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المؤلفون: Karissa Barthelson, Lachlan Baer, Yang Dong, Melanie Hand, Zac Pujic, Morgan Newman, Geoffrey J. Goodhill, Robert I. Richards, Stephen M. Pederson, Michael Lardelli
المصدر: Frontiers in Genetics, Vol 12 (2021)
مصطلحات موضوعية: Genetics, Mutation, congenital, hereditary, and neonatal diseases and abnormalities, biology, Morpholino, Chromosome, chromosome evolution, QH426-470, biology.organism_classification, medicine.disease_cause, zebrafish, FMR1, transcriptome analysis, transcriptional adaptation, Homologous chromosome, medicine, Molecular Medicine, Allele, fragile X syndrome, Zebrafish, Gene, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e915969dcb2534a7b92a6039e9ed30dTest
https://www.frontiersin.org/articles/10.3389/fgene.2021.625466/fullTest -
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المؤلفون: Karissa, Barthelson, Lachlan, Baer, Yang, Dong, Melanie, Hand, Zac, Pujic, Morgan, Newman, Geoffrey J, Goodhill, Robert I, Richards, Stephen M, Pederson, Michael, Lardelli
المصدر: Frontiers in Genetics
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, transcriptome analysis, transcriptional adaptation, homeostasis, Genetics, chromosome evolution, fragile X syndrome, zebrafish, FMR1, linkage disequilibrium, Original Research
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::5f44c504aa4443976804a92c7260df47Test
https://pubmed.ncbi.nlm.nih.gov/34135935Test -
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المؤلفون: Shuying Wu, Ge Huang, Manhua Cui, He Zhu, Tianmin Xu
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 10 (2019)مصطلحات موضوعية: FMR4, 0301 basic medicine, Untranslated region, congenital, hereditary, and neonatal diseases and abnormalities, Down syndrome, Ataxia, lcsh:QH426-470, BC1, FMR6, Review, Biology, fragile X-related primary ovarian insufficiency, 03 medical and health sciences, Exon, 0302 clinical medicine, Genetics, medicine, long noncoding RNA, fragile X syndrome, Genetics (clinical), fragile X-associated tremor/ataxia syndrome, medicine.disease, TUG1, FMR1, Long non-coding RNA, Fragile X syndrome, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, Molecular Medicine, medicine.symptom, Fragile X-associated tremor/ataxia syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6272a2659e1d3b778b1e09c5a52ee9ffTest
https://doi.org/10.3389/fgene.2019.00446Test -
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المؤلفون: Yafang Zhou, Yacen Hu, Qiying Sun, Nina Xie
المصدر: Frontiers in Genetics, Vol 10 (2019)
Frontiers in Geneticsمصطلحات موضوعية: 0301 basic medicine, Untranslated region, congenital, hereditary, and neonatal diseases and abnormalities, potential converging mechanisms, lcsh:QH426-470, non-coding RNA, Review, Biology, medicine.disease_cause, 03 medical and health sciences, 0302 clinical medicine, Translational regulation, microRNA, medicine, Genetics, microRNA mediated translational regulation, Genetics (clinical), RNAi mediated epigenetic silencing, Mutation, medicine.disease, Non-coding RNA, FMR1, Fragile X syndrome, lcsh:Genetics, 030104 developmental biology, 030220 oncology & carcinogenesis, Molecular Medicine, Autism
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15b5bc6d380ffe0240e4673d0c9a462fTest
https://www.frontiersin.org/article/10.3389/fgene.2019.00139/fullTest -
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المصدر: Frontiers in Genetics, Vol 9 (2018)
Frontiers in Geneticsمصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, lcsh:QH426-470, Biology, Melting curve analysis, 03 medical and health sciences, 0302 clinical medicine, Genotype, medicine, Genetics, Allele, fragile X syndrome, FMR1, Genetics (clinical), Original Research, medicine.disease, DNA extraction, Molecular biology, dried blood spot, Dried blood spot, nervous system diseases, triplet-primed PCR (TP-PCR), Fragile X syndrome, lcsh:Genetics, 030104 developmental biology, Molecular Medicine, Trinucleotide repeat expansion, melt curve analysis (MCA), 030217 neurology & neurosurgery, trinucleotide repeat
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36ff5abaca91c7c0ea2352feff71b6eeTest
https://www.frontiersin.org/article/10.3389/fgene.2018.00582/fullTest -
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المؤلفون: Eleonora Napoli, Andrea Schneider, Randi Hagerman, Gyu Song, Sarah Wong, Flora Tassone, Cecilia Giulivi
المصدر: Frontiers in Genetics, Vol 9 (2018)
