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Tytuł:
Integrated CGH/WES Analyses Advance Understanding of Aggressive Neuroblastoma Evolution: A Case Study.
Autorzy:
Corallo D; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Zanon C; Bioinformatics Core Service, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Pantile M; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Tonini GP; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.
Zin A; Advanced Diagnostics and Target Discovery in Rare Pediatric Solid Tumors, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Francescato S; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Rossi B; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Trevisson E; Clinical Genetics Unit, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Pinato C; Clinical Genetics Unit, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Monferrer E; Pathology Department, Medical School, University of Valencia-INCLIVA, 46010 Valencia, Spain.
Noguera R; Pathology Department, Medical School, University of Valencia-INCLIVA, 46010 Valencia, Spain.
Aliño SF; Pharmacogenetics Unit, Instituto Investigación Sanitaria La Fe and Department Pharmacology, University of Valencia, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Herrero MJ; Pharmacogenetics Unit, Instituto Investigación Sanitaria La Fe and Department Pharmacology, University of Valencia, Avda. Fernando Abril Martorell 106, 46026 Valencia, Spain.
Biffi A; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Viscardi E; Pediatric Hematology, Oncology, and Stem Cell Transplant Center, Department of Woman's and Child's Health, University of Padova, Via Gustiniani 3, 35128 Padova, Italy.
Aveic S; Laboratory of Target Discovery and Biology of Neuroblastoma, Fondazione Istituto di Ricerca Pediatrica Città della Speranza, C.so Stati Uniti 4, 35127 Padova, Italy.; Department of Dental Materials and Biomaterials Research, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.
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Źródło:
Cells [Cells] 2021 Oct 09; Vol. 10 (10). Date of Electronic Publication: 2021 Oct 09.
Typ publikacji:
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Comparative Genomic Hybridization*
Exome Sequencing*
Neuroblastoma/*genetics
Child, Preschool ; Disease Progression ; Drug Resistance, Neoplasm/genetics ; Fatal Outcome ; Humans ; Immunophenotyping ; Polymorphism, Single Nucleotide/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Correspondence of aCGH and long-read genome assembly for detection of copy number differences: A proof-of-concept with cichlid genomes.
Autorzy:
Preising GA; Department of Biology, Reed College, Portland, OR, United States of America.
Faber-Hammond JJ; Department of Biology, Reed College, Portland, OR, United States of America.
Renn SCP; Department of Biology, Reed College, Portland, OR, United States of America.
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Źródło:
PloS one [PLoS One] 2021 Oct 07; Vol. 16 (10), pp. e0258193. Date of Electronic Publication: 2021 Oct 07 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Comparative Genomic Hybridization*
Genome*
Proof of Concept Study*
Cichlids/*genetics
DNA Copy Number Variations/*genetics
Animals ; Bias ; Gene Ontology ; Sequence Alignment ; Species Specificity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiers.
Autorzy:
Viailly PJ; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France. .; Centre Henri Becquerel, Rouen, France. .
Sater V; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
Viennot M; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Bohers E; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Vergne N; LMRS UMRS 6085, Normandie Univ, UNIROUEN, Rouen, France.
Berard C; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
Dauchel H; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
Lecroq T; LITIS EA 4108, Normandie Univ, UNIROUEN, Rouen, France.
Celebi A; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.; Master Bioinformatique BIM, Normandie Univ, UNIROUEN, Rouen, France.
Ruminy P; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Marchand V; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Lanic MD; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Dubois S; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Penther D; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Tilly H; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
Mareschal S; INSERM U1052 UMR CNRS 5286, Cancer Research Center of Lyon, Lyon, France.
Jardin F; INSERM U1245, Team Genomics and Biomarkers of Lymphoma and Solid Tumors, Normandie Univ, UNIROUEN, Rouen, France.; Centre Henri Becquerel, Rouen, France.
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Źródło:
BMC bioinformatics [BMC Bioinformatics] 2021 Mar 12; Vol. 22 (1), pp. 120. Date of Electronic Publication: 2021 Mar 12.
Typ publikacji:
Journal Article; Multicenter Study
MeSH Terms:
Comparative Genomic Hybridization*
DNA Copy Number Variations*
High-Throughput Nucleotide Sequencing*
Adult ; Humans ; Male ; Middle Aged ; Prospective Studies ; Sequence Analysis, DNA
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Reducing misdiagnosis caused by maternal cell contamination in genetic testing for early pregnancy loss.
