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Tytuł:
Functional analysis of Cdc20 reveals a critical role of CRY box in mitotic checkpoint signaling.
Autorzy:
Zhang Y; Cancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Young R; Chester Beatty Laboratories, Structural Biology Division, Institute of Cancer Research, London, UK.
Garvanska DH; The NNF Center for Protein Research, University of Copenhagen, Copenhagen, Denmark.
Song C; Cancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Zhai Y; School of Public Health, Qingdao University, Qingdao, China.
Wang Y; School of Public Health, Qingdao University, Qingdao, China.
Jiang H; Cancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Fang J; Cancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Nilsson J; The NNF Center for Protein Research, University of Copenhagen, Copenhagen, Denmark.
Alfieri C; Chester Beatty Laboratories, Structural Biology Division, Institute of Cancer Research, London, UK. .
Zhang G; Cancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, China. zhanggang_.
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Źródło:
Communications biology [Commun Biol] 2024 Feb 09; Vol. 7 (1), pp. 164. Date of Electronic Publication: 2024 Feb 09.
Typ publikacji:
Journal Article
MeSH Terms:
Cdc20 Proteins*/chemistry
Cdc20 Proteins*/genetics
Cdc20 Proteins*/metabolism
M Phase Cell Cycle Checkpoints*/genetics
Spindle Apparatus*/genetics
Spindle Apparatus*/metabolism
Anaphase-Promoting Complex-Cyclosome/genetics ; Anaphase-Promoting Complex-Cyclosome/metabolism ; Cell Cycle Proteins/genetics ; Cell Cycle Proteins/metabolism ; Signal Transduction ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
MAPK-dependent control of mitotic progression in S. pombe.
Autorzy:
Iglesias-Romero AB; Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide, Seville, 41013, Spain.
Soto T; Yeast Physiology Group, Department of Genetics and Microbiology, Facultad de Biología, Universidad de Murcia, Murcia, 30071, Spain.
Flor-Parra I; Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide, Seville, 41013, Spain.
Salas-Pino S; Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide, Seville, 41013, Spain.
Ruiz-Romero G; Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide, Seville, 41013, Spain.
Gould KL; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN, 37240, USA.
Cansado J; Yeast Physiology Group, Department of Genetics and Microbiology, Facultad de Biología, Universidad de Murcia, Murcia, 30071, Spain. .
Daga RR; Centro Andaluz de Biología del Desarrollo, Universidad Pablo de Olavide, Seville, 41013, Spain. .
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Źródło:
BMC biology [BMC Biol] 2024 Mar 25; Vol. 22 (1), pp. 71. Date of Electronic Publication: 2024 Mar 25.
Typ publikacji:
Journal Article
MeSH Terms:
Schizosaccharomyces*/genetics
Schizosaccharomyces*/metabolism
Schizosaccharomyces pombe Proteins*/genetics
Schizosaccharomyces pombe Proteins*/metabolism
Anaphase-Promoting Complex-Cyclosome/genetics ; Anaphase-Promoting Complex-Cyclosome/metabolism ; Cdc20 Proteins/genetics ; Cdc20 Proteins/metabolism ; Cell Cycle Proteins/metabolism ; Mitosis ; Spindle Apparatus/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Functional analysis of recurrent CDC20 promoter variants in human melanoma.
Autorzy:
Godoy PM; Division of Medical Oncology, Department of Medicine and Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO, USA.
Oyedeji A; Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.; Siteman Cancer Center, Washington University in Saint Louis, St. Louis, MO, USA.
Mudd JL; Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.; Siteman Cancer Center, Washington University in Saint Louis, St. Louis, MO, USA.
Morikis VA; Departments of Medicine (Oncology) and Cell Biology and Physiology and the ICCE Institute, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Zarov AP; Division of Medical Oncology, Department of Medicine and Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO, USA.
Longmore GD; Siteman Cancer Center, Washington University in Saint Louis, St. Louis, MO, USA.; Departments of Medicine (Oncology) and Cell Biology and Physiology and the ICCE Institute, Washington University School of Medicine, St. Louis, MO, 63110, USA.
Fields RC; Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.; Siteman Cancer Center, Washington University in Saint Louis, St. Louis, MO, USA.
Kaufman CK; Division of Medical Oncology, Department of Medicine and Department of Developmental Biology, Washington University School of Medicine, St. Louis, MO, USA. .; Siteman Cancer Center, Washington University in Saint Louis, St. Louis, MO, USA. .
