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Wyszukujesz frazę ""Genetic Heterogeneity"" wg kryterium: Temat


Tytuł:
ASO Author Reflections: Genetic Heterogeneity in HER2-Low Breast Cancers Reflects Different Treatment Responses.
Autorzy:
Yang L; Department of Pathology/Institute of Clinical Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China. .
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Źródło:
Annals of surgical oncology [Ann Surg Oncol] 2023 Sep; Vol. 30 (9), pp. 5663-5664. Date of Electronic Publication: 2023 Apr 10.
Typ publikacji:
Journal Article; Comment
MeSH Terms:
Genetic Heterogeneity*
Breast Neoplasms*/genetics
Humans ; Female ; Breast ; Receptor, ErbB-2/genetics
Czasopismo naukowe
Tytuł:
Emergence of NDM-1 and KPC-3 carbapenemases in Kluyvera cryocrescens: Investigating genetic heterogeneity and acquisition routes of bla NDM-1 in Enterobacterales species in Portugal.
Autorzy:
Loiodice M; UCIBIO - Applied Molecular Biosciences Unit, Faculty of Pharmacy, University of Porto, Porto, Portugal; Associate Laboratory i4HB - Institute for Health and Bioeconomy, Faculty of Pharmacy, University of Porto, Porto, Portugal.
Ribeiro M; Service of Clinical Pathology, Hospital University Centre São João, Porto, Portugal.
Peixe L; UCIBIO - Applied Molecular Biosciences Unit, Faculty of Pharmacy, University of Porto, Porto, Portugal; Associate Laboratory i4HB - Institute for Health and Bioeconomy, Faculty of Pharmacy, University of Porto, Porto, Portugal.
Novais Â; UCIBIO - Applied Molecular Biosciences Unit, Faculty of Pharmacy, University of Porto, Porto, Portugal; Associate Laboratory i4HB - Institute for Health and Bioeconomy, Faculty of Pharmacy, University of Porto, Porto, Portugal. Electronic address: .
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Źródło:
Journal of global antimicrobial resistance [J Glob Antimicrob Resist] 2023 Sep; Vol. 34, pp. 195-198. Date of Electronic Publication: 2023 Jul 17.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Heterogeneity*
Escherichia coli*/genetics
Humans ; Portugal
SCR Organism:
Kluyvera cryocrescens
Czasopismo naukowe
Tytuł:
DGH-GO: dissecting the genetic heterogeneity of complex diseases using gene ontology.
Autorzy:
Asif M; Biomedical Data Science Lab, Department of Bioinformatics and Biotechnology, Government College University Faisalabad, Faisalabad, 38000, Pakistan. .; LASIGE, Departamento de Informática, Faculdade de Ciências, Universidade de Lisboa, Lisboa, Portugal. .
Martiniano HFMC; Instituto Nacional de Saúde Doutor Ricardo Jorge, Avenida Padre Cruz, 1649-016, Lisbon, Portugal.; BioISI - Instituto de Biosistemas e Ciências Integrativas, Faculdade de Ciências, Universidade de Lisboa, 1749-016, Lisboa, Portugal.
Lamurias A; Department of Computer Science, Aalborg University, Ålborg, Denmark.; NOVA LINCS, NOVA School of Science and Technology, Lisboa, Portugal.
Kausar S; DeepOmicsVision, Avenue de Luminy, 13009, Marseille, France.
Couto FM; LASIGE, Departamento de Informática, Faculdade de Ciências, Universidade de Lisboa, Lisboa, Portugal. .
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Źródło:
BMC bioinformatics [BMC Bioinformatics] 2023 Apr 26; Vol. 24 (1), pp. 171. Date of Electronic Publication: 2023 Apr 26.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Heterogeneity*
Autism Spectrum Disorder*/genetics
Humans ; Gene Ontology ; Software
Czasopismo naukowe
Tytuł:
Hallmarks of transcriptional intratumour heterogeneity across a thousand tumours.
Autorzy:
Gavish A; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Tyler M; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Greenwald AC; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Hoefflin R; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.; Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Simkin D; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Tschernichovsky R; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.; Davidoff Cancer Center, Rabin Medical Center, Petah Tikva, Israel.
