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Wyszukujesz frazę ""Chromosomes, Human, Pair 1"" wg kryterium: Temat


Tytuł :
Duplication 1q is highly correlated with poor prognosis in high hyperdiploid pediatric B-acute lymphoblastic leukemia.
Autorzy :
El Ashry MS; Clinical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Elsayed GM; Clinical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Madney Y; Pediatric Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Arafah O; Pediatric Oncology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Allam RM; Biostatistics and Cancer Epidemiology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
Rasekh EO; Clinical Pathology Department, National Cancer Institute, Cairo University, Cairo, Egypt.
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Źródło :
International journal of laboratory hematology [Int J Lab Hematol] 2021 Apr; Vol. 43 (2), pp. 235-243. Date of Electronic Publication: 2020 Oct 19.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Duplication*
Chromosomes, Human, Pair 1*
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/*mortality
Adolescent ; Biomarkers ; Child ; Child, Preschool ; Chromosome Aberrations ; Cytogenetic Analysis ; Egypt/epidemiology ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/diagnosis ; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/epidemiology ; Prognosis ; Proportional Hazards Models ; Translocation, Genetic
Czasopismo naukowe
Tytuł :
A Scalable Computational Approach for Simulating Complexes of Multiple Chromosomes.
Autorzy :
Oliveira Junior AB; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; ICTP South American Institute for Fundamental Research, Instituto de Física Teórica, UNESP - 01140-070, São Paulo, SP, Brazil. Electronic address: .
Contessoto VG; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; Instituto de Biociências, Letras e Ciências Exatas, UNESP - Univ. Estadual Paulista, Departamento de Física, São José do Rio Preto, SP, Brazil. Electronic address: .
Mello MF; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; Chemical Engineering Department, Military Institute of Engineering, Rio de Janeiro, RJ, Brazil.
Onuchic JN; Center for Theoretical Biological Physics, Rice University, Houston, TX, USA; ICTP South American Institute for Fundamental Research, Instituto de Física Teórica, UNESP - 01140-070, São Paulo, SP, Brazil. Electronic address: .
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Źródło :
Journal of molecular biology [J Mol Biol] 2021 Mar 19; Vol. 433 (6), pp. 166700. Date of Electronic Publication: 2020 Nov 06.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Molecular Dynamics Simulation*
Software*
Chromatin/*chemistry
Chromosomes, Human, Pair 1/*chemistry
Chromosomes, Human, Pair 2/*chemistry
Chromosomes, Human, Pair 3/*chemistry
Chromosomes, Human, Pair 4/*chemistry
Animals ; Cell Line, Tumor ; Chromatin/metabolism ; Chromatin/ultrastructure ; Chromosomes, Human, Pair 1/metabolism ; Chromosomes, Human, Pair 1/ultrastructure ; Chromosomes, Human, Pair 2/metabolism ; Chromosomes, Human, Pair 2/ultrastructure ; Chromosomes, Human, Pair 3/metabolism ; Chromosomes, Human, Pair 3/ultrastructure ; Chromosomes, Human, Pair 4/metabolism ; Chromosomes, Human, Pair 4/ultrastructure ; Drosophila melanogaster/genetics ; Drosophila melanogaster/metabolism ; Humans ; Lymphocytes/cytology ; Lymphocytes/metabolism ; Saccharum/genetics ; Saccharum/metabolism ; Thermodynamics ; Triticum/genetics ; Triticum/metabolism
Czasopismo naukowe
Tytuł :
Age Dependency of the Prognostic Impact of Tumor Genomics in Localized Resectable MYCN -Nonamplified Neuroblastomas. Report From the SIOPEN Biology Group on the LNESG Trials and a COG Validation Group.
Autorzy :
Ambros IM; Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.
Tonini GP; Paediatric Research Institute, Fondazione Città della Speranza, Neuroblastoma Laboratory, Padua, Italy.
Pötschger U; Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.
Gross N; Pediatric Oncology Research, Department of Pediatrics, University Hospital, Lausanne, Switzerland.
