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1دورية أكاديمية
المؤلفون: Mark Kiel, Amina Kozaric, Moriel Singer-Berk, Jordan Wood, Emily Evangelista, Amanda Hope, Leena Panwala, Stephanie Heinrich, Samantha Baxter
المصدر: Genetics in Medicine Open, Vol 2, Iss , Pp 101067- (2024)
وصف الملف: electronic resource
العلاقة: http://www.sciencedirect.com/science/article/pii/S2949774424002139Test; https://doaj.org/toc/2949-7744Test
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2دورية أكاديمية
المؤلفون: Guang Lin, Burak Tepe, Geoff McGrane, Regine C Tipon, Gist Croft, Leena Panwala, Amanda Hope, Agnes JH Liang, Zhongyuan Zuo, Seul Kee Byeon, Lily Wang, Akhilesh Pandey, Hugo J Bellen
المصدر: eLife, Vol 12 (2023)
مصطلحات موضوعية: INAD, Parkinson's disease, gene therapy, ceramides, lysosome, drug screen, Medicine, Science, Biology (General), QH301-705.5
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Patricia L. Babin, Sudheendra N. R. Rao, Anita Chacko, Fidelia B. Alvina, Anil Panwala, Leena Panwala, Danielle C. Fumagalli
المصدر: Frontiers in Genetics, Vol 9 (2018)
مصطلحات موضوعية: infantile neuroaxonal dystrophy, rare disease, exome sequencing, enzyme replacement therapy, vector gene therapy, CRISPR/Cas9, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://www.frontiersin.org/article/10.3389/fgene.2018.00597/fullTest; https://doaj.org/toc/1664-8021Test
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المؤلفون: Guang Lin, Burak Tepe, Geoff McGrane, Regine C Tipon, Gist Croft, Leena Panwala, Amanda Hope, Agnes JH Liang, Zhongyuan Zuo, Seul Kee Byeon, Lily Wang, Akhilesh Pandey, Hugo J Bellen
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::5737f82bb244b9dc487fd1679729501dTest
https://doi.org/10.7554/elife.82555.sa2Test -
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المؤلفون: Guang Lin, Burak Tepe, Geoff McGrane, Regine C. Tipon, Gist Croft, Leena Panwala, Amanda Hope, Agnes J.H. Liang, Zongyuan Zuo, Lily Wang, Hugo J. Bellen
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::7c5bbf7ed2829b58a3d5128cc556e2c2Test
https://doi.org/10.1101/2022.08.16.504080Test -
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المؤلفون: Anil Panwala, Sudheendra N.R. Rao, Fidelia B. Alvina, Danielle C. Fumagalli, Leena Panwala, Patricia L. Babin, Anita Chacko
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 9 (2018)مصطلحات موضوعية: 0301 basic medicine, lcsh:QH426-470, rare disease, Disease, infantile neuroaxonal dystrophy, Bioinformatics, vector gene therapy, Infantile neuroaxonal dystrophy, 03 medical and health sciences, Gene panel, Hypothesis and Theory, medicine, Genetics, CRISPR/Cas9, Genetics (clinical), Exome sequencing, business.industry, Molecular pathology, Enzyme replacement therapy, Molecular diagnostics, medicine.disease, lcsh:Genetics, 030104 developmental biology, Molecular Medicine, business, exome sequencing, Rare disease, enzyme replacement therapy
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c6b283875763e3f881ce21f479c341aTest
http://europepmc.org/articles/PMC6295457Test