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Nodes: 1364,
Authors: 3358,
Journals: 307,
Outer References: 11901,
Words: 2507
Collection span: 1995 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1201 | 1 | 5 | 1201 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(4):731-732 Salomons GS; Ropers HH Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation - Reply | 0 | 0 |
| 1202 | 8 | 29 | 1202 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):129-132 Rife M; Nadal A; Mila M; Willemsen R Immunohistochemical FMRP studies in a full mutated female fetus | 0 | 0 |
| 1203 | 3 | 16 | 1203 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 124A(2):213-215 Marshall I; Betensky BP; Goseco A; Vogiatzi MV; Flieder D Fragile x and mosaic 45,X/46,XY mixed gonadal dysgenesis in a girl with ambiguous genitalia | 0 | 0 |
| 1204 | 3 | 5 | 1204 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 125A(3):320-320 Milunsky JM; Maher TA Fragile X carrier screening and spinocerebellar ataxia in older males | 0 | 3 |
| 1205 | 14 | 48 | 1205 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 126A(1):9-17 Kau ASM; Tierney E; Bukelis I; Stump MH; Kates WR; et al. Social behavior profile in young males with fragile X syndrome: Characteristics and specificity | 0 | 2 |
| 1206 | 18 | 38 | 1206 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 128A(3):250-255 Penagarikano O; Gil A; Telez M; Ortega B; Flores P; et al. A new insight into fragile X syndrome among Basque population | 0 | 0 |
| 1207 | 16 | 40 | 1207 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(2):184-189 Zeesman S; Zwaigenbaum L; Whelan DT; Hagerman RJ; Tassone F; et al. Paternal transmission of fragile X syndrome | 0 | 0 |
| 1208 | 17 | 26 | 1208 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):218-224 Biancalana V; Beldjord C; Taillandier A; Szpiro-Tapia S; Cusin V; et al. Five years of molecular diagnosis of Fragile X syndrome(1997-2001): A collaborative study reporting 95% of the activity in France | 0 | 1 |
| 1209 | 15 | 59 | 1209 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):225-234 Kaufmann WE; Cortell R; Kau CSM; Bukelis I; Tierney E; et al. Autism spectrum disorder in fragile X syndrome: Communication, social interaction, and specific behaviors | 0 | 0 |
| 1210 | 7 | 16 | 1210 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):326-328 Clarke NF; Mowat D; Kooy RF; Reyniers E; Willemsen R Fragile X syndrome phenotype with normal FMR1 gene studies | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1211 | 0 | 42 | 1211 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 126B(1):46-50 Devlin B; Bennett P; Dawson G; Figlewicz DA; Grigorenko EL; et al. Alleles of a Reelin CGG repeat do not convey liability to autism in a sample from the CPEA network | 0 | 3 |
| 1212 | 11 | 51 | 1212 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):208-218 Philofsky A; Hepburn SL; Hayes A; Hagerman R; Rogers SJ Linguistic and cognitive functioning and autism symptoms in young children with fragile X syndrome | 0 | 1 |
| 1213 | 13 | 79 | 1213 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):237-254 Abbeduto L; Seltzer MM; Shattuck P; Krauss MW; Orsmond G; et al. Psychological well-being and coping in mothers of youths with autism, Down syndrome, or fragile X syndrome | 0 | 1 |
| 1214 | 0 | 0 | 1214 2004 ANNALS OF NEUROLOGY 56:S104-S104 Cortell R; Bukelis I; Gray RM; Cox C; Tierney E; et al. Autism spectrum disorder in boys with Fragile X: Serial evaluation | 0 | 0 |
| 1215 | 6 | 50 | 1215 2004 ARCHIVES OF GENERAL PSYCHIATRY 61(3):281-288 Garrett AS; Menon V; MacKenzie K; Reiss AL Here's looking at you, kid - Neural systems underlying face and gaze processing in fragile X syndrome | 0 | 1 |
| 1216 | 0 | 0 | 1216 2004 BEHAVIOR GENETICS 34(6):638-638 Fisch GS; Simensen RJ; Schroer RJ Longitudinal assessment of cognitive-behavioral features of children and adolescents with either autism or the fragile X mutation | 0 | 0 |
| 1217 | 0 | 0 | 1217 2004 BIOLOGICAL PSYCHIATRY 55:159S-159S Daly EM; Moore CJ; Simmons A; Tassone F; Tysoe C; et al. A H-1 magnetic resonance spectroscopy study of males with premutation expansion of CGG trinucleoticle repeats | 0 | 0 |
| 1218 | 21 | 62 | 1218 2004 BRAIN 127:591-601 Kogan CS; Boutet I; Cornish K; Zangenehpour S; Mullen KT; et al. Differential impact of the FMR1 gene on visual processing in fragile X syndrome | 2 | 2 |
