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    1. Cuajungco, MP; Leyne, M; Mull, J; Gill, SP; Gusella, JF; Slaugenhaupt, SA
      Cloning, characterization, and genomic structure of the mouse Ikbkap gene

      DNA AND CELL BIOLOGY
    2. 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
    3. 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
    4. Slaugenhaupt, SA; Blumenfeld, A; Gill, SP; Leyne, M; Mull, J; Cuajungco, MP; Liebert, CB; Chadwick, B; Idelson, M; Reznik, L; Robbins, CM; Makalowska, I; Brownstein, MJ; Krappmann, D; Scheidereit, C; Maayan, C; Axelrod, FB; Gusella, JF
      Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia

      AMERICAN JOURNAL OF HUMAN GENETICS
    5. Gusella, JF; MacDonald, ME
      Molecular genetics: Unmasking polyglutamine triggers in neurodegenerative disease

      NATURE REVIEWS NEUROSCIENCE
    6. 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
    7. 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
    8. Chadwick, BP; Leyne, M; Gill, S; Liebert, CB; Mull, J; Mezey, E; Robbins, CM; Pinkett, HW; Makalowska, I; Maayan, C; Blumenfeld, A; Axelrod, FB; Brownstein, M; Gusella, JF; Slaugenhaupt, SA
      Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31

      MAMMALIAN GENOME
    9. Lim, DJ; Rubenstein, AE; Evans, DG; Jacks, T; Seizinger, BG; Baser, ME; Beebe, D; Brackmann, DE; Chiocca, EA; Fehon, RG; Giovannini, M; Glazer, R; Gusella, JF; Gutmann, DH; Korf, B; Lieberman, F; Martuza, R; McClatchey, AI; Parry, DM; Pulst, SM; Ramesh, V; Ramsey, WJ; Ratner, N; Rutkowski, JL; Ruttledge, M; Weinstein, DE
      Advances in neurofibromatosis 2 (NF2): A workshop report

      JOURNAL OF NEUROGENETICS
    10. Castells, A; Gusella, JF; Ramesh, V; Rustgi, AK
      A region of deletion on chromosome 22q13 is common to human breast and colorectal cancers

      CANCER RESEARCH
    11. 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
    12. 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
    13. 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
    14. 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
    15. Chadwick, BP; Mull, J; Helbling, LA; Gill, S; Leyne, M; Robbins, CM; Pinkett, HW; Makalowska, I; Maayan, C; Blumenfeld, A; Axelrod, FB; Brownstein, N; Gusella, JF; Slaugenhaupt, SA
      Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familiar dysautonomia candidate region on 9q31

      GENOMICS
    16. Gusella, JF; Ramesh, V; MacCollin, M; Jacoby, LB
      Merlin: the neurofibromatosis 2 tumor suppressor

      BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER
    17. Zhu, JJG; Maruyama, T; Jacoby, LB; Herman, JG; Gusella, JF; Black, PM; Wu, JK
      Clonal analysis of a case of multiple meningiomas using multiple moleculargenetic approaches: Pathology case report

      NEUROSURGERY
    18. 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
    19. Castells, A; Ino, Y; Louis, DN; Ramesh, V; Gusella, JF; Rustgi, AK
      Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer

      GASTROENTEROLOGY
    20. Slaugenhaupt, SA; Acierno, JS; Helbling, LA; Bove, C; Goldin, E; Bach, G; Schiffmann, R; Gusella, JF
      Mapping of the mucolipidosis type IV gene to chromosome 19p and definitionof founder haplotypes

      AMERICAN JOURNAL OF HUMAN GENETICS
    21. Blumenfeld, A; Slaugenhaupt, SA; Liebert, CB; Temper, V; Maayan, C; Gill, S; Lucente, DE; Idelson, M; MacCormack, K; Monahan, MA; Mull, J; Leyne, M; Mendillo, M; Schiripo, T; Mishori, E; Breakefield, X; Axelrod, FB; Gusella, JF
      Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31

