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Tytuł :
Genome collinearity analysis illuminates the evolution of donkey chromosome 1 and horse chromosome 5 in perissodactyls: A comparative study.
Autorzy :
Li S; Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.; College of Basic Medicine, Inner Mongolia Medical University, Hohhot, 010110, China.; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Zhao G; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Han H; Department of Physical Education, Hohhot Minzu College, Hohhot, 010051, China.
Li Y; Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Sciences, Inner Mongolia University, Hohhot, 010070, China.; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Li J; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China.
Wang J; College of Basic Medicine, Inner Mongolia Medical University, Hohhot, 010110, China.
Cao G; College of Veterinary Science, Inner Mongolia Agricultural University, Hohhot, 010018, China.
Li X; Research Center for Animal Genetic Resources of Mongolia Plateau, College of Life Sciences, Inner Mongolia University, Hohhot, 010070, China. .; Inner Mongolia Saikexing Institute of Breeding and Reproductive Biotechnology in Domestic Animal, Hohhot, 011517, China. .
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Źródło :
BMC genomics [BMC Genomics] 2021 Sep 15; Vol. 22 (1), pp. 665. Date of Electronic Publication: 2021 Sep 15.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosomes, Human, Pair 1*
Equidae*/genetics
Animals ; Chromosomes/genetics ; Chromosomes, Human, Pair 5 ; Genome ; Horses/genetics ; Humans
Czasopismo naukowe
Tytuł :
A prenatal case with multiple supernumerary markers identified as derivatives of chromosomes 13, 15, and 20: molecular cytogenetic characterization and review of the literature.
Autorzy :
Bertini V; Cytogenetics Unit, Department of Laboratory Medicine, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Giuliani C; Cytogenetics Unit, Department of Laboratory Medicine, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Ferreri MI; Cytogenetics Unit, Department of Laboratory Medicine, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Orsini A; Section Of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Bonuccelli A; Section Of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Peroni D; Section Of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Bonaglia C; Cytogenetics Laboratory, Scientific Institute, IRCSS Eugenio Medea, Bosisio Parini, Italy.
Valetto A; Cytogenetics Unit, Department of Laboratory Medicine, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
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Źródło :
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians [J Matern Fetal Neonatal Med] 2021 Sep; Vol. 34 (17), pp. 2918-2922. Date of Electronic Publication: 2019 Oct 01.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Chromosome Aberrations*
Chromosomes, Human, Pair 13*/genetics
Chromosomes ; Cytogenetic Analysis ; Female ; Genetic Markers ; Humans ; Pregnancy
Czasopismo naukowe
Tytuł :
Molecular characterization of the Yp11.2 region deletion in the Chinese Han population.
Autorzy :
Pang Q; Jining Medical University, Jining, 272067, China. .; Center for Forensic Science, Jining Medical University, Jining, 272067, China. .
Lin Q; Jining Medical University, Jining, 272067, China.
Wang D; Jining Medical University, Jining, 272067, China.
Sun Z; Jining Medical University, Jining, 272067, China.
Wang J; Jining Medical University, Jining, 272067, China.
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Źródło :
International journal of legal medicine [Int J Legal Med] 2021 Jul; Vol. 135 (4), pp. 1351-1358. Date of Electronic Publication: 2021 Apr 26.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Deletion*
Chromosomes, Human, Y*
Genetic Loci*
Sequence Tagged Sites*
Amelogenin/genetics ; Asian Continental Ancestry Group/genetics ; Cadherins/genetics ; Cell Cycle Proteins/genetics ; Chromosome Breakpoints ; Chromosomes, Human, Pair 11 ; Humans ; Male ; Microsatellite Repeats ; Protein-Serine-Threonine Kinases/genetics ; Transducin/genetics
SCR Disease Name :
Chromosome 11, deletion 11p
Czasopismo naukowe
Tytuł :
Sex chromosomes in the Vizcacheras' White-lipped frog, Leptodactylus bufonius (Anura, Leptodactylidae).
Autorzy :
Schneider RG; Laboratorio de Genética Evolutiva 'Claudio Juan Bidau', Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Félix de Azara 1552, 6to Piso, CPA N3300LQF, Posadas, Misiones, Argentina.
