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Wyszukujesz frazę ""Translocation, Genetic"" wg kryterium: Wszystkie pola


Tytuł:
Alterations in Genome Organization in Lymphoma Cell Nuclei due to the Presence of the t(14;18) Translocation.
Autorzy:
Garimberti E; Clinical Genomics Laboratory, Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
Federico C; Department of Biological, Geological, and Environmental Sciences, University of Catania, Via Androne 81, 95124 Catania, Italy.
Ragusa D; Centre for Genome Engineering and Maintenance (CenGEM), College of Health, Medicine and Life Sciences, Brunel University London, Kingston Lane, Uxbridge UB8 3PH, UK.
Bruno F; Department of Biological, Geological, and Environmental Sciences, University of Catania, Via Androne 81, 95124 Catania, Italy.
Saccone S; Department of Biological, Geological, and Environmental Sciences, University of Catania, Via Androne 81, 95124 Catania, Italy.
Bridger JM; Centre for Genome Engineering and Maintenance (CenGEM), College of Health, Medicine and Life Sciences, Brunel University London, Kingston Lane, Uxbridge UB8 3PH, UK.
Tosi S; Centre for Genome Engineering and Maintenance (CenGEM), College of Health, Medicine and Life Sciences, Brunel University London, Kingston Lane, Uxbridge UB8 3PH, UK.; Leukaemia and Chromosome Research Laboratory, College of Health, Medicine and Life Sciences, Brunel University London, Kingston Lane, Uxbridge UB8 3PH, UK.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2024 Feb 17; Vol. 25 (4). Date of Electronic Publication: 2024 Feb 17.
Typ publikacji:
Journal Article
MeSH Terms:
Translocation, Genetic*
Lymphoma*/genetics
Humans ; In Situ Hybridization, Fluorescence ; Proto-Oncogene Proteins c-bcl-2/genetics ; Cell Nucleus/genetics
Czasopismo naukowe
Tytuł:
Identification and interruption of inheritance of familial cryptic translocations: A case report.
Autorzy:
Ou J; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Sun J; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Yang CC; School of Basic Medical Sciences, Guangdong Medical University, Zhanjiang, Guangdong, China.
Ni MX; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Zou QY; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Xing SY; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Lin CH; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Meng QX; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Ding J; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Zheng AY; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Zhang Y; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
Kong LY; Basecare Medical Device Co., Ltd., Suzhou, Jiangsu, China.
Liang B; State Key Laboratory of Microbial Metabolism, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Li H; Center for Reproduction and Genetics, The affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Suzhou, Jiangsu, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2024 Jan; Vol. 12 (1), pp. e2356.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Translocation, Genetic*
Genetic Testing*
Humans ; Chromosome Breakpoints ; Gene Rearrangement
Czasopismo naukowe
Tytuł:
t(1;4) translocation in a child with acute lymphoblastic leukemia: a case report.
Autorzy:
El Mahdaoui C; Laboratory of Cellular and Molecular Pathology, Faculty of Medicine and Pharmacy, Hassan II University of Casablanca, Casablanca, Morocco. .
Hda N; Hda Laboratories of Medical Biology Analysis, Casablanca, Morocco.
Oukkache B; Hematology Laboratory, Ibn Rochd University Hospital, Casablanca, Morocco.
Dehbi H; Laboratory of Cellular and Molecular Pathology, Faculty of Medicine and Pharmacy, Hassan II University of Casablanca, Casablanca, Morocco.; Laboratory of Medical Genetics, Ibn Rochd University Hospital, Casablanca, Morocco.; Hematology and Pediatric Oncology Department of August 20 Hospital, Ibn Rochd University Hospital, Casablanca, Morocco.
Khoubila N; Hematology and Pediatric Oncology Department of August 20 Hospital, Ibn Rochd University Hospital, Casablanca, Morocco.
Madani A; Hematology and Pediatric Oncology Department of August 20 Hospital, Ibn Rochd University Hospital, Casablanca, Morocco.