Autorzy:
Volozonoka L; Scientific Laboratory of Molecular Genetics, Riga Stradins University , Riga, Latvia.
Gailite L; Scientific Laboratory of Molecular Genetics, Riga Stradins University , Riga, Latvia.
Perminov D; Egila Gulbja Laboratory , Riga, Latvia.
Kornejeva L; IVF Riga Clinic , Riga, Latvia.
Fodina V; IVF Riga Clinic , Riga, Latvia.
Kempa I; Scientific Laboratory of Molecular Genetics, Riga Stradins University , Riga, Latvia.
Miskova A; Department of Obstetrics and Gynecology, Riga Stradins University , Riga, Latvia.
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Źródło:
Systems biology in reproductive medicine [Syst Biol Reprod Med] 2020 Dec; Vol. 66 (6), pp. 410-420. Date of Electronic Publication: 2020 Oct 15.
Typ publikacji:
Journal Article
MeSH Terms:
Comparative Genomic Hybridization*
Genetic Testing*
Specimen Handling*
Abortion, Spontaneous/*genetics
Abortion, Spontaneous/diagnosis ; Diagnostic Errors ; Female ; Genetic Predisposition to Disease ; Gestational Age ; Humans ; Karyotype ; Karyotyping ; Predictive Value of Tests ; Pregnancy ; Reproducibility of Results
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Comparative analysis of alignment-free genome clustering and whole genome alignment-based phylogenomic relationship of coronaviruses.
Autorzy:
Kirichenko AD; Department of Genomics and Bioinformatics, Institute of Fundamental Biology and Biotechnology, Siberian Federal University, Krasnoyarsk, Russian Federation.
Poroshina AA; Laboratory of Molecular Systematics, Limnological Institute, Siberian Branch of Russian Academy of Sciences, Irkutsk, Russian Federation.
Sherbakov DY; Laboratory of Molecular Systematics, Limnological Institute, Siberian Branch of Russian Academy of Sciences, Irkutsk, Russian Federation.; Faculty of Biology and Soil Studies, Irkutsk State University, Irkutsk, Russian Federation.; Novosibirsk State University, Faculty of Natural Sciences, Novosibirsk, Russian Federation.
Sadovsky MG; Institute of Computational Modelling, Siberian Branch of Russian Academy of Sciences, Krasnoyarsk, Russian Federation.; V.F. Voino-Yasenetsky Krasnoyarsk State Medical University, Krasnoyarsk, Russian Federation.; Federal Research and Clinical Center, Federal Medical-Biological Agency, Krasnoyarsk, Russian Federation.
Krutovsky KV; Department of Genomics and Bioinformatics, Institute of Fundamental Biology and Biotechnology, Siberian Federal University, Krasnoyarsk, Russian Federation.; Department of Forest Genetics and Forest Tree Breeding, Georg-August University of Göttingen, Göttingen, Germany.; Center for Integrated Breeding Research, Georg-August University of Göttingen, Göttingen, Germany.; Laboratory of Forest Genomics, Genome Research and Education Center, Institute of Fundamental Biology and Biotechnology, Siberian Federal University, Krasnoyarsk, Russian Federation.; Laboratory of Population Genetics, N.I. Vavilov Institute of General Genetics, Russian Academy of Sciences, Moscow, Russian Federation.; Scientific and methodological center, G. F. Morozov Voronezh State University of Forestry and Technologies, Voronezh, Russian Federation.
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Źródło:
PloS one [PLoS One] 2022 Mar 08; Vol. 17 (3), pp. e0264640. Date of Electronic Publication: 2022 Mar 08 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genome, Viral*
Comparative Genomic Hybridization/*methods
Coronavirus/*genetics
Chromosome Mapping ; Cluster Analysis ; Coronavirus/classification ; Humans ; Phylogeny ; SARS-CoV-2/classification ; SARS-CoV-2/genetics ; Sequence Alignment
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Appropriateness of array-CGH in the ADHD clinics: A comparative study.
Autorzy:
Baccarin M; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.
Picinelli C; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.
Tomaiuolo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.
Castronovo P; Mafalda Luce Center for Pervasive Developmental Disorders, Milan, Italy.
