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Title:
Relaxation Along a Fictitious Field, continuous wave T1rho, adiabatic T1rho and adiabatic T2rho imaging of human gliomas at 3T: A feasibility study.
Authors:
Jambor I; Department of Radiology, University of Turku, Turku, Finland.; Enterprise Service Group-Radiology, Mass General Brigham, Boston, MA, United States of America.
Steiner A; Department of Radiology, University of Turku, Turku, Finland.; Medical Imaging Centre of Southwest Finland, Turku University Hospital, Turku, Finland.
Pesola M; Department of Radiology, University of Turku, Turku, Finland.
Gardberg M; Tyks Laboratories, Pathology, Turku University Hospital and Institute of Biomedicine, University of Turku Turku, Finland.
Frantzén J; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Turku, Finland.
Jokinen P; Division of Clinical Neurosciences, Department of Neurosurgery, Turku University Hospital and University of Turku, Turku, Finland.
Liimatainen T; Department of Radiology, University of Oulu, Oulu, Finland.; Department of Biotechnology and Molecular Medicine, A.I. Virtanen Institute for Molecular Sciences, University of Eastern Finland, Kuopio, Finland.
Minn H; Department of Oncology and Radiotherapy, Turku University Hospital, Turku, Finland.; Turku PET Centre, Turku University and Turku University Hospital, Turku, Finland, Finland.
Aronen H; Department of Radiology, University of Turku, Turku, Finland.; Medical Imaging Centre of Southwest Finland, Turku University Hospital, Turku, Finland.
Merisaari H; Department of Radiology, University of Turku, Turku, Finland.; Medical Imaging Centre of Southwest Finland, Turku University Hospital, Turku, Finland.
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Source:
PloS one [PLoS One] 2024 Apr 01; Vol. 19 (4), pp. e0296958. Date of Electronic Publication: 2024 Apr 01 (Print Publication: 2024).
Publication Type:
Journal Article
MeSH Terms:
Brain Neoplasms*/diagnostic imaging
Brain Neoplasms*/pathology
Glioma*/diagnostic imaging
Glioma*/pathology
Humans ; Feasibility Studies ; Prospective Studies ; Magnetic Resonance Imaging/methods ; Mutation ; Chromosome Aberrations ; Isocitrate Dehydrogenase/genetics ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 19
Academic Journal
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Title:
Genome-Wide Identification and Expression Pattern Analysis of BAHD Acyltransferase Family in Taxus mairei .
Authors:
Xu D; Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing 210014, China.; Co-Innovation Center for Sustainable Forestry in Southern China, College of Life Sciences, Nanjing Forestry University, Nanjing 210037, China.
Wang Z; Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing 210014, China.
Zhuang W; Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing 210014, China.
Zhang F; Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing 210014, China.; Co-Innovation Center for Sustainable Forestry in Southern China, College of Life Sciences, Nanjing Forestry University, Nanjing 210037, China.
Xie Y; Co-Innovation Center for Sustainable Forestry in Southern China, College of Life Sciences, Nanjing Forestry University, Nanjing 210037, China.
Wang T; Jiangsu Key Laboratory for the Research and Utilization of Plant Resources, Institute of Botany, Jiangsu Province and Chinese Academy of Sciences (Nanjing Botanical Garden Mem. Sun Yat-Sen), Nanjing 210014, China.
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Source:
International journal of molecular sciences [Int J Mol Sci] 2024 Mar 28; Vol. 25 (7). Date of Electronic Publication: 2024 Mar 28.
Publication Type:
Journal Article
MeSH Terms:
Taxus*/genetics
Humans ; Phylogeny ; Acyltransferases ; Chromosomes, Human, Pair 1 ; Paclitaxel
Academic Journal
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Title:
Strong selection signatures for Aleutian disease tolerance acting on novel candidate genes linked to immune and cellular responses in American mink (Neogale vison).
