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Wyszukujesz frazę ""Chromosome Banding"" wg kryterium: Temat


Tytuł :
A DAPI-Based Modified C-banding Technique for a Rapid Achieving High Photographic Contrast of Centromeres on Chromosomes.
Autorzy :
Gonen R; Nuclear Research Center Negev, 84190, Beer-Sheba, Israel. .; Department of Biomedical Engineering, Ben Gurion University, Beer Sheva, Israel. .
Platkov M; Nuclear Research Center Negev, 84190, Beer-Sheba, Israel.
Gardos Z; Sami Shamoon College of Engineering, Beer-Sheba, Israel.
Shayir S; Department of Biomedical Engineering, Ben Gurion University, Beer Sheva, Israel.
Levitsky I; Sami Shamoon College of Engineering, Beer-Sheba, Israel.
Weinstein M; Nuclear Research Center Negev, 84190, Beer-Sheba, Israel.
Manor E; Department of Virology and Developmental Genetics, Faculty of Health Sciences, Ben Gurion University of the Negev, Beersheba, Israel.; Institute of Genetics, Soroka Medical Center and Faculty of Health Sciences, Ben Gurion University, Beer Sheba, Israel.
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Źródło :
Cell biochemistry and biophysics [Cell Biochem Biophys] 2022 Jun; Vol. 80 (2), pp. 375-384. Date of Electronic Publication: 2022 Feb 08.
Typ publikacji :
Journal Article
MeSH Terms :
Centromere*
Indoles*
Chromosome Aberrations ; Chromosome Banding ; Humans
Czasopismo naukowe
Tytuł :
[Clinical genetic analysis of an infant with 1q21.3-qter duplication and Xpter-p11 deletion caused by maternal balanced chromosomal translocation].
Autorzy :
Lin L; Institute of Genetics, Linyi People's Hospital, Linyi, Shandong 276000, China. .
Zhao C
Lv Y
Zhao X
Li L
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2022 May 10; Vol. 39 (5), pp. 514-517.
Typ publikacji :
Journal Article
MeSH Terms :
Genetic Testing*
Translocation, Genetic*
Chromosome Banding ; Chromosome Deletion ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping
Czasopismo naukowe
Tytuł :
[A rare case of dicentric ring chromosome and derivative ring chromosome Chimera].
Autorzy :
Zhu J; Hebei Maternal Hospital, Shijiazhuang, Hebei 050000, China. .
Yu X
Qi X
Cao Q
Zhu W
Yang D
Zhang H
Song Z
Wang S
Wang C
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2022 May 10; Vol. 39 (5), pp. 534-536.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosome Disorders*/genetics
Infertility*/genetics
Ring Chromosomes*
Adult ; Chimera ; Chromosome Banding ; Chromosome Deletion ; Dacarbazine ; Female ; Humans
Czasopismo naukowe
Tytuł :
[Genetic analysis and prenatal diagnosis of a fetus with Xq25 microduplication].
Autorzy :
Jing X; Prenatal Diagnostic Center, Guangzhou Women and Children' s Medical Centre, Guangzhou, Guangdong 510623, China. .
Pan M
Li R
Zhang Y
Li F
Li D
Liao C
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2022 Apr 10; Vol. 39 (4), pp. 425-427.
Typ publikacji :
Journal Article
MeSH Terms :
Fetus*
Prenatal Diagnosis*
Chromosome Banding ; Female ; Genetic Testing ; Humans ; Karyotyping ; Pregnancy
Czasopismo naukowe
Tytuł :
[Cytogenetic and molecular genetic analysis of three cases with small supernumerary marker chromosomes].
Autorzy :
Fan J; Shaoxing Women and Children's Health Care Hospital, Shaoxing, Zhejiang 312000, China. .
