Temat: "Chromosomes" - OpacWWW

Skocz do pozycji: 1 1.

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.; Pokaż więcej
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

Szczegóły

Skocz do pozycji: 2 2.

Tytuł :: Computer vision for pattern detection in chromosome contact maps.
Autorzy :: Matthey-Doret C; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France.; Sorbonne Université, Collège Doctoral, F-75005, Paris, France.
Baudry L; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France.; Sorbonne Université, Collège Doctoral, F-75005, Paris, France.
Breuer A; ENGIE, Global Energy Management, Paris, France.
Montagne R; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France.
Guiglielmoni N; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France.
Scolari V; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France.
Jean E; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France.
Campeas A; ENGIE, Global Energy Management, Paris, France.
Chanut PH; ENGIE, Global Energy Management, Paris, France.
Oriol E; ENGIE, Global Energy Management, Paris, France.
Méot A; ENGIE, Global Energy Management, Paris, France.
Politis L; ENGIE, Global Energy Management, Paris, France.
Vigouroux A; Institut Pasteur, Synthetic Biology Group, Paris, France.
Moreau P; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France.
Koszul R; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France. .
Cournac A; Institut Pasteur, Unité Régulation Spatiale des Génomes, CNRS, UMR 3525, C3BI USR 3756, Paris, France. .; Pokaż więcej
Źródło :: Nature communications [Nat Commun] 2020 Nov 16; Vol. 11 (1), pp. 5795. Date of Electronic Publication: 2020 Nov 16.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :: Computers*
Pattern Recognition, Automated*
Chromosomes/*genetics
Algorithms ; Chromosomes, Fungal/genetics ; Chromosomes, Human/genetics ; Genome, Fungal ; Humans ; Saccharomyces cerevisiae/genetics ; Workflow
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 3 3.

Tytuł :: Myelodysplastic syndromes in a pediatric patient with Cri du Chat syndrome with a ring chromosome 5.
Autorzy :: Nozawa A; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Ozeki M; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan. .
Yasue S; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Endo S; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Kadowaki T; Department of Pediatrics, National Hospital Organization Nagara Medical Center, Gifu, 502-8558, Japan.
Ohnishi H; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Muramatsu H; Department of Pediatrics, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, 466-8650, Japan.
Hama A; Department of Hematology and Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nakamura-ku, Nagoya, 453-8511, Japan.
Takahashi Y; Department of Pediatrics, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, 466-8650, Japan.
Kojima S; Department of Pediatrics, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, 466-8650, Japan.
Fukao T; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.; Pokaż więcej
Źródło :: International journal of hematology [Int J Hematol] 2020 Nov; Vol. 112 (5), pp. 728-733. Date of Electronic Publication: 2020 Jun 09.
Typ publikacji :: Case Reports; Journal Article
MeSH Terms :: Chromosome Deletion*
Ring Chromosomes*
Azacitidine/*administration & dosage
Chromosomes, Human, Pair 5/*genetics
Cri-du-Chat Syndrome/*genetics
Myelodysplastic Syndromes/*drug therapy
Myelodysplastic Syndromes/*etiology
Myelodysplastic Syndromes/*genetics
Adolescent ; Age Factors ; Cri-du-Chat Syndrome/etiology ; Cytogenetic Analysis/methods ; Female ; Humans ; Myelodysplastic Syndromes/blood ; Quality of Life ; Treatment Outcome
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 4 4.

Tytuł :: [Identification of a critical region on chromosome 4p16.3 for Wolf-Hirschhorn syndrome-associated fetal growth retardation].
Autorzy :: Zheng W; Department of Laboratory Medicine, Xiaolan Hospital of Southern Medical University, Zhongshan, Guangdong 528415, China. .
Chen B
Yin Z
Huang X
Liang Y; Pokaż więcej
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] 2020 Jul 10; Vol. 37 (7), pp. 731-735.
Typ publikacji :: Journal Article
MeSH Terms :: Chromosomes, Human, Pair 3*
Fetal Growth Retardation*/genetics
Wolf-Hirschhorn Syndrome*/genetics
Carrier Proteins ; Chromosome Aberrations ; Chromosome Deletion ; Chromosomes, Human, Pair 4/genetics ; Female ; Humans ; Microtubule-Associated Proteins/genetics ; Nuclear Proteins/genetics ; Phenotype ; Pregnancy ; mRNA Cleavage and Polyadenylation Factors/genetics
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 5 5.