Costa A; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy.
Verdecchia M; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy.
Cannizzaro C; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy.
Barbieri G; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy.
Sacco R; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy.
Persico AM; Interdepartmental Program 'Autism 0-90', 'Gaetano Martino' University Hospital, University of Messina, Messina, Italy.
Lintas C; Service for Neurodevelopmental Disorders, Department of Medicine, University Campus Bio-Medico, Rome, Italy.
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Źródło:
Genes, brain, and behavior [Genes Brain Behav] 2020 Jul; Vol. 19 (6), pp. e12651. Date of Electronic Publication: 2020 Apr 12.
Typ publikacji:
Comparative Study; Evaluation Study; Journal Article
MeSH Terms:
Attention Deficit Disorder with Hyperactivity/*genetics
Comparative Genomic Hybridization/*methods
Genetic Testing/*methods
Adolescent ; Attention Deficit Disorder with Hyperactivity/diagnosis ; Child ; Comparative Genomic Hybridization/standards ; DNA Copy Number Variations ; Female ; Genetic Testing/standards ; Humans ; Male ; Sensitivity and Specificity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Small Cell Carcinoma of the Ovary, Hypercalcemic Type (SCCOHT) beyond SMARCA4 Mutations: A Comprehensive Genomic Analysis.
Autorzy:
Auguste A; Medical Oncologist, Gynecology Unit, Lead Translational Research Team, INSERM U981, Gustave Roussy, 94805 Villejuif, France.
Blanc-Durand F; Gynecological Unit, Department of Medicine, Gustave Roussy, 94805 Villejuif, France.
Deloger M; Bioinformatics Core Facility, Gustave Roussy Cancer Center, UMS CNRS 3655/INSERM 23 AMMICA, 94805 Villejuif, France.
Le Formal A; Medical Oncologist, Gynecology Unit, Lead Translational Research Team, INSERM U981, Gustave Roussy, 94805 Villejuif, France.
Bareja R; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY 10001, USA.; Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY 10001, USA.
Wilkes DC; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY 10001, USA.
Richon C; Genomic Platform Gustave Roussy Cancer Institute, 94805 Villejuif, France.
Brunn B; Gynecological Unit, Department of Medicine, Gustave Roussy, 94805 Villejuif, France.
Caron O; Genomic Platform Gustave Roussy Cancer Institute, 94805 Villejuif, France.
Devouassoux-Shisheboran M; Department of Pathology, Hospital de la Croix Rousse, 69000 Lyon, France.
Gouy S; Gynecological Unit, Department of Medicine, Gustave Roussy, 94805 Villejuif, France.
Morice P; Gynecological Unit, Department of Medicine, Gustave Roussy, 94805 Villejuif, France.
Bentivegna E; Gynecological Unit, Department of Medicine, Gustave Roussy, 94805 Villejuif, France.
Sboner A; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY 10001, USA.; Institute for Computational Biomedicine, Weill Cornell Medicine, New York, NY 10001, USA.; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY 10001, USA.
Elemento O; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY 10001, USA.; Department of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York, NY 10001, USA.
Rubin MA; Department for BioMedical Research, University of Bern, 3001 Bern, Switzerland.
Pautier P; Gynecological Unit, Department of Medicine, Gustave Roussy, 94805 Villejuif, France.
Genestie C; Department of Pathology, Gustave Roussy, 94805 Villejuif, France.
Cyrta J; Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY 10001, USA.; Department for BioMedical Research, University of Bern, 3001 Bern, Switzerland.; Department of Pathology, Institut Curie, Universite Paris Sciences et Lettres, 6 rue d'Ulm, 75005 Paris, France.
Leary A; Medical Oncologist, Gynecology Unit, Lead Translational Research Team, INSERM U981, Gustave Roussy, 94805 Villejuif, France.; Gynecological Unit, Department of Medicine, Gustave Roussy, 94805 Villejuif, France.
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Źródło:
Cells [Cells] 2020 Jun 19; Vol. 9 (6). Date of Electronic Publication: 2020 Jun 19.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Comparative Genomic Hybridization*/methods
Carcinoma, Small Cell/*genetics
DNA Helicases/*genetics
Mutation/*genetics
Nuclear Proteins/*genetics
Transcription Factors/*genetics
Antigens, Neoplasm/genetics ; Carcinoma, Small Cell/drug therapy ; Carcinoma, Small Cell/pathology ; Cohort Studies ; Female ; Humans ; Hypercalcemia/genetics ; Hypercalcemia/pathology ; Ovarian Neoplasms/genetics ; Ovary/pathology
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing.
