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    1. Chun, WJ; Lesort, M; Tucholski, J; Faber, PW; MacDonald, ME; Ross, CA; Johnson, GVW
      Tissue transglutaminase selectively modifies proteins associated with truncated mutant huntingtin in intact cells

      NEUROBIOLOGY OF DISEASE
    2. Auerbach, W; Hurlbert, MS; Hilditch-Maguire, P; Wadghiri, YZ; Wheeler, VC; Cohen, SI; Joyner, AL; MacDonald, ME; Turnbull, DH
      The HD mutation causes progressive lethal neurological disease in mice expressing reduced levels of huntingtin

      HUMAN MOLECULAR GENETICS
    3. Gomez-Tortosa, E; MacDonald, ME; Friend, JC; Taylor, SAM; Weiler, LJ; Cupples, LA; Srinidhi, J; Gusella, JF; Bird, ED; Vonsattel, JP; Myers, RH
      Quantitative neuropathological changes in presymptomatic Huntington's disease

      ANNALS OF NEUROLOGY
    4. Zuccato, C; Ciammola, A; Rigamonti, D; Leavitt, BR; Goffredo, D; Conti, L; MacDonald, ME; Friedlander, RM; Silani, V; Hayden, MR; Timmusk, T; Sipione, S; Cattaneo, E
      Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease

      SCIENCE
    5. DeStefano, AL; Golbe, LI; Mark, MH; Lazzarini, AM; Maher, NE; Saint-Hilaire, M; Feldman, RG; Guttman, M; Watts, RL; Suchowersky, O; Lafontaine, AL; Labelle, N; Lew, MF; Waters, CH; Growdon, JH; Singer, C; Currie, LJ; Wooten, GF; Vieregge, P; Pramstaller, PP; Klein, C; Hubble, JP; Stacy, M; Montgomery, E; MacDonald, ME; Gusella, JF; Myers, RH
      Genome-wide scan for Parkinson's disease: The GenePD study

      NEUROLOGY
    6. MacDonald, ME; Hall, BK
      Altered timing of the extracellular-matrix-mediated epithelial-mesenchymalinteraction that initiates mandibular skeletogenesis in three inbred strains of mice: Development, heterochrony, and evolutionary change in morphology

      JOURNAL OF EXPERIMENTAL ZOOLOGY
    7. MacDonald, ME; Passani, L; Hilditch-Maguire, P
      Huntingtin-associated proteins

      MOLECULAR MECHANISMS OF NEURODEGENERATIVE DISEASES
    8. Gusella, JF; MacDonald, ME
      Molecular genetics: Unmasking polyglutamine triggers in neurodegenerative disease

      NATURE REVIEWS NEUROSCIENCE
    9. Wheeler, VC; White, JK; Gutekunst, CA; Vrbanac, V; Weaver, M; Li, XJ; Li, SH; Yi, H; Vonsattel, JP; Gusella, JF; Hersch, S; Auerbach, W; Joyner, AL; MacDonald, ME
      Long glutamine tracts cause nuclear localization of a novel form of huntingtin in medium spiny striatal neurons in Hdh(Q92) and Hdh(Q111) knock-in mice

      HUMAN MOLECULAR GENETICS
    10. Hilditch-Maguire, P; Trettel, F; Passani, LA; Auerbach, A; Persichetti, F; MacDonald, ME
      Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles

      HUMAN MOLECULAR GENETICS
    11. Trettel, F; Rigamonti, D; Hilditch-Maguire, P; Wheeler, VC; Sharp, AH; Persichetti, F; Cattaneo, E; MacDonald, ME
      Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells

      HUMAN MOLECULAR GENETICS
    12. Passani, LA; Bedford, MT; Faber, PW; McGinnis, KM; Sharp, AH; Gusella, JF; Vonsattel, JP; MacDonald, ME
      Huntingtin's WW domain partners in Huntington's disease post-mortem brain fulfill genetic criteria for direct involvement in Huntington's disease pathogenesis

      HUMAN MOLECULAR GENETICS
    13. MacDonald, ME; Alexanian, A; York, RA; Popovic, Z; Grossman, EN
      Spectral transmittance of lossy printed resonant-grid terahertz bandpass filters

      IEEE TRANSACTIONS ON MICROWAVE THEORY AND TECHNIQUES
    14. Plant, MR; MacDonald, ME; Grad, LI; Ritchie, SJ; Richman, JM
      Locally released retinoic acid repatterns the first branchial arch cartilages in vivo

      DEVELOPMENTAL BIOLOGY
    15. MacDonald, ME
      Gadzooks!

