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Tytuł:
Enzymatic Supercoiling of Bacterial Chromosomes Facilitates Genome Manipulation.
Autorzy:
Fujita H; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
Osaku A; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
Sakane Y; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
Yoshida K; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
Yamada K; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
Nara S; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
Mukai T; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
Su'etsugu M; Department of Life Science, College of Science, Rikkyo University, Tokyo 171-8501, Japan.
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Źródło:
ACS synthetic biology [ACS Synth Biol] 2022 Sep 16; Vol. 11 (9), pp. 3088-3099. Date of Electronic Publication: 2022 Aug 23.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Bacterial*/genetics
Escherichia coli*/genetics
Chromosomes/genetics ; DNA ; DNA, Bacterial/genetics ; Genome, Bacterial/genetics ; Synthetic Biology
Czasopismo naukowe
Tytuł:
Chromosome dynamics: Rearranging the choreography of a multipartite bacterial genome.
Autorzy:
Funnell BE; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1M1, Canada. Electronic address: .
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Źródło:
Current biology : CB [Curr Biol] 2022 Aug 22; Vol. 32 (16), pp. R889-R891.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosomes, Bacterial*/genetics
DNA Replication*
Bacteria/genetics ; Chromosomes ; Genome, Bacterial
Czasopismo naukowe
Tytuł:
B-cell acute lymphoblastic leukemia with iAMP21 in a patient with Down syndrome due to a constitutional isodicentric chromosome 21.
Autorzy:
Verdoni AM; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Zilla ML; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Bullock G; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Guinipero TL; Department of Hematology, Oncology, BMT, Division of Pediatrics, Nationwide Children's Hospital, The Ohio State University College of Medicine, Columbus, Ohio, USA.
Meade J; Department of Pediatrics, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Yatsenko SA; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.; Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
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Źródło:
American journal of medical genetics. Part A [Am J Med Genet A] 2022 Aug; Vol. 188 (8), pp. 2325-2330. Date of Electronic Publication: 2022 Jun 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Burkitt Lymphoma*/complications
Down Syndrome*/complications
Down Syndrome*/diagnosis
Down Syndrome*/genetics
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/genetics
Ring Chromosomes*
Child ; Chromosome Aberrations ; Chromosomes, Human, Pair 21/genetics ; Humans ; Translocation, Genetic
Czasopismo naukowe
Tytuł:
Imputation-free reconstructions of three-dimensional chromosome architectures in human diploid single-cells using allele-specified contacts.
Autorzy:
Hirata Y; Faculty of Engineering, Information and Systems, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8573, Japan. .
Oda AH; Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Meguro-ku, Tokyo, 153-8902, Japan.
Motono C; Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology, Koto-ku, Tokyo, 135-0064, Japan.; Computational Bio Big-Data Open Innovation Laboratory (CBBD-OIL), National Institute of Advanced Industrial Science and Technology (AIST), Waseda University, 3-4-1 Okubo, Shinjuku-ku, Tokyo, 169-0072, Japan.
Shiro M; Mathematical Neuroscience Research Group, Human Informatics and Interaction Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Ibaraki, 305-8568, Japan.
Ohta K; Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Meguro-ku, Tokyo, 153-8902, Japan.; Research Center for Complex Systems Biology, Universal Biology Institute, 3-8-1 Komaba, Meguro-ku, Tokyo, 153-8902, Japan.
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Źródło:
Scientific reports [Sci Rep] 2022 Jul 11; Vol. 12 (1), pp. 11757. Date of Electronic Publication: 2022 Jul 11.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes*
Diploidy*
Algorithms ; Alleles ; Chromosome Structures ; Chromosomes, Human/genetics ; Humans
Czasopismo naukowe
Tytuł:
Tempo of Degeneration Across Independently Evolved Nonrecombining Regions.
Autorzy:
Carpentier F; Laboratoire Ecologie Systématique et Evolution, Bâtiment 360, CNRS, AgroParisTech, Université Paris-Saclay, 91400 Orsay, France.; Université de Lille, CNRS, UMR 8198-Evo-Eco-Paleo F-59000, Lille, France.
Rodríguez de la Vega RC; Laboratoire Ecologie Systématique et Evolution, Bâtiment 360, CNRS, AgroParisTech, Université Paris-Saclay, 91400 Orsay, France.
Jay P; Laboratoire Ecologie Systématique et Evolution, Bâtiment 360, CNRS, AgroParisTech, Université Paris-Saclay, 91400 Orsay, France.
