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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 2101 | 1 | 1 | 2294 2003 NATURE REVIEWS NEUROSCIENCE 4(10):776-777 Casci T Neurological disorders - Fragile X: a class of its own | 0 | 0 |
| 2102 | 1 | 2 | 2361 2004 NATURE REVIEWS NEUROSCIENCE 5(1):4-4 Jones R Neurological disorders: Fragile X functions | 0 | 0 |
| 2103 | 7 | 34 | 1620 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 5 | 40 |
| 2104 | 1 | 1 | 1621 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; Nilges M; Pastore A The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997) | 0 | 0 |
| 2105 | 4 | 13 | 1141 1993 NERVENHEILKUNDE 12(2):84-86 FROSTER UG CLINICAL AND MOLECULAR ASPECTS OF THE FRAGILE-X FORM OF MENTAL-RETARDATION (MARTIN-BELL SYNDROME) | 0 | 0 |
| 2106 | 8 | 27 | 2177 2002 NEUROBIOLOGY OF DISEASE 10(3):211-218 D'Agata V; Warren ST; Zhao WQ; Torre ER; Alkon DL; Cavallaro S Gene expression profiles in a transgenic animal model of fragile X syndrome | 0 | 10 |
| 2107 | 17 | 39 | 2178 2002 NEUROBIOLOGY OF DISEASE 11(1):53-63 Schenck A; Van de Bor V; Bardoni B; Giangrande A Novel features of dFMR1, the Drosophila orthologue of the fragile X mental retardation protein | 3 | 3 |
| 2108 | 23 | 59 | 2179 2002 NEUROBIOLOGY OF DISEASE 11(1):221-229 Castren M; Lampinen KE; Miettinen R; Koponen E; Sipola I; Bakker CE; Oostra BA; Castren E BDNF regulates the expression of fragile X mental retardation protein mRNA in the hippocampus | 2 | 3 |
| 2109 | 4 | 13 | 1952 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 73(1):87-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation | 20 | 25 |
| 2110 | 6 | 14 | 1953 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000) | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2111 | 0 | 0 | 2046 2001 NEUROIMAGE 13(6):S1076-S1076 Moore CJ; Daly EM; Schmitz N; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of Fragile X syndrome | 0 | 0 |
| 2112 | 0 | 0 | 657 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME | 1 | 1 |
| 2113 | 0 | 0 | 79 1982 NEUROLOGY 32(4):A190-A190 ROSENBERGER PB; WILSONCIAMBRONE S; MILUNSKY A SPEECH FLUENCY DISORDER IN THE FRAGILE-X SYNDROME | 2 | 2 |
| 2114 | 3 | 10 | 721 1990 NEUROLOGY 40(2):378-380 DESAI HB; DONAT J; SHOKEIR MHK; MUNOZ DG AMYOTROPHIC LATERAL SCLEROSIS IN A PATIENT WITH FRAGILE X-SYNDROME | 5 | 7 |
| 2115 | 0 | 0 | 1250 1994 NEUROLOGY 44(4):A400-A400 GUERREIRO M; MOURARIBEIRO MVL; CAMARGO EE; KATO M; MENEZES JR; GUERREIRO CAM NEUROBIOLOGY OF FRAGILE-X-SYNDROME (FXS) | 0 | 0 |
| 2116 | 22 | 61 | 1251 1994 NEUROLOGY 44(7):1317-1324 REISS AL; LEE J; FREUND L NEUROANATOMY OF FRAGILE-X SYNDROME - THE TEMPORAL-LOBE | 49 | 83 |
| 2117 | 0 | 0 | 1622 1997 NEUROLOGY 48(3):5062-5062 Mostofsky SH; Mazzocco MM; Aakalu G; Warsofsky IS; Denckla MB; Reiss AL Aberrant posterior vermis size in fragile X syndrome: Correlation with neurocognitive performance | 0 | 0 |
| 2118 | 18 | 63 | 1693 1998 NEUROLOGY 50(1):121-130 Mostofsky SH; Mazzocco MMM; Aakalu G; Warsofsky IS; Denckla MB; Reiss AL Decreased cerebellar posterior vermis size in fragile X syndrome - Correlation with neurocognitive performance | 18 | 44 |