Cherkaoui S; Laboratory of Cellular and Molecular Pathology, Faculty of Medicine and Pharmacy, Hassan II University of Casablanca, Casablanca, Morocco.; Hematology and Pediatric Oncology Department of August 20 Hospital, Ibn Rochd University Hospital, Casablanca, Morocco.
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Źródło:
Journal of medical case reports [J Med Case Rep] 2023 Dec 12; Vol. 17 (1), pp. 537. Date of Electronic Publication: 2023 Dec 12.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/drug therapy
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/genetics
Translocation, Genetic*
Child, Preschool ; Female ; Humans ; Chromosome Aberrations ; Prognosis
Czasopismo naukowe
Tytuł:
Effects of chromosomal translocation characteristics on fertilization and blastocyst development - a retrospective cohort study.
Autorzy:
Wu S; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Zhang J; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Guan Y; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Ren B; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Zhang Y; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Liu X; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Wang K; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Zhang M; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Li Z; Reproductive Medicine Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2023 Nov 01; Vol. 16 (1), pp. 273. Date of Electronic Publication: 2023 Nov 01.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Translocation, Genetic*
Preimplantation Diagnosis*
Pregnancy ; Humans ; Male ; Female ; Retrospective Studies ; Fertilization in Vitro ; Pregnancy Rate ; Blastocyst ; Embryonic Development/genetics ; Fertilization ; Genetic Testing
Czasopismo naukowe
Tytuł:
11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four-way balanced chromosomal translocation.
Autorzy:
Zhang Q; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Wang Y; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Zhou J; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Zhou R; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Liu A; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Meng L; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Ji X; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Hu P; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
Xu Z; Department of Prenatal Diagnosis, Women's Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2023 Oct; Vol. 11 (10), pp. e2248. Date of Electronic Publication: 2023 Jul 21.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Translocation, Genetic*
Chromosome Aberrations*
Humans ; Female ; Adolescent ; DNA Copy Number Variations ; Karyotyping ; Chromosome Structures
Czasopismo naukowe
Tytuł:
Gene sequencing and result analysis of balanced translocation carriers by third-generation gene sequencing technology.
Autorzy:
Zeng X; Fujian Provincial Sperm Bank, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China. .; Obstetrics Department of Longyan First Hospital of Fujian Medical University, Fuzhou, China. .
Lin D; Fujian Provincial Sperm Bank, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Liang D; Fujian Provincial Sperm Bank, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Huang J; Fujian Provincial Sperm Bank, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Yi J; Fujian Provincial Sperm Bank, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
Lin D; Fujian Provincial Sperm Bank, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China. .
Zhang Z; Fujian Provincial Sperm Bank, Fujian Maternity and Child Health Hospital College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou, China.
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Źródło:
Scientific reports [Sci Rep] 2023 Apr 28; Vol. 13 (1), pp. 7004. Date of Electronic Publication: 2023 Apr 28.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Translocation, Genetic*
Chromosome Disorders*/genetics
Female ; Pregnancy ; Humans ; Chromosome Breakpoints ; Heterozygote ; Genetic Testing
Czasopismo naukowe
Tytuł:
The oncogenic properties of the EWSR1::CREM fusion gene are associated with polyamine metabolism.
Autorzy:
Kaprio H; Department of Pathology, Turku University Hospital, Kiinamyllynkatu 10 D, Turku, Finland. .; Institute of Biomedicine, University of Turku, Turku, Finland. .
Siddiqui A; Department of Obstetrics and Gynecology, Turku University Hospital, Turku, Finland.
Saustila L; Institute of Biomedicine, University of Turku, Turku, Finland.
Heuser VD; Department of Pathology, Turku University Hospital, Kiinamyllynkatu 10 D, Turku, Finland.; Institute of Biomedicine, University of Turku, Turku, Finland.
Gardberg M; Department of Pathology, Turku University Hospital, Kiinamyllynkatu 10 D, Turku, Finland.; Institute of Biomedicine, University of Turku, Turku, Finland.
