GeneRIFs

Entrez Gene GeneRIFs are recent publications from the PubMed® catalog that contain relevant information about FMR1.

• Adinolfi S, Ramos A, Martin SR, Dal Piaz F, Pucci P, Bardoni B, Mandel JL, Pastore A. The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding. Biochemistry. 2003 Sep 9;42(35):10437-44. PubMed citation
• Allen EG, Sullivan AK, Marcus M, Small C, Dominguez C, Epstein MP, Charen K, He W, Taylor KC, Sherman SL. Examination of reproductive aging milestones among women who carry the FMR1 premutation. Hum Reprod. 2007 Aug;22(8):2142-52. Epub 2007 Jun 22. PubMed citation
• Allen EG, Sullivan AK, Marcus M, Small C, Dominguez C, Epstein MP, Charen K, He W, Taylor KC, Sherman SL. Examination of reproductive aging milestones among women who carry the FMR1 premutation. Hum Reprod. 2007 Aug;22(8):2142-52. Epub 2007 Jun 22. PubMed citation
• Bagni C, Greenough WT. From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome. Nat Rev Neurosci. 2005 May;6(5):376-87. Review. PubMed citation
• Bailey DB Jr, Raspa M, Olmsted M, Holiday DB. Co-occurring conditions associated with FMR1 gene variations: findings from a national parent survey. Am J Med Genet A. 2008 Aug 15;146A(16):2060-9. PubMed citation
• Bardoni B, Castets M, Huot ME, Schenck A, Adinolfi S, Corbin F, Pastore A, Khandjian EW, Mandel JL. 82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization. Hum Mol Genet. 2003 Jul 15;12(14):1689-98. PubMed citation
• Bardoni B, Castets M, Huot ME, Schenck A, Adinolfi S, Corbin F, Pastore A, Khandjian EW, Mandel JL. 82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization. Hum Mol Genet. 2003 Jul 15;12(14):1689-98. PubMed citation
• Bardoni B, Castets M, Huot ME, Schenck A, Adinolfi S, Corbin F, Pastore A, Khandjian EW, Mandel JL. 82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization. Hum Mol Genet. 2003 Jul 15;12(14):1689-98. PubMed citation
• Bardoni B, Castets M, Huot ME, Schenck A, Adinolfi S, Corbin F, Pastore A, Khandjian EW, Mandel JL. 82-FIP, a novel FMRP (fragile X mental retardation protein) interacting protein, shows a cell cycle-dependent intracellular localization. Hum Mol Genet. 2003 Jul 15;12(14):1689-98. PubMed citation
• Bardoni B, Schenck A, Mandel JL. A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein. Hum Mol Genet. 1999 Dec;8(13):2557-66. PubMed citation
• Barros-Núñez P, Rosales-Reynoso MA, Sandoval L, Romero-Espinoza P, Troyo-Sanromán R, Ibarra B. Genetic variation of the FMR1 gene among four Mexican populations: Mestizo, Huichol, Purepecha, and Tarahumara. Am J Hum Biol. 2008 May-Jun;20(3):259-63. PubMed citation
• Bhattacharyya A, McMillan E, Wallace K, Tubon TC Jr, Capowski EE, Svendsen CN. Normal Neurogenesis but Abnormal Gene Expression in Human Fragile X Cortical Progenitor Cells. Stem Cells Dev. 2008 Feb;17(1):107-17. PubMed citation
• Bodega B, Bione S, Dalprà L, Toniolo D, Ornaghi F, Vegetti W, Ginelli E, Marozzi A. Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation. Hum Reprod. 2006 Apr;21(4):952-7. Epub 2005 Dec 16. PubMed citation
• Bretherick KL, Fluker MR, Robinson WP. FMR1 repeat sizes in the gray zone and high end of the normal range are associated with premature ovarian failure. Hum Genet. 2005 Aug;117(4):376-82. Epub 2005 Jun 2. PubMed citation