Authors:
Vahedi SM; Department of Animal Science and Aquaculture, Dalhousie University, Bible Hill, NS, B2N5E3, Canada.
Salek Ardestani S; Department of Animal Science, University of Zanjan, Zanjan, 4537138791, Zanjan, Iran.
Banabazi MH; Department of Animal Breeding and Genetics (HGEN), Centre for Veterinary Medicine and Animal Science (VHC), Swedish University of Agricultural Sciences (SLU), 75007, Uppsala, Sweden. .; Department of Biotechnology, Animal Science Research Institute of IRAN (ASRI),, Agricultural Research, Education & Extension Organization (AREEO), Karaj, 3146618361, Iran. .
Clark KF; Department of Animal Science and Aquaculture, Dalhousie University, Bible Hill, NS, B2N5E3, Canada. .
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Source:
Scientific reports [Sci Rep] 2024 Jan 10; Vol. 14 (1), pp. 1035. Date of Electronic Publication: 2024 Jan 10.
Publication Type:
Journal Article
MeSH Terms:
Aleutian Mink Disease*/genetics
Aleutian Mink Disease Virus*/genetics
Animals ; Humans ; Mink/genetics ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 6
Academic Journal
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Title:
Deletion in 1p36.33-p36.32 is associated with pancytopenia: a case report.
Authors:
Yang H; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China.; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Huang J; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China.; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Zheng H; Department of Pediatrics, Fujian Union Hospital, Fuzhou, China.
Zhang Y; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China.; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Zhang Y; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.; Department of Pediatrics, Affiliated Dongfang Hospital, Xiamen University, Fuzhou, China.
Liu W; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Wu J; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Chen X; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Lin J; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Ni Y; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China.
Nie X; Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China. .; Department of Pediatrics, The 900th Hospital of Joint Logistic Support Force, PLA, Fuzhou, China. .; Department of Pediatrics, Affiliated Dongfang Hospital, Xiamen University, Fuzhou, China. .
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Source:
BMC medical genomics [BMC Med Genomics] 2023 Nov 09; Vol. 16 (1), pp. 282. Date of Electronic Publication: 2023 Nov 09.
Publication Type:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Intellectual Disability*/genetics
Pancytopenia*/genetics
Chromosome Disorders*/genetics
Humans ; DNA Copy Number Variations ; Chromosome Deletion ; Syndrome ; Phenotype ; Chromosomes, Human, Pair 1
SCR Disease Name:
Chromosome 1p36 Deletion Syndrome
Academic Journal
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Title:
Homozygosity for a Novel DOCK7 Variant Due to Segmental Uniparental Isodisomy of Chromosome 1 Associated with Early Infantile Epileptic Encephalopathy (EIEE) and Cortical Visual Impairment.
Authors:
Kivrak Pfiffner F; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Koller S; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Ménétrey A; Department of Pediatric Neurology, University Children's Hospital, University of Zurich, 8032 Zurich, Switzerland.
Graf U; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Bähr L; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Maspoli A; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.
Hackenberg A; Department of Pediatric Neurology, University Children's Hospital, University of Zurich, 8032 Zurich, Switzerland.
Kottke R; Department of Diagnostic Imaging, University Children's Hospital, University of Zurich, 8032 Zurich, Switzerland.
Gerth-Kahlert C; Department of Ophthalmology, University Hospital, 8091 Zurich, Switzerland.
Berger W; Institute of Medical Molecular Genetics, University of Zurich, Wagistrasse 12, 8952 Schlieren, Switzerland.; Neuroscience Center Zurich, University and ETH Zurich, 8057 Zurich, Switzerland.; Center for Integrative Human Physiology, University of Zurich, 8057 Zurich, Switzerland.
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Source:
International journal of molecular sciences [Int J Mol Sci] 2022 Jul 02; Vol. 23 (13). Date of Electronic Publication: 2022 Jul 02.