      NATURE GENETICS
    16. Persichetti, F; Trettel, F; Huang, CC; Fraefel, C; Timmers, HTM; Gusella, JF; MacDonald, ME
      Mutant huntingtin forms in vivo complexes with distinct context-dependent conformations of the polyglutamine segment

      NEUROBIOLOGY OF DISEASE
    17. Leeflang, EP; Tavare, S; Marjoram, P; Neal, COS; Srinidhi, J; MacFarlane, H; MacDonald, ME; Gusella, JF; de Young, M; Wexler, NS; Arnheim, N
      Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism (vol 8, pg 173, 1999)

      HUMAN MOLECULAR GENETICS
    18. Leeflang, EP; Tavare, S; Marjoram, P; Neal, COS; Srinidhi, J; MacDonald, ME; de Young, M; Wexler, NS; Gusella, JF; Arnheim, N
      Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism

      HUMAN MOLECULAR GENETICS
    19. Wheeler, VC; Auerbach, W; White, JK; Srinidhi, J; Auerbach, A; Ryan, A; Duyao, MP; Vrbanac, V; Weaver, M; Gusella, JF; Joyner, AL; MacDonald, ME
      Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse

      HUMAN MOLECULAR GENETICS
    20. MacDonald, ME; Vonsattel, MP; Shrinidhi, J; Couropmitree, NN; Cupples, LA; Bird, ED; Gusella, JF; Myers, RH
      Evidence for the GluR6 gene associated with younger onset age of Huntington's disease

      NEUROLOGY
    21. Faber, PW; Alter, JR; MacDonald, ME; Hart, AC
      Polyglutamine-mediated dysfunction and apoptotic death of a Caenorhabditiselegans sensory neuron

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    22. FABER PW; BARNES GT; SRINIDHI J; CHEN JM; GUSELLA JF; MACDONALD ME
      HUNTINGTIN INTERACTS WITH A FAMILY OF WW DOMAIN PROTEINS

      Human molecular genetics (Print)
    23. GUSELLA JF; MACDONALD ME
      HUNTINGTIN - A SINGLE BAIT HOOKS MANY SPECIES

      Current opinion in neurobiology
    24. JACKSON GR; SALECKER I; DONG XZ; YAO X; ARNHEIM N; FABER PW; MACDONALD ME; ZIPURSKY SL
      POLYGLUTAMINE-EXPANDED HUMAN HUNTINGTIN TRANSGENES INDUCE DEGENERATION OF DROSOPHILA PHOTORECEPTOR NEURONS

      Neuron (Cambridge, Mass.)
    25. Huang, CC; Faber, PW; Persichetti, F; Mittal, V; Vonsattel, JP; MacDonald, ME; Gusella, JF
      Amyloid formation by mutant huntingtin: Threshold, progressivity and recruitment of normal polyglutamine proteins

      SOMATIC CELL AND MOLECULAR GENETICS
    26. PENNEY JB; VONSATTEL JP; MACDONALD ME; GUSELLA JF; MYERS RH
      ON THE PATHOLOGICAL PROGRESSION OF HUNTINGTONS-DISEASE - REPLY

      Annals of neurology
    27. GUSELLA JF; PERSICHETTI F; MACDONALD ME
      THE GENETIC-DEFECT CAUSING HUNTINGTONS-DISEASE - REPEATED IN OTHER CONTEXTS

      Molecular medicine
    28. WHITE JK; AUERBACH W; DUYAO MP; VONSATTEL JP; GUSELLA JF; JOYNER AL; MACDONALD ME
      HUNTINGTIN IS REQUIRED FOR NEUROGENESIS AND IS NOT IMPAIRED BY THE HUNTINGTONS-DISEASE CAG EXPANSION