| 2119 | 0 | 0 | 1694 1998 NEUROLOGY 50(4):A86-A86 Mostofsky SH; Reiss AL; Freund L Examination of posterior vermis size in young males with fragile X syndrome | 0 | 0 |
| 2120 | 3 | 10 | 2047 2001 NEUROLOGY 57(1):127-130 Hagerman RJ; Leehey M; Heinrichs W; Tassone F; Wilson R; Hills J; Grigsby J; Gage B; Hagerman PJ Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 29 | 45 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2121 | 0 | 0 | 2180 2002 NEUROLOGY 58(6):987-987 Munoz DG Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 0 | 0 |
| 2122 | 0 | 0 | 2181 2002 NEUROLOGY 58(6):987-988 Hagerman RJ; Greco C; Jacquemont S; Leehy M; Hagerman P Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X - Reply | 0 | 0 |
| 2123 | 0 | 0 | 2182 2002 NEUROLOGY 58(7):A481-A482 Leehey MA; Brunberg JA; Lang AE; Jacquemont S; Rubinstein D; Greco C; Grigsby J; Tassone F; Hagerman R; Hagerman PJ MRI increased T2 signal intensity in the cerebellar peduncles: Specific for the fragile X premutation tremor/ataxia syndrome? | 0 | 0 |
| 2124 | 0 | 0 | 2183 2002 NEUROLOGY 58(7):A482-A482 Munhoz RP; Lozano AM; Lang AE Fragile X syndrome premutation mistaken as essential tremor: An unrecognized source of diagnostic confusion | 0 | 0 |
| 2125 | 0 | 0 | 2362 2004 NEUROLOGY 62(7):A48-A48 Hagerman PJ; 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 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 |
| 2126 | 9 | 20 | 2184 2002 NEURON 34(6):859-862 Gao FB Understanding fragile X syndrome: Insights from retarded flies | 3 | 6 |
| 2127 | 20 | 52 | 2185 2002 NEURON 34(6):961-972 Morales J; Hiesinger PR; Schroeder AJ; Kume K; Verstreken P; Jackson FR; Nelson DL; Hassan BA Drosophila fragile X protein, DFXR, regulates neuronal morphology and function in the brain | 17 | 25 |
| 2128 | 7 | 10 | 2295 2003 NEURON 38(6):843-845 Billuart P; Chelly J From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP | 1 | 1 |
| 2129 | 21 | 64 | 2296 2003 NEURON 38(6):887-898 Schenck A; Bardoni B; Langmann C; Harden N; Mandel JL; Giangrande A CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein | 5 | 9 |
| 2130 | 5 | 35 | 2297 2003 NEURON 39(5):739-747 Jin P; Zarnescu DC; Zhang FP; Pearson CE; Lucchesi JC; Moses K; Warren ST RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2131 | 0 | 0 | 306 1985 NEUROPEDIATRICS 16(3):171-172 GRANSTROM ML; SIMOLA KOJ; YLINEN A; RINTAHAKA P THE FRAGILE-X SYNDROME IN CHILDHOOD - A THERAPEUTIC TRIAL WITH FOLIC-ACID | 0 | 0 |
| 2132 | 3 | 12 | 1142 1993 NEUROPEDIATRICS 24(4):211-213 REES M; DIEBOLD U; PARKER K; DOOSE H; GARDINER RM; WHITEHOUSE WP BENIGN CHILDHOOD EPILEPSY WITH CENTROTEMPORAL SPIKES AND THE FOCAL SHARP WAVE TRAIT IS NOT LINKED TO THE FRAGILE-X REGION | 6 | 23 |
| 2133 | 7 | 41 | 1252 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; BERGONZI P BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| 2134 | 4 | 16 | 403 1986 NEUROPSYCHOLOGIA 24(3):405-409 MIEZEJESKI CM; JENKINS EC; HILL AL; WISNIEWSKI K; FRENCH JH; BROWN WT A PROFILE OF COGNITIVE DEFICIT IN FEMALES FROM FRAGILE-X FAMILIES | 47 | 60 |