Tytuł :: Tumor-specific transcript variants of cyclin D1 in mantle cell lymphoma and multiple myeloma with chromosome 11q13 abnormalities.
Autorzy :: Chinen Y; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan. Electronic address: .
Tsukamoto T; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Maegawa-Matsui S; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Matsumura-Kimoto Y; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Takimoto-Shimomura T; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Tanba K; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Mizuno Y; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Fujibayashi Y; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kuwahara-Ota S; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Shimura Y; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kobayashi T; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Horiike S; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Taniwaki M; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Kuroda J; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.; Pokaż więcej
Źródło :: Experimental hematology [Exp Hematol] 2020 Apr; Vol. 84, pp. 45-53.e1. Date of Electronic Publication: 2020 Mar 05.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :: Chromosomes, Human, Pair 11*/genetics
Chromosomes, Human, Pair 11*/metabolism
Cyclin D1*/biosynthesis
Cyclin D1*/genetics
Gene Expression Regulation, Neoplastic*
Lymphoma, Mantle-Cell*/genetics
Lymphoma, Mantle-Cell*/metabolism
Lymphoma, Mantle-Cell*/pathology
Multiple Myeloma*/genetics
Multiple Myeloma*/metabolism
Multiple Myeloma*/pathology
Transcription, Genetic*
Translocation, Genetic*
5' Untranslated Regions ; Cell Line, Tumor ; Chromosomes, Human, Pair 14/genetics ; Chromosomes, Human, Pair 14/metabolism ; Exons ; HEK293 Cells ; Humans ; Signal Transduction/genetics ; TOR Serine-Threonine Kinases/genetics ; TOR Serine-Threonine Kinases/metabolism
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 6 6.

Tytuł :: [Acute myeloid leukemia with inversion of chromosome 16: cytological, immunophenotypic and cytogenetic disruption].
Autorzy :: Mghinia S; Laboratoire d'hématologie, CHU Ibn Rochd, Casablanca, Maroc.
Zaidani M; Unité d'hématologie, Hôpital Hassan II, Settat, Maroc.
Hda N; Laboratoire HDA d'analyses médicales, Casablanca, Maroc.
Gamraoui K; Laboratoire d'hématologie, CHU Ibn Rochd, Casablanca, Maroc.
Oukkache B; Laboratoire d'hématologie, CHU Ibn Rochd, Casablanca, Maroc.; Pokaż więcej
Transliterated Title :: Leucémie aiguë myéloïde avec inversion du chromosome 16 : discordance cytologique, immunophénotypique et cytogénétique.
Źródło :: Annales de biologie clinique [Ann Biol Clin (Paris)] 2020 Apr 01; Vol. 78 (2), pp. 187-190.
Typ publikacji :: Case Reports; Journal Article
MeSH Terms :: Chromosome Inversion*
Chromosomes, Human, Pair 16*
Leukemia, Myeloid, Acute/*diagnosis
Adolescent ; Chromosomes, Human, Pair 22/genetics ; Cytodiagnosis ; Cytogenetic Analysis ; Humans ; Immunophenotyping ; Karyotyping ; Leukemia, Myeloid, Acute/complications ; Leukemia, Myeloid, Acute/genetics ; Male ; Trisomy/diagnosis ; Trisomy/genetics
SCR Disease Name :: Chromosome 22, trisomy
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 7 7.

