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Wyszukujesz frazę ""Chromosomes, Human, Pair 8"" wg kryterium: Temat


Tytuł :
The structure, function and evolution of a complete human chromosome 8.
Autorzy :
Logsdon GA; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Vollger MR; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Hsieh P; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Mao Y; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Liskovykh MA; Developmental Therapeutics Branch, National Cancer Institute, Bethesda, MD, USA.
Koren S; Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Nurk S; Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Mercuri L; Department of Biology, University of Bari, Aldo Moro, Bari, Italy.
Dishuck PC; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Rhie A; Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
de Lima LG; Stowers Institute for Medical Research, Kansas City, MO, USA.
Dvorkina T; Center for Algorithmic Biotechnology, Institute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, Russia.
Porubsky D; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Harvey WT; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Mikheenko A; Center for Algorithmic Biotechnology, Institute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, Russia.
Bzikadze AV; Graduate Program in Bioinformatics and Systems Biology, University of California, San Diego, San Diego, CA, USA.
Kremitzki M; McDonnell Genome Institute, Department of Genetics, Washington University School of Medicine, St Louis, MO, USA.
Graves-Lindsay TA; McDonnell Genome Institute, Department of Genetics, Washington University School of Medicine, St Louis, MO, USA.
Jain C; Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Hoekzema K; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Murali SC; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.; Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA.
Munson KM; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Baker C; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Sorensen M; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Lewis AM; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA.
Surti U; Department of Pathology, University of Pittsburgh, Pittsburgh, PA, USA.
Gerton JL; Stowers Institute for Medical Research, Kansas City, MO, USA.
Larionov V; Developmental Therapeutics Branch, National Cancer Institute, Bethesda, MD, USA.
Ventura M; Department of Biology, University of Bari, Aldo Moro, Bari, Italy.
Miga KH; Center for Biomolecular Science and Engineering, University of California, Santa Cruz, Santa Cruz, CA, USA.
Phillippy AM; Genome Informatics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Eichler EE; Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA. .; Howard Hughes Medical Institute, University of Washington, Seattle, WA, USA. .
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Źródło :
Nature [Nature] 2021 May; Vol. 593 (7857), pp. 101-107. Date of Electronic Publication: 2021 Apr 07.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Evolution, Molecular*
Chromosomes, Human, Pair 8/*chemistry
Chromosomes, Human, Pair 8/*genetics
Animals ; Cell Line ; Centromere/chemistry ; Centromere/genetics ; Centromere/metabolism ; Chromosomes, Human, Pair 8/physiology ; DNA Methylation ; DNA, Satellite/genetics ; Epigenesis, Genetic ; Female ; Humans ; Macaca mulatta/genetics ; Male ; Minisatellite Repeats/genetics ; Pan troglodytes/genetics ; Phylogeny ; Pongo abelii/genetics ; Telomere/chemistry ; Telomere/genetics ; Telomere/metabolism
Czasopismo naukowe
Tytuł :
Therapy-related Myeloid Leukemia With the Translocation t(8;19)(p11;q13) Leading to a KAT6A-LEUTX Fusion Gene.
Autorzy :
Panagopoulos I; Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway; .
Andersen K; Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
Ramslien LF; Department of Cancer and Hematological Diseases, Telemark Hospital, Skien, Norway.
Ikonomou IM; Department of Pathology, Oslo University Hospital, Oslo, Norway.
Micci F; Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
Heim S; Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
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Źródło :
Anticancer research [Anticancer Res] 2021 Apr; Vol. 41 (4), pp. 1753-1760.
Typ publikacji :
Case Reports
MeSH Terms :
Chromosomes, Human, Pair 19*
Chromosomes, Human, Pair 8*
Gene Fusion*
Translocation, Genetic*
Biomarkers, Tumor/*genetics
Chemoradiotherapy/*adverse effects
Histone Acetyltransferases/*genetics
Homeodomain Proteins/*genetics
Leukemia, Myeloid, Acute/*etiology
Aged ; Female ; Gene Expression Regulation, Leukemic ; Humans ; Leukemia, Myeloid, Acute/diagnosis ; Leukemia, Myeloid, Acute/drug therapy ; Leukemia, Myeloid, Acute/genetics ; Treatment Outcome ; Uterine Cervical Neoplasms/therapy
Raport
Tytuł :
Acute myeloid leukemia with a severe coagulopathy and t(8;16)(p11;p13).