• Brylawski BP, Chastain PD 2nd, Cohen SM, Cordeiro-Stone M, Kaufman DG. Mapping of an origin of DNA replication in the promoter of fragile X gene FMR1. Exp Mol Pathol. 2007 Apr;82(2):190-6. Epub 2006 Dec 28. PubMed citation
• Bussani C, Papi L, Sestini R, Baldinotti F, Bucciantini S, Bruni V, Scarselli G. Premature ovarian failure and fragile X premutation: a study on 45 women. Eur J Obstet Gynecol Reprod Biol. 2004 Feb 10;112(2):189-91. PubMed citation
• Capelli LP, Gonçalves MR, Kok F, Leite CC, Nitrini R, Barbosa ER, Vianna-Morgante AM. Fragile X-associated tremor/ataxia syndrome: intrafamilial variability and the size of the FMR1 premutation CGG repeat. Mov Disord. 2007 Apr 30;22(6):866-70. PubMed citation
• Cecconi M, Forzano F, Rinaldi R, Cappellacci S, Grammatico P, Faravelli F, Dagna Bricarelli F, Di Maria E, Grasso M. A single nucleotide variant in the FMR1 CGG repeat results in a "Pseudodeletion" and is not associated with the fragile X syndrome phenotype. J Mol Diagn. 2008 May;10(3):272-5. Epub 2008 Apr 10. PubMed citation
• Ceman S, Brown V, Warren ST. Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex. Mol Cell Biol. 1999 Dec;19(12):7925-32. PubMed citation
• Ceman S, Brown V, Warren ST. Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex. Mol Cell Biol. 1999 Dec;19(12):7925-32. PubMed citation
• Ceman S, Brown V, Warren ST. Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex. Mol Cell Biol. 1999 Dec;19(12):7925-32. PubMed citation
• Ceman S, Brown V, Warren ST. Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex. Mol Cell Biol. 1999 Dec;19(12):7925-32. PubMed citation
• Ceman S, O'Donnell WT, Reed M, Patton S, Pohl J, Warren ST. Phosphorylation influences the translation state of FMRP-associated polyribosomes. Hum Mol Genet. 2003 Dec 15;12(24):3295-305. Epub 2003 Oct 21. PubMed citation
• Chen L, Yun SW, Seto J, Liu W, Toth M. The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences. Neuroscience. 2003;120(4):1005-17. PubMed citation
• Chen Y, Sittler A, Yu M, Bardoni B, Wu G. [Screening of proteins interact with FMR1 by yeast two-hybrid system] Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1998 Jun;20(3):173-8. Chinese. PubMed citation
• Chen Y, Sittler A, Yu M, Bardoni B, Wu G. [Screening of proteins interact with FMR1 by yeast two-hybrid system] Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 1998 Jun;20(3):173-8. Chinese. PubMed citation
• Coffee B, Ikeda M, Budimirovic DB, Hjelm LN, Kaufmann WE, Warren ST. Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literature. Am J Med Genet A. 2008 May 15;146A(10):1358-67. Review. PubMed citation
• Coffee B, Zhang F, Ceman S, Warren ST, Reines D. Histone modifications depict an aberrantly heterochromatinized FMR1 gene in fragile x syndrome. Am J Hum Genet. 2002 Oct;71(4):923-32. Epub 2002 Sep 13. PubMed citation
• Cornish K, Kogan C, Turk J, Manly T, James N, Mills A, Dalton A. The emerging fragile X premutation phenotype: evidence from the domain of social cognition. Brain Cogn. 2005 Feb;57(1):53-60. PubMed citation
• Cornish KM, Li L, Kogan CS, Jacquemont S, Turk J, Dalton A, Hagerman RJ, Hagerman PJ. Age-dependent cognitive changes in carriers of the fragile X syndrome. Cortex. 2008 Jun;44(6):628-36. Epub 2007 Dec 23. PubMed citation
• Crawford DC, Acuña JM, Sherman SL. FMR1 and the fragile X syndrome: human genome epidemiology review. Genet Med. 2001 Sep-Oct;3(5):359-71. Review. PubMed citation