      AMERICAN JOURNAL OF HUMAN GENETICS
    22. JAMES MF; GONZALEZAGOSTI C; PINNEY D; GUSELLA JF; HARTWIG JH; RAMESH V
      THE NEUROFIBROMATOSIS-2 PROTEIN, MERLIN, BINDS ACTIN DIRECTLY

      Molecular biology of the cell
    23. GONZALEZAGOSTI C; WIEDERHOLD T; HERNDON ME; GUSELLA JF; RAMESH V
      HOMOTYPIC AND HETEROTYPIC INTERACTION OF MERLIN AND THE ERM PROTEINS,DIFFERENCES BETWEEN ISOFORM-1 AND ISOFORM-2 OF MERLIN

      Molecular biology of the cell
    24. 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)
    25. GUSELLA JF; MACDONALD ME
      HUNTINGTIN - A SINGLE BAIT HOOKS MANY SPECIES

      Current opinion in neurobiology
    26. GREEN T; HEINEMANN SF; GUSELLA JF
      MOLECULAR NEUROBIOLOGY AND GENETICS - INVESTIGATION OF NEURAL FUNCTION AND DYSFUNCTION

      Neuron
    27. STEMMERRACHAMIMOV AO; JACOBY LB; GUSELLA JF; RAMESH V; LOUIS DN
      UNIVERSAL ABSENCE OF MERLIN, BUT NOT ERM FAMILY MEMBERS, IN SCHWANNOMAS

      Modern pathology
    28. MCCLATCHEY AI; SAOTOME I; MERCER K; CROWLEY D; GUSELLA JF; BRONSON RT; JACKS T
      MICE HETEROZYGOUS FOR A MUTATION AT THE NF2 TUMOR-SUPPRESSOR LOCUS DEVELOP A RANGE OF HIGHLY METASTATIC TUMORS

      Genes & development
    29. 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
    30. Cowley, GS; Murthy, AE; Parry, DM; Schneider, G; Korf, B; Upadhyaya, M; Harper, P; MacCollin, M; Bernards, A; Gusella, JF
      Genetic variation in the 3 ' untranslated region of the neurofibromatosis 1 gene: Application to unequal allelic expression

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

      Annals of neurology
    32. Chadwick, BP; Helbling, LA; Angrist, M; Chakravarti, A; Gusella, JF; Slaugenhaupt, SA
      Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR

      CYTOGENETICS AND CELL GENETICS
    33. Stemmer-Rachamimov, AO; Ino, Y; Lim, ZY; Jacoby, LB; MacCollin, M; Gusella, JF; Ramesh, V; Louis, DN
      Loss of the NF2 gene and merlin occur by the tumorlet stage of schwannoma development in neurofibromatosis 2

      JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
    34. GUSELLA JF
      INFLAMMATORY BOWEL-DISEASE - IS IT IN THE GENES

      Gastroenterology (New York, N.Y. 1943)
    35. Rutter, JL; Mitchell, TI; Buttice, G; Meyers, J; Gusella, JF; Ozelius, LJ; Brinckerhoff, CE
      A single nucleotide polymorphism in the matrix metalloproteinase-1 promoter creates an Ets binding site and augments transcription

      CANCER RESEARCH
    36. GUSELLA JF; PERSICHETTI F; MACDONALD ME
      THE GENETIC-DEFECT CAUSING HUNTINGTONS-DISEASE - REPEATED IN OTHER CONTEXTS

      Molecular medicine
    37. 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
    38. OZELIUS LJ; HEWETT JW; PAGE CE; BRESSMAN SB; KRAMER PL; SHALISH C; DELEON D; BRIN MF; RAYMOND D; COREY DP; FAHN S; RISCH NJ; BUCKLER AJ; GUSELLA JF; BREAKEFIELD XO
      THE EARLY-ONSET TORSION DYSTONIA GENE (DYT1) ENCODES AN ATP BINDING-PROTEIN

      Nature genetics
    39. GONZALEZAGOSTI C; MURTHY A; CORDERO E; PINNEY D; CANDIA C; SOLOMON F; GUSELLA JF; RAMESH V
      IDENTIFICATION AND CHARACTERIZATION OF A NOVEL INTERACTOR FOR MERLIN THAT INTERACTS WITH THE ERM PROTEINS