Autorzy :
Hastings A; Department of Haematology, Hammersmith Hospital, London, UK.
Apperley JF; Centre for Haematology, Hammersmith Hospital Campus, Imperial College London, London, UK.
Nadal-Melsio E; Specialist Integrated Haematological Malignancy Diagnostic Service, Hammersmith Hospital, London, UK.
Brown L; Specialist Integrated Haematological Malignancy Diagnostic Service, Hammersmith Hospital, London, UK.
Bain BJ; Centre for Haematology, St Mary's Hospital Campus, Imperial College London, St Mary's Hospital, Praed Street, London, UK.
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Źródło :
American journal of hematology [Am J Hematol] 2021 Jan; Vol. 96 (1), pp. 163-164. Date of Electronic Publication: 2020 Jul 28.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Blood Coagulation Disorders*/drug therapy
Blood Coagulation Disorders*/genetics
Blood Coagulation Disorders*/metabolism
Blood Coagulation Disorders*/pathology
Chromosomes, Human, Pair 16*/genetics
Chromosomes, Human, Pair 16*/metabolism
Chromosomes, Human, Pair 8*/genetics
Chromosomes, Human, Pair 8*/metabolism
Leukemia, Myeloid, Acute*/drug therapy
Leukemia, Myeloid, Acute*/genetics
Leukemia, Myeloid, Acute*/metabolism
Leukemia, Myeloid, Acute*/pathology
Translocation, Genetic*
Antineoplastic Combined Chemotherapy Protocols/*administration & dosage
Adult ; Cytarabine/administration & dosage ; Daunorubicin/administration & dosage ; Dexamethasone/administration & dosage ; Gemtuzumab/administration & dosage ; Humans ; Male ; Tretinoin/administration & dosage
Czasopismo naukowe
Tytuł :
Association of 3 single nucleotide polymorphisms of the eighth chromosome with remodeling of the myocardium and carotid arteries in the Kazakh population.
Autorzy :
Raushan K; Medical Centre Hospital of President's Affairs Administration of the Republic of Kazakhstan.
Benberin V; Medical Centre Hospital of President's Affairs Administration of the Republic of Kazakhstan.
Vochshenkova T; Medical Centre Hospital of President's Affairs Administration of the Republic of Kazakhstan.
Babenko D; Karaganda Medical University, Kazakhstan.
Sibagatova A; Medical Centre Hospital of President's Affairs Administration of the Republic of Kazakhstan.
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Źródło :
Medicine [Medicine (Baltimore)] 2021 Feb 12; Vol. 100 (6), pp. e24608.
Typ publikacji :
Journal Article; Observational Study
MeSH Terms :
Carotid Intima-Media Thickness*
Chromosomes, Human, Pair 8*
Carotid Arteries/*physiology
Hypertension/*genetics
Ventricular Remodeling/*genetics
Adult ; Carotid Arteries/diagnostic imaging ; Case-Control Studies ; Female ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide
Czasopismo naukowe
Tytuł :
Transcriptome of Breast Tumors With Different Amplification Status of the Long Arm of Chromosome 8.
Autorzy :
Ibragimova MK; Tomsk National Research Medical Center of the Russian Academy of Sciences, Cancer Research Institute, Tomsk, Russian Federation .
Tsyganov MM; Tomsk National Research Medical Center of the Russian Academy of Sciences, Cancer Research Institute, Tomsk, Russian Federation.
Pevzner AM; Tomsk National Research Medical Center of the Russian Academy of Sciences, Cancer Research Institute, Tomsk, Russian Federation.
Litviakov NV; Tomsk National Research Medical Center of the Russian Academy of Sciences, Cancer Research Institute, Tomsk, Russian Federation.