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Źródło:
Communications biology [Commun Biol] 2023 Nov 29; Vol. 6 (1), pp. 1216. Date of Electronic Publication: 2023 Nov 29.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural
MeSH Terms:
Melanoma*/genetics
Melanoma*/metabolism
Humans ; Mutation ; Promoter Regions, Genetic ; Regulatory Sequences, Nucleic Acid ; Genome ; Cdc20 Proteins/genetics ; Cdc20 Proteins/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Knockdown of CDC20 promotes adipogenesis of bone marrow-derived stem cells by modulating β-catenin.
Autorzy:
Du Y; Department of Prosthodontics, National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, National Clinical Research Center for Oral Diseases, Beijing Key Laboratory of Digital Stomatology, Peking University School and Hospital of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing, 100081, People's Republic of China.
Liu Y; Department of Prosthodontics, National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, National Clinical Research Center for Oral Diseases, Beijing Key Laboratory of Digital Stomatology, Peking University School and Hospital of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing, 100081, People's Republic of China.
Zhou Y; Department of Prosthodontics, National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, National Clinical Research Center for Oral Diseases, Beijing Key Laboratory of Digital Stomatology, Peking University School and Hospital of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing, 100081, People's Republic of China. .
Zhang P; Department of Prosthodontics, National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, National Clinical Research Center for Oral Diseases, Beijing Key Laboratory of Digital Stomatology, Peking University School and Hospital of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing, 100081, People's Republic of China. .
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Źródło:
Stem cell research & therapy [Stem Cell Res Ther] 2022 Sep 02; Vol. 13 (1), pp. 443. Date of Electronic Publication: 2022 Sep 02.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Adipogenesis*
Mesenchymal Stem Cells*/metabolism
Cdc20 Proteins/*metabolism
Animals ; Bone Marrow/metabolism ; Bone Marrow Cells ; Cdc20 Proteins/genetics ; Cell Differentiation ; Cells, Cultured ; Humans ; Mice ; Mice, Knockout ; Mice, Nude ; Osteogenesis/genetics ; beta Catenin/genetics ; beta Catenin/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
REC8 inhibits proliferation, migration and invasion of breast cancer cells by targeting CDC20.
Autorzy:
He S; Department of Emergency Medicine, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi 710068, P.R. China.
Liu D; Department of Emergency Medicine, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi 710068, P.R. China.
Chen Z; Department of Emergency Medicine, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi 710068, P.R. China.
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Źródło:
Molecular medicine reports [Mol Med Rep] 2022 Jul; Vol. 26 (1). Date of Electronic Publication: 2022 May 26.
Typ publikacji:
Journal Article
MeSH Terms:
Breast Neoplasms*/genetics
Cdc20 Proteins*/genetics
Cdc20 Proteins*/metabolism
Cell Cycle Proteins*/genetics
Cell Cycle Proteins*/metabolism
Matrix Metalloproteinase 2*/metabolism
Apoptosis/genetics ; Caspase 3/metabolism ; Cell Line, Tumor ; Cell Movement/genetics ; Cell Proliferation ; Female ; Gene Expression Regulation, Neoplastic ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Septin 9 controls CCNB1 stabilization via APC/C during meiotic metaphase I/anaphase I transition in mouse oocytes.
Autorzy:
Chen L; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.; University of Chinese Academy of Sciences, Beijing, China.
Ouyang YC; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Gu LJ; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.; University of Chinese Academy of Sciences, Beijing, China.
Guo JN; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.; University of Chinese Academy of Sciences, Beijing, China.
Han ZM; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Wang ZB; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.; University of Chinese Academy of Sciences, Beijing, China.
Hou Y; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Schatten H; Department of Veterinary Pathobiology, University of Missouri, Columbia, Missouri, USA.
Sun QY; Fertility Preservation Lab, Guangdong-Hong Kong Metabolism & Reproduction Joint Laboratory, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou, China.
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Źródło:
Cell proliferation [Cell Prolif] 2023 Feb; Vol. 56 (2), pp. e13359. Date of Electronic Publication: 2022 Nov 10.