Autorzy:
Lu G; Department of Pathology, Laboratory of Translational Medicine Research, Deyang Key Laboratory of Tumor Molecular Research, Deyang People's Hospital, No. 173 First Section of TaishanBei Road, Jiangyang District, Deyang, 618000, China. .
Peng Q; Department of Child Healthcare, Shenzhen Baoan Women's and Children's Hospital, Jinan University, 56 Yulyu Road, Baoan District, Shenzhen, 518000, China.
Wu L; Department of Pathology, Laboratory of Translational Medicine Research, Deyang Key Laboratory of Tumor Molecular Research, Deyang People's Hospital, No. 173 First Section of TaishanBei Road, Jiangyang District, Deyang, 618000, China.
Zhang J; Department of Pathology, Laboratory of Translational Medicine Research, Deyang Key Laboratory of Tumor Molecular Research, Deyang People's Hospital, No. 173 First Section of TaishanBei Road, Jiangyang District, Deyang, 618000, China.
Ma L; Department of Child Healthcare, Shenzhen Baoan Women's and Children's Hospital, Jinan University, 56 Yulyu Road, Baoan District, Shenzhen, 518000, China. .
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Źródło:
BMC medical genomics [BMC Med Genomics] 2021 Nov 14; Vol. 14 (1), pp. 270. Date of Electronic Publication: 2021 Nov 14.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Point Mutation*
Sequence Deletion*
Abnormalities, Multiple/*genetics
Comparative Genomic Hybridization/*methods
DNA-Binding Proteins/*genetics
Face/*abnormalities
Hand Deformities, Congenital/*genetics
Haploinsufficiency/*genetics
Intellectual Disability/*genetics
Micrognathism/*genetics
Neck/*abnormalities
Transcription Factors/*genetics
Exome Sequencing/*methods
Chromosomes, Human, Pair 6 ; Female ; Humans ; Infant ; Infant, Newborn ; Polymorphism, Single Nucleotide
SCR Disease Name:
Coffin-Siris syndrome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Cytogenetics and Cytogenomics Evaluation in Cancer.
Autorzy:
Ribeiro IP; Cytogenetics and Genomics Laboratory, Faculty of Medicine, University of Coimbra, 3004-531 Coimbra, Portugal. .; iCBR-CIMAGO, Center of Investigation on Environment, Genetics and Oncobiology, Faculty of Medicine, University of Coimbra, 3004-531 Coimbra, Portugal. .
Melo JB; Cytogenetics and Genomics Laboratory, Faculty of Medicine, University of Coimbra, 3004-531 Coimbra, Portugal. .; iCBR-CIMAGO, Center of Investigation on Environment, Genetics and Oncobiology, Faculty of Medicine, University of Coimbra, 3004-531 Coimbra, Portugal. .; CNC, IBILI, Group of Aging and Brain Diseases: Advanced Diagnosis and Biomarkers, 3004-531 Coimbra, Portugal. .
Carreira IM; Cytogenetics and Genomics Laboratory, Faculty of Medicine, University of Coimbra, 3004-531 Coimbra, Portugal. .; iCBR-CIMAGO, Center of Investigation on Environment, Genetics and Oncobiology, Faculty of Medicine, University of Coimbra, 3004-531 Coimbra, Portugal. .; CNC, IBILI, Group of Aging and Brain Diseases: Advanced Diagnosis and Biomarkers, 3004-531 Coimbra, Portugal. .
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2019 Sep 23; Vol. 20 (19). Date of Electronic Publication: 2019 Sep 23.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Chromosome Aberrations*
Comparative Genomic Hybridization*
High-Throughput Nucleotide Sequencing*
Neoplasms*/diagnosis
Neoplasms*/genetics
Precision Medicine*
Biomarkers, Tumor/*genetics
Humans ; Prognosis
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay.
Autorzy:
Wayhelova M; Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlarska 267/2, Brno, Czech Republic. .; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic. .