Tytuł :: Deciphering Ancestral Sex Chromosome Turnovers Based on Analysis of Male Mutation Bias.
Autorzy :: Acosta A; Center for Genome Sciences, UNAM, Cuernavaca, Mexico.
Martínez-Pacheco ML; Center for Genome Sciences, UNAM, Cuernavaca, Mexico.
Díaz-Barba K; Center for Genome Sciences, UNAM, Cuernavaca, Mexico.
Porras N; Center for Genome Sciences, UNAM, Cuernavaca, Mexico.
Gutiérrez-Mariscal M; Biotechnology Institute, UNAM, Cuernavaca, Mexico.
Cortez D; Center for Genome Sciences, UNAM, Cuernavaca, Mexico.; Pokaż więcej
Źródło :: Genome biology and evolution [Genome Biol Evol] 2019 Nov 01; Vol. 11 (11), pp. 3054-3067.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :: Phylogeny*
Sex Chromosomes*/genetics
Animals ; Chromosomes, Mammalian ; Eutheria/genetics ; Evolution, Molecular ; Female ; Genome ; Lizards/genetics ; Male ; Monotremata/genetics ; Mutation ; X Chromosome ; Y Chromosome
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 8 8.

Tytuł :: An extraordinarily stable karyotype of the woody Populus species revealed by chromosome painting.
Autorzy :: Xin H; Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Forest Genetics and Biotechnology of Ministry of Education, Jiangsu Key Laboratory for Poplar Germplasm Enhancement and Variety Improvement, Nanjing Forestry University, Nanjing, 210037, China.; Department of Plant Biology, Michigan State University, East Lansing, Michigan, 48824, USA.
Zhang T; Jiangsu Key Laboratory of Crop Genetics and Physiology, Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding, Co-Innovation Centre for Modern Production Technology of Grain Crops, Key Laboratory of Plant Functional Genomics of the Ministry of Education, Yangzhou University, Yangzhou, 225009, China.
Wu Y; The State Key Laboratory of Crop Genetics and Germplasm Enhancement, Jiangsu Collaborative Innovation Center for Modern Crop Production, Nanjing Agricultural University, Nanjing, 210095, China.
Zhang W; The State Key Laboratory of Crop Genetics and Germplasm Enhancement, Jiangsu Collaborative Innovation Center for Modern Crop Production, Nanjing Agricultural University, Nanjing, 210095, China.
Zhang P; National Engineering Laboratory for Tree Breeding, College of Bioscience and Biotechnology, Beijing Forestry University, Beijing, 100083, China.
Xi M; Co-Innovation Center for Sustainable Forestry in Southern China, Key Laboratory of Forest Genetics and Biotechnology of Ministry of Education, Jiangsu Key Laboratory for Poplar Germplasm Enhancement and Variety Improvement, Nanjing Forestry University, Nanjing, 210037, China.
Jiang J; Department of Plant Biology, Michigan State University, East Lansing, Michigan, 48824, USA.; Department of Horticulture, Michigan State University, East Lansing, MI, 48824, USA.; Michigan State University AgBioResearch, East Lansing, MI, 48824, USA.; Pokaż więcej
Źródło :: The Plant journal : for cell and molecular biology [Plant J] 2020 Jan; Vol. 101 (2), pp. 253-264. Date of Electronic Publication: 2019 Oct 17.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :: Chromosomes, Plant*
Karyotype*
Chromosome Painting/*methods
Populus/*genetics
Chromosome Aberrations ; DNA, Ribosomal ; Evolution, Molecular ; Genome, Plant ; In Situ Hybridization, Fluorescence ; Karyotyping ; Metaphase ; Sex Chromosomes ; Species Specificity ; Synteny
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 9 9.

Tytuł :: Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis.
Autorzy :: Chen CP; Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; Department of Biotechnology, Asia University, Taichung, Taiwan; School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan; Institute of Clinical and Community Health Nursing, National Yang-Ming University, Taipei, Taiwan; Department of Obstetrics and Gynecology, School of Medicine, National Yang-Ming University, Taipei, Taiwan. Electronic address: .
Lin YH; Department of Obstetrics and Gynecology, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
Chern SR; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
Wu PS; Gene Biodesign Co. Ltd, Taipei, Taiwan.
Chen SW; Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan.
Wu FT; Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan.
Lee MS; Department of Obstetrics and Gynecology, MacKay Memorial Hospital, Taipei, Taiwan.
Chen YY; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan.
Wang W; Department of Medical Research, MacKay Memorial Hospital, Taipei, Taiwan; Department of Bioengineering, Tatung University, Taipei, Taiwan.; Pokaż więcej
Źródło :: Taiwanese journal of obstetrics & gynecology [Taiwan J Obstet Gynecol] 2020 Jan; Vol. 59 (1), pp. 146-149.
Typ publikacji :: Case Reports
MeSH Terms :: Chromosomes, Human, Pair 7*
Amniocentesis/*methods
Amnion/*cytology
Trisomy/*diagnosis
Adult ; Cells, Cultured ; Chromosomes, Human, Pair 20/genetics ; Female ; Humans ; Mosaicism ; Pregnancy ; Trisomy/genetics
SCR Disease Name :: Chromosome 20, trisomy
: Raport