• Cronister A, Teicher J, Rohlfs EM, Donnenfeld A, Hallam S. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis. Obstet Gynecol. 2008 Mar;111(3):596-601. PubMed citation
• Darnell JC, Fraser CE, Mostovetsky O, Stefani G, Jones TA, Eddy SR, Darnell RB. Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes. Genes Dev. 2005 Apr 15;19(8):903-18. Epub 2005 Apr 1. PubMed citation
• Davidovic L, Jaglin XH, Lepagnol-Bestel AM, Tremblay S, Simonneau M, Bardoni B, Khandjian EW. The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules. Hum Mol Genet. 2007 Dec 15;16(24):3047-58. Epub 2007 Sep 19. PubMed citation
• De Diego Otero Y, Severijnen LA, van Cappellen G, Schrier M, Oostra B, Willemsen R. Transport of fragile X mental retardation protein via granules in neurites of PC12 cells. Mol Cell Biol. 2002 Dec;22(23):8332-41. PubMed citation
• Denman RB. Methylation of the arginine-glycine-rich region in the fragile X mental retardation protein FMRP differentially affects RNA binding. Cell Mol Biol Lett. 2002;7(3):877-83. PubMed citation
• Dobson T, Kube E, Timmerman S, Krushel LA. Identifying intrinsic and extrinsic determinants that regulate internal initiation of translation mediated by the FMR1 5' leader. BMC Mol Biol. 2008 Oct 15;9:89. PubMed citation
• Dolzhanskaya N, Bolton DC, Denman RB. Chemical and structural probing of the N-terminal residues encoded by FMR1 exon 15 and their effect on downstream arginine methylation. Biochemistry. 2008 Aug 19;47(33):8491-503. Epub 2008 Jul 26. PubMed citation
• Dolzhanskaya N, Merz G, Aletta JM, Denman RB. Methylation regulates the intracellular protein-protein and protein-RNA interactions of FMRP. J Cell Sci. 2006 May 1;119(Pt 9):1933-46. PubMed citation
• Dolzhanskaya N, Sung YJ, Conti J, Currie JR, Denman RB. The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system. Biochem Biophys Res Commun. 2003 May 30;305(2):434-41. PubMed citation
• Dombrowski C, Lévesque S, Morel ML, Rouillard P, Morgan K, Rousseau F. Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles. Hum Mol Genet. 2002 Feb 15;11(4):371-8. PubMed citation
• Ennis S, Murray A, Brightwell G, Morton NE, Jacobs PA. Closely linked cis-acting modifier of expansion of the CGG repeat in high risk FMR1 haplotypes. Hum Mutat. 2007 Dec;28(12):1216-24. PubMed citation
• Felix-López XA, Argüello-García R, Cerda-Flores RM, Peñaloza-Espinoza RI, Buentello-Malo L, Estrada-Mena FJ, Ramos-Kuri M, Gómez FS, Arenas-Aranda DJ. FMR1 CGG repeat distribution and linked microsatellite-SNP haplotypes in normal Mexican Mestizo and indigenous populations. Hum Biol. 2006 Oct;78(5):579-98. PubMed citation
• Gabus C, Mazroui R, Tremblay S, Khandjian EW, Darlix JL. The fragile X mental retardation protein has nucleic acid chaperone properties. Nucleic Acids Res. 2004 Apr 19;32(7):2129-37. Print 2004. PubMed citation
• Gagné JP, Bonicalzi ME, Gagné P, Ouellet ME, Hendzel MJ, Poirier GG. Poly(ADP-ribose) glycohydrolase is a component of the FMRP-associated messenger ribonucleoparticles. Biochem J. 2005 Dec 15;392(Pt 3):499-509. PubMed citation
• Gheldof N, Tabuchi TM, Dekker J. The active FMR1 promoter is associated with a large domain of altered chromatin conformation with embedded local histone modifications. Proc Natl Acad Sci U S A. 2006 Aug 15;103(33):12463-8. Epub 2006 Aug 4. PubMed citation