Typ publikacji:
Journal Article
MeSH Terms:
Oocytes*/cytology
Oocytes*/metabolism
Septins*/genetics
Septins*/metabolism
Cell Cycle*
Animals ; Mice ; Anaphase ; Anaphase-Promoting Complex-Cyclosome/genetics ; Anaphase-Promoting Complex-Cyclosome/metabolism ; Cdc20 Proteins/genetics ; Cdc20 Proteins/metabolism ; Cell Cycle Proteins/metabolism ; Metaphase ; RNA, Messenger/metabolism ; RNA, Small Interfering/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Recovery from spindle checkpoint-mediated arrest requires a novel Dnt1-dependent APC/C activation mechanism.
Autorzy:
Bai S; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Sun L; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Wang X; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Wang SM; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Luo ZQ; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Wang Y; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
Jin QW; State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, Xiamen, Fujian, China.
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Źródło:
PLoS genetics [PLoS Genet] 2022 Sep 15; Vol. 18 (9), pp. e1010397. Date of Electronic Publication: 2022 Sep 15 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cell Cycle Proteins*/genetics
Cell Cycle Proteins*/metabolism
Thiabendazole*/metabolism
Anaphase-Promoting Complex-Cyclosome/genetics ; Anaphase-Promoting Complex-Cyclosome/metabolism ; Cdc20 Proteins/genetics ; Cdc20 Proteins/metabolism ; Kinetochores/metabolism ; M Phase Cell Cycle Checkpoints/genetics ; Securin/genetics ; Spindle Apparatus/genetics ; Spindle Apparatus/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
CDK1 and CDC20 overexpression in patients with colorectal cancer are associated with poor prognosis: evidence from integrated bioinformatics analysis.
Autorzy:
Li J; Department of Gastrointestinal Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, People's Republic of China.
Wang Y; Department of Gastrointestinal Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, People's Republic of China.
Wang X; Department of Gastrointestinal Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, People's Republic of China.
Yang Q; Department of Gastrointestinal Surgery, The Affiliated Hospital of Southwest Medical University, Luzhou, 646000, Sichuan, People's Republic of China. .
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Źródło:
World journal of surgical oncology [World J Surg Oncol] 2020 Mar 04; Vol. 18 (1), pp. 50. Date of Electronic Publication: 2020 Mar 04.
Typ publikacji:
Journal Article
MeSH Terms:
Computational Biology*
CDC2 Protein Kinase/*genetics
Cdc20 Proteins/*genetics
Colorectal Neoplasms/*etiology
CDC2 Protein Kinase/physiology ; Cdc20 Proteins/physiology ; Colorectal Neoplasms/genetics ; Colorectal Neoplasms/mortality ; Gene Ontology ; Humans ; Prognosis ; Protein Interaction Maps
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Analysis of TET2 and EZH2 gene functions in chromosome instability in acute myeloid leukemia.
Autorzy:
Wang J; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.; Department of Hematology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, 250011, P.R. China.
He N; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.
Wang R; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.
Tian T; Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
Han F; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.
Zhong C; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.
Zhang C; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.
Hua M; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.
Ji C; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China.
Ma D; Department of Hematology, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, P.R. China. .
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Źródło:
Scientific reports [Sci Rep] 2020 Feb 17; Vol. 10 (1), pp. 2706. Date of Electronic Publication: 2020 Feb 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomal Instability*
Gene Expression Regulation, Leukemic*
Cdc20 Proteins/*genetics
DNA-Binding Proteins/*genetics
Enhancer of Zeste Homolog 2 Protein/*genetics
Leukemia, Myeloid, Acute/*genetics
Mad2 Proteins/*genetics
Proto-Oncogene Proteins/*genetics
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antimetabolites, Antineoplastic/therapeutic use ; Cdc20 Proteins/metabolism ; Cell Line, Tumor ; Chromosomes, Human ; DNA Methylation ; DNA-Binding Proteins/antagonists & inhibitors ; DNA-Binding Proteins/metabolism ; Decitabine/therapeutic use ; Dioxygenases ; Enhancer of Zeste Homolog 2 Protein/antagonists & inhibitors ; Enhancer of Zeste Homolog 2 Protein/metabolism ; Epigenesis, Genetic ; Female ; Humans ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/metabolism ; Leukemia, Myeloid, Acute/pathology ; Mad2 Proteins/metabolism ; Male ; Middle Aged ; Proto-Oncogene Proteins/antagonists & inhibitors ; Proto-Oncogene Proteins/metabolism ; RNA, Small Interfering/genetics ; RNA, Small Interfering/metabolism ; Remission Induction ; Transcription, Genetic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
GTSE1, CDC20, PCNA, and MCM6 Synergistically Affect Regulations in Cell Cycle and Indicate Poor Prognosis in Liver Cancer.