Zeng Y
Luo T
Che M
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Mar 10; Vol. 38 (3), pp. 264-267.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosome Banding*
Chromosome Disorders*
Karyotyping*
Cytogenetics ; Humans ; In Situ Hybridization, Fluorescence
Czasopismo naukowe
Tytuł :
Molecular Cytogenetics (Fluorescence In Situ Hybridization - FISH and Fluorochrome Banding): Resolving Species Relationships and Genome Organization.
Autorzy :
Siljak-Yakovlev S; University Paris-Saclay, CNRS, AgroParisTech, Ecologie Systématique Evolution, Orsay, France. .
Pustahija F; Faculty of Forestry, University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Vičić-Bočkor V; Faculty of Science, Department of Molecular Biology, University of Zagreb, Zagreb, Croatia.
Robin O; University Paris-Saclay, CNRS, AgroParisTech, Ecologie Systématique Evolution, Orsay, France.
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Źródło :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2021; Vol. 2222, pp. 363-379.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Banding*/methods
Cytogenetic Analysis*/methods
Genome*
Genomics*/methods
In Situ Hybridization, Fluorescence*/methods
Phylogeny*
Chromomycins/pharmacology ; DNA Barcoding, Taxonomic ; DNA, Ribosomal/genetics ; Pinus/classification ; Pinus/genetics
Czasopismo naukowe
Tytuł :
Chromosome Mapping of U2 snDNA in Species of Leptodactylus (Anura, Leptodactylidae).
Autorzy :
Gazoni T; Departamento de Biologia Geral e Aplicada, Instituto de Biociências, Universidade Estadual Paulista - UNESP, Rio Claro, Brazil.
Dorigon NS; Departamento de Biologia Geral e Aplicada, Instituto de Biociências, Universidade Estadual Paulista - UNESP, Rio Claro, Brazil.
da Silva MJ; Departamento de Biologia Geral e Aplicada, Instituto de Biociências, Universidade Estadual Paulista - UNESP, Rio Claro, Brazil.
Cholak LR; Departamento de Biologia Geral e Aplicada, Instituto de Biociências, Universidade Estadual Paulista - UNESP, Rio Claro, Brazil.
Haddad CFB; Departamento de Biodiversidade e Centro de Aquicultura, Instituto de Biociências, Universidade Estadual Paulista - UNESP, Rio Claro, Brazil.
Parise-Maltempi PP; Departamento de Biologia Geral e Aplicada, Instituto de Biociências, Universidade Estadual Paulista - UNESP, Rio Claro, Brazil.
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Źródło :
Cytogenetic and genome research [Cytogenet Genome Res] 2021; Vol. 161 (1-2), pp. 63-69. Date of Electronic Publication: 2021 Apr 06.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Banding*
Karyotype*
Anura/*genetics
Animals ; Chromosome Mapping ; Conserved Sequence ; Cytogenetics ; In Situ Hybridization, Fluorescence ; Karyotyping ; RNA, Small Nuclear/genetics ; Repetitive Sequences, Nucleic Acid ; Species Specificity
Czasopismo naukowe
Tytuł :
Chromosome banding analysis and genomic microarrays are both useful but not equivalent methods for genomic complexity risk stratification in chronic lymphocytic leukemia patients.
Autorzy :
Ramos-Campoy S; Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain; Translational Research on Hematological Neoplasms Group, Cancer Research Program, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain.
Puiggros A; Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain; Translational Research on Hematological Neoplasms Group, Cancer Research Program, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain. .
Beà S; Hematopathology Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBERONC, Barcelona, Spain.
Bougeon S; Oncogenomic Laboratory, Hematology Service, Lausanne University Hospital, Lausanne, Switzerland.
Larráyoz MJ; Cytogenetics and Hematological Genetics Services, Department of Genetics, University of Navarra, Pamplona, Spain.
Costa D; Hematopathology Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBERONC, Barcelona, Spain.
Parker H; Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Rigolin GM; Hematology Section, St. Anna University Hospital, Ferrara, Italy.