Galili Darnell N; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Somech E; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Barbolin C; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Antman T; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Kovarsky D; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Barrett T; Department of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St Louis, MO, USA.; Department of Genetics, Washington University School of Medicine, St Louis, MO, USA.
Gonzalez Castro LN; Department of Pathology and Center for Cancer Research, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Neuro-Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.; Department of Neurology, Brigham and Women's Hospital, Boston, MA, USA.
Halder D; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Chanoch-Myers R; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Laffy J; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Mints M; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.; Department of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.
Wider A; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Tal R; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Spitzer A; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Hara T; Department of Pathology and Center for Cancer Research, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Raitses-Gurevich M; The Oncology Institute, Chaim Sheba Medical Center, Ramat Gan, Israel.
Stossel C; The Oncology Institute, Chaim Sheba Medical Center, Ramat Gan, Israel.; The Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Golan T; The Oncology Institute, Chaim Sheba Medical Center, Ramat Gan, Israel.; The Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
Tirosh A; The Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.; Division of Endocrinology, Diabetes and Metabolism, Chaim Sheba Medical Center, Ramat Gan, Israel.
Suvà ML; Department of Pathology and Center for Cancer Research, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Puram SV; Department of Otolaryngology-Head and Neck Surgery, Washington University School of Medicine, St Louis, MO, USA.; Siteman Cancer Center, Washington University School of Medicine, St Louis, MO, USA.
Tirosh I; Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel. .
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Źródło:
Nature [Nature] 2023 Jun; Vol. 618 (7965), pp. 598-606. Date of Electronic Publication: 2023 May 31.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Expression Regulation, Neoplastic*
Genetic Heterogeneity*
Neoplasms*/classification
Neoplasms*/genetics
Neoplasms*/pathology
Single-Cell Gene Expression Analysis*
Humans ; Epithelial Cells/cytology ; Epithelial Cells/metabolism ; Tumor Microenvironment
Czasopismo naukowe
Tytuł:
Genetic Heterogeneity Shapes Brain Connectivity in Psychiatry.
Autorzy:
Moreau CA; Human Genetics and Cognitive Functions, Institut Pasteur, Université Paris Cité, Paris, France; Sainte-Justine Research Center, University of Montréal, Montréal, Canada; Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montreal, Canada. Electronic address: .
Harvey A; Sainte-Justine Research Center, University of Montréal, Montréal, Canada; Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montreal, Canada.
Kumar K; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Huguet G; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Urchs SGW; Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montreal, Canada; Montreal Neurological Institute, McGill University, Montreal, Canada.
Douard EA; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Schultz LM; Lifespan Brain Institute, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.
Sharmarke H; Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montreal, Canada.
Jizi K; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Martin CO; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Younis N; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Tamer P; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Rolland T; Human Genetics and Cognitive Functions, Institut Pasteur, Université Paris Cité, Paris, France.
Martineau JL; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Orban P; Centre de Recherche de l'Institut Universitaire en Santé Mentale de Montréal, Montréal, Canada; Département de Psychiatrie et d'Addictologie, Université de Montréal, Montréal, Canada.
Silva AI; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, United Kingdom; School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, The Netherlands.
Hall J; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, United Kingdom.
van den Bree MBM; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, United Kingdom.
Owen MJ; Neuroscience and Mental Health Research Institute, Cardiff University, Cardiff, United Kingdom; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, United Kingdom.
Linden DEJ; MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, United Kingdom; School for Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, The Netherlands.
Labbe A; Département des Sciences de la Décision, HEC, Québec, Montréal, Canada.
Lippé S; Sainte-Justine Research Center, University of Montréal, Montréal, Canada.
Bearden CE; Integrative Center for Neurogenetics, Semel Institute for Neuroscience and Human Behavior, Departments of Psychiatry and Biobehavioral Sciences and Psychology, University of California, Los Angeles, Los Angeles, California.
Almasy L; Department of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Pennsylvania; Department of Genetics, University of Pennsylvania, Philadelphia, Pennsylvania; Lifespan Brain Institute, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania.
Glahn DC; Harvard Medical School, Department of Psychiatry, Boston, Massachusetts; Boston Children's Hospital, Tommy Fuss Center for Neuropsychiatric Disease Research, Boston, Massachusetts.