Autorzy:
Zheng Y; Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Shi Y; Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Yu S; Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Han Y; Center of Tree Shrew Germplasm Resources, Institute of Medical Biology, The Chinese Academy of Medical Sciences and Peking Union Medical College, Yunnan Key Laboratory of Vaccine Research and Development on Severe Infectious Diseases, Kunming, Yunnan 650118, China.
Kang K; Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Xu H; Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Gu H; Department of Hepatobiliary Surgery, Affiliated Hospital of Guizhou Medical University, No. 28, Guiyi Street, Yunyan District, 550004 Guiyang, China.
Sang X; Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Chen Y; MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, Bioinformatics Division, BNRist, Department of Automation, Tsinghua University, Beijing 100084, China.
Wang J; MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systems Biology, Bioinformatics Division, BNRist, Department of Automation, Tsinghua University, Beijing 100084, China.; Department of Basic Medical Science, Tsinghua-Peking Joint Center for Life Sciences, School of Medicine, Tsinghua University, Beijing 100084, China.
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Źródło:
Analytical cellular pathology (Amsterdam) [Anal Cell Pathol (Amst)] 2019 Dec 30; Vol. 2019, pp. 1038069. Date of Electronic Publication: 2019 Dec 30 (Print Publication: 2019).
Typ publikacji:
Journal Article
MeSH Terms:
Carcinoma, Hepatocellular/*metabolism
Cdc20 Proteins/*metabolism
Liver Neoplasms/*metabolism
Microtubule-Associated Proteins/*metabolism
Minichromosome Maintenance Complex Component 6/*metabolism
Proliferating Cell Nuclear Antigen/*metabolism
S Phase Cell Cycle Checkpoints/*genetics
Adult ; Biomarkers, Tumor/genetics ; Biomarkers, Tumor/metabolism ; Carcinoma, Hepatocellular/genetics ; Carcinoma, Hepatocellular/pathology ; Cdc20 Proteins/genetics ; Cell Line, Tumor ; Cell Movement/genetics ; Cell Proliferation/genetics ; Databases, Nucleic Acid ; Gene Expression Regulation, Neoplastic ; Gene Ontology ; Humans ; Liver Neoplasms/genetics ; Liver Neoplasms/pathology ; Microtubule-Associated Proteins/genetics ; Minichromosome Maintenance Complex Component 6/genetics ; Prognosis ; Proliferating Cell Nuclear Antigen/genetics ; Tissue Array Analysis ; Up-Regulation
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
CDC20 in and out of mitosis: a prognostic factor and therapeutic target in hematological malignancies.
Autorzy:
Bruno S; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna and Institute of Hematology 'L. e A. Seràgnoli', Bologna, Italy.
Ghelli Luserna di Rorà A; Biosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) 'Dino Amadori', via Piero Maroncelli 40, 47014, Meldola, FC, Italy. .
Napolitano R; Biosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) 'Dino Amadori', via Piero Maroncelli 40, 47014, Meldola, FC, Italy.
Soverini S; Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna and Institute of Hematology 'L. e A. Seràgnoli', Bologna, Italy.
Martinelli G; Scientific Directorate, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) 'Dino Amadori', via Piero Maroncelli 40, 47014, Meldola, FC, Italy.
Simonetti G; Biosciences Laboratory, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) 'Dino Amadori', via Piero Maroncelli 40, 47014, Meldola, FC, Italy.
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Źródło:
Journal of experimental & clinical cancer research : CR [J Exp Clin Cancer Res] 2022 Apr 30; Vol. 41 (1), pp. 159. Date of Electronic Publication: 2022 Apr 30.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Hematologic Neoplasms*/drug therapy
Hematologic Neoplasms*/genetics
Neoplasms*
Cdc20 Proteins/genetics ; Cdc20 Proteins/metabolism ; Cell Cycle Proteins/genetics ; Cell Cycle Proteins/metabolism ; Humans ; Mitosis ; Prognosis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
CDC20 regulates sensitivity to chemotherapy and radiation in glioblastoma stem cells.
Autorzy:
Mao DD; Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Cleary RT; Department of Neurological Surgery, Saint Louis University School of Medicine, St. Louis, Missouri, United States of America.
Gujar A; The Jackson Laboratory in Genomic Medicine, Farmington, Connecticut, United States of America.
Mahlokozera T; Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Kim AH; Department of Neurological Surgery, Washington University School of Medicine, St. Louis, Missouri, United States of America.; The Brain Tumor Center, Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, United States of America.