      Nature genetics
    29. MCNEIL SM; NOVELLETTO A; SRINIDHI J; BARNES G; KORNBLUTH I; ALTHERR MR; WASMUTH JJ; GUSELLA JF; MACDONALD ME; MYERS RH
      REDUCED PENETRANCE OF THE HUNTINGTONS-DISEASE MUTATION

      Human molecular genetics
    30. PRIBILL I; BARNES GT; CHEN JM; CHURCH D; BUCKLER A; BAXENDALE S; BATES GP; LEHRACH H; GUSELLA MJ; DUYAO MP; AMBROSE CM; GUSELLA JF; MACDONALD ME
      EXON TRAPPING AND SEQUENCE-BASED METHODS OF GENE FINDING IN TRANSCRIPT MAPPING OF HUMAN 4P16.3

      Somatic cell and molecular genetics
    31. JONES RM; MACDONALD ME; BRANDA J; ALTHERR MR; LOUIS DN; SCHMIDT EV
      ASSIGNMENT OF THE HUMAN GENE ENCODING EUKARYOTIC INITIATION-FACTOR 4E(EIF4E) TO THE REGION Q21-25 ON CHROMOSOME-4

      Somatic cell and molecular genetics
    32. PRILLER J; SCHERZER CR; FABER PW; MACDONALD ME; YOUNG AB
      FRATAXIN GENE OF FRIEDREICHS-ATAXIA IS TARGETED TO MITOCHONDRIA

      Annals of neurology
    33. PENNEY JB; VONSATTEL JP; MACDONALD ME; GUSELLA JF; MYERS RH
      CAG REPEAT NUMBER GOVERNS THE DEVELOPMENT RATE OF PATHOLOGY IN HUNTINGTONS-DISEASE

      Annals of neurology
    34. FERRANTE RJ; GUTEKUNST CA; PERSICHETTI F; MCNEIL SM; KOWALL NW; GUSELLA JF; MACDONALD ME; BEAL MF; HERSCH SM
      HETEROGENEOUS TOPOGRAPHIC AND CELLULAR-DISTRIBUTION OF HUNTINGTON EXPRESSION IN THE NORMAL HUMAN NEOSTRIATUM

      The Journal of neuroscience
    35. FERRANTE RJ; GUTEKUNST CA; PERSICHETTI F; KOWALL NW; GUSELLA JF; BEAL F; MACDONALD ME; HERSCH SM
      HETEROGENEOUS EXPRESSION OF HUNTINGTIN IMMUNOREACTIVITY IN THE NORMALHUMAN NEOSTRIATUM

      Neurology
    36. TAMMINGA CA; SCHWARCZ R; MACDONALD ME
      HUNTINGTONS-DISEASE - FROM DISEASE TO GENE

      The American journal of psychiatry
    37. CALZONETTI T; WHITE JK; WEAVER MA; VRBANAC V; GUSELLA JF; MACDONALD ME
      HUNTINGTIN IS REQUIRED AT SEVERAL STAGES OF MURINE EMBRYOGENESIS

      American journal of human genetics
    38. DOMPE C; FABER PW; CARLEE LM; CALZONETTI T; BARNES GT; GUSELLA JF; MACDONALD ME
      HUNTINGTONS-DISEASE - NEW MOUSE HUNGTINTIN INTERACTING PROTEINS

      American journal of human genetics
    39. WHEELER VC; RYAN A; AUERBACH A; CALZONETTI T; DUYAO MP; WHITE JK; VRBANAC V; ALLEN MJ; GUSELLA JF; SRINIDHI J; JOYNER AL; MACDONALD ME
      INHERITANCE OF THE HUNTINGTONS-DISEASE CAG REPEAT IN MICE

      American journal of human genetics
    40. WHITE JK; AUERBACH W; CALZONETTI T; WEAVER M; VRBANAC V; VONSATTEL JP; GUSELLA JF; JOYNER AL; MACDONALD ME
      HUNTINGTIN FUNCTION IS REQUIRED FOR MOUSE-BRAIN DEVELOPMENT AND IS NOT IMPAIRED BY THE HUNTINGTONS-DISEASE CAG EXPANSION MUTATION

      American journal of human genetics
    41. PERSICHETTI F; CARLEE L; FABER PW; MCNEIL SM; AMBROSE CM; SRINIDHI J; ANDERSON M; BARNES GT; GUSELLA JF; MACDONALD ME
      DIFFERENTIAL EXPRESSION OF NORMAL AND MUTANT HUNTINGTONS-DISEASE GENEALLELES