Thompson PM; Imaging Genetics Center, Stevens Institute for Neuroimaging and Informatics, Keck USC School of Medicine, Marina del Rey, California.
Bourgeron T; Human Genetics and Cognitive Functions, Institut Pasteur, Université Paris Cité, Paris, France.
Bellec P; Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal, Montreal, Canada.
Jacquemont S; Sainte-Justine Research Center, University of Montréal, Montréal, Canada. Electronic address: .
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Źródło:
Biological psychiatry [Biol Psychiatry] 2023 Jan 01; Vol. 93 (1), pp. 45-58. Date of Electronic Publication: 2022 Sep 02.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Heterogeneity*
Psychiatry*
Humans ; Genetic Predisposition to Disease ; Multifactorial Inheritance/genetics ; Brain/diagnostic imaging ; DNA Copy Number Variations/genetics ; Genome-Wide Association Study
Czasopismo naukowe
Tytuł:
Treatments, prognostic factors, and genetic heterogeneity in advanced cholangiocarcinoma: A multicenter real-world study.
Autorzy:
Ottaiano A; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Santorsola M; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Diana A; Medical Oncology Unit, Ospedale del Mare, Napoli, Italy.
Belli A; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Lentini Graziano ML; Medical Oncology Unit, AORN Ospedali dei Colli-Monaldi-Cotugno-CTO, Napoli, Italy.
Orefice J; Medical Oncology Unit, Ospedale del Mare, Napoli, Italy.
Patrone R; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Di Mauro A; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Scognamiglio G; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Tatangelo F; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
De Bellis M; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Piccirillo M; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Fiore F; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Stilo S; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Tarotto L; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Correra M; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Di Lorenzo S; Medical Oncology Unit, Ospedale del Mare, Napoli, Italy.
Capuozzo M; Coordinamento Farmaceutico, ASL-Naples-3, Ercolano, Italy.
Avallone A; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Silvestro L; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Bianco A; Medical Oncology Unit, AORN Ospedali dei Colli-Monaldi-Cotugno-CTO, Napoli, Italy.
Granata V; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Federico P; Medical Oncology Unit, Ospedale del Mare, Napoli, Italy.
Montesarchio V; Medical Oncology Unit, AORN Ospedali dei Colli-Monaldi-Cotugno-CTO, Napoli, Italy.
Daniele B; Medical Oncology Unit, Ospedale del Mare, Napoli, Italy.
Izzo F; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
Nasti G; Istituto Nazionale Tumori di Napoli, IRCCS 'G. Pascale', Napoli, Italy.
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Źródło:
Cancer medicine [Cancer Med] 2024 Feb; Vol. 13 (4), pp. e6892.
Typ publikacji:
Multicenter Study; Journal Article
MeSH Terms:
Cholangiocarcinoma*/drug therapy
Cholangiocarcinoma*/genetics
Cholangiocarcinoma*/pathology
Bile Duct Neoplasms*/drug therapy
Bile Duct Neoplasms*/genetics
Humans ; Aged ; Prognosis ; Genetic Heterogeneity ; Bile Ducts, Intrahepatic/pathology ; Antineoplastic Combined Chemotherapy Protocols/therapeutic use
Czasopismo naukowe
Tytuł:
Measures of genetic diversification in somatic tissues at bulk and single-cell resolution.
Autorzy:
Moeller ME; Department of Mathematics, Queen Mary University of London, London, United Kingdom.
Mon Père NV; Evolutionary Dynamics Group, Centre for Cancer Genomics and Computational Biology, Barts Cancer Centre, Queen Mary University of London, London, United Kingdom.; Interuniversity Institute of Bioinformatics in Brussels, Université Libre de Bruxelles, Ixelles, Belgium.
Werner B; Evolutionary Dynamics Group, Centre for Cancer Genomics and Computational Biology, Barts Cancer Centre, Queen Mary University of London, London, United Kingdom.
Huang W; Department of Mathematics, Queen Mary University of London, London, United Kingdom.; Group of Theoretical Biology, The State Key Laboratory of Biocontrol, School of Life Science, Sun Yat-sen University, Guangzhou, China.