| 1219 | 16 | 40 | 1219 2004 BRAIN 127:2672-2681 Moore CJ; Daly EM; Tassone F; Tysoe C; Schmitz N; et al. The effect of pre-mutation of X chromosome CGG trinucleotide repeats on brain anatomy | 0 | 0 |
| 1220 | 3 | 21 | 1220 2004 BRAIN & DEVELOPMENT 26(6):380-383 Suwa K; Momoi MY Non-invasive screening of fragile X syndrome A using urine and hair roots | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1221 | 3 | 6 | 1221 2004 BRAIN AND COGNITION 54(3):235-239 Cornish K; Swainson R; Cunnington R; Wilding J; Morris P; et al. Do women with fragile X syndrome have problems in switching attention: Preliminary findings from ERP and fMRI | 0 | 0 |
| 1222 | 0 | 0 | 1222 2004 BRAIN AND COGNITION 56(1):121-121 Kogan C; Boutet I; Cornish K; Andermann E; DerKaloustian V; et al. Evidence for a transient channel visual deficit in Fragile X Syndrome | 0 | 0 |
| 1223 | 51 | 135 | 1223 2004 CELLULAR AND MOLECULAR LIFE SCIENCES 61(14):1714-1728 Denman RB; Dolzhanskaya N; Sung YJ Regulating a translational regulator: mechanisms cells use to control the activity of the fragile X mental retardation protein | 1 | 2 |
| 1224 | 25 | 120 | 1224 2004 CNS DRUGS 18(11):687-703 Tsiouris JA; Brown WT Neuropsychiatric symptoms of fragile X syndrome - Pathophysiology and pharmacotherapy | 0 | 0 |
| 1225 | 5 | 47 | 1225 2004 COGNITIVE NEUROPSYCHOLOGY 21(6):579-596 Keenan JM; Simon JA Inference deficits in women with Fragile X Syndrome: A problem in working memory | 0 | 0 |
| 1226 | 14 | 47 | 1226 2004 CURRENT BIOLOGY 14(12):1025-1034 Xu KY; Bogert BA; Li WJ; Su K; Lee A; et al. The fragile X-related gene affects the crawling behavior of Drosophila larvae by regulating the mRNA level of the DEG/ENaC protein pickpocket1 | 2 | 3 |
| 1227 | 16 | 37 | 1227 2004 CURRENT BIOLOGY 14(20):1863-1870 Pan LY; Zhang YQ; Woodruff E; Broadie K The Drosophila fragile X gene negatively regulates neuronal elaboration and synaptic differentiation | 2 | 2 |
| 1228 | 13 | 38 | 1228 2004 CYTOGENETIC AND GENOME RESEARCH 105(2-4):448-454 Errijgers V; Kooy RF Genetic modifiers in mice: the example of the fragile X mouse model | 0 | 0 |
| 1229 | 12 | 58 | 1229 2004 DEVELOPMENTAL BIOLOGY 270(2):290-307 Zhang YQ; Matthies HJG; Mancuso J; Andrews HK; Woodruff E; et al. The Drosophila fragile X-related gene regulates axoneme differentiation during spermatogenesis | 3 | 3 |
| 1230 | 5 | 41 | 1230 2004 DEVELOPMENTAL SCIENCE 7(1):116-130 Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1231 | 15 | 55 | 1231 2004 EMBO JOURNAL 23(16):3346-3355 Rackham O; Brown CM Visualization of RNA-protein interactions in living cells: FMRP and IMP1 interact on mRNAs | 3 | 4 |
| 1232 | 4 | 19 | 1232 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; et al. Premature ovarian failure and fragile X premutation: a study on 45 women | 0 | 0 |
| 1233 | 27 | 49 | 1233 2004 EXPERIMENTAL NEUROLOGY 189(2):343-353 Schrier M; Severijnen LA; Reis S; Rife M; van't Padje S; et al. Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells | 0 | 0 |
| 1234 | 0 | 0 | 1234 2004 FERTILITY AND STERILITY 82:S246-S247 Malcov M; Carmon A; Mey-Raz N; Ben Yosef D; Lessing JB; et al. Preimplantation genetic diagnosis for fragile X syndrome in Israel | 0 | 0 |
| 1235 | 17 | 34 | 1235 2004 GENE 343(2):231-238 Guduric-Fuchs J; Mohrlen F; Frohme M; Frank U A fragile X mental retardation-like gene in a cnidarian | 0 | 0 |
| 1236 | 29 | 114 | 1236 2004 GENES BRAIN AND BEHAVIOR 3(6):337-359 Yan QJ; Asafo-Adjei PK; Arnold HM; Brown RE; Bauchwitz RP A phenotypic and molecular characterization of the fmr1-tm1Cgr Fragile X mouse | 1 | 1 |
| 1237 | 0 | 0 | 1237 2004 GENETIC COUNSELING 15(2):239-286 [Anon] Abstracts of the 11(th) International Workshop on Fragile X and X-Linked Mental Retardation - 27-30 August 2003, Pafos, Cyprus | 0 | 0 |
| 1238 | 12 | 42 | 1238 2004 GENETIC EPIDEMIOLOGY 26(4):294-304 Huggins RM; Loesch DZ; Qian GQ; Bui QM; Mitchell RJ; et al. Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X | 0 | 0 |
| 1239 | 0 | 0 | 1239 2004 GENETICS IN MEDICINE 6(4):300-300 MacKenzie JJ; Sumargo IV; Taylor SA A cryptic full mutation in a male with a classical fragile X phenotype. | 0 | 0 |