• Gothelf D, Furfaro JA, Hoeft F, Eckert MA, Hall SS, O'Hara R, Erba HW, Ringel J, Hayashi KM, Patnaik S, Golianu B, Kraemer HC, Thompson PM, Piven J, Reiss AL. Neuroanatomy of fragile X syndrome is associated with aberrant behavior and the fragile X mental retardation protein (FMRP). Ann Neurol. 2008 Jan;63(1):40-51. PubMed citation
• Gray SJ, Gerhardt J, Doerfler W, Small LE, Fanning E. An origin of DNA replication in the promoter region of the human fragile X mental retardation (FMR1) gene. Mol Cell Biol. 2007 Jan;27(2):426-37. Epub 2006 Nov 13. PubMed citation
• Grigsby J, Brega AG, Engle K, Leehey MA, Hagerman RJ, Tassone F, Hessl D, Hagerman PJ, Cogswell JB, Bennett RE, Cook K, Hall DA, Bounds LS, Paulich MJ, Reynolds A. Cognitive profile of fragile X premutation carriers with and without fragile X-associated tremor/ataxia syndrome. Neuropsychology. 2008 Jan;22(1):48-60. PubMed citation
• Hagerman RJ, Leavitt BR, Farzin F, Jacquemont S, Greco CM, Brunberg JA, Tassone F, Hessl D, Harris SW, Zhang L, Jardini T, Gane LW, Ferranti J, Ruiz L, Leehey MA, Grigsby J, Hagerman PJ. Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. Am J Hum Genet. 2004 May;74(5):1051-6. Epub 2004 Apr 2. PubMed citation
• Han JY, Shin JH, Han MS, Je GH, Shaffer LG. Microarray detection of a de novo der(X)t(X;11)(q28;p13) in a girl with premature ovarian failure and features of Beckwith-Wiedemann syndrome. J Hum Genet. 2006;51(7):641-3. Epub 2006 May 18. PubMed citation
• Harikrishnan KN, Chow MZ, Baker EK, Pal S, Bassal S, Brasacchio D, Wang L, Craig JM, Jones PL, Sif S, El-Osta A. Brahma links the SWI/SNF chromatin-remodeling complex with MeCP2-dependent transcriptional silencing. Nat Genet. 2005 Mar;37(3):254-64. Epub 2005 Feb 6. PubMed citation
• Hessl D, Tassone F, Loesch DZ, Berry-Kravis E, Leehey MA, Gane LW, Barbato I, Rice C, Gould E, Hall DA, Grigsby J, Wegelin JA, Harris S, Lewin F, Weinberg D, Hagerman PJ, Hagerman RJ. Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):115-21. PubMed citation
• Holoch K, Stein Q, Flanagan J, Hansen K. Premature ovarian failure: a phenotypic expression of fragile X premutation. S D Med. 2008 Jan;61(1):13, 15. PubMed citation
• Huber KM. The fragile X-cerebellum connection. Trends Neurosci. 2006 Apr;29(4):183-5. Epub 2006 Feb 28. Review. PubMed citation
• Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SL. Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers. Behav Genet. 2008 Sep;38(5):493-502. Epub 2008 Jun 6. PubMed citation
• Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SL. No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50. Am J Hum Genet. 2008 Dec;83(6):692-702. Epub 2008 Nov 20. PubMed citation
• Hunter JE, Allen EG, Abramowitz A, Rusin M, Leslie M, Novak G, Hamilton D, Shubeck L, Charen K, Sherman SL. No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50. Am J Hum Genet. 2008 Dec;83(6):692-702. Epub 2008 Nov 20. PubMed citation
• Hunter JE, Epstein MP, Tinker SW, Charen KH, Sherman SL. Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity. Genet Epidemiol. 2008 Sep;32(6):553-9. PubMed citation
• Jacquemont S, Hagerman RJ, Leehey MA, Hall DA, Levine RA, Brunberg JA, Zhang L, Jardini T, Gane LW, Harris SW, Herman K, Grigsby J, Greco CM, Berry-Kravis E, Tassone F, Hagerman PJ. Penetrance of the fragile X-associated tremor/ataxia syndrome in a premutation carrier population. JAMA. 2004 Jan 28;291(4):460-9. PubMed citation