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Źródło:
Scientific reports [Sci Rep] 2023 Mar 25; Vol. 13 (1), pp. 4884. Date of Electronic Publication: 2023 Mar 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Translocation, Genetic*
Polyamines*
Humans ; RNA-Binding Protein EWS/genetics ; RNA-Binding Protein EWS/metabolism ; Oncogene Proteins, Fusion/genetics ; Oncogene Proteins, Fusion/metabolism ; Gene Fusion ; Cyclic AMP Response Element Modulator/genetics
Czasopismo naukowe
Tytuł:
A New Case of Translocation T(2;7)(p23;q35) in Recurrent Pregnancy Loss.
Autorzy:
Yildirim A; Department of Medical Genetics, School of Medicine, Erciyes University, Kayseri, Turkey.
Taskin D; Department of Medical Genetics, School of Medicine, Erciyes University, Kayseri, Turkey.
Atasay R; Department of Medical Genetics, School of Medicine, Erciyes University, Kayseri, Turkey.
Dundar M; Department of Medical Genetics, School of Medicine, Erciyes University, Kayseri, Turkey. .
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Źródło:
Clinical medicine & research [Clin Med Res] 2023 Mar; Vol. 21 (1), pp. 53-55.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Translocation, Genetic*
Abortion, Habitual*/genetics
Humans ; Pregnancy ; Male ; Female ; In Situ Hybridization, Fluorescence ; Karyotyping ; Karyotype
Czasopismo naukowe
Tytuł:
The most common recurrent reciprocal translocation: T(11; 22)(q23; q11).
Autorzy:
Chen X; Department of Obstetrics and Gynecology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Yu Z; Department of Colorectal Surgery, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Chen S; Department of Obstetrics and Gynecology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
Zhou Y; Department of Obstetrics and Gynecology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
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Źródło:
Andrologia [Andrologia] 2022 Dec; Vol. 54 (11), pp. e14618. Date of Electronic Publication: 2022 Oct 28.
Typ publikacji:
Letter
MeSH Terms:
Translocation, Genetic*
Humans ; In Situ Hybridization, Fluorescence
Opinia redakcyjna
Tytuł:
Nonamer dependent RAG cleavage at CpGs can explain mechanism of chromosomal translocations associated to lymphoid cancers.
Autorzy:
Paranjape AM; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Desai SS; Institute of Bioinformatics and Applied Biotechnology, Electronics City, Bangalore, India.; Manipal Academy of Higher Education, Manipal, Karnataka, India.
Nishana M; Department of Biochemistry, Indian Institute of Science, Bangalore, India.; Indian Institute of Science Education and Research, Thiruvananthapuram, Kerala, India.
Roy U; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Nilavar NM; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Mondal A; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Kumari R; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Radha G; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Katapadi VK; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
Choudhary B; Institute of Bioinformatics and Applied Biotechnology, Electronics City, Bangalore, India.
Raghavan SC; Department of Biochemistry, Indian Institute of Science, Bangalore, India.
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Źródło:
PLoS genetics [PLoS Genet] 2022 Oct 13; Vol. 18 (10), pp. e1010421. Date of Electronic Publication: 2022 Oct 13 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Neoplasms*/genetics
Translocation, Genetic*/genetics
Humans ; Chromatin ; Cytidine Deaminase/genetics ; DNA/genetics ; Homeodomain Proteins/metabolism ; CpG Islands
Czasopismo naukowe
Tytuł:
DNA replication timing directly regulates the frequency of oncogenic chromosomal translocations.
Autorzy:
Peycheva M; Research Institute of Molecular Pathology (IMP), Vienna Biocenter, 1030 Vienna, Austria.
Neumann T; Research Institute of Molecular Pathology (IMP), Vienna Biocenter, 1030 Vienna, Austria.; Vienna BioCenter PhD Program, Doctoral School of the University of Vienna and Medical University of Vienna, Vienna Biocenter, 1030 Vienna, Austria.
Malzl D; Research Institute of Molecular Pathology (IMP), Vienna Biocenter, 1030 Vienna, Austria.