Ferro JM; Laboratorio de Genética Evolutiva 'Claudio Juan Bidau', Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Félix de Azara 1552, 6to Piso, CPA N3300LQF, Posadas, Misiones, Argentina.
Reinko IN; Laboratorio de Genética Evolutiva 'Claudio Juan Bidau', Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Félix de Azara 1552, 6to Piso, CPA N3300LQF, Posadas, Misiones, Argentina.
Boeris JM; Laboratorio de Genética Evolutiva 'Claudio Juan Bidau', Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Félix de Azara 1552, 6to Piso, CPA N3300LQF, Posadas, Misiones, Argentina.
Cardozo DE; Laboratorio de Genética Evolutiva 'Claudio Juan Bidau', Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Félix de Azara 1552, 6to Piso, CPA N3300LQF, Posadas, Misiones, Argentina.
Baldo D; Laboratorio de Genética Evolutiva 'Claudio Juan Bidau', Instituto de Biología Subtropical (CONICET-UNaM), Facultad de Ciencias Exactas, Químicas y Naturales, Universidad Nacional de Misiones, Félix de Azara 1552, 6to Piso, CPA N3300LQF, Posadas, Misiones, Argentina.
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Źródło :
Anais da Academia Brasileira de Ciencias [An Acad Bras Cienc] 2021 Jun 04; Vol. 93 (2), pp. e20190426. Date of Electronic Publication: 2021 Jun 04 (Print Publication: 2021).
Typ publikacji :
Journal Article
MeSH Terms :
Anura*/genetics
Sex Chromosomes*/genetics
Animals ; Argentina ; Chromosome Banding ; Chromosomes/genetics ; Female ; In Situ Hybridization, Fluorescence ; Male
Czasopismo naukowe
Tytuł :
A novel aberration of COL1A1-PDGFB fusion as an insertion in chromosome 15 in one case of dermatofibrosarcoma protuberans involving a rare location.
Autorzy :
Daoud A; Department of Dermatology, Stony Brook University, Stony Brook, New York, USA.
Cunningham CR; Department of Pathology, University of Missouri, Columbia, Missouri, USA.
Kozel JA; MAWD Pathology Group, 9705 Lenexa Dr, Lenexa, Kansas, USA.
Slutsky JB; Department of Dermatology, Stony Brook University, Stony Brook, New York, USA.
Varade R; DuPage Medical Group, Joliet, Illinois, USA.
Batanian JR; Department of Pediatrics and Pathology, Saint Louis University Medical School, St. Louis, Missouri, USA.
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Źródło :
Journal of cutaneous pathology [J Cutan Pathol] 2021 Feb; Vol. 48 (2), pp. 285-289. Date of Electronic Publication: 2020 Jul 06.
Typ publikacji :
Case Reports
MeSH Terms :
Chromosomes, Human, Pair 15*/genetics
Chromosomes, Human, Pair 15*/metabolism
Facial Neoplasms*/genetics
Facial Neoplasms*/metabolism
Facial Neoplasms*/pathology
Fibrosarcoma*/genetics
Fibrosarcoma*/metabolism
Fibrosarcoma*/pathology
Mutagenesis, Insertional*
Oncogene Proteins, Fusion*/genetics
Oncogene Proteins, Fusion*/metabolism
Skin Neoplasms*/genetics
Skin Neoplasms*/metabolism
Skin Neoplasms*/pathology
Adult ; Chromosomes, Human, Pair 17/genetics ; Chromosomes, Human, Pair 17/metabolism ; Chromosomes, Human, Pair 22/genetics ; Chromosomes, Human, Pair 22/metabolism ; Humans ; Male ; Translocation, Genetic
Raport
Tytuł :
Robbing Peter to Pay Paul: Competition for Radiogenic Breaks During Rejoining Diminishes Curvature in the Dose Response for Simple Chromosome Exchanges.
Autorzy :
Shuryak I; Center for Radiological Research, Columbia University Irving Medical Center, New York, New York.
Loucas BD; Department of Radiation Oncology, University of Texas Medical Branch, Galveston, Texas.
Cornforth MN; Department of Radiation Oncology, University of Texas Medical Branch, Galveston, Texas.