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Źródło:
ELife [Elife] 2024 Jan 24; Vol. 12. Date of Electronic Publication: 2024 Jan 24.
Typ publikacji:
Journal Article
MeSH Terms:
Adult Stem Cells*
Adult ; Humans ; Cell Self Renewal ; Environmental Exposure ; Genetic Heterogeneity ; Genomics
Czasopismo naukowe
Tytuł:
Glioblastoma evolution and heterogeneity from a 3D whole-tumor perspective.
Autorzy:
Mathur R; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Wang Q; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Schupp PG; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Nikolic A; Department of Biochemistry & Molecular Biology, University of Calgary, Calgary, AB.
Hilz S; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Hong C; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Grishanina NR; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Kwok D; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Stevers NO; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Jin Q; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Youngblood MW; Department of Neurological Surgery, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Stasiak LA; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Hou Y; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Wang J; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Yamaguchi TN; Department of Human Genetics, University of California, Los Angeles, Los Angees, CA, USA.
Lafontaine M; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Shai A; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Smirnov IV; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Solomon DA; Department of Pathology, University of California San Francisco, San Francisco, CA, USA.
Chang SM; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Hervey-Jumper SL; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Berger MS; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Lupo JM; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Okada H; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Phillips JJ; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Boutros PC; Department of Human Genetics, University of California, Los Angeles, Los Angees, CA, USA.
Gallo M; Department of Biochemistry & Molecular Biology, University of Calgary, Calgary, AB; Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX, USA.
Oldham MC; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA.
Yue F; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA; Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. Electronic address: .
Costello JF; Department of Neurological Surgery, University of California San Francisco, San Francisco, CA, USA. Electronic address: .
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Źródło:
Cell [Cell] 2024 Jan 18; Vol. 187 (2), pp. 446-463.e16.
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Brain Neoplasms*/genetics
Brain Neoplasms*/pathology
Glioblastoma*/genetics
Glioblastoma*/pathology
Models, Biological*
Humans ; Epigenomics ; Genomics ; Single-Cell Analysis ; Tumor Microenvironment ; Genetic Heterogeneity
Czasopismo naukowe
Tytuł:
Genetic heterogeneity in p53-null leukemia increases transiently with spindle assembly checkpoint inhibition and is not rescued by p53.
Autorzy:
Wang M; Molecular & Cell Biophysics Lab, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Phan S; Molecular & Cell Biophysics Lab, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Hayes BH; Molecular & Cell Biophysics Lab, University of Pennsylvania, Philadelphia, PA, 19104, USA.
Discher DE; Molecular & Cell Biophysics Lab, University of Pennsylvania, Philadelphia, PA, 19104, USA. .
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Źródło:
Chromosoma [Chromosoma] 2024 Jan; Vol. 133 (1), pp. 77-92. Date of Electronic Publication: 2023 May 31.
Typ publikacji:
Journal Article
MeSH Terms:
Neoplasms*/genetics
Neoplasms*/metabolism
Leukemia*/genetics
Leukemia*/metabolism
Humans ; M Phase Cell Cycle Checkpoints ; Tumor Suppressor Protein p53/genetics ; Tumor Suppressor Protein p53/metabolism ; DNA Copy Number Variations ; Genetic Heterogeneity ; Aneuploidy ; Spindle Apparatus/metabolism
Czasopismo naukowe
Tytuł:
Understanding genetic heterogeneity in gene-edited hematopoietic stem cell products.
Autorzy:
Becker HJ; Laboratory for Stem Cell Therapy, Faculty of Medicine, Tsukuba University, Tsukuba, Japan; Division of Cell Regulation, Center of Experimental Medicine and Systems Biology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan. Electronic address: .
Yamazaki S; Laboratory for Stem Cell Therapy, Faculty of Medicine, Tsukuba University, Tsukuba, Japan; Division of Cell Regulation, Center of Experimental Medicine and Systems Biology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan. Electronic address: .
