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Wyświetlanie 41-60 z 343
Tytuł:
MicroRNA-124 regulates lens epithelial cell apoptosis by affecting Fas alternative splicing by targeting polypyrimidine tract-binding protein in age-related cataract.
Autorzy:
Zhang K; Department of Ophthalmology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Yin Y; School of Public Health, Xi'an Jiaotong University, Xi'an, China.
Pei C; Department of Ophthalmology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Wu C; Department of Ophthalmology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
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Źródło:
Clinical & experimental ophthalmology [Clin Exp Ophthalmol] 2021 Aug; Vol. 49 (6), pp. 591-605. Date of Electronic Publication: 2021 May 29.
Typ publikacji:
Journal Article
MeSH Terms:
Cataract*/genetics
Lens, Crystalline*
MicroRNAs*/genetics
Alternative Splicing ; Apoptosis ; Cell Line ; Epithelial Cells ; Humans ; Polypyrimidine Tract-Binding Protein ; fas Receptor/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Polypyrimidine tract-binding protein binds to the 5' untranslated region of the mouse mammary tumor virus mRNA and stimulates cap-independent translation initiation.
Autorzy:
Cáceres CJ; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Contreras N; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Angulo J; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Vera-Otarola J; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Pino-Ajenjo C; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Llorian M; Department of Biochemistry, University of Cambridge, UK.
Ameur M; Centre national de la Recherche Scientifique, Unité Mixte de Recherche 8015, Laboratoire de Cristallographie et RMN Biologique, Université Paris Descartes, France.
Lisboa F; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Pino K; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Lowy F; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Sargueil B; Centre national de la Recherche Scientifique, Unité Mixte de Recherche 8015, Laboratoire de Cristallographie et RMN Biologique, Université Paris Descartes, France.
López-Lastra M; Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
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Źródło:
The FEBS journal [FEBS J] 2016 May; Vol. 283 (10), pp. 1880-901. Date of Electronic Publication: 2016 Apr 05.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
5' Untranslated Regions*
RNA Caps*
Mammary Tumor Virus, Mouse/*genetics
Polypyrimidine Tract-Binding Protein/*metabolism
RNA, Messenger/*genetics
Binding Sites ; Gene Knockdown Techniques ; Genes, Viral ; HEK293 Cells ; Humans ; Internal Ribosome Entry Sites ; Polypyrimidine Tract-Binding Protein/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Validation of suitable genes for normalization of diurnal gene expression studies in Chenopodium quinoa.
Autorzy:
Maldonado-Taipe N; Plant Breeding Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
Patirange DSR; Plant Breeding Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
Schmöckel SM; King Abdullah University of Science and Technology (KAUST), Biological and Environmental Sciences & Engineering Division (BESE), Thuwal, Saudi Arabia.; Institute of Crop Science, University of Hohenheim, Stuttgart, Germany.
Jung C; Plant Breeding Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
Emrani N; Plant Breeding Institute, Christian-Albrechts-University of Kiel, Kiel, Germany.
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Źródło:
PloS one [PLoS One] 2021 Mar 11; Vol. 16 (3), pp. e0233821. Date of Electronic Publication: 2021 Mar 11 (Print Publication: 2021).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation, Plant*
Chenopodium quinoa/*genetics
Plant Proteins/*genetics
Algorithms ; Chenopodium quinoa/metabolism ; Isocitrate Dehydrogenase/genetics ; Isocitrate Dehydrogenase/metabolism ; Plant Proteins/metabolism ; Polypyrimidine Tract-Binding Protein/genetics ; Polypyrimidine Tract-Binding Protein/metabolism ; RNA, Plant/metabolism ; Real-Time Polymerase Chain Reaction ; Transcriptome
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
hnRNP I regulates neonatal immune adaptation and prevents colitis and colorectal cancer.
Autorzy:
Jin Z; Department of comparative Biosciences, College of veterinary medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.
Liang F; Department of statistics, University of Illinois at Urbana-Champaign, Champaign, Illinois, United States of America.
Yang J; Department of comparative Biosciences, College of veterinary medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.
Mei W; Department of comparative Biosciences, College of veterinary medicine, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States of America.
