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Results: 1-18 |
Results: 18
THE GENETIC-DEFECT CAUSING HUNTINGTONS-DISEASE - REPEATED IN OTHER CONTEXTS
Authors: GUSELLA JF PERSICHETTI F MACDONALD ME
Citation: Jf. Gusella et al., THE GENETIC-DEFECT CAUSING HUNTINGTONS-DISEASE - REPEATED IN OTHER CONTEXTS, Molecular medicine, 3(4), 1997, pp. 238-246
HETEROGENEOUS TOPOGRAPHIC AND CELLULAR-DISTRIBUTION OF HUNTINGTON EXPRESSION IN THE NORMAL HUMAN NEOSTRIATUM
Authors: FERRANTE RJ GUTEKUNST CA PERSICHETTI F MCNEIL SM KOWALL NW GUSELLA JF MACDONALD ME BEAL MF HERSCH SM
Citation: Rj. Ferrante et al., HETEROGENEOUS TOPOGRAPHIC AND CELLULAR-DISTRIBUTION OF HUNTINGTON EXPRESSION IN THE NORMAL HUMAN NEOSTRIATUM, The Journal of neuroscience, 17(9), 1997, pp. 3052-3063
HUNTINGTON IMMUNOREACTIVITY IN THE RAT NEOTRIATUM - DIFFERENTIAL ACCUMULATION AND SELECTIVE VULNERABILITY
Authors: KOSINSKI CM CHA JH YOUNG AB PERSICHETTI F MACDONALD M GUSELLA JF PENNEY JB STANDAERT DG
Citation: Cm. Kosinski et al., HUNTINGTON IMMUNOREACTIVITY IN THE RAT NEOTRIATUM - DIFFERENTIAL ACCUMULATION AND SELECTIVE VULNERABILITY, Neurology, 48(6), 1997, pp. 7-7
HETEROGENEOUS EXPRESSION OF HUNTINGTIN IMMUNOREACTIVITY IN THE NORMALHUMAN NEOSTRIATUM
Authors: FERRANTE RJ GUTEKUNST CA PERSICHETTI F KOWALL NW GUSELLA JF BEAL F MACDONALD ME HERSCH SM
Citation: Rj. Ferrante et al., HETEROGENEOUS EXPRESSION OF HUNTINGTIN IMMUNOREACTIVITY IN THE NORMALHUMAN NEOSTRIATUM, Neurology, 48(3), 1997, pp. 22006-22006
HUNTINGTIN IMMUNOREACTIVITY IN THE RAT NEOSTRIATUM - DIFFERENTIAL ACCUMULATION IN PROJECTION AND INTERNEURONS
Authors: KOSINSKI CM CHA JH YOUNG AB PERSICHETTI F MACDONALD M GUSELLA JF PENNEY JB STANDAERT DG
Citation: Cm. Kosinski et al., HUNTINGTIN IMMUNOREACTIVITY IN THE RAT NEOSTRIATUM - DIFFERENTIAL ACCUMULATION IN PROJECTION AND INTERNEURONS, Experimental neurology, 144(2), 1997, pp. 239-247
DIFFERENTIAL EXPRESSION OF NORMAL AND MUTANT HUNTINGTONS-DISEASE GENEALLELES
Authors: PERSICHETTI F CARLEE L FABER PW MCNEIL SM AMBROSE CM SRINIDHI J ANDERSON M BARNES GT GUSELLA JF MACDONALD ME
Citation: F. Persichetti et al., DIFFERENTIAL EXPRESSION OF NORMAL AND MUTANT HUNTINGTONS-DISEASE GENEALLELES, Neurobiology of disease, 3(3), 1996, pp. 183-190
HUNTINGTONS-DISEASE
Authors: GUSELLA JF MCNEIL S PERSICHETTI F SRINIDHI J NOVELLETTO A BIRD E FABER P VONSATTEL JP MYERS RH MACDONALD ME
Citation: Jf. Gusella et al., HUNTINGTONS-DISEASE, Cold Spring Harbor Symposia on Quantitative Biology, 61, 1996, pp. 615-626
NORMAL AND EXPANDED HUNTINGTONS-DISEASE GENE ALLELES PRODUCE DISTINGUISHABLE PROTEINS DUE TO TRANSLATION ACROSS THE CAG REPEAT
Authors: 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
Citation: F. Persichetti et al., NORMAL AND EXPANDED HUNTINGTONS-DISEASE GENE ALLELES PRODUCE DISTINGUISHABLE PROTEINS DUE TO TRANSLATION ACROSS THE CAG REPEAT, Molecular medicine, 1(4), 1995, pp. 374-383
CEPH CONSORTIUM MAP OF CHROMOSOME-14
Authors: COX DW BILLINGSLEY GD BALE AE DONISKELLER H EDWARDS JH LITT M MCBRIDE W PERSICHETTI F SPURR NK WEBER JL WEISSENBACH J WHITE RL
Citation: Dw. Cox et al., CEPH CONSORTIUM MAP OF CHROMOSOME-14, Cytogenetics and cell genetics, 69(3-4), 1995, pp. 175-178
INACTIVATION OF THE MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG HDH
Authors: DUYAO MP AUERBACH AB RYAN A PERSICHETTI F BARNES GT MCNEIL SM GE P VONSATTEL JP GUSELLA JF JOYNER AL MACDONALD ME
Citation: Mp. Duyao et al., INACTIVATION OF THE MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG HDH, Science, 269(5222), 1995, pp. 407-410
RECURRENT SIMPLE TANDEM REPEAT MUTATIONS DURING HUMAN Y-CHROMOSOME RADIATION IN CAUCASIAN SUBPOPULATIONS