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Źródło :
Anticancer research [Anticancer Res] 2021 Jan; Vol. 41 (1), pp. 187-195.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosomes, Human, Pair 8*
Gene Amplification*
Transcriptome*
Breast Neoplasms/*genetics
Adult ; Aged ; Biomarkers, Tumor ; Breast Neoplasms/diagnosis ; Breast Neoplasms/therapy ; Combined Modality Therapy ; Computational Biology/methods ; Female ; Gene Expression Profiling/methods ; Gene Expression Regulation, Neoplastic ; Gene Frequency ; Humans ; Middle Aged ; Neoplasm Staging ; Young Adult
Czasopismo naukowe
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: .
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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
Tytuł :
Behçet disease (BD) and BD-like clinical phenotypes: NF-κB pathway in mucosal ulcerating diseases.
Autorzy :
Perazzio SF; Seattle Children's Research Institute, University of Washington and Center for Immunity and Immunotherapies, Seattle, WA, USA.; Division of Rheumatology, Federal University of Sao Paulo, Sao Paulo, Brazil.
Allenspach EJ; Seattle Children's Research Institute, University of Washington and Center for Immunity and Immunotherapies, Seattle, WA, USA.
Eklund KK; Division of Rheumatology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; ORTON Orthopaedic Hospital of the Orton Foundation, Helsinki, Finland.
Varjosalo M; Division of Rheumatology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; ORTON Orthopaedic Hospital of the Orton Foundation, Helsinki, Finland.; Molecular Systems Biology Research Group and Proteomics Unit, Institute of Biotechnology, University of Helsinki, Helsinki, Finland.
Shinohara MM; Divisions of Dermatology and Dermatopathology, University of Washington, Seattle, WA, USA.
Torgerson TR; Allen Institute for Immunology, Seattle, WA, USA.
Seppänen MRJ; Rare Disease and Pediatric Research Centers, Hospital for Children and Adolescents and Adult Immunodeficiency Unit, Inflammation Center, University of Helsinki and HUS Helsinki University Hospital, Helsinki, Finland.
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Źródło :
Scandinavian journal of immunology [Scand J Immunol] 2020 Nov; Vol. 92 (5), pp. e12973. Date of Electronic Publication: 2020 Oct 10.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Behcet Syndrome/*immunology
Chromosomes, Human, Pair 8/*immunology
NF-kappa B/*immunology
Trisomy/*immunology
Behcet Syndrome/genetics ; Behcet Syndrome/pathology ; Chromosomes, Human, Pair 8/genetics ; Genetic Predisposition to Disease/genetics ; Humans ; Interleukin-10/genetics ; Interleukin-10/immunology ; Mouth Mucosa/immunology ; Mouth Mucosa/metabolism ; Mouth Mucosa/pathology ; NF-kappa B/genetics ; NF-kappa B/metabolism ; Phenotype ; Skin Ulcer/genetics ; Skin Ulcer/immunology ; Skin Ulcer/pathology ; Trisomy/genetics
Czasopismo naukowe
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. .
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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
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 :
Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development.
Autorzy :
Bademci G; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Abad C; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Cengiz FB; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Seyhan S; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Incesulu A; Department of Otolaryngology, Eskisehir Osmangazi University School of Medicine, Eskisehir, Turkey.
Guo S; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Fitoz S; Department of Diagnostic Radiology, Ankara University School of Medicine, Ankara, Turkey.
Atli EI; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Gosstola NC; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Demir S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Colbert BM; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.; Medical Scientist Training Program, University of Miami Miller School of Medicine, Miami, Florida, USA.
Seyhan GC; Department of Dermatology, Bakirkoy Sadi Konuk Training and Research Hospital, Istanbul, Turkey.
Sineni CJ; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.
Duman D; Department of Audiology, Ankara University School of Medicine, Ankara, Turkey.
Gurkan H; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.
Morton CC; Department of Obstetrics and Gynecology, Brigham and Women's Hospital, Boston, Massachusetts, USA.; Harvard Medical School, Boston, Massachusetts, USA.; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.; Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts, USA.; Manchester Centre for Audiology and Deafness, School of Health Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom.