      Neurobiology of disease
    42. MACDONALD ME; GUSELLA JF
      HUNTINGTONS-DISEASE - TRANSLATING A CAG REPEAT INTO A PATHOGENIC MECHANISM

      Current opinion in neurobiology
    43. LIU R; PAXTON WA; CHOE S; CERADINI D; MARTIN SR; HORUK R; MACDONALD ME; STUHLMANN H; KOUP RA; LANDAU NR
      HOMOZYGOUS DEFECT IN HIV-1 CORECEPTOR ACCOUNTS FOR RESISTANCE OF SOMEMULTIPLY-EXPOSED INDIVIDUALS TO HIV-1 INFECTION

      Cell
    44. GUSELLA JF; MCNEIL S; PERSICHETTI F; SRINIDHI J; NOVELLETTO A; BIRD E; FABER P; VONSATTEL JP; MYERS RH; MACDONALD ME
      HUNTINGTONS-DISEASE

      Cold Spring Harbor Symposia on Quantitative Biology
    45. MACDONALD ME; DUYAO M; CALZONETTI T; AUERBACH A; RYAN A; BARNES G; WHITE JK; AUERBACH W; VONSATTEL JP; GUSELLA JF; JOYNER AL
      TARGETED INACTIVATION OF THE MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG HDH

      Cold Spring Harbor Symposia on Quantitative Biology
    46. GUSELLA JF; MACDONALD ME
      TRINUCLEOTIDE INSTABILITY - A REPEATING THEME IN HUMAN INHERITED DISORDERS

      Annual review of medicine
    47. DUYAO MP; AUERBACH A; RYAN A; WHITE JK; AUERBACH W; MCNEIL S; GUSELLA JF; JOYNER A; MACDONALD ME
      HUNTINGTONS-DISEASE AND MOUSE MODELS

      Journal of neurochemistry
    48. PREMONT RT; MACRAE AD; STOFFEL RH; CHUNG NJ; PITCHER JA; AMBROSE C; INGLESE J; MACDONALD ME; LEFKOWITZ RJ
      CHARACTERIZATION OF THE G-PROTEIN-COUPLED RECEPTOR KINASE GRK4 - IDENTIFICATION OF 4 SPLICE VARIANTS

      The Journal of biological chemistry
    49. RUBIO A; STEINBERG K; FIGLEWICZ DA; MACDONALD ME; GREENAMYRE T; HAMILL R; SHOULSON I; POWERS JM
      COEXISTENCE OF HUNTINGTONS-DISEASE AND FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS - CASE PRESENTATION

      Acta Neuropathologica
    50. PERSICHETTI F; AMBROSE CM; GE P; MCNEIL SM; SRINIDHI J; ANDERSON MA; JENKINS B; BARNES GT; DUYAO MP; KANALEY L; WEXLER NS; MYERS RH; BIRD ED; VONSATTEL JP; MACDONALD ME; GUSELLA JF
      NORMAL AND EXPANDED HUNTINGTONS-DISEASE GENE ALLELES PRODUCE DISTINGUISHABLE PROTEINS DUE TO TRANSLATION ACROSS THE CAG REPEAT

      Molecular medicine
    51. GUSELLA JF; MACDONALD ME
      HUNTINGTONS-DISEASE

      Seminars in cell biology
    52. LEEFLANG EP; ZHANG L; TAVARE S; HUBERT R; SRINIDHI J; MACDONALD ME; MYERS RH; DEYOUNG M; WEXLER NS; GUSELLA JF; ARNHEIM N
      SINGLE SPERM ANALYSIS OF THE TRINUCLEOTIDE REPEATS IN THE HUNTINGTONS-DISEASE GENE - QUANTIFICATION OF THE MUTATION FREQUENCY-SPECTRUM