Publication Type:
Case Reports
MeSH Terms:
Chromosomes, Human, Pair 1*
Uniparental Disomy*
Female ; GTPase-Activating Proteins/genetics ; Guanine Nucleotide Exchange Factors/genetics ; Humans ; Infant ; Polymorphism, Single Nucleotide ; Spasms, Infantile ; Vision Disorders
SCR Disease Name:
Infantile Epileptic-Dyskinetic Encephalopathy
Report
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Title:
Chromosome 1p36 candidate gene ZNF436 predicts the prognosis of neuroblastoma: a bioinformatic analysis.
Authors:
Wang H; Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China. .
Wang X; Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
Xu L; Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
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Source:
Italian journal of pediatrics [Ital J Pediatr] 2023 Oct 31; Vol. 49 (1), pp. 145. Date of Electronic Publication: 2023 Oct 31.
Publication Type:
Journal Article
MeSH Terms:
Neuroblastoma*/genetics
Humans ; Infant ; Adolescent ; N-Myc Proto-Oncogene Protein/genetics ; Prognosis ; Chromosome Aberrations ; Chromosomes ; Chromosomes, Human, Pair 1/genetics ; Chromosome Deletion ; Transcription Factors/genetics
Academic Journal
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Title:
CRISPR imaging reveals chromatin fluctuation at the centromere region related to cellular senescence.
Authors:
Takata H; Biomedical Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Ikeda, Osaka, 563-8577, Japan. .
Masuda Y; Graduate School of Human Development and Environment, Kobe University, Nada-ku, Kobe, 657-8501, Japan.
Ohmido N; Graduate School of Human Development and Environment, Kobe University, Nada-ku, Kobe, 657-8501, Japan.
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Source:
Scientific reports [Sci Rep] 2023 Sep 05; Vol. 13 (1), pp. 14609. Date of Electronic Publication: 2023 Sep 05.
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromatin*
Clustered Regularly Interspaced Short Palindromic Repeats*
Humans ; Centromere ; Cellular Senescence ; Chromosomes, Human, Pair 1 ; Decitabine
Academic Journal
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Title:
Tandem NBPF 3mer HORs (Olduvai triplets) in Neanderthal and two novel HOR tandem arrays in human chromosome 1 T2T-CHM13 assembly.
Authors:
Glunčić M; Faculty of Science, University of Zagreb, 10000, Zagreb, Croatia. .
Vlahović I; Algebra University College, 10000, Zagreb, Croatia.
Rosandić M; University Hospital Centre Zagreb (Ret.), 10000, Zagreb, Croatia.; Croatian Academy of Sciences and Arts, 10000, Zagreb, Croatia.
Paar V; Faculty of Science, University of Zagreb, 10000, Zagreb, Croatia.; Croatian Academy of Sciences and Arts, 10000, Zagreb, Croatia.
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Source:
Scientific reports [Sci Rep] 2023 Sep 02; Vol. 13 (1), pp. 14420. Date of Electronic Publication: 2023 Sep 02.
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Neanderthals*/genetics
Neuroblastoma*
Humans ; Animals ; Chromosomes, Human ; Chromosomes, Human, Pair 1 ; Family ; Pan troglodytes
Academic Journal
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Title:
Uncovering the phenotypic consequences of multi-locus imprinting disturbances using genome-wide methylation analysis in genomic imprinting disorders.
Authors:
Kim HY; Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, Seoul National University Bundang Hospital, Seongnam, Korea.
Shin CH; Department of Pediatrics, Division of Pediatric Endocrinology and Metabolism, Seoul National University College of Medicine, Seoul, Korea.
Shin CH; Department of Orthopaedics, Division of Pediatric Orthopedics, Seoul National University College of Medicine, Seoul, Korea.
Ko JM; Department of Pediatrics, Division of Clinical Genetics, Seoul National University College of Medicine, Seoul, Korea.; Rare Disease Center, Seoul National University Hospital, Seoul, Korea.