Duhamel M; Laboratoire Ecologie Systématique et Evolution, Bâtiment 360, CNRS, AgroParisTech, Université Paris-Saclay, 91400 Orsay, France.; Evolution der Pflanzen und Pilze, Ruhr-Universität Bochum, Universitätsstraße 150, 44780, Bochum, Germany.
Shykoff JA; Laboratoire Ecologie Systématique et Evolution, Bâtiment 360, CNRS, AgroParisTech, Université Paris-Saclay, 91400 Orsay, France.
Perlin MH; Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA.
Wallen RM; Department of Biology, Program on Disease Evolution, University of Louisville, Louisville, KY 40292, USA.
Hood ME; Department of Biology, Amherst College, Amherst, MA, USA.
Giraud T; Laboratoire Ecologie Systématique et Evolution, Bâtiment 360, CNRS, AgroParisTech, Université Paris-Saclay, 91400 Orsay, France.
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Źródło:
Molecular biology and evolution [Mol Biol Evol] 2022 Apr 11; Vol. 39 (4).
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromosomes, Fungal*
Genes, Mating Type, Fungal*
Codon/genetics ; Evolution, Molecular ; Recombination, Genetic ; Sex Chromosomes
Czasopismo naukowe
Tytuł:
Single-base editing of rs12603332 on chromosome 17q21 with a cytosine base editor regulates ORMDL3 and ATF6α expression.
Autorzy:
Weng N; Department of Medicine, University of California San Diego, La Jolla, California, USA.
Miller M; Department of Medicine, University of California San Diego, La Jolla, California, USA.
Pham AK; Department of Medicine, University of California San Diego, La Jolla, California, USA.
Komor AC; Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, California, USA.
Broide DH; Department of Medicine, University of California San Diego, La Jolla, California, USA.
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Źródło:
Allergy [Allergy] 2022 Apr; Vol. 77 (4), pp. 1139-1149. Date of Electronic Publication: 2021 Sep 24.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural
MeSH Terms:
Asthma*/genetics
Chromosomes, Human, Pair 17*
Cytosine*
Case-Control Studies ; Chromosomes ; Genetic Predisposition to Disease ; Humans ; Membrane Proteins/genetics ; Polymorphism, Single Nucleotide ; RNA, Messenger ; Transcription Factors/genetics
Czasopismo naukowe
Tytuł:
Somatic homozygous loss of SH2B3, and a non-Robertsonian translocation t(15;21)(q25.3;q22.1) with NTRK3 rearrangement, in an adolescent with progenitor B-cell acute lymphoblastic leukemia with the iAMP21.
Autorzy:
Capela de Matos RR; Cytogenetics Department, Bone Marrow Transplantation Unit, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil; Post-Graduate Programme in Oncology, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil.
Othman M; Jena University Hospital, Institute of Human Genetics, Jena, Germany.
Ferreira GM; Stem Cells Department, Bone Marrow Transplantation Unit, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil.
Monteso K; Cytogenetics Department, Bone Marrow Transplantation Unit, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil; Post-Graduate Programme in Oncology, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil.
de Souza MT; Cytogenetics Department, Bone Marrow Transplantation Unit, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil.
Rouxinol M; Lagoa Federal Hospital, Rio de Janeiro, Brazil.
Melo JB; Cytogenetics and Genomics Laboratory, Faculty of Medicine, University of Coimbra, Coimbra, Portugal; Centre of Investigation on Environment Genetics and Oncobiology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Carreira IM; Cytogenetics and Genomics Laboratory, Faculty of Medicine, University of Coimbra, Coimbra, Portugal; Centre of Investigation on Environment Genetics and Oncobiology, Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Abdelhay E; Stem Cells Department, Bone Marrow Transplantation Unit, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil; Post-Graduate Programme in Oncology, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil.
Liehr T; Jena University Hospital, Institute of Human Genetics, Jena, Germany.
Ribeiro RC; Departments of Oncology and Global Pediatric Medicine, St. Jude Children's Research Hospital, Memphis, TN, USA.
Silva M; Cytogenetics Department, Bone Marrow Transplantation Unit, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil; Post-Graduate Programme in Oncology, Instituto Nacional de Câncer José de Alencar Gomes da Silva (INCA-RJ), Rio de Janeiro, Brazil. Electronic address: .