Szczegóły

Skocz do pozycji: 10 10.

Tytuł :: A database of amphibian karyotypes.
Autorzy :: Perkins RD; Department of Biology, TAMU 3258 Texas A&M, College Station, TX, 77843, USA.
Gamboa JR; Department of Biology, TAMU 3258 Texas A&M, College Station, TX, 77843, USA.
Jonika MM; Department of Biology, TAMU 3258 Texas A&M, College Station, TX, 77843, USA.
Lo J; Department of Biology, TAMU 3258 Texas A&M, College Station, TX, 77843, USA.
Shum A; Department of Biology, TAMU 3258 Texas A&M, College Station, TX, 77843, USA.
Adams RH; Department of Biology, University of Texas at Arlington, 501 S. Nedderman Dr, Arlington, TX, 76019, USA.
Blackmon H; Department of Biology, TAMU 3258 Texas A&M, College Station, TX, 77843, USA. .; Pokaż więcej
Źródło :: Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology [Chromosome Res] 2019 Dec; Vol. 27 (4), pp. 313-319. Date of Electronic Publication: 2019 Jul 23.
Typ publikacji :: Journal Article
MeSH Terms :: Chromosomes*
Databases, Genetic*
Karyotype*
Amphibians/*genetics
Genomics/*methods
Animals ; Female ; Male ; Sex Chromosomes
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 11 11.

Tytuł :: A case of "double hit" mantle cell lymphoma carrying CCND1 and MYC translocations relapsed/refractory to rituximab bendamustine cytarabine (R-BAC) and ibrutinib.
Autorzy :: Scapinello G; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.
Riva M; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.; Hematology Division, San Bortolo Hospital, Vicenza, Italy.
Branca A; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.
Pizzi M; Surgical Pathology/Cytopathology Units - Department of Medicine - DIMED, University of Padova, Padova, Italy.
Bonaldi L; Immunology and Molecular Oncology Unit, Veneto Institute of Oncology, IOV-IRCCS, Padova, Italy.
Martines A; Immunology and Molecular Oncology Unit, Veneto Institute of Oncology, IOV-IRCCS, Padova, Italy.
Manni S; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.; Laboratory of Myeloma and Lymphoma Pathobiology, Venetian Institute of Molecular Medicine, Padova, Italy.
Visentin A; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.
Trentin L; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.
Semenzato G; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.
Gurrieri C; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.
Piazza F; Hematology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy. .; Laboratory of Myeloma and Lymphoma Pathobiology, Venetian Institute of Molecular Medicine, Padova, Italy. .; Pokaż więcej
Źródło :: Annals of hematology [Ann Hematol] 2020 Nov; Vol. 99 (11), pp. 2715-2717. Date of Electronic Publication: 2020 Jul 15.
Typ publikacji :: Case Reports; Letter
MeSH Terms :: Genes, myc*
Translocation, Genetic*
Antineoplastic Combined Chemotherapy Protocols/*therapeutic use
Chromosomes, Human, Pair 11/*ultrastructure
Chromosomes, Human, Pair 14/*ultrastructure
Chromosomes, Human, Pair 8/*ultrastructure
Cyclin D1/*genetics
Lymphoma, Mantle-Cell/*genetics
Oncogene Proteins, Fusion/*genetics
Abnormal Karyotype ; Aged ; Bendamustine Hydrochloride/administration & dosage ; Biomarkers, Tumor ; Bortezomib/administration & dosage ; Chromosomes, Human, Pair 11/genetics ; Chromosomes, Human, Pair 14/genetics ; Chromosomes, Human, Pair 8/genetics ; Cytarabine/administration & dosage ; Drug Resistance, Neoplasm ; Fatal Outcome ; Gene Duplication ; Humans ; Lymphoma, Mantle-Cell/drug therapy ; Lymphoma, Mantle-Cell/pathology ; Male ; Pyrazoles/administration & dosage ; Pyrimidines/administration & dosage ; Recurrence ; Rituximab/administration & dosage
: Raport