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Źródło :
Radiation research [Radiat Res] 2021 Aug 01; Vol. 196 (2), pp. 147-155.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Radiation Dosage*
Chromosome Aberrations/*radiation effects
Chromosome Breakage/*radiation effects
Chromosomes, Human/*radiation effects
Chromosomes/genetics ; Chromosomes/radiation effects ; Dose-Response Relationship, Radiation ; Gamma Rays/adverse effects ; Humans ; In Situ Hybridization, Fluorescence ; Lymphocytes/radiation effects ; Models, Theoretical ; X-Rays/adverse effects
Czasopismo naukowe
Tytuł :
Genome-wide association mapping uncovers sex-associated copy number variation markers and female hemizygous regions on the W chromosome in Salix viminalis.
Autorzy :
Hallingbäck HR; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Box 7080, SE-750 07, Uppsala, Sweden.; Present Address: Skogforsk (The Forestry Research Institute of Sweden), Uppsala Science Park, SE-751 83, Uppsala, Sweden.
Pucholt P; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Box 7080, SE-750 07, Uppsala, Sweden.
Ingvarsson PK; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Box 7080, SE-750 07, Uppsala, Sweden.
Rönnberg-Wästljung AC; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Box 7080, SE-750 07, Uppsala, Sweden. .
Berlin S; Department of Plant Biology, Uppsala BioCenter, Swedish University of Agricultural Sciences and Linnean Center for Plant Biology, Box 7080, SE-750 07, Uppsala, Sweden.
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Źródło :
BMC genomics [BMC Genomics] 2021 Oct 02; Vol. 22 (1), pp. 710. Date of Electronic Publication: 2021 Oct 02.
Typ publikacji :
Journal Article
MeSH Terms :
DNA Copy Number Variations*
Salix*/genetics
Chromosomes, Plant/*genetics
Genetic Markers ; Genome-Wide Association Study ; Sex Chromosomes/genetics
Czasopismo naukowe
Tytuł :
Acute myeloid leukemia with 11q23 rearrangements: A study of therapy-related disease and therapeutic outcomes.
Autorzy :
Menghrajani K; Memorial Sloan Kettering Cancer Center, USA. Electronic address: .
Zhang Y; Memorial Sloan Kettering Cancer Center, USA.
Famulare C; Memorial Sloan Kettering Cancer Center, USA.
Devlin SM; Memorial Sloan Kettering Cancer Center, USA.
Tallman MS; Memorial Sloan Kettering Cancer Center, USA; Weill-Cornell Medical College, USA.
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Źródło :
Leukemia research [Leuk Res] 2020 Nov; Vol. 98, pp. 106453. Date of Electronic Publication: 2020 Sep 16.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Breast Neoplasms*/drug therapy
Breast Neoplasms*/genetics
Breast Neoplasms*/metabolism
Breast Neoplasms*/pathology
Chromosomes, Human, Pair 11*/genetics
Chromosomes, Human, Pair 11*/metabolism
Leukemia, Myeloid, Acute*/drug therapy
Leukemia, Myeloid, Acute*/genetics
Leukemia, Myeloid, Acute*/metabolism
Leukemia, Myeloid, Acute*/pathology
Neoplasms, Second Primary*/drug therapy
Neoplasms, Second Primary*/genetics
Neoplasms, Second Primary*/metabolism
Neoplasms, Second Primary*/pathology
Translocation, Genetic*
Anthracyclines/*administration & dosage
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Chromosomes, Human, Pair 19/genetics ; Chromosomes, Human, Pair 19/metabolism ; Chromosomes, Human, Pair 9/genetics ; Chromosomes, Human, Pair 9/metabolism ; Female ; Humans ; Male ; Middle Aged
Czasopismo naukowe
Tytuł :
Xp;Yq Unbalanced Translocation with Pseudoautosomal Region Aberrations in a Natural Two-Generation Transmission.
Autorzy :
Jiang Y; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital of Jilin University, Changchun, China.; Jilin Engineering Research Center for Reproductive Medicine and Genetics, Changchun, China.
Yu Y; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital of Jilin University, Changchun, China.; Jilin Engineering Research Center for Reproductive Medicine and Genetics, Changchun, China.
Zhang H; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital of Jilin University, Changchun, China.; Jilin Engineering Research Center for Reproductive Medicine and Genetics, Changchun, China.