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Źródło:
PLoS genetics [PLoS Genet] 2017 Mar 15; Vol. 13 (3), pp. e1006672. Date of Electronic Publication: 2017 Mar 15 (Print Publication: 2017).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Adaptive Immunity/*genetics
Colitis/*genetics
Colorectal Neoplasms/*genetics
Heterogeneous-Nuclear Ribonucleoproteins/*genetics
Polypyrimidine Tract-Binding Protein/*genetics
Animals ; Animals, Newborn ; Blotting, Western ; Colitis/metabolism ; Colorectal Neoplasms/metabolism ; Epithelial Cells/metabolism ; Female ; Gene Expression ; Heterogeneous-Nuclear Ribonucleoproteins/metabolism ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Interleukin-1 Receptor-Associated Kinases/metabolism ; Intestinal Mucosa/metabolism ; Intestinal Mucosa/pathology ; Male ; Mice, Inbred C57BL ; Mice, Knockout ; NF-kappa B/metabolism ; Polypyrimidine Tract-Binding Protein/metabolism ; Reverse Transcriptase Polymerase Chain Reaction
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
A Novel Combination RNAi toward Warburg Effect by Replacement with miR-145 and Silencing of PTBP1 Induces Apoptotic Cell Death in Bladder Cancer Cells.
Autorzy:
Takai T; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. .; Department of Urology, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Yoshikawa Y; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. .; Department of Urology, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Inamoto T; Department of Urology, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Minami K; Department of Urology, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Taniguchi K; Department of General and Gastroenterological Surgery, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Sugito N; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. .
Kuranaga Y; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. .
Shinohara H; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. .
Kumazaki M; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. .
Tsujino T; Department of Urology, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Takahara K; Department of Urology, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Ito Y; Department of Anatomy and Cell Biology, Division of Life Sciences, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
Akao Y; United Graduate School of Drug Discovery and Medical Information Sciences, Gifu University, 1-1 Yanagido, Gifu 501-1193, Japan. .
Azuma H; Department of Urology, Osaka Medical College, 2-7 Daigaku-machi, Takatsuki, Osaka 569-8686, Japan. .
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Źródło:
International journal of molecular sciences [Int J Mol Sci] 2017 Jan 17; Vol. 18 (1). Date of Electronic Publication: 2017 Jan 17.
Typ publikacji:
Journal Article
MeSH Terms:
RNA Interference*
Apoptosis/*genetics
Glycolysis/*genetics
Heterogeneous-Nuclear Ribonucleoproteins/*genetics
MicroRNAs/*genetics
Polypyrimidine Tract-Binding Protein/*genetics
Urinary Bladder Neoplasms/*genetics
Aged ; Aged, 80 and over ; Animals ; Blotting, Western ; Cell Line, Tumor ; Cell Proliferation/genetics ; Female ; Gene Expression Regulation, Neoplastic ; Heterogeneous-Nuclear Ribonucleoproteins/metabolism ; Humans ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Nude ; Middle Aged ; Models, Genetic ; Polypyrimidine Tract-Binding Protein/metabolism ; RNAi Therapeutics/methods ; Reverse Transcriptase Polymerase Chain Reaction ; Signal Transduction/genetics ; Urinary Bladder Neoplasms/metabolism ; Urinary Bladder Neoplasms/therapy ; Xenograft Model Antitumor Assays/methods
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
U2AF65-Dependent SF3B1 Function in SMN Alternative Splicing.
Autorzy:
Choi N; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Liu Y; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Oh J; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Ha J; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Zheng X; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
Shen H; School of Life Sciences, Gwangju Institute of Science and Technology, Gwangju 500-712, Korea.