• Karmon Y, Gadoth N. Fragile X associated tremor/ataxia syndrome (FXTAS) with dementia in a female harbouring FMR1 premutation. J Neurol Neurosurg Psychiatry. 2008 Jun;79(6):738-9. No abstract available. PubMed citation
• Khaniani MS, Kalitsis P, Burgess T, Slater HR. An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1). Mol Cytogenet. 2008 Apr 8;1(1):5. PubMed citation
• Koekkoek SK, Yamaguchi K, Milojkovic BA, Dortland BR, Ruigrok TJ, Maex R, De Graaf W, Smit AE, VanderWerf F, Bakker CE, Willemsen R, Ikeda T, Kakizawa S, Onodera K, Nelson DL, Mientjes E, Joosten M, De Schutter E, Oostra BA, Ito M, De Zeeuw CI. Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome. Neuron. 2005 Aug 4;47(3):339-52. PubMed citation
• Kogan CS, Turk J, Hagerman RJ, Cornish KM. Impact of the Fragile X mental retardation 1 (FMR1) gene premutation on neuropsychiatric functioning in adult males without fragile X-associated Tremor/Ataxia syndrome: a controlled study. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):859-72. PubMed citation
• Kraff J, Tang HT, Cilia R, Canesi M, Pezzoli G, Goldwurm S, Hagerman PJ, Tassone F. Screen for excess FMR1 premutation alleles among males with parkinsonism. Arch Neurol. 2007 Jul;64(7):1002-6. PubMed citation
• Lachiewicz AM, Dawson DV, Spiridigliozzi GA, McConkie-Rosell A. Arithmetic difficulties in females with the fragile X premutation. Am J Med Genet A. 2006 Apr 1;140(7):665-72. PubMed citation
• Leehey MA, Berry-Kravis E, Goetz CG, Zhang L, Hall DA, Li L, Rice CD, Lara R, Cogswell J, Reynolds A, Gane L, Jacquemont S, Tassone F, Grigsby J, Hagerman RJ, Hagerman PJ. FMR1 CGG repeat length predicts motor dysfunction in premutation carriers. Neurology. 2008 Apr 15;70(16 Pt 2):1397-402. Epub 2007 Dec 5. PubMed citation
• Liang S, Bass HN, Gao H, Astbury C, Jamehdor MR, Qu Y. A pseudo-full mutation identified in fragile X assay reveals a novel base change abolishing an EcoRI restriction site. J Mol Diagn. 2008 Sep;10(5):469-74. Epub 2008 Aug 7. PubMed citation
• Lim JH, Booker AB, Luo T, Williams T, Furuta Y, Lagutin O, Oliver G, Sargent TD, Fallon JR. AP-2alpha selectively regulates fragile X mental retardation-1 gene transcription during embryonic development. Hum Mol Genet. 2005 Jul 15;14(14):2027-34. Epub 2005 Jun 1. PubMed citation
• Linder B, Plöttner O, Kroiss M, Hartmann E, Laggerbauer B, Meister G, Keidel E, Fischer U. Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP. Hum Mol Genet. 2008 Oct 15;17(20):3236-46. Epub 2008 Jul 28. PubMed citation
• Lisik MZ. [Abnormal function of ovaries in women carriers of premutation in the FMR1 gene] Wiad Lek. 2007;60(5-6):265-9. Review. Polish. PubMed citation
• Livshyts' HB, Kravchenko SA, Tatars'kyĭ PF, Sudoma IA, Livshyts' LA. [Molecular-genetic analysis of natural and stimulated ovulation impairment] Tsitol Genet. 2008 Mar-Apr;42(2):63-9. Ukrainian. PubMed citation
• Loat CS, Craig G, Plomin R, Craig IW. Investigating the relationship between FMR1 allele length and cognitive ability in children: a subtle effect of the normal allele range on the normal ability range? Ann Hum Genet. 2006 Sep;70(Pt 5):555-65. PubMed citation