Nazarova M; Research Institute of Molecular Pathology (IMP), Vienna Biocenter, 1030 Vienna, Austria.
Schoeberl UE; Research Institute of Molecular Pathology (IMP), Vienna Biocenter, 1030 Vienna, Austria.
Pavri R; Research Institute of Molecular Pathology (IMP), Vienna Biocenter, 1030 Vienna, Austria.
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Źródło:
Science (New York, N.Y.) [Science] 2022 Sep 16; Vol. 377 (6612), pp. eabj5502. Date of Electronic Publication: 2022 Sep 16.
Typ publikacji:
Journal Article
MeSH Terms:
Carcinogenesis*/genetics
DNA Replication Timing*
Lymphoma, B-Cell*/genetics
Proto-Oncogene Proteins c-myc*/genetics
Translocation, Genetic*
DNA Breaks, Double-Stranded ; Humans ; Immunoglobulin Heavy Chains/genetics
Czasopismo naukowe
Tytuł:
Replication timing and genetic instability.
Autorzy:
Méchali M; Institute of Human Genetics, CNRS-University of Montpellier, Montpellier, France.
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Źródło:
Science (New York, N.Y.) [Science] 2022 Sep 16; Vol. 377 (6612), pp. 1259-1260. Date of Electronic Publication: 2022 Sep 15.
Typ publikacji:
Journal Article; Comment
MeSH Terms:
DNA Replication Timing*
Genomic Instability*
Immunoglobulin Heavy Chains*/genetics
Lymphoma, B-Cell*/genetics
Proto-Oncogene Proteins c-myc*/genetics
Replication Origin*
Translocation, Genetic*
Humans
Czasopismo naukowe
Tytuł:
Recurrent Translocations in Topoisomerase Inhibitor-Related Leukemia Are Determined by the Features of DNA Breaks Rather Than by the Proximity of the Translocating Genes.
Autorzy:
Lomov NA; Department of Molecular Biology, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.
Viushkov VS; Department of Molecular Biology, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.
Ulianov SV; Department of Molecular Biology, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.; Institute of Gene Biology, Russian Academy of Sciences, Moscow 119334, Russia.
Gavrilov AA; Institute of Gene Biology, Russian Academy of Sciences, Moscow 119334, Russia.
Alexeyevsky DA; A.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119234, Russia.
Artemov AV; Department of Neuroimmunology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria.
Razin SV; Department of Molecular Biology, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.; Institute of Gene Biology, Russian Academy of Sciences, Moscow 119334, Russia.
Rubtsov MA; Department of Molecular Biology, Faculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.; Department of Biochemistry, Center for Industrial Technologies and Entrepreneurship I.M., Sechenov First Moscow State Medical University (Sechenov University), Moscow 119435, Russia.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Aug 29; Vol. 23 (17). Date of Electronic Publication: 2022 Aug 29.
Typ publikacji:
Journal Article
MeSH Terms:
Leukemia, Myeloid, Acute*/genetics
Translocation, Genetic*
DNA ; DNA Breaks, Double-Stranded ; Etoposide/adverse effects ; Humans ; In Situ Hybridization, Fluorescence ; Topoisomerase II Inhibitors/adverse effects
Czasopismo naukowe
Tytuł:
A sustainable mouse karyotype created by programmed chromosome fusion.
Autorzy:
Wang LB; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Li ZK; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Wang LY; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Xu K; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Ji TT; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
Mao YH; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Ma SN; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; College of Life Science, Northeast Agricultural University, Harbin 150030, China.
Liu T; Annoroad Gene Technology (Beijing) Co., Ltd., Beijing 100176, China.
Tu CF; Annoroad Gene Technology (Beijing) Co., Ltd., Beijing 100176, China.
Zhao Q; Annoroad Gene Technology (Beijing) Co., Ltd., Beijing 100176, China.
Fan XN; Annoroad Gene Technology (Beijing) Co., Ltd., Beijing 100176, China.
Liu C; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Wang LY; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.
Shu YJ; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
Yang N; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; University of Chinese Academy of Sciences, Beijing 100049, China.