Mosseri V; Service de Biostatistiques, Institut Curie, Paris, France.
Beiske K; Department of Pathology, Oslo University Hospital Rikshospitalet, Oslo, Norway.
Berbegall AP; Department of Pathology, Medical School, University of Valencia-Fundación de Investigación del Hospital Clínico Universitario de Valencia, Valencia, Spain.; Centro de Investigación Biomédica en Red de Cáncer, Madrid, Spain.
Bénard J; Département de Biologie et de Pathologie Médicales, Service de Pathologie Moléculaire, Institut Gustave Roussy, Villejuif, France.
Bown N; Northern Genetics Service, Newcastle upon Tyne, United Kingdom.
Caron H; Department of Pediatric Oncology, Emma Children's Hospital, Academic Medical Center, Amsterdam, the Netherlands.
Combaret V; Centre Léon Bérard, Laboratoire de Recherche Translationnelle, Lyon, France.
Couturier J; Unité de Génétique Somatique et Cytogénétique, Institut Curie, Paris, France.
Defferrari R; Department of Pathology, Istituto G. Gaslini, Genoa, Italy.
Delattre O; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Paris, France.
Jeison M; Ca-Cytogenetic Laboratory, Pediatric Hematology Oncology Department, Schneider Children's Medical Center of Israel, Petah Tikvah, Israel.
Kogner P; Childhood Cancer Research Unit, Karolinska Institutet, Astrid Lindgren Children's Hospital, Stockholm, Sweden.
Lunec J; Biosciences Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Marques B; Centro de Genética Humana, Instituto Nacional de Saude doutor Ricardo Jorge, Lisbon, Portugal.
Martinsson T; Department of Clinical Genetics, Institute of Biomedicine, University of Gothenburg, Sahlgrenska University Hospital, Göteborg, Sweden.
Mazzocco K; Department of Pathology, Istituto G. Gaslini, Genoa, Italy.
Noguera R; Department of Pathology, Medical School, University of Valencia-Fundación de Investigación del Hospital Clínico Universitario de Valencia, Valencia, Spain.; Centro de Investigación Biomédica en Red de Cáncer, Madrid, Spain.
Schleiermacher G; INSERM U830, Laboratoire de Génétique et Biologie des Cancers, Paris, France.; Département de Pédiatrie, Institut Curie, Paris, France.
Valent A; Département de Biologie et de Pathologie Médicales, Service de Pathologie Moléculaire, Institut Gustave Roussy, Villejuif, France.
Van Roy N; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Villamon E; Department of Pathology, Medical School, University of Valencia-Fundación de Investigación del Hospital Clínico Universitario de Valencia, Valencia, Spain.; Centro de Investigación Biomédica en Red de Cáncer, Madrid, Spain.
Janousek D; Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.
Pribill I; Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.
Glogova E; Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.
Attiyeh EF; Division of Oncology, The Children's Hospital of Philadelphia, Philadelphia, PA.
Hogarty MD; Division of Oncology, The Children's Hospital of Philadelphia, Philadelphia, PA.
Monclair TF; Section for Paediatric Surgery, Division of Surgery, Rikshospitalet University Hospital, Oslo, Norway.
Holmes K; Department of Paediatric Surgery, St George's Hospital, London, UK.
Valteau-Couanet D; Département de Cancérologie de l'Enfant et de l'Adolescent, Gustave Roussy, Villejuif, France.
Castel V; Unidad de Oncologia Pediatrica Hospital Universitario La Fe, Valencia, Spain.
Tweddle DA; Wolfson Childhood Cancer Research Centre, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
Park JR; Seattle Children's Hospital and University of Washington School of Medicine, Seattle, WA.
Cohn S; Department of Pediatrics, The University of Chicago, Chicago, IL.
Ladenstein R; Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.; Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
Beck-Popovic M; Pediatric Hematology Oncology Unit, University Hospital of Lausanne, Lausanne, Switzerland.