• Loesch DZ, Bui QM, Dissanayake C, Clifford S, Gould E, Bulhak-Paterson D, Tassone F, Taylor AK, Hessl D, Hagerman R, Huggins RM. Molecular and cognitive predictors of the continuum of autistic behaviours in fragile X. Neurosci Biobehav Rev. 2007;31(3):315-26. Epub 2006 Nov 9. Review. PubMed citation
• Loesch DZ, Bui QM, Grigsby J, Butler E, Epstein J, Huggins RM, Taylor AK, Hagerman RJ. Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X. Neuropsychology. 2003 Oct;17(4):646-57. PubMed citation
• Loesch DZ, Bui QM, Huggins RM, Mitchell RJ, Hagerman RJ, Tassone F. Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats. J Med Genet. 2007 Mar;44(3):200-4. Epub 2006 Aug 11. PubMed citation
• Loesch DZ, Cook M, Litewka L, Gould E, Churchyard A, Tassone F, Slater HR, Storey E. A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes. J Med Genet. 2008 Mar;45(3):179-81. Epub 2007 Dec 5. PubMed citation
• Loesch DZ, Litewka L, Brotchie P, Huggins RM, Tassone F, Cook M. Magnetic resonance imaging study in older fragile X premutation male carriers. Ann Neurol. 2005 Aug;58(2):326-30. PubMed citation
• Martínez R, Bonilla-Henao V, Jiménez A, Lucas M, Vega C, Ramos I, Sobrino F, Pintado E. Skewed X inactivation of the normal allele in fully mutated female carriers determines the levels of FMRP in blood and the fragile X phenotype. Mol Diagn. 2005;9(3):157-62. PubMed citation
• Menon RP, Gibson TJ, Pastore A. The C terminus of fragile X mental retardation protein interacts with the multi-domain Ran-binding protein in the microtubule-organising centre. J Mol Biol. 2004 Oct 8;343(1):43-53. PubMed citation
• Menon RP, Gibson TJ, Pastore A. The C terminus of fragile X mental retardation protein interacts with the multi-domain Ran-binding protein in the microtubule-organising centre. J Mol Biol. 2004 Oct 8;343(1):43-53. PubMed citation
• Menon V, Leroux J, White CD, Reiss AL. Frontostriatal deficits in fragile X syndrome: relation to FMR1 gene expression. Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3615-20. Epub 2004 Mar 1. PubMed citation
• Mononen T, von Koskull H, Airaksinen RL, Juvonen V. A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat instability. Clin Genet. 2007 Dec;72(6):528-31. Epub 2007 Oct 7. PubMed citation
• Moore CJ, Daly EM, Schmitz N, Tassone F, Tysoe C, Hagerman RJ, Hagerman PJ, Morris RG, Murphy KC, Murphy DG. A neuropsychological investigation of male premutation carriers of fragile X syndrome. Neuropsychologia. 2004;42(14):1934-47. PubMed citation
• Napierala M, Michalowski D, de Mezer M, Krzyzosiak WJ. Facile FMR1 mRNA structure regulation by interruptions in CGG repeats. Nucleic Acids Res. 2005 Jan 19;33(2):451-63. Print 2005. PubMed citation
• Noguchi E, Yokouchi Y, Zhang J, Shibuya K, Shibuya A, Bannai M, Tokunaga K, Doi H, Tamari M, Shimizu M, Shirakawa T, Shibasaki M, Ichikawa K, Arinami T. Positional identification of an asthma susceptibility gene on human chromosome 5q33. Am J Respir Crit Care Med. 2005 Jul 15;172(2):183-8. Epub 2005 May 5. PubMed citation
• Nolin SL, Brown WT, Glicksman A, Houck GE Jr, Gargano AD, Sullivan A, Biancalana V, Bröndum-Nielsen K, Hjalgrim H, Holinski-Feder E, Kooy F, Longshore J, Macpherson J, Mandel JL, Matthijs G, Rousseau F, Steinbach P, Väisänen ML, von Koskull H, Sherman SL. Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles. Am J Hum Genet. 2003 Feb;72(2):454-64. Epub 2003 Jan 14. PubMed citation
