Citation: Nt. Potter et J. Tarleton, NEUROGENETICS IN DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS - ADVANCES IN MOLECULAR DIAGNOSIS, Journal of developmental and behavioral pediatrics, 19(2), 1998, pp. 117-130
Authors:
KNIGHT SP
RICHARDSON MM
OSMAND AP
STAKKESTAD A
POTTER NT
Citation: Sp. Knight et al., EXPRESSION AND DISTRIBUTION OF THE DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY GENE-PRODUCT (ATROPHIN-1 DRPLAP) IN NEURONAL AND NONNEURONAL TISSUES/, Journal of the neurological sciences, 146(1), 1997, pp. 19-26
Citation: Nt. Potter, MEIOTIC INSTABILITY ASSOCIATED WITH THE CAGR1 TRINUCLEOTIDE REPEAT AT13Q13, Journal of Medical Genetics, 34(5), 1997, pp. 411-413
Citation: Kl. Legge et al., PRESENTATION OF A T-CELL RECEPTOR ANTAGONIST PEPTIDE BY IMMUNOGLOBULINS ABLATES ACTIVATION OF T-CELLS BY A SYNTHETIC PEPTIDE OR PROTEINS REQUIRING ENDOCYTIC PROCESSING, The Journal of experimental medicine, 185(6), 1997, pp. 1043-1053
Citation: Nt. Potter, INITIAL CHARACTERIZATION OF THE CAGR1 GENE-PRODUCT - A NOVEL GENE CONTAINING A MEIOTICALLY UNSTABLE TRINUCLEOTIDE REPEAT, American journal of human genetics, 61(4), 1997, pp. 1858-1858
Authors:
YANAGISAWA H
FUJII K
NAGAFUCHI S
NAKAHORI Y
NAKAGOME Y
AKANE A
NAKAMURA M
SANO A
KOMURE O
KONDO I
JIN DK
SORENSEN SA
POTTER NT
YOUNG SR
NAKAMURA K
NUKINA N
NAGAO Y
TADOKORO K
OKUYAMA T
MIYASHITA T
INOUE T
KANAZAWA I
YAMADA M
Citation: H. Yanagisawa et al., A UNIQUE ORIGIN AND MULTISTEP PROCESS FOR THE GENERATION OF EXPANDED DRPLA TRIPLET REPEATS, Human molecular genetics, 5(3), 1996, pp. 373-379
Citation: Ts. Stephens et al., IDENTIFICATION AND CHARACTERIZATION OF A B-CELL DETERMINANT WITHIN THE AMPHIPATHIC DOMAIN (RESIDUES-178-238) OF THE MYELIN PROTEOLIPID PROTEIN, Journal of neuroscience research, 43(5), 1996, pp. 545-553
Citation: Nt. Potter et al., DIFFERENT ORIGINS OF EXPANDED REPEATS FOR HAW-RIVER-SYNDROME AND DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY, Lancet, 347(9010), 1996, pp. 1271-1271
Citation: Nt. Potter, THE RELATIONSHIP BETWEEN (CAG)(N) REPEAT NUMBER AND AGE-OF-ONSET IN AFAMILY WITH DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA) - DIAGNOSTICIMPLICATIONS OF CONFIRMATORY AND PREDICTIVE TESTING, Journal of Medical Genetics, 33(2), 1996, pp. 168-170
Authors:
POTTER NT
MEYER MA
ZIMMERMAN AW
EISENSTADT ML
ANDERSON IJ
Citation: Nt. Potter et al., MOLECULAR AND CLINICAL FINDINGS IN A FAMILY WITH DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY, Annals of neurology, 37(2), 1995, pp. 273-277
Citation: Ma. Meyer et Nt. Potter, ISSUES AND OPINIONS - SPORADIC ALS AND CHROMOSOME-22 - EVIDENCE FOR APOSSIBLE NEUROFILAMENT GENE DEFECT, Muscle & nerve, 18(5), 1995, pp. 536-539
Citation: Nt. Potter et al., GENOTYPE PHENOTYPE CORRELATIONS IN A NORTH-AMERICAN FAMILY WITH DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA)/, American journal of human genetics, 57(4), 1995, pp. 1442-1442
Citation: Nt. Potter et Ts. Stephens, HUMORAL IMMUNE RECOGNITION OF PROTEOLIPID PROTEIN (PLP)-SPECIFIC ENCEPHALITOGENIC EPITOPES IN THE SJL J MOUSE/, Journal of neuroscience research, 37(1), 1994, pp. 15-22