteins, Fusion/genetics, Translocation, Genetic/*genetics, Alternative Splicing
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0711p15p15ID1360.html; Aurelia M, Meloni-Ehrig. t(7;11)(p15;p15) NUP98/HOXA13. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2017, 10, p. 372-374; http://hdl.handle.net/2042/68741; https://doi.org/10.4267/2042/68741
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14
Autori:
Prispievatelia:
Predmety: chromosome 3, t(3, 7)(q26, q21), MECOM, Leukaemia Section, Cell Cycle Checkpoints/genetics, Cyclin-Dependent Kinase 6/*genetics/*metabolism, Transcriptional Activation, Adult, Aged, 80 and over, Chromosome Aberrations, Chromosomes, Human, Pair 3/genetics, Pair 7/genetics, Cohort Studies, Cytogenetics, DNA-Binding Proteins/*genetics/metabolism
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0307q26q21ID1672.html; Jean-Loup, Huret. t(3;7)(q26;q21) CDK6/MECOM. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2017, 5, p. 187-188; http://hdl.handle.net/2042/68246; https://doi.org/10.4267/2042/68246
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15
Autori:
Prispievatelia:
Predmety: hromosome 3, chromosome 21, t(3, 21)(q26, q11), MECOM, NRIP1, Leukaemia Section, Adaptor Proteins, Signal Transducing/*physiology, Estrogens/metabolism, Female, Humans, Male, Neoplasms/classification/*metabolism, Nuclear Proteins/*physiology, Signal Transduction, Transcription, Genetic, Wnt Proteins/metabolism, Adult, Aged, 80 and over, Chromosome Aberrations, Chromosomes, Human, Pair 3/genetics, Pair 7/genetics
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/t0321q26q11ID1464.html; Jean-Loup, Huret. t(3;21)(q26;q11) NRIP1/MECOM. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2017, 4, p. 164-165; http://hdl.handle.net/2042/68239; https://doi.org/10.4267/2042/68239
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16
Autori:
Prispievatelia:
Predmety: chromosome 3, inv(3)(p24q26), MECOM, Leukaemia Section, Adult, Aged, 80 and over, Chromosome Aberrations, Chromosomes, Human, Pair 3/genetics, Pair 7/genetics, Cohort Studies, Cytogenetics, DNA-Binding Proteins/*genetics/metabolism, Female, Humans, In Situ Hybridization, Fluorescence, Karyotyping, Leukemia, Myeloid, Acute/*genetics/metabolism/pathology, MDS1 and EVI1 Complex Locus Protein
Relation: Atlas of Genetics and Cytogenetics in Oncology and Haematology; http://AtlasGeneticsOncology.org/Anomalies/inv3p24q26ID1441.html; Jean-Loup, Huret. inv(3)(p24q26) ?/MECOM. Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2017, 4, p. 160-161; http://hdl.handle.net/2042/68237; https://doi.org/10.4267/2042/68237
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17
Autori: a ďalší
Prispievatelia: a ďalší
Zdroj: Journal of Medical Genetics. 43:625-633
Predmety: Male, 0301 basic medicine, diagnosis, Gene Dosage, CHILDREN, amplification, Chromosomes, Human, Pair 7/genetics, array-cgh, TELOMERES, Abnormalities, Multiple/genetics, rearrangements, COMPARATIVE GENOMIC HYBRIDIZATION, Child, microarrays, 11 Medical and Health Sciences, Genetics & Heredity, 0303 health sciences, SISTA, copy number variation, REARRANGEMENTS, Nucleic Acid Hybridization, Middle Aged, 3. Good health, Child, Preschool, Female, Life Sciences & Biomedicine, Chromosomes, Human, Pair 7, Adult, MICRODUPLICATION, Child, preschool, Adolescent, Bioinformatics, comparative genomic hybridization, DIAGNOSIS, 3105 Genetics, 03 medical and health sciences, children, Intellectual Disability, Humans, Abnormalities, Multiple, COPY NUMBER VARIATION, Chromosome Aberrations, Science & Technology, Genome, Human, microduplication, 3202 Clinical sciences, Infant, Microarray analysis, AMPLIFICATION, Gene Dosage/genetics, 06 Biological Sciences, telomeres, Intellectual Disability/genetics, MICROARRAYS, Clinical bio informatics, Genome, Human/genetics, ARRAY-CGH
Prístupová URL adresa: https://europepmc.org/articles/pmc2564583?pdf=render
https://pubmed.ncbi.nlm.nih.gov/16490798
https://www.ncbi.nlm.nih.gov/pubmed/16490798
https://jmg.bmj.com/content/43/8/625
https://jmg.bmj.com/lookup/doi/10.1136/jmg.2005.039453