      Human molecular genetics
    53. LANDWEHRMEYER GB; MCNEIL SM; DURE LS; GE P; AIZAWA H; HUANG Q; AMBROSE CM; DUYAO MP; BIRD ED; BONILLA E; DEYOUNG M; AVILAGONZALES AJ; WEXLER NS; DIFIGLIA M; GUSELLA JF; MACDONALD ME; PENNEY JB; YOUNG AB; VONSATTEL JP
      HUNTINGTONS-DISEASE GENE - REGIONAL AND CELLULAR EXPRESSION IN BRAIN OF NORMAL AND AFFECTED INDIVIDUALS

      Annals of neurology
    54. DUYAO MP; AUERBACH AB; RYAN A; PERSICHETTI F; BARNES GT; MCNEIL SM; GE P; VONSATTEL JP; GUSELLA JF; JOYNER AL; MACDONALD ME
      INACTIVATION OF THE MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG HDH

      Science
    55. MACDONALD ME; GROSSMAN EN
      NIOBIUM MICROBOLOMETERS FOR FAR-INFRARED DETECTION

      IEEE transactions on microwave theory and techniques
    56. NOVELLETTO A; PERSICHETTI F; SABBADINI G; MANDICH P; BELLONE E; AJMAR F; SQUITIERI F; CAMPANELLA G; BOZZA A; MACDONALD ME; GUSELLA JF; FRONTALI M
      POLYMORPHISM ANALYSIS OF THE HUNTINGTIN GENE IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE

      Human molecular genetics
    57. HUMMERICH H; BAXENDALE S; MOTT R; KIRBY SF; MACDONALD ME; GUSELLA J; LEHRACH H; BATES GP
      DISTRIBUTION OF TRINUCLEOTIDE REPEAT SEQUENCES ACROSS A 2-MBP REGION CONTAINING THE HUNTINGTONS-DISEASE GENE

      Human molecular genetics
    58. NOVELLETTO A; PERSICHETTI F; SABBADINI G; MANDICH P; BELLONE E; AJMAR F; PERGOLA M; DELSENNO L; MACDONALD ME; GUSELLA JF; FRONTALI M
      ANALYSIS OF THE TRINUCLEOTIDE REPEAT EXPANSION IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE

      Human molecular genetics
    59. GROSSON CLS; MACDONALD ME; DUYAO MP; AMBROSE CM; ROFFLERTARLOV S; GUSELLA JF
      SYNTENY CONSERVATION OF THE HUNTINGTONS-DISEASE GENE AND SURROUNDING LOCI ON MOUSE CHROMOSOME-5

      Mammalian genome
    60. BARNES GT; DUYAO MP; AMBROSE CM; MCNEIL S; PERSICHETTI F; SRINIDHI J; GUSELLA JF; MACDONALD ME
      MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG (HDH)

      Somatic cell and molecular genetics
    61. AMBROSE CM; DUYAO MP; BARNES G; BATES GP; LIN CS; SRINIDHI J; BAXENDALE S; HUMMERICH H; LEHRACH H; ALTHERR M; WASMUTH J; BUCKLER A; CHURCH D; HOUSMAN D; BERKS M; MICKLEM G; DURBIN R; DODGE A; READ A; GUSELLA J; MACDONALD ME
      STRUCTURE AND EXPRESSION OF THE HUNTINGTONS-DISEASE GENE - EVIDENCE AGAINST SIMPLE INACTIVATION DUE TO AN EXPANDED CAG REPEAT

      Somatic cell and molecular genetics
    62. GUSELLA JF; MACDONALD ME
      HUNTINGTONS-DISEASE AND REPEATING TRINUCLEOTIDES

      The New England journal of medicine
    63. DURE LS; LANDWEHRMEYER GB; GOLDEN J; MCNEIL SM; GE P; AIZAWA H; HUANG Q; AMBROSE CM; DUYAO MP; BIRD ED; DIFIGLIA M; GUSELLA JF; MACDONALD ME; PENNEY JB; YOUNG AB; VONSATTEL JP
      IT15 GENE-EXPRESSION IN FETAL HUMAN BRAIN

      Brain research
    64. MYERS RH; MACDONALD ME; GUSELLA JF
      DISCREPANCY RESOLVED

      Nature genetics
    65. MYERS RH; MACDONALD ME; KOROSHETZ WJ; DUYAO MP; AMBROSE CM; TAYLOR SAM; BARNES G; SRINIDHI J; LIN CS; WHALEY WL; LAZZARINI AM; SCHWARZ M; WOLFF G; BIRD ED; VONSATTEL JPG; GUSELLA JF
      DE-NOVO EXPANSION OF A (CAG)(N) REPEAT IN SPORADIC HUNTINGTONS-DISEASE

