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    1. Kenneson, A; Warren, ST
      The female and the fragile X reviewed

      SEMINARS IN REPRODUCTIVE MEDICINE
    2. Kenneson, A; Zhang, FP; Hagedorn, CH; Warren, ST
      Reduced FMRP and increased FMR1 transcription is proportionally associatedwith CGG repeat number in intermediate-length and premutation carriers

      HUMAN MOLECULAR GENETICS
    3. Li, ZZ; Zhang, YY; Ku, L; Wilkinson, KD; Warren, ST; Feng, Y
      The fragile X mental retardation protein inhibits translation via interacting with mRNA

      NUCLEIC ACIDS RESEARCH
    4. Brown, V; Jin, P; Ceman, S; Darnell, JC; O'Donnell, WT; Tenenbaum, SA; Jin, XK; Feng, Y; Wilkinson, KD; Keene, JD; Darnell, RB; Warren, ST
      Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

      CELL
    5. Darnell, JC; Jensen, KB; Jin, P; Brown, V; Warren, ST; Darnell, RB
      Fragile X mental retardation protein targets G quartet mRNAs important forneuronal function

      CELL
    6. Hegde, MR; Chong, B; Fawkner, M; Lambiris, N; Peters, H; Kenneson, A; Warren, ST; Love, DR; McGaughran, J
      Microdeletion in the FMR-1 gene: an apparent null allele using routine clinical PCR amplification

      JOURNAL OF MEDICAL GENETICS
    7. Peier, AM; McIlwain, KL; Kenneson, A; Warren, ST; Paylor, R; Nelson, DL
      (Over)correction of FMR1 deficiency with YAC transgenics: behavioral and physical features

      HUMAN MOLECULAR GENETICS
    8. Jin, P; Warren, ST
      Understanding the molecular basis of fragile X syndrome

      HUMAN MOLECULAR GENETICS
    9. Crawford, DC; Zhang, FP; Wilson, B; Warren, ST; Sherman, SL
      Fragile X CGG repeat structures among African-Americans: identification ofa novel factor responsible for repeat instability

      HUMAN MOLECULAR GENETICS
    10. Fryns, JP; Borghgraef, M; Brown, TW; Chelly, J; Fisch, GS; Hamel, B; Hanauer, A; Lacombe, D; Luo, L; MacPherson, JN; Mandel, JL; Moraine, C; Mulley, J; Nelson, D; Oostra, B; Partington, M; Ramakers, GJA; Ropers, HH; Rousseau, F; Schwartz, C; Steinbach, P; Stoll, C; Tranebjaerg, L; Turner, G; Van Bokhoven, H; Vianna-Morgante, A; Villard, L; Warren, ST
      9th international workshop on fragile X syndrome and X-linked mental retardation

      AMERICAN JOURNAL OF MEDICAL GENETICS
    11. Ping, DS; Boekhoudt, G; Zhang, FP; Morris, A; Philipsen, S; Warren, ST; Boss, JM
      Sp1 binding is critical for promoter assembly and activation of the MCP-1 gene by tumor necrosis factor

      JOURNAL OF BIOLOGICAL CHEMISTRY
    12. Conway, KE; McConnell, BB; Bowring, CE; Donald, CD; Warren, ST; Vertino, PM
      TMS1, a novel proapoptotic caspase recruitment domain protein, is a targetof methylation-induced gene silencing in human breast cancers

      CANCER RESEARCH
    13. Tsui, SL; Dai, TN; Warren, ST; Salido, EC; Yen, PH
      Association of the mouse infertility factor DAZL1 with actively translating polyribosomes

      BIOLOGY OF REPRODUCTION
    14. Ceman, S; Nelson, R; Warren, ST
      Identification of mouse YB1/p50 as a component of the FMRP-associated mRNPparticle

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    15. Crawford, DC; Schwartz, CE; Meadows, KL; Newman, JL; Taft, LF; Gunter, C; Brown, WT; Carpenter, NJ; Howard-Peebles, PN; Monaghan, KG; Nolin, SL; Reiss, AL; Feldman, GL; Rohlfs, EM; Warren, ST; Sherman, SL
      Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population

      AMERICAN JOURNAL OF HUMAN GENETICS
    16. Warren, ST
      A new millennium and a new editor