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Źródło:
Cancer genetics [Cancer Genet] 2022 Apr; Vol. 262-263, pp. 16-22. Date of Electronic Publication: 2021 Dec 22.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Burkitt Lymphoma*/genetics
Chromothripsis*
Precursor Cell Lymphoblastic Leukemia-Lymphoma*/genetics
Ring Chromosomes*
Adolescent ; Chromosomes, Human, Pair 21/genetics ; Core Binding Factor Alpha 2 Subunit/genetics ; Homozygote ; Humans ; Precursor Cells, B-Lymphoid ; Sequence Deletion ; Translocation, Genetic
Czasopismo naukowe
Tytuł:
First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15.
Autorzy:
Receveur A; Service D'Histologie Embryologie Cytogénétique, APHP.Université Paris Saclay, Antoine Béclère Hospital, 157 Rue de La Porte de Trivaux, 92141, Clamart Cedex, France. Electronic address: .
Puisney-Dakhli C; Service D'Histologie Embryologie Cytogénétique, APHP.Université Paris Saclay, Antoine Béclère Hospital, 157 Rue de La Porte de Trivaux, 92141, Clamart Cedex, France.
Kleinfinger P; Laboratoire CERBA, 95310 Saint-Ouen l'Aumône, France.
Gitz L; Service de Gynécologie et Obstétrique, Hôpital Du Sud Francilien, 91 Evry, France.
Grevoul-Fesquet J; Service de Gynécologie et Obstétrique, Hôpital Du Sud Francilien, 91 Evry, France.
Jouni D; Service D'Histologie Embryologie Cytogénétique, APHP.Université Paris Saclay, Antoine Béclère Hospital, 157 Rue de La Porte de Trivaux, 92141, Clamart Cedex, France.
Diot R; Service D'Histologie Embryologie Cytogénétique, APHP.Université Paris Saclay, Antoine Béclère Hospital, 157 Rue de La Porte de Trivaux, 92141, Clamart Cedex, France.
Tachdjian G; Service D'Histologie Embryologie Cytogénétique, APHP.Université Paris Saclay, Antoine Béclère Hospital, 157 Rue de La Porte de Trivaux, 92141, Clamart Cedex, France.
Petit F; Laboratoire de Génétique Moléculaire, APHP.Université Paris Saclay, Antoine Béclère Hospital, 157 Rue de La Porte de Trivaux, 92141 Clamart, Cedex, France.
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Źródło:
Taiwanese journal of obstetrics & gynecology [Taiwan J Obstet Gynecol] 2022 Mar; Vol. 61 (2), pp. 382-384.
Typ publikacji:
Case Reports
MeSH Terms:
Chromosomes, Human, Pair 15*
Uniparental Disomy*/genetics
Chromosomes ; Chromosomes, Human, Pair 14 ; Female ; Genetic Markers ; Humans ; Pregnancy
Raport
Tytuł:
Mosaic ring chromosome 18 in a Chinese child with epilepsy: a case report and review of the literature.
Autorzy:
Wang J; Department of Neurology, Dingxi Second People's Hospital, Dingxi, Gansu, People's Republic of China.
Xiao L; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Wang J; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.; Laboratory of Medical Genetics, Central South University, Changsha, Hunan, People's Republic of China.; Key Laboratory of Hunan Province in Neurodegenerative Disorders, Central South University, Changsha, Hunan, People's Republic of China.; National Clinical Research Centre for Geriatric Diseases, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Ding Z; Department of Anesthesiology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.
Ni J; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China.; Laboratory of Medical Genetics, Central South University, Changsha, Hunan, People's Republic of China.
Long X; Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan, People's Republic of China. .
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Źródło:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2021 Dec; Vol. 42 (12), pp. 5231-5239. Date of Electronic Publication: 2021 Apr 08.
Typ publikacji:
Case Reports; Journal Article; Review
MeSH Terms:
Epilepsy*/diagnostic imaging
Epilepsy*/genetics
Ring Chromosomes*
Child ; Chromosomes, Human, Pair 18/genetics ; Female ; Humans ; Seizures
SCR Disease Name:
Chromosome 18 ring
Czasopismo naukowe
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:
Multiple desmoplastic Spitz nevi with BRAF fusions in a patient with ring chromosome 7 syndrome.
Autorzy:
Roy SF; Department of Pathology, University of Montréal, Montréal, OC, Canada.
Bastian BC; Department of Dermatology, University of California in San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California in San Francisco, San Francisco, CA, USA.