| 1240 | 0 | 0 | 1240 2004 GENETICS IN MEDICINE 6(4):352-352 Han X; Chehab F; Powell B; Phalin-Rague J A high mental functioning fragile X male with a de novo 103bp deletion including entire CGG repeat region in > 50% of his peripheral leukocytes. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1241 | 11 | 49 | 1241 2004 GENOMICS 83(1):106-118 Naumann F; Remus R; Schmitz B; Doerfler W Gene structure and expression of the 5 '-(CGG)(n)-3 '-binding protein (CGGBP1) | 0 | 1 |
| 1242 | 1 | 40 | 1242 2004 GENOMICS 84(1):69-81 Sarafidou T; Kahl C; Martinez-Garay I; Mangelsdorf M; Gesk S; et al. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein | 0 | 0 |
| 1243 | 31 | 55 | 1243 2004 GROWTH HORMONE & IGF RESEARCH 14:S158-S165 Mandel JL; Biancalana V Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues | 0 | 0 |
| 1244 | 0 | 9 | 1244 2004 HEMOGLOBIN 28(3):173-176 Regtuijt ME; Harteveld CL; Van Delft P; Akkermans N; Giordano PC Hb Suan-Dok [alpha 109(G16)Leu -> Arg; CTG--> CGG (alpha 2)] - Described in a patient of African ancestry | 0 | 0 |
| 1245 | 18 | 42 | 1245 2004 HUMAN MOLECULAR GENETICS 13(1):79-89 Wang HP; Ku L; Osterhout DJ; Li W; Ahmadian A; et al. Developmentally-programmed FMRP expression in oligodendrocytes: a potential role of FMRP in regulating translation in oligodendroglia progenitors | 1 | 3 |
| 1246 | 9 | 32 | 1246 2004 HUMAN MOLECULAR GENETICS 13(5):543-549 Beilina A; Tassone F; Schwartz PH; Sahota P; Hagerman PJ Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element | 4 | 6 |
| 1247 | 1 | 5 | 1247 2004 ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES 41(1):70-70 Kandil ST; Bilici M; Aksu HB; Celep F; Karaguzel A Early infantile autism and fragile X anomaly | 0 | 0 |
| 1248 | 15 | 55 | 1248 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(4):460-469 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al. Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population | 6 | 15 |
| 1249 | 1 | 1 | 1249 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2945 Barrett SK; Drazin T; Rosa D; Kupchik GS Genetic counseling for families of patients with fragile X syndrome | 0 | 0 |
| 1250 | 2 | 6 | 1250 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2946 Hagerman PJ; Hagerman RJ; Gane LW Genetic counseling for families of patients with fragile X syndrome - In reply | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1251 | 1 | 1 | 1251 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 292(17):2086-2086 Hagerman P Genetic counseling for families of patients with fragile X syndrome (vol 291, pg 2945, 2004) | 0 | 0 |
| 1252 | 5 | 50 | 1252 2004 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 34(1):41-48 Seltzer MM; Abbeduto L; Krauss MW; Greenberg J; Swe A Comparison groups in autism family research: Down syndrome, fragile X syndrome, and schizophrenia | 0 | 2 |
| 1253 | 40 | 103 | 1253 2004 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY 45(6):1042-1053 Cornish KM; Turk J; Wilding J; Sudhalter V; Munir F; et al. Annotation: Deconstructing the attention deficit in fragile X syndrome: a developmental neuropsychological approach | 0 | 0 |
| 1254 | 13 | 57 | 1254 2004 JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM 89(9):4569-4574 Welt CK; Smith PC; Taylor AE Evidence of early ovarian aging in fragile X premutation carriers | 0 | 0 |
| 1255 | 0 | 30 | 1255 2004 JOURNAL OF CLINICAL MICROBIOLOGY 42(8):3538-3548 Otsuka Y; Parniewski P; Zwolska Z; Kai M; Fujino T; et al. Characterization of a trinucleotide repeat sequence (CGG)(5) and potential use in restriction fragment length polymorphism typing of Mycobacterium tuberculosis | 0 | 1 |
| 1256 | 6 | 36 | 1256 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(1):21-27 Mirrett PL; Bailey DB; Roberts JE; Hatton DD Developmental screening and detection of developmental delays in infants and toddlers with fragile X syndrome | 0 | 0 |
| 1257 | 20 | 54 | 1257 2004 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 25(6):392-398 Goodlin-Jones BL; Tassone F; Gane LW Autistic spectrum disorder and the fragile X premutation | 0 | 0 |
| 1258 | 0 | 1 | 1258 2004 JOURNAL OF FORENSIC SCIENCES 49(1):192-193 Brenner CH; Inman K Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. | 0 | 0 |
| 1259 | 0 | 3 | 1259 2004 JOURNAL OF FORENSIC SCIENCES 49(1):194-195 Thompson WC; Taroni PF; Aitken CGG 'Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. - Response | 0 | 0 |