| 2135 | 3 | 36 | 484 1987 NEUROPSYCHOLOGIA 25(6):881-891 GRIGSBY JP; KEMPER MB; HAGERMAN RJ DEVELOPMENTAL GERSTMANN SYNDROME WITHOUT APHASIA IN FRAGILE-X SYNDROME | 16 | 27 |
| 2136 | 10 | 29 | 722 1990 NEUROPSYCHOLOGIA 28(1):9-16 CROWE SF; HAY DA NEUROPSYCHOLOGICAL DIMENSIONS OF THE FRAGILE X-SYNDROME - SUPPORT FOR A NONDOMINANT HEMISPHERE DYSFUNCTION HYPOTHESIS | 36 | 52 |
| 2137 | 17 | 36 | 1695 1998 NEUROPSYCHOLOGIA 36(11):1239-1246 Cornish KM; Munir F; Cross G The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective | 10 | 14 |
| 2138 | 13 | 47 | 1954 2000 NEUROPSYCHOLOGIA 38(9):1261-1270 Munir F; Cornish KM; Wilding J A neuropsychological profile of attention deficits in young males with fragile X syndrome | 13 | 15 |
| 2139 | 15 | 32 | 2186 2002 NEUROPSYCHOLOGIA 40(8):1343-1349 Wilding J; Cornish K; Munir F Further delineation of the executive deficit in males with fragile-X syndrome | 4 | 4 |
| 2140 | 27 | 61 | 1382 1995 NEUROPSYCHOLOGY 9(4):470-480 MAZZOCCO MMM; FREUND LS; BAUMGARDNER TL; FORMAN L; REISS AL NEUROPSYCHOLOGICAL AND PSYCHOSOCIAL EFFECTS OF THE FMR-1 FULL MUTATION - CASE-REPORT OF MONOZYGOTIC TWINS DISCORDANT FOR THE FRAGILE-X SYNDROME | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2141 | 26 | 47 | 2048 2001 NEUROPSYCHOLOGY 15(2):290-299 Bennetto L; Pennington BF; Porter D; Taylor AK; Hagerman RJ Profile of cognitive functioning in women with the fragile X mutation | 9 | 11 |
| 2142 | 41 | 101 | 2298 2003 NEUROPSYCHOLOGY 17(4):646-657 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 | 1 | 1 |
| 2143 | 6 | 11 | 1696 1998 NEUROREPORT 9(3):477-481 Steward O; Bakker CE; Willems PJ; Oostra BA No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome | 10 | 16 |
| 2144 | 8 | 20 | 2049 2001 NEUROREPORT 12(11):2573-2576 Rojas DC; Benkers TL; Rogers SJ; Teale PD; Reite ML; Hagerman RJ Auditory evoked magnetic fields in adults with fragile X syndrome | 2 | 3 |
| 2145 | 17 | 53 | 1820 1999 NEUROSCIENCE 94(1):185-192 Paradee W; Melikian HE; Rasmussen DL; Kenneson A; Conn PJ; Warren ST Fragile X mouse: Strain effects of knockout phenotype and evidence suggesting deficient amygdala function | 19 | 37 |
| 2146 | 15 | 43 | 2050 2001 NEUROSCIENCE 103(4):1043-1050 Chen L; Toth M Fragile X mice develop sensory hyperreactivity to auditory stimuli | 16 | 26 |
| 2147 | 14 | 26 | 2299 2003 NEUROSCIENCE 119(1):9-13 D'Antuono M; Merlo D; Avoli M Involvement of cholinergic and GABAergic systems in the fragile X knockout mice | 0 | 1 |
| 2148 | 21 | 39 | 2300 2003 NEUROSCIENCE 120(4):1005-1017 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 | 3 | 3 |
| 2149 | 27 | 53 | 1955 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):255-263 de Vries BBA; Oostra BA The fragile X syndrome: A model for mental retardation | 0 | 0 |
| 2150 | 8 | 18 | 1956 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; Nieuwenhuizen I; De Vries BBA; Reyniers E; Hoogeveen AT; Willems PJ; De Deyn PP; Oostra BA Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2151 | 0 | 0 | 606 1988 NEUROTOXICOLOGY 9(1):139-140 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 2152 | 5 | 9 | 607 1988 NEUROTOXICOLOGY 9(3):359-365 EDWARDS DR; KEPPEN LD; RANELLS JD; GOLLIN SM AUTISM IN ASSOCIATION WITH FRAGILE X-SYNDROME IN FEMALES - IMPLICATIONS FOR DIAGNOSIS AND TREATMENT IN CHILDREN | 4 | 7 |