Maguiness S; Department of Dermatology, University of Minnesota, Minneapolis, MN, USA.
Giubellino A; Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA.
Vemula SS; Department of Pathology, University of California in San Francisco, San Francisco, CA, USA.
McCalmont TH; Department of Dermatology, University of California in San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California in San Francisco, San Francisco, CA, USA.
Yeh I; Department of Dermatology, University of California in San Francisco, San Francisco, CA, USA.; Department of Pathology, University of California in San Francisco, San Francisco, CA, USA.
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Źródło:
Pigment cell & melanoma research [Pigment Cell Melanoma Res] 2021 Sep; Vol. 34 (5), pp. 987-993. Date of Electronic Publication: 2021 Mar 17.
Typ publikacji:
Case Reports; Research Support, N.I.H., Extramural
MeSH Terms:
Chromosome Disorders*/genetics
Chromosome Disorders*/metabolism
Ear Neoplasms*/genetics
Ear Neoplasms*/metabolism
Ear Neoplasms*/pathology
Nevus, Epithelioid and Spindle Cell*/genetics
Nevus, Epithelioid and Spindle Cell*/metabolism
Nevus, Epithelioid and Spindle Cell*/pathology
Oncogene Proteins, Fusion*/genetics
Oncogene Proteins, Fusion*/metabolism
Proto-Oncogene Proteins B-raf*/genetics
Proto-Oncogene Proteins B-raf*/metabolism
Ring Chromosomes*
Skin Neoplasms*/genetics
Skin Neoplasms*/metabolism
Skin Neoplasms*/pathology
Adult ; Chromosomes, Human, Pair 7/genetics ; Chromosomes, Human, Pair 7/metabolism ; Chromosomes, Human, Pair 7/physiology ; Humans ; Male
SCR Disease Name:
Chromosome 7 ring syndrome
Raport
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 ; Asians/genetics ; Cadherins/genetics ; Cell Cycle Proteins/genetics ; Chromosome Breakpoints ; Chromosomes, Human, Pair 11 ; Humans ; Male ; Microsatellite Repeats ; Protein Serine-Threonine Kinases/genetics ; Protocadherins ; Transducin/genetics
SCR Disease Name:
Chromosome 11, deletion 11p
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:
Gonadal hormones and sex chromosome complement differentially contribute to ethanol intake, preference, and relapse-like behaviour in four core genotypes mice.
Autorzy:
Sneddon EA; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Rasizer LN; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Cavalco NG; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Jaymes AH; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Ostlie NJ; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Minshall BL; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Masters BM; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
Hughes MR; Department of Statistics, Miami University, Oxford, Ohio, USA.
Hrncir H; Department of Integrative Biology and Physiology, and Laboratory of Neuroendocrinology of the Brain Research Institute, University of California, Los Angeles, California, USA.
Arnold AP; Department of Integrative Biology and Physiology, and Laboratory of Neuroendocrinology of the Brain Research Institute, University of California, Los Angeles, California, USA.
Radke AK; Department of Psychology and Center for Neuroscience and Behavior, Miami University, Oxford, Ohio, USA.
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Źródło:
Addiction biology [Addict Biol] 2022 Sep; Vol. 27 (5), pp. e13222.
Typ publikacji:
Journal Article
MeSH Terms:
Ethanol*/pharmacology
Sex Chromosomes*
Alcohol Drinking/genetics ; Animals ; Female ; Genotype ; Gonadal Hormones ; Gonadal Steroid Hormones ; Humans ; Male ; Mice ; Mice, Inbred C57BL ; Recurrence
Czasopismo naukowe
Tytuł:
The evolution of gene regulation on sex chromosomes.
Autorzy:
Shaw DE; Department of Genetics, University of Georgia, Athens, GA 30602, USA.
White MA; Department of Genetics, University of Georgia, Athens, GA 30602, USA. Electronic address: .
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Źródło:
Trends in genetics : TIG [Trends Genet] 2022 Aug; Vol. 38 (8), pp. 844-855. Date of Electronic Publication: 2022 May 13.
Typ publikacji:
Journal Article; Review; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Evolution, Molecular*
Sex Chromosomes*/genetics
Alleles ; Gene Expression Regulation/genetics ; Y Chromosome
Czasopismo naukowe
Tytuł:
Sex-limited chromosomes and non-reproductive traits.