| 1260 | 1 | 13 | 1260 2004 JOURNAL OF HUMAN GENETICS 49(2):97-101 Nagao K; Fujii K; Yamada M; Miyashita T Identification of a novel polymorphism involving a CGG repeat in the PTCH gene and a genome-wide screening of CGG-containing genes | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1261 | 0 | 0 | 1261 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:287-287 Brown W; Nolin S; Dobkin C; Houck G; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families | 0 | 0 |
| 1262 | 0 | 0 | 1262 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:288-288 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. The fragile X syndrome (FXS): Screening and prenatal diagnosis | 0 | 0 |
| 1263 | 0 | 0 | 1263 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Einfeld SL; Tonge BJ; Turner G; Smith E Longitudinal course of behavioural and emotional problems in Prader-Willi, Fragile X, Williams and Down syndromes | 0 | 0 |
| 1264 | 0 | 0 | 1264 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:294-294 Turk J; Das D; Howlin P; Barber N; Mottaleb M; et al. A follow-up of intellectual, social, communicatory & adaptive functioning in boys & young men with fragile X syndrome | 0 | 0 |
| 1265 | 0 | 0 | 1265 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:324-324 Abbeduto L; Murphy MM Language, communication, and the behavioural phenotype of Down syndrome (DS): Insights from fragile X syndrome (FXS) and typical development | 0 | 0 |
| 1266 | 0 | 0 | 1266 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:325-325 Abbeduto L; Murphy MM; Giles N; Bruno L; Richmond EK; et al. Understanding language in context: Comparisons of Down syndrome (DS) with fragile X syndrome and typical development | 0 | 0 |
| 1267 | 0 | 0 | 1267 2004 JOURNAL OF INVESTIGATIVE MEDICINE 52(1):S101-S101 Nowicki ST; Jacquemont S; Li L; Nguyen DV; Gregg JP; et al. An approach to identify epistatic genes involved in the development of autism spectrum disorder in patients with fragile X syndrome | 0 | 0 |
| 1268 | 0 | 0 | 1268 2004 JOURNAL OF MEDICAL GENETICS 41:S64-S64 Turner A; Myring J; Stephens M; Antoniadi T; Butler R The Problem with Premutations: Assessment of new methods for fragile-X screening. | 0 | 0 |
| 1269 | 0 | 0 | 1269 2004 JOURNAL OF MEDICAL GENETICS 41:S82-S82 McConachie M; Conlin L; McKay F; Gillespie K; Berg J A false negative PCR result in a boy with Fragile X syndrome | 0 | 0 |
| 1270 | 11 | 15 | 1270 2004 JOURNAL OF MEDICAL GENETICS 41(4) Tassone F; Hagerman RJ; Garcia-Arocena D; Khandjian EW; Greco CM; et al. Intranuclear inclusions in neural cells with premutation alleles in fragile X associated tremor/ataxia syndrome | 0 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1271 | 3 | 16 | 1271 2004 JOURNAL OF MEDICAL GENETICS 41(4) Zhou Y; Law HY; Boehm CD; Yoon CS; Cutting GR; et al. Robust fragile X (CGG)(n) genotype classification using a methylation specific triple PCR assay | 0 | 0 |
| 1272 | 33 | 65 | 1272 2004 JOURNAL OF MOLECULAR BIOLOGY 343(1):43-53 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 | 0 | 0 |
| 1273 | 0 | 0 | 1273 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Williams J; Lyon E; Miller C; Mao R Chromosome aneuploidy detected by fragile X southern blot and PCR analysis | 0 | 0 |
| 1274 | 0 | 0 | 1274 2004 JOURNAL OF MOLECULAR DIAGNOSTICS 6(4):409-409 Lee JY; Zhang YT; Hopcus-Niccum D; Mulvihill JJ; Li SB A mosaicism of 45,X/46,XX/47,XXX uncovered by molecular fragile X testing | 0 | 0 |
| 1275 | 9 | 34 | 1275 2004 JOURNAL OF MOLECULAR HISTOLOGY 35(4):389-395 Reis SA; Willemsen R; van Unen L; Hoogeveen AT; Oostra BA Prospects of TAT-mediated protein therapy for fragile X syndrome | 0 | 0 |
| 1276 | 12 | 37 | 1276 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655 Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses | 10 | 15 |
| 1277 | 36 | 97 | 1277 2004 JOURNAL OF NEUROSCIENCE 24(25):5798-5809 Michel CI; Kraft R; Restifo LL Defective neuronal development in the mushroom bodies of Drosophila Fragile X Mental Retardation 1 Mutants | 6 | 7 |
| 1278 | 21 | 34 | 1278 2004 JOURNAL OF NEUROSCIENCE 24(33):7272-7276 Stefani G; Fraser CE; Darnell JC; Darnell RB Fragile X mental retardation protein is associated with translating polyribosomes in neuronal cells | 2 | 3 |
| 1279 | 16 | 25 | 1279 2004 JOURNAL OF NEUROSCIENCE 24(47):10579-10583 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of Fragile X mental retardation protein | 1 | 1 |