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Źródło:
Experimental hematology [Exp Hematol] 2024 Jan; Vol. 129, pp. 104133. Date of Electronic Publication: 2023 Nov 29.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Gene Editing*
CRISPR-Cas Systems*
Genetic Heterogeneity ; Hematopoietic Stem Cells/metabolism ; Mutation
Czasopismo naukowe
Tytuł:
New evidence of genetic heterogeneity causing hereditary gingival fibromatosis and ALK and CD36 as new candidate genes.
Autorzy:
Machado RA; Department of Oral Diagnosis, School of Dentistry, University of Campinas (FOP/UNICAMP), Piracicaba, São Paulo, Brazil.; Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, São Paulo, Brazil.
de Andrade RS; Department of Oral Diagnosis, School of Dentistry, University of Campinas (FOP/UNICAMP), Piracicaba, São Paulo, Brazil.
Pêgo SPB; Stomatology Clinic, Dental School, State University of Montes Claros (Unimontes), Montes Claros, Minas Gerais, Brazil.
Krepischi ACV; Department of Genetics and Evolutionary Biology, Human Genome and Stem-Cell Research Center, Institute of Biosciences, University of São Paulo (IB/USP), São Paulo, Brazil.
Coletta RD; Department of Oral Diagnosis, School of Dentistry, University of Campinas (FOP/UNICAMP), Piracicaba, São Paulo, Brazil.; Graduate Program in Oral Biology, School of Dentistry, University of Campinas, Piracicaba, São Paulo, Brazil.
Martelli-Júnior H; Stomatology Clinic, Dental School, State University of Montes Claros (Unimontes), Montes Claros, Minas Gerais, Brazil.; Center for Rehabilitation of Craniofacial Anomalies, Dental School, University of José Rosario Vellano (Unifenas), Alfenas, Minas Gerais, Brazil.
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Źródło:
Journal of periodontology [J Periodontol] 2023 Jan; Vol. 94 (1), pp. 108-118. Date of Electronic Publication: 2022 Jul 01.
Typ publikacji:
Journal Article
MeSH Terms:
Genetic Heterogeneity*
Fibromatosis, Gingival*/genetics
Fibromatosis, Gingival*/pathology
Humans ; CD36 Antigens/genetics ; Pedigree ; Receptor Protein-Tyrosine Kinases/genetics
SCR Disease Name:
Fibromatosis, Gingival, Hereditary
Czasopismo naukowe
Tytuł:
Genetic heterogeneity: Challenges, impacts, and methods through an associative lens.
Autorzy:
Woodward AA; Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Urbanowicz RJ; Department of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Naj AC; Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Moore JH; Department of Computational Biomedicine, Cedars-Sinai Medical Center, Los Angeles, California, USA.
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Źródło:
Genetic epidemiology [Genet Epidemiol] 2022 Dec; Vol. 46 (8), pp. 555-571. Date of Electronic Publication: 2022 Aug 04.
Typ publikacji:
Journal Article; Review; Research Support, N.I.H., Extramural
MeSH Terms:
Genetic Heterogeneity*
Precision Medicine*/methods
Humans ; Machine Learning ; Phenotype
Czasopismo naukowe
Tytuł:
Multiregional Sequencing Analysis Reveals Extensive Genetic Heterogeneity in Gastric Tumors from Latinos.
Autorzy:
Toal TW; Genome Center, University of California, Davis, California.
Estrada-Florez AP; Genome Center, University of California, Davis, California.; Grupo de Citogenética, Filogenia y Evolución de las Poblaciones, Universidad del Tolima, Ibagué, Colombia.
Polanco-Echeverry GM; Genome Center, University of California, Davis, California.
Sahasrabudhe RM; Genome Center, University of California, Davis, California.
Lott PC; Genome Center, University of California, Davis, California.
Suarez-Olaya JJ; Grupo de Citogenética, Filogenia y Evolución de las Poblaciones, Universidad del Tolima, Ibagué, Colombia.
Guevara-Tique AA; Grupo de Citogenética, Filogenia y Evolución de las Poblaciones, Universidad del Tolima, Ibagué, Colombia.
Rocha S; Genome Center, University of California, Davis, California.
Morales-Arana A; Genome Center, University of California, Davis, California.
Castro-Valencia F; Grupo de Citogenética, Filogenia y Evolución de las Poblaciones, Universidad del Tolima, Ibagué, Colombia.