Authors: CIMINELLI BM POMPEI F MALASPINA P HAMMER M PERSICHETTI F PIGNATTI P PALENA A ANAGNOU N GUANTI G JODICE C TERRENATO L NOVELLETTO A
Citation: Bm. Ciminelli et al., RECURRENT SIMPLE TANDEM REPEAT MUTATIONS DURING HUMAN Y-CHROMOSOME RADIATION IN CAUCASIAN SUBPOPULATIONS, Journal of molecular evolution, 41(6), 1995, pp. 966-973
POLYMORPHISM ANALYSIS OF THE HUNTINGTIN GENE IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE
Authors: NOVELLETTO A PERSICHETTI F SABBADINI G MANDICH P BELLONE E AJMAR F SQUITIERI F CAMPANELLA G BOZZA A MACDONALD ME GUSELLA JF FRONTALI M
Citation: A. Novelletto et al., POLYMORPHISM ANALYSIS OF THE HUNTINGTIN GENE IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE, Human molecular genetics, 3(7), 1994, pp. 1129-1132
ANALYSIS OF THE TRINUCLEOTIDE REPEAT EXPANSION IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE
Authors: NOVELLETTO A PERSICHETTI F SABBADINI G MANDICH P BELLONE E AJMAR F PERGOLA M DELSENNO L MACDONALD ME GUSELLA JF FRONTALI M
Citation: A. Novelletto et al., ANALYSIS OF THE TRINUCLEOTIDE REPEAT EXPANSION IN ITALIAN FAMILIES AFFECTED WITH HUNTINGTON DISEASE, Human molecular genetics, 3(1), 1994, pp. 93-98
MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG (HDH)
Authors: BARNES GT DUYAO MP AMBROSE CM MCNEIL S PERSICHETTI F SRINIDHI J GUSELLA JF MACDONALD ME
Citation: Gt. Barnes et al., MOUSE HUNTINGTONS-DISEASE GENE HOMOLOG (HDH), Somatic cell and molecular genetics, 20(2), 1994, pp. 87-97
EFFECT OF TRINUCLEOTIDE REPEAT LENGTH AND PARENTAL SEX ON PHENOTYPIC VARIATION IN SPINOCEREBELLAR ATAXIA-I
Authors: JODICE C MALASPINA P PERSICHETTI F NOVELLETTO A SPADARO M GIUNTI P MOROCUTTI C TERRENATO L HARDING AE FRONTALI M
Citation: C. Jodice et al., EFFECT OF TRINUCLEOTIDE REPEAT LENGTH AND PARENTAL SEX ON PHENOTYPIC VARIATION IN SPINOCEREBELLAR ATAXIA-I, American journal of human genetics, 54(6), 1994, pp. 959-965
TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE
Authors: DUYAO M AMBROSE C MYERS R NOVELLETTO A PERSICHETTI F FRONTALI M FOLSTEIN S ROSS C FRANZ M ABBOTT M GRAY J CONNEALLY P YOUNG A PENNEY J HOLLINGSWORTH Z SHOULSON I LAZZARINI A FALEK A KOROSHETZ W SAX D BIRD E VONSATTEL J BONILLA E ALVIR J CONDE JB CHA JH DURE L GOMEZ F RAMOS M SANCHEZRAMOS J SNODGRASS S DEYOUNG M WEXLER N MOSCOWITZ C PENCHASZADEH G MACFARLANE H ANDERSON M JENKINS B SRINIDHI J BARNES G GUSELLA J MACDONALD M
Citation: M. Duyao et al., TRINUCLEOTIDE REPEAT LENGTH INSTABILITY AND AGE-OF-ONSET IN HUNTINGTONS-DISEASE, Nature genetics, 4(4), 1993, pp. 387-392
THE GENE FOR SPINAL CEREBELLAR ATAXIA-1 (SCA1) IS FLANKED BY 2 CLOSELY LINKED HIGHLY POLYMORPHIC MICROSATELLITE LOCI
Authors: JODICE C FRONTALI M PERSICHETTI F NOVELLETTO A PANDOLFO M SPADARO M GIUNTI P SCHINAIA G LULLI P MALASPINA P PLASMATI R TOLA R ANTONELLI A DIDONATO S MOROCUTTI C WEISSENBACH J CANN HM TERRENATO L
Citation: C. Jodice et al., THE GENE FOR SPINAL CEREBELLAR ATAXIA-1 (SCA1) IS FLANKED BY 2 CLOSELY LINKED HIGHLY POLYMORPHIC MICROSATELLITE LOCI, Human molecular genetics, 2(9), 1993, pp. 1383-1387
THE GENE FOR AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA (SCA1) MAPS CENTROMERIC TO D6S89 AND SHOWS NO RECOMBINATION, IN 9 LARGE KINDREDS, WITH A DINUCLEOTIDE REPEAT AT THE AM10 LOCUS
Authors: KWIATKOWSKI TJ ORR HT BANFI S MCCALL AE JODICE C PERSICHETTI F NOVELLETTO A LEBORGNEDEMARQUOY F DUVICK LA FRONTALI M SUBRAMONY SH BEAUDET AL TERRENATO L ZOGHBI HY RANUM LPW
Citation: Tj. Kwiatkowski et al., THE GENE FOR AUTOSOMAL-DOMINANT SPINOCEREBELLAR ATAXIA (SCA1) MAPS CENTROMERIC TO D6S89 AND SHOWS NO RECOMBINATION, IN 9 LARGE KINDREDS, WITH A DINUCLEOTIDE REPEAT AT THE AM10 LOCUS, American journal of human genetics, 53(2), 1993, pp. 391-400
Risultati: 1-18 |