| 1280 | 1 | 1 | 1280 2004 JOURNAL OF NEUROSCIENCE 24(50):CP3-CP4 Gabel LA; Won S; Kawai H; McKinney M; Tartakoff AM; et al. Visual experience regulates transient expression and dendritic localization of fragile X mental retardation protein (vol 24, pg 10579, 2004) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1281 | 7 | 21 | 1281 2004 JOURNAL OF THE NEUROLOGICAL SCIENCES 227(1):115-118 Garland EM; Vnencak-Jones CL; Biaggioni I; Davis TL; Montine TJ; et al. Fragile X gene premutation in multiple system atrophy | 0 | 0 |
| 1282 | 0 | 0 | 1282 2004 LANCET NEUROLOGY 3(12):701-701 Nelson R Drosophila model increases understanding of fragile-X syndrome | 0 | 0 |
| 1283 | 0 | 0 | 1283 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):1-2 Crnic LS; Hagerman R Preface: Fragile X syndrome: Frontiers of understanding gene-brain-behavior relationships | 0 | 0 |
| 1284 | 15 | 48 | 1284 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10 Bailey DB Newborn screening for fragile X syndrome | 0 | 1 |
| 1285 | 18 | 67 | 1285 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):11-16 Cornish K; Sudhalter V; Turk J Attention and language in fragile X | 1 | 1 |
| 1286 | 24 | 74 | 1286 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):17-24 Hessl D; Rivera SM; Reiss AL The neuroanatomy and neuroendocrinotogy of fragile X syndrome | 1 | 2 |
| 1287 | 24 | 55 | 1287 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):25-30 Hagerman PJ; Hagerman RJ Fragile X-associated tremor/ataxia syndrome (FXTAS) | 0 | 1 |
| 1288 | 29 | 66 | 1288 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):31-41 Loesch DZ; Huggins RM; Hagerman RJ Phenotypic variation and FMRP levels in fragile X | 1 | 1 |
| 1289 | 9 | 45 | 1289 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):42-48 Berry-Kravis E; Potanos K Psychopharmacology in fragile X syndrome - Present and future | 0 | 0 |
| 1290 | 15 | 32 | 1290 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):49-52 Darnell JC; Warren ST; Darnell RB The fragile X mental retardation protein, FMRP, recognizes G-quartets | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1291 | 21 | 54 | 1291 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):53-59 Beckel-Mitchener A; Greenough WT Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome | 0 | 2 |
| 1292 | 35 | 102 | 1292 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):60-67 Willemsen R; Oostra BA; Bassell GJ; Dictenberg J The fragile X syndrome: From molecular genetics to neurobiology | 2 | 5 |
| 1293 | 18 | 82 | 1293 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):68-74 Siomi H; Ishizuka A; Siomi MC RNA interference: A new mechanism by which FMRP acts in the normal brain? What can drosophila teach us? | 1 | 4 |
| 1294 | 7 | 66 | 1294 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):75-81 Rattazzi MC; LaFauci G; Brown WT Prospects for gene therapy in the fragile X syndrome | 0 | 0 |
| 1295 | 9 | 36 | 1295 2004 MOLECULAR BRAIN RESEARCH 131(1-2):101-109 Lauterborn JC Stress induced changes in cortical and hypothalamic c-fos expression are altered in fragile X mutant mice | 0 | 0 |
| 1296 | 6 | 11 | 1296 2004 MOLECULAR HUMAN REPRODUCTION 10(10):773-776 Rife M; Badenas C; Quinto L; Puigoriol E; Tazon B; et al. Analysis of CGG variation through 642 meioses in Fragile X families | 1 | 1 |
| 1297 | 1 | 50 | 1297 2004 MOLECULAR MICROBIOLOGY 54(3):742-754 Blaha B; Semsey S; Ferenczi S; Csiszovszki Z; Papp PP; et al. A proline tRNA(CGG) gene encompassing the attachment site of temperate phage 16-3 is functional and convertible to suppressor tRNA | 0 | 0 |
| 1298 | 9 | 41 | 1298 2004 MOLECULAR PSYCHIATRY 9(4):417-425 Frankland PW; Wang Y; Rosner B; Shimizu T; Balleine BW; et al. Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice | 0 | 1 |
| 1299 | 0 | 0 | 1299 2004 MOVEMENT DISORDERS 19:S20-S20 Zhao Y; Puong K; Law H; Wong M; Ng I; et al. Fragile X premutation alleles in patients with sporadic cerebellar ataxia | 0 | 0 |
| 1300 | 0 | 0 | 1300 2004 MOVEMENT DISORDERS 19:S21-S21 Hall DA; Pelak VS; Hagerman RJ; Hagerman PJ; Leehey MA Ocular motility in Fragile X premutation carriers and Fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1301 | 0 | 0 | 1301 2004 MOVEMENT DISORDERS 19:S338-S338 Leehey MA; Berry-Kravis E; Jacquemont S; Zhang L; Hagerman R; et al. Misdiagnosis of fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 1302 | 0 | 0 | 1302 2004 MOVEMENT DISORDERS 19:S339-S339 Leehey MA; Zhang L; Wheelock V; Tassone F; Hagerman R; et al. A preliminary observation: Increased frequency of fragile X expanded alleles in patients that meet diagnostic criteria for MSA | 0 | 0 |
