Suchergebnisse - "DNA-Binding Proteins: genetics"
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1
Autoren: et al.
Quelle: N Engl J Med
The New England journal of medicine, vol. 392, no. 16, pp. 1594-1608Schlagwörter: Male, Lung Neoplasms, Middle Aged, Article, Monocytes, Dioxygenases, DNA-Binding Proteins, Mice, Observational Studies as Topic, Cell Movement, Carcinoma, Non-Small-Cell Lung, Cell Line, Tumor, Mutation, Tumor Microenvironment, Animals, Humans, Female, Prospective Studies, Clonal Hematopoiesis, Neoplasm Recurrence, Local, Aged, Carcinoma, Non-Small-Cell Lung/genetics, Carcinoma, Non-Small-Cell Lung/immunology, Carcinoma, Non-Small-Cell Lung/mortality, Carcinoma, Non-Small-Cell Lung/pathology, Clonal Hematopoiesis/genetics, Clonal Hematopoiesis/immunology, Dioxygenases/genetics, DNA-Binding Proteins/genetics, Lung Neoplasms/genetics, Lung Neoplasms/mortality, Lung Neoplasms/pathology, Neoplasm Recurrence, Local/epidemiology, Neoplasm Recurrence, Local/genetics, Neoplasm Recurrence, Local/pathology, Tumor Microenvironment/immunology, Monocytes/immunology, Monocytes/pathology, Cell Movement/genetics, Cell Movement/immunology, Neoplasm Transplantation
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/40267425
https://ora.ox.ac.uk/objects/uuid:e20d5bce-3d87-4ac2-9e89-b887ca4cc72b
https://doi.org/10.1056/nejmoa2413361
https://serval.unil.ch/notice/serval:BIB_435B0ABCF518
https://serval.unil.ch/resource/serval:BIB_435B0ABCF518.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_435B0ABCF5187 -
2
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Scientia
Scientia. Dipòsit d'Informació Digital del Departament de Salut
instname
Annals of Oncology, 35, 10, pp. 892-901
Allen, S, Balmaña, J, Domchek, S M, Evans, D G, Hoogerbrugge, N, Nathanson, K L, Tischkowitz, M, Foulkes, W D & Turnbull, C 2024, 'Population-based germline breast cancer gene association studies and meta-analysis to inform wider mainstream testing', Annals of oncology : official journal of the European Society for Medical Oncology, vol. 35, no. 10, pp. 892-901. https://doi.org/10.1016/j.annonc.2024.07.244Schlagwörter: Other subheadings::Other subheadings::Other subheadings::/genetics, Ubiquitin-Protein Ligases, Breast Neoplasms, Ataxia Telangiectasia Mutated Proteins, Breast Neoplasms/genetics, Checkpoint Kinase 2/genetics, breast cancer, ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Genetic Testing, Ataxia Telangiectasia Mutated Proteins/genetics, Otros calificadores::Otros calificadores::Otros calificadores::/genética, Humans, Genetic Predisposition to Disease, Ubiquitin-Protein Ligases/genetics, Genetic Testing, Germ-Line Mutation, Genetic Association Studies, BRCA2 Protein, BRCA1 Protein, Tumor Suppressor Proteins, mainstream genetic testing, Cromosomes humans - Anomalies - Diagnòstic, Fanconi Anemia Complementation Group N Protein/genetics, BRCA2 Protein/genetics, 3. Good health, DNA-Binding Proteins, Meta-analysis, Checkpoint Kinase 2, TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::diagnóstico::técnicas y procedimientos diagnósticos::técnicas de laboratorio clínico::pruebas genéticas, Case-Control Studies, multi-gene panel testing, BRCA1 Protein/genetics, Mama - Càncer - Aspectes genètics, Human Genetics - Radboud University Medical Center, Female, Fanconi Anemia Complementation Group N Protein, ENFERMEDADES::neoplasias::neoplasias por localización::neoplasias de la mama, case-control, DNA-Binding Proteins/genetics, Genetic Testing/methods, DISEASES::Neoplasms::Neoplasms by Site::Breast Neoplasms