Ortega M; Department of Hematology, University Hospital Vall d'Hebron, Barcelona, Spain.
Blanco ML; Department of Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Collado R; Department of Hematology, Consorcio Hospital General Universitario, Valencia, Spain.
Salgado R; Cytogenetics Laboratory, Hematology Department, Fundación Jiménez Díaz, Madrid, Spain.
Baumann T; Hematopathology Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), CIBERONC, Barcelona, Spain.
Gimeno E; Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain; Applied Clinical Research in Hematological Malignances, Cancer Research Program, IMIMHospital del Mar, Barcelona, Spain.
Moreno C; Department of Hematology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Bosch F; Department of Hematology, University Hospital Vall d'Hebron, Barcelona, Spain.
Calvo X; Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain; Translational Research on Hematological Neoplasms Group, Cancer Research Program, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain.
Calasanz MJ; Cytogenetics and Hematological Genetics Services, Department of Genetics, University of Navarra, Pamplona, Spain.
Cuneo A; Hematology Section, St. Anna University Hospital, Ferrara, Italy.
Strefford JC; Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK.
Nguyen-Khac F; Hematology Department and Sorbonne Université, Hopital Pitie-Salpetriere, APHP, INSERM U1138, Paris, France.
Oscier D; Department of Molecular Pathology, Royal Bournemouth Hospital, Bournemouth, UK.
Haferlach C; MLL Munich Leukemia Laboratory, Munich, Germany.
Schoumans J; Oncogenomic Laboratory, Hematology Service, Lausanne University Hospital, Lausanne, Switzerland.
Espinet B; Molecular Cytogenetics Laboratory, Pathology Department, Hospital del Mar, Barcelona, Spain; Translational Research on Hematological Neoplasms Group, Cancer Research Program, Institut Hospital del Mar d'Investigacions Mèdiques (IMIM), Barcelona, Spain. .
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Źródło :
Haematologica [Haematologica] 2022 Mar 01; Vol. 107 (3), pp. 593-603. Date of Electronic Publication: 2022 Mar 01.
Typ publikacji :
Journal Article
MeSH Terms :
Leukemia, Lymphocytic, Chronic, B-Cell*/diagnosis
Leukemia, Lymphocytic, Chronic, B-Cell*/genetics
Chromosome Aberrations ; Chromosome Banding ; Genomics ; Humans ; Mutation ; Prognosis ; Risk Assessment
Czasopismo naukowe
Tytuł :
Prognostic heterogeneity of adult B-cell precursor acute lymphoblastic leukaemia patients with t(1;19)(q23;p13)/TCF3-PBX1 treated with measurable residual disease-oriented protocols.
Autorzy :
Ribera J; Josep Carreras Leukaemia Research Institute, ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
Granada I; Josep Carreras Leukaemia Research Institute, ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
Morgades M; Josep Carreras Leukaemia Research Institute, ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
González T; Hospital Universitario de Salamanca, Universidad de Salamanca, IBMCC (CSIC/USAL), IBSAL and CIBERONC, Salamanca, Spain.
Ciudad J; Cytometry Service (NUCLEUS) and Department of Medicine, Cancer Research Center (IBMCC-CSIC/USAL-IBSAL), University of Salamanca, Salamanca, Spain.; Centro de Investigación Biomédica en Red de Cáncer (CIBER-ONC) CB16/12/00400, Instituto de Salud Carlos III, Madrid, Spain.
Such E; Hematology Department, Hospital Universitari Politècnic La Fe, Valencia, Spain.
Calasanz MJ; Centro de Investigación Clínica Aplicada (CIMA), Universidad de Navarra, Pamplona, Spain.
Mercadal S; Hematology Department, ICO-Hospital Duran i Reynals, Hospitalet de Llobregat, Spain.
Coll R; Hematology Department, ICO-Hospital Josep Trueta, Girona, Spain.
