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Wyświetlanie 21-40 z 1547
Tytuł:
Antinuclear antibody pattern and autoantibody profiling of systemic sclerosis patients in a tertiary referral center in North India.
Autorzy:
Machhua S; Department of Immunopathology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Sharma SK; Department of Internal Medicine, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Kumar Y; Department of Immunopathology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Anand S; Department of Immunopathology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Handa S; Department of Dermatology Venereology Leprology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Minz RW; Department of Immunopathology, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
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Źródło:
Pathology international [Pathol Int] 2022 May; Vol. 72 (5), pp. 283-292. Date of Electronic Publication: 2022 Mar 23.
Typ publikacji:
Journal Article
MeSH Terms:
Antibodies, Antinuclear*
Scleroderma, Systemic*/complications
Scleroderma, Systemic*/diagnosis
Adult ; Autoantibodies ; Humans ; RNA Polymerase III ; Tertiary Care Centers
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Novel de novo POLR3B mutations responsible for demyelinating Charcot-Marie-Tooth disease in Japan.
Autorzy:
Ando M; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Higuchi Y; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Yuan JH; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Yoshimura A; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Kitao R; Department of Neurology, National Hospital Organization Hakone Hospital, Kanagawa, Japan.
Morimoto T; Department of Pediatrics, Asahigawaso Minamiehime Rehabilitation Hospital, Ehime, Japan.
Taniguchi T; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.; Department of Neurology, Imakiire General Hospital, Kagoshima, Japan.
Takeuchi M; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Takei J; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Hiramatsu Y; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Sakiyama Y; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Hashiguchi A; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Okamoto Y; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.; Department of Physical Therapy, School of Health Sciences, Faculty of Medicine, Kagoshima University, Kagoshima, Japan.
Mitsui J; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Chiba, Japan.
Ishiura H; Department of Neurology, Faculty of Medicine, The University of Tokyo, Chiba, Japan.
Tsuji S; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Chiba, Japan.; Institute of Medical Genomics, International University of Health and Welfare, Chiba, Japan.
Takashima H; Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
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Źródło:
Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2022 May; Vol. 9 (5), pp. 747-755. Date of Electronic Publication: 2022 Apr 28.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Charcot-Marie-Tooth Disease*/genetics
Ataxia ; Atrophy ; Female ; Humans ; Japan ; Mutation ; Phenotype ; RNA Polymerase III/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery.
Autorzy:
Saghi M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
InanlooRahatloo K; School of Biology, College of Science, University of Tehran, Tehran, Iran. .
Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
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Źródło:
BMC medical genomics [BMC Med Genomics] 2022 Apr 18; Vol. 15 (1), pp. 89. Date of Electronic Publication: 2022 Apr 18.
Typ publikacji:
Journal Article
MeSH Terms:
Intellectual Disability*/pathology
Humans ; Mutation ; Mutation, Missense ; Pedigree ; RNA Polymerase III/genetics ; Ribosomal Proteins/genetics ; Spliceosomes/genetics ; Spliceosomes/pathology ; Transcription Factors/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
An RNA Polymerase III General Transcription Factor Engages in Cell Type-Specific Chromatin Looping.
Autorzy:
de Llobet Cucalon L; Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Dr. Aiguader 88, 08003 Barcelona, Spain.
Di Vona C; Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Dr. Aiguader 88, 08003 Barcelona, Spain.; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), 28029 Madrid, Spain.
Morselli M; Department of Chemistry, Life Sciences and Environmental, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.
Vezzoli M; Department of Chemistry, Life Sciences and Environmental, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.
Montanini B; Department of Chemistry, Life Sciences and Environmental, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.
Teichmann M; Bordeaux Institute of Oncology (BRIC), University of Bordeaux Inserm U1312, 33076 Bordeaux, France.
de la Luna S; Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology (BIST), Dr. Aiguader 88, 08003 Barcelona, Spain.; Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), 28029 Madrid, Spain.; Institució Catalana de Recerca i Estudis Avançats (ICREA), Passeig Lluís Companys 23, 08010 Barcelona, Spain.
Ferrari R; Department of Chemistry, Life Sciences and Environmental, University of Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2022 Feb 18; Vol. 23 (4). Date of Electronic Publication: 2022 Feb 18.