Urayama S; UC Davis Comprehensive Cancer Center, Sacramento, California.; Division of Gastroenterology & Hepatology, University of California, Davis, California.
Kirane A; UC Davis Comprehensive Cancer Center, Sacramento, California.
Wei D; Department of Pathology and Laboratory Medicine, University of California, Davis, California.
Rios-Sarabia N; Unidad de Investigación en Enfermedades Infecciosas y Parasitarias, Unidad Médica de Alta Especialidad en Pediatría, Instituto Mexicano del Seguro Social, México City, México.
Medrano R; Departamento de Sarcomas y Tubo Digestivo Alto, Unidad Medica de Alta Especialidad en Oncología Instituto Mexicano del Seguro Social (IMSS), México City, México.
Mantilla A; Departamento de Patología, Unidad Medica de Alta Especialidad en Oncología, Instituto Mexicano del Seguro Social (IMSS), México City, México.
Echeverry de Polanco M; Grupo de Citogenética, Filogenia y Evolución de las Poblaciones, Universidad del Tolima, Ibagué, Colombia.
Torres J; Unidad de Investigación en Enfermedades Infecciosas y Parasitarias, Unidad Médica de Alta Especialidad en Pediatría, Instituto Mexicano del Seguro Social, México City, México.
Bohorquez-Lozano ME; Grupo de Citogenética, Filogenia y Evolución de las Poblaciones, Universidad del Tolima, Ibagué, Colombia.
Carvajal-Carmona LG; Genome Center, University of California, Davis, California.; UC Davis Comprehensive Cancer Center, Sacramento, California.; Department of Biochemistry and Molecular Medicine, School of Medicine, University of California, Davis, California.
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Źródło:
Cancer research communications [Cancer Res Commun] 2022 Nov 28; Vol. 2 (11), pp. 1487-1496. Date of Electronic Publication: 2022 Nov 28 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Heterogeneity*
Hispanic or Latino*/genetics
Stomach Neoplasms*/genetics
Humans ; Carcinogenesis ; Eye Proteins/genetics ; Mutation ; Asian ; White ; Prognosis
Czasopismo naukowe
Tytuł:
STS pathogenic variants in a Dutch patient cohort clinically suspected for X-linked ichthyosis show genetic heterogeneity.
Autorzy:
Nagtzaam IF; Department of Dermatology.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
van Leersum FS; Department of Dermatology.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
Kouwenberg LCM; Department of Dermatology.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
Blok MJ; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.; Department of Clinical Genetics, Maastricht University Medical Centre+, Maastricht, the Netherlands.
Vreeburg M; Department of Clinical Genetics, Maastricht University Medical Centre+, Maastricht, the Netherlands.
Steijlen PM; Department of Dermatology.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
Gostyński A; Department of Dermatology.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
van Geel M; Department of Dermatology.; GROW-School for Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.; Department of Clinical Genetics, Maastricht University Medical Centre+, Maastricht, the Netherlands.
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Źródło:
The British journal of dermatology [Br J Dermatol] 2022 Nov; Vol. 187 (5), pp. 820-822. Date of Electronic Publication: 2022 Aug 11.
Typ publikacji:
Letter
MeSH Terms:
Genetic Heterogeneity*
Ichthyosis, X-Linked*/diagnosis
Ichthyosis, X-Linked*/genetics
Humans ; Steryl-Sulfatase/genetics ; Cohort Studies
Opinia redakcyjna
Tytuł:
Gene expression-based dissection of inter-histotypes, intra-histotype and intra-tumor heterogeneity in pediatric tumors.
Autorzy:
Ciceri S; Molecular Bases of Genetic Risk and Genetic Testing Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Dei Tumori, Via Venezian 1, 20133, Milano, Italy.
Carenzo A; Molecular Mechanisms Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Dei Tumori, Via Venezian 1, 20133, Milano, Italy.
Iannó MF; Integrated Biology Platform, Department of Applied Research and Technology Development, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Bertolotti A; Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Morosi C; Department of Radiology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Luksch R; Pediatric Oncology Unit, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Spreafico F; Pediatric Oncology Unit, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Collini P; Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
Radice P; Molecular Bases of Genetic Risk and Genetic Testing Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Dei Tumori, Via Venezian 1, 20133, Milano, Italy.