González-Campos J; Hematology Department, Hospital Universitario Virgen del Rocío, Sevilla, Spain.
Tormo M; Hematology Department, Hospital Clínico Universitario, Valencia, Spain.
García-Cadenas I; Hematology Department, Hospital de Sant Pau, Josep Carreras Leukaemia Research Institute, Barcelona, Spain.
Gil C; Hematology Department, Hospital General de Alicante, Alicante, Spain.
Cervera M; Hematology Department, ICO-Hospital Joan XXIII, Tarragona, Spain.
Barba P; Hematology Department, Hospital Universitari Vall d'Hebrón, Barcelona, Spain.
Costa D; Haematopathology Section, Department of Pathology, Hospital Clínic, Barcelona, Spain.
Ayala R; Hematology Department, Hospital Universitario Doce de Octubre, Madrid, Spain.
Bermúdez A; Hematology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain.
Orfao A; Cytometry Service (NUCLEUS) and Department of Medicine, Cancer Research Center (IBMCC-CSIC/USAL-IBSAL), University of Salamanca, Salamanca, Spain.; Centro de Investigación Biomédica en Red de Cáncer (CIBER-ONC) CB16/12/00400, Instituto de Salud Carlos III, Madrid, Spain.
Ribera JM; Josep Carreras Leukaemia Research Institute, ICO-Hospital Germans Trias i Pujol, Universitat Autònoma de Barcelona, Badalona, Spain.
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Corporate Authors :
Programa para el Tratamiento de Hemopatias Malignas (PETHEMA) Group (Spanish Society of Hematology, SEHH)
Źródło :
British journal of haematology [Br J Haematol] 2022 Feb; Vol. 196 (3), pp. 670-675. Date of Electronic Publication: 2021 Sep 21.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 1*
Chromosomes, Human, Pair 19*
Translocation, Genetic*
Neoplasm, Residual/*therapy
Oncogene Proteins, Fusion/*genetics
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/*therapy
Adolescent ; Adult ; Antineoplastic Combined Chemotherapy Protocols/adverse effects ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Chromosome Banding ; Disease Management ; Female ; Humans ; Male ; Middle Aged ; Neoplasm Metastasis ; Neoplasm Staging ; Neoplasm, Residual/diagnosis ; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/diagnosis ; Precursor B-Cell Lymphoblastic Leukemia-Lymphoma/mortality ; Prognosis ; Remission Induction ; Treatment Outcome ; Young Adult
Czasopismo naukowe
Tytuł :
[Genetic analysis of a case with 2q37 microdeletion syndrome].
Autorzy :
Lian X; Laboratory of Basic Medicine, Dongfang Hospital (900th Hospital of Joint Logistics Support Force), Xiamen University, Fuzhou, Fujian 350025, China. .
Zhang X
Huang M
Lin J
Zeng J
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2022 Jan 10; Vol. 39 (1), pp. 81-84.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Deletion*
Chromosome Banding ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Phenotype
Czasopismo naukowe
Tytuł :
Classification of fluorescent R-Band metaphase chromosomes using a convolutional neural network is precise and fast in generating karyograms of hematologic neoplastic cells.
Autorzy :
Vajen B; Department of Human Genetics, Hannover Medical School, Hannover 30625, Germany. Electronic address: .
Hänselmann S; MetaSystems Hard and Software GmbH, Robert-Bosch-Str. 6, Altlussheim 68804, Germany.
Lutterloh F; Department of Human Genetics, Hannover Medical School, Hannover 30625, Germany.
Käfer S; Department of Human Genetics, Hannover Medical School, Hannover 30625, Germany.
Espenkötter J; Department of Human Genetics, Hannover Medical School, Hannover 30625, Germany.
Beening A; Department of Human Genetics, Hannover Medical School, Hannover 30625, Germany.
Bogin J; MetaSystems Hard and Software GmbH, Robert-Bosch-Str. 6, Altlussheim 68804, Germany.