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Source:
PloS one [PLoS One] 2023 Aug 18; Vol. 18 (8), pp. e0290450. Date of Electronic Publication: 2023 Aug 18 (Print Publication: 2023).
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genomic Imprinting*
DNA Methylation*
Humans ; Exome ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 6
Academic Journal
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Title:
Characterization and Gene Mapping of an Open-Glume Oryza sativa L. Mutant.
Authors:
Mao X; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
Zheng X; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
Chen W; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
Li C; Rice Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou 510640, China.; Guangdong Key Laboratory of New Technology in Rice Breeding, Guangzhou 510640, China.
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Source:
International journal of molecular sciences [Int J Mol Sci] 2023 Aug 11; Vol. 24 (16). Date of Electronic Publication: 2023 Aug 11.
Publication Type:
Journal Article
MeSH Terms:
Oryza*/genetics
Humans ; Chromosome Mapping ; Agriculture ; Chromosomes, Human, Pair 1 ; Codon, Initiator
Academic Journal
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Title:
Role of 1q21 in Multiple Myeloma: From Pathogenesis to Possible Therapeutic Targets.
Authors:
Burroughs Garcìa J; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.; Department of Medical-Veterinary Science, University of Parma, 43121 Parma, Italy.
Eufemiese RA; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
Storti P; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
Sammarelli G; Hematology, Azienda Ospedaliero-Universitaria di Parma, 43126 Parma, Italy.
Craviotto L; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.; Hematology, Azienda Ospedaliero-Universitaria di Parma, 43126 Parma, Italy.
Todaro G; Hematology, Azienda Ospedaliero-Universitaria di Parma, 43126 Parma, Italy.
Toscani D; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
Marchica V; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.
Giuliani N; Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy.; Hematology, Azienda Ospedaliero-Universitaria di Parma, 43126 Parma, Italy.
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Source:
Cells [Cells] 2021 Jun 01; Vol. 10 (6). Date of Electronic Publication: 2021 Jun 01.
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms:
Chromosomes, Human, Pair 1*/genetics
Chromosomes, Human, Pair 1*/metabolism
Gene Amplification*
Multiple Myeloma*/genetics
Multiple Myeloma*/metabolism
Multiple Myeloma*/therapy
Neoplasm Proteins*/genetics
Neoplasm Proteins*/metabolism
Signal Transduction*
Humans
Academic Journal
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Title:
Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient.
Authors:
Wang H; Department of Pediatric Neurology, Shengjing Hospital of China Medical University, Shenyang, P.R. China.
Huo L; Department of Pediatric Neurology, Shengjing Hospital of China Medical University, Shenyang, P.R. China.
Wang Y; Chigene (Beijing) Translational Medical Research Center Co., Ltd., Beijing, P.R. China.
Sun W; Chigene (Beijing) Translational Medical Research Center Co., Ltd., Beijing, P.R. China.
Gu W; Chigene (Beijing) Translational Medical Research Center Co., Ltd., Beijing, P.R. China.
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Source:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Oct; Vol. 9 (10), pp. e1779. Date of Electronic Publication: 2021 Aug 18.
Publication Type:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Paternal Inheritance*
Uniparental Disomy*
Glycogen Storage Disease Type III/*complications
Glycogen Storage Disease Type III/*diagnosis
Usher Syndromes/*complications
Usher Syndromes/*diagnosis
Adult ; Biomarkers ; Child, Preschool ; DNA Copy Number Variations ; Female ; Genetic Association Studies ; Genetic Predisposition to Disease ; Glycogen Debranching Enzyme System/chemistry ; Glycogen Debranching Enzyme System/genetics ; Glycogen Storage Disease Type III/etiology ; Glycogen Storage Disease Type III/metabolism ; Humans ; Male ; Middle Aged ; Models, Molecular ; Pedigree ; Sequence Analysis, DNA ; Structure-Activity Relationship ; Usher Syndromes/etiology ; Usher Syndromes/metabolism ; Exome Sequencing
SCR Disease Name:
Usher syndrome, type 2A
Academic Journal
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Title:
Genome collinearity analysis illuminates the evolution of donkey chromosome 1 and horse chromosome 5 in perissodactyls: A comparative study.