| 2153 | 1 | 7 | 30 1981 NEW ENGLAND JOURNAL OF MEDICINE 305(22):1348-1348 NIELSEN KB; TOMMERUP N; DYGGVE H; SCHOU C MACROORCHIDISM, MENTAL-RETARDATION, AND THE FRAGILE-X | 8 | 12 |
| 2154 | 1 | 6 | 80 1982 NEW ENGLAND JOURNAL OF MEDICINE 306(25):1551-1552 POPOVICH B; VEKEMANS M; ROSENBLATT D; MONROE P FRAGILE-X | 17 | 21 |
| 2155 | 2 | 6 | 154 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(5):285-286 HECHT F; GLOVER TW ANTIBIOTICS CONTAINING TRIMETHOPRIM AND THE FRAGILE X-CHROMOSOME | 4 | 6 |
| 2156 | 2 | 6 | 155 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(23):1424-1424 HAGERMAN RJ; LEVITAS A DILANTIN AND THE FRAGILE X-SYNDROME | 0 | 2 |
| 2157 | 6 | 11 | 225 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1462-1462 WATSON MS; LECKMAN JF; ANNEX B; BREG WR; BOLES D; VOLKMAR FR; COHEN DJ; CARTER C FRAGILE X IN A SURVEY OF 75 AUTISTIC MALES | 34 | 56 |
| 2158 | 0 | 1 | 226 1984 NEW ENGLAND JOURNAL OF MEDICINE 310(22):1471-1471 STEIN M THE FRAGILE X SYNDROME - DIAGNOSIS, BIOCHEMISTRY, AND INTERVENTION - HAGERMAN,RJ, MCBOGG,PM | 0 | 0 |
| 2159 | 1 | 6 | 404 1986 NEW ENGLAND JOURNAL OF MEDICINE 315(10):607-609 TURNER G; ROBINSON H; LAING S; PURVISSMITH S PREVENTIVE SCREENING FOR THE FRAGILE-X SYNDROME | 95 | 123 |
| 2160 | 4 | 4 | 485 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2161 | 0 | 1 | 486 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 TURNER G THE FRAGILE X-CHROMOSOME - REPLY | 1 | 1 |
| 2162 | 0 | 0 | 487 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 HECHT F; HECHT BK THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 2163 | 15 | 28 | 885 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1673-1681 ROUSSEAU F; HEITZ D; BIANCALANA V; BLUMENFELD S; KRETZ C; BOUE J; TOMMERUP N; VANDERHAGEN C; DELOZIERBLANCHET C; CROQUETTE MF; GILGENKRANTZ S; JALBERT P; VOELCKEL MA; OBERLE I; MANDEL JL DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION | 268 | 438 |
| 2164 | 6 | 11 | 886 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1720-1722 SUTHERLAND GR; GEDEON A; KORNMAN L; DONNELLY A; BYARD RW; MULLEY JC; KREMER E; LYNCH M; PRITCHARD M; YU S; RICHARDS RI PRENATAL-DIAGNOSIS OF FRAGILE X-SYNDROME BY DIRECT DETECTION OF THE UNSTABLE DNA-SEQUENCE | 61 | 86 |
| 2165 | 7 | 11 | 887 1991 NEW ENGLAND JOURNAL OF MEDICINE 325(24):1736-1738 SHAPIRO LR THE FRAGILE X-SYNDROME - A PECULIAR PATTERN OF INHERITANCE | 2 | 5 |
| 2166 | 0 | 0 | 1383 1995 NEW SCIENTIST 147(1985):10-10 WEBB J QUESTION MARK HANGS OVER FRAGILE-X TEST IN NEWBORNS | 0 | 0 |
| 2167 | 11 | 14 | 1384 1995 NEW ZEALAND MEDICAL JOURNAL 108(1009):404-406 NEVILLE L; COCHRANE J; FITZGERALD P; KENNEDY M FRAGILE-X MENTAL-RETARDATION SYNDROME - DNA DIAGNOSIS AND CARRIER DETECTION IN NEW-ZEALAND FAMILIES | 0 | 0 |
| 2168 | 13 | 45 | 1504 1996 NIMHANS JOURNAL 14(3):201-207 Suresh KP; Girimaji SR; Manjunatha KR Newer genetics in mental retardation .1. Fragile X syndrome and triplet repeat mutations | 0 | 1 |