Zhang H; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital of Jilin University, Changchun, China.; Jilin Engineering Research Center for Reproductive Medicine and Genetics, Changchun, China.
Sun M; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital of Jilin University, Changchun, China.; Jilin Engineering Research Center for Reproductive Medicine and Genetics, Changchun, China.
Liu R; Center for Reproductive Medicine, Center for Prenatal Diagnosis, First Hospital of Jilin University, Changchun, China.; Jilin Engineering Research Center for Reproductive Medicine and Genetics, Changchun, China.
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Źródło :
BioMed research international [Biomed Res Int] 2020 Dec 01; Vol. 2020, pp. 4976204. Date of Electronic Publication: 2020 Dec 01 (Print Publication: 2020).
Typ publikacji :
Journal Article
MeSH Terms :
Chromosomes, Human, X*
Chromosomes, Human, Y*
In Situ Hybridization, Fluorescence*
Translocation, Genetic*
Chromosome Aberrations ; Chromosome Deletion ; Chromosome Duplication ; Chromosomes ; Comparative Genomic Hybridization ; Cytogenetics ; Gene Deletion ; Humans ; Karyotyping ; Male ; Metaphase ; Oligonucleotide Array Sequence Analysis ; Pseudoautosomal Regions ; Risk Factors ; Spermatogenesis ; User-Computer Interface
Czasopismo naukowe
Tytuł :
Bacillus subtilis Smc condenses chromosomes in a heterologous cell system, which is down-regulated by ScpAB.
Autorzy :
Knust T; Agilent Technologies R&D and Marketing GmbH & Co. KG, Hewlett-Packard-Strasse 8, 76337, Waldbronn, Germany.
Graumann PL; SYNMIKRO, LOEWE-Zentrum Für Synthetische Mikrobiologie, Hans-Meerwein-Straße, 35043, Marburg, Germany. .; Fachbereich Chemie, Hans-Meerwein-Straße 4, 35032, Marburg, Germany. .
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Źródło :
BMC research notes [BMC Res Notes] 2020 Nov 11; Vol. 13 (1), pp. 524. Date of Electronic Publication: 2020 Nov 11.
Typ publikacji :
Journal Article
MeSH Terms :
Bacillus subtilis*/genetics
Bacterial Proteins*/genetics
Chromosomes, Bacterial*/genetics
Cell Cycle Proteins/genetics ; Chromosomes ; Escherichia coli
Czasopismo naukowe
Tytuł :
Hypospadias in ring X syndrome.
Autorzy :
Elghezal H; Cytogenetics and Molecular Genetics Division, Prince Sultan Military Medical City, Riyadh, Saudi Arabia. Electronic address: .
Alfayez K; Cytogenetics and Molecular Genetics Division, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Ben Abdallah I; Cytogenetics and Molecular Genetics Division, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Alfares A; Division of Genetic and Metabolic Medicine, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Almazyad A; Cytogenetics and Molecular Genetics Division, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Al Jasser A; Division of Endocrinology, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Almobadel N; Cytogenetics and Molecular Genetics Division, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Alsuhaibani O; Central Military Laboratory and Blood Bank Department, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.
Alhashem A; Division of Genetic and Metabolic Medicine, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.
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Źródło :
European journal of medical genetics [Eur J Med Genet] 2021 Jul; Vol. 64 (7), pp. 104225. Date of Electronic Publication: 2021 Apr 16.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Ring Chromosomes*
Chromosome Disorders/*genetics
Chromosomes, Human, X/*genetics
Hypospadias/*genetics
Microcephaly/*genetics
Child, Preschool ; Chromosome Disorders/pathology ; Gene Deletion ; Gene Duplication ; Humans ; Hypospadias/pathology ; Male ; Microcephaly/pathology ; Short Stature Homeobox Protein/genetics ; Syndrome
Czasopismo naukowe
Tytuł :
3D genomics across the tree of life reveals condensin II as a determinant of architecture type.
Autorzy :
Hoencamp C; Division of Gene Regulation, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Dudchenko O; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.; Center for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.
Elbatsh AMO; Division of Gene Regulation, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Brahmachari S; Center for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.