Authors:
Li S; Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.; College of Basic Medicine, Inner Mongolia Medical University, Hohhot, 010110, China.; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Zhao G; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Han H; Department of Physical Education, Hohhot Minzu College, Hohhot, 010051, China.
Li Y; Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Li J; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Wang J; College of Basic Medicine, Inner Mongolia Medical University, Hohhot, 010110, China.
Cao G; College of Veterinary Science, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Li X; Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Sciences, Inner Mongolia University, Hohhot, 010070, China. .; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China. .
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Source:
BMC genomics [BMC Genomics] 2021 Sep 15; Vol. 22 (1), pp. 665. Date of Electronic Publication: 2021 Sep 15.
Publication Type:
Journal Article
MeSH Terms:
Chromosomes, Human, Pair 1*
Equidae*/genetics
Animals ; Chromosomes/genetics ; Chromosomes, Human, Pair 5 ; Genome ; Horses/genetics ; Humans
Academic Journal
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Title:
WHO grade I meningiomas that show regrowth after gamma knife radiosurgery often show 1p36 loss.
Authors:
Damen PJJ; Department of Pathology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, P. Debyelaan 25, Postbox 5800, 6202 AZ, Maastricht, The Netherlands.
Bulthuis VJ; Department of Neurosurgery, Maastricht University Medical Center, Maastricht, The Netherlands.
Hanssens PEJ; Gamma Knife Center Tilburg, ETZ-Elisabeth Hospital, Tilburg, The Netherlands.
Lie ST; Gamma Knife Center Tilburg, ETZ-Elisabeth Hospital, Tilburg, The Netherlands.
Fleischeuer R; Department of Pathology, ETZ-Elisabeth Hospital, Tilburg, The Netherlands.
Melotte V; Department of Pathology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, P. Debyelaan 25, Postbox 5800, 6202 AZ, Maastricht, The Netherlands.
Wouters KA; Department of Pathology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, P. Debyelaan 25, Postbox 5800, 6202 AZ, Maastricht, The Netherlands.
Ruland A; Department of Pathology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, P. Debyelaan 25, Postbox 5800, 6202 AZ, Maastricht, The Netherlands.
Beckervordersandforth J; Department of Pathology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, P. Debyelaan 25, Postbox 5800, 6202 AZ, Maastricht, The Netherlands.
Speel EJM; Department of Pathology, GROW School for Oncology and Developmental Biology, Maastricht University Medical Centre, P. Debyelaan 25, Postbox 5800, 6202 AZ, Maastricht, The Netherlands. .
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Source:
Scientific reports [Sci Rep] 2021 Aug 12; Vol. 11 (1), pp. 16432. Date of Electronic Publication: 2021 Aug 12.
Publication Type:
Journal Article
MeSH Terms:
Chromosome Deletion*
Chromosomes, Human, Pair 1*
Meningeal Neoplasms/*pathology
Meningeal Neoplasms/*radiotherapy
Meningioma/*pathology
Meningioma/*radiotherapy
Neoplasm Recurrence, Local/*pathology
Radiosurgery/*methods
Female ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Survival Rate ; Treatment Outcome ; World Health Organization
Academic Journal
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Title:
Effects of SMC1A on immune microenvironment and cancer stem cells in colon adenocarcinoma.
Authors:
Li J; Department of Oncology, The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian, China.
Zhou Q; The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian, China.
Liu L; The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian, China.
He J; Department of Oncology, The Affiliated Huaian No.1 People's Hospital of Nanjing Medical University, Huaian, China.