Dateibeschreibung: application/pdf; Print-Electronic
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/38986768
https://hdl.handle.net/11351/11965
https://research.manchester.ac.uk/en/publications/590e571d-7ad9-4fb3-b723-57aaa7277a35
https://doi.org/10.1016/j.annonc.2024.07.244
https://repository.ubn.ru.nl/handle/2066/310405
https://repository.ubn.ru.nl//bitstream/handle/2066/310405/310405.pdf
https://research.manchester.ac.uk/en/publications/590e571d-7ad9-4fb3-b723-57aaa7277a35
http://www.scopus.com/inward/record.url?scp=85201586788&partnerID=8YFLogxK
https://doi.org/10.1016/j.annonc.2024.07.244 -
3
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Fam Cancer
Familial Cancer, 23, 4, pp. 447-457Schlagwörter: 0301 basic medicine, Cancer Research, 0303 health sciences, Meeting report, Review, Europe [MeSH], C, European C, Brain Neoplasms/genetics [MeSH], Humans [MeSH], Neoplastic Syndromes, Hereditary/genetics [MeSH], DNA-Binding Proteins/genetics [MeSH], Paris [MeSH], Neoplastic Syndromes, Hereditary/diagnosis [MeSH], Mismatch Repair Endonuclease PMS2/genetics [MeSH], Germ-Line Mutation [MeSH], Neoplastic Syndromes, Hereditary/therapy [MeSH], MutS Homolog 2 Protein/genetics [MeSH], CMMRD, Brain Neoplasms/therapy [MeSH], MutL Protein Homolog 1/genetics [MeSH], Medical Biosciences - Radboud University Medical Center, 03 medical and health sciences, Oncology, Genetics, Genetics(clinical), CCMMRD, European CCMMRD consortium
Dateibeschreibung: application/pdf
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Autoren: et al.
Quelle: Gastric Cancer
Schlagwörter: Male, Adult, 0301 basic medicine, LRP1B, 03 medical and health sciences, Stomach Neoplasms, ARID1A, EGC, Pen, Prognosis, Biomarkers, Tumor, Humans, Aged, Aged, 80 and over, 0303 health sciences, Genomics, Middle Aged, DNA-Binding Proteins, Receptors, LDL, Aged, 80 and over [MeSH], Aged [MeSH], Transcription Factors/genetics [MeSH], Stomach Neoplasms/pathology [MeSH], Stomach Neoplasms/surgery [MeSH], Neoplasm Recurrence, Local/pathology [MeSH], Stomach Neoplasms/mortality [MeSH], DNA-Binding Proteins/genetics [MeSH], Original Article, Male [MeSH], Neoplasm Recurrence, Local/genetics [MeSH], Stomach Neoplasms/genetics [MeSH], Female [MeSH], Follow-Up Studies [MeSH], Mutation [MeSH], Adult [MeSH], Humans [MeSH], Genomics/methods [MeSH], Middle Aged [MeSH], Microsatellite Instability [MeSH], Receptors, LDL [MeSH], Biomarkers, Tumor/genetics [MeSH], Prognosis [MeSH], Mutation, Female, Microsatellite Instability, Neoplasm Recurrence, Local, Transcription Factors, Follow-Up Studies
Dateibeschreibung: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document
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5
Autoren: et al.
Quelle: Science
Schlagwörter: Male, Eukaryotic Initiation Factor-2/metabolism, Article, Mice, Genes, Y-Linked, Y Chromosome, Male/genetics, Testis, Humans, Animals, Spermatogenesis, Infertility, Male, Cell Proliferation, Spermatogenesis/genetics, Nuclear Proteins, Y-Linked, Spermatogonia, DNA-Binding Proteins, Chromosome Pairing, Meiosis, Genes, Meiosis/genetics, Spermatogonia/metabolism, Infertility, Testis/metabolism, Y Chromosome/genetics, Chromosome Deletion, Transcriptome, DNA-Binding Proteins/genetics, Gene Deletion, Transcription Factors
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/39847625
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Autoren: et al.