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Źródło:
PloS one [PLoS One] 2022 Jun 23; Vol. 17 (6), pp. e0270251. Date of Electronic Publication: 2022 Jun 23 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
MeSH Terms:
Brain Neoplasms*/drug therapy
Brain Neoplasms*/genetics
Brain Neoplasms*/radiotherapy
Glioblastoma*/pathology
Cdc20 Proteins/genetics ; Cdc20 Proteins/metabolism ; Cell Cycle Proteins/genetics ; Cell Cycle Proteins/metabolism ; Cell Line, Tumor ; Humans ; Neoplasm Recurrence, Local/pathology ; Neoplastic Stem Cells/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Bioinformatics analysis and experimental validation reveal that CDC20 overexpression promotes bladder cancer progression and potential underlying mechanisms
Autorzy:
Liu, Yuan
Zou, Shao-hui
Gao, XinAff1, Aff2, IDs1325802401505x_cor3
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Źródło:
Genes & Genomics. 46(4):437-449
Czasopismo naukowe
Szczegóły
Tytuł:
A Novel Gene Signature Based on CDC20 and FCN3 for Prediction of Prognosis and Immune Features in Patients with Hepatocellular Carcinoma.
Autorzy:
Lai X; Department of Hepatobiliary Surgery, The Tongnan District People's Hospital, Chongqing, China.
Wu YK; Department of Hepatobiliary Surgery, The Suining Central Hospital, Suining, China.
Hong GQ; Department of Hepatobiliary Surgery, The Tongnan District People's Hospital, Chongqing, China.
Li JK; Department of Hepatobiliary Surgery, The Tongnan District People's Hospital, Chongqing, China.
Luo Q; Department of Hepatobiliary Surgery, The Tongnan District People's Hospital, Chongqing, China.
Yuan J; Department of Infection Diseases, the Chongqing University Jiangjin Hospital, School of Medicine, Chongqing University, Chongqing, China.
Dai GH; Department of Hepatobiliary Surgery, the Chongqing University Jiangjin Hospital, School of Medicine, Chongqing University, Chongqing, China.
Liu SQ; Department of Hepatobiliary Surgery, the Chongqing University Jiangjin Hospital, School of Medicine, Chongqing University, Chongqing, China.
Feng HG; Department of Hepatobiliary Surgery, the Chongqing University Jiangjin Hospital, School of Medicine, Chongqing University, Chongqing, China.
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Źródło:
Journal of immunology research [J Immunol Res] 2022 Mar 30; Vol. 2022, pp. 9117205. Date of Electronic Publication: 2022 Mar 30 (Print Publication: 2022).
Typ publikacji:
Journal Article
MeSH Terms:
Carcinoma, Hepatocellular*/diagnosis
Carcinoma, Hepatocellular*/genetics
Carcinoma, Hepatocellular*/pathology
Liver Neoplasms*/genetics
Liver Neoplasms*/pathology
Cdc20 Proteins/genetics ; Cell Cycle Proteins ; Humans ; Lectins ; Prognosis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Ubc1 turnover contributes to the spindle assembly checkpoint in Saccharomyces cerevisiae.
Autorzy:
Arsenault HE; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Ghizzoni JM; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Leech CM; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Diers AR; BERG, Framingham, MA 01710, USA.
Gesta S; BERG, Framingham, MA 01710, USA.
Vishnudas VK; BERG, Framingham, MA 01710, USA.
Narain NR; BERG, Framingham, MA 01710, USA.
Sarangarajan R; BERG, Framingham, MA 01710, USA.
Benanti JA; Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
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Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2021 Dec 08; Vol. 11 (12).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Saccharomyces cerevisiae*/genetics
Saccharomyces cerevisiae Proteins*/genetics
Anaphase ; Anaphase-Promoting Complex-Cyclosome/genetics ; Cdc20 Proteins ; Cell Cycle Proteins/genetics ; M Phase Cell Cycle Checkpoints ; Mitosis ; Spindle Apparatus ; Ubiquitin-Conjugating Enzymes/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
SETDB2 interacts with BUBR1 to induce accurate chromosome segregation independently of its histone methyltransferase activity
Autorzy:
Yanhong Tu
Haomiao Zhang
Jialin Xia
Yu Zhao
Ruifang Yang
Jing Feng
Xueyun Ma
Jing Li
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Temat:
APC/C
BUBR1
CDC20
chromosome segregation
mitosis
SETDB2
Biology (General)
QH301-705.5
Źródło:
FEBS Open Bio, Vol 14, Iss 3, Pp 444-454 (2024)
Opis pliku:
electronic resource
Relacje:
https://doaj.org/toc/2211-5463
Dostęp URL:
https://doaj.org/article/ed055d30364e40cfbd691798711217b0  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Reciprocal interaction between SIRT6 and APC/C regulates genomic stability.
