المؤلفون: Marjolein Carron, Attila Placido Sachslehner, Munevver Burcu Cicekdal, Inge Bruggeman, Suzan Demuynck, Bahar Golabi, Elfride De Baere, Wim Declercq, Erwin Tschachler, Kris Vleminckx, Leopold Eckhart

المصدر: Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2041-1723Test

الوصول الحر: https://doaj.org/article/a710d9a58fc84d2b8c16e5cff7cd038fTest

المؤلفون: Kris Vleminckx, Marjolein Carron, Attila Sachslehner, Leopold Eckart

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::ae9f97ba1341667b327d07d2e747cbd6Test
https://doi.org/10.26226/m.64199a115cbd02001a87debcTest

المؤلفون: Suzan Demuynck, Aaron M. Zorn, Kris Vleminckx, Marjolein Carron, Andy Willaert, Nicole A. Edwards, Marcin Wlizla, Thomas Naert, Dieter Tulkens, Paul Coucke, Annekatrien Boel, Nikko-Ideen Shaidani, Marko E. Horb

المصدر: SCIENTIFIC REPORTS
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)

مصطلحات موضوعية: 0301 basic medicine, Xenopus, lcsh:Medicine, Penetrance, Context (language use), Computational biology, Article, Mice, Xenopus laevis, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Genome editing, CRISPR-Associated Protein 9, Medicine and Health Sciences, Animals, Humans, CRISPR, Clustered Regularly Interspaced Short Palindromic Repeats, Guide RNA, lcsh:Science, Frameshift Mutation, Zebrafish, Gene Editing, Multidisciplinary, biology, Cas9, lcsh:R, Biology and Life Sciences, Mouse Embryonic Stem Cells, Genetic models, biology.organism_classification, HEK293 Cells, 030104 developmental biology, Genetic engineering, lcsh:Q, CRISPR-Cas Systems, Genetic techniques, Functional genomics, 030217 neurology & neurosurgery, RNA, Guide, Kinetoplastida

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::462bc8461d063a25887d564380b7f954Test
https://doi.org/10.1038/s41598-020-71412-0Test

المؤلفون: Dionysia Dimitrakopoulou, Liza Eeckhout, Kris Vleminckx, Christian Vanhove, Rivka Noelanders, Jo Van Dorpe, Gert Van Isterdael, Dieter Tulkens, Suzan Demuynck, Marjolein Carron, Dieter Deforce, Thomas Naert, David Creytens

المصدر: Oncogene. 39(13)

مصطلحات موضوعية: 0301 basic medicine, Cancer Research, Xenopus, Retinoblastoma-Like Protein p107, Biology, Xenopus Proteins, medicine.disease_cause, Retinoblastoma-like protein 1, Animals, Genetically Modified, 03 medical and health sciences, 0302 clinical medicine, Glioma, Pancreatic cancer, Genetics, medicine, Animals, Humans, Carcinoma, Small Cell, neoplasms, Molecular Biology, Gene Editing, Retinoblastoma, Retinoblastoma protein, medicine.disease, Choroid plexus papilloma, eye diseases, Carcinoma, Neuroendocrine, Pancreatic Neoplasms, Disease Models, Animal, 030104 developmental biology, 030220 oncology & carcinogenesis, Cancer research, biology.protein, Choroid plexus, CRISPR-Cas Systems, Carcinogenesis, Glioblastoma, Signal Transduction

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb0e6a50d81baaa4f3994202df0effeaTest
https://pubmed.ncbi.nlm.nih.gov/32001819Test

المؤلفون: Kristof Van Schil, Sarah Naessens, Stijn Van de Sompele, Marjolein Carron, Alexander Aslanidis, Caroline Van Cauwenbergh, Anja K. Mayer, Mattias Van Heetvelde, Miriam Bauwens, Hannah Verdin, Frauke Coppieters, Michael E. Greenberg, Marty G. Yang, Marcus Karlstetter, Thomas Langmann, Katleen De Preter, Susanne Kohl, Timothy J. Cherry, Bart P. Leroy, Elfride De Baere, James R Lupski, Claudia Carvalho, Max van Min, Petra Klous, Sarah De Jaegere, Sally Hooghe

المصدر: Genetics in Medicine

مصطلحات موضوعية: RNA, Untranslated, DNA Copy Number Variations, Genome, Human, Correction, Cadherin Related Proteins, Chromosome Mapping, Genetic mapping, Genomics, Sequence Analysis, DNA, Regulatory Sequences, Nucleic Acid, Cadherins, Retinal diseases, Open Reading Frames, Databases, Genetic, Humans, Genetic Predisposition to Disease, Genetic variation, Eye Proteins, Alleles, Genetics (clinical), Genome-Wide Association Study, Sequence Deletion

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9d961174ea556c6c2050d6c13fdeb22Test
https://doi.org/10.1038/s41436-018-0305-0Test

المؤلفون: Kristof Van Schil, Sarah Naessens, Stijn Van de Sompele, Marjolein Carron, Alexander Aslanidis, Caroline Van Cauwenbergh, Anja K. Mayer, Mattias Van Heetvelde, Miriam Bauwens, Hannah Verdin, Frauke Coppieters, Michael E. Greenberg, Marty G. Yang, Marcus Karlstetter, Thomas Langmann, Katleen De Preter, Susanne Kohl, Timothy J. Cherry, Bart P. Leroy, James R. Lupski, Claudia Carvalho, Max van Min, Petra Klous, Sarah De Jaegere, Sally Hooghe, Elfride De Baere

المصدر: GENETICS IN MEDICINE
Genetics in Medicine

مصطلحات موضوعية: 0301 basic medicine, Genomics, Genome-wide association study, Computational biology, Biology, VARIANTS, Genome, 03 medical and health sciences, 0302 clinical medicine, Gene mapping, MEDIATED DELETION, parasitic diseases, RETINITIS-PIGMENTOSA, Medicine and Health Sciences, genomic features, Original Research Article, Copy-number variation, TRANSCRIPTION, Gene, Genetics (clinical), Genetics, Disease gene, DIAGNOSTIC YIELD, MUTATIONS, copy-number variations, Biology and Life Sciences, DYSTROPHY, DEGENERATIONS, inherited retinal disease genes, ENHANCERS, 030104 developmental biology, predisposition, targeted locus amplification (TLA), Human genome, EXOME SEQUENCING DATA, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9afc86b76ee1eb917ae11e695592fc3Test
https://biblio.ugent.be/publication/8529931Test