| 2169 | 1 | 1 | 723 1990 NUCLEIC ACIDS RESEARCH 18(3):690-690 YU S; SUTHERS GK; MULLEY JC A BCLI RFLP FOR DXS296 (VK21) NEAR THE FRAGILE-X | 2 | 6 |
| 2170 | 0 | 2 | 724 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692 HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369) | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2171 | 10 | 25 | 888 1991 NUCLEIC ACIDS RESEARCH 19(10):2567-2572 DIETRICH A; KIOSCHIS P; MONACO AP; GROSS B; KORN B; WILLIAMS SV; SHEER D; HEITZ D; OBERLE I; TONIOLO D; WARREN ST; LEHRACH H; POUSTKA A MOLECULAR-CLONING AND ANALYSIS OF THE FRAGILE X-REGION IN MAN | 23 | 45 |
| 2172 | 9 | 25 | 889 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; FLYNN G; CHRISTADOULOU Z; MACKINNON RN; FRANCIS M; LITTLER AJ; ANAND R; POUSTKA AM; LEHRACH H; SCHLESSINGER D; DURSO M; BUCKLE VJ; DAVIES KE A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| 2173 | 10 | 20 | 890 1991 NUCLEIC ACIDS RESEARCH 19(16):4355-4359 NAKAHORI Y; KNIGHT SJL; HOLLAND J; SCHWARTZ C; ROCHE A; TARLETON J; WONG S; FLINT TJ; FROSTERISKENIUS U; BENTLEY D; DAVIES KE; HIRST MC MOLECULAR HETEROGENEITY OF THE FRAGILE-X SYNDROME | 61 | 91 |
| 2174 | 11 | 34 | 1385 1995 NUCLEIC ACIDS RESEARCH 23(11):1876-1881 MITCHELL JE; NEWBURY SF; MCCLELLAN JA COMPACT STRUCTURES OF D(CNG)(N) OLIGONUCLEOTIDES IN SOLUTION AND THEIR POSSIBLE RELEVANCE TO FRAGILE-X AND RELATED HUMAN GENETIC-DISEASES | 2 | 31 |
| 2175 | 5 | 27 | 1505 1996 NUCLEIC ACIDS RESEARCH 24(4):784-792 Mariappan SVS; Catasti P; Chen X; Ratliff R; Moyzis RK; Bradbury EM; Gupta G Solution structures of the individual single strands of the fragile X DNA triplets (GCC)(n)center dot(GGC)(n) | 10 | 48 |
| 2176 | 26 | 45 | 1957 2000 NUCLEIC ACIDS RESEARCH 28(7):1535-1541 Weisman-Shomer P; Cohen E; Fry M Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures | 5 | 11 |
| 2177 | 12 | 42 | 1958 2000 NUCLEIC ACIDS RESEARCH 28(10):2141-2152 Genc B; Muller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; Majewski F; von Gontard A; Doerfler W Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals | 3 | 6 |
| 2178 | 18 | 36 | 2051 2001 NUCLEIC ACIDS RESEARCH 29(11):2276-2283 Li ZZ; Zhang YY; Ku L; Wilkinson KD; Warren ST; Feng Y The fragile X mental retardation protein inhibits translation via interacting with mRNA | 46 | 67 |
| 2179 | 5 | 47 | 2052 2001 NUCLEIC ACIDS RESEARCH 29(22):4684-4690 Fojtik P; Vorlickova M The fragile X chromosome (GCC) repeat folds into a DNA tetraplex at neutral pH | 0 | 1 |
| 2180 | 16 | 36 | 2187 2002 NUCLEIC ACIDS RESEARCH 30(14):3278-3285 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; Neri G Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 3 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2181 | 7 | 58 | 2188 2002 NUCLEIC ACIDS RESEARCH 30(17):3672-3681 Weisman-Shomer P; Cohen E; Fry M Distinct domains in the CArG-box binding factor A destabilize tetraplex forms of the fragile X expanded sequence d(CGG)(n) | 1 | 2 |
| 2182 | 16 | 50 | 2301 2003 NUCLEIC ACIDS RESEARCH 31(14):3963-3970 Weisman-Shomer P; Cohen E; Hershco I; Khateb S; Wolfovitz-Barchad O; Hurley LH; Fry M The cationic porphyrin TMPyP4 destabilizes the tetraplex form of the fragile X syndrome expanded sequence d(CGG)(n) | 2 | 3 |