Autorzy:
Wang H; MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systematic Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Feng K; MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systematic Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Wang Q; Beijing Chaoyang Hospital Affiliated to Capital Medical University, Beijing, 100043, China.
Deng H; MOE Key Laboratory of Bioinformatics, Center for Synthetic and Systematic Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China. .
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Źródło:
Scientific reports [Sci Rep] 2021 Jul 09; Vol. 11 (1), pp. 14253. Date of Electronic Publication: 2021 Jul 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Anaphase-Promoting Complex-Cyclosome/*metabolism
Cell Cycle Proteins/*metabolism
Sirtuins/*metabolism
Anaphase-Promoting Complex-Cyclosome/genetics ; Antigens, CD/genetics ; Antigens, CD/metabolism ; Cadherins/genetics ; Cadherins/metabolism ; Cdc20 Proteins/genetics ; Cdc20 Proteins/metabolism ; Cell Cycle Proteins/genetics ; Cell Line ; Cell Line, Tumor ; Chromosomal Instability/genetics ; Chromosomal Instability/physiology ; HeLa Cells ; Humans ; Protein Binding ; Sirtuins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
CDC20 promotes the progression of hepatocellular carcinoma by regulating epithelial‑mesenchymal transition.
Autorzy:
Yang G; Department of Hepatocellular Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637007, P.R. China.
Wang G; Physical Examination Center, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637007, P.R. China.
Xiong Y; Department of Hepatocellular Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637007, P.R. China.
Sun J; Department of Hepatocellular Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637007, P.R. China.
Li W; Department of Hepatocellular Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637007, P.R. China.
Tang T; Department of Hepatocellular Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637007, P.R. China.
Li J; Department of Hepatocellular Surgery, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan 637007, P.R. China.
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Źródło:
Molecular medicine reports [Mol Med Rep] 2021 Jul; Vol. 24 (1). Date of Electronic Publication: 2021 Apr 28.
Typ publikacji:
Journal Article
MeSH Terms:
Carcinoma, Hepatocellular/*metabolism
Cdc20 Proteins/*genetics
Cdc20 Proteins/*metabolism
Epithelial-Mesenchymal Transition/*physiology
Liver Neoplasms/*metabolism
Adult ; Aged ; Antigens, CD ; Cadherins/metabolism ; Carcinoma, Hepatocellular/genetics ; Carcinoma, Hepatocellular/pathology ; Cell Line, Tumor ; Cell Movement ; Cell Proliferation ; Female ; Gene Expression Regulation, Neoplastic ; Gene Knockdown Techniques ; Humans ; Liver Neoplasms/genetics ; Liver Neoplasms/pathology ; Male ; Middle Aged ; Transcriptome ; Vimentin/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The kinetochore-dependent and -independent formation of the CDC20-MAD2 complex and its functions in HeLa cells.
Autorzy:
Li J; Institute for Cell and Molecular Biosciences, Newcastle University, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
Dang N; Institute for Cell and Molecular Biosciences, Newcastle University, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
Wood DJ; Institute for Cell and Molecular Biosciences, Newcastle University, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
Huang JY; Institute for Cell and Molecular Biosciences, Newcastle University, Framlington Place, Newcastle upon Tyne, NE2 4HH, UK.
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Źródło:
Scientific reports [Sci Rep] 2017 Jan 23; Vol. 7, pp. 41072. Date of Electronic Publication: 2017 Jan 23.
Typ publikacji:
Journal Article
MeSH Terms:
Kinetochores*
Cdc20 Proteins/*genetics
Mad2 Proteins/*genetics
Multiprotein Complexes/*genetics
Cdc20 Proteins/chemistry ; Cell Cycle/genetics ; Cell Cycle Proteins/genetics ; Cell Nucleus/genetics ; Cyclin B1/genetics ; HeLa Cells ; Humans ; Mad2 Proteins/chemistry ; Mitosis/genetics ; Multiprotein Complexes/chemistry
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Wyświetlanie 1-20 z 814

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