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Źródło:
Cells [Cells] 2020 Dec 09; Vol. 9 (12). Date of Electronic Publication: 2020 Dec 09.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alternative Splicing*
Phosphoproteins/*metabolism
RNA Splicing Factors/*metabolism
Splicing Factor U2AF/*metabolism
Survival of Motor Neuron 1 Protein/*genetics
Survival of Motor Neuron 2 Protein/*genetics
Cell Line ; Exons ; Humans ; Muscular Atrophy, Spinal/metabolism ; Muscular Atrophy, Spinal/pathology ; Phosphoproteins/antagonists & inhibitors ; Phosphoproteins/genetics ; Polypyrimidine Tract-Binding Protein/genetics ; Polypyrimidine Tract-Binding Protein/metabolism ; Protein Binding ; RNA Interference ; RNA Precursors/genetics ; RNA Precursors/metabolism ; RNA Splicing Factors/antagonists & inhibitors ; RNA Splicing Factors/genetics ; RNA, Small Interfering/metabolism ; Splicing Factor U2AF/chemistry ; Survival of Motor Neuron 1 Protein/metabolism ; Survival of Motor Neuron 2 Protein/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
In situ direct reprogramming of astrocytes to neurons via polypyrimidine tract-binding protein 1 knockdown in a mouse model of ischemic stroke
Autorzy:
Meng Yuan
Yao Tang
Tianwen Huang
Lining Ke
En Huang
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Temat:
astrocyte
in situ direct reprogramming
ischemic stroke
mir-30 based shrna
neuron
polypyrimidine tract-binding protein 1
transdifferentiation
Neurology. Diseases of the nervous system
RC346-429
Źródło:
Neural Regeneration Research, Vol 19, Iss 10, Pp 2240-2248 (2024)
Opis pliku:
electronic resource
Relacje:
http://www.nrronline.org/article.asp?issn=1673-5374;year=2024;volume=19;issue=10;spage=2240;epage=2248;aulast=; https://doaj.org/toc/1673-5374
Dostęp URL:
https://doaj.org/article/b6727f0bca5b4c33b6d80e63fff4d6c3  Link otwiera się w nowym oknie
Czasopismo naukowe
Szczegóły
Tytuł:
Quantitative proteomics study of the neuroprotective effects of B12 on hydrogen peroxide-induced apoptosis in SH-SY5Y cells.
Autorzy:
Zhong L; Medical and Health Analytical Center, Peking University Health Science Center, Beijing 100191, China.
Zhou J; Department of Pathology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China.
Chen X; Medical and Health Analytical Center, Peking University Health Science Center, Beijing 100191, China.
Lou Y; Medical and Health Analytical Center, Peking University Health Science Center, Beijing 100191, China.
Liu D; Medical and Health Analytical Center, Peking University Health Science Center, Beijing 100191, China.
Zou X; Medical and Health Analytical Center, Peking University Health Science Center, Beijing 100191, China.
Yang B; Medical and Health Analytical Center, Peking University Health Science Center, Beijing 100191, China.
Yin Y; Institute of Systems Biomedicine, Department of Pathology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, 100191, China.; Beijing Key Laboratory of Tumor Systems Biology, Beijing, 100191, China.
Pan Y; Department of Pharmacology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China.
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Źródło:
Scientific reports [Sci Rep] 2016 Mar 08; Vol. 6, pp. 22635. Date of Electronic Publication: 2016 Mar 08.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Anti-Inflammatory Agents/*pharmacology
Antioxidants/*pharmacology
Cobamides/*pharmacology
Heterogeneous-Nuclear Ribonucleoproteins/*metabolism
Hydrogen Peroxide/*toxicity
Neuroprotective Agents/*pharmacology
Polypyrimidine Tract-Binding Protein/*metabolism
Apoptosis/drug effects ; Cell Line, Tumor ; Cell Survival/drug effects ; Heterogeneous-Nuclear Ribonucleoproteins/genetics ; Humans ; Neuroblastoma/metabolism ; Neurodegenerative Diseases/drug therapy ; Oxidative Stress/drug effects ; Polypyrimidine Tract-Binding Protein/genetics ; Proteomics ; RNA Interference ; RNA, Small Interfering/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
High Throughput Sequencing Identifies Misregulated Genes in the Drosophila Polypyrimidine Tract-Binding Protein (hephaestus) Mutant Defective in Spermatogenesis.
Autorzy:
Sridharan V; Department of Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, Colorado, United States of America.
Heimiller J; Department of Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, Colorado, United States of America.
Robida MD; Department of Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, Colorado, United States of America.
Singh R; Department of Molecular, Cellular and Developmental Biology, University of Colorado at Boulder, Boulder, Colorado, United States of America.
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Źródło:
PloS one [PLoS One] 2016 Mar 04; Vol. 11 (3), pp. e0150768. Date of Electronic Publication: 2016 Mar 04 (Print Publication: 2016).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation*
Drosophila Proteins/*genetics
Drosophila melanogaster/*genetics
High-Throughput Nucleotide Sequencing/*methods
Mutation/*genetics
Polypyrimidine Tract-Binding Protein/*genetics
Spermatogenesis/*genetics
Animals ; Base Sequence ; Binding Sites ; Conserved Sequence ; Drosophila Proteins/metabolism ; Gene Expression Profiling ; Gene Ontology ; Male ; Molecular Sequence Data ; Phylogeny ; Polypyrimidine Tract-Binding Protein/metabolism ; Protein Isoforms/genetics ; Protein Isoforms/metabolism ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; Real-Time Polymerase Chain Reaction ; Transcription Initiation Site ; Transcriptome/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
PTBP1 and PTBP2 impaired autoregulation of SRSF3 in cancer cells.
