يعرض 1 - 10 نتائج من 18 نتيجة بحث عن '"Maria C. Sterrett"', وقت الاستعلام: 0.80s تنقيح النتائج
  1. 1
    دورية أكاديمية
    A Drosophila model of Pontocerebellar Hypoplasia reveals a critical role for the RNA exosome in neurons.

    المؤلفون: Derrick J Morton, Binta Jalloh, Lily Kim, Isaac Kremsky, Rishi J Nair, Khuong B Nguyen, J Christopher Rounds, Maria C Sterrett, Brianna Brown, Thalia Le, Maya C Karkare, Kathryn D McGaughey, Shaoyi Sheng, Sara W Leung, Milo B Fasken, Kenneth H Moberg, Anita H Corbett

    المصدر: PLoS Genetics, Vol 16, Iss 7, p e1008901 (2020)

    مصطلحات موضوعية: Genetics, QH426-470

    وصف الملف: electronic resource

    العلاقة: https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

    الوصول الحر: https://doaj.org/article/8fcdad56f18443738042e0b80b7add26Test

    View record in DOAJ النص الكامل

    أضف إلى المفضلة
  2. 2
    In vivo characterization of the critical interaction between the RNA exosome and the essential RNA helicase Mtr4 inSaccharomyces cerevisiae

    المؤلفون: Maria C Sterrett, Daniela Farchi, Sarah E Strassler, Lawrence H Boise, Milo B Fasken, Anita H Corbett

    المصدر: G3 Genes|Genomes|Genetics.

    مصطلحات موضوعية: Genetics, Molecular Biology, Genetics (clinical)

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::61742397218e41e5c3eb40466d460b9eTest
    https://doi.org/10.1093/g3journal/jkad049Test


    أضف إلى المفضلة
  3. 3
    In vivoCharacterization of the Critical Interaction between the RNA Exosome and the Essential RNA Helicase Mtr4 inSaccharomyces cerevisiae

    المؤلفون: Maria C. Sterrett, Daniela Farchi, Sarah E. Strassler, Lawrence H. Boise, Milo B. Fasken, Anita H. Corbett

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::249c5be31d88688ff5c17567619962b1Test
    https://doi.org/10.1101/2022.10.31.514520Test


    أضف إلى المفضلة
  4. 4
    A budding yeast model for human disease mutations in the EXOSC2 cap subunit of the RNA exosome complex

    المؤلفون: Sara W. Leung, Richard Baker, Richard S. Lee, Sarah E. Strassler, Munira A. Basrai, Liz Enyenihi, Laurie Hess, Elise S. Withers, Isaac Kremsky, Maria C. Sterrett, Anita H. Corbett, Milo B. Fasken, Daniela Farchi, Ambro van Hoof

    المصدر: RNA. 27:1046-1067

    مصطلحات موضوعية: Transcriptome, Exosome complex, Protein subunit, Exoribonuclease complex, RNA, Missense mutation, Biology, Molecular Biology, Gene, Exosome Multienzyme Ribonuclease Complex, Cell biology

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::c9676bd9b83a84f217103e157cc78e7cTest
    https://doi.org/10.1261/rna.078618.120Test


    أضف إلى المفضلة
  5. 5
    Hox proteins interact to pattern neuronal subtypes in Caenorhabditis elegans males

    المؤلفون: Andrea K Kalis, Maria C Sterrett, Cecily Armstrong, Amarantha Ballmer, Kylie Burkstrand, Elizabeth Chilson, Estee Emlen, Emma Ferrer, Seanna Loeb, Taylor Olin, Kevin Tran, Andrew Wheeler, Jennifer Ross Wolff

    المصدر: Genetics

    مصطلحات موضوعية: Investigation, Homeodomain Proteins, Male, Neurons, Genetics, Animals, Gene Expression Regulation, Developmental, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Transcription Factors

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc250d8c28c0da161940cfae3d587a88Test
    https://doi.org/10.1093/genetics/iyac010Test


    أضف إلى المفضلة
  6. 6
    Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness

    المؤلفون: Juvianee I. Estrada-Veras, Eirik Frengen, Linda Mathisen, Liz Enyenihi, Hans Einar Treidene, Daniah Beleford, Yue Si, Ganka Douglas, Michelle Foreman, Jacque L. Duncan, Jennifer E. Hurtig, Anne Slavotinek, Erik-Jan Kamsteeg, Charlotte A. Haaxma, Sara W. Leung, Milo B. Fasken, Ambro van Hoof, Anita H. Corbett, Dina Schneidman-Duhovny, Stephanie Htun, Doriana Misceo, Maria C. Sterrett, Vivian Xia

    المصدر: Human Molecular Genetics, 29, 13, pp. 2218-2239
    Hum Mol Genet
    Human molecular genetics, vol 29, iss 13
    Human Molecular Genetics, 29, 2218-2239