De Bernardi B; Department of Paediatric Haematology and Oncology, Giannina Gaslini Children's Hospital, Genova, Italy.
Michon J; Département de Pédiatrie, Institut Curie, Paris, France.
Pearson ADJ; Institute of Cancer Research, Royal Marsden Hospital, Sutton, Surrey, United Kingdom.
Ambros PF; Children's Cancer Research Institute, St Anna Kinderkrebsforschung, Vienna, Austria.; Department of Pediatrics, Medical University of Vienna, Vienna, Austria.
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Źródło :
Journal of clinical oncology : official journal of the American Society of Clinical Oncology [J Clin Oncol] 2020 Nov 01; Vol. 38 (31), pp. 3685-3697. Date of Electronic Publication: 2020 Sep 09.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Aberrations*
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 11*
N-Myc Proto-Oncogene Protein/*genetics
Neuroblastoma/*genetics
Age Factors ; Clinical Trials as Topic ; Diploidy ; Gene Amplification ; Genomics ; Humans ; Infant ; Neoplasm Staging ; Neuroblastoma/pathology ; Neuroblastoma/surgery ; Prognosis ; Progression-Free Survival ; Survival Rate
Czasopismo naukowe
Tytuł :
Acute megakaryoblastic leukaemia with t(1;22)(p13·3;q13·1)/RBM15-MKL1 in an adult patient following a non-mediastinal germ cell tumour.
Autorzy :
Saito Y; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.; Department of Pathology, National Cancer Center Hospital, Tokyo, Japan.
Makita S; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Chinen S; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Kito M; Department of Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan.
Fujino T; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Ida H; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Hosoba R; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Tanaka T; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Fukuhara S; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Munakata W; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.
Suzuki T; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.
Maruyama D; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.
Miyagi-Maeshima A; Department of Pathology, National Cancer Center Hospital, Tokyo, Japan.
Matsushita H; Department of Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan.
Izutsu K; Department of Hematology, National Cancer Center Hospital, Tokyo, Japan.; Rare Cancer Center, National Cancer Center Hospital, Tokyo, Japan.
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Źródło :
British journal of haematology [Br J Haematol] 2020 Sep; Vol. 190 (6), pp. e329-e332. Date of Electronic Publication: 2020 Jun 23.
Typ publikacji :
Case Reports; Letter
MeSH Terms :
Chromosomes, Human, Pair 1*/genetics
Chromosomes, Human, Pair 1*/metabolism
Chromosomes, Human, Pair 22*/genetics
Chromosomes, Human, Pair 22*/metabolism
Leukemia, Megakaryoblastic, Acute*/genetics
Leukemia, Megakaryoblastic, Acute*/metabolism
Leukemia, Megakaryoblastic, Acute*/pathology
Neoplasms, Germ Cell and Embryonal*/genetics
Neoplasms, Germ Cell and Embryonal*/metabolism
Neoplasms, Germ Cell and Embryonal*/pathology
Neoplasms, Second Primary*/genetics
Neoplasms, Second Primary*/metabolism
Neoplasms, Second Primary*/pathology
Oncogene Proteins, Fusion*/genetics
Oncogene Proteins, Fusion*/metabolism
Retroperitoneal Neoplasms*/genetics
Retroperitoneal Neoplasms*/metabolism
Retroperitoneal Neoplasms*/pathology
Translocation, Genetic*
Adult ; Humans ; Male
Raport
Tytuł :
A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups.
Autorzy :
Ritzmann TA; Children's Brain Tumor Research Centre, School of Medicine, University of Nottingham, Nottingham, UK.
Rogers HA; Children's Brain Tumor Research Centre, School of Medicine, University of Nottingham, Nottingham, UK.
Paine SML; Department of Neuropathology, Nottingham University Hospital, Nottingham, UK.
Storer LCD; Children's Brain Tumor Research Centre, School of Medicine, University of Nottingham, Nottingham, UK.
Jacques TS; Developmental Biology and Cancer Programme, UCL GOS Institute of Child Health and Department of Histopathology, Great Ormond Street Hospital for Children NHS Trust, London, UK.