Zhou Q; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
Li W; State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China.; Institute for Stem Cell and Regeneration, Chinese Academy of Sciences, Beijing 100101, China.; Bejing Institute for Stem Cell and Regenerative Medicine, Beijing 100101, China.
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Źródło:
Science (New York, N.Y.) [Science] 2022 Aug 26; Vol. 377 (6609), pp. 967-975. Date of Electronic Publication: 2022 Aug 25.
Typ publikacji:
Journal Article
MeSH Terms:
Artificial Gene Fusion*/methods
Gene Editing*/methods
Karyotype*
Translocation, Genetic*
Animals ; Chromatin/chemistry ; Embryonic Stem Cells ; Haploidy ; Mice ; Mitosis
Czasopismo naukowe
Tytuł:
Ku70 affects the frequency of chromosome translocation in human lymphocytes after radiation and T-cell acute lymphoblastic leukemia.
Autorzy:
Cheng Z; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China.; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China.
Wang Y; Department of Medical Laboratory, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, 410005, People's Republic of China.
Guo L; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China.; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China.
Li J; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China.; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China.
Zhang W; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China.; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China.
Zhang C; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China.; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China.
Liu Y; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China.; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China.
Huang Y; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China.; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China.
Xu K; Department of Laboratory Medicine, The Third Xiangya Hospital, Central South University, Changsha, 410013, People's Republic of China. .; Department of Laboratory Medicine, Xiangya School of Medicine, Central South University, Changsha, 410013, People's Republic of China. .
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Źródło:
Radiation oncology (London, England) [Radiat Oncol] 2022 Aug 19; Vol. 17 (1), pp. 144. Date of Electronic Publication: 2022 Aug 19.
Typ publikacji:
Journal Article
MeSH Terms:
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma*
Translocation, Genetic*
Humans ; In Situ Hybridization, Fluorescence ; Lymphocytes/radiation effects ; RNA, Messenger ; T-Lymphocytes
Czasopismo naukowe
Tytuł:
The mechanisms of human lymphoid chromosomal translocations and their medical relevance.
Autorzy:
Liu D; Department of Pathology & Laboratory Medicine, Department of Biochemistry & Molecular Biology, Department of Molecular Microbiology and Immunology, and Section of Computational Biology in the Department of Biological Sciences, USC Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Lieber MR; Department of Pathology & Laboratory Medicine, Department of Biochemistry & Molecular Biology, Department of Molecular Microbiology and Immunology, and Section of Computational Biology in the Department of Biological Sciences, USC Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
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Źródło:
Critical reviews in biochemistry and molecular biology [Crit Rev Biochem Mol Biol] 2022 Jun; Vol. 57 (3), pp. 227-243. Date of Electronic Publication: 2021 Dec 07.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Immunoglobulin Class Switching*
Translocation, Genetic*
Base Sequence ; DNA ; Humans
Czasopismo naukowe
Tytuł:
Evaluation of optical genome mapping for detecting chromosomal translocation in clinical cytogenetics.
Autorzy:
Dai P; The Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Zhu X; The Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Pei Y; GrandOmics Diagnostic, Wuhan, China.
Chen P; Department of Neurology, The First Hospital of Yulin, Yulin, China.
Li J; GrandOmics Diagnostic, Wuhan, China.
Gao Z; The Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Liang Y; GrandOmics Diagnostic, Wuhan, China.
Kong X; The Genetics and Prenatal Diagnosis Center, The Department of Obstetrics and Gynecology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2022 Jun; Vol. 10 (6), pp. e1936. Date of Electronic Publication: 2022 Apr 06.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosome Disorders*/genetics
Translocation, Genetic*
Chromosome Aberrations ; Chromosome Mapping ; Cytogenetic Analysis/methods ; Cytogenetics/methods ; Female ; Humans ; Pregnancy
Czasopismo naukowe
Tytuł:
A Single-Institute Experience with C-ros Oncogene 1 Translocation in Non-Small Cell Lung Cancers in Taiwan.