    مصطلحات موضوعية: Exosome complex, Developmental Disabilities, Medical and Health Sciences, Sensory disorders Donders Center for Medical Neuroscience [Radboudumc 12], Exon, 0302 clinical medicine, Cerebellum, 2.1 Biological and endogenous factors, Missense mutation, Aetiology, Frameshift Mutation, Zebrafish, Genetics (clinical), Genetics & Heredity, Genetics, 0303 health sciences, Exosome Multienzyme Ribonuclease Complex, Homozygote, RNA-Binding Proteins, General Medicine, Biological Sciences, Disorders of movement Donders Center for Medical Neuroscience [Radboudumc 3], Hypotonia, Pedigree, General Article, medicine.symptom, Mutation, Missense, Dwarfism, Biology, Nervous System Malformations, Frameshift mutation, 03 medical and health sciences, Rare Diseases, Clinical Research, Antigens, Neoplasm, medicine, Animals, Humans, Antigens, Molecular Biology, Gene, Loss function, 030304 developmental biology, Neurosciences, Mutation, Neoplasm, Missense, 030217 neurology & neurosurgery

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::619de630446be920565ee1a38cd9d0d6Test
    https://doi.org/10.1093/hmg/ddaa108Test


    أضف إلى المفضلة
  7. 7
    A budding yeast model for human disease mutations in the

    المؤلفون: Maria C, Sterrett, Liz, Enyenihi, Sara W, Leung, Laurie, Hess, Sarah E, Strassler, Daniela, Farchi, Richard S, Lee, Elise S, Withers, Isaac, Kremsky, Richard E, Baker, Munira A, Basrai, Ambro, van Hoof, Milo B, Fasken, Anita H, Corbett

    المصدر: RNA

    مصطلحات موضوعية: Models, Molecular, Aspartic Acid, Saccharomyces cerevisiae Proteins, Exosome Multienzyme Ribonuclease Complex, Sequence Homology, Amino Acid, Protein Conformation, Glycine, Mutation, Missense, Facies, Gene Expression, RNA-Binding Proteins, Dwarfism, RNA, Fungal, Saccharomyces cerevisiae, Syndrome, Models, Biological, Article, Amino Acid Substitution, Exoribonucleases, Humans, Amino Acid Sequence, Hearing Loss, Retinitis Pigmentosa

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::e5d64bfa72e5212a1b375190661795c4Test
    https://pubmed.ncbi.nlm.nih.gov/34162742Test


    أضف إلى المفضلة
  8. 8
    A Budding Yeast Model for Human Disease Mutations in the EXOSC2 Cap Subunit of the RNA Exosome

    المؤلفون: Maria C. Sterrett, Liz Enyenihi, Sara W. Leung, Laurie Hess, Sarah E. Strassler, Daniela Farchi, Richard S. Lee, Elise S. Withers, Isaac Kremsky, Richard E. Baker, Munira A. Basrai, Ambro van Hoof, Milo B. Fasken, Anita H. Corbett

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::dbff2b129e62f025530ef4f7c2747a73Test
    https://doi.org/10.1101/2020.12.06.413658Test


    أضف إلى المفضلة
  9. 9
    Biallelic variants in the RNA exosome gene EXOSC5 are associated with developmental delays, short stature, cerebellar hypoplasia and motor weakness

    المؤلفون: Yue Si, Eirik Frengen, Linda Mathisen, Ambro van Hoof, Daniah Beleford, Hans Einar Treidene, Michelle Foreman, Liz Enyenihi, Sara W. Leung, Anne Slavotinek, Stephanie Htun, Ganka Douglas, Juvianee I. Estrada-Veras, Jacque L. Duncan, Jennifer E. Hurtig, Doriana Misceo, Maria C. Sterrett, Vivian Xia, Anita H. Corbett, Dina Schneidman-Duhovny, Milo B. Fasken

    مصطلحات موضوعية: Genetics, 0303 health sciences, Exosome complex, Biology, medicine.disease, Hypotonia, 03 medical and health sciences, Exon, 0302 clinical medicine, Chromosome 19, medicine, Missense mutation, medicine.symptom, Gene, Cerebellar hypoplasia, 030217 neurology & neurosurgery, Loss function, 030304 developmental biology

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c95b9e06cfd6bad82401d0a25d8c1dd1Test


    أضف إلى المفضلة
  10. 10
    ADrosophilaModel of Pontocerebellar Hypoplasia Reveals a Critical Role for the RNA Exosome in Neurons

    المؤلفون: Derrick J. Morton, Binta Jalloh, Lily Kim, Isaac Kremsky, Rishi J. Nair, Khuong B. Nguyen, J. Christopher Rounds, Maria C. Sterrett, Brianna Brown, Thalia Le, Maya C. Karkare, Kathryn D. McGaughey, Shaoyi Sheng, Sara W. Leung, Milo B. Fasken, Kenneth H. Moberg, Anita H. Corbett

    مصطلحات موضوعية: 0303 health sciences, Cas9, Exosome complex, Mutant, RNA, Biology, Cell biology, 03 medical and health sciences, 0302 clinical medicine, RNA interference, Gene expression, CRISPR, Gene, 030217 neurology & neurosurgery, 030304 developmental biology

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e92c3198268f436b8a7d2e54b0f09bfTest
    https://doi.org/10.1101/727693Test


    أضف إلى المفضلة
أدوات البحث: أحصل على تغذية RSS — أرسل هذا البحث بالبريد الإلكتروني — حفظ البحث