Smetana J; Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlarska 267/2, Brno, Czech Republic.; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Vallova V; Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlarska 267/2, Brno, Czech Republic.; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Hladilkova E; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Filkova H; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Hanakova M; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Vilemova M; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Nikolova P; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Gromesova B; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Gaillyova R; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
Kuglik P; Institute of Experimental Biology, Faculty of Science, Masaryk University, Kotlarska 267/2, Brno, Czech Republic.; Department of Medical Genetics, University Hospital Brno, Cernopolni 212/9, Brno, Czech Republic.
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Źródło:
BMC medical genomics [BMC Med Genomics] 2019 Jul 23; Vol. 12 (1), pp. 111. Date of Electronic Publication: 2019 Jul 23.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Comparative Genomic Hybridization*
DNA Copy Number Variations*
Oligonucleotide Array Sequence Analysis*
Developmental Disabilities/*genetics
Intellectual Disability/*genetics
Adolescent ; Child ; Child, Preschool ; Cohort Studies ; Czech Republic ; Female ; Humans ; Infant ; Infant, Newborn ; Male
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
History of radiation genetics: light and darkness.
Autorzy:
Nakamura N; a Department of Molecular Biosciences , RERF , Hiroshima , Japan.
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Źródło:
International journal of radiation biology [Int J Radiat Biol] 2019 Jul; Vol. 95 (7), pp. 999-1014. Date of Electronic Publication: 2019 Feb 20.
Typ publikacji:
Historical Article; Journal Article; Review
MeSH Terms:
Comparative Genomic Hybridization*
Radiation Injuries/*genetics
Radiation Injuries/*history
Animals ; Chromosome Aberrations/radiation effects ; DNA Repair ; Gene Deletion ; Genome, Human ; Germ Cells ; Germ-Line Mutation ; Haploidy ; Heterozygote ; History, 20th Century ; History, 21st Century ; Humans ; Mice ; Oligonucleotide Array Sequence Analysis ; Oocytes/radiation effects ; Phenotype ; Radioactive Hazard Release ; Risk
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
An atypical chondroid syringoma with malignant degeneration: Utility of comparative genomic hybridization in confirming the diagnosis.
Autorzy:
Zia S; Department of Pathology and Laboratory Medicine, Henry Ford Hospital, Detroit, Michigan, USA.
Shaw B; Department of Pathology and Laboratory Medicine, Henry Ford Hospital, Detroit, Michigan, USA.
Chapman S; Department of Dermatology, Henry Ford Hospital, Detroit, Michigan, USA.
Friedman BJ; Department of Pathology and Laboratory Medicine, Henry Ford Hospital, Detroit, Michigan, USA.; Department of Dermatology, Henry Ford Hospital, Detroit, Michigan, USA.
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Źródło:
Journal of cutaneous pathology [J Cutan Pathol] 2021 Jun; Vol. 48 (6), pp. 775-780. Date of Electronic Publication: 2021 Feb 01.
Typ publikacji:
Case Reports
MeSH Terms:
Adenoma, Pleomorphic/*genetics
Cell Transformation, Neoplastic/*genetics
Comparative Genomic Hybridization/*methods
Sweat Gland Neoplasms/*pathology
Adenoma, Pleomorphic/diagnosis ; Adenoma, Pleomorphic/pathology ; Adenoma, Pleomorphic/surgery ; Aged, 80 and over ; Biomarkers, Tumor ; Cell Transformation, Neoplastic/pathology ; Humans ; Male ; Mixed Tumor, Malignant/pathology ; Skin Neoplasms/pathology ; Treatment Outcome
Raport
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Comparative transcriptome analysis of unripe and ripe banana (cv. Nendran) unraveling genes involved in ripening and other related processes.
Autorzy:
Kaur K; Department of Biotechnology, Plant Tissue Culture and Genetic Engineering Lab, National Agri-Food Biotechnology Institute (NABI), Ministry of Science and Technology (Government of India), Mohali, Punjab, India.
Awasthi P; Department of Biotechnology, Plant Tissue Culture and Genetic Engineering Lab, National Agri-Food Biotechnology Institute (NABI), Ministry of Science and Technology (Government of India), Mohali, Punjab, India.
Tiwari S; Department of Biotechnology, Plant Tissue Culture and Genetic Engineering Lab, National Agri-Food Biotechnology Institute (NABI), Ministry of Science and Technology (Government of India), Mohali, Punjab, India.