Szczegóły

Skocz do pozycji: 12 12.

Tytuł :: Human metaphase chromosome consists of randomly arranged chromatin fibres with up to 30-nm diameter.
Autorzy :: Wako T; Institute of Crop Sciences, National Agriculture and Food Research Organization, 2-1-1 Kannondai, Tsukuba, Ibaraki, 305-8602, Japan.
Yoshida A; Morphological Research Laboratory, Toray Research Center Inc., 3-3-7 Sonoyama, Otsu, Shiga, 520-8567, Japan.
Kato J; Morphological Research Laboratory, Toray Research Center Inc., 3-3-7 Sonoyama, Otsu, Shiga, 520-8567, Japan.
Otsuka Y; Morphological Research Laboratory, Toray Research Center Inc., 3-3-7 Sonoyama, Otsu, Shiga, 520-8567, Japan.
Ogawa S; Nanoelectronics Research Institute, National Institute of Advanced Industrial Science and Technology, 1-1-1 Umezono, Tsukuba, Ibaraki, 305-8568, Japan.
Kaneyoshi K; Graduate School of Engineering, Osaka University, 2-1 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Takata H; Kansai Center, National Institute of Advanced Industrial Science and Technology, Midorigaoka, Ikeda, Osaka, 563-8577, Japan.
Fukui K; Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan. .; Pokaż więcej
Źródło :: Scientific reports [Sci Rep] 2020 Jun 02; Vol. 10 (1), pp. 8948. Date of Electronic Publication: 2020 Jun 02.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :: Chromatin/*physiology
Chromosomes/*metabolism
Metaphase/*physiology
Chromatids/metabolism ; Chromatids/physiology ; Chromatin/metabolism ; Chromosomes/genetics ; Chromosomes, Human ; HeLa Cells ; Humans ; Microscopy, Electron, Scanning ; Nucleosomes/physiology
: Czasopismo naukowe

Szczegóły Pełny tekst Pełny tekst

Skocz do pozycji: 13 13.

Tytuł :: Ultrastructural Details of Mammalian Chromosome Architecture.
Autorzy :: Krietenstein N; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Abraham S; Insitute for Medical Engineering and Sciences and Department of Physics, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA; Center for 3D Structure and Physics of the Genome, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA.
Venev SV; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Program in Systems Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Abdennur N; Insitute for Medical Engineering and Sciences and Department of Physics, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA; Center for 3D Structure and Physics of the Genome, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA.
Gibcus J; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Program in Systems Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Hsieh TS; Department of Molecular and Cell Biology, Li Ka Shing Center for Biomedical and Health Sciences, CIRM Center of Excellence, University of California, Berkeley, Berkeley, CA 94720, USA.
Parsi KM; Program in Molecular Medicine, Diabetes Center of Excellence, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Yang L; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Program in Systems Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Maehr R; Program in Molecular Medicine, Diabetes Center of Excellence, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Mirny LA; Insitute for Medical Engineering and Sciences and Department of Physics, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA; Center for 3D Structure and Physics of the Genome, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA.
Dekker J; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Program in Systems Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA; Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA.
Rando OJ; Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA. Electronic address: .; Pokaż więcej
Źródło :: Molecular cell [Mol Cell] 2020 May 07; Vol. 78 (3), pp. 554-565.e7. Date of Electronic Publication: 2020 Mar 25.
Typ publikacji :: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :: Chromosomes, Human/*ultrastructure
Animals ; CCCTC-Binding Factor/metabolism ; Cells, Cultured ; Chromatin/chemistry ; Chromosomes, Mammalian/ultrastructure ; Embryonic Stem Cells/cytology ; Fibroblasts/cytology ; Humans ; Male ; Mammals/genetics ; Nucleosomes/metabolism ; Nucleosomes/ultrastructure ; Signal-To-Noise Ratio
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 14 14.