Massimino M; Pediatric Oncology Unit, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale Dei Tumori, Milan, Italy.
De Cecco L; Molecular Mechanisms Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Dei Tumori, Via Venezian 1, 20133, Milano, Italy. .
Perotti D; Molecular Bases of Genetic Risk and Genetic Testing Unit, Department of Research, Fondazione IRCCS Istituto Nazionale Dei Tumori, Via Venezian 1, 20133, Milano, Italy. .
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Źródło:
Scientific reports [Sci Rep] 2022 Oct 25; Vol. 12 (1), pp. 17837. Date of Electronic Publication: 2022 Oct 25.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genetic Heterogeneity*
Neoplasm Recurrence, Local*/genetics
Child ; Humans ; Mutation ; Epigenomics ; Gene Expression ; Tumor Microenvironment
Czasopismo naukowe
Tytuł:
Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy.
Autorzy:
Martínez-Rubio D; Rare Neurodegenerative Diseases Laboratory, Valencia Biomedical Research Foundation, Centro de Investigación Príncipe Felipe (CIPF), 46012 València, Spain.; Joint Unit CIPF-IIS La Fe Rare Diseases, 46012 València, Spain.
Hinarejos I; Rare Neurodegenerative Diseases Laboratory, Valencia Biomedical Research Foundation, Centro de Investigación Príncipe Felipe (CIPF), 46012 València, Spain.; Joint Unit CIPF-IIS La Fe Rare Diseases, 46012 València, Spain.
Argente-Escrig H; Department of Neurology, Hospital Universitari Arnau de Vilanova, 46012 València, Spain.
Marco-Marín C; Structural Enzymopathology Unit, Instituto de Biomedicina de Valencia (IBV), Consejo Superior de Investigaciones Científicas (CSIC), 46022 València, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), 28220 Madrid, Spain.
Lozano MA; Rare Neurodegenerative Diseases Laboratory, Valencia Biomedical Research Foundation, Centro de Investigación Príncipe Felipe (CIPF), 46012 València, Spain.
Gorría-Redondo N; Paediatric Neurology Unit, Department of Paediatrics, Hospital Universitario de Navarra, Navarrabiomed, 31008 Pamplona, Spain.
Lupo V; Rare Neurodegenerative Diseases Laboratory, Valencia Biomedical Research Foundation, Centro de Investigación Príncipe Felipe (CIPF), 46012 València, Spain.
Martí-Carrera I; Paediatric Neurology Unit, Department of Paediatrics, Hospital Universitario Donostia, 20014 Donostia, Spain.
Miranda C; Paediatric Neurology Unit, Department of Paediatrics, Hospital General Universitario Gregorio Marañón, 28027 Madrid, Spain.
Vázquez-López M; Paediatric Neurology Unit, Department of Paediatrics, Hospital General Universitario Gregorio Marañón, 28027 Madrid, Spain.
García-Pérez A; Paediatric Neurology Unit, Department of Paediatrics, Hospital Universitario Fundación Alcorcón, Alcorcón, 28922 Madrid, Spain.
Marco-Hernández AV; Paediatric Neurology Unit, Department of Paediatrics, Hospital Universitari Doctor, Peset, 46017 València, Spain.
Tomás-Vila M; Paediatric Neurology Unit, Department of Paediatrics, Hospital Universitari i Politècnic La Fe, 46026 València, Spain.
Aguilera-Albesa S; Paediatric Neurology Unit, Department of Paediatrics, Hospital Universitario de Navarra, Navarrabiomed, 31008 Pamplona, Spain.
Espinós C; Rare Neurodegenerative Diseases Laboratory, Valencia Biomedical Research Foundation, Centro de Investigación Príncipe Felipe (CIPF), 46012 València, Spain.; Joint Unit CIPF-IIS La Fe Rare Diseases, 46012 València, Spain.; Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III (ISCIII), 28220 Madrid, Spain.; Biotechnology Department, Universitat Politècnica de València, 46022 València, Spain.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2023 Nov 16; Vol. 24 (22). Date of Electronic Publication: 2023 Nov 16.