Raaijmakers JA; Division of Cell Biology, Oncode Institute, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
van Schaik T; Division of Gene Regulation, Oncode Institute, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Sedeño Cacciatore Á; Division of Gene Regulation, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Contessoto VG; Center for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.; Department of Physics, Institute of Biosciences, Letters and Exact Sciences, São Paulo State University (UNESP), São José do Rio Preto - SP, 15054-000, Brazil.
van Heesbeen RGHP; Division of Cell Biology, Oncode Institute, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
van den Broek B; BioImaging Facility, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Mhaskar AN; Division of Gene Regulation, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Teunissen H; Division of Gene Regulation, Oncode Institute, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
St Hilaire BG; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Weisz D; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Omer AD; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.
Pham M; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.
Colaric Z; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.
Yang Z; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech, Pudong 201210, China.
Rao SSP; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.; Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Mitra N; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Lui C; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.
Yao W; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.
Khan R; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Moroz LL; Whitney Laboratory and Department of Neuroscience, University of Florida, Gainesville, FL 32611, USA.
Kohn A; Whitney Laboratory and Department of Neuroscience, University of Florida, Gainesville, FL 32611, USA.
St Leger J; Department of Biosciences, Cornell University College of Veterinary Medicine, Ithaca, NY 14853, USA.
Mena A; SeaWorld San Diego, San Diego, CA 92109, USA.
Holcroft K; Moody Gardens, Galveston, TX 77554, USA.
Gambetta MC; Center for Integrative Genomics, University of Lausanne, 1015 Lausanne, Switzerland.
Lim F; Department of Medicine and Molecular Biology, University of California, San Diego, La Jolla, CA 92093, USA.
Farley E; Department of Medicine and Molecular Biology, University of California, San Diego, La Jolla, CA 92093, USA.
Stein N; Leibniz Institute of Plant Genetics and Crop Plant Research (IPK Gatersleben), 06466 Seeland, Germany.; Center of Integrated Breeding Research (CiBreed), Department of Crop Sciences, Georg-August-University Göttingen, 37075 Göttingen, Germany.; UWA School of Agriculture and Environment, The University of Western Australia, Perth, WA 6009, Australia.
Haddad A; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA.
Chauss D; National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Mutlu AS; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.
Wang MC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.; Huffington Center on Aging, Baylor College of Medicine, Houston, TX 77030, USA.; Howard Hughes Medical Institute, Baylor College of Medicine, Houston, TX 77030, USA.
Young ND; Faculty of Veterinary and Agricultural Sciences, University of Melbourne, Parkville, VIC 3010, Australia.
Hildebrandt E; Avian Diseases and Oncology Laboratory, US Department of Agriculture, Agricultural Research Service, East Lansing, MI 48823, USA.
Cheng HH; Avian Diseases and Oncology Laboratory, US Department of Agriculture, Agricultural Research Service, East Lansing, MI 48823, USA.
Knight CJ; Hopkins Marine Station, Stanford University, Pacific Grove, CA 93950, USA.
Burnham TLU; Department of Wildlife, Fish, and Conservation Biology, University of California, Davis, Davis, CA 95616, USA.; Coastal and Marine Institute and Department of Biology, San Diego State University, San Diego, CA 92106, USA.
Hovel KA; Coastal and Marine Institute and Department of Biology, San Diego State University, San Diego, CA 92106, USA.
Beel AJ; Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Mattei PJ; Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Kornberg RD; Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Warren WC; Department of Animal Sciences, University of Missouri, Columbia, MO 65211, USA.
Cary G; The Jackson Laboratory, Bar Harbor, ME 04609, USA.
Gómez-Skarmeta JL; Centro Andaluz de Biología del Desarrollo CSIC, Universidad Pablo de Olavide, 41013 Sevilla, Spain.
Hinman V; Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA.
Lindblad-Toh K; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.; Science for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, 751 23 Uppsala, Sweden.
Di Palma F; Department of Biological Sciences, University of East Anglia, Norwich NR4 7TJ, UK.
Maeshima K; Genome Dynamics Laboratory, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan.; Department of Genetics, Sokendai (Graduate University for Advanced Studies), Mishima, Shizuoka 411-8540, Japan.
Multani AS; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Pathak S; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Nel-Themaat L; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Behringer RR; Department of Genetics, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Kaur P; UWA School of Agriculture and Environment, The University of Western Australia, Perth, WA 6009, Australia.