Tytuł :: A Rare Cytogenetic Variant of Monosomy 18p Syndrome as a Consequence of Whole-Arm Translocation between Chromosomes 13 and 18.
Autorzy :: Safavi M; Molecular Pathology and Cytogenetics Division, Pathology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Haghi Ashtiani MT; Molecular Pathology and Cytogenetics Division, Pathology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Badv RS; Pediatric Neurology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Azari-Yam A; Molecular Pathology and Cytogenetics Division, Pathology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Vasei M; Molecular Pathology and Cytogenetics Division, Pathology Department, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.; Pokaż więcej
Źródło :: Archives of Iranian medicine [Arch Iran Med] 2019 Oct 01; Vol. 22 (10), pp. 627-628. Date of Electronic Publication: 2019 Oct 01.
Typ publikacji :: Case Reports; Journal Article
MeSH Terms :: Chromosomes, Human, Pair 13*
Translocation, Genetic*
Chromosome Disorders/*genetics
Chromosome Deletion ; Chromosome Disorders/diagnosis ; Chromosomes, Human, Pair 18/genetics ; Cytogenetic Analysis ; Humans ; Infant ; Male ; Ring Chromosomes
SCR Disease Name :: Chromosome 18 ring; Chromosome 18p deletion syndrome
: Czasopismo naukowe

Szczegóły Pełny tekst

Skocz do pozycji: 15 15.

Tytuł :: Landscape of snake' sex chromosomes evolution spanning 85 MYR reveals ancestry of sequences despite distinct evolutionary trajectories.
Autorzy :: Viana PF; Coordenação de Biodiversidade, Laboratory of Animal Genetics, Instituto Nacional de Pesquisas da Amazônia, Av. André Araújo 2936, Petrópolis, Manaus, AM, 69067-375, Brazil. .
Ezaz T; Institute for Applied Ecology, Faculty of Science and Technology, University of Canberra, ACT 12, Canberra, 2616, Australia.
de Bello Cioffi M; Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, Brazil.; Institute of Human Genetics, University Hospital Jena, Am Klinikum 1, 07747, Jena, Germany.
Liehr T; Institute of Human Genetics, University Hospital Jena, Am Klinikum 1, 07747, Jena, Germany.
Al-Rikabi A; Institute of Human Genetics, University Hospital Jena, Am Klinikum 1, 07747, Jena, Germany.
Goll LG; Coordenação de Biodiversidade, Laboratory of Animal Genetics, Instituto Nacional de Pesquisas da Amazônia, Av. André Araújo 2936, Petrópolis, Manaus, AM, 69067-375, Brazil.
Rocha AM; Faculdade Cathedral, Laboratório de Zoologia Aplicada de Vertebrados Terrestres E Aquáticos, Av. Luis Canuto Chaves 293, Boa Vista, RR, Brazil.
Feldberg E; Coordenação de Biodiversidade, Laboratory of Animal Genetics, Instituto Nacional de Pesquisas da Amazônia, Av. André Araújo 2936, Petrópolis, Manaus, AM, 69067-375, Brazil.; Pokaż więcej
Źródło :: Scientific reports [Sci Rep] 2020 Jul 27; Vol. 10 (1), pp. 12499. Date of Electronic Publication: 2020 Jul 27.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :: Evolution, Molecular*
Phylogeny*
Sex Chromosomes/*genetics
Snakes/*genetics
Animals ; Chromosome Painting ; Chromosomes, Artificial, Bacterial/genetics ; Comparative Genomic Hybridization ; DNA/genetics ; Female ; Genome ; Heterochromatin/genetics ; Male ; Species Specificity
: Czasopismo naukowe

Szczegóły Pełny tekst Pełny tekst

Skocz do pozycji: 16 16.