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Source:
Cancer medicine [Cancer Med] 2023 Jun; Vol. 12 (11), pp. 12881-12895. Date of Electronic Publication: 2023 Apr 25.
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adenocarcinoma*/genetics
Colonic Neoplasms*/genetics
Animals ; Humans ; Mice ; Chromosomes, Human, Pair 1 ; DNA Copy Number Variations ; Neoplastic Stem Cells ; Tumor Microenvironment
Academic Journal
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Title:
Whole-genome optical mapping of bone-marrow myeloma cells reveals association of extramedullary multiple myeloma with chromosome 1 abnormalities.
Authors:
Kriegova E; Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Hnevotinska 3, 779 00, Olomouc, Czech Republic. .
Fillerova R; Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Hnevotinska 3, 779 00, Olomouc, Czech Republic.
Minarik J; Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
Savara J; Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Hnevotinska 3, 779 00, Olomouc, Czech Republic.; Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VŠB-Technical University of Ostrava, Ostrava, Czech Republic.
Manakova J; Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Hnevotinska 3, 779 00, Olomouc, Czech Republic.
Petrackova A; Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Hnevotinska 3, 779 00, Olomouc, Czech Republic.
Dihel M; Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Hnevotinska 3, 779 00, Olomouc, Czech Republic.
Balcarkova J; Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
Krhovska P; Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
Pika T; Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
Gajdos P; Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VŠB-Technical University of Ostrava, Ostrava, Czech Republic.
Behalek M; Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VŠB-Technical University of Ostrava, Ostrava, Czech Republic.
Vasinek M; Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VŠB-Technical University of Ostrava, Ostrava, Czech Republic.
Papajik T; Department of Hemato-Oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Olomouc, Czech Republic.
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Source:
Scientific reports [Sci Rep] 2021 Jul 19; Vol. 11 (1), pp. 14671. Date of Electronic Publication: 2021 Jul 19.
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 1*/genetics
Bone Marrow/*pathology
Multiple Myeloma/*genetics
Aged ; Aged, 80 and over ; Bone Marrow/diagnostic imaging ; Bone Marrow/metabolism ; Bone Marrow Cells/pathology ; Cohort Studies ; Cytogenetic Analysis/methods ; Czech Republic ; Female ; Genome-Wide Association Study/methods ; Humans ; Male ; Middle Aged ; Multiple Myeloma/pathology ; Pilot Projects
Academic Journal
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Title:
CBFB gene rearrangement due to a novel t(1;16) with deceptive morphology.
Authors:
Gupta A; Department of Hematopathology and Molecular Genetics, AMPATH, Hyderabad, Telangana, India.
Reddy KG; Manipal Super specialty Hospital, Vijaywada, Andhra Pradesh, India.
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Source:
International journal of laboratory hematology [Int J Lab Hematol] 2021 Jun; Vol. 43 (3), pp. e128-e129. Date of Electronic Publication: 2020 Dec 04.
Publication Type:
Letter
MeSH Terms:
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 22*
Gene Rearrangement*
Phenotype*
Protein Biosynthesis*
Core Binding Factor beta Subunit/*genetics
Genetic Association Studies/methods ; Genetic Predisposition to Disease ; Humans
Editorial & Opinion
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Title:
MiR-3130-5p is an intermediate modulator of 2q33 and influences the invasiveness of lung adenocarcinoma by targeting NDUFS1.
Authors:
Zhan J; Department of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.; Department of Oncology, Zhongshan Hospital, Xiamen University, Xiamen, China.
Sun S; Department of Pulmonary and Critical Care Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Chen Y; Laboratory, Xiamen Cancer Center, The First Affiliated Hospital of Xiamen University, Xiamen, China.
Xu C; National Institute for Data Science in Health and Medicine, School of Medicine, Xiamen University, Xiamen, China.
Chen Q; National Institute for Data Science in Health and Medicine, School of Medicine, Xiamen University, Xiamen, China.