https://pubmed.ncbi.nlm.nih.gov/16490798/
https://jmg.bmj.com/content/jmedgenet/43/8/625.full.pdf
https://researchportal.vub.be/en/publications/emerging-patterns-of-cryptic-chromosomal-imbalance-in-patients-wi
https://biblio.vub.ac.be/vubir/(5769424d-4ff4-4bb3-9126-36109e75ea71).html -
18
Autori: a ďalší
Zdroj: American Journal of Human Genetics, Vol. 65, No 3 (1999) pp. 645-655
Predmety: Male, 0301 basic medicine, Genotype, Genetic Linkage, DNA Mutational Analysis, Molecular Sequence Data, Kruppel-Like Transcription Factors, India, Nerve Tissue Proteins, Xenopus Proteins, GLI3, 03 medical and health sciences, Chromosomes, Human, Pair 7/genetics, Exons/genetics, DNA-Binding Proteins/genetics/ metabolism, Linkage (Genetics)/genetics, Genetics, Codon/genetics, Humans, Genetics(clinical), Amino Acid Sequence, Polymorphism, Genetic/genetics, Codon, Genes, Dominant, ddc:616, Family Health, 0303 health sciences, Chromosome 7, Base Sequence, Syndrome, Exons, Transcription Factors/genetics/ metabolism, Pedigree, Repressor Proteins, DNA-Binding Proteins, Polydactyly, Genes, Dominant/ genetics, Phenotype, Limb abnormalities, Mutation, Female, Polydactyly/ genetics/physiopathology, Mutations, Chromosomes, Human, Pair 7
Popis súboru: application/pdf
Prístupová URL adresa: http://www.cell.com/article/S0002929707623155/pdf
https://pubmed.ncbi.nlm.nih.gov/10441570
https://www.ncbi.nlm.nih.gov/pubmed/10441570
https://pubmed.ncbi.nlm.nih.gov/10441570/
https://archive-ouverte.unige.ch/unige:8979
https://www.cell.com/ajhg/fulltext/S0002-9297(07)62315-5
https://www.pubmedcentral.nih.gov/pmc/articles/PMC1377970/
https://www.cell.com/AJHG/abstract/S0002-9297(07)62315-5
https://archive-ouverte.unige.ch/unige:8979
https://doi.org/10.1086/302557
https://archive-ouverte.unige.ch/unige:8979 -
19
Autori: a ďalší
Zdroj: Nature Genetics. 14:199-202
Predmety: 0301 basic medicine, Chromosomes, Human, Pair 3/genetics, Genotype, Sciences de la santé humaine, Nuclear Family, 03 medical and health sciences, Crohn Disease, Chromosomes, Human, Pair 7/genetics, Humans, Genetic Predisposition to Disease, Genetic Testing, Human health sciences, Colitis, Ulcerative/genetics, Chromosomes, Human, Pair 12/genetics, Crohn Disease/genetics, 0303 health sciences, Chromosomes, Human, Pair 12, Genetic Screening, Genome, Human, Chromosome Mapping, Gastroentérologie & hépatologie, 3. Good health, Colitis, Ulcerative, Chromosomes, Human, Pair 3, Lod Score, Gastroenterology & hepatology, Chromosomes, Human, Pair 7, Microsatellite Repeats
Prístupová URL adresa: https://pubmed.ncbi.nlm.nih.gov/8841195
https://www.ncbi.nlm.nih.gov/pubmed/8841195
https://orbi.uliege.be/handle/2268/31925
https://europepmc.org/article/MED/8841195
https://pubmed.ncbi.nlm.nih.gov/8841195/
https://www.expmedndm.ox.ac.uk/publications/135430
https://www.nature.com/articles/ng1096-199.pdf -
20
Autori: a ďalší
Zdroj: Benyamin, B, Esko, T, Ried, J S, Radhakrishnan, A, Vermeulen, S H, Traglia, M, Gögele, M, Anderson, D, Broer, L, Podmore, C, Luan, J, Kutalik, Z, Sanna, S, van der Meer, P, Tanaka, T, Wang, F, Westra, H-J, Franke, L, Mihailov, E, Milani, L, Hälldin, J, Häldin, J, Winkelmann, J, Meitinger, T, Thiery, J, Peters, A, Waldenberger, M, Rendon, A, Jolley, J, Sambrook, J, Kiemeney, L A, Sweep, F C, Sala, C F, Schwienbacher, C, Pichler, I, Hui, J, Demirkan, A, Isaacs, A, Amin, N, Steri, M, Waeber, G, Verweij, N, Powell, J E, Nyholt, D R, Heath, A ....
Predmety: Adult, Chromosomes, Human, Pair 7/genetics, Ferritins/metabolism, Gene Expression Regulation, Genetic Association Studies, Genetic Loci, Genetic Predisposition to Disease, Hemochromatosis/blood, Homeostasis/genetics, Humans, Iron/blood, Lipids/blood, Phenotype, Polymorphism, Single Nucleotide/genetics, Reproducibility of Results, Risk Factors, Transferrin/metabolism
Relation: info:eu-repo/semantics/altIdentifier/pmid/25352340; info:eu-repo/semantics/altIdentifier/wos/000343934300001; info:eu-repo/semantics/altIdentifier/pissn/2041-1723; info:eu-repo/semantics/reference/pmid/25817829; info:eu-repo/semantics/reference/wos/000352720000032
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