Typ publikacji:
Journal Article
MeSH Terms:
Chromatin/*genetics
RNA Polymerase III/*genetics
Transcription Factors, TFIII/*genetics
CCCTC-Binding Factor/genetics ; Cells, Cultured ; Chromatin Immunoprecipitation Sequencing/methods ; DNA/genetics ; Humans ; Promoter Regions, Genetic/genetics ; Repetitive Sequences, Nucleic Acid/genetics ; Transcription, Genetic/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Spinal cord-predominant neuropathology in an adult-onset case of POLR3A-related spastic ataxia.
Autorzy:
Sytsma TM; Neuropathology Division, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.
Chen DH; Department of Neurology, University of Washington School of Medicine, Seattle, Washington, USA.
Rolf B; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
Dorschner M; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
Jayadev S; Neuropathology Division, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.; Department of Neurology, University of Washington School of Medicine, Seattle, Washington, USA.; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
Keene CD; Neuropathology Division, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.
Zhang J; Neuropathology Division, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.
Bird TD; Department of Neurology, University of Washington School of Medicine, Seattle, Washington, USA.; Division of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA.; Geriatric Research Education and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington, USA.
Latimer CS; Neuropathology Division, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.
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Źródło:
Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2022 Feb; Vol. 42 (1), pp. 58-65. Date of Electronic Publication: 2021 Nov 09.
Typ publikacji:
Case Reports
MeSH Terms:
Optic Atrophy*
Spinocerebellar Ataxias*
Aged ; Humans ; Intellectual Disability ; Male ; Muscle Spasticity ; RNA Polymerase III
SCR Disease Name:
Spastic Ataxia
Raport
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients.
Autorzy:
Di Donato I; Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci, 16, 50055, Siena, Italy. .
Gallo A; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Ricca I; Molecular Medicine and Neurogenetics, IRCCS Fondazione Stella Maris, via dei Giacinti 2, Calambrone, 56128, Pisa, Italy.
Fini N; Neurology Unit, Department of Neurosciences, Azienda Ospedaliero Universitaria di Modena, Modena, Italy.
Silvestri G; Fondazione Policlinico Universitario 'A. Gemelli' IRCCS, UOC Neurologia, Rome, Italy.; Department of Neurosciences, Università Cattolica del Sacro Cuore, Rome, Italy.
Gurrieri F; Medical Genetics, Università Campus Bio-Medico, 00128, Rome, Italy.
Cirillo M; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Cerase A; Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci, 16, 50055, Siena, Italy.
Natale G; Molecular Medicine and Neurogenetics, IRCCS Fondazione Stella Maris, via dei Giacinti 2, Calambrone, 56128, Pisa, Italy.
Matrone F; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.
Riso V; Fondazione Policlinico Universitario 'A. Gemelli' IRCCS, UOC Neurologia, Rome, Italy.; Department of Neurosciences, Università Cattolica del Sacro Cuore, Rome, Italy.
Melone MAB; Department of Advanced Medical and Surgical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.; Sbarro Institute for Cancer Research and Molecular Medicine, Center for Biotechnology, Temple University, Philadelphia, PA, USA.
Tessa A; Molecular Medicine and Neurogenetics, IRCCS Fondazione Stella Maris, via dei Giacinti 2, Calambrone, 56128, Pisa, Italy.
De Michele G; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
Federico A; Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci, 16, 50055, Siena, Italy.
Filla A; Department of Neurosciences, Reproductive and Odontostomatological Sciences, Federico II University, Naples, Italy.
Dotti MT; Department of Medicine, Surgery and Neurosciences, University of Siena, viale Bracci, 16, 50055, Siena, Italy.
Santorelli FM; Molecular Medicine and Neurogenetics, IRCCS Fondazione Stella Maris, via dei Giacinti 2, Calambrone, 56128, Pisa, Italy. .
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Źródło:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology [Neurol Sci] 2022 Feb; Vol. 43 (2), pp. 1071-1077. Date of Electronic Publication: 2021 Jul 23.
Typ publikacji:
Journal Article
MeSH Terms:
Optic Atrophy*
Paraparesis, Spastic*
Spastic Paraplegia, Hereditary*/diagnostic imaging
Spastic Paraplegia, Hereditary*/genetics
Spinocerebellar Ataxias*
Ataxia/diagnostic imaging ; Ataxia/genetics ; Child ; Humans ; Mutation ; Phenotype ; RNA Polymerase III/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
African swine fever virus I267L acts as an important virulence factor by inhibiting RNA polymerase III-RIG-I-mediated innate immunity.