Dykxhoorn DM; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.; John T. Macdonald Foundation Department of Human Genetics, and.
Walz K; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.; John T. Macdonald Foundation Department of Human Genetics, and.
Tekin M; John P. Hussman Institute for Human Genomics, University of Miami Miller School of Medicine, Miami, Florida, USA.; John T. Macdonald Foundation Department of Human Genetics, and.; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, Florida, USA.
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Źródło :
The Journal of clinical investigation [J Clin Invest] 2020 Aug 03; Vol. 130 (8), pp. 4213-4217.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Chromosomes, Human, Pair 8*/genetics
Chromosomes, Human, Pair 8*/metabolism
Cochlea*/embryology
Cochlea*/pathology
Cochlear Diseases*/embryology
Cochlear Diseases*/genetics
Cochlear Diseases*/pathology
Growth Differentiation Factor 6*/biosynthesis
Growth Differentiation Factor 6*/genetics
Response Elements*
Animals ; Female ; Humans ; Male ; Mice ; Mice, Transgenic
Czasopismo naukowe
Tytuł :
AML1-ETO inhibits acute myeloid leukemia immune escape by CD48.
Autorzy :
Wang Z; Department of Hematology-Oncology, International Cancer Center, Shenzhen University General Hospital, Shenzhen University Health Science Center, Shenzhen, China.; Department of Hematology, Chinese PLA General Hospital, Beijing, China.
Guan W; Department of Hematology, Chinese PLA General Hospital, Beijing, China.
Wang M; Department of Hematology, Chinese PLA General Hospital, Beijing, China.
Chen J; Department of Hematology-Oncology, International Cancer Center, Shenzhen University General Hospital, Shenzhen University Health Science Center, Shenzhen, China.
Zhang L; Department of Hematology, Chinese PLA General Hospital, Beijing, China.
Xiao Y; Department of Hematology, Chinese PLA General Hospital, Beijing, China.
Wang L; Department of Hematology-Oncology, International Cancer Center, Shenzhen University General Hospital, Shenzhen University Health Science Center, Shenzhen, China.
Li Y; Department of Hematology-Oncology, International Cancer Center, Shenzhen University General Hospital, Shenzhen University Health Science Center, Shenzhen, China.
Yu L; Department of Hematology-Oncology, International Cancer Center, Shenzhen University General Hospital, Shenzhen University Health Science Center, Shenzhen, China.; Department of Hematology, Chinese PLA General Hospital, Beijing, China.
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Źródło :
Leukemia & lymphoma [Leuk Lymphoma] 2021 Apr; Vol. 62 (4), pp. 937-943. Date of Electronic Publication: 2020 Nov 21.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Core Binding Factor Alpha 2 Subunit*/genetics
Leukemia, Myeloid, Acute*/genetics
Chromosomes, Human, Pair 21 ; Chromosomes, Human, Pair 8 ; Humans ; Oncogene Proteins, Fusion/genetics ; RUNX1 Translocation Partner 1 Protein/genetics ; Translocation, Genetic
Czasopismo naukowe
Tytuł :
Morphological characteristics, cytogenetic profile, and outcome of RUNX1-RUNX1T1-positive acute myeloid leukemia: Experience of an Indian tertiary care center.
Autorzy :
Gupta R; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
Yadav S; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
Parashar Y; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
Rahman K; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
Singh MK; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
Chandra D; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
Gupta A; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
Nityanand S; Department of Hematology, Sanjay Gandhi Post Graduate Institute of Medical Sciences (SGPGIMS), Uttar Pradesh, Lucknow, India.
