The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
The fragile X mental retardation protein is associated with ribosomes
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“FMRP co-IP’d with rpP0-containing complexes, as did the ribosomal proteins rpL5 and rpS6 (Figure 7H), demonstrating a direct association of FMRP with ribosome-containing complexes, reminiscent of previous findings in cultured cells (Khandjian et al., 1996; Siomi et al., 1996).”
From FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism (2011) · cites this paper as Khandjian et al., 1996
Citations
Cites
Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y.-H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., et al. (1991) · Cell · doi:10.1016/0092-8674(91)90397-h · Cited by 3,481
Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome
Oberlé, I., Rousseau, F., Heitz, D., Kretz, C., Devys, D., Hanauer, A., Boué, J., Bertheas, M. F., & Mandel, J. L. (1991) · Science · doi:10.1126/science.252.5009.1097 · Cited by 1,499
Self-citationAbsence of expression of the FMR-1 gene in fragile X syndrome
Pieretti, M., Zhang, F., Fu, Y.-H., Warren, S. T., Oostra, B. A., Caskey, C. T., & Nelson, D. L. (1991) · Cell · doi:10.1016/0092-8674(91)90125-i · Cited by 1,476
Fmr1 knockout mice: A model to study fragile X mental retardation
THEDUTCHBELGIANFRAGILEXCONSOR (1994) · Cell · doi:10.1016/0092-8674(94)90569-x · Cited by 1,108
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
Kremer, E., Pritchard, M., Lynch, M., Yu, S., Holman, K., Baker, E., Warren, S., Schlessinger, D., Sutherland, G., & Richards, R. (1991) · Science · doi:10.1126/science.1675488 · Cited by 929
Devys, D., Lutz, Y., Rouyer, N., Bellocq, J., & Mandel, J. (1993) · Nature Genetics · doi:10.1038/ng0893-335 · Cited by 781
Ross, M. (1974) · Annals of Internal Medicine · doi:10.7326/0003-4819-81-2-286_5 · Cited by 758
FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding
Ashley, C. T., Wilkinson, K. D., Reines, D., & Warren, S. T. (1993) · Science · doi:10.1126/science.7692601 · Cited by 752
Lerner, E. A., Lerner, M. R., Janeway, C. A., & STEITZ, J. A. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.5.2737 · Cited by 718
DNA methylation represses FMR-1 transcription in fragile X syndrome
Sutcliffe, J. S., Nelson, D. L., Zhang, F., Pieretti, M., Caskey, C. T., Saxe, D., & Warren, S. T. (1992) · Human Molecular Genetics · doi:10.1093/hmg/1.6.397 · Cited by 680
Research works printed but not linked: 2
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Leguay, K., Acevedo, M., Colic, E., Patel, P. U., Abadi, S. S. K., Chan, H. L., Sun, S., Lang-Ouellette, D., Chan, B., Zhan, X., et al. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110341 · Cited by 2
Molecular aspects of X-linked mental retardation loci
Essop, F. (2010) · University of the Witwatersrand, Johannesburg Institutional Repository on DSpace (University of the Witwatersrand, Johannesburg) · Cited by 1
Insights into the human Fragile X syndrome gene family using Drosophila melanogaster
Coffee, R. L. (2011) · Cited by 1
Huot, M. (2005) · Corpus Université Laval (Université Laval) · Cited by 1
Differentiation of neural stem cells in fragile X syndrome
Tervonen, T. A. (2008) · Työväentutkimus Vuosikirja
Molekulare Grundlagen neurologischer Trinukleotidblockexpansionssyndrome