Autorzy:
Ran Y; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; African Swine Fever Regional Laboratory of China, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Li D; State Key Laboratory of Veterinary Etiological Biology, OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.; African Swine Fever Regional Laboratory of China, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Xiong MG; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; African Swine Fever Regional Laboratory of China, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; University of Chinese Academy of Sciences Beijing, China.
Liu HN; State Key Laboratory of Veterinary Etiological Biology, OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.; African Swine Fever Regional Laboratory of China, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Feng T; State Key Laboratory of Veterinary Etiological Biology, OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.; African Swine Fever Regional Laboratory of China, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Shi ZW; State Key Laboratory of Veterinary Etiological Biology, OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.; African Swine Fever Regional Laboratory of China, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Li YH; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; African Swine Fever Regional Laboratory of China, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; University of Chinese Academy of Sciences Beijing, China.
Wu HN; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; African Swine Fever Regional Laboratory of China, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; University of Chinese Academy of Sciences Beijing, China.
Wang SY; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; African Swine Fever Regional Laboratory of China, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
Zheng HX; State Key Laboratory of Veterinary Etiological Biology, OIE/National Foot and Mouth Disease Reference Laboratory, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.; African Swine Fever Regional Laboratory of China, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, China.
Wang YY; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.; African Swine Fever Regional Laboratory of China, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, China.
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Źródło:
PLoS pathogens [PLoS Pathog] 2022 Jan 28; Vol. 18 (1), pp. e1010270. Date of Electronic Publication: 2022 Jan 28 (Print Publication: 2022).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
African Swine Fever Virus/*pathogenicity
Immunity, Innate/*immunology
Virulence/*immunology
Virulence Factors/*immunology
African Swine Fever/immunology ; African Swine Fever Virus/immunology ; Animals ; RNA Polymerase III/immunology ; Receptors, Cell Surface/immunology ; Swine
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Analysis of SINE Families B2, Dip, and Ves with Special Reference to Polyadenylation Signals and Transcription Terminators.
Autorzy:
Vassetzky NS; Laboratory of Eukaryotic Genome Evolution, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Borodulina OR; Laboratory of Eukaryotic Genome Evolution, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Ustyantsev IG; Laboratory of Eukaryotic Genome Evolution, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Kosushkin SA; Laboratory of Eukaryotic Genome Evolution, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
Kramerov DA; Laboratory of Eukaryotic Genome Evolution, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2021 Sep 13; Vol. 22 (18). Date of Electronic Publication: 2021 Sep 13.
Typ publikacji:
Journal Article
MeSH Terms:
Evolution, Molecular*
Transcription Termination, Genetic*
Retroelements/*genetics
Short Interspersed Nucleotide Elements/*genetics
Animals ; Humans ; Mice ; Poly A/genetics ; Polyadenylation/genetics ; RNA/genetics ; RNA 3' Polyadenylation Signals/genetics ; RNA Polymerase III/genetics ; RNA, Messenger/genetics ; Transcription, Genetic/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
tRNA biogenesis and specific aminoacyl-tRNA synthetases regulate senescence stability under the control of mTOR.
Autorzy:
Guillon J; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Coquelet H; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Leman G; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Toutain B; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Petit C; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Henry C; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Boissard A; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Guette C; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
Coqueret O; Centre de Recherche en Cancérologie et Immunologie Nantes Angers (CRCINA), INSERM U1232 Paul Papin ICO Cancer Center, Université d'Angers, Angers, France.
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Źródło:
PLoS genetics [PLoS Genet] 2021 Dec 20; Vol. 17 (12), pp. e1009953. Date of Electronic Publication: 2021 Dec 20 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Amino Acyl-tRNA Synthetases/*genetics
Cellular Senescence/*genetics
E2F1 Transcription Factor/*genetics
TATA-Binding Protein Associated Factors/*genetics
TOR Serine-Threonine Kinases/*genetics
Apoptosis/genetics ; Breast Neoplasms/genetics ; Breast Neoplasms/pathology ; Cell Cycle Checkpoints/genetics ; Cell Proliferation/genetics ; Colorectal Neoplasms/genetics ; Colorectal Neoplasms/pathology ; Female ; Gene Expression Regulation, Neoplastic/genetics ; Humans ; MCF-7 Cells ; RNA Polymerase III/genetics ; RNA, Transfer/biosynthesis ; RNA, Transfer/genetics ; Transcription, Genetic/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Identification of hub genes with prognostic values in multiple myeloma by bioinformatics analysis.