      Molecular biology of the cell
    40. OZELIUS LJ; HEWETT J; KRAMER P; BRESSMAN SB; SHALISH C; DELEON D; RUTTER M; RISCH N; BRIN MF; MARKOVA ED; LIMBORSKA SA; IVANOVASMOLENSKAYA IA; MCCORMICK MK; FAHN S; BUCKLER AJ; GUSELLA JF; BREAKEFIELD XO
      FINE LOCALIZATION OF THE TORSION DYSTONIA GENE (DYT1) ON HUMAN-CHROMOSOME 9Q34 - YAC MAP AND LINKAGE DISEQUILIBRIUM

      PCR methods and applications
    41. 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
    42. MENON AG; RUTTER JL; VONSATTEL JP; SYNDER H; MURDOCH C; BLUMENFELD A; MARTUZA RL; VONDEIMLING A; GUSELLA JF; HOUSEAL TW
      FREQUENT LOSS OF CHROMOSOME-14 IN ATYPICAL AND MALIGNANT MENINGIOMA -IDENTIFICATION OF A PUTATIVE TUMOR PROGRESSION LOCUS

      Oncogene
    43. MCCLATCHEY AI; SAOTOME I; RAMESH V; GUSELLA JF; JACKS T
      THE NF2 TUMOR-SUPPRESSOR GENE-PRODUCT IS ESSENTIAL FOR EXTRAEMBRYONICDEVELOPMENT IMMEDIATELY PRIOR TO GASTRULATION

      Genes & development
    44. 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
    45. 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
    46. 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
    47. THE I; HANNIGAN GE; COWLEY GS; REGINALD S; ZHONG Y; GUSELLA JF; HARIHARAN IK; BERNARDS A
      RESCUE OF A DROSOPHILA NF1 MUTANT PHENOTYPE BY PROTEIN-KINASE-A

      Science
    48. KOSINSKI CM; CHA JH; YOUNG AB; PERSICHETTI F; MACDONALD M; GUSELLA JF; PENNEY JB; STANDAERT DG
      HUNTINGTON IMMUNOREACTIVITY IN THE RAT NEOTRIATUM - DIFFERENTIAL ACCUMULATION AND SELECTIVE VULNERABILITY

      Neurology
    49. 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
    50. KOSINSKI CM; CHA JH; YOUNG AB; PERSICHETTI F; MACDONALD M; GUSELLA JF; PENNEY JB; STANDAERT DG
      HUNTINGTIN IMMUNOREACTIVITY IN THE RAT NEOSTRIATUM - DIFFERENTIAL ACCUMULATION IN PROJECTION AND INTERNEURONS

      Experimental neurology
    51. SLAUGHENHAUPT SA; MOODY D; LIEBERT CB; POVEY S; REBELLO M; ATTWOOD J; GUSELLA JF
      SATURATION OF THE GENETIC-MAP AND EXPANSION OF THE PHYSICAL MAP SURROUNDING THE FAMILIAL DYSAUTONOMIA GENE ON HUMAN-CHROMOSOME-9

      Annals of Human Genetics
    52. STEMMERRACHAMIMOV AO; XU L; GONZALEZAGOSTI C; BURWICK JA; PINNEY D; BEAUCHAMP R; JACOBY LB; GUSELLA JF; RAMESH V; LOUIS DN
      UNIVERSAL ABSENCE OF MERLIN, BUT NOT OTHER ERM FAMILY MEMBERS, IN SCHWANNOMAS

      The American journal of pathology
    53. OZELIUS LJ; HEWETT JW; SHALISH C; PAGE CE; BRESSMAN SB; KRAMER PL; DELEON D; BUCKLER AJ; BRIN MF; COREY DP; FAHN S; RISCH NJ; GUSELLA JF; BREAKEFIELD XO
      EARLY-ONSET TORSION DYSTONIA GENE (DYT1) ENCODES AN ATP-BINDING PROTEIN