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Źródło:
PloS one [PLoS One] 2021 Jul 27; Vol. 16 (7), pp. e0254709. Date of Electronic Publication: 2021 Jul 27 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Transcriptome*
Comparative Genomic Hybridization/*methods
Musa/*genetics
Carotenoids/chemistry ; Carotenoids/metabolism ; Down-Regulation ; Fruit/genetics ; Geranylgeranyl-Diphosphate Geranylgeranyltransferase/genetics ; Geranylgeranyl-Diphosphate Geranylgeranyltransferase/metabolism ; Intramolecular Lyases/genetics ; Intramolecular Lyases/metabolism ; Plant Proteins/genetics ; Plant Proteins/metabolism ; Transcription Factors/genetics ; Transcription Factors/metabolism ; Up-Regulation
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Array CGH-based detection of CNV regions and their potential association with reproduction and other economic traits in Holsteins.
Autorzy:
Liu M; College of Animal Science and Technology, Northwest A&F University, Shaanxi Key Laboratory of Agricultural Molecular Biology, Yangling, 712100, Shaanxi, China.; Animal Genomics and Improvement Laboratory, BARC, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
Fang L; Animal Genomics and Improvement Laboratory, BARC, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.; Department of Animal and Avian Sciences, University of Maryland, College Park, MD, USA.
Liu S; Animal Genomics and Improvement Laboratory, BARC, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.; College of Animal Science and Technology, China Agricultural University, Beijing, 100193, China.
Pan MG; Animal Genomics and Improvement Laboratory, BARC, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
Seroussi E; Agricultural Research Organization (ARO), Volcani Center, Institute of Animal Science, Department of Quantitative and Molecular Genetics, HaMaccabim Road, P.O.B 15159, 7528809, Rishon LeTsiyon, Israel.
Cole JB; Animal Genomics and Improvement Laboratory, BARC, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA.
Ma L; Department of Animal and Avian Sciences, University of Maryland, College Park, MD, USA.
Chen H; College of Animal Science and Technology, Northwest A&F University, Shaanxi Key Laboratory of Agricultural Molecular Biology, Yangling, 712100, Shaanxi, China. .
Liu GE; Animal Genomics and Improvement Laboratory, BARC, Agricultural Research Service, USDA, Beltsville, MD, 20705, USA. .
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Źródło:
BMC genomics [BMC Genomics] 2019 Mar 07; Vol. 20 (1), pp. 181. Date of Electronic Publication: 2019 Mar 07.
Typ publikacji:
Journal Article
MeSH Terms:
Comparative Genomic Hybridization*
DNA Copy Number Variations*
Cattle/*genetics
Cattle/*physiology
Reproduction/*genetics
Animals ; Male
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Refining the Phenotype of Recurrent Rearrangements of Chromosome 16.
Autorzy:
Redaelli S; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. .
Maitz S; Clinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, S. Gerardo Hospital, 20900 Monza, Italy. .
Crosti F; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. .
Sala E; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. .
Villa N; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. .
Spaccini L; Clinical Genetics Unit, Department of Obstetrics and Gynecology, V. Buzzi Children's Hospital, University of Milan, 20154 Milan, Italy. .
Selicorni A; Clinical Pediatric Unit, ASST Lariana, 22042 Como, Italy. .
Rigoldi M; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. .
Conconi D; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. .
Dalprà L; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. .
Roversi G; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. .; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. .
Bentivegna A; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. .; NeuroMI, Milan center of Neuroscience, University of Milano-Bicocca, Dept. of Neurology and Neuroscience, San Gerardo Hospital, 20900 Monza, Italy. .
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2019 Mar 04; Vol. 20 (5). Date of Electronic Publication: 2019 Mar 04.
Typ publikacji:
Journal Article
MeSH Terms:
Comparative Genomic Hybridization*
Abnormalities, Multiple/*genetics
Chromosomes, Human, Pair 16/*genetics
Developmental Disabilities/*genetics
Abnormalities, Multiple/classification ; Abnormalities, Multiple/physiopathology ; Adolescent ; Adult ; Child ; Child, Preschool ; Chromosome Aberrations ; Chromosome Deletion ; DNA Copy Number Variations/genetics ; Developmental Disabilities/classification ; Developmental Disabilities/physiopathology ; Female ; Homologous Recombination/genetics ; Humans ; Infant ; Infant, Newborn ; Karyotype ; Male ; Phenotype ; Segmental Duplications, Genomic/genetics ; Young Adult
Czasopismo naukowe
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Tytuł:
Comparative genomic analysis revealed rapid differentiation in the pathogenicity-related gene repertoires between Pyricularia oryzae and Pyricularia penniseti isolated from a Pennisetum grass.