Autorzy:
Yang J; Department of Hematology and Oncology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, People's Republic of China.
Wang F; Department of Hematology and Oncology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, People's Republic of China.
Zhong S; Center of Clinical Laboratory Science, Jiangsu Cancer Hospital Affiliated to Nanjing Medical University, Nanjing, People's Republic of China.
Chen B; Department of Hematology and Oncology, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, People's Republic of China.
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Źródło:
Hematology (Amsterdam, Netherlands) [Hematology] 2021 Dec; Vol. 26 (1), pp. 453-459.
Typ publikacji:
Journal Article
MeSH Terms:
Gene Expression Regulation, Neoplastic*
Multiple Myeloma/*genetics
Carbohydrate Epimerases/genetics ; Databases, Genetic ; Gene Expression Profiling ; Gene Ontology ; Gene Regulatory Networks ; Genomics ; Humans ; Ketone Oxidoreductases/genetics ; Multiple Myeloma/diagnosis ; Prognosis ; RNA Polymerase III/genetics ; Transcriptome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Duplication and Loss of Function of Genes Encoding RNA Polymerase III Subunit C4 Causes Hybrid Incompatibility in Rice.
Autorzy:
Nguyen GN; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Yamagata Y; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Shigematsu Y; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Watanabe M; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Miyazaki Y; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Doi K; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Tashiro K; Molecular Gene Technics Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Kuhara S; Molecular Gene Technics Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Kanamori H; Agrogenomics Research Center, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8634, Japan.
Wu J; Agrogenomics Research Center, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8634, Japan.
Matsumoto T; Agrogenomics Research Center, National Institute of Agrobiological Sciences, Tsukuba, Ibaraki 305-8634, Japan.
Yasui H; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan.
Yoshimura A; Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan .
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Źródło:
G3 (Bethesda, Md.) [G3 (Bethesda)] 2017 Aug 07; Vol. 7 (8), pp. 2565-2575. Date of Electronic Publication: 2017 Aug 07.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Duplication*
Genes, Plant*
Hybridization, Genetic*
Oryza/*enzymology
Oryza/*genetics
Plant Proteins/*genetics
Protein Subunits/*genetics
RNA Polymerase III/*genetics
Chromosome Mapping ; Chromosome Segregation/genetics ; Cloning, Molecular ; Crosses, Genetic ; Epistasis, Genetic ; Fertility/genetics ; Gene Expression Regulation, Plant ; Genetic Linkage ; Genotype ; Germination/genetics ; Heterozygote ; Plant Infertility/genetics ; Plant Proteins/metabolism ; Pollen/genetics ; Protein Subunits/metabolism ; RNA Polymerase III/metabolism ; Time Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Transcribing RNA polymerase III observed by electron cryomicroscopy.
Autorzy:
Hoffmann NA; European Molecular Biology Laboratory (EMBL), Structural and Computational Biology Unit, Heidelberg, Germany.
Jakobi AJ; European Molecular Biology Laboratory (EMBL), Structural and Computational Biology Unit, Heidelberg, Germany.
Vorländer MK; European Molecular Biology Laboratory (EMBL), Structural and Computational Biology Unit, Heidelberg, Germany.
Sachse C; European Molecular Biology Laboratory (EMBL), Structural and Computational Biology Unit, Heidelberg, Germany.
Müller CW; European Molecular Biology Laboratory (EMBL), Structural and Computational Biology Unit, Heidelberg, Germany.
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Źródło:
The FEBS journal [FEBS J] 2016 Aug; Vol. 283 (15), pp. 2811-9. Date of Electronic Publication: 2016 Apr 28.