Tytuł :: A distal enhancer at risk locus 11q13.5 promotes suppression of colitis by T reg cells.
Autorzy :: Nasrallah R; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.
Imianowski CJ; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK. .; Department of Pathology, University of Cambridge, Cambridge, UK. .
Bossini-Castillo L; Immune Genomics Group, Wellcome Sanger Institute, Cambridge, UK.
Grant FM; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.
Dogan M; The Jackson Laboratory, Farmington, CT, USA.
Placek L; The Jackson Laboratory, Farmington, CT, USA.
Kozhaya L; The Jackson Laboratory, Farmington, CT, USA.
Kuo P; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.; Department of Pathology, University of Cambridge, Cambridge, UK.
Sadiyah F; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.; Department of Pathology, University of Cambridge, Cambridge, UK.
Whiteside SK; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.; Department of Pathology, University of Cambridge, Cambridge, UK.
Mumbach MR; Howard Hughes Medical Institute and Center for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA, USA.
Glinos D; Immune Genomics Group, Wellcome Sanger Institute, Cambridge, UK.
Vardaka P; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.; Department of Pathology, University of Cambridge, Cambridge, UK.
Whyte CE; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.
Lozano T; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.
Fujita T; Chromatin Biochemistry Research Group, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.; Department of Biochemistry and Genome Biology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Fujii H; Chromatin Biochemistry Research Group, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.; Department of Biochemistry and Genome Biology, Hirosaki University Graduate School of Medicine, Hirosaki, Japan.
Liston A; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.
Andrews S; Bioinformatics Group, The Babraham Institute, Cambridge, UK.
Cozzani A; Inserm UMR1277/CNRS9020, Institut pour la Recherche sur le Cancer de Lille, Lille, France.
Yang J; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK.; Department of Pathology, University of Cambridge, Cambridge, UK.
Mitra S; Inserm UMR1277/CNRS9020, Institut pour la Recherche sur le Cancer de Lille, Lille, France.
Lugli E; Humanitas Clinical and Research Center, Milan, Italy.
Chang HY; Howard Hughes Medical Institute and Center for Personal Dynamic Regulomes, Stanford University School of Medicine, Stanford, CA, USA.
Unutmaz D; The Jackson Laboratory, Farmington, CT, USA.
Trynka G; Immune Genomics Group, Wellcome Sanger Institute, Cambridge, UK. .; Open Targets, Wellcome Genome Campus, Cambridge, UK. .
Roychoudhuri R; Laboratory of Lymphocyte Signalling and Development, The Babraham Institute, Cambridge, UK. .; Department of Pathology, University of Cambridge, Cambridge, UK. .; Pokaż więcej
Źródło :: Nature [Nature] 2020 Jul; Vol. 583 (7816), pp. 447-452. Date of Electronic Publication: 2020 May 13.
Typ publikacji :: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :: Chromosomes, Human, Pair 11/*genetics
Colitis/*genetics
Colitis/*immunology
Enhancer Elements, Genetic/*genetics
Genetic Predisposition to Disease/*genetics
T-Lymphocytes, Regulatory/*immunology
Acetylation ; Alleles ; Animals ; Chromosomes, Mammalian/genetics ; Female ; Forkhead Transcription Factors/metabolism ; Histones/metabolism ; Humans ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Mice ; Synteny/genetics
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 17 17.