Medema RH; Division of Cell Biology, Oncode Institute, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
van Steensel B; Division of Gene Regulation, Oncode Institute, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
de Wit E; Division of Gene Regulation, Oncode Institute, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands.
Onuchic JN; Center for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.; Departments of Physics and Astronomy, Chemistry, and Biosciences, Rice University, Houston, TX 77005, USA.
Di Pierro M; Center for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.; Department of Physics, Northeastern University, Boston, MA 02115, USA.
Lieberman Aiden E; The Center for Genome Architecture, Baylor College of Medicine, Houston, TX 77030, USA. .; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.; Center for Theoretical Biological Physics, Rice University, Houston, TX 77005, USA.; Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech, Pudong 201210, China.; UWA School of Agriculture and Environment, The University of Western Australia, Perth, WA 6009, Australia.; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Rowland BD; Division of Gene Regulation, Netherlands Cancer Institute, 1066 CX Amsterdam, Netherlands. .
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Źródło :
Science (New York, N.Y.) [Science] 2021 May 28; Vol. 372 (6545), pp. 984-989.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Biological Evolution*
Genome*
Adenosine Triphosphatases/*genetics
Adenosine Triphosphatases/*physiology
Chromosomes/*ultrastructure
DNA-Binding Proteins/*genetics
DNA-Binding Proteins/*physiology
Eukaryota/*genetics
Multiprotein Complexes/*genetics
Multiprotein Complexes/*physiology
Adenosine Triphosphatases/chemistry ; Algorithms ; Animals ; Cell Nucleolus/ultrastructure ; Cell Nucleus/ultrastructure ; Centromere/ultrastructure ; Chromosomes/chemistry ; Chromosomes, Human/chemistry ; Chromosomes, Human/ultrastructure ; DNA-Binding Proteins/chemistry ; Genome, Human ; Genomics ; Heterochromatin/ultrastructure ; Humans ; Interphase ; Mitosis ; Models, Biological ; Multiprotein Complexes/chemistry ; Telomere/ultrastructure
Czasopismo naukowe
Tytuł :
Generation of iPSC line ICGi024-A from human skin fibroblasts of a patient with ring chromosome 18.
Autorzy :
Khabarova AA; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russia. Electronic address: .
Pristyazhnyuk IE; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russia.
Orlova PA; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russia.
Nikitina TV; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia.
Kashevarova AA; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia.
Lopatkina ME; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia.
Belyaeva EO; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia.
Sukhanova NN; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia.
Nazarenko LP; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia; Siberian State Medical University, Tomsk, Russia.
Lebedev IN; Research Institute of Medical Genetics, Tomsk NRMC, Tomsk, Russia; Siberian State Medical University, Tomsk, Russia.
Serov OL; Institute of Cytology and Genetics, SB RAS, Novosibirsk, Russia.
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Źródło :
Stem cell research [Stem Cell Res] 2020 Dec; Vol. 49, pp. 102076. Date of Electronic Publication: 2020 Nov 03.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Induced Pluripotent Stem Cells*
Ring Chromosomes*
Cell Line ; Chromosomes, Human, Pair 18 ; Fibroblasts ; Humans
SCR Disease Name :
Chromosome 18 ring
Czasopismo naukowe
Tytuł :
[Myelodysplastic syndrome with chromosome 5q deletion and philadelphia chromosome: case report and literatures review].
Autorzy :
Zhang YQ; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Liu RT; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Pan JQ; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Xu P; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Li XY; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Yu LQ; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Gao HY; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
Jiang YF; Department of Hematology, the Second Affiliated Hospital of Harbin Medical University, Harbin 150001, China.
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Źródło :
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi [Zhonghua Xue Ye Xue Za Zhi] 2020 Nov 14; Vol. 41 (11), pp. 940-942.
Typ publikacji :
Case Reports; Journal Article; Review
MeSH Terms :
Chromosome Aberrations*
Chromosomes, Human, Pair 5*/genetics
Myelodysplastic Syndromes*/genetics
Philadelphia Chromosome*
Chromosome Deletion ; Chromosomes ; Humans
Czasopismo naukowe
Tytuł :
Chromosome heteromorphisms: do they entail a reproductive risk for male carriers?
