M. Hergersberg, K. Matsuo, M. Gassmann, W. Schaffner, B. Luscher, T. Rülicke, A. Aguzzi (1995)
Tissue-specific expression of a FMR1/β-galactosidase fusion gene in transgenic miceHuman Molecular Genetics, 4
Feng (1995)
Quantitative comparison of FMR1 gene expression in normal and premutation allelesAm. J. Hum. Genet, 56
Harold JefferiesS, Thomas, George ThomasSn (1994)
Elongation factor-1 alpha mRNA is selectively translated following mitogenic stimulation.The Journal of biological chemistry, 269 6
C. Ashley, K. Wilkinson, D. Reines, S. Warren (1993)
FMR1 protein: conserved RNP family domains and selective RNA binding.Science, 262 5133
E. Bonfa, A. Parnassa, D. Rhoads, D. Roufa, I. Wool, K. Elkon (1989)
Antiribosomal S10 antibodies in humans and MRL/lpr mice with systemic lupus erythematosus.Arthritis and rheumatism, 32 10
D. Eberhart, H. Malter, Yue Feng, S. Warren (1996)
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals.Human molecular genetics, 5 8
Filippo Tamanini, Nicolle Meijer, C. Verheij, Patrick Willems, Hans Galjaard, B. Oostra, A. Hoogeveen (1996)
FMRP is associated to the ribosomes via RNA.Human molecular genetics, 5 6
Rudelli (1985)
Adult fragile X syndromeActa Neuropathol, 67
G. Dreyfuss, M. Matunis, S. Piñol-Roma, C. Burd (1993)
hnRNP proteins and the biogenesis of mRNA.Annual review of biochemistry, 62
H. Urlaub, V. Kruft, O. Bischof, E. Müller, B. Wittmann-Liebold (1995)
Protein‐rRNA binding features and their structural and functional implications in ribosomes as determined by cross‐linking studies.The EMBO Journal, 14
H. Hinds, C. Ashley, J. Sutcliffe, D. Nelson, S. Warren, D. Housman, M. Schalling (1993)
Tissue specific expression of FMR–1 provides evidence for a functional role in fragile X syndromeNature Genetics, 3
H. Leffers, Kurt Dejgaard, J. Celis (1995)
Characterisation of two major cellular poly(rC)-binding human proteins, each containing three K-homologous (KH) domains.European journal of biochemistry, 230 2
M. Kiledjian, Xiaoming Wang, S. Liebhaber (1995)
Identification of two KH domain proteins in the alpha‐globin mRNP stability complex.The EMBO Journal, 14
H. Meljer, E. Graaff, D. Merckx, Roselle Jongbloed, C. Die-Smulders, J. Engelen, J. Fryns, Paul Curfs, B. Oostra (1994)
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.Human molecular genetics, 3 4
(1996)
Dreyfuss for antibodies
Derek Eberhart, Stephen Warren (1996)
The molecular basis of fragile X syndrome.Cold Spring Harbor symposia on quantitative biology, 61
S. Warren, D. Nelson (1994)
Advances in molecular analysis of fragile X syndrome.JAMA, 271 7
Mahone (1995)
Localized Bicaudal-C RNA encodes a protein containing a KH domain, the RNA binding motif of FMR1EMBO J, 14
D. Devys, Y. Lutz, N. Rouyer, J. Bellocq, J. Mandel (1993)
The FMR–1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationNature Genetics, 4
J. Ch'ng, D. Shoemaker, P. Schimmel, E. Holmes (1990)
Reversal of creatine kinase translational repression by 3' untranslated sequences.Science, 248 4958
M. Morelli, G. Stier, T. Gibson, C. Joseph, G. Musco, A. Pastore, G. Travé (1995)
The KH module has an αβ foldFEBS Letters, 358
Leffers (1995)
Characterization of two major cellular poly(rC)-binding human proteins, each containing three K-homologous (KH) domainsEur. J. Biochem, 230
H. Siomi, M. Choi, M. Siomi, R. Nussbaum, G. Dreyfuss (1994)
Essential role for KH domains in RNA binding: Impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndromeCell, 77
H. Berg (1989)
Cold Spring Harbor Symposia on Quantitative Biology.: Vol. LII. Evolution of Catalytic Functions. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY, 1987, ISBN 0-87969-054-2, xix + 955 pp., US $150.00.Journal of Electroanalytical Chemistry, 276
K. Lugenbeel, A. Peier, N. Carson, A. Chudley, D. Nelson (1995)
Intragenic loss of function mutations demonstrate the primary role of FMR1 in fragile X syndromeNature Genetics, 10
R. Fridell, R. Benson, J. Hua, H. Bogerd, Bryan Cullen (1996)
A nuclear role for the Fragile X mental retardation protein.The EMBO Journal, 15
C. Ashley, J. Sutcliffe, Catherine Kunst, Harold Leiner, E. Eichler, D. Nelson, S. Warren (1993)
Human and murine FMR-1: alternative splicing and translational initiation downstream of the CGG–repeatNature Genetics, 4
Veronica Hinton, Veronica Hinton, W. Brown, K. Wisniewski, R. Rudelli (1991)
Analysis of neocortex in three males with the fragile X syndrome.American journal of medical genetics, 41 3
Yue Feng, C. Gutekunst, D. Eberhart, Hong Yi, S. Warren, S. Hersch (1997)
Fragile X Mental Retardation Protein: Nucleocytoplasmic Shuttling and Association with Somatodendritic RibosomesThe Journal of Neuroscience, 17
Yan Zhang, James O'Connor, M. Siomi, S. Srinivasan, A. Dutra, R. Nussbaum, G. Dreyfuss (1995)
The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2.The EMBO Journal, 14