Autorzy:
Zheng H; National Engineering Research Center of JUNCAO Technology, College of Life Science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Zhong Z; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Shi M; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Zhang L; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Lin L; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of life science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Hong Y; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of life science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Fang T; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Zhu Y; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Guo J; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Zhang L; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Fang J; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of life science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Lin H; National Engineering Research Center of JUNCAO Technology, College of Life Science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Norvienyeku J; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.; College of life science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Chen X; Institute of Oceanography, Minjiang University, Fuzhou, 350108, China.
Lu G; National Engineering Research Center of JUNCAO Technology, College of Life Science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. .; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. .
Hu H; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. .; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. .
Wang Z; State Key Laboratory of Ecological Pest Control for Fujian and Taiwan Crops, College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. .; College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. .; College of life science, Fujian Agriculture and Forestry University, Fuzhou, 350002, China. .
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Źródło:
BMC genomics [BMC Genomics] 2018 Dec 13; Vol. 19 (1), pp. 927. Date of Electronic Publication: 2018 Dec 13.
Typ publikacji:
Journal Article
MeSH Terms:
Comparative Genomic Hybridization*
Genes, Fungal*
Ascomycota/*genetics
Pennisetum/*microbiology
Ascomycota/classification ; Ascomycota/pathogenicity ; DNA, Fungal/chemistry ; DNA, Fungal/isolation & purification ; DNA, Fungal/metabolism ; Gene Rearrangement ; Host-Pathogen Interactions/genetics ; Magnaporthe/classification ; Magnaporthe/genetics ; Magnaporthe/pathogenicity ; Phylogeny ; Plant Diseases/microbiology ; Sequence Analysis, DNA ; Virulence/genetics
Czasopismo naukowe
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Tytuł:
Comparative genomic analysis of Parageobacillus thermoglucosidasius strains with distinct hydrogenogenic capacities.
Autorzy:
Mohr T; Section II: Technical Biology, Institute of Process engineering in Life Science, Karlsruhe Institute of Technology, Kaiserstrasse 12, 76131, Karlsruhe, Germany. .
Aliyu H; Section II: Technical Biology, Institute of Process engineering in Life Science, Karlsruhe Institute of Technology, Kaiserstrasse 12, 76131, Karlsruhe, Germany.
Küchlin R; Section II: Technical Biology, Institute of Process engineering in Life Science, Karlsruhe Institute of Technology, Kaiserstrasse 12, 76131, Karlsruhe, Germany.
Zwick M; Section II: Technical Biology, Institute of Process engineering in Life Science, Karlsruhe Institute of Technology, Kaiserstrasse 12, 76131, Karlsruhe, Germany.
Cowan D; Centre for Microbial Ecology and Genomics, Department of Biochemistry, Genetics and Microbiology, University of Pretoria, Hatfield, Pretoria, 0028, South Africa.
Neumann A; Section II: Technical Biology, Institute of Process engineering in Life Science, Karlsruhe Institute of Technology, Kaiserstrasse 12, 76131, Karlsruhe, Germany. .
de Maayer P; School of Molecular & Cell Biology, Faculty of Science, University of the Witwatersrand, WITS, Johannesburg, 2050, South Africa.
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Źródło:
BMC genomics [BMC Genomics] 2018 Dec 06; Vol. 19 (1), pp. 880. Date of Electronic Publication: 2018 Dec 06.
Typ publikacji:
Journal Article
MeSH Terms:
Comparative Genomic Hybridization*
Genome, Bacterial*
Geobacillus/*genetics
Hydrogen/*metabolism
Bacterial Proteins/genetics ; Base Sequence ; Carbon Monoxide/chemistry ; Carbon Monoxide/metabolism ; Genetic Loci ; Hydrogenase/genetics ; INDEL Mutation ; Multienzyme Complexes/genetics ; Sequence Alignment
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Molecular characterization of a series of 990 index patients with albinism.