Typ publikacji:
Journal Article; Review; Research Support, Non-U.S. Gov't
MeSH Terms:
Transcription, Genetic*
RNA Polymerase III/*chemistry
Cryoelectron Microscopy ; Humans ; Models, Molecular ; RNA Polymerase III/antagonists & inhibitors ; RNA Polymerase III/metabolism ; RNA Polymerase III/ultrastructure
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation.
Autorzy:
Choquet K; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada.; Department of Human Genetics, McGill University, Montréal, Québec, Canada.; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Québec, Canada.
Yang S; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada.
Moir RD; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, USA.
Forget D; Translational Proteomics Laboratory, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Larivière R; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada.
Bouchard A; Translational Proteomics Laboratory, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Poitras C; Translational Proteomics Laboratory, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.
Sgarioto N; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada.
Dicaire MJ; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada.
Noohi F; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada.; Department of Human Genetics, McGill University, Montréal, Québec, Canada.
Kennedy TE; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada.
Rochford J; Douglas Institute Research Center, Montréal, Québec, Canada.
Bernard G; Departments of Neurology and Neurosurgery, and Pediatrics, McGill University, Montreal, Canada.; Department of Medical Genetics, Montreal Children's Hospital, McGill University Health Center, Montreal, Canada.; Child Health and Human Development Program, Research Institute of the McGill University Health Center, Montreal, Canada.
Teichmann M; INSERM U1212 - CNRS UMR5320, Université de Bordeaux, Bordeaux, France.
Coulombe B; Translational Proteomics Laboratory, Institut de recherches cliniques de Montréal (IRCM), Montréal, Québec, Canada.; Département de biochimie et médecine moléculaire, Université de Montréal, Montréal, Québec, Canada.
Willis IM; Department of Biochemistry, Albert Einstein College of Medicine, Bronx, New York, USA.
Kleinman CL; Department of Human Genetics, McGill University, Montréal, Québec, Canada.; Lady Davis Institute for Medical Research, Jewish General Hospital, Montréal, Québec, Canada.
Brais B; Montreal Neurological Institute, McGill University, 3801 University Street, room 622, Montréal, Québec, H3A 2B4, Canada. .; Department of Human Genetics, McGill University, Montréal, Québec, Canada. .
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Źródło:
Molecular brain [Mol Brain] 2017 Apr 13; Vol. 10 (1), pp. 13. Date of Electronic Publication: 2017 Apr 13.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Hereditary Central Nervous System Demyelinating Diseases/*genetics
Mutation/*genetics
Myelin Sheath/*metabolism
RNA Polymerase III/*genetics
Animals ; Cerebellum/pathology ; Cerebellum/physiopathology ; Gene Knock-In Techniques ; Hereditary Central Nervous System Demyelinating Diseases/physiopathology ; Homozygote ; Humans ; Mice, Inbred C57BL ; Mice, Knockout ; Motor Activity ; Purkinje Cells/metabolism ; Purkinje Cells/pathology ; RNA Polymerase III/metabolism ; Transcription, Genetic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
High-resolution RNA allelotyping along the inactive X chromosome: evidence of RNA polymerase III in regulating chromatin configuration.
Autorzy:
Hong R; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive 637551, Singapore.
Lin B; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive 637551, Singapore.
Lu X; Genome Institute of Singapore, 138672, Singapore.
Lai LT; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive 637551, Singapore.
Chen X; Division of Mathematical Sciences, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link 637371, Singapore.
Sanyal A; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive 637551, Singapore.
Ng HH; Genome Institute of Singapore, 138672, Singapore.
Zhang K; Department of Bioengineering, University of California at San Diego, La Jolla, CA 92093, USA.
Zhang LF; School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive 637551, Singapore.
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Źródło:
Scientific reports [Sci Rep] 2017 Apr 03; Vol. 7, pp. 45460. Date of Electronic Publication: 2017 Apr 03.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Chromatin/*metabolism
RNA Polymerase III/*metabolism
X Chromosome/*genetics
Alleles ; Animals ; Cell Line ; Databases, Genetic ; Genes, X-Linked ; Mice ; Polymorphism, Single Nucleotide ; RNA Interference ; RNA Polymerase III/antagonists & inhibitors ; RNA Polymerase III/genetics ; RNA, Long Noncoding/genetics ; RNA, Long Noncoding/metabolism ; RNA, Small Interfering/metabolism ; Transcription Factors, TFIII/antagonists & inhibitors ; Transcription Factors, TFIII/genetics ; Transcription Factors, TFIII/metabolism ; X Chromosome/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
A de novo variant of POLR3B causes demyelinating Charcot-Marie-Tooth disease in a Chinese patient: a case report.