Autorzy:
Guo J; Hubei-MOST KLOS &KLOBME, School &Hospital of Stomatology, Wuhan University, Wuhan, 430079, PR China.
Jia J; Hubei-MOST KLOS &KLOBME, School &Hospital of Stomatology, Wuhan University, Wuhan, 430079, PR China.
Jia R; Hubei-MOST KLOS &KLOBME, School &Hospital of Stomatology, Wuhan University, Wuhan, 430079, PR China.
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Źródło:
Scientific reports [Sci Rep] 2015 Sep 29; Vol. 5, pp. 14548. Date of Electronic Publication: 2015 Sep 29.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation, Neoplastic*
Carcinoma, Squamous Cell/*metabolism
Heterogeneous-Nuclear Ribonucleoproteins/*metabolism
Mouth Neoplasms/*metabolism
Nerve Tissue Proteins/*metabolism
Polypyrimidine Tract-Binding Protein/*metabolism
RNA, Messenger/*metabolism
RNA-Binding Proteins/*metabolism
Alternative Splicing ; Base Sequence ; Binding Sites ; Carcinoma, Squamous Cell/genetics ; Carcinoma, Squamous Cell/pathology ; Codon, Terminator/metabolism ; Exons ; Gene Expression Profiling ; HEK293 Cells ; Heterogeneous-Nuclear Ribonucleoproteins/genetics ; Humans ; Molecular Sequence Data ; Mouth Neoplasms/genetics ; Mouth Neoplasms/pathology ; Nerve Tissue Proteins/genetics ; Polypyrimidine Tract-Binding Protein/genetics ; Protein Binding ; RNA Precursors/genetics ; RNA Precursors/metabolism ; RNA Stability ; RNA, Messenger/genetics ; RNA-Binding Proteins/genetics ; Serine-Arginine Splicing Factors ; Signal Transduction ; Tissue Array Analysis ; Tumor Cells, Cultured
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
PTB binds to the 3' untranslated region of the human astrovirus type 8: a possible role in viral replication.
Autorzy:
Espinosa-Hernández W; Programa Institucional de Biomedicina Molecular, Sección de Estudios de Posgrado e Investigación, ENMH, Instituto Politécnico Nacional, Col. Fracc. La Escalera-Ticomán, México D.F., México.
Velez-Uriza D; Programa Institucional de Biomedicina Molecular, Sección de Estudios de Posgrado e Investigación, ENMH, Instituto Politécnico Nacional, Col. Fracc. La Escalera-Ticomán, México D.F., México.
Valdés J; Departamento de Bioquímica, Centro de Investigación y de Estudios Avanzados del IPN, Col. San Pedro Zacatenco, México D.F., México.
Vélez-Del Valle C; Departamento de Biología Celular, Centro de Investigación y de Estudios Avanzados del IPN, Col. San Pedro Zacatenco, México D.F., México.
Salas-Benito J; Programa Institucional de Biomedicina Molecular, Sección de Estudios de Posgrado e Investigación, ENMH, Instituto Politécnico Nacional, Col. Fracc. La Escalera-Ticomán, México D.F., México.
Martínez-Contreras R; Centro de Investigaciones en Ciencias Microbiológicas, Edificio 103, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla (BUAP), Col. San Manuel, Puebla, México.
García-Espítia M; Programa Institucional de Biomedicina Molecular, Sección de Estudios de Posgrado e Investigación, ENMH, Instituto Politécnico Nacional, Col. Fracc. La Escalera-Ticomán, México D.F., México.
Salas-Benito M; Programa Institucional de Biomedicina Molecular, Sección de Estudios de Posgrado e Investigación, ENMH, Instituto Politécnico Nacional, Col. Fracc. La Escalera-Ticomán, México D.F., México.
Vega-Almeida T; Facultad de Medicina, Departamento de Microbiología y Parasitología, Universidad Nacional Autónoma de México, Circuito interior, Ciudad Universitaria, México D.F., México.