Autorzy:
Lasseaux E; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.
Plaisant C; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.
Michaud V; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.
Pennamen P; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.; INSERM U1211, Maladies Rares, Génétique et Métabolisme, Université de Bordeaux, Bordeaux, France.
Trimouille A; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.; INSERM U1211, Maladies Rares, Génétique et Métabolisme, Université de Bordeaux, Bordeaux, France.
Gaston L; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.
Monfermé S; Service d'Ophtalmologie, CHU de Bordeaux, Bordeaux, France.
Lacombe D; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.; INSERM U1211, Maladies Rares, Génétique et Métabolisme, Université de Bordeaux, Bordeaux, France.
Rooryck C; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.; INSERM U1211, Maladies Rares, Génétique et Métabolisme, Université de Bordeaux, Bordeaux, France.
Morice-Picard F; Service de Dermatologie, CHU de Bordeaux, Bordeaux, France.
Arveiler B; Service de Génétique Médicale, CHU de Bordeaux, Bordeaux, France.; INSERM U1211, Maladies Rares, Génétique et Métabolisme, Université de Bordeaux, Bordeaux, France.
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Źródło:
Pigment cell & melanoma research [Pigment Cell Melanoma Res] 2018 Jul; Vol. 31 (4), pp. 466-474. Date of Electronic Publication: 2018 Feb 14.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alleles*
Comparative Genomic Hybridization*
Gene Rearrangement*
High-Throughput Nucleotide Sequencing*
Molecular Diagnostic Techniques*
Albinism/*diagnosis
Albinism/*genetics
Female ; Humans ; Male
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing.
Autorzy:
Li FX; Department of Obstetrics and Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Xie MJ; Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Qu SF; National Institutes for Food and Drug Control, Beijing 100050, P.R. China.
He D; Guangzhou Darui Biotechnology Co. Ltd., Guangzhou, Guangdong 510665, P.R. China.
Wu L; Guangzhou Darui Biotechnology Co. Ltd., Guangzhou, Guangdong 510665, P.R. China.
Liang ZK; Guangzhou Darui Biotechnology Co. Ltd., Guangzhou, Guangdong 510665, P.R. China.
Wu YS; Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Yang F; Department of Obstetrics and Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
Yang XX; Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.
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Źródło:
Molecular medicine reports [Mol Med Rep] 2020 Aug; Vol. 22 (2), pp. 1269-1276. Date of Electronic Publication: 2020 Jun 03.
Typ publikacji:
Journal Article
MeSH Terms:
Abortion, Spontaneous*/diagnosis
Abortion, Spontaneous*/genetics
Chromosome Aberrations*
DNA Copy Number Variations*
Chromosome Disorders/*diagnosis
Comparative Genomic Hybridization/*methods
Adolescent ; Adult ; Case-Control Studies ; Female ; High-Throughput Nucleotide Sequencing/methods ; Humans ; Middle Aged ; Pregnancy ; Prospective Studies ; Retrospective Studies ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Comparative genomic analysis provides insight into the phylogeny and virulence of atypical enteropathogenic Escherichia coli strains from Brazil.
Autorzy:
Hernandes RT; Departamento de Microbiologia e Imunologia, Instituto de Biociências, Universidade Estadual Paulista 'Júlio de Mesquita Filho' (UNESP), Botucatu, SP, Brasil.
Hazen TH; Institute for Genome Sciences, Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Dos Santos LF; Instituto Adolfo Lutz, São Paulo, SP, Brasil.
Richter TKS; Institute for Genome Sciences, Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Michalski JM; Institute for Genome Sciences, Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
Rasko DA; Institute for Genome Sciences, Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.
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Źródło:
PLoS neglected tropical diseases [PLoS Negl Trop Dis] 2020 Jun 01; Vol. 14 (6), pp. e0008373. Date of Electronic Publication: 2020 Jun 01 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Genome, Bacterial*
Phylogeny*
Comparative Genomic Hybridization/*methods
Enteropathogenic Escherichia coli/*classification
Enteropathogenic Escherichia coli/*genetics
Virulence Factors/*genetics
Brazil ; Escherichia coli Infections ; Escherichia coli Proteins/genetics ; Humans ; Multilocus Sequence Typing ; Serotyping ; Virulence
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
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