| 1303 | 0 | 0 | 1303 2004 MOVEMENT DISORDERS 19:S359-S360 Di Maria E; Grasso M; Abbruzzese G; Mandich P; Ratto S; et al. The role for Fragile X premutation in essential tremor and spinocerebellar ataxia: Findings from two cohorts of Italian patients | 0 | 0 |
| 1304 | 0 | 0 | 1304 2004 MOVEMENT DISORDERS 19:S444-S444 Puong K; Zhao Y; Law H; Wong M; Ng I; et al. Screening for Fragile X premutation alleles in patients with essential tremor | 0 | 0 |
| 1305 | 0 | 0 | 1305 2004 MOVEMENT DISORDERS 19(9):1122-1122 Leehey MA; Hall D; Rice C; Jacquemont S; Zhang L; et al. The clinical course of fragile X-associated tremor/ataxia syndrome (FXTAS). | 0 | 0 |
| 1306 | 0 | 0 | 1306 2004 MOVEMENT DISORDERS 19(9):1127-1127 Hall DA; Rice CD; Hagerman RR; Hagerman PR; Berry-Kravis E; et al. Medical treatment for the fragile x-associated tremor/ataxia syndrome. | 0 | 0 |
| 1307 | 41 | 73 | 1307 2004 NATURE CELL BIOLOGY 6(11):1048-1053 Jin P; Alisch RS; Warren ST RNA and microRNAs in fragile X mental retardation | 2 | 3 |
| 1308 | 20 | 39 | 1308 2004 NATURE NEUROSCIENCE 7(2):113-117 Jin P; Zarnescu DC; Ceman S; Nakamoto M; Mowrey J; et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway | 16 | 38 |
| 1309 | 1 | 2 | 1309 2004 NATURE REVIEWS NEUROSCIENCE 5(1):4-4 Jones R Neurological disorders: Fragile X functions | 0 | 0 |
| 1310 | 0 | 0 | 1310 2004 NEUROBIOLOGY OF AGING 25:S434-S434 Westmark CJ; Malter JS FMRP mediates mGluR1-activated translation of APP | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1311 | 0 | 0 | 1311 2004 NEUROLOGY 62(7):A48-A48 Hagerman PJ; Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; et al. Penetrance of the Fragile X-associated Tremor/Ataxia Syndrome (FXTAS) in a premutation carrier population: Initial results from a California family-based study | 0 | 0 |
| 1312 | 7 | 10 | 1312 2004 NEUROLOGY 63(2):362-363 Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; et al. Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort | 0 | 4 |
| 1313 | 5 | 37 | 1313 2004 NEUROLOGY 63(9):1634-1639 Kogan CS; Bertone A; Cornish K; Boutet I; Kaloustian VMD; et al. Integrative cortical dysfunction and pervasive motion perception deficit in fragile X syndrome | 0 | 0 |
| 1314 | 5 | 7 | 1314 2004 NEUROLOGY 63(11):2188-2189 Pugliese P; Annesi G; Cutuli N; Arabia G; Nicoletti G; et al. The fragile X premutation presenting as postprandial hypotension | 0 | 0 |
| 1315 | 22 | 75 | 1315 2004 NEUROLOGY INDIA 52(1):36-42 Pandey UB; Phadke SR; Mittal B Molecular diagnosis and genetic counseling for fragile X mental retardation | 0 | 0 |
| 1316 | 29 | 101 | 1316 2004 NEUROPSYCHOLOGIA 42(14):1934-1947 Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; et al. A neuropsychological investigation of male premutation carriers of fragile X syndrome | 0 | 0 |
| 1317 | 2 | 23 | 1317 2004 NEUROREPORT 15(10):1579-1583 Greicius MD; Boyett-Anderson JM; Menon V; Reiss AL Reduced basal forebrain and hippocampal activation during memory encoding in girls with fragile X syndrome | 0 | 0 |
| 1318 | 22 | 42 | 1318 2004 NEUROREPORT 15(16):2447-2450 Veneri M; Zalfa F; Bagni C FMRP and its target RNAs: fishing for the specificity | 0 | 0 |
| 1319 | 16 | 41 | 1319 2004 NUCLEIC ACIDS RESEARCH 32(1):298-306 Fojtik P; Kejnovska I; Vorlickova M The guanine-rich fragile X chromosome repeats are reluctant to form tetraplexes | 0 | 2 |
| 1320 | 23 | 40 | 1320 2004 NUCLEIC ACIDS RESEARCH 32(7):2129-2137 Gabus C; Mazroui R; Tremblay S; Khandjian EW; Darlix JL The fragile X mental retardation protein has nucleic acid chaperone properties | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1321 | 16 | 44 | 1321 2004 NUCLEIC ACIDS RESEARCH 32(14):4145-4154 Khateb S; Weisman-Shomer P; Hershco I; Loeb LA; Fry M Destabilization of tetraplex structures of the fragile X repeat sequence (CGG)(n) is mediated by homolog-conserved domains in three members of the hnRNP family | 0 | 0 |
| 1322 | 0 | 1 | 1322 2004 PRAXIS DER KINDERPSYCHOLOGIE UND KINDERPSYCHIATRIE 53(8):593-594 Irblich D The fragile X syndrome - A guide for parents | 0 | 0 |
| 1323 | 3 | 8 | 1323 2004 PRENATAL DIAGNOSIS 24(1):67-68 Delatycki MB; Sheffield LJ; Wake S; Cohen J Screening approach for Fragile X syndrome | 0 | 0 |