Quelle: BMC Microbiol
BMC Microbiology, Vol 25, Iss 1, Pp 1-16 (2025)
BMC microbiology, vol. 25, no. 1, pp. 286Schlagwörter: SOS response, H-NS regulators, Research, Mitomycin, Gene Expression Regulation, Bacterial, Microbiology, QR1-502, DNA-Binding Proteins, Repressor Proteins, Tailocin, Pyocin, Bacterial Proteins, Pseudomonas, Pseudomonas/genetics, Pseudomonas/metabolism, Pseudomonas/virology, Bacterial Proteins/genetics, Bacterial Proteins/metabolism, DNA-Binding Proteins/metabolism, DNA-Binding Proteins/genetics, Repressor Proteins/metabolism, Repressor Proteins/genetics, Mitomycin/pharmacology, Regulation
Dateibeschreibung: application/pdf
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/40350448
https://doaj.org/article/4bf0f9778db242b384e6e5a8d7e8ab4b
https://serval.unil.ch/resource/serval:BIB_941D5210DB6B.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_941D5210DB6B1
https://serval.unil.ch/notice/serval:BIB_941D5210DB6B -
7
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Nat Cell Biol
Schlagwörter: 0301 basic medicine, KMT2C protein, human, Oncologie, Triple Negative Breast Neoplasms/pathology, Triple Negative Breast Neoplasms, Histone-Lysine N-Methyltransferase/genetics, Sciences de la santé humaine, Article, Epigenesis, Genetic, Mice, 03 medical and health sciences, Neoplasm Proteins/genetics, KMT2D protein, human, Cell Line, Tumor, Matrix Metalloproteinase 3/metabolism, Neoplasm Proteins/metabolism, Animals, Humans, Human health sciences, Histone-Lysine N-Methyltransferase/metabolism, Brain Neoplasms/genetics, Histone Demethylases, Mice, Knockout, 0303 health sciences, DNA-Binding Proteins/metabolism, Brain Neoplasms, KDM6A protein, human, Cell Biology, Histone-Lysine N-Methyltransferase, Kmt2d protein, mouse, MMP3 protein, human, Up-Regulation, Neoplasm Proteins, Gene Expression Regulation, Neoplastic, DNA-Binding Proteins, Oncology, Triple Negative Breast Neoplasms/metabolism, Brain Neoplasms/pathology, Histone Demethylases/genetics, Brain Neoplasms/secondary, Matrix Metalloproteinase 3, Female, Histone Demethylases/metabolism, Triple Negative Breast Neoplasms/genetics, Matrix Metalloproteinase 3/genetics, DNA-Binding Proteins/genetics, Myeloid-Lymphoid Leukemia Protein, Brain Neoplasms/metabolism
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/38926506
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8
Autoren: et al.
Quelle: Hum Genet
Schlagwörter: Male, 0301 basic medicine, 0303 health sciences, Micrognathism, Face/abnormalities [MeSH], Mutation [MeSH], Protein Aggregates [MeSH], Transcription Factors/genetics [MeSH], Abnormalities, Multiple/genetics [MeSH], Humans [MeSH], Intellectual Disability/genetics [MeSH], Micrognathism/genetics [MeSH], DNA-Binding Proteins/genetics [MeSH], DNA-Binding Proteins/metabolism [MeSH], Original Investigation, Hand Deformities, Congenital/genetics [MeSH], Male [MeSH], Neck/abnormalities [MeSH], Transcription Factors/metabolism [MeSH], 3. Good health, DNA-Binding Proteins, Protein Aggregates, 03 medical and health sciences, Intellectual Disability, Face, Mutation, Humans, Abnormalities, Multiple, Hand Deformities, Congenital, Neck, Transcription Factors
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Autoren: et al.