Schlegelberger B; Department of Human Genetics, Hannover Medical School, Hannover 30625, Germany.
Göhring G; Department of Human Genetics, Hannover Medical School, Hannover 30625, Germany.
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Źródło :
Cancer genetics [Cancer Genet] 2022 Jan; Vol. 260-261, pp. 23-29. Date of Electronic Publication: 2021 Nov 20.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Banding/*methods
Hematologic Neoplasms/*genetics
Spectral Karyotyping/*methods
Algorithms ; Female ; Humans ; Male ; Metaphase ; Neural Networks, Computer ; Reproducibility of Results ; Time Factors
Czasopismo naukowe
Tytuł :
Cryptic TCF3 fusions in childhood leukemia: Detection by RNA sequencing.
Autorzy :
Salim M; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Heldt F; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Thomay K; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Lentes J; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Behrens YL; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Kaune B; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Möricke A; General Paediatrics, University Hospital Schleswig-Holstein, Kiel, Germany.
Cario G; General Paediatrics, University Hospital Schleswig-Holstein, Kiel, Germany.
Schieck M; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Hofmann W; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Davenport C; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Steinemann D; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Schrappe M; General Paediatrics, University Hospital Schleswig-Holstein, Kiel, Germany.
Schlegelberger B; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
Göhring G; Department of Human Genetics, Hannover Medical School, Hannover, Germany.
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Źródło :
Genes, chromosomes & cancer [Genes Chromosomes Cancer] 2022 Jan; Vol. 61 (1), pp. 22-26. Date of Electronic Publication: 2021 Sep 13.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Sequence Analysis, RNA*
Basic Helix-Loop-Helix Transcription Factors/*genetics
Oncogene Proteins, Fusion/*genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma/*genetics
Child ; Chromosome Banding ; Humans ; In Situ Hybridization, Fluorescence ; Pilot Projects ; Polymerase Chain Reaction ; Prognosis ; Proto-Oncogene Protein c-fli-1/genetics ; Translocation, Genetic
Czasopismo naukowe
Tytuł :
Characterizing the Genetic Stability of Human Naïve and Primed Pluripotent Stem Cells.
Autorzy :
Baker D; Sheffield Diagnostic Genetic Services, Sheffield Children's Hospital, Sheffield, UK.
Barbaric I; Centre for Stem Cell Biology, Department of Biomedical Science, The University of Sheffield, Western Bank, Sheffield, UK. .
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Źródło :
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2022; Vol. 2416, pp. 267-284.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Pluripotent Stem Cells*
Cell Differentiation ; Chromosome Aberrations ; Chromosome Banding ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping
Czasopismo naukowe
Tytuł :
[Genetic analysis of a pedigree with atypical partial 4q trisomy].
Autorzy :
Zhang Q; Henan Provincial Key Laboratory of Medical Genetics, Institute of Medical Genetics, Henan Provincial People's Hospital, Zhengzhou, Henan 450003, China. .
Wu D
Zhang M
Zhang X
Xiao H
Gao Y
Li X
Wang F
Zhang X
Yan F
Liao S
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Dec 10; Vol. 38 (12), pp. 1245-1249.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Genetic Testing*
Trisomy*/genetics
Adult ; Chromosome Banding ; Female ; Humans ; Karyotyping ; Male ; Pedigree
Czasopismo naukowe
Tytuł :
Detailed chromosome analysis of wild-type, immortalized fibroblasts with SV40T, E6E7, combinational introduction of cyclin dependent kinase 4, cyclin D1, telomerase reverse transcriptase.
Autorzy :
Takada H; Graduate School of Science and Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate, 020-8551, Japan.
Miura T; Department of Risk Analysis and Biodosimetry, Institute of Radiation Emergency Medicine, Hirosaki University, Aomori, 036-8564, Japan. .