      AMERICAN JOURNAL OF HUMAN GENETICS
    17. Coffee, B; Zhang, FP; Warren, ST; Reines, D
      Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells

      NATURE GENETICS
    18. 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

      NEUROSCIENCE
    19. Zacharias, AS; Wagener, ME; Warren, ST; Hopkins, LC
      Emery-Dreifuss muscular dystrophy

      SEMINARS IN NEUROLOGY
    20. 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 componentsof the complex

      MOLECULAR AND CELLULAR BIOLOGY
    21. Kaytor, MD; Warren, ST
      Aberrant protein deposition and neurological disease

      JOURNAL OF BIOLOGICAL CHEMISTRY
    22. GUNTER C; PARADEE W; CRAWFORD DC; MEADOWS KA; NEWMAN J; KUNST CB; NELSON DL; SCHWARTZ C; MURRAY A; MACPHERSON JN; SHERMAN SL; WARREN ST
      REEXAMINATION OF FACTORS ASSOCIATED WITH EXPANSION OF CGG REPEATS USING A SINGLE NUCLEOTIDE POLYMORPHISM IN FMR1

      Human molecular genetics (Print)
    23. SMALL K; WARREN ST
      EMERIN DELETIONS OCCURRING ON BOTH XQ28 INVERSION BACKGROUNDS

      Human molecular genetics
    24. GUNTER C; WARREN ST
      POLYMORPHISM IN THE FMR1 GENE

      Human genetics
    25. CHOU HH; TAKEMATSU H; DIAZ S; IBER J; NICKERSON E; WRIGHT KL; MUCHMORE EA; NELSON DL; WARREN ST; VARKI A
      A MUTATION IN HUMAN CMP-SIALIC ACID HYDROXYLASE OCCURRED AFTER THE HOMO-PAN DIVERGENCE

      Proceedings of the National Academy of Sciences of the United Statesof America
    26. BROWN V; SMALL K; LAKKIS L; FENG Y; GUNTER C; WILKINSON KD; WARREN ST
      PURIFIED RECOMBINANT FMRP EXHIBITS SELECTIVE RNA-BINDING AS AN INTRINSIC PROPERTY OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN

      The Journal of biological chemistry
    27. ZABAWA RE; WARREN ST
      FROM COMPANY TO COMMUNITY - AGRICULTURAL COMMUNITY-DEVELOPMENT IN MACON COUNTY, ALABAMA, 1881 TO THE NEW-DEAL

      Agricultural history
    28. WARREN ST; ZABAWA RE
      THE ORIGINS OF THE TUSKEGEE NATIONAL FOREST - 19TH-CENTURY AND 20TH-CENTURY RESETTLEMENT AND LAND-DEVELOPMENT PROGRAMS IN THE BLACK-BELT REGION OF ALABAMA

      Agricultural history
    29. WARREN ST
      TRINUCLEOTIDE REPETITION AND FRAGILE-X-SYNDROME

      Hospital practice
    30. FENG Y; ABSHER D; EBERHART DE; BROWN V; MALTER HE; WARREN ST
      FMRP ASSOCIATES WITH POLYRIBOSOMES AS AN MRNP, AND THE I304N MUTATIONOF SEVERE FRAGILE-X-SYNDROME ABOLISHES THIS ASSOCIATION

      MOLECULAR CELL
    31. SMALL K; IBER J; WARREN ST
      EMERIN DELETION REVEALS A COMMON X-CHROMOSOME INVERSION MEDIATED BY INVERTED REPEATS

      Nature genetics
    32. MALTER HE; IBER JC; WILLEMSEN R; DEGRAAFF E; TARLETON JC; LEISTI J; WARREN ST; OOSTRA BA
      CHARACTERIZATION OF THE FULL FRAGILE-X-SYNDROME MUTATION IN FETAL GAMETES

      Nature genetics
    33. SMALL K; WAGENER M; WARREN ST
      ISOLATION AND CHARACTERIZATION OF THE COMPLETE MOUSE EMERIN GENE

      Mammalian genome
    34. FENG Y; GUTEKUNST CA; EBERHART DE; YI H; WARREN ST; HERSCH SM
      FRAGILE-X MENTAL-RETARDATION PROTEIN - NUCLEOCYTOPLASMIC SHUTTLING AND ASSOCIATION WITH SOMATODENDRITIC RIBOSOMES