Autorzy :
Anton E; Genetics of Male Fertility Group, Cell Biology Unit, Faculty of Biosciences, Autonomous University of Barcelona, Bellaterra (Cerdanyola del Vallès) 08193, Spain.
Garcia-Guixé E; Reprogenetics Spain, Barcelona 08006, Spain.
Ramos-Muntada M; Genetics of Male Fertility Group, Cell Biology Unit, Faculty of Biosciences, Autonomous University of Barcelona, Bellaterra (Cerdanyola del Vallès) 08193, Spain.
Godo A; Genetics of Male Fertility Group, Cell Biology Unit, Faculty of Biosciences, Autonomous University of Barcelona, Bellaterra (Cerdanyola del Vallès) 08193, Spain.
Sandalinas M; Reprogenetics Spain, Barcelona 08006, Spain.
Blanco J; Genetics of Male Fertility Group, Cell Biology Unit, Faculty of Biosciences, Autonomous University of Barcelona, Bellaterra (Cerdanyola del Vallès) 08193, Spain.
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Źródło :
Asian journal of andrology [Asian J Androl] 2020 Sep-Oct; Vol. 22 (5), pp. 544-546.
Typ publikacji :
Letter; Research Support, Non-U.S. Gov't
MeSH Terms :
Aneuploidy*
Chromosomes, Human*
Spermatozoa*
Adult ; Chromosomes, Human, Pair 1 ; Chromosomes, Human, Pair 13 ; Chromosomes, Human, Pair 18 ; Chromosomes, Human, Pair 21 ; Chromosomes, Human, Pair 22 ; Chromosomes, Human, Pair 9 ; Chromosomes, Human, X ; Chromosomes, Human, Y ; Humans ; In Situ Hybridization, Fluorescence ; Male ; Middle Aged ; Reproduction ; Young Adult
Raport
Tytuł :
Characterization of axolotl lampbrush chromosomes by fluorescence in situ hybridization and immunostaining.
Autorzy :
Keinath MC; Carnegie Institution for Science, Baltimore, MD, USA.
Davidian A; Carnegie Institution for Science, Baltimore, MD, USA; Saint Petersburg State University, Saint Petersburg, Russia.
Timoshevskiy V; University of Kentucky, Lexington, KY, USA.
Timoshevskaya N; University of Kentucky, Lexington, KY, USA.
Gall JG; Carnegie Institution for Science, Baltimore, MD, USA. Electronic address: .
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Źródło :
Experimental cell research [Exp Cell Res] 2021 Apr 15; Vol. 401 (2), pp. 112523. Date of Electronic Publication: 2021 Mar 03.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
In Situ Hybridization, Fluorescence*
Transcription, Genetic*
Ambystoma mexicanum/*genetics
Centromere/*ultrastructure
Chromosomes/*genetics
Ambystoma mexicanum/immunology ; Animals ; Centromere/genetics ; Chromosome Mapping ; Chromosomes/immunology ; Chromosomes, Artificial, Bacterial/genetics ; Chromosomes, Artificial, Bacterial/immunology ; Oocytes/growth & development ; Oocytes/ultrastructure
Czasopismo naukowe
Tytuł :
8p23.2p22 deletion: a case report of a large deletion encompassing 8p23.1 with additional clinical features.
Autorzy :
LaBranche JTN; Departments of Medical Genetics.; Pediatrics, University of Calgary.
Argiropoulos B; Departments of Medical Genetics.; Cytogenetics Laboratory, Alberta Public Laboratories, Calgary, Alberta, Canada.
Thomas MA; Departments of Medical Genetics.; Pediatrics, University of Calgary.
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Źródło :
Clinical dysmorphology [Clin Dysmorphol] 2020 Oct; Vol. 29 (4), pp. 207-209.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosome Deletion*
Chromosomes, Human, Pair 8*
Genetic Association Studies*
Phenotype*
Chromosome Disorders/*diagnosis
Chromosome Disorders/*genetics
Child ; Chromosomes, Human, Pair 2 ; Comparative Genomic Hybridization ; Facies ; Genetic Testing ; Humans ; Male
SCR Disease Name :
Chromosome 2, monosomy 2p22
Czasopismo naukowe
Tytuł :
Fluorescence In Situ Hybridization on DNA Halo Preparations to Reveal Whole Chromosomes, Telomeres and Gene Loci.