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Źródło :
International journal of laboratory hematology [Int J Lab Hematol] 2020 Feb; Vol. 42 (1), pp. 37-45. Date of Electronic Publication: 2019 Nov 14.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosomes, Human, Pair 21*/genetics
Chromosomes, Human, Pair 21*/metabolism
Chromosomes, Human, Pair 8*/genetics
Chromosomes, Human, Pair 8*/metabolism
Core Binding Factor Alpha 2 Subunit*/blood
Core Binding Factor Alpha 2 Subunit*/genetics
Leukemia, Myeloid, Acute*/blood
Leukemia, Myeloid, Acute*/drug therapy
Leukemia, Myeloid, Acute*/genetics
Leukemia, Myeloid, Acute*/mortality
Sarcoma, Myeloid*/blood
Sarcoma, Myeloid*/drug therapy
Sarcoma, Myeloid*/genetics
Sarcoma, Myeloid*/mortality
Translocation, Genetic*
Antineoplastic Combined Chemotherapy Protocols/*administration & dosage
Adolescent ; Adult ; Aged ; Asparaginase/administration & dosage ; Child ; Child, Preschool ; Daunorubicin/administration & dosage ; Disease-Free Survival ; Female ; Humans ; Male ; Middle Aged ; Prednisone/administration & dosage ; RUNX1 Translocation Partner 1 Protein/blood ; RUNX1 Translocation Partner 1 Protein/genetics ; Retrospective Studies ; Survival Rate ; Vincristine/administration & dosage
SCR Protocol :
PVDA protocol
Czasopismo naukowe
Tytuł :
Pediatric Idiopathic Basal Ganglia Calcification and Spherocytosis With Chromosome 8p11 Deletion.
Autorzy :
Morris M; From the Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Kwon R; From the Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Chen L; From the Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
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Źródło :
Journal of neuropathology and experimental neurology [J Neuropathol Exp Neurol] 2020 Feb 01; Vol. 79 (2), pp. 238-241.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosome Deletion*
Chromosomes, Human, Pair 8*
Basal Ganglia Diseases/*genetics
Basal Ganglia Diseases/*pathology
Brain/*pathology
Calcinosis/*genetics
Calcinosis/*pathology
Spherocytosis, Hereditary/*genetics
Spherocytosis, Hereditary/*pathology
Basal Ganglia Diseases/complications ; Calcinosis/complications ; Female ; Humans ; Sodium-Phosphate Cotransporter Proteins, Type III/genetics ; Spherocytosis, Hereditary/complications
SCR Disease Name :
Idiopathic basal ganglia calcification, childhood onset
Czasopismo naukowe
Tytuł :
[Genetic analysis of a family with congenital heart defects caused by chromosome 8p23.1 deletion].
Autorzy :
Feng Q; Shenzhen Maternal and Child Health Care Hospital Affiliated to Southern Medical University, Shenzhen, Guangdong 518017, China. .
Xie J
Liu Y
Geng Q
Wu W
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2020 Jan 10; Vol. 37 (1), pp. 44-47.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosome Deletion*
Chromosomes, Human, Pair 8*/genetics
Heart Defects, Congenital*/genetics
GATA4 Transcription Factor/genetics ; Genetic Testing ; Humans ; Karyotyping
Czasopismo naukowe
Tytuł :
[A case with 8q22.2q22.3 deletion syndrome].
Autorzy :
Lei K; Pediatric Institute of Pediatric Center, Affiliated Hospital of Qingdao University, Qingdao 266003, China.
Zhang Y; Neurological and Endocrine Department of Pediatric Center, Affiliated Hospital of Qingdao University, Qingdao 266003, China.
Sun Y; Department of Ophthalmology, Affiliated Central Hospital of Qingdao University, Qingdao 266042, China.
Yuan SY; Department of Cerebral Surgery, Affiliated Central Hospital of Qingdao University, Qingdao 266042, China.
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Źródło :
Zhonghua er ke za zhi = Chinese journal of pediatrics [Zhonghua Er Ke Za Zhi] 2020 Jan 02; Vol. 58 (1), pp. 56-57.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Deletion*
Chromosomes, Human, Pair 2*
Chromosomes, Human, Pair 8*
Humans ; Syndrome
Czasopismo naukowe
Tytuł :
Expression of ERV3-1 in leukocytes of acute myelogenous leukemia patients.
Autorzy :
Nakagawa S; Department of Molecular Life Science, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan; Division of Genome Sciences, Institute of Medical Sciences, Tokai University, Isehara, Kanagawa 259-1193, Japan. Electronic address: .