      The Journal of neuroscience
    35. WARREN ST
      POLYALANINE EXPANSION IN SYNPOLYDACTYLY MIGHT RESULT FROM UNEQUAL CROSSING-OVER OF HOXD13

      Science
    36. KUNST CB; LEEFLANG EP; IBER JC; ARNHEIM N; WARREN ST
      THE EFFECT OF FMR1 CGG REPEAT INTERRUPTIONS ON MUTATION FREQUENCY AS MEASURED BY SPERM TYPING

      Journal of Medical Genetics
    37. LOSEKOOT M; HOOGENDOORN E; OLMER R; JANSEN CCAM; OOSTERWIJK JC; VANDENOUWELAND AMW; HALLEY DJJ; WARREN ST; WILLEMSEN R; OOSTRA BA; BAKKER E
      PRENATAL-DIAGNOSIS OF THE FRAGILE-X-SYNDROME - LOSS OF MUTATION OWINGTO A DOUBLE RECOMBINANT OR GENE CONVERSION EVENT AT THE FMR1 LOCUS

      Journal of Medical Genetics
    38. KENNESON A; CRAMER DW; WARREN ST
      FRAGILE-X PREMUTATIONS ARE NOT A MAJOR CAUSE OF EARLY MENOPAUSE

      American journal of human genetics
    39. KENNESON A; CRAMER DW; WARREN ST
      THE FRAGILE-X PREMUTATION IS NOT A MAJOR RISK FOR EARLY MENOPAUSE

      American journal of human genetics
    40. WINKELER KA; LAKKIS L; WARREN ST
      DIFFERENTIATION OF PC12 CELLS RESULTS IN ALTERNATIVE SPLICING CHANGESIN THE FMR1 GENE LEADING TO HIGH EXPRESSION OF ISOFORM-4

      American journal of human genetics
    41. BROWN VL; SMALL K; LAKKIS L; WILKINSON KD; WARREN ST
      PURIFICATION AND CHARACTERIZATION OF THE FRAGILE-X MENTAL-RETARDATIONPROTEIN

      American journal of human genetics
    42. GUNTER C; PARADEE W; NEWMAN J; SHERMAN SL; WARREN ST
      A NOVEL BIALLELIC POLYMORPHISM IN THE FMR1 GENE SHOWS STRONG LINKAGE DISEQUILIBRIUM WITH CGG REPEATS AND FLANKING MICROSATELLITE MARKERS

      American journal of human genetics
    43. PARADEE W; RASMUSSEN D; MELIKIAN H; CONN PJ; WARREN ST
      HIPPOCAMPUS-INDEPENDENT DEFICITS IN THE FRAGILE-X MOUSE

      American journal of human genetics
    44. FENG Y; ABSHER D; BROWN V; EBERHART DE; MALTER HE; WARREN ST
      FMRP ASSOCIATES WITH POLYRIBOSOMES AS AN MRNP AND THE I304N MUTATION CAUSING SEVERE FRAGILE-X-SYNDROME ABOLISHES THIS ASSOCIATION

      American journal of human genetics
    45. SMALL K; WAGENER M; WARREN ST
      COMPLETE EMERIN DELETIONS LEADING TO EMERY-DREIFUSS MUSCULAR-DYSTROPHY OCCUR ON COMMON XQ28 INVERSION BACKGROUNDS

      American journal of human genetics
    46. LINDBLAD K; BURGESS CE; YUAN QP; LAKKIS L; HUDSON TJ; WARREN ST; SCHALLING M
      A STRATEGY FOR IDENTIFICATION OF SEQUENCE FLANKING TRINUCLEOTIDE REPEAT EXPANSION LOCI

      American journal of human genetics
    47. EBERHART DE; MALTER HE; FENG Y; WARREN ST
      THE FRAGILE-X MENTAL-RETARDATION PROTEIN IS A RIBONUCLEOPROTEIN CONTAINING BOTH NUCLEAR-LOCALIZATION AND NUCLEAR EXPORT SIGNALS

      Human molecular genetics
    48. DIMARCO SP; GLOVER TW; MILLER DE; REINES D; WARREN ST
      TRANSCRIPTION ELONGATION-FACTOR SII (TCEA) MAPS TO HUMAN-CHROMOSOME 3P22-]P21.3