Autorzy:
Xue YY; Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, China.
Cheng HL; Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, China.; Department of Neurology, First Affiliated Hospital, Fujian Medical University, Fuzhou, China.
Dong HL; Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, China.
Yin HM; Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, China.
Yuan Y; Department of Neurology, Peking University First Hospital, Beijing, China.
Meng LC; Department of Neurology, Peking University First Hospital, Beijing, China.
Wu ZY; Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, China. .
Yu H; Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, Key Laboratory of Medical Neurobiology of Zhejiang Province, Zhejiang University School of Medicine, 88 Jiefang Road, Hangzhou, China. .
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Źródło:
BMC neurology [BMC Neurol] 2021 Oct 20; Vol. 21 (1), pp. 402. Date of Electronic Publication: 2021 Oct 20.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Charcot-Marie-Tooth Disease*/genetics
Adult ; China ; Heterozygote ; Humans ; Male ; Mutation/genetics ; Phenotype ; RNA Polymerase III ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Molecular Determinants for RNA Release into Extracellular Vesicles.
Autorzy:
Mosbach ML; Institute of Biochemistry, Justus Liebig University of Gießen, 35392 Gießen, Germany.
Pfafenrot C; Institute of Biochemistry, Justus Liebig University of Gießen, 35392 Gießen, Germany.
von Strandmann EP; Institute for Tumor Immunology, Center for Tumor Biology and Immunology (ZTI), Philipps University of Marburg, 35043 Marburg, Germany.
Bindereif A; Institute of Biochemistry, Justus Liebig University of Gießen, 35392 Gießen, Germany.
Preußer C; Institute for Tumor Immunology, Center for Tumor Biology and Immunology (ZTI), Philipps University of Marburg, 35043 Marburg, Germany.
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Źródło:
Cells [Cells] 2021 Oct 06; Vol. 10 (10). Date of Electronic Publication: 2021 Oct 06.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Extracellular Vesicles/*metabolism
RNA, Messenger/*metabolism
RNA, Small Nuclear/*metabolism
Cell Line ; Extracellular Vesicles/ultrastructure ; Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)/genetics ; Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)/metabolism ; Humans ; Poly A/metabolism ; Polyadenylation ; RNA Caps/metabolism ; RNA Polymerase III/metabolism ; RNA, Messenger/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Characterization of new RNA polymerase III and RNA polymerase II transcriptional promoters in the Bovine Leukemia Virus genome.
Autorzy:
Van Driessche B; Service of Molecular Virology, Department of Molecular Biology (DBM), Université Libre de Bruxelles (ULB), Gosselies, B-6041, Belgium.
Rodari A; Service of Molecular Virology, Department of Molecular Biology (DBM), Université Libre de Bruxelles (ULB), Gosselies, B-6041, Belgium.
Delacourt N; Service of Molecular Virology, Department of Molecular Biology (DBM), Université Libre de Bruxelles (ULB), Gosselies, B-6041, Belgium.
Fauquenoy S; Service of Molecular Virology, Department of Molecular Biology (DBM), Université Libre de Bruxelles (ULB), Gosselies, B-6041, Belgium.
Vanhulle C; Service of Molecular Virology, Department of Molecular Biology (DBM), Université Libre de Bruxelles (ULB), Gosselies, B-6041, Belgium.
Burny A; Service of Molecular Virology, Department of Molecular Biology (DBM), Université Libre de Bruxelles (ULB), Gosselies, B-6041, Belgium.
Rohr O; Institut Universitaire de Technologie Louis Pasteur de Schiltigheim, University of Strasbourg, Schiltigheim, F-67300, France.; Institut de Parasitologie et de Pathologie Tropicale, Laboratory of Dynamic of Host-Pathogen Interactions (DHPI), EA7292, University of Strasbourg, Strasbourg, F-67000, France.
Van Lint C; Service of Molecular Virology, Department of Molecular Biology (DBM), Université Libre de Bruxelles (ULB), Gosselies, B-6041, Belgium.