| 1324 | 0 | 1 | 1324 2004 PRENATAL DIAGNOSIS 24(1):68-69 Wald NJ; Morris JK Reply: Prenatal screen for Fragile X syndrome | 0 | 0 |
| 1325 | 4 | 12 | 1325 2004 PRIMARY CARE 31(3):621-+ Wiesner GL; Cassidy SB; Grimes SJ; Matthews AL; Acheson LS Clinical consult: developmental delay/fragile X syndrome | 0 | 0 |
| 1326 | 7 | 57 | 1326 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(10):3615-3620 Menon V; Leroux J; White CD; Reiss AL Frontostriatal deficits in fragile X syndrome: Relation to FMR1 gene expression | 0 | 0 |
| 1327 | 24 | 61 | 1327 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(36):13357-13362 Khandjian EW; Huot ME; Tremblay S; Davidovic L; Mazroui R; et al. Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles | 6 | 7 |
| 1328 | 23 | 53 | 1328 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(42):15201-15206 Lu R; Wang HP; Liang Z; Ku L; O'Donnell WT; et al. The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development | 3 | 3 |
| 1329 | 15 | 21 | 1329 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17329-17330 Miyashiro K; Eberwine J Fragile X syndrome: (What's) lost in translation? | 0 | 0 |
| 1330 | 17 | 61 | 1330 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17428-17433 Ling SC; Fahrner PS; Greenough WT; Gelfand VI Transport of Drosophila fragile X rental retardation protein-containing ribonucleoprotein granules by kinesin-1 and cytoplasmic dynein | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1331 | 22 | 50 | 1331 2004 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 101(50):17504-17509 Weiler IJ; Spangler CC; Klintsova AY; Grossman AW; Kim SH; et al. Fragile X mental retardation protein is necessary for neurotransmitter-activated protein translation at synapses | 0 | 0 |
| 1332 | 1 | 1 | 1332 2004 PROTEIN EXPRESSION AND PURIFICATION 37(1):264-264 McNulty DE; Claffee BA; Huddleston MJ; Kane JF Mistranslational errors associated with the rare arginine codon CGG in Escherichia coli (vol 27, pg 365, 2003) | 0 | 0 |
| 1333 | 1 | 53 | 1333 2004 QUALITATIVE HEALTH RESEARCH 14(6):741-759 Medved MI; Brockmeier J Making sense of traumatic experiences: Telling your life with fragile X syndrome | 0 | 0 |
| 1334 | 0 | 1 | 1334 2004 REPRODUCTIVE BIOMEDICINE ONLINE 8(3):337-337 [Anon] Late onset fragile X syndrome | 0 | 0 |
| 1335 | 2 | 7 | 1335 2004 REVISTA DE NEUROLOGIA 38(1):7-11 Artigas-Pallares J; Brun-Gasca C Can the behavioural phenotype of Fragile X syndrome be attributed to mental retardation and to attention deficit hyperactivity disorder? | 0 | 0 |
| 1336 | 30 | 95 | 1336 2004 TRENDS IN NEUROSCIENCES 27(7):370-377 Bear MF; Huber KM; Warren ST The mGIuR theory of fragile X mental retardation | 8 | 10 |
| 1337 | 12 | 41 | 1337 2005 AMERICAN JOURNAL OF HUMAN GENETICS 76(2):302-311 Edamura KN; Leonard MR; Pearson CE Role of replication and CpG methylation in fragile X syndrome CGG deletions in primate cells | 0 | 0 |
| 1338 | 18 | 50 | 1338 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(1):25-32 Skinner M; Hooper S; Hatton DD; Robert J; Mirrett P; et al. Mapping nonverbal IQ in young boys with fragile X syndrome | 0 | 0 |
| 1339 | 10 | 18 | 1339 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(2):210-214 Angeli CB; Capelli LP; Auricchio MTBM; Vianna-Morgante AM; Mingroni-Netto RC; et al. AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations | 0 | 0 |
| 1340 | 9 | 20 | 1340 2005 ANNALS OF NEUROLOGY 57(1):144-147 Berry-Kravis E; Potanos K; Weinberg D; Zhou LL; Goetz CG Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1341 | 9 | 98 | 1341 2005 APPLIED PSYCHOLINGUISTICS 26(1):7-27 Rice ML; Warren SF; Betz SK Language symptoms of developmental language disorders: An overview of autism, Down syndrome, fragile X, specific language impairment, and Williams syndrome | 0 | 1 |
| 1342 | 0 | 13 | 1342 2005 ARCHIVES DE PEDIATRIE 12(2):176-179 Vantalon V; Briard-Luginbuhl V; Mouren MC Fragile X syndrome and very early onset schizophrenia: a female case study | 0 | 0 |
| 1343 | 8 | 47 | 1343 2005 BIOCHEMICAL JOURNAL 386:297-303 Kumari D; Gabrielian A; Wheeler D; Usdin K The roles of Sp1, Sp3, USF1/USF2 and NRF-1 in the regulation and three-dimensional structure of the Fragile X mental retardation gene promoter | 0 | 0 |