      Nature genetics
    66. SNELL RG; MACMILLAN JC; CHEADLE JP; FENTON I; LAZAROU LP; DAVIES P; MACDONALD ME; GUSELLA JF; HARPER PS; SHAW DJ
      RELATIONSHIP BETWEEN TRINUCLEOTIDE REPEAT EXPANSION AND PHENOTYPIC VARIATION IN HUNTINGTONS-DISEASE

      Nature genetics
    67. BAXENDALE S; MACDONALD ME; MOTT R; FRANCIS F; LIN C; KIRBY SF; JAMES M; ZEHETNER G; HUMMERICH H; VALDES J; COLLINS FS; DEAVEN LJ; GUSELLA JF; LEHRACH H; BATES GP
      A COSMID CONTIG AND HIGH-RESOLUTION RESTRICTION MAP OF THE 2 MEGABASEREGION CONTAINING THE HUNTINGTONS-DISEASE GENE

      Nature genetics
    68. DUYAO MP; TAYLOR SAM; BUCKLER AJ; AMBROSE CM; LIN C; GROOT N; CHURCH D; BARNES G; WASMUTH JJ; HOUSMAN DE; MACDONALD ME; GUSELLA JF
      A GENE FROM CHROMOSOME-4P16.3 WITH SIMILARITY TO A SUPERFAMILY OF TRANSPORTER PROTEINS

      Human molecular genetics
    69. MACDONALD ME; BARNES G; SRINIDHI J; DUYAO MP; AMBROSE CM; MYERS RH; GRAY J; CONNEALLY PM; YOUNG A; PENNEY J; SHOULSON I; HOLLINGSWORTH Z; KOROSHETZ W; BIRD E; VONSATTEL JP; BONILLA E; MOSCOWITZ C; PENCHASZADEH G; BRZUSTOWICZ L; ALVIR J; CONDE JB; CHA JH; DURE L; GOMEZ F; RAMOSARROYO M; SANCHEZRAMOS J; SNODGRASS SR; DEYOUNG M; WEXLER NS; MACFARLANE H; ANDERSON MA; JENKINS B; GUSELLA JF
      GAMETIC BUT NOT SOMATIC INSTABILITY OF CAG REPEAT LENGTH IN HUNTINGTONS-DISEASE

      Journal of Medical Genetics
    70. GUSELLA JF; MACDONALD ME; AMBROSE CM; DUYAO MP
      MOLECULAR-GENETICS OF HUNTINGTONS-DISEASE

      Archives of neurology
    71. MYERS RH; MACDONALD ME; KOROSHETZ WJ; DUYAO MP; AMBROSE CM; TAYLOR SA; BARNES G; SRINIDHI J; LIN CS; WHALEY WL; LAZZARINI AM; SCHWARZ M; WOLFF G; BIRD ED; VONSATTEL JPG; GUSELLA JF
      DE-NOVO EXPANSION OF A CAG REPEAT IN SPORADIC HUNTINGTONS-DISEASE

      American journal of human genetics
    72. HUBERT R; MACDONALD ME; GUSELLA JF; ARNHEIM N
      LINKAGE ANALYSIS OF THE RECOMBINATION HOTSPOT NEAR THE HUNTINGTONS-DISEASE GENE USING SPERM TYPING

      American journal of human genetics
    73. AMBROSE CM; DUYAO MP; CHURCH DM; DARIGO KL; BARNES G; BUCKLER AJ; GUSELLA JF; MACDONALD ME
      GENOMIC STRUCTURE OF THE HUNTINGTONS-DISEASE GENE, IT15

      American journal of human genetics
    74. DUYAO MP; AMBROSE CM; MYERS RH; NOVELLETTO A; PERSICHETTI E; BARNES G; SRINIDHI J; BIRD E; VONSATTEL JP; MACDONALD ME; GUSELLA JF
      TRINUCLEOTIDE REPEAT LENGTH - INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE

      American journal of human genetics


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Documento generato il 12/08/20 alle ore 15:04:18