| 2183 | 7 | 23 | 2302 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248 Handa V; Saha T; Usdin K The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer | 0 | 2 |
| 2184 | 11 | 41 | 2363 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 | 0 |
| 2185 | 21 | 40 | 2364 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 | 0 | 0 |
| 2186 | 3 | 11 | 227 1984 OBSTETRICS AND GYNECOLOGY 63(3):S19-S21 HOGGE WA; SCHONBERG SA; GLOVER TW; HECHT F; GOLBUS MS PRENATAL-DIAGNOSIS OF FRAGILE (X) SYNDROME | 7 | 14 |
| 2187 | 26 | 80 | 2189 2002 OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA 29(2):367-+ Wenstrom KD Fragile X and other trinucleotide repeat diseases | 1 | 3 |
| 2188 | 0 | 0 | 891 1991 OPTOMETRY AND VISION SCIENCE 68(8):634-640 MAINO DM; WESSON M; SCHLANGE D; CIBIS G; MAINO JH OPTOMETRIC FINDINGS IN THE FRAGILE X-SYNDROME | 5 | 9 |
| 2189 | 19 | 33 | 1697 1998 OPTOMETRY AND VISION SCIENCE 75(12):856-859 Kranjc BS; Brezigar A; Peterlin B Bilateral macular dysplasia in fragile X syndrome | 0 | 0 |
| 2190 | 32 | 54 | 1959 2000 OPTOMETRY AND VISION SCIENCE 77(11):592-599 Block SS; Brusca-Vega R; Pizzi WJ; Berry-Kravis E; Maino DM; Treitman TM Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2191 | 0 | 10 | 2190 2002 PANMINERVA MEDICA 44(1):7-10 Bargagna S; Canepa G; Tinelli F Social adjustment in children with Down mental retardation (MRD) and Fragile-X mental retardation (MRX) | 0 | 1 |
| 2192 | 7 | 11 | 725 1990 PATHOBIOLOGY 58(4):236-240 JENKINS EC; DUNCAN CJ; SANZ MM; GENOVESE M; GU H; SCHWARTZRICHSTEIN C; LELE KP; SALANDI ML; KRAWCZUN MS PROGRESS TOWARD AN INTERNAL CONTROL-SYSTEM FOR FRAGILE-X INDUCTION BY 5-FLUORODEOXYURIDINE IN WHOLE-BLOOD CULTURES | 3 | 6 |
| 2193 | 0 | 0 | 156 1983 PATHOLOGY 15(1):105-106 JACKY PB; SUTHERLAND GR FRAGILE-X EXPRESSION IN FIBROBLASTS | 0 | 0 |
| 2194 | 0 | 0 | 228 1984 PATHOLOGY 16(1):108-108 THEOBALD TM; HAY DA INDIVIDUAL VARIATION AND SPECIFIC COGNITIVE DEFICITS IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 2195 | 0 | 0 | 229 1984 PATHOLOGY 16(1):108-108 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 0 | 0 |
| 2196 | 7 | 10 | 1960 2000 PEDIATRIC HEMATOLOGY AND ONCOLOGY 17(7):597-600 Ferrari A; Meazza C; Casanova M Nasopharyngeal carcinoma in a boy with fragile X syndrome | 0 | 0 |
| 2197 | 0 | 0 | 488 1987 PEDIATRIC NEUROLOGY 3(5):284-287 MATSUISHI T; SHIOTSUKI Y; NIIKAWA N; KATAFUCHI Y; OTAKI E; ANDO H; YAMASHITA Y; HORIKAWA M; URABE F; KURIYA N; YAMASHITA F FRAGILE-X SYNDROME IN JAPANESE PATIENTS WITH INFANTILE-AUTISM | 4 | 6 |
| 2198 | 18 | 33 | 1010 1992 PEDIATRIC NEUROLOGY 8(4):272-274 WONG VCN; LAM STS FRAGILE X POSITIVITY IN CHINESE CHILDREN WITH AUTISTIC SPECTRUM DISORDER | 3 | 5 |
| 2199 | 12 | 14 | 1506 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 2200 | 0 | 0 | 31 1981 PEDIATRIC RESEARCH 15(4):560-560 CARPENTER NJ; LEICHTMAN LG; SAY B STUDIES ON THE FRAGILE X-SYNDROME IN SUBJECTS WITH MENTAL-RETARDATION OF UNKNOWN ETIOLOGY | 0 | 0 |
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