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Źródło:
Scientific reports [Sci Rep] 2016 Aug 22; Vol. 6, pp. 31125. Date of Electronic Publication: 2016 Aug 22.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Genome, Viral*
Leukemia Virus, Bovine/*enzymology
Leukemia Virus, Bovine/*genetics
RNA Polymerase II/*genetics
RNA Polymerase III/*genetics
3' Untranslated Regions ; Animals ; Binding Sites/genetics ; Cattle ; Cell Line ; Epigenesis, Genetic ; Gene Knockdown Techniques ; HEK293 Cells ; Humans ; MicroRNAs/genetics ; MicroRNAs/metabolism ; Promoter Regions, Genetic ; Protein Subunits ; RNA Polymerase II/chemistry ; RNA Polymerase II/metabolism ; RNA Polymerase III/chemistry ; RNA Polymerase III/metabolism ; RNA, Small Interfering/genetics ; Sheep ; Transcription, Genetic
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
CRISPR/Cas-9 mediated knock-in by homology dependent repair in the West Nile Virus vector Culex quinquefasciatus Say.
Autorzy:
Purusothaman DK; Arthropod Genetics, The Pirbright Institute, Ash Road, Pirbright, GU24 0NF, Surrey, UK.
Shackleford L; Arthropod Genetics, The Pirbright Institute, Ash Road, Pirbright, GU24 0NF, Surrey, UK.
Anderson MAE; Arthropod Genetics, The Pirbright Institute, Ash Road, Pirbright, GU24 0NF, Surrey, UK.
Harvey-Samuel T; Arthropod Genetics, The Pirbright Institute, Ash Road, Pirbright, GU24 0NF, Surrey, UK.
Alphey L; Arthropod Genetics, The Pirbright Institute, Ash Road, Pirbright, GU24 0NF, Surrey, UK. .
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Źródło:
Scientific reports [Sci Rep] 2021 Jul 22; Vol. 11 (1), pp. 14964. Date of Electronic Publication: 2021 Jul 22.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Culex/*growth & development
Gene Knock-In Techniques/*veterinary
Kynurenine 3-Monooxygenase/*genetics
RNA Polymerase III/*genetics
Animals ; CRISPR-Cas Systems ; Culex/genetics ; Culex/virology ; DNA Repair ; Disease Vectors ; Female ; Genes, Recessive ; Germ Cells/growth & development ; Germ Cells/metabolism ; Insect Proteins/genetics ; Male ; Pest Control, Biological ; Promoter Regions, Genetic ; West Nile virus/pathogenicity
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Whole-exome sequencing reveals POLR3B variants associated with progeria-related Wiedemann-Rautenstrauch syndrome.
Autorzy:
Wu SW; Department of Obstetrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, Chaoyang, China.; Beijing Maternal and Child Health Care Hospital, Beijing, 100026, Chaoyang, China.
Li L; Beijing Maternal and Child Health Care Hospital, Beijing, 100026, Chaoyang, China.; Central Laboratory, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, Chaoyang, China.
Feng F; Department of Basic Medical Sciences, School of Medicine, Tsinghua University, Haidian, Beijing, 100084, China.
Wang L; Beijing Maternal and Child Health Care Hospital, Beijing, 100026, Chaoyang, China.; Department of Ultrasound, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, Chaoyang, China.
Kong YY; Beijing Maternal and Child Health Care Hospital, Beijing, 100026, Chaoyang, China.; Department of Newborn Screening, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, Chaoyang, China.
Liu XW; Department of Obstetrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, Chaoyang, China. .; Beijing Maternal and Child Health Care Hospital, Beijing, 100026, Chaoyang, China. .
Yin C; Beijing Maternal and Child Health Care Hospital, Beijing, 100026, Chaoyang, China. .; Central Laboratory, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, Chaoyang, China. .
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Źródło:
Italian journal of pediatrics [Ital J Pediatr] 2021 Jul 21; Vol. 47 (1), pp. 160. Date of Electronic Publication: 2021 Jul 21.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Exome Sequencing*
Fetal Growth Retardation/*genetics
Progeria/*genetics
RNA Polymerase III/*genetics
Child ; Genotype ; Humans ; Male ; Pedigree ; Phenotype
SCR Disease Name:
Progeroid syndrome, neonatal
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 21-40 z 1547

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