Chapman RJ; Children's Brain Tumor Research Centre, School of Medicine, University of Nottingham, Nottingham, UK.
Ellison D; Department of Pathology, St Jude Children's Hospital, Memphis, Tennessee.
Donson AM; Department of Pediatrics, University of Colorado, Denver, Aurora, Colorado.
Foreman NK; Department of Pediatrics, University of Colorado, Denver, Aurora, Colorado.
Grundy RG; Children's Brain Tumor Research Centre, School of Medicine, University of Nottingham, Nottingham, UK.
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Źródło :
Pediatric blood & cancer [Pediatr Blood Cancer] 2020 Sep; Vol. 67 (9), pp. e28426. Date of Electronic Publication: 2020 Jul 02.
Typ publikacji :
Clinical Trial; Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't
MeSH Terms :
Brain Neoplasms*/genetics
Brain Neoplasms*/metabolism
Brain Neoplasms*/mortality
Brain Neoplasms*/therapy
Chromosomes, Human, Pair 1*/genetics
Chromosomes, Human, Pair 1*/metabolism
DNA Methylation*
DNA, Neoplasm*/genetics
DNA, Neoplasm*/metabolism
Ependymoma*/genetics
Ependymoma*/metabolism
Ependymoma*/mortality
Ependymoma*/therapy
Neoplasm Recurrence, Local*/genetics
Neoplasm Recurrence, Local*/metabolism
Neoplasm Recurrence, Local*/mortality
Neoplasm Recurrence, Local*/therapy
Adolescent ; Child ; Child, Preschool ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Retrospective Studies ; Risk Factors
Czasopismo naukowe
Tytuł :
Giant Cell Tumor of Tendon Sheath With a t(1;1)(p13;p34) Chromosomal Translocation.
Autorzy :
Nakayama S; Department of Orthopaedic Surgery, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Nishio J; Department of Orthopaedic Surgery, Faculty of Medicine, Fukuoka University, Fukuoka, Japan .
Nakatani K; Department of Orthopaedic Surgery, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Nabeshima K; Department of Pathology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Yamamoto T; Department of Orthopaedic Surgery, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
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Źródło :
Anticancer research [Anticancer Res] 2020 Aug; Vol. 40 (8), pp. 4373-4377.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosomes, Human, Pair 1*
Translocation, Genetic*
Giant Cell Tumor of Tendon Sheath/*genetics
Aged ; Biopsy, Needle ; Giant Cell Tumor of Tendon Sheath/diagnostic imaging ; Giant Cell Tumor of Tendon Sheath/pathology ; Humans ; Magnetic Resonance Imaging ; Male
Czasopismo naukowe
Tytuł :
Globular C1q Receptor (gC1qR/p32/HABP1) Suppresses the Tumor-Inhibiting Role of C1q and Promotes Tumor Proliferation in 1q21-Amplified Multiple Myeloma.
Autorzy :
Xu J; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Sun Y; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Jiang J; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xu Z; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Li J; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Xu T; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
Liu P; Department of Hematology, Zhongshan Hospital, Fudan University, Shanghai, China.
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Źródło :
Frontiers in immunology [Front Immunol] 2020 Jul 14; Vol. 11, pp. 1292. Date of Electronic Publication: 2020 Jul 14 (Print Publication: 2020).
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 1*
Gene Amplification*
Carrier Proteins/*metabolism
Complement C1q/*immunology
Mitochondrial Proteins/*metabolism
Multiple Myeloma/*genetics
Multiple Myeloma/*immunology
Adult ; Aged ; Bone Marrow/pathology ; Cell Line, Tumor ; Cell Proliferation ; Complement C1q/metabolism ; Female ; Gene Expression Regulation, Neoplastic ; Humans ; Immunophenotyping ; Male ; Middle Aged ; Multiple Myeloma/mortality ; Multiple Myeloma/pathology ; Prognosis
Czasopismo naukowe
Tytuł :
Dissecting Molecular Genetic Mechanisms of 1q21.1 CNV in Neuropsychiatric Disorders.