Fujibayashi S; Graduate School of Science and Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate, 020-8551, Japan.
Sasaki N; Department of Risk Analysis and Biodosimetry, Institute of Radiation Emergency Medicine, Hirosaki University, Aomori, 036-8564, Japan.
Takahashi K; Graduate School of Science and Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate, 020-8551, Japan.
Sugano E; Graduate School of Science and Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate, 020-8551, Japan.
Tomita H; Graduate School of Science and Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate, 020-8551, Japan.
Ozaki T; Graduate School of Science and Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate, 020-8551, Japan.
Kiyono T; Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, 6-5-1 Kashiwanoha, Kashiwa-city, Chiba, 277-8577, Japan. .
Yoshida MA; Institute of Chromosome Life Science (ICLS), 2-11-5-409 Fukuokachuo, Fujimino, Saitama, 356-0031, Japan.
Fukuda T; Graduate School of Science and Engineering, Iwate University, 4-3-5 Ueda, Morioka, Iwate, 020-8551, Japan. .
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Źródło :
In vitro cellular & developmental biology. Animal [In Vitro Cell Dev Biol Anim] 2021 Dec; Vol. 57 (10), pp. 998-1005. Date of Electronic Publication: 2021 Dec 10.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosomes, Human*
Cyclin D1/*genetics
Cyclin-Dependent Kinase 4/*genetics
Fibroblasts/*cytology
Telomerase/*genetics
Antigens, Polyomavirus Transforming/genetics ; Cell Cycle/genetics ; Cell Line, Transformed ; Chromosome Banding ; Humans ; Karyotyping ; Oncogene Proteins, Viral/genetics
Czasopismo naukowe
Tytuł :
Recurrence of an early postzygotic rescue of an inherited unbalanced translocation resulting in mosaic segmental uniparental isodisomy of chromosome 11q in siblings.
Autorzy :
Blanluet M; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Chantot-Bastaraud S; Department of Medical Genetics and Embryology, Armand-Trousseau Children Hospital, AP-HP, Paris, France.
Chambon P; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Cassinari K; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Vera G; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Goldenberg A; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Keren B; Genetics Department, La Pitié-Salpêtrière Hospital, AP-HP, Paris, France.
Le Meur N; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Hannequin D; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Mace B; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Siffroi JP; Department of Medical Genetics and Embryology, Armand-Trousseau Children Hospital, AP-HP, Paris, France.
Frebourg T; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Nicolas G; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
Joly-Helas G; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000, Rouen, France.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2021 Oct; Vol. 185 (10), pp. 3057-3061. Date of Electronic Publication: 2021 May 27.
Typ publikacji :
Case Reports
MeSH Terms :
Uniparental Disomy*
Abnormalities, Multiple/*genetics
Intellectual Disability/*genetics
Kyphosis/*genetics
Scoliosis/*genetics
Abnormalities, Multiple/pathology ; Cervical Vertebrae/pathology ; Chromosome Banding ; Chromosome Deletion ; Chromosomes/genetics ; Chromosomes, Human, Pair 11/genetics ; Chromosomes, Human, Pair 2/genetics ; Female ; Genetic Predisposition to Disease ; Humans ; In Situ Hybridization, Fluorescence ; Intellectual Disability/pathology ; Karyotyping ; Kyphosis/pathology ; Male ; Mosaicism ; Scoliosis/pathology ; Siblings ; Translocation, Genetic/genetics
SCR Disease Name :
Kyphoscoliosis 1
Raport
Tytuł :
Faint gray bands in Drosophila melanogaster polytene chromosomes are formed by coding sequences of housekeeping genes.
Autorzy :
Demakova OV; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Demakov SA; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Boldyreva LV; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Zykova TY; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Levitsky VG; Novosibirsk State University, Novosibirsk, 630090, Russia.; Institute of Cytology and Genetics, SB RAS, 630090, Novosibirsk, Russia.