Autorzy:
Wang HS; Department of Pathology, Chang Gung Memorial Hospital, Chang Gung University School of Medicine, Kwei-Shan, Taoyuan 33305, Taiwan.
Liu CY; Department & Centers of Lung Cancer and Interventional Bronchoscopy, Chang Gung Memorial Hospital, Chang Gung University School of Medicine, Kwei-Shan, Taoyuan 33305, Taiwan.
Hsu SC; Department of Pathology, Chang Gung Memorial Hospital, Chang Gung University School of Medicine, Kwei-Shan, Taoyuan 33305, Taiwan.
Huang SC; Department of Pathology, Chang Gung Memorial Hospital, Chang Gung University School of Medicine, Kwei-Shan, Taoyuan 33305, Taiwan.
Hung TH; Institute of Stem Cell & Translational Cancer Research, Chang Gung Memorial Hospital at Linkou and Chang Gung University, Taoyuan 33305, Taiwan.
Ng KF; Department of Pathology, Chang Gung Memorial Hospital, Chang Gung University School of Medicine, Kwei-Shan, Taoyuan 33305, Taiwan.
Chen TC; Department of Pathology, Chang Gung Memorial Hospital, Chang Gung University School of Medicine, Kwei-Shan, Taoyuan 33305, Taiwan.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 May 21; Vol. 23 (10). Date of Electronic Publication: 2022 May 21.
Typ publikacji:
Journal Article
MeSH Terms:
Carcinoma, Non-Small-Cell Lung*/drug therapy
Carcinoma, Non-Small-Cell Lung*/genetics
Carcinoma, Non-Small-Cell Lung*/pathology
Crizotinib*/therapeutic use
Lung Neoplasms*/drug therapy
Lung Neoplasms*/genetics
Lung Neoplasms*/pathology
Protein-Tyrosine Kinases*/genetics
Protein-Tyrosine Kinases*/metabolism
Proto-Oncogene Proteins*/genetics
Proto-Oncogene Proteins*/metabolism
Translocation, Genetic*
ErbB Receptors/genetics ; Humans ; In Situ Hybridization, Fluorescence ; Oncogenes ; Prospective Studies ; Retrospective Studies ; Taiwan/epidemiology
Czasopismo naukowe
Tytuł:
Genetic analysis and clinical significance of a rare t(1;12)(q21;p13) in a patient with high-risk myelodysplastic syndrome.
Autorzy:
Fang F; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Jia R; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Liu C; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Zhao H; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing, China.
Sun W; Department of Hematology, Xuanwu Hospital, Capital Medical University, Beijing, China.
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Źródło:
Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2022 Apr; Vol. 10 (4), pp. e1893. Date of Electronic Publication: 2022 Feb 22.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Myelodysplastic Syndromes*/genetics
Translocation, Genetic*
Humans ; In Situ Hybridization, Fluorescence/methods ; Karyotyping ; Male ; Trisomy
Czasopismo naukowe
Tytuł:
Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6).
Autorzy:
Jurčenko M; Clinic of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital, Riga, Latvia.
Auzenbaha M; Clinic of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital, Riga, Latvia.; Department of Biology and Microbiology, Rīga Stradiņš University, Riga, Latvia.
Mičule I; Clinic of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital, Riga, Latvia.
Grīnfelde I; Clinic of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital, Riga, Latvia.; Department of Biology and Microbiology, Rīga Stradiņš University, Riga, Latvia.
Dzalbs A; Clinic of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital, Riga, Latvia.
Mālniece I; Clinic of Medical Genetics and Prenatal Diagnostics, Children's Clinical University Hospital, Riga, Latvia.
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Źródło:
The American journal of case reports [Am J Case Rep] 2022 Feb 22; Vol. 23, pp. e935370. Date of Electronic Publication: 2022 Feb 22.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Chromosome Disorders*/genetics
Translocation, Genetic*
Amniocentesis ; Child ; Female ; Genetic Testing ; Humans ; Infant, Newborn ; Pregnancy ; Pregnancy Outcome
Czasopismo naukowe

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