| 1344 | 21 | 49 | 1344 2005 BRAIN AND COGNITION 57(1):53-60 Cornish K; Kogan C; Turk J; Manly T; James N; et al. The emerging fragile X premutation phenotype: Evidence from the domain of social cognition | 0 | 0 |
| 1345 | 17 | 20 | 1345 2005 CELLULAR AND MOLECULAR LIFE SCIENCES 62(2):251-252 Zalfa F; Bagni C Another view of the role of FMRP in translational regulation | 0 | 0 |
| 1346 | 15 | 52 | 1346 2005 DEVELOPMENTAL CELL 8(1):43-52 Zarnescu DC; Jin P; Betschinger J; Nakamoto M; Wang Y; et al. Fragile X protein functions with Lgl and the PAR complex in flies and mice | 0 | 0 |
| 1347 | 9 | 43 | 1347 2005 DEVELOPMENTAL CELL 8(3):331-342 Costa A; Wang Y; Dockendorff TC; Erdjument-Bromage H; Tempst P; et al. The Drosophila fragile X protein functions as a negative regulator in the orb autoregulatory pathway | 0 | 0 |
| 1348 | 1 | 33 | 1348 2005 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 47(2):94-104 Weiskop S; Richdale A; Matthews J Behavioural treatment to reduce sleep problems in children with autism or fragile X syndrome | 0 | 0 |
| 1349 | 0 | 1 | 1349 2005 EDUCATIONAL REVIEW 57(2):258-260 Reid G Educating children with Fragile X syndrome | 0 | 0 |
| 1350 | 14 | 26 | 1350 2005 FEBS JOURNAL 272(3):872-878 Pozdnyakova I; Regan L New insights into Fragile X syndrome - Relating genotype to phenotype at the molecular level | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1351 | 19 | 68 | 1351 2005 HUMAN MOLECULAR GENETICS 14(6):835-844 Castets M; Schaeffer C; Bechara E; Schenck A; Khandjian EW; et al. FMRP interferes with the Rac1 pathway and controls actin cytoskeleton dynamics in murine fibroblasts | 0 | 0 |
| 1352 | 2 | 4 | 1352 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-296 Toft M; Farrer M Premutation alleles and fragile X-associated tremor/ataxia syndrome | 0 | 0 |
| 1353 | 1 | 3 | 1353 2005 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 293(3):296-297 Deng H; Le WD; Jankovic J Premutation alleles and fragile X-associated tremor/ataxia syndrome - Reply | 0 | 0 |
| 1354 | 17 | 46 | 1354 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(6):4498-4503 Mulvihill DJ; Edamura KN; Hagerman KA; Pearson CE; Wang YH Effect of CAT or AGG interruptions and CpG methylation on nucleosome assembly upon trinucleotide repeats on spinocerebellar ataxia, type 1 and fragile X syndrome | 0 | 0 |
| 1355 | 21 | 47 | 1355 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280(7):5750-5763 Garnon J; Lachance C; Di Marco S; Hel Z; Marion D; et al. Fragile X-related protein FXR1P regulates proinflammatory cytokine tumor necrosis factor expression at the post-transcriptional level | 0 | 0 |
| 1356 | 3 | 8 | 1356 2005 JOURNAL OF CLINICAL NEUROSCIENCE 12(1):42-43 Storey E; Billimoria P Increased T-2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome | 0 | 0 |
| 1357 | 0 | 0 | 1357 2005 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 76(1):151-151 Ealing J; Mavrogiannis LA; Kingston H; Cockburn DJ; Taylor GR; et al. An atypical tetra nucleotide expansion in DM2 (PROMM) | 0 | 0 |
| 1358 | 24 | 61 | 1358 2005 MOLECULAR & CELLULAR PROTEOMICS 4(3):278-290 Zhang YQ; Friedman DB; Wang Z; Woodruff E; Pan LY; et al. Protein expression profiling of the Drosophila fragile X mutant brain reveals up-regulation of monoamine synthesis | 0 | 0 |
| 1359 | 4 | 10 | 1359 2005 NEURON 45(5):642-644 Dolen G; Bear MF Courting a cure for Fragile X | 0 | 0 |
| 1360 | 11 | 56 | 1360 2005 NEURON 45(5):753-764 McBride SMJ; Choi CH; Wang Y; Liebelt D; Braunstein E; et al. Pharmacological rescue of synaptic plasticity, courtship behavior, and mushroom body defects in a Drosophila model of fragile X syndrome | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1361 | 16 | 34 | 1361 2005 NEUROSCIENCE LETTERS 377(3):141-146 El Idrissi A; Ding XH; Scalia J; Trenkner E; Brown WT; et al. Decreased GABA(A) receptor expression in the seizure-prone fragile X mouse | 0 | 0 |
| 1362 | 17 | 45 | 1362 2005 NUCLEIC ACIDS RESEARCH 33(2):451-463 Napierala M; Michalowski D; de Mezer M; Krzyzosiak WJ Facile FMR1 mRNA structure regulation by interruptions in CGG repeats | 0 | 0 |
| 1363 | 26 | 46 | 1363 2005 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 102(6):2180-2185 Aschrafi A; Cunningham BA; Edelman GM; Vanderklish PW The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain | 0 | 0 |
| 1364 | 54 | 77 | 1364 2005 TRENDS IN GENETICS 21(1):37-45 Zhang YQ; Broadie K Fathoming fragile X in fruit flies | 1 | 1 |