De Nova-Ocampo M; Programa Institucional de Biomedicina Molecular, Sección de Estudios de Posgrado e Investigación, ENMH, Instituto Politécnico Nacional, Col. Fracc. La Escalera-Ticomán, México D.F., México.
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Źródło:
PloS one [PLoS One] 2014 Nov 18; Vol. 9 (11), pp. e113113. Date of Electronic Publication: 2014 Nov 18 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
3' Untranslated Regions/*genetics
Macromolecular Substances/*metabolism
Mamastrovirus/*metabolism
Polypyrimidine Tract-Binding Protein/*metabolism
Virus Replication/*physiology
Blotting, Western ; Caco-2 Cells ; DNA Primers/genetics ; Electrophoretic Mobility Shift Assay ; Fluorescent Antibody Technique ; Humans ; Mamastrovirus/genetics ; Polymerase Chain Reaction ; Polypyrimidine Tract-Binding Protein/genetics ; RNA, Small Interfering/genetics ; Real-Time Polymerase Chain Reaction
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Regulation of mRNA abundance by polypyrimidine tract-binding protein-controlled alternate 5' splice site choice.
Autorzy:
Hamid FM; School of Biological Sciences, Nanyang Technological University, Singapore.
Makeyev EV; School of Biological Sciences, Nanyang Technological University, Singapore; MRC Centre for Developmental Neurobiology, King's College London, London, United Kingdom.
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Źródło:
PLoS genetics [PLoS Genet] 2014 Nov 06; Vol. 10 (11), pp. e1004771. Date of Electronic Publication: 2014 Nov 06 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alternative Splicing/*genetics
Hermanski-Pudlak Syndrome/*genetics
Polypyrimidine Tract-Binding Protein/*genetics
RNA, Messenger/*genetics
Animals ; Exons ; Gene Expression Regulation ; HeLa Cells ; Hermanski-Pudlak Syndrome/pathology ; Humans ; Membrane Proteins/biosynthesis ; Membrane Proteins/genetics ; Mice ; Polypyrimidine Tract-Binding Protein/biosynthesis ; RNA Splice Sites/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Drosophila polypyrimidine tract-binding protein (DmPTB) regulates dorso-ventral patterning genes in embryos.
Autorzy:
Heimiller J; Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, United States of America.
Sridharan V; Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, United States of America.
Huntley J; BioFrontiers Next-Gen Sequencing Facility, University of Colorado, Boulder, Colorado, United States of America.
Wesley CS; Departments of Genetics and Medical Genetics, University of Wisconsin, Madison, Wisconsin, United States of America.
Singh R; Department of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, United States of America.
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Źródło:
PloS one [PLoS One] 2014 Jul 11; Vol. 9 (7), pp. e98585. Date of Electronic Publication: 2014 Jul 11 (Print Publication: 2014).
Typ publikacji:
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation, Developmental*
Body Patterning/*genetics
Drosophila Proteins/*genetics
Drosophila melanogaster/*genetics
Polypyrimidine Tract-Binding Protein/*genetics
RNA, Messenger/*genetics
Alternative Splicing ; Animals ; Drosophila Proteins/deficiency ; Drosophila Proteins/metabolism ; Drosophila melanogaster/embryology ; Drosophila melanogaster/metabolism ; Embryo, Nonmammalian ; High-Throughput Nucleotide Sequencing ; Homeodomain Proteins/genetics ; Homeodomain Proteins/metabolism ; In Situ Hybridization ; Mutation ; Polypyrimidine Tract-Binding Protein/deficiency ; RNA, Messenger/metabolism ; Repressor Proteins/genetics ; Repressor Proteins/metabolism ; Reverse Transcriptase Polymerase Chain Reaction ; Signal Transduction ; Transforming Growth Factor beta/genetics ; Transforming Growth Factor beta/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Alternative Splicing of Cdh23 Exon 68 Is Regulated by RBM24, RBM38, and PTBP1.
Autorzy:
Li N; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong Province, China.
Du H; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong Province, China.
Ren R; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong Province, China.
Wang Y; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong Province, China.
Xu Z; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao, Shandong Province, China.; Shandong Provincial Collaborative Innovation Center of Cell Biology, Shandong Normal University, Jinan, Shandong Province, China.
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Źródło:
Neural plasticity [Neural Plast] 2020 Jul 25; Vol. 2020, pp. 8898811. Date of Electronic Publication: 2020 Jul 25 (Print Publication: 2020).