• Nolin SL, Ding XH, Houck GE, Brown WT, Dobkin C. Fragile X full mutation alleles composed of few alleles: implications for CGG repeat expansion. Am J Med Genet A. 2008 Jan 1;146A(1):60-5. PubMed citation
• Orlov SV, Kuteykin-Teplyakov KB, Ignatovich IA, Dizhe EB, Mirgorodskaya OA, Grishin AV, Guzhova OB, Prokhortchouk EB, Guliy PV, Perevozchikov AP. Novel repressor of the human FMR1 gene - identification of p56 human (GCC)(n)-binding protein as a Krüppel-like transcription factor ZF5. FEBS J. 2007 Sep;274(18):4848-62. Epub 2007 Aug 21. PubMed citation
• Piazzon N, Rage F, Schlotter F, Moine H, Branlant C, Massenet S. In vitro and in cellulo evidences for association of the survival of motor neuron complex with the fragile X mental retardation protein. J Biol Chem. 2008 Feb 29;283(9):5598-610. Epub 2007 Dec 19. PubMed citation
• Pietrobono R, Tabolacci E, Zalfa F, Zito I, Terracciano A, Moscato U, Bagni C, Oostra B, Chiurazzi P, Neri G. Molecular dissection of the events leading to inactivation of the FMR1 gene. Hum Mol Genet. 2005 Jan 15;14(2):267-77. Epub 2004 Nov 24. PubMed citation
• Poon PM, Chen QL, Zhong N, Lam ST, Lai KY, Wong CK, Pang CP. AGG interspersion analysis of the FMR1 CGG repeats in mental retardation of unspecific cause. Clin Biochem. 2006 Mar;39(3):244-8. Epub 2005 Dec 7. PubMed citation
• Primerano B, Tassone F, Hagerman RJ, Hagerman P, Amaldi F, Bagni C. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations. RNA. 2002 Dec;8(12):1482-8. PubMed citation
• Ramos A, Hollingworth D, Adinolfi S, Castets M, Kelly G, Frenkiel TA, Bardoni B, Pastore A. The structure of the N-terminal domain of the fragile X mental retardation protein: a platform for protein-protein interaction. Structure. 2006 Jan;14(1):21-31. PubMed citation
• Reis AH, Ferreira AC, Gomes KB, Aguiar MJ, Fonseca CG, Cardoso FE, Pardini VC, Carvalho MR. Frequency of FMR1 premutation in individuals with ataxia and/or tremor and/or parkinsonism. Genet Mol Res. 2008 Jan 29;7(1):74-84. PubMed citation
• Rivera SM, Menon V, White CD, Glaser B, Reiss AL. Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMR1 protein expression. Hum Brain Mapp. 2002 Aug;16(4):206-18. PubMed citation
• Rodriguez-Revenga L, Gómez-Anson B, Muñoz E, Jiménez D, Santos M, Tintoré M, Martín G, Brieva L, Milà M. FXTAS in spanish patients with ataxia: support for female FMR1 premutation screening. Mol Neurobiol. 2007 Jun;35(3):324-8. PubMed citation
• Rosales-Reynoso MA, Mendoza-Carrera F, Troyo-Sanromán R, Medina C, Barros-Núñez P. Genetic diversity at the FMR1 locus in Mexican population. Arch Med Res. 2005 Jul-Aug;36(4):412-7. PubMed citation
• Schenck A, Bardoni B, Moro A, Bagni C, Mandel JL. A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P. Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8844-9. Epub 2001 Jul 3. PubMed citation
• Schenck A, Bardoni B, Moro A, Bagni C, Mandel JL. A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P. Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8844-9. Epub 2001 Jul 3. PubMed citation
• Schenck A, Bardoni B, Moro A, Bagni C, Mandel JL. A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P. Proc Natl Acad Sci U S A. 2001 Jul 17;98(15):8844-9. Epub 2001 Jul 3. PubMed citation
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