      American journal of human genetics
    54. LIEBERT CB; MULL J; LEBEL A; MACCORMACK K; GILL S; LEYNE M; MOODY D; BUCKLER A; MAAYAN C; BLUMENFELD A; AXELROD F; GUSELLA JF; SLAUGENHAUPT SA
      CLONING OF A NOVEL BAND-4.1 SUPERFAMILY GENE FROM THE FAMILIAL DYSAUTONOMIA CANDIDATE REGION ON HUMAN-CHROMOSOME-9

      American journal of human genetics
    55. 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
    56. 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
    57. 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
    58. 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
    59. HAINES JL; TERMINASSIAN M; BAZYK A; GUSELLA JF; KIM DJ; TERWEDOW H; PERICAKVANCE MA; RIMMLER JB; HAYNES CS; ROSES AD; LEE A; SHANER B; MENOLD M; SEBOUN E; FITOUSSI RP; GARTIOUX C; REYES C; RIBIERRE F; GYAPAY G; WEISSENBACH J; HAUSER SL; GOODKIN DE; LINCOLN R; USUKU K; GARCIAMERINO A; GATTO N; YOUNG S; OKSENBERG JR
      A COMPLETE GENOMIC SCREEN FOR MULTIPLE-SCLEROSIS UNDERSCORES A ROLE FOR THE MAJOR HISTOCOMPATABILITY COMPLEX

      Nature genetics
    60. GONZALEZAGOSTI C; XU L; PINNEY D; BEAUCHAMP R; HOBBS W; GUSELLA JF; RAMESH V
      THE NF2 TUMOR-SUPPRESSOR PROTEIN, MERLIN, LOCALIZES PREFERENTIALLY INMEMBRANE RUFFLES

      Molecular biology of the cell
    61. JACOBY LB; MACCOLLIN M; BARONE R; RAMESH V; GUSELLA JF
      FREQUENCY AND DISTRIBUTION OF NF2 MUTATIONS IN SCHWANNOMAS

      Genes, chromosomes & cancer
    62. MURTHY AE; BERNARDS A; CHURCH D; WASMUTH J; GUSELLA JF
      IDENTIFICATION AND CHARACTERIZATION OF 2 NOVEL TETRATRICOPEPTIDE REPEAT-CONTAINING GENES

      DNA and cell biology
    63. 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
    64. GROSSON CLS; ESTEBAN J; MCKENNAYASEK D; GUSELLA JF; BROWN RH
      HYPOKALEMIC PERIODIC PARALYSIS MUTATIONS - CONFIRMATION OF MUTATION AND ANALYSIS OF FOUNDER EFFECT

      Neuromuscular disorders
    65. MACDONALD ME; GUSELLA JF
      HUNTINGTONS-DISEASE - TRANSLATING A CAG REPEAT INTO A PATHOGENIC MECHANISM

      Current opinion in neurobiology
    66. GUSELLA JF; RAMESH V; MACCOLLIN M; JACOBY LB
      NEUROFIBROMATOSIS-2 - LOSS OF MERLIN PROTECTIVE SPELL

      Current opinion in genetics & development
    67. HAINES JL; PRITCHARD ML; SAUNDERS AM; SCHILDKRAUT JM; GROWDON JH; GASKELL PC; FARRER LA; AUERBACH SA; GUSELLA JF; LOCKE PA; ROSI BL; YAMAOKA L; SMALL GW; CONNEALLY PM; ROSES AD; PERICAKVANCE MA
      NO GENETIC EFFECT OF ALPHA(1)-ANTICHYMOTRYPSIN IN ALZHEIMER-DISEASE

      Genomics
    68. CHUNG WK; POWERKEHOE L; GUSELLA JF; CONNEALLY PM; WEXLER NS; LEIBEL RL
      GENETIC-MAP OF 1P31 IN REGION HOMOLOGOUS TO MIDMURINE CHROMOSOME-4

      Cytogenetics and cell genetics
    69. GROSSON CLS; CANNON SC; COREY DP; GUSELLA JF
      SEQUENCE OF THE VOLTAGE-GATED SODIUM-CHANNEL BETA(1)-SUBUNIT IN WILD-TYPE AND IN QUIVERING MICE