Li M; Department of Thoracic Surgery, Zhongshan Hospital, Xiamen University, Xiamen, China.
Pei Y; Central Laboratory, Zhongshan Hospital, Xiamen University, Xiamen, China.
Li Q; National Institute for Data Science in Health and Medicine, School of Medicine, Xiamen University, Xiamen, China.
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Source:
Cancer medicine [Cancer Med] 2021 Jun; Vol. 10 (11), pp. 3700-3714. Date of Electronic Publication: 2021 May 12.
Publication Type:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Human, Pair 1*
Adenocarcinoma of Lung/*genetics
Lung Neoplasms/*genetics
MicroRNAs/*metabolism
NADH Dehydrogenase/*metabolism
Quantitative Trait Loci/*genetics
Adenocarcinoma of Lung/pathology ; Animals ; Cell Line, Tumor ; Cell Movement ; Epithelial-Mesenchymal Transition/genetics ; Genes, Tumor Suppressor ; Genome-Wide Association Study ; Heterografts ; Humans ; Lung Neoplasms/pathology ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Neoplasm Invasiveness/genetics ; Phenotype ; Prognosis ; Tumor Suppressor Proteins/metabolism
Academic Journal
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Title:
Duplication 1q is highly correlated with poor prognosis in high hyperdiploid pediatric B-acute lymphoblastic leukemia.
Authors:
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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Source:
International journal of laboratory hematology [Int J Lab Hematol] 2021 Apr; Vol. 43 (2), pp. 235-243. Date of Electronic Publication: 2020 Oct 19.
Publication Type:
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
Academic Journal
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Title:
Loss of IDH mutation or secondary tumour manifestation? Evolution of an IDH-mutant and 1p/19q-codeleted oligodendroglioma after 15 years of continuous temozolomide treatment and radiotherapy: A case report.
Authors:
Ehret F; Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Radiation Oncology, Berlin, Germany.; Charité - Universitätsmedizin Berlin, Berlin, Germany; German Cancer Consortium (DKTK), Partner Site Berlin, and German Cancer Research Center (DKFZ), Heidelberg, Germany.
Hansch A; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Radiation Oncology, Berlin, Germany.
Meinhardt J; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Neuropathology, Berlin, Germany.
Hain EG; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Neuropathology, Berlin, Germany.
Misch M; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Neurosurgery, Berlin, Germany.
Onken J; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Neurosurgery, Berlin, Germany.
Roohani S; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Radiation Oncology, Berlin, Germany.
Koch A; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Neuropathology, Berlin, Germany.
Schweizer L; Charité - Universitätsmedizin Berlin, Berlin, Germany; German Cancer Consortium (DKTK), Partner Site Berlin, and German Cancer Research Center (DKFZ), Heidelberg, Germany.; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Neuropathology, Berlin, Germany.
Radke J; Charité - Universitätsmedizin Berlin, Berlin, Germany; German Cancer Consortium (DKTK), Partner Site Berlin, and German Cancer Research Center (DKFZ), Heidelberg, Germany.; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Neuropathology, Berlin, Germany.; Department of Pathology, University Medicine Greifswald, Greifswald, Germany.
Kaul D; Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Department of Radiation Oncology, Berlin, Germany.; Charité - Universitätsmedizin Berlin, Berlin, Germany; German Cancer Consortium (DKTK), Partner Site Berlin, and German Cancer Research Center (DKFZ), Heidelberg, Germany.
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Source:
Neuropathology and applied neurobiology [Neuropathol Appl Neurobiol] 2023 Feb; Vol. 49 (1), pp. e12859. Date of Electronic Publication: 2022 Dec 14.
Publication Type:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Oligodendroglioma*/pathology
Glioma*/pathology
Brain Neoplasms*/pathology
Humans ; Temozolomide ; Mutation ; Isocitrate Dehydrogenase/genetics ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 19
Academic Journal
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Showing 1-20 from 939 results

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