Epplen, J. T., & Haupt, A. (2000) · Springer eBooks · doi:10.1007/978-3-642-57043-8_18
Fragile X Syndrome: From Pathophysiology to New Therapeutic Perspectives
D’Antoni, S., Spatuzza, M., Carmela, M., Aloisi, E., Musumeci, S. A., & Vincenza, M. (2012) · InTech eBooks · doi:10.5772/31387
Trinukleotid-Repeat-Erkrankungen
Klockgether, T., & Weller, M. (1999) · Springer eBooks · doi:10.1007/978-3-662-07096-3_3
Biochemistry and modeling of human Dicer, a key protein involved in RNA interference
Zhang, H. (2004) · edoc (University of Basel) · doi:10.5451/unibas-003602075
Variabilidade do domínio KH-2 da proteína do retardo mental do X frágil (FMRP)
Velloso, F. J. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2013.tde-21032014-090729
Expressão de isoformas da proteína do retardo mental do X frágil (FMRP) e sua regulação
Velloso, F. J. (2008) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.41.2008.tde-19032009-144613
Romancino, D. P., Guarneri, P., Cascio, C., Dalmazio, S., Guarneri, R., & Carlo, M. D. (2001) · Molecular Cell Biology Research Communications · doi:10.1006/mcbr.2001.0305
Corrêa, J. D. C. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.41.2014.tde-01092014-085006
FRAGILE X SYNDROME IN NORTHERN FINLAND
Väisänen, M. (1999)
Rôle de la protéine FMRP dans la formation et le dynamisme des granules à ARN
Mellaoui, S. (2012) · Corpus Université Laval (Université Laval)
Blancquaert, I. R., & Caron, L. (2002)
Funktionelle Charakterisierung von FMRP, dem Krankheitsgenprodukt des Fragilen X-Syndroms
München, L.-M.-U. (2004)
FMRP and the Pathophysiology of Fragile X Syndrome
Barnes, S. A., Thomson, S. R., Kind, P. C., & Osterweil, E. K. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800109-7.00008-x
Dysregulated Translation in Autism Spectrum Disorder
Santini, E., & Borgkvist, A. (2020) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780190686307.013.24
Targeting Translation Regulation for the Development of Novel Drugs
Alroy, I., Mansour, W., & Sheinberger, Y. (2020) · Royal Society of Chemistry eBooks · doi:10.1039/9781839160691-00254
Functional characterization of the TTF complex and its role in neurodevelopmental disorders
Brosi, C. (2018) · Online Publication Service of Würzburg University (Würzburg University) · doi:10.25972/opus-15778
What Can the Study of Behavioral Phenotypes Teach Us About the Pathway from Genes to Behavior?
Flint, J. (2003) · Humana Press eBooks · doi:10.1007/978-1-59259-353-8_4
Tamanini, F. (2009) · Springer eBooks · doi:10.1007/978-3-540-29676-8_652
Excessive Cap-dependent Translation as a Molecular Mechanism Underlying ASD
Klann, E. (2014) · Defense Technical Information Center (DTIC) · doi:10.21236/ada612864
Nairn, A. C., & Wiseman, S. L. (2011) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.12154956.13994054
Fmr1 exon 14 skipping in late embryonic development of the rat forebrain
Corrêa-Velloso, J. C., Linardi, A., Glaser, T., Velloso, F. J., Rivas, M. P., Leite, R. E. P., Grinberg, L. T., Ulrich, H., Akins, M. R., Chiavegatto, S., et al. (2022) · BMC Neuroscience · doi:10.1186/s12868-022-00711-1 · Cited by 1
Dubuc, K., Marchais, M., Gilbert, I., Bastien, A., Nenonene, E. K., Khandjian, E. W., Viger, R. S., & Robert, C. (2022) · Research Square · doi:10.21203/rs.3.rs-2026855/v1
Self-citationOxytocin and Vasopressin in Autism and Genetic Syndromes