      Molecular brain research
    70. 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
    71. 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
    72. GUSELLA JF; MACDONALD ME
      TRINUCLEOTIDE INSTABILITY - A REPEATING THEME IN HUMAN INHERITED DISORDERS

      Annual review of medicine
    73. HAUSER SL; HAINES JL; SEBOUN E; OKSENBERG J; GOODKIN DE; LINCOLN R; GUSELLA JF; ROSES AD; PERICAKVANCE MA
      GENETIC-ANALYSIS OF THE HLA REGION IN MULTIPLE-SCLEROSIS

      Neurology
    74. HAINES JL; SEBOUN E; RIMMLER J; GOODKIN DE; LINCOLN R; BAZYK A; LEE A; OKSENBERG J; GUSELLA JF; ROSES AD; HAUSER SA; PERICAKVANCE MA
      A COMPLETE GENOMIC SCREEN FOR MULTIPLE-SCLEROSIS

      Neurology
    75. SEBOUN E; CARSIQUE R; PAHMDINH D; BOESPFLUGTANGUY O; GOODKIN DE; LATHROP M; RIMMLER J; HAINES JL; OKSENBERG J; FIZAMES C; LINCOLN R; PERICAKVANCE MA; GUSELLA JF; ROSES AD; WEISSENBACH J; DAUTIGNY A; HAUSER SL
      GENETIC SUSCEPTIBILITY TO MULTIPLE-SCLEROSIS - THE ROLE OF MAG, MBP, MOG, OMGP, AND PLP

      Neurology
    76. 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
    77. XU L; AGOSTI CG; PINNEY D; BEAUCHAMP R; HOBBS W; GUSELLA JF; RAMESH V
      THE NF2 TUMOR-SUPPRESSOR PROTEIN, MERLIN, LOCALIZES PREFERENTIALLY INMEMBRANE RUFFLES

      The Journal of general physiology
    78. DEGASPERI R; SOSA MAG; SARTORATO EL; BATTISTINI S; MACFARLANE H; GUSELLA JF; KRIVIT W; KOLODNY EH
      MOLECULAR HETEROGENEITY OF LATE-ONSET FORMS OF GLOBOID-CELL LEUKODYSTROPHY

      American journal of human genetics
    79. PARRY DM; MACCOLLIN MM; KAISERKUPFER MI; PULASKI K; NICHOLSON HS; BOLESTA M; ELDRIDGE R; GUSELLA JF
      GERM-LINE MUTATIONS IN THE NEUROFIBROMATOSIS-2 GENE - CORRELATIONS WITH DISEASE SEVERITY AND RETINAL ABNORMALITIES

      American journal of human genetics
    80. 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
    81. JOHNSON EW; IYER LM; RICH SS; ORR HT; GILNAGEL A; KURTH JH; ZABRAMSKI JM; MARCHUK DA; WEISSENBACH J; CLERICUZIO CL; DAVIS LE; HART BL; GUSELLA JF; KOSOFSKY BE; LOUIS DN; MORRISON LA; GREEN ED; WEBER JL
      REFINED LOCALIZATION OF THE CEREBRAL CAVERNOUS MALFORMATION GENE (CCM1) TO A 4-CM INTERVAL OF CHROMOSOME 7Q CONTAINED IN A WELL-DEFINED YACCONTIG

      PCR methods and applications
    82. TROFATTER JA; LONG KR; MURRELL JR; STOTLER CJ; GUSELLA JF; BUCKLER AJ
      AN EXPRESSION-INDEPENDENT CATALOG OF GENES FROM HUMAN-CHROMOSOME 22

      PCR methods and applications
    83. GUSELLA JF; MACDONALD ME
      HUNTINGTONS-DISEASE