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Alternative Splicing*
Cadherins/*genetics
Ear, Inner/*metabolism
Heterogeneous-Nuclear Ribonucleoproteins/*genetics
Polypyrimidine Tract-Binding Protein/*genetics
RNA-Binding Proteins/*genetics
Animals ; Cell Line ; Chlorocebus aethiops ; Exons ; Mice
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Abnormal PTBP1 Expression Sustains the Disease Progression of Multiple Myeloma.
Autorzy:
Bai H; Department of Hematology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China.
Chen B; Department of Hematology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China.
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Źródło:
Disease markers [Dis Markers] 2020 Jun 18; Vol. 2020, pp. 4013658. Date of Electronic Publication: 2020 Jun 18 (Print Publication: 2020).
Typ publikacji:
Journal Article
MeSH Terms:
Up-Regulation*
Carrier Proteins/*genetics
Heterogeneous-Nuclear Ribonucleoproteins/*genetics
Membrane Proteins/*genetics
Multiple Myeloma/*genetics
Polypyrimidine Tract-Binding Protein/*genetics
Thyroid Hormones/*genetics
Alternative Splicing ; Cell Line, Tumor ; Cell Movement ; Cell Proliferation ; Disease Progression ; Female ; Gene Expression Profiling ; Gene Expression Regulation, Neoplastic ; Glycolysis ; Humans ; Male ; Prognosis ; Thyroid Hormone-Binding Proteins
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Remodelling of a polypyrimidine tract-binding protein complex during apoptosis activates cellular IRESs.
Autorzy:
King HA; Medical Research Council Toxicology Unit, Lancaster Road, Leicester LE1 9HN, UK.
Cobbold LC
Pichon X
Pöyry T
Wilson LA
Booden H
Jukes-Jones R
Cain K
Lilley KS
Bushell M
Willis AE
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Źródło:
Cell death and differentiation [Cell Death Differ] 2014 Jan; Vol. 21 (1), pp. 161-71. Date of Electronic Publication: 2013 Oct 18.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Apoptosis/*drug effects
Polypyrimidine Tract-Binding Protein/*metabolism
TNF-Related Apoptosis-Inducing Ligand/*pharmacology
Cell Nucleus/metabolism ; Cyclin T/genetics ; Cyclin T/metabolism ; DNA-Binding Proteins ; HeLa Cells ; Histone-Lysine N-Methyltransferase/genetics ; Histone-Lysine N-Methyltransferase/metabolism ; Humans ; MCF-7 Cells ; Nuclear Matrix-Associated Proteins/antagonists & inhibitors ; Nuclear Matrix-Associated Proteins/genetics ; Nuclear Matrix-Associated Proteins/metabolism ; Octamer Transcription Factors/antagonists & inhibitors ; Octamer Transcription Factors/genetics ; Octamer Transcription Factors/metabolism ; PTB-Associated Splicing Factor ; Polypyrimidine Tract-Binding Protein/antagonists & inhibitors ; Polypyrimidine Tract-Binding Protein/genetics ; RNA Interference ; RNA, Messenger/metabolism ; RNA, Small Interfering/metabolism ; RNA-Binding Proteins/antagonists & inhibitors ; RNA-Binding Proteins/genetics ; RNA-Binding Proteins/metabolism ; Y-Box-Binding Protein 1/metabolism
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Mapping and characterization of the interaction interface between two polypyrimidine-tract binding proteins and a nova-type protein of Solanum tuberosum.
Autorzy:
Shah S; Roy J. Carver Department of Biochemistry Biophysics and Molecular Biology, Iowa State University, Ames, Iowa, United States of America.
Butler NM
Hannapel DJ
Rao AG
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Źródło:
PloS one [PLoS One] 2013 May 24; Vol. 8 (5), pp. e64783. Date of Electronic Publication: 2013 May 24 (Print Publication: 2013).