Quelle: EMBO Rep
EMBO reports, vol. 26, no. 14, pp. 3554-3573
Ammitsoe, T, Ebstrup, E, Blanco-Tourinan, N, Hansen, J, Hardtke, C S, Petersen, M & Rodriguez, E 2025, ' BZR1 promotes pluripotency acquisition and callus development through direct regulation of ARF7 and ARF19 ', EMBO Reports, vol. 26, no. 14, pp. 3554-3573 . https://doi.org/10.1038/s44319-025-00433-5Schlagwörter: Callus, Pluripotency, Transcriptional Regulation, Bzr1, Arabidopsis Proteins/genetics, Arabidopsis Proteins/metabolism, Arabidopsis/genetics, Arabidopsis/growth & development, Arabidopsis/metabolism, Gene Expression Regulation, Plant, Transcription Factors/genetics, Transcription Factors/metabolism, DNA-Binding Proteins/metabolism, DNA-Binding Proteins/genetics, Indoleacetic Acids/metabolism, Nuclear Proteins/genetics, Nuclear Proteins/metabolism, Promoter Regions, Genetic, Signal Transduction, Mutation, Protein Binding, ARFs, BZR1, Article
Dateibeschreibung: application/pdf
Zugangs-URL: https://serval.unil.ch/notice/serval:BIB_A4AB9CE03B09
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_A4AB9CE03B092
https://serval.unil.ch/resource/serval:BIB_A4AB9CE03B09.P001/REF.pdf
https://curis.ku.dk/ws/files/461316792/ammits_e-et-al-bzr1-promotes-pluripotency-acquisition-and-callus-development-through-direct-regulation-of-arf7-and-arf19.pdf -
10
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Acta Neuropathol
Schlagwörter: Male, Glioma / genetics, Adolescent, Colorectal Neoplasms, Hereditary Nonpolyposis / genetics, DNA-Binding Proteins / genetics, DNA Mismatch Repair, DNA Mismatch Repair / genetics, Neoplastic Syndromes, Hereditary / genetics, MutS Homolog 2 Protein / genetics, Immunohistochemistry / methods, Brain Neoplasms / pathology, MutL Protein Homolog 1 / genetics, Neoplastic Syndromes, Hereditary, Germ-Line Mutation / genetics, Humans, Child, Mismatch Repair Endonuclease PMS2, Brain Neoplasms, Mismatch Repair Endonuclease PMS2 / metabolism, Glioma / metabolism, Infant, Colorectal Neoplasms, Hereditary Nonpolyposis / pathology, DNA-Binding Proteins / metabolism, Glioma, Brain Neoplasms / genetics, Immunohistochemistry, Colorectal Neoplasms, Hereditary Nonpolyposis, Mismatch Repair Endonuclease PMS2 / genetics, DNA-Binding Proteins, Lynch syndrome, MutS Homolog 2 Protein, Colorectal Neoplasms, Hereditary Nonpolyposis / diagnosis, Pediatric high-grade glioma, Neoplastic Syndromes, Hereditary / diagnosis, Child, Preschool, Glioma / pathology, Original Article, Female, Colorectal Neoplasms, MutL Protein Homolog 1, Constitutional mismatch repair deficiency, MutS Homolog 2 Protein / metabolism
Dateibeschreibung: application/pdf
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11
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Science Immunology. 10
Schlagwörter: Male, sequence analysis, cell maturation, severe combined immune deficiency disease, preschool child, DISEASE, immunology, rituximab, cellular indexing of transcriptome and epitope by sequencing, nuclear protein, genetic variability, T lymphocyte, RAG1 protein, genetics, gene mutation, Child, IMMUNODEFICIENCY, epitope, child, B-Lymphocytes, adult, steroid, allele, RAG gene, Nuclear Proteins, B-Lymphocytes/immunology, EXPANSION, interferon, Inflammation/immunology, I IFNS, RAG-1 protein, autoantigen, 3204 Immunology, DNA-Binding Proteins, DIFFERENTIATION, female, Phenotype, Child, Preschool, Female, Omenn syndrome, Centralized Sequencing Program Group§§, Life Sciences & Biomedicine, Centralized Sequencing Program Group, phenotype, Immunology, leaky severe combined immune deficiency disease, Article, male, immune dysregulation, Humans, controlled study, cyclosporine, human, IMMUNOGLOBULIN-SECRETING CELLS, Preschool, Inflammation, Homeodomain Proteins, Science & Technology, B lymphocyte, MUTATIONS, RAG2 protein, human, human cell, 3202 Clinical sciences, RAG2 protein, immune deficiency, Multiomics, major clinical study, DNA binding protein, human tissue, Th2 cell, inflammation, homeodomain protein, adolescent, ANTIBODIES, Mutation, T-CELLS, AUTOANTIBODIES, genetic disorder, Homeodomain Proteins/genetics, mutation, transcriptome, DNA-Binding Proteins/genetics, autoantibody, multiomics
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/39792639
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Autoren: et al.