Typ publikacji:
Journal Article
MeSH Terms:
Cerebellar Ataxia*/genetics
Cerebellar Ataxia*/diagnosis
Cerebellar Diseases*
Spastic Paraplegia, Hereditary*/genetics
Neurodegenerative Diseases*
Child ; Humans ; Genetic Heterogeneity ; Mutation ; Ataxia ; Phenotype ; Paraplegia ; Pedigree ; Atrophy ; Microtubule-Associated Proteins/genetics ; Membrane Proteins/genetics
Czasopismo naukowe
Tytuł:
Genetic heterogeneity of cardiomyopathy and its correlation with patient care.
Autorzy:
Kim MJ; Division of Pediatric Cardiology, Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Cha S; Division of Pediatric Cardiology, Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Baek JS; Division of Pediatric Cardiology, Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Yu JJ; Division of Pediatric Cardiology, Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Seo GH; 3billion, Inc, Seoul, Korea.
Kang M; Genome Research Center for Birth Defects and Genetic Diseases, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Do HS; Genome Research Center for Birth Defects and Genetic Diseases, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Lee SE; Department of Cardiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. .
Lee BH; Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicines, Seoul, Korea. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2023 Oct 30; Vol. 16 (1), pp. 270. Date of Electronic Publication: 2023 Oct 30.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Cardiomyopathies*/genetics
Cardiomyopathy, Dilated*/genetics
Cardiomyopathy, Dilated*/pathology
Cardiomyopathy, Hypertrophic*/genetics
Male ; Female ; Humans ; Genetic Heterogeneity ; Patient Care
Czasopismo naukowe
Tytuł:
Development and validation of an individualized gene expression-based signature to predict overall survival of patients with high-grade serous ovarian carcinoma.
Autorzy:
Yuan D; Department of Obstertrics and Gynecology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Zhu H; Department of Gynecological Oncology, Renji Hospital Affiliated to Medical College of Shanghai Jiaotong University, Shanghai, 200000, China.
Wang T; Department of Hepatological Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Zhang Y; Department of Obstertrics and Gynecology, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.
Zheng X; Department of Gynecology, The First Hospital of Jiaxing City, Jiaxing, 314000, China.
Qu Y; Department of Obstertrics and Gynecology, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China. .
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Źródło:
European journal of medical research [Eur J Med Res] 2023 Oct 27; Vol. 28 (1), pp. 465. Date of Electronic Publication: 2023 Oct 27.
Typ publikacji:
Journal Article
MeSH Terms:
Transcriptome*/genetics
Ovarian Neoplasms*/genetics
Humans ; Female ; Autophagy ; Genetic Heterogeneity ; Prognosis
Czasopismo naukowe
Tytuł:
Intratumor heterogeneity in colorectal cancer: Distribution of tumor suppressor gene variants with regard to patient lymph node status.
Autorzy:
Wątor G; Center for Medical Genomics OMICRON, Jagiellonian University Medical College, Krakow, Poland.
Seweryn M; Center for Medical Genomics OMICRON, Jagiellonian University Medical College, Krakow, Poland.
Kapusta P; Center for Medical Genomics OMICRON, Jagiellonian University Medical College, Krakow, Poland.
Świrta J; Department of Endocrine Surgery, Third Chair of General Surgery, Jagiellonian University Medical College, Kraków, Poland.
Wałęga P; Department of Endocrine Surgery, Third Chair of General Surgery, Jagiellonian University Medical College, Kraków, Poland.
Barczyński M; Department of Endocrine Surgery, Third Chair of General Surgery, Jagiellonian University Medical College, Kraków, Poland.
Wołkow PP; Center for Medical Genomics OMICRON, Jagiellonian University Medical College, Krakow, Poland.
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Źródło:
Clinical genetics [Clin Genet] 2023 Oct; Vol. 104 (4), pp. 406-417. Date of Electronic Publication: 2023 Jun 20.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Colorectal Neoplasms*/genetics
Colorectal Neoplasms*/pathology
Humans ; Mutation ; Genes, Tumor Suppressor ; Lymph Nodes/pathology ; Genetic Heterogeneity
Czasopismo naukowe

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