مصطلحات موضوعية: 0301 basic medicine, Mitochondrial ROS, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, lcsh:QH426-470, Mitochondrion, bioenergetics, 03 medical and health sciences, Internal medicine, mitochondrial dysfunction, Genetics, oxidative stress, Medicine, Epigenetics, Allele, Genetics (clinical), Depression (differential diagnoses), business.industry, FMR1, Phenotype, 3. Good health, lcsh:Genetics, premutation, 030104 developmental biology, Endocrinology, Molecular Medicine, FXTAS, business, Asymptomatic carrier
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6c963371d658b6d307ae8a67135868fTest
https://doi.org/10.3389/fgene.2018.00338Test -
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المؤلفون: Keri J. Heilman, Anne Wheeler, Jacek Kolacz, Melissa Raspa, Anne Edwards, Amanda Wylie, Stephen W. Porges
المصدر: Frontiers in Genetics, Vol 9 (2018)
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Sensory processing, hyposensitivity, lcsh:QH426-470, medicine.medical_treatment, feeding behavior, Sensory system, Family income, 03 medical and health sciences, 0302 clinical medicine, 030225 pediatrics, Genetics, medicine, Early childhood, fragile X syndrome, sensory processing, Full mutation, Genetics (clinical), business.industry, medicine.disease, FMR1, Fragile X syndrome, lcsh:Genetics, Molecular Medicine, Autism, hypersensitivity, business, FMR1 premutation, 030217 neurology & neurosurgery, Clinical psychology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf4514124fb304ea57d32b223fe8e155Test
https://www.frontiersin.org/article/10.3389/fgene.2018.00351/fullTest -
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المؤلفون: Veronica Julia Peschansky, Chiara ePastori, Zane eZeier, Dario eMotti, Katya eWentzel, Dmitry eVelmeshev, Marco eMagistri, John L Bixby, Vance P Lemmon, José P Silva, Claes eWahlestedt
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 6 (2015)مصطلحات موضوعية: FMR4, congenital, hereditary, and neonatal diseases and abnormalities, lcsh:QH426-470, Biology, chromatin remodeling, 03 medical and health sciences, 0302 clinical medicine, lncRNA, Gene expression, medicine, Genetics, Gene silencing, Epigenetics, Gene, Genetics (clinical), 030304 developmental biology, Original Research, 0303 health sciences, epigenetics, differentiation, medicine.disease, FMR1, Long non-coding RNA, Fragile X syndrome, lcsh:Genetics, intellectual disability, Fragile X Syndrome, Fragile X, Molecular Medicine, MBD4, Trinucleotide repeat expansion, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa0e26b8bdbc770ce8faa2b5c7fc905eTest
http://europepmc.org/articles/PMC4530595Test -
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المؤلفون: Karen Usdin, Daman Kumari
المصدر: Frontiers in Genetics, Vol 6 (2015)
Frontiers in Geneticsمصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, lcsh:QH426-470, Review, R loops, Biology, Bioinformatics, polycomb repressive complex 2, 03 medical and health sciences, 0302 clinical medicine, Trinucleotide Repeats, Tandem repeat, Genetics, medicine, Gene silencing, Gene Silencing, fragile X syndrome, Allele, Genetics (clinical), 030304 developmental biology, Repeat-mediated gene silencing, 0303 health sciences, epigenetics, fragile X-associated tremor/ataxia syndrome, Chromosomal fragile site, medicine.disease, FMR1, Fragile X syndrome, lcsh:Genetics, Molecular Medicine, FXS, Trinucleotide repeat expansion, 030217 neurology & neurosurgery, fragile X-associated primary ovarian insufficiency, Fragile X-associated tremor/ataxia syndrome
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10474be2adb316e2a171855fe940fb28Test
https://doi.org/10.3389/fgene.2015.00192Test -
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المؤلفون: Marsha eMailick, Jinkuk eHong, Paul eRathouz, Mei eBaker, Jan eGreenberg, Leann eSmith, Matthew eMaenner
المصدر: Frontiers in Genetics
Frontiers in Genetics, Vol 5 (2014)مصطلحات موضوعية: low-normal FMR1 CGG repeats, congenital, hereditary, and neonatal diseases and abnormalities, genotype-phenotype correlations, lcsh:QH426-470, Population, genotype–phenotype correlations, Odds, breast cancer, Uterine Cancer, Uterine cancer, Genetics, Medicine, Original Research Article, fragile X syndrome, Allele, education, Genetics (clinical), education.field_of_study, FMR1 CGG expansions, cognitive aging, business.industry, Cognition, medicine.disease, Mental health, FMR1, nervous system diseases, Fragile X syndrome, lcsh:Genetics, Molecular Medicine, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a303cfcec30a4e7cf40f317a65fab1aTest
https://doi.org/10.3389/fgene.2014.00309Test