Quelle: Mol Imaging Biol
Schlagwörter: Heart Failure, 0301 basic medicine, Endonucleases/metabolism [MeSH], Heart failure, Heart Failure/diagnostic imaging [MeSH], Endonucleases/genetics [MeSH], Ercc1, Animals [MeSH], Apoptosis [MeSH], DNA-Binding Proteins/genetics [MeSH], Myocardium/pathology [MeSH], DNA-Binding Proteins/metabolism [MeSH], Molecular imaging, FMT, CT, Aging, Mice [MeSH], Heart Failure/pathology [MeSH], Research Article, DNA repair, X-Ray Microtomography [MeSH], 0303 health sciences, Myocardium, Apoptosis, X-Ray Microtomography, Endonucleases, DNA-Binding Proteins, Mice, 03 medical and health sciences, 0302 clinical medicine, SDG 3 - Good Health and Well-being, Animals
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Autoren: et al.
Quelle: J Neurol
Journal of NeurologySchlagwörter: Adult, 0301 basic medicine, 0303 health sciences, Adolescent, ddc, 3. Good health, Short Commentary, Movement disorders, Dystonia, Exome sequencing, Autism, DNA-Binding Proteins, Young Adult, 03 medical and health sciences, Phenotype, Neurodevelopmental Disorders, Dystonic Disorders, Child, Preschool, Humans, Female, Child, Frameshift Mutation, Dystonia/genetics [MeSH], Dystonia/diagnosis [MeSH], Transcription Factors/genetics [MeSH], Frameshift Mutation [MeSH], Neurodevelopmental Disorders/diagnosis [MeSH], DNA-Binding Proteins/genetics [MeSH], Neurodevelopmental Disorders/genetics [MeSH], Dystonia/etiology [MeSH], Dystonic Disorders/complications [MeSH], Phenotype [MeSH], Dystonic Disorders/diagnosis [MeSH], Child [MeSH], Adolescent [MeSH], Female [MeSH], Adult [MeSH], Humans [MeSH], Dystonic Disorders/physiopathology [MeSH], Dystonic Disorders/genetics [MeSH], Young Adult [MeSH], Dystonia/physiopathology [MeSH], Child, Preschool [MeSH], Transcription Factors
Dateibeschreibung: application/pdf
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Autoren: et al.
Quelle: Graefes Arch Clin Exp Ophthalmol
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, vol. 262, no. 6, pp. 1737-1744Schlagwörter: Male, Fundus Oculi, Visual Acuity, DNA, Hematologic Diseases, Multimodal Imaging, Neoplasm Proteins, 3. Good health, DNA-Binding Proteins, Macular Degeneration, Phenotype, Vestibular Diseases, Face, Electroretinography, Retinal Disorders, Humans, Abnormalities, Multiple, Female, Fluorescein Angiography, Vestibular Diseases/genetics, Vestibular Diseases/diagnosis, Vestibular Diseases/physiopathology, Face/abnormalities, Hematologic Diseases/genetics, Hematologic Diseases/diagnosis, Hematologic Diseases/physiopathology, Tomography, Optical Coherence/methods, Abnormalities, Multiple/genetics, Abnormalities, Multiple/diagnosis, Follow-Up Studies, Neoplasm Proteins/genetics, Fluorescein Angiography/methods, DNA-Binding Proteins/genetics, Macular Degeneration/genetics, Macular Degeneration/diagnosis, Macular Degeneration/physiopathology, Neck, DNA/genetics, Exome Sequencing, DNA Mutational Analysis, Macula Lutea/pathology, Time Factors, Adult, Adolescent, KMTD2 gene, Adaptive optics, Autofluorescence imaging, Dystrophy, Kabuki syndrome, Macula, Multimodal imaging, Retinal imaging, Tomography, Optical Coherence
Dateibeschreibung: application/pdf
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15
Autoren: et al.
Quelle: Eur J Hum Genet
Schlagwörter: Adult, 0301 basic medicine, 0303 health sciences, Base Sequence, Article, DNA-Binding Proteins, 03 medical and health sciences, Phenotype, SDG 3 - Good Health and Well-being, Neurodevelopmental Disorders, Intellectual Disability, Humans, Female, Autistic Disorder, Female [MeSH], 631/208, Adult [MeSH], Transcription Factors/genetics [MeSH], 692/308/2056, Humans [MeSH], Intellectual Disability/genetics [MeSH], DNA-Binding Proteins/genetics [MeSH], Neurodevelopmental Disorders/genetics [MeSH], Autistic Disorder/genetics [MeSH], 45/23, 45/91, Phenotype [MeSH], Base Sequence [MeSH], article, Transcription Factors
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Autoren: et al.