Tytuł :: RUNX1/ETO and mutant KIT both contribute to programming the transcriptional and chromatin landscape in t(8;21) acute myeloid leukemia.
Autorzy :: Chin PS; Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Assi SA; Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Ptasinska A; Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Imperato MR; Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Cockerill PN; Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Bonifer C; Institute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK. Electronic address: .; Pokaż więcej
Źródło :: Experimental hematology [Exp Hematol] 2020 Dec; Vol. 92, pp. 62-74. Date of Electronic Publication: 2020 Nov 02.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :: Chromosomes, Human, Pair 21*/genetics
Chromosomes, Human, Pair 21*/metabolism
Chromosomes, Human, Pair 8*/genetics
Chromosomes, Human, Pair 8*/metabolism
Leukemia, Myeloid, Acute*/genetics
Leukemia, Myeloid, Acute*/metabolism
Leukemia, Myeloid, Acute*/pathology
Mutation, Missense*
Transcription, Genetic*
Translocation, Genetic*
Chromatin/*metabolism
Core Binding Factor Alpha 2 Subunit/*metabolism
Proto-Oncogene Proteins c-kit/*metabolism
RUNX1 Translocation Partner 1 Protein/*metabolism
Amino Acid Substitution ; Chromatin/pathology ; Core Binding Factor Alpha 2 Subunit/genetics ; Female ; Gene Expression Regulation, Leukemic ; HEK293 Cells ; Humans ; Male ; Proto-Oncogene Proteins c-kit/genetics ; RUNX1 Translocation Partner 1 Protein/genetics
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 18 18.

Tytuł :: Hyperosmotic stress: in situ chromatin phase separation.
Autorzy :: Olins AL; Department of Pharmaceutical Sciences, College of Pharmacy, University of New England, Portland, ME, USA.
Gould TJ; Department of Physics & Astronomy, Bates College, Lewiston, ME,USA.
Boyd L; Department of Physics & Astronomy, Bates College, Lewiston, ME,USA.
Sarg B; Division of Clinical Biochemistry, Biocenter, Innsbruck Medical University, Innsbruck, Austria.
Olins DE; Department of Pharmaceutical Sciences, College of Pharmacy, University of New England, Portland, ME, USA.; Pokaż więcej
Źródło :: Nucleus (Austin, Tex.) [Nucleus] 2020 Dec; Vol. 11 (1), pp. 1-18.
Typ publikacji :: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :: Osmotic Pressure*
Chromatin/*metabolism
Chromosomes/*metabolism
Chromatin/chemistry ; Chromatin/genetics ; Chromosomes/chemistry ; Chromosomes/genetics ; HL-60 Cells ; Humans ; Microscopy, Confocal ; Microscopy, Fluorescence ; Mitosis ; Optical Imaging ; Tumor Cells, Cultured
: Czasopismo naukowe

Szczegóły Pełny tekst Pełny tekst

Skocz do pozycji: 19 19.

Tytuł :: [Prenatal diagnosis and genetic analysis of a fetus with der(X)t(X;Y)(p22.3;q11.2)].
Autorzy :: Li J; Center of Prenatal Diagnosis, the First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China. .
Dong Y
Li J
Luo J
Li C
Qi H; Pokaż więcej
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] 2020 Nov 10; Vol. 37 (11), pp. 1287-1290.
Typ publikacji :: Journal Article
MeSH Terms :: Chromosomes, Human, X*/genetics
Chromosomes, Human, Y*/genetics
Prenatal Diagnosis*
Chromosome Banding ; Chromosome Deletion ; Female ; Fetus ; Humans ; Karyotyping ; Male ; Pregnancy ; Translocation, Genetic
: Czasopismo naukowe

Szczegóły

Skocz do pozycji: 20 20.

Tytuł :: Sexual conflict through mother's curse and father's curse.
Autorzy :: Ågren JA; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, 14583, USA.
Munasinghe M; Department of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, 14853, USA.
Clark AG; Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, 14583, USA; Department of Biological Statistics and Computational Biology, Cornell University, Ithaca, NY, 14853, USA. Electronic address: .; Pokaż więcej
Źródło :: Theoretical population biology [Theor Popul Biol] 2019 Oct; Vol. 129, pp. 9-17. Date of Electronic Publication: 2019 May 02.
Typ publikacji :: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :: Fathers*
Mothers*
Selection, Genetic*
Sex Chromosome Aberrations*
Sex Chromosomes*
Chromosomes, Human, Y ; DNA, Mitochondrial ; Female ; Humans ; Male ; Models, Theoretical
: Czasopismo naukowe

Szczegóły

Informacja

Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Chromosomes"" wg kryterium: Temat

Źródło danych

Ogranicz do:

Ogranicz do bazy

Typ dokumentu

Temat

Wydawca

Publikacja

Język