المؤلفون: Grainok, Janya, Pitout, Ianthe L, Chen, Fred K, McLenachan, Samuel, Heath Jeffery, Rachael C, Mitrpant, Chalermchai, Fletcher, Sue

مصطلحات موضوعية: Codon, Nonsense, Eye Proteins - genetics, Eye Proteins - metabolism, Humans, Mutation, Oligonucleotides, Antisense - genetics, Antisense - therapeutic use, Open Reading Frames, Pedigree, Retinitis Pigmentosa, RNA Precursors - genetics

وصف الملف: pdf

العلاقة: ispartof: International journal of molecular sciences issue 6 vol 25; WOS:001193446500001; 991005652870007891; https://researchportal.murdoch.edu.au/esploro/outputs/journalArticle/A-Precision-Therapy-Approach-for-Retinitis/991005652870007891Test; https://researchportal.murdoch.edu.au/view/delivery/61MUN_INST/12160737560007891/13160737550007891Test; alma:61MUN_INST/bibs/991005652870007891

الإتاحة: https://doi.org/10.3390/ijms25063391Test
https://researchportal.murdoch.edu.au/esploro/outputs/journalArticle/A-Precision-Therapy-Approach-for-Retinitis/991005652870007891Test
https://researchportal.murdoch.edu.au/view/delivery/61MUN_INST/12160737560007891/13160737550007891Test

المؤلفون: Flynn, Loren L., Li, Ruohan, Pitout, Ianthe L., Aung-Htut, May T., Larcher, Leon M., Cooper, Jack A. L., Greer, Kane L., Hubbard, Alysia, Griffiths, Lisa, Bond, Charles S., Wilton, Steve D., Fox, Archa H., Fletcher, Sue

المساهمون: National Health and Medical Research Council

المصدر: Frontiers in Genetics ; volume 13 ; ISSN 1664-8021

الإتاحة: https://doi.org/10.3389/fgene.2022.791416Test

المؤلفون: Larcher, Leon M., Pitout, Ianthe L., Keegan, Niall P., Veedu, Rakesh N., Fletcher, Sue

المصدر: Nucleic Acid Therapeutics ; volume 33, issue 3, page 178-192 ; ISSN 2159-3337 2159-3345

الإتاحة: https://doi.org/10.1089/nat.2022.0066Test

المؤلفون: Mejzini, Rita, Flynn, Loren L., Pitout, Ianthe L., Fletcher, Sue, Wilton, Steve D., Akkari, P. Anthony

المصدر: Frontiers in Neuroscience ; volume 13 ; ISSN 1662-453X

الإتاحة: https://doi.org/10.3389/fnins.2019.01310Test

المؤلفون: Flynn, Loren L., Mitrpant, Chalermchai, Pitout, Ianthe L., Fletcher, Sue, Wilton, Steve D.

المساهمون: Parry Foundation, Spinal Muscular Atrophy Association of Australia, NHMRC, Team Spencer and Muscular Dystrophy WA

المصدر: Molecular Therapy - Nucleic Acids ; volume 11, page 91-102 ; ISSN 2162-2531

الإتاحة: https://doi.org/10.1016/j.omtn.2018.01.011Test
https://api.elsevier.com/content/article/PII:S216225311830012X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S216225311830012X?httpAccept=text/plainTest

المؤلفون: Daniels, Willie M. U., Pitout, Ianthe L., Afullo, Thomas J. O., Mabandla, Musa V.

المصدر: Metabolic Brain Disease ; volume 24, issue 4, page 629-641 ; ISSN 0885-7490 1573-7365

مصطلحات موضوعية: Cellular and Molecular Neuroscience, Neurology (clinical), Biochemistry

الإتاحة: https://doi.org/10.1007/s11011-009-9164-3Test

المؤلفون: Flynn, Loren L., Mitrpant, Chalermchai, Adams, Abbie, Pitout, Ianthe L., Stirnweiss, Anja, Fletcher, Sue, Wilton, Steve D., Lebleu, Bernard

المصدر: Biomedicines; May2021, Vol. 9 Issue 5, p552, 1p

مصطلحات موضوعية: GENE targeting, OLIGONUCLEOTIDES, MOTOR neurons

المؤلفون: Aung-Htut, May T., McIntosh, Craig S., Ham, Kristin A., Pitout, Ianthe L., Flynn, Loren L., Greer, Kane, Fletcher, Sue, Wilton, Steve D.

المصدر: International Journal of Molecular Sciences; Oct2019, Vol. 20 Issue 20, p5030, 1p, 1 Diagram, 4 Charts, 2 Graphs

مصطلحات موضوعية: RNA splicing, SPINAL muscular atrophy, OLIGONUCLEOTIDES, DUCHENNE muscular dystrophy, HUMAN genes, NEUROMUSCULAR diseases