Autorzy:
Cīrulis A; Department of Biology, Lund University, 223 62, Lund, Sweden. .
Hansson B; Department of Biology, Lund University, 223 62, Lund, Sweden.
Abbott JK; Department of Biology, Lund University, 223 62, Lund, Sweden. .
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Źródło:
BMC biology [BMC Biol] 2022 Jul 06; Vol. 20 (1), pp. 156. Date of Electronic Publication: 2022 Jul 06.
Typ publikacji:
Journal Article; Review; Research Support, Non-U.S. Gov't
MeSH Terms:
Biological Evolution*
Sex Chromosomes*/genetics
Phenotype ; Reproduction/genetics
Czasopismo naukowe
Tytuł:
Nuclear chromosome locations dictate segregation error frequencies.
Autorzy:
Klaasen SJ; Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Truong MA; Oncode Institute, Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
van Jaarsveld RH; Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Koprivec I; Ruđer Bošković Institute, Zagreb, Croatia.
Štimac V; Ruđer Bošković Institute, Zagreb, Croatia.
de Vries SG; Oncode Institute, Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Risteski P; Ruđer Bošković Institute, Zagreb, Croatia.
Kodba S; Ruđer Bošković Institute, Zagreb, Croatia.
Vukušić K; Ruđer Bošković Institute, Zagreb, Croatia.
de Luca KL; Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Marques JF; Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Gerrits EM; Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Bakker B; Department of Ageing Biology/ERIBA, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Foijer F; Department of Ageing Biology/ERIBA, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Kind J; Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.; Department of Molecular Biology, Faculty of Science, Radboud Institute for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands.
Tolić IM; Ruđer Bošković Institute, Zagreb, Croatia.
Lens SMA; Oncode Institute, Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Kops GJPL; Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands. .
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Źródło:
Nature [Nature] 2022 Jul; Vol. 607 (7919), pp. 604-609. Date of Electronic Publication: 2022 Jul 13.
Typ publikacji:
Journal Article
MeSH Terms:
Aneuploidy*
Chromosome Positioning*
Chromosome Segregation*/genetics
Chromosomes*/genetics
Chromosomes*/metabolism
CRISPR-Associated Protein 9 ; Cell Line ; Cell Line, Tumor ; Chromothripsis ; Growth and Development/genetics ; Humans ; Interphase ; Micronuclei, Chromosome-Defective ; Mitosis ; Neoplasms/genetics ; Neoplasms/pathology ; Organoids/cytology ; Organoids/metabolism ; Sequence Analysis, DNA ; Single-Cell Analysis
Czasopismo naukowe
Tytuł:
Chromosome 10 abnormality predicts prognosis of neuroblastoma patients with bone marrow metastasis.
Autorzy:
Jiang CY; Medical Oncology Department, Pediatric Oncology Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, 100045, China.
Xu X; Medical Oncology Department, Pediatric Oncology Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, 100045, China.
Jian BL; Medical Oncology Department, Pediatric Oncology Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, 100045, China.
Zhang X; Medical Oncology Department, Pediatric Oncology Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, 100045, China.
Yue ZX; Medical Oncology Department, Pediatric Oncology Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, 100045, China.
Guo W; MILS (Beijing) Medical Labortory, Beijing, China.
Ma XL; Medical Oncology Department, Pediatric Oncology Center, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing Key Laboratory of Pediatric Hematology Oncology, Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, 100045, China. .
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Źródło:
Italian journal of pediatrics [Ital J Pediatr] 2021 Jun 09; Vol. 47 (1), pp. 134. Date of Electronic Publication: 2021 Jun 09.
Typ publikacji:
Journal Article
MeSH Terms:
Chromosome Aberrations*
Chromosomes, Human, Pair 10*
Bone Marrow Neoplasms/*secondary
Neuroblastoma/*genetics
Neuroblastoma/*pathology
Adrenal Gland Neoplasms/genetics ; Adrenal Gland Neoplasms/pathology ; Bone Marrow Neoplasms/genetics ; Child, Preschool ; Chromosomes, Human, Pair 1 ; Female ; Humans ; Infant ; Male ; Mediastinal Neoplasms/genetics ; Mediastinal Neoplasms/pathology ; N-Myc Proto-Oncogene Protein/genetics ; Orbital Neoplasms/genetics ; Orbital Neoplasms/secondary ; Prognosis ; Retroperitoneal Neoplasms/genetics ; Retroperitoneal Neoplasms/pathology
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

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