Quelle: Virchows Arch
Schlagwörter: Male, Adult, Aged, 80 and over, Aged, 80 and over [MeSH], Neoplasm Grading [MeSH], Aged [MeSH], Rhabdoid, Transcription Factors/genetics [MeSH], DNA-Binding Proteins/deficiency [MeSH], DNA-Binding Proteins/genetics [MeSH], Diagnosis, Differential [MeSH], Yolk sac-like, Original Article, SMARCB1-deficient adenocarcinoma, SMARCB1 Protein/deficiency [MeSH], Male [MeSH], Paranasal Sinus Neoplasms/genetics [MeSH], Adenocarcinoma/pathology [MeSH], SWI/SNF complex, Next-generation sequencing, Sinonasal, Myoepithelioma/genetics [MeSH], Transcription Factors/deficiency [MeSH], Female [MeSH], Mutation [MeSH], Adult [MeSH], Head and neck, Humans [MeSH], Myoepithelioma/pathology [MeSH], Middle Aged [MeSH], Paranasal Sinus Neoplasms/pathology [MeSH], Biomarkers, Tumor/genetics [MeSH], Adenocarcinoma/genetics [MeSH], SMARCB1 Protein/genetics [MeSH], In Situ Hybridization, Fluorescence [MeSH], High-Throughput Nucleotide Sequencing [MeSH], High-Throughput Nucleotide Sequencing, SMARCB1 Protein, Middle Aged, Adenocarcinoma, Myoepithelioma, 3. Good health, DNA-Binding Proteins, Diagnosis, Differential, Mutation, Biomarkers, Tumor, Humans, Female, Neoplasm Grading, Paranasal Sinus Neoplasms, In Situ Hybridization, Fluorescence, Aged, Transcription Factors
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17
Autoren: et al.
Weitere Verfasser: et al.
Quelle: Nat Genet
Franco, E D, Owens, N, Montaser, H, Wakeling, M, Saarimäki-Vire, J, Triantou, A, Ibrahim, H G, Balboa, D, Caswell, R, Jennings, R E, Kvist, J, Johnson, M B, Muralidharan, S, Ellard, S, Wright, C F, Maddirevula, S, Alkuraya, F S, Laimon, W, Hassan, S S, Abdullah, M A, Fritzberg, A, Wakeling, E, Nathwani, N, Elbarbary, N, Osman, A, Alkandari, H, alTararwa, A, Habeb, A, Al-Agha, A E, Ahmad, I A, Aldulaimi, M N N, Ustyol, A, Binomar, H M A, Shagrani, M, Pancreatic Agenesis Gene Discovery Consortium, Hanley, N, Flanagan, S, Otonkoski, T, Hattersley, A & Imbeault, M 2023, ' Primate-specific ZNF808 is essential for pancreatic development in humans ', Nature Genetics, vol. 55 . https://doi.org/10.1038/s41588-023-01565-x
Pancreatic Agenesis Gene Discovery Consortium 2023, 'Primate-specific ZNF808 is essential for pancreatic development in humans', Nature Genetics, vol. 55, no. 12, pp. 2075-2081. https://doi.org/10.1038/s41588-023-01565-x, https://doi.org/10.1038/s41588-023-01565-xSchlagwörter: Gata4, Primates, Letter, Primates/abnormalities, Pancreas/abnormalities, Gene, Congenital Abnormalities/genetics, Congenital Abnormalities, Visceral endoderm, Developmental biology, Sequencing, Animals, Humans, Methyltransferase, Pancreas, Onset, Genome, Genome, Human, Diabetes, Cell Differentiation, Gene regulation, DNA-Binding Proteins, Zinc-finger proteins, Genetics, developmental biology, physiology, Differentiation, DNA Transposable Elements, Mutations, DNA-Binding Proteins/genetics, Enhancer, Human
Dateibeschreibung: application/pdf; application/zip; text/xml
Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/37973953
https://research.manchester.ac.uk/en/publications/f3675a85-119c-4809-8e52-3f9d4da9c279
https://doi.org/10.1038/s41588-023-01565-x
http://hdl.handle.net/10138/569488
https://research.manchester.ac.uk/en/publications/fc355949-5dac-41c8-9249-b27c9a316fc8
https://doi.org/10.1038/s41588-023-01565-x -
18
Autoren: et al.