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms:
Antigens, Neoplasm/*genetics
Antigens, Neoplasm/*metabolism
Nerve Tissue Proteins/*genetics
Nerve Tissue Proteins/*metabolism
Polypyrimidine Tract-Binding Protein/*genetics
Polypyrimidine Tract-Binding Protein/*metabolism
RNA-Binding Proteins/*genetics
RNA-Binding Proteins/*metabolism
Solanum tuberosum/*genetics
Solanum tuberosum/*metabolism
Amino Acid Motifs ; Amino Acid Sequence ; Antigens, Neoplasm/chemistry ; Binding Sites ; Carrier Proteins/genetics ; Carrier Proteins/metabolism ; Cell Surface Display Techniques ; Molecular Sequence Data ; Mutation ; Nerve Tissue Proteins/chemistry ; Neuro-Oncological Ventral Antigen ; Peptide Library ; Polypyrimidine Tract-Binding Protein/chemistry ; Protein Binding ; Protein Interaction Domains and Motifs ; Protein Interaction Mapping ; RNA-Binding Proteins/chemistry ; Sequence Alignment
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknieSzczegóły
Tytuł:
Long non-coding RNA ARAP1-AS1 promotes tumorigenesis and metastasis through facilitating proto-oncogene c-Myc translation via dissociating PSF/PTB dimer in cervical cancer.
Autorzy:
Zhang Y; Department of Gynaecology and Obstetrics, Shengjing Hospital of China Medical University, Shenyang, China.
Wu D; Department of Gynaecology and Obstetrics, Shengjing Hospital of China Medical University, Shenyang, China.
Wang D; Department of Gynaecology and Obstetrics, Shengjing Hospital of China Medical University, Shenyang, China.
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Źródło:
Cancer medicine [Cancer Med] 2020 Mar; Vol. 9 (5), pp. 1855-1866. Date of Electronic Publication: 2020 Jan 17.
Typ publikacji:
Journal Article; Retracted Publication
MeSH Terms:
Carcinogenesis/*genetics
Lung Neoplasms/*genetics
Proto-Oncogene Proteins c-myc/*genetics
RNA, Long Noncoding/*metabolism
Uterine Cervical Neoplasms/*genetics
Animals ; Cell Line, Tumor ; E-Box Elements/genetics ; Feedback, Physiological ; Female ; Gene Expression Regulation, Neoplastic ; Gene Knockdown Techniques ; Humans ; Internal Ribosome Entry Sites/genetics ; Lung Neoplasms/secondary ; Mice ; PTB-Associated Splicing Factor/metabolism ; Polypyrimidine Tract-Binding Protein/metabolism ; Promoter Regions, Genetic/genetics ; Protein Biosynthesis ; Protein Multimerization/genetics ; Proto-Oncogene Mas ; Proto-Oncogene Proteins c-myc/metabolism ; RNA, Long Noncoding/genetics ; Transcriptional Activation ; Uterine Cervical Neoplasms/pathology ; Xenograft Model Antitumor Assays
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
PTBP1-mediated regulation of AXL mRNA stability plays a role in lung tumorigenesis.
Autorzy:
Cho CY; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Chung SY; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Lin S; Inflammation Research & Drug Development Center, Changhua Christian Hospital, Changhua, Taiwan.
Huang JS; Department of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Chen YL; Department of Pathology, Cardinal Tien Hospital, School of Medicine, Fu-Jen Catholic University, New Taipei City, Taiwan.
Jiang SS; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Cheng LC; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.; Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.
Kuo TH; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.; Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan.
Lay JD; Department of Nursing, National Taichung University of Science and Technology, Taichung, Taiwan.
Yang YY; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Lai GM; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.; Comprehensive Cancer Center, Taipei Medical University, Taipei, Taiwan.; Cancer Center, Wan Fang Hospital, Taipei Medical University, Taipei, Taiwan.
Chuang SE; National Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan. .
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Źródło:
Scientific reports [Sci Rep] 2019 Nov 15; Vol. 9 (1), pp. 16922. Date of Electronic Publication: 2019 Nov 15.
Typ publikacji:
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:
Gene Expression Regulation*
RNA Stability*
Cell Transformation, Neoplastic/*genetics
Cell Transformation, Neoplastic/*metabolism
Heterogeneous-Nuclear Ribonucleoproteins/*metabolism
Polypyrimidine Tract-Binding Protein/*metabolism
Proto-Oncogene Proteins/*genetics
RNA, Messenger/*genetics
Receptor Protein-Tyrosine Kinases/*genetics
5' Untranslated Regions ; Apoptosis ; Cell Line, Tumor ; Cell Movement ; Cell Survival ; Gene Expression ; Genes, Reporter ; Humans ; Lung Neoplasms/genetics ; Lung Neoplasms/metabolism ; Lung Neoplasms/pathology ; Axl Receptor Tyrosine Kinase
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 41-60 z 343

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