      Genomics
    49. PRICE DK; ZHANG FP; ASHLEY CT; WARREN ST
      THE CHICKEN FMR1 GENE IS HIGHLY CONSERVED WITH A CCT 5'-UNTRANSLATED REPEAT AND ENCODES AN RNA-BINDING PROTEIN

      Genomics
    50. EBERHART DE; WARREN ST
      NUCLEASE SENSITIVITY OF PERMEABILIZED CELLS CONFIRMS ALTERED CHROMATIN FORMATION AT THE FRAGILE-X LOCUS

      Somatic cell and molecular genetics
    51. LACHIEWICZ AM; SPIRIDIGLIOZZI GA; MCCONKIEROSELL A; BURGESS D; FENG Y; WARREN ST; TARLETON J
      A FRAGILE-X MALE WITH A BROAD SMEAR ON SOUTHERN BLOT ANALYSIS REPRESENTING 100-500 CGG REPEATS AND NO METHYLATION AT THE EAGI SITE OF THE FMR-1 GENE

      American journal of medical genetics
    52. EBERHART DE; WARREN ST
      THE MOLECULAR-BASIS OF FRAGILE-X-SYNDROME

      Cold Spring Harbor Symposia on Quantitative Biology
    53. WARREN ST
      THE EXPANDING WORLD OF TRINUCLEOTIDE REPEATS

      Science
    54. KUNST CB; ZERYLNICK C; KARICKHOFF L; EICHLER E; BULLARD J; CHALIFOUX M; HOLDEN JJA; TORRONI A; NELSON DL; WARREN ST
      FMR1 IN GLOBAL POPULATIONS

      American journal of human genetics
    55. EICHLER EE; KUNST CB; LUGENBEEL KA; RYDER OA; DAVISON D; WARREN ST; NELSON DL
      EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT

      Nature genetics
    56. ANDERSSON B; LU F; MUZNY DM; WARREN ST; GIBBS RA
      COMPLETE SEQUENCE OF A 38.4-KB HUMAN COSMID INSERT CONTAINING THE POLYMORPHIC MARKER DXS455 FROM XQ28

      DNA sequence
    57. BIONE S; SMALL K; AKSMANOVIC VMA; DURSO M; CICCODICOLA A; MERLINI L; MORANDI L; KRESS W; YATES JRW; WARREN ST; TONIOLO D
      IDENTIFICATION OF NEW MUTATIONS IN THE EMERY-DREIFUSS MUSCULAR-DYSTROPHY GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY OF THE DISEASE

      Human molecular genetics
    58. GREGOR P; NASH SR; CARON MG; SELDIN MF; WARREN ST
      ASSIGNMENT OF THE CREATINE TRANSPORTER GENE (SLC6A8) TO HUMAN-CHROMOSOME XQ28 TELOMERIC TO G6PD

      Genomics
    59. WARREN ST; ASHLEY CT
      TRIPLET REPEAT EXPANSION MUTATIONS - THE EXAMPLE OF FRAGILE-X SYNDROME

      Annual review of neuroscience
    60. ASHLEY CT; WARREN ST
      TRINUCLEOTIDE REPEAT EXPANSION AND HUMAN-DISEASE

      Annual review of genetics
    61. FENG Y; ZHANG FP; LOKEY LK; CHASTAIN JL; LAKKIS L; EBERHART D; WARREN ST
      TRANSLATIONAL SUPPRESSION BY TRINUCLEOTIDE REPEAT EXPANSION AT FMR1

      Science
    62. KIRCHGESSNER CU; WARREN ST; WILLARD HF
      X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE

      Journal of Medical Genetics
    63. FENG Y; EBERHART DE; WARREN ST
      THE PROTEIN ABSENT IN FRAGILE-X SYNDROME (FMRP) IS A RIBOSOME-ASSOCIATED PROTEIN

      American journal of human genetics
    64. EBERHART DE; FENG Y; WARREN ST
      IDENTIFICATION OF A CYTOPLASMIC ANCHOR DOMAIN RESPONSIBLE FOR THE SUBCELLULAR-LOCALIZATION OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN, FMRP