Semeshin VF; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Pokholkova GV; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Sidorenko DS; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Goncharov FP; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Belyaeva ES; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia.
Zhimulev IF; Institute of Molecular and Cellular Biology, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave. 8/2, Novosibirsk, 630090, Russia. .; Novosibirsk State University, Novosibirsk, 630090, Russia. .
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Źródło :
Chromosoma [Chromosoma] 2020 Mar; Vol. 129 (1), pp. 25-44. Date of Electronic Publication: 2019 Dec 09.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosome Banding*
Genes, Essential*
Open Reading Frames*
Drosophila melanogaster/*genetics
Polytene Chromosomes/*genetics
Animals ; Arabidopsis Proteins/metabolism ; Chromatin/genetics ; Computational Biology/methods ; Drosophila Proteins/metabolism ; Female ; Gene Rearrangement ; Histones/metabolism ; In Situ Hybridization, Fluorescence ; Ion Channels/metabolism ; Male ; Mutation ; Protein Serine-Threonine Kinases/metabolism ; Sex Chromosomes
Czasopismo naukowe
Tytuł :
Comparative Cytogenetics of Four Sea Turtle Species (Cheloniidae): G-Banding Pattern and in situ Localization of Repetitive DNA Units.
Autorzy :
Machado CRD; Programa de Pós-Graduação em Biologia Evolutiva, Universidade Estadual de Ponta Grossa, Ponta Grossa, Brazil.
Glugoski L; Programa de Pós-Graduação em Biologia Evolutiva, Universidade Estadual de Ponta Grossa, Ponta Grossa, Brazil.
Domit C; Laboratório de Ecologia e Conservação, Universidade Federal do Paraná, Pontal do Paraná, Brazil.
Pucci MB; Departamento de Saúde II, Universidade Nove de Julho, Bauru, Brazil.
Goldberg DW; E-conservation, Universidade Santa Úrsula, Rio de Janeiro, Brazil.
Marinho LA; Prefeitura Municipal de Natal, Natal, Brazil.
da Costa GWWF; Departamento de Biologia Celular e Genética, Universidade Federal do Rio Grande do Norte, Natal, Brazil.
Nogaroto V; Programa de Pós-Graduação em Biologia Evolutiva, Universidade Estadual de Ponta Grossa, Ponta Grossa, Brazil.
Vicari MR; Programa de Pós-Graduação em Biologia Evolutiva, Universidade Estadual de Ponta Grossa, Ponta Grossa, Brazil, .
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Źródło :
Cytogenetic and genome research [Cytogenet Genome Res] 2020; Vol. 160 (9), pp. 531-538. Date of Electronic Publication: 2020 Oct 29.
Typ publikacji :
Comparative Study; Journal Article
MeSH Terms :
Chromosome Banding*
Repetitive Sequences, Nucleic Acid*
DNA/*genetics
Turtles/*genetics
Animals ; DNA, Ribosomal/genetics ; Evolution, Molecular ; Female ; In Situ Hybridization, Fluorescence ; Karyotype ; Male ; RNA, Ribosomal, 18S/genetics ; Species Specificity
Czasopismo naukowe
Tytuł :
[Genetic testing and prenatal diagnosis for a family with 10q22.3q23.2 microdeletion].
Autorzy :
Zeng L; Center of Prenatal Diagnosis, the Affiliated Hospital of Putian College, Putian, Fujian 351100, China. .
Zhang Y
Lin L
Dong X
Li L
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Aug 10; Vol. 38 (8), pp. 768-770.
Typ publikacji :
Journal Article
MeSH Terms :
Genetic Testing*
Prenatal Diagnosis*
Cadherin Related Proteins ; Cadherins ; Chromosome Banding ; Chromosome Deletion ; Female ; Fetus ; Humans ; Karyotyping ; Nerve Tissue Proteins ; Pregnancy
Czasopismo naukowe

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