      Seminars in cell biology
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      Brain pathology
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      Brain pathology
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      Human molecular genetics
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      Oncogene
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      Genomics
    89. MARCHUK DA; GALLIONE CJ; MORRISON LA; CLERICUZIO CL; HART BL; KOSOFSKY BE; LOUIS DN; GUSELLA JF; DAVIS LE; PRENGER VL
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      Genomics
    90. SLAUGENHAUPT SA; ROCA AL; LIEBERT CB; ALTHERR MR; GUSELLA JF; REPPERT SM
      MAPPING OF THE GENE FOR THE MEL(1A)-MELATONIN RECEPTOR TO HUMAN-CHROMOSOME-4 (MTNR1A) AND MOUSE CHROMOSOME-8 (MTNR1A)

      Genomics
    91. SLAUGENHAUPT SA; BLUMENFELD A; LIEBERT CB; MULL J; LUCENTE DE; MONAHAN M; BREAKEFIELD XO; MAAYAN C; PARADA L; AXELROD FB; GUSELLA JF
      THE HUMAN GENE FOR NEUROTROPHIC TYROSINE KINASE RECEPTOR-TYPE-2 (NTRK2) IS LOCATED ON CHROMOSOME-9 BUT IS NOT THE FAMILIAL DYSAUTONOMIA GENE

      Genomics
    92. LOCKE PA; CONNEALLY PM; TANZI RE; GUSELLA JF; HAINES JL
      APOLIPOPROTEIN-E4 ALLELE AND ALZHEIMERS-DISEASE - EXAMINATION OF ALLELIC ASSOCIATION AND EFFECT ON AGE AT ONSET IN BOTH EARLY-ONSET AND LATE-ONSET CASES

      Genetic epidemiology
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      PERIPHERIN GENE IS LINKED TO KERATIN-18 GENE ON HUMAN-CHROMOSOME-12

      Somatic cell and molecular genetics
    94. 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
    95. LOUIS DN; GUSELLA JF
      A TIGER BEHIND MANY DOORS - MULTIPLE GENETIC PATHWAYS TO MALIGNANT GLIOMA

      Trends in genetics
    96. RUSTGI AK; XU L; PINNEY D; STERNER C; BEAUCHAMP R; SCHMIDT S; GUSELLA JF; RAMESH V
      NEUROFIBROMATOSIS-2 GENE IN HUMAN COLORECTAL-CANCER

      Cancer genetics and cytogenetics
    97. ENG CM; SLAUGENHAUPT SA; BLUMENFELD A; AXELROD FB; GUSELLA JF; DESNICK RJ
      PRENATAL-DIAGNOSIS OF FAMILIAL DYSAUTONOMIA BY ANALYSIS OF LINKED CA-REPEAT POLYMORPHISMS ON CHROMOSOME 9Q31-Q33

      American journal of medical genetics
    98. LERNER TJ; BOUSTANY RMN; ANDERSON JW; DARIGO KL; SCHLUMPF K; BUCKLER AJ; GUSELLA JF; HAINES JL; KREMMIDIOTIS G; LENSINK IL; SUTHERLAND GR; CALLEN DF; TASCHNER PEM; DEVOS N; VANOMMEN GJB; BREUNING MH; DOGGETT NA; MEINCKE LJ; LIU ZY; GOODWIN LA; TESMER JG; MITCHISON HM; ORAWE AM; MUNROE PB; JARVELA IE; GARDINER RM; MOLE SE
      ISOLATION OF A NOVEL GENE UNDERLYING BATTEN-DISEASE, CLN3

      Cell
    99. DUYAO MP; AUERBACH AB; RYAN A; PERSICHETTI F; BARNES GT; MCNEIL SM; GE P; VONSATTEL JP; GUSELLA JF; JOYNER AL; MACDONALD ME
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      Science
    100. CORDER EH; SAUNDERS AM; STRITTMATTER WJ; SCHMECHEL DE; GASKELL PC; RIMMLER JB; LOCKE PA; CONNEALLY PM; SCHMADER KE; TANZI RE; GUSELLA JF; SMALL GW; ROSES AD; PERICAKVANCE MA; HAINES JL
      APOLIPOPROTEIN-E, SURVIVAL IN ALZHEIMERS-DISEASE PATIENTS, AND THE COMPETING RISKS OF DEATH AND ALZHEIMERS-DISEASE

      Neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 10/08/20 alle ore 05:13:01