Kawashima M; Division of Clinical Oncology and Hematology, The Jikei University School of Medicine, Minato-ku, Tokyo 105-8471, Japan; Department of Hematological Malignancy, Institute of Medical Science, Tokai University, Isehara, Kanagawa 259-1193, Japan.
Miyatake Y; Department of Hematological Malignancy, Institute of Medical Science, Tokai University, Isehara, Kanagawa 259-1193, Japan; Department of Advanced Medical Science, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.
Kudo K; Department of Hematological Malignancy, Institute of Medical Science, Tokai University, Isehara, Kanagawa 259-1193, Japan; Department of Advanced Medical Science, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.
Kotaki R; Department of Hematological Malignancy, Institute of Medical Science, Tokai University, Isehara, Kanagawa 259-1193, Japan.
Ando K; Department of Hematological Malignancy, Institute of Medical Science, Tokai University, Isehara, Kanagawa 259-1193, Japan; Department of Hematology and Oncology, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan.
Kotani A; Department of Hematological Malignancy, Institute of Medical Science, Tokai University, Isehara, Kanagawa 259-1193, Japan; Department of Advanced Medical Science, Tokai University School of Medicine, Isehara, Kanagawa 259-1193, Japan. Electronic address: .
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Źródło :
Gene [Gene] 2021 Mar 20; Vol. 773, pp. 145363. Date of Electronic Publication: 2020 Dec 16.
Typ publikacji :
Journal Article
MeSH Terms :
Gene Products, env/*genetics
Leukemia, Myeloid, Acute/*genetics
Leukocytes/*metabolism
Monocytes/*metabolism
Adult ; Aged ; Aged, 80 and over ; Cell Lineage ; Chromosomes, Human, Pair 8/genetics ; Female ; Gene Expression Regulation, Neoplastic/genetics ; Genome, Human/genetics ; Humans ; Leukemia, Myeloid, Acute/blood ; Leukemia, Myeloid, Acute/pathology ; Leukocytes/virology ; Male ; Middle Aged ; Monocytes/virology ; Retroviridae/genetics ; Trisomy/genetics ; Trisomy/pathology
SCR Disease Name :
Chromosome 8, trisomy
Czasopismo naukowe
Tytuł :
[Prenatal diagnosis of a fetus with 8q13.3 microdeletion through chromosomal microarray analysis].
Autorzy :
Rao H; Prenatal Diagnosis Center, Jiangxi Provincial Maternal and Child Health Care Hospital, Nanchang, Jiangxi 330006, China. .
Liu Y
Xiao J
Zou Y
Yuan H
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Mar 10; Vol. 38 (3), pp. 268-270.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosome Aberrations*
Prenatal Diagnosis*
Chromosome Deletion ; Chromosomes, Human, Pair 8 ; DNA Copy Number Variations ; Female ; Fetus ; Humans ; Karyotyping ; Microarray Analysis ; Pregnancy
Czasopismo naukowe
Tytuł :
Hemophagocytic lymphohistiocytosis and myelodysplastic syndrome: a case report and review of the literature.
Autorzy :
Sun Y; Section of Hematology/Oncology, Baylor St Luke Medical Center, Houston, TX, 77030, USA.
Blieden C; Department of Molecular and Human Genetics, Baylor Genetics, Baylor College of Medicine, Houston, TX, USA.
Merritt BY; Department of Pathology and Immunology, Baylor St. Luke's Medical Center, Baylor College of Medicine, Houston, TX, USA.
Sosa R; Section of Hematology/Oncology, Baylor St Luke Medical Center, Houston, TX, 77030, USA.; The Dan L. Duncan Comprehensive Cancer Center at Baylor College of Medicine, 1 Baylor Plaza, Houston, TX, 77030, USA.
Rivero G; Section of Hematology/Oncology, Baylor St Luke Medical Center, Houston, TX, 77030, USA. .; The Dan L. Duncan Comprehensive Cancer Center at Baylor College of Medicine, 1 Baylor Plaza, Houston, TX, 77030, USA. .