F. Nielsen, L. Østergaard, Jacob Nielsen, J. Christiansen (1995)
Growth-dependent translation of IGF-II mRNA by a rapamycin-sensitive pathwayNature, 377
(1997)
were performed at room temperature with the primary antibody titers
C. Burd, G. Dreyfuss (1994)
Conserved structures and diversity of functions of RNA-binding proteins.Science, 265 5172
R. Nelson, T. Ziegelhoffer, C. Nicolet, M. Werner-Washburne, E. Craig (1992)
The translation machinery and 70 kd heat shock protein cooperate in protein synthesisCell, 71
M. Mahone, E. Saffman, P. Lasko (1995)
Localized Bicaudal‐C RNA encodes a protein containing a KH domain, the RNA binding motif of FMR1The EMBO Journal, 16
A. Verkerk, M. Pieretti, J. Sutcliffe, Ying-Hui Fu, D. Kuhl, A. Pizzuti, O. Reiner, S. Richards, Maureen Victoria, Fuping Zhang, Bert Eussen, G. Ommen, L. Blonden, G. Riggins, J. Chastain, Catherine Kunst, H. Galjaard, C. Caskey, D. Nelson, B. Oostra, S. Warren (1991)
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeCell, 65
Jones (1995)
Mutations in gld-1, a female germ cell-specific tumor suppresser gene in Caenorhabditis elegans, affect a conserved domain also found in Src-associated protein Sam68EMBO J, 9
F. Corbin, M. Bouillon, A. Fortin, Stanislas Morin, François Rousseau, É. Khandjian (1997)
The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes.Human molecular genetics, 6 9
Ying-Hui Fu, D. Kuhl, A. Pizzuti, M. Pieretti, J. Sutcliffe, S. Richards, Annemieke Verkert, J. Holden, R. Fenwick, S. Warren, B. Oostra, D. Nelson, C. Caskey (1991)
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 67
I. Oberle, François Rousseau, D. Heitz, C. Kretz, D. Devys, A. Hanauer, J. Boué, M. Bertheas, J. Mandel (1991)
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndromeScience, 252
(1995)
Two new cases of FMR1 deletions Urlaub associated with mental impairment
C. Gravholt, U. Friedrich (1995)
Quantitative comparison of FMR1 gene expression in normal and premutation alleles.American Journal of Medical Genetics, 56
Allan Jones, T. Schedl (1995)
Mutations in gld-1, a female germ cell-specific tumor suppressor gene in Caenorhabditis elegans, affect a conserved domain also found in Src-associated protein Sam68.Genes & development, 9 12
K. Boulle, A. Verkerk, E. Reyniers, L. Vits, J. Hendrickx, B. Roy, Feikje Bos, E. Graaff, B. Oostra, P. Willems (1993)
A point mutation in the FMR-1 gene associated with fragile X mental retardationNature Genetics, 3
É. Khandjian, F. Corbin, S. Woerly, F. Rousseau (1996)
The fragile X mental retardation protein is associated with ribosomesNature Genetics, 12
Molecular basis of fragile Xunderlined position , which results in the I 304 N mutation . The mis - syndrome
T. Comery, J. Harris, P. Willems, B. Oostra, S. Irwin, I. Weiler, W. Greenough (1997)
Abnormal dendritic spines in fragile X knockout mice: maturation and pruning deficits.Proceedings of the National Academy of Sciences of the United States of America, 94 10
(1995)
lymphoblastoids, respectively, in a total volume
A. Sittler, D. Devys, C. Weber, J. Mandel (1996)
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms.Human molecular genetics, 5 1
(1996)
pFLAG-Mc2.17 into the EcoRI–SnaBI sites
(1995)
amino acids 2 and 3 to form pFLAG-Mc2.17 (Brown et
(1993)
FXR2 monoclonal antibody
J. Sutcliffe, D. Nelson, Fuping Zhang, M. Pieretti, C. Caskey, D. Saxe, S. Warren (1992)
DNA methylation represses FMR-1 transcription in fragile X syndrome.Human molecular genetics, 1 6
The protein product of the fragile X gene, FMR1, has characteristics of an RNA binding protein
F. Herrera, L. Triana, I. Bosch (1988)
Importance of polysomal mRNA-associated polypeptides for protein synthesis initiation in yeast.European journal of biochemistry, 175 1
J. Scott, S. Wenger, M. Steele, A. Chakravarti (1995)
Down syndrome consequent to a cryptic maternal 12p;21q chromosome translocation.American journal of medical genetics, 56 1
G. Musco, G. Stier, C. Joseph, M. Morelli, M. Nilges, T. Gibson, A. Pastore (1996)
Three-Dimensional Structure and Stability of the KH Domain: Molecular Insights into the Fragile X SyndromeCell, 85
M. Siomi, H. Siomi, W. Sauer, S. Srinivasan, R. Nussbaum, G. Dreyfuss (1995)
FXR1, an autosomal homolog of the fragile X mental retardation gene.The EMBO Journal, 14
J. Hensold, Diane Barth-Baus, C. Stratton (1996)
Inducers of Erythroleukemic Differentiation Cause Messenger RNAs That Lack Poly(A)-binding Protein to Accumulate in Translationally Inactive, Salt-labile 80 S Ribosomal Complexes*The Journal of Biological Chemistry, 271
M. Siomi, Yan Zhang, H. Siomi, G. Dreyfuss (1996)
Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among themMolecular and Cellular Biology, 16
Molecular Cell – Unpaywall
Published: Dec 1, 1997
Access the full text.
Sign up today, get DeepDyve free for 14 days.