Weitere Verfasser: et al.
Quelle: ISSN: 0014-2980.
Schlagwörter: CST, Class switch recombination, DSB repair, Shieldin, MESH: Animals, MESH: B-Lymphocytes* / immunology, MESH: Immunoglobulin Class Switching* / genetics, MESH: Immunoglobulin Class Switching* / immunology, MESH: Immunoglobulin Heavy Chains* / genetics, MESH: Immunoglobulin Heavy Chains* / immunology, MESH: Mice, Inbred C57BL, Knockout, MESH: Telomere-Binding Proteins* / genetics, MESH: Telomere-Binding Proteins* / metabolism, MESH: Tumor Suppressor p53-Binding Protein 1, MESH: Cytidine Deaminase / genetics, MESH: Cytidine Deaminase / metabolism, MESH: DNA Breaks, Double-Stranded, MESH: DNA End-Joining Repair, MESH: DNA Repair, MESH: DNA-Binding Proteins* / genetics, MESH: DNA-Binding Proteins* / metabolism, MESH: Epistasis, Genetic, [SDV.IMM]Life Sciences [q-bio]/Immunology, [SDV.GEN]Life Sciences [q-bio]/Genetics
Relation: info:eu-repo/semantics/altIdentifier/pmid/40178294; PUBMED: 40178294; PUBMEDCENTRAL: PMC11967320
Verfügbarkeit: https://u-paris.hal.science/hal-05121552
https://u-paris.hal.science/hal-05121552v1/document
https://u-paris.hal.science/hal-05121552v1/file/Eur%20J%20Immunol%20-%202025%20-%20Lescale%20-%20CST%20Is%20Epistatic%20With%20Shieldin%20to%20Limit%20DNA%20Double%E2%80%90Strand%20Break%20End%20Resection%20and%20Promote.pdf
https://doi.org/10.1002/eji.202451585 -
19
Autoren: et al.
Weitere Verfasser: et al.
Quelle: ISSN: 2375-2548 ; Science Advances ; https://hal.science/hal-05326520 ; Science Advances , 2025, 11 (8), pp.eadq2475. ⟨10.1126/sciadv.adq2475⟩.
Schlagwörter: MESH: DNA-Binding Proteins* / chemistry, MESH: DNA-Binding Proteins* / genetics, MESH: Protein Inhibitors of Activated STAT / metabolism, MESH: Small Ubiquitin-Related Modifier Proteins* / genetics, MESH: Small Ubiquitin-Related Modifier Proteins* / metabolism, MESH: Stress Granules / metabolism, MESH: Sumoylation, MESH: Ubiquitins* / genetics, MESH: Ubiquitins* / metabolism, MESH: DNA-Binding Proteins* / metabolism, MESH: Humans, MESH: Oxidative Stress, MESH: Poly-ADP-Ribose Binding Proteins, MESH: Protein Aggregates, MESH: Protein Aggregation, Pathological* / metabolism, MESH: Protein Binding, MESH: Protein Inhibitors of Activated STAT / genetics, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, [SDV.NEU.NB]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]/Neurobiology
Relation: info:eu-repo/semantics/altIdentifier/pmid/39982984; info:eu-repo/grantAgreement//725836/EU/The chemistry and physics of RNP granules: how they form, age and cause disease/PhaseAge; PUBMED: 39982984; PUBMEDCENTRAL: PMC11844728
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20
Autoren: et al.
Weitere Verfasser: et al.
Quelle: ISSN: 0305-1048.
Schlagwörter: MESH: Bacterial Proteins* / genetics, MESH: Bacterial Proteins* / metabolism, MESH: Streptococcus pneumoniae* / genetics, MESH: Streptococcus pneumoniae* / metabolism, MESH: Chromosomes, Bacterial* / chemistry, Bacterial* / genetics, Bacterial* / metabolism, MESH: DNA Replication, MESH: DNA, Bacterial / genetics, MESH: DNA-Binding Proteins* / genetics, MESH: DNA-Binding Proteins* / metabolism, MESH: Replication Origin, [SDV]Life Sciences [q-bio]
Relation: https://doi.org/10.6084/m9.figshare.c.7486716.v1; info:eu-repo/semantics/altIdentifier/pmid/40263708; PUBMED: 40263708; PUBMEDCENTRAL: PMC12014288
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