      American journal of human genetics
    65. NELSON DL; KUNST CB; LUGENBEEL KA; RYDER OA; WARREN ST; EICHLER EE
      EVOLUTION OF THE CRYPTIC FMR1 CGG REPEAT

      American journal of human genetics
    66. WYDNER KL; MCNEIL JA; BYRON M; ZHANG F; WARREN ST; LIN F; WORMAN HJ; LAWRENCE JB
      CHROMOSOME AND NUCLEAR MAPPING OF THE HUMAN NUCLEAR LAMINS AND THE FMR-1 GENE USING FLUORESCENT IN-SITU HYBRIDIZATION

      American journal of human genetics
    67. WINKELER KA; WARREN ST
      VARIATIONS IN THE LENGTH OF THE CGG-REPEAT OF FMR-1 AFFECT GENE-EXPRESSION

      American journal of human genetics
    68. FENG Y; LAKKIS L; DEVYS D; WARREN ST
      QUANTITATIVE COMPARISON OF FMRI GENE-EXPRESSION IN NORMAL AND PREMUTATION ALLELES

      American journal of human genetics
    69. ZERYLNICK C; TORRONI A; SHERMAN SL; WARREN ST
      NORMAL VARIATION AT THE MYOTONIC-DYSTROPHY LOCUS IN GLOBAL HUMAN-POPULATIONS

      American journal of human genetics
    70. RIGGINS GJ; ZHANG FP; WARREN ST
      LACK OF IMPRINTING OF BCR

      Nature genetics
    71. RIGGINS GJ; SHERMAN SL; PHILLIPS CN; STOCK W; WESTBROOK CA; WARREN ST
      CGG-REPEAT POLYMORPHISM OF THE BCR GENE RULES OUT PREDISPOSING ALLELES LEADING TO THE PHILADELPHIA-CHROMOSOME

      Genes, chromosomes & cancer
    72. VANDENOUWELAND AMW; DEELEN WH; KUNST CB; UZIELLI MLG; NELSON DL; WARREN ST; OOSTRA BA; HALLEY DJJ
      LOSS OF MUTATION AT THE FMR1 LOCUS THROUGH MULTIPLE EXCHANGES BETWEENMATERNAL X-CHROMOSOMES

      Human molecular genetics
    73. WARREN ST
      OVERVIEW AND UPDATE ON FMR1 AND FRAGILE-X SYNDROME

      Journal of cellular biochemistry
    74. WARREN ST; NELSON DL
      ADVANCES IN MOLECULAR ANALYSIS OF FRAGILE-X SYNDROME

      JAMA, the journal of the American Medical Association
    75. KUNST CB; WARREN ST
      CRYPTIC AND POLAR VARIATION OF THE FRAGILE-X REPEAT COULD RESULT IN PREDISPOSING NORMAL ALLELES

      Cell
    76. HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; HOUSMAN DE; SCHALLING M
      TISSUE-SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE X-SYNDROME (VOL 3, PG 36, 1993)

      Nature genetics
    77. NELSON DL; WARREN ST
      TRINUCLEOTIDE REPEAT INSTABILITY - WHEN AND WHERE (VOL 4, PG 107, 1993)

      Nature genetics
    78. ASHLEY CT; SUTCLIFFE JS; KUNST CB; LEINER HA; EICHLER EE; NELSON DL; WARREN ST
      HUMAN AND MURINE FMR-1 - ALTERNATIVE SPLICING AND TRANSLATIONAL INITIATION DOWNSTREAM OF THE CGG-REPEAT

      Nature genetics
    79. NELSON DL; WARREN ST
      TRINUCLEOTIDE REPEAT INSTABILITY - WHEN AND WHERE

      Nature genetics
    80. HORNSTRA IK; NELSON DL; WARREN ST; YANG TP
      HIGH-RESOLUTION METHYLATION ANALYSIS OF THE FMR1 GENE TRINUCLEOTIDE REPEAT REGION IN FRAGILE X-SYNDROME

      Human molecular genetics
    81. GORLIN JB; HENSKE E; WARREN ST; KUNST CB; DURSO M; PALMIERI G; HARTWIG JH; BRUNS G; KWIATKOWSKI DJ
      ACTIN-BINDING PROTEIN (ABP-280) FILAMIN GENE (FLN) MAPS TELOMERIC TO THE COLOR-VISION LOCUS (R GCP) AND CENTROMERIC TO G6PD IN XQ28/