Levin‐Decanini, T., Francis, S. M., Sagar, A., Liu, W., Carter, C. S., & Jacob, S. (2015) · Contemporary clinical neuroscience · doi:10.1007/978-1-4939-2190-4_14
Additional file 1 of Fmr1 exon 14 skipping in late embryonic development of the rat forebrain
Corrêa-Velloso, J. C., Linardi, A., Glaser, T., Velloso, F. J., Rivas, M. P., Leite, R. E. P., Grinberg, L. T., Ulrich, H., Akins, M. R., Chiavegatto, S., et al. (2022) · Figshare · doi:10.6084/m9.figshare.19947736
Dubuc, K., Marchais, M., Gilbert, I., Bastien, A., Nenonene, E. K., Khandjian, E. W., Viger, R. S., Delbès, G., & Robert, C. (2023) · Figshare · doi:10.6084/m9.figshare.22799941
Self-citationDubuc, K., Marchais, M., Gilbert, I., Bastien, A., Nenonene, E. K., Khandjian, E. W., Viger, R. S., Delbès, G., & Robert, C. (2023) · Figshare · doi:10.6084/m9.figshare.22799944
Self-citationDubuc, K., Marchais, M., Gilbert, I., Bastien, A., Nenonene, E. K., Khandjian, E. W., Viger, R. S., Delbès, G., & Robert, C. (2023) · Figshare · doi:10.6084/m9.figshare.22799947
Self-citationDubuc, K., Marchais, M., Gilbert, I., Bastien, A., Nenonene, E. K., Khandjian, E. W., Viger, R. S., Delbès, G., & Robert, C. (2023) · Figshare · doi:10.6084/m9.figshare.22799938
Self-citationHuang, J. Q., Kadijk, E., Schreiber, K. J., Liu, Z. H., Chiang, R., Zhang, Z., Guttman, K. M., Huang, T. H., Almeida, S. M. T., Zhulyn, O., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.24.707808
Involvement of mGluR5/Homer crosstalk disruption in the pathophysiology of Fragile X Syndrome
Aloisi, E. (2015) · theses.fr (ABES) · doi:10.70675/e628d840zb6adz4e63z9d1fz71559b23fe24
Bermudez-Martin, P. (2020) · theses.fr (ABES) · doi:10.70675/d0d223ffzbc0ez44d9z8475z153f265e94f5
Rôle de la phosphodiestérase 2A dans la physiopathologie du syndrome de l’X fragile
Delhaye, S. (2021) · theses.fr (ABES) · doi:10.70675/e0fac395z63d4z46a4z944aza4037215ca98
Molekulargenetische Grundlagen des fra(X)-Syndroms—Diagnostik und therapeutische Hilfen
Steinbach, P. J. (2000) · Springer eBooks · doi:10.1007/978-3-642-57043-8_17
Turner (1996) · doi:10.1002/(sici)1096-8628(19960712)64:1
Metadata
- Authors
- Khandjian, E. W., Corbin, F., Woerly, S., & Rousseau, F.
- Affiliations
- Hôpital Saint-François d'Assise (CA)
- Venue
- Nature Genetics
- Published
- 1996-01
- Volume
- 12
- Issue
- 1
- Pages
- 91-93
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W2026456570
- Cited by
- 251
- References
- 30
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 1 · 2023: 6 · 2022: 4 · 2021: 3 · 2020: 10 · 2019: 7 · 2018: 4 · 2017: 6 · 2016: 8 · 2015: 6 · 2014: 12 · 2013: 8 · 2012: 5
- FWCI
- 9.81
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Genetics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Keywords
- FMRP, fragile X syndrome, ribosome association, 60S ribosomal subunit, CGG repeat expansion, FMR1 gene silencing, RNA-binding proteins, translation machinery, neurons, polysomes
- MeSH terms
- Animals, Cell Compartmentation, Fragile X Syndrome, HeLa Cells, Humans, Nerve Tissue Proteins, Protein Binding, Ribosomes, Protein Biosynthesis, 3T3 Cells, RNA-Binding Proteins, Fluorescent Antibody Technique, Indirect, Mice, Fragile X Messenger Ribonucleoprotein 1, Fragile X Mental Retardation Protein
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