Autorzy :
Godwin LS; Laboratory of Nuclear and Genomic Health, Centre for Genome Engineering and Maintenance, Division of Biosciences, Department of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London.
Bridger JM; Laboratory of Nuclear and Genomic Health, Centre for Genome Engineering and Maintenance, Division of Biosciences, Department of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London; .
Foster HA; Biosciences, Department of Clinical, Pharmaceutical and Biological Science, School of Life and Medical Sciences, University of Hertfordshire.
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Źródło :
Journal of visualized experiments : JoVE [J Vis Exp] 2021 Mar 04 (169). Date of Electronic Publication: 2021 Mar 04.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Video-Audio Media
MeSH Terms :
Genetic Loci*
In Situ Hybridization, Fluorescence*
Chromosomes/*metabolism
DNA/*metabolism
Telomere/*metabolism
Cell Nucleus/metabolism ; Cells, Cultured ; Chromosomes, Artificial, Bacterial/metabolism ; Dermis/cytology ; Fibroblasts/metabolism ; Humans ; Image Processing, Computer-Assisted
Czasopismo naukowe
Tytuł :
Partial trisomy 16q and partial monosomy 7p of a fetus derivated from paternal balanced translocation: A case report.
Autorzy :
Xie HH; Department of Prenatal Diagnosis Medical Center of Xuzhou Central Hospital, Xuzhou Clinical Schools of Xuzhou Medical University and Nanjing Medical University, Xuzhou, Jiangsu, China.
Liu T
Zhang JB
Zhai JF
Liu Y
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Źródło :
Medicine [Medicine (Baltimore)] 2021 Feb 19; Vol. 100 (7), pp. e24382.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosomes, Human, Pair 7/*genetics
Monosomy/*diagnosis
Trisomy/*genetics
Abortion, Eugenic ; Adult ; Amniocentesis ; Chromosomes, Human, Pair 16/genetics ; Female ; Humans ; Pregnancy ; Translocation, Genetic/genetics ; Trisomy/diagnosis ; Whole Genome Sequencing
SCR Disease Name :
Chromosome 16, trisomy 16q
Czasopismo naukowe
Tytuł :
Cytogenomics Unveil Possible Transposable Elements Driving Rearrangements in Chromosomes 2 and 4 of Solea senegalensis .
Autorzy :
Rodríguez ME; Área de Genética, Facultad de Ciencias del Mar y Ambientales, Instituto Universitario de Investigación Marina (INMAR), Universidad de Cádiz, 11510 Cádiz, Spain.
Cross I; Área de Genética, Facultad de Ciencias del Mar y Ambientales, Instituto Universitario de Investigación Marina (INMAR), Universidad de Cádiz, 11510 Cádiz, Spain.
Arias-Pérez A; Área de Genética, Facultad de Ciencias del Mar y Ambientales, Instituto Universitario de Investigación Marina (INMAR), Universidad de Cádiz, 11510 Cádiz, Spain.
Portela-Bens S; Área de Genética, Facultad de Ciencias del Mar y Ambientales, Instituto Universitario de Investigación Marina (INMAR), Universidad de Cádiz, 11510 Cádiz, Spain.
Merlo MA; Área de Genética, Facultad de Ciencias del Mar y Ambientales, Instituto Universitario de Investigación Marina (INMAR), Universidad de Cádiz, 11510 Cádiz, Spain.
Liehr T; Institute of Human Genetics, University Clinic Jena, 07747 Jena, Germany.
Rebordinos L; Área de Genética, Facultad de Ciencias del Mar y Ambientales, Instituto Universitario de Investigación Marina (INMAR), Universidad de Cádiz, 11510 Cádiz, Spain.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2021 Feb 05; Vol. 22 (4). Date of Electronic Publication: 2021 Feb 05.
Typ publikacji :
Journal Article
MeSH Terms :
DNA Transposable Elements*
Chromosomes/*genetics
Cytogenetics/*methods
Flatfishes/*genetics
Animals ; Chromosome Aberrations ; Chromosome Mapping ; Chromosomes, Artificial, Bacterial/genetics ; Evolution, Molecular ; In Situ Hybridization, Fluorescence ; Karyotype ; Phylogeny ; Synteny
Czasopismo naukowe

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