      Genomics
    82. EICHLER EE; ASHLEY C; WARREN ST; RICHARDS S; GIBBS RA; NELSON DL
      STRUCTURE OF THE FMR1 GENE AT XQ27.3

      Cytogenetics and cell genetics
    83. ONODERA O; KOBAYASHI H; KANEKO K; WARREN ST; MIYATAKE T; TSUJI S
      ISOLATION OF 11 NEW EXPRESSED SEQUENCE-TAGGED SITES FROM HUMAN-CHROMOSOME REGION XQ24-]QTER

      Cytogenetics and cell genetics
    84. KANEKO K; WARREN ST; MIYATAKE T; TSUJI S
      ISOLATION OF 353 NOTL-LINKING CLONES AND 62 DNA MARKERS (DXS607-DXS668) FROM HUMAN-CHROMOSOME XQ24-]QTER

      Cytogenetics and cell genetics
    85. ASHLEY CT; WILKINSON KD; REINES D; WARREN ST
      FMR1 PROTEIN - CONSERVED RNP FAMILY DOMAINS AND SELECTIVE RNA-BINDING

      Science
    86. ASHLEY CT; WILKINSON KD; WARREN ST
      FMR-1 IS A RNA-BINDING PROTEIN WITH 2 HIGHLY CONSERVED FUNCTIONAL DOMAINS

      American journal of human genetics
    87. ZERYLNICK C; KUNST C; TORRONI A; SHERMAN SL; WARREN ST
      NORMAL TRINUCLEOTIDE REPEAT VARIATION AT THE FMR-1, DM, AND HD LOCI IN HUMAN-POPULATIONS

      American journal of human genetics
    88. KUNST C; KARICKHOFF L; ZERYLNICK C; HOLDEN J; NELSON DL; SHERMAN SL; WARREN ST
      IDENTIFICATION OF 2 POLYMORPHIC LOCI NEAR FMR-1 AND DEMONSTRATION OF MARKED LINKAGE DISEQUILIBRIUM WITHIN NORMAL AND BETWEEN ABNORMAL CGG-REPEAT LENGTHS

      American journal of human genetics
    89. HOLDEN JJA; CHALIFOUX M; WING M; WHITE BN; GLOVER T; STEIN C; ZEESMAN S; CHITAYAT D; TESHIMA I; BROWN C; WARREN ST
      THE FRAGILE-X SYNDROME AND PREMATURE MENOPAUSE

      American journal of human genetics
    90. EBERHART DE; WARREN ST
      ABNORMAL CHROMATIN STRUCTURE ASSOCIATED WITH THE FULL FRAGILE-X MUTATION

      American journal of human genetics
    91. FENG Y; WARREN ST
      FMR-1 TRANSCRIPTIONAL STUDIES DEMONSTRATE NO DIFFERENCE BETWEEN NORMAL AND PREMUTATION ALLELES

      American journal of human genetics
    92. IBER H; WARREN ST
      PROTEIN-BINDING TO THE 5' UNTRANSLATED REGION OF FMR-1 MESSENGER-RNA

      American journal of human genetics
    93. PRICE DK; ASHLEY CT; LEINER HA; WARREN ST
      THE 3' UNTRANSLATED REGION OF FMR-1 IS HIGHLY CONSERVED AND IDENTIFIES GENES WITH SIMILAR 3' UTRS FROM YEAST TO HUMANS

      American journal of human genetics
    94. RIGGINS GJ; SHERMAN SL; PHILLIPS CN; STOCK W; WESTBROOK CA; WARREN ST
      A POLYMORPHIC CGG-REPEAT OF THE BCR GENE DEMONSTRATES A LACK OF IMPRINTING AND ALLELIC ASSOCIATION WITH PH1-POSITIVE LEUKEMIA

      American journal of human genetics
    95. MALTER HE; KARICKHOFF L; TUCKER M; WIKER S; WRIGHT G; MORTON P; MASSEY JB; ELSNER C; WARREN ST
      SINGLE-CELL ANALYSIS OF THE REPEAT EXPANSION MUTATION ASSOCIATED WITHFRAGILE X-SYNDROME

      American journal of human genetics


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Documento generato il 26/02/20 alle ore 06:21:00