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Źródło :
Journal of medical case reports [J Med Case Rep] 2021 Mar 01; Vol. 15 (1), pp. 98. Date of Electronic Publication: 2021 Mar 01.
Typ publikacji :
Case Reports; Journal Article; Review
MeSH Terms :
Lymphohistiocytosis, Hemophagocytic/*diagnosis
Lymphohistiocytosis, Hemophagocytic/*genetics
Myelodysplastic Syndromes/*diagnosis
Myelodysplastic Syndromes/*genetics
Aged, 80 and over ; Bone Marrow/pathology ; Chromosomes, Human, Pair 8 ; Fatal Outcome ; Female ; Humans ; Karyotype ; Trisomy
SCR Disease Name :
Chromosome 8, trisomy
Czasopismo naukowe
Tytuł :
[Clinical characterization and genetic analysis of a newborn with chromosome 8q21.11 deletion syndrome].
Autorzy :
Li S; Medical Genetics Center, Shenzhen Maternal and Child Health Care Hospital Affiliated to Southern Medical University, Shenzhen, Guangdong 518017, China. .
Wu W
Xie J
Li H
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Feb 10; Vol. 38 (2), pp. 145-149.
Typ publikacji :
Journal Article
MeSH Terms :
DNA Copy Number Variations*
Genetic Testing*
Monosomy/*genetics
Chromosome Banding ; Chromosomes, Human, Pair 8/genetics ; Female ; Homeodomain Proteins/genetics ; Humans ; Infant, Newborn ; Karyotyping ; Peroxisomal Biogenesis Factor 2/genetics ; Polymorphism, Single Nucleotide ; Transcription Factors/genetics
SCR Disease Name :
Chromosome 8 deletion
Czasopismo naukowe
Tytuł :
Hematopoietic stem cell transplantation for diffuse large B-cell lymphoma having 8q24/MYC rearrangement in Japan.
Autorzy :
Takahashi T; Department of Oncology/Hematology, Shimane University Hospital, Izumo, Japan.; The Adult Malignant Lymphoma Working Group of the JSHCT, Nagoya, Japan.
Suzuki R; Department of Oncology/Hematology, Shimane University Hospital, Izumo, Japan.; The Adult Malignant Lymphoma Working Group of the JSHCT, Nagoya, Japan.
Yamamoto G; Department of Hematology, Toranomon Hospital, Tokyo, Japan.
Nakazawa H; Division of Hematology, Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.
Kurosawa M; Department of Hematology, National Hospital Organization Hokkaido Cancer Center, Sapporo, Japan.
Kobayashi T; Division of Hematology and Oncology, Department of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Okada M; Division of Hematology, Department of Internal Medicine, Hyogo College of Medicine, Nishinomiya, Japan.
Akasaka T; Department of Hematology, Tenri Hospital, Tenri, Japan.
Kim SW; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Fukuda T; Department of Hematopoietic Stem Cell Transplantation, National Cancer Center Hospital, Tokyo, Japan.
Ichinohe T; Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan.
Atsuta Y; Japanese Data Center for Hematopoietic Cell Transplantation, Nagoya, Japan.; Department of Healthcare Administration, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Suzumiya J; Department of Oncology/Hematology, Shimane University Hospital, Izumo, Japan.; The Adult Malignant Lymphoma Working Group of the JSHCT, Nagoya, Japan.
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Źródło :
Hematological oncology [Hematol Oncol] 2021 Feb; Vol. 39 (1), pp. 66-74. Date of Electronic Publication: 2020 Oct 05.
Typ publikacji :
Journal Article
MeSH Terms :
Chromosome Aberrations*
Hematopoietic Stem Cell Transplantation*
Lymphoma, Large B-Cell, Diffuse*/genetics
Lymphoma, Large B-Cell, Diffuse*/mortality
Lymphoma, Large B-Cell, Diffuse*/therapy
Chromosomes, Human, Pair 8/*genetics
Proto-Oncogene Proteins c-myc/*genetics
Adult ; Aged ; Autografts ; Disease-Free Survival ; Female ; Humans ; Male ; Middle Aged ; Retrospective Studies ; Survival Rate
Czasopismo naukowe

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