Autorzy :
Yoon J; Department of Biology, Eberly College of Science, Pennsylvania State University, University Park, PA 16802, USA.
Mao Y; Department of Biology, Eberly College of Science, Pennsylvania State University, University Park, PA 16802, USA.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 May 28; Vol. 22 (11). Date of Electronic Publication: 2021 May 28.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Genetic Predisposition to Disease*
Abnormalities, Multiple/*genetics
DNA Copy Number Variations/*genetics
Megalencephaly/*genetics
Mental Disorders/*genetics
Autism Spectrum Disorder/genetics ; Chromosome Deletion ; Chromosome Duplication ; Chromosomes, Human, Pair 1/genetics ; Genome-Wide Association Study ; Humans ; Microcephaly/genetics ; Neurodegenerative Diseases/genetics ; Neurodevelopmental Disorders/genetics ; Schizophrenia/genetics
SCR Disease Name :
Chromosome 1q21.1 Deletion Syndrome, 1.35-Mb
Czasopismo naukowe
Tytuł :
MGMT promoter methylation is associated with patient age and 1p/19q status in IDH-mutant gliomas.
Autorzy :
Horbinski C; Department of Pathology, Northwestern University, Chicago, Illinois, USA.; Department of Neurological Surgery, Northwestern University, Chicago, Illinois, USA.
McCortney K; Department of Neurological Surgery, Northwestern University, Chicago, Illinois, USA.
Stupp R; Department of Neurological Surgery, Northwestern University, Chicago, Illinois, USA.; Department of Neurology, Northwestern University, Chicago, Illinois, USA.; Department of Medicine, Northwestern University, Chicago, Illinois, USA.
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Źródło :
Neuro-oncology [Neuro Oncol] 2021 May 05; Vol. 23 (5), pp. 858-860.
Typ publikacji :
Letter; Research Support, N.I.H., Extramural
MeSH Terms :
Brain Neoplasms*/genetics
Glioma*/genetics
Chromosomes, Human, Pair 1/genetics ; Chromosomes, Human, Pair 19 ; DNA Modification Methylases/genetics ; DNA Repair Enzymes/genetics ; Humans ; Infant ; Isocitrate Dehydrogenase/genetics ; Methylation ; Mutation ; Promoter Regions, Genetic/genetics ; Tumor Suppressor Proteins/genetics
Raport
Tytuł :
Transcription factor networks of oligodendrogliomas treated with adjuvant radiotherapy or observation inform prognosis.
Autorzy :
So J; Radiation Medicine Program, Princess Margaret Cancer Center, University of Toronto, Toronto, Ontario, Canada.
Mamatjan Y; Department of Laboratory Medicine and Pathobiology, Princess Margaret Cancer Centre, University of Toronto and MacFeeters-Hamilton Centre for Neuro-Oncology Research, Toronto, Ontario, Canada.
Zadeh G; Department of Laboratory Medicine and Pathobiology, Princess Margaret Cancer Centre, University of Toronto and MacFeeters-Hamilton Centre for Neuro-Oncology Research, Toronto, Ontario, Canada.; Department of Neurosurgery, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.
Aldape K; Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland.
Moraes FY; Department of Radiation Oncology, Kingston General Hospital, Queen's University, Kingston, Ontario, Canada.
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Źródło :
Neuro-oncology [Neuro Oncol] 2021 May 05; Vol. 23 (5), pp. 795-802.
Typ publikacji :
Journal Article
MeSH Terms :
Brain Neoplasms*/genetics
Brain Neoplasms*/radiotherapy
Oligodendroglioma*/genetics
Oligodendroglioma*/radiotherapy
Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 19 ; Humans ; Isocitrate Dehydrogenase/genetics ; Mutation ; Prognosis ; Radiotherapy, Adjuvant ; Transcription Factors
Czasopismo naukowe

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