AAAAAA

   
Results: 1-25 | 26-28
Results: 1-25/28
Volunteer monitoring of nonindigenous invasive plant species in the Adirondack Park, New York, USA
Authors: Brown, WT Krasny, ME Schoch, N
Citation: Wt. Brown et al., Volunteer monitoring of nonindigenous invasive plant species in the Adirondack Park, New York, USA, NAT AREA J, 21(2), 2001, pp. 189-196
Haplotype analysis at the FRAXA locus in Thai subjects
Authors: Limprasert, P Saechan, V Ruangdaraganon, N Sura, T Vasiknanote, P Jaruratanasirikul, S Brown, WT
Citation: P. Limprasert et al., Haplotype analysis at the FRAXA locus in Thai subjects, AM J MED G, 98(3), 2001, pp. 224-229
Metabolism of the 2-oxoaldehyde methylglyoxal by aldose reductase and by glyoxalase-I: roles for glutathione in both enzymes and implications for diabetic complications
Authors: Vander Jagt, DL Hassebrook, RK Hunsaker, LA Brown, WT Royer, RE
Citation: Dl. Vander Jagt et al., Metabolism of the 2-oxoaldehyde methylglyoxal by aldose reductase and by glyoxalase-I: roles for glutathione in both enzymes and implications for diabetic complications, CHEM-BIO IN, 130(1-3), 2001, pp. 549-562
The digital transformation of oral health care - Teledentistry and electronic commerce
Authors: Bauer, JC Brown, WT
Citation: Jc. Bauer et Wt. Brown, The digital transformation of oral health care - Teledentistry and electronic commerce, J AM DENT A, 132(2), 2001, pp. 204-209
Heterogeneity of late-infantile neuronal ceroid lipofuscinosis
Authors: Zhong, N Moroziewicz, DN Ju, WN Jurkiewicz, A Johnston, L Wisniewski, KE Brown, WT
Citation: N. Zhong et al., Heterogeneity of late-infantile neuronal ceroid lipofuscinosis, GENET MED, 2(6), 2000, pp. 312-318
The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA
Authors: Velinov, M Gu, H Genovese, M Duncan, C Brown, WT Jenkins, E
Citation: M. Velinov et al., The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNA, MOL GEN MET, 69(1), 2000, pp. 81-83
Apparent FMR1 allele instability in non-Fragile X males - Invited commentary
Authors: Brown, WT Nolin, SL
Citation: Wt. Brown et Sl. Nolin, Apparent FMR1 allele instability in non-Fragile X males - Invited commentary, GENET TEST, 4(3), 2000, pp. 241-242
Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses
Authors: Zhong, NA Wisniewski, KE Ju, WN Moroziewicz, DN Jurkiewicz, A McLendon, L Jenkins, EC Brown, WT
Citation: Na. Zhong et al., Molecular diagnosis of and carrier screening for the neuronal ceroid lipofuscinoses, GENET TEST, 4(3), 2000, pp. 243-248
Effect of crosslinker reaction rate on film properties for thermoset coatings
Authors: Brown, WT
Citation: Wt. Brown, Effect of crosslinker reaction rate on film properties for thermoset coatings, J COAT TECH, 72(904), 2000, pp. 63-70
Fmr1 knockout mouse has a distinctive strain-specific learning impairment
Authors: Dobkin, C Rabe, A Dumas, R El Idrissi, A Haubenstock, H Brown, WT
Citation: C. Dobkin et al., Fmr1 knockout mouse has a distinctive strain-specific learning impairment, NEUROSCIENC, 100(2), 2000, pp. 423-429
RNAs that interact with the Fragile X syndrome RNA binding protein FMRP
Authors: Sung, YJ Conti, J Currie, JR Brown, WT Denman, RB
Citation: Yj. Sung et al., RNAs that interact with the Fragile X syndrome RNA binding protein FMRP, BIOC BIOP R, 275(3), 2000, pp. 973-980
Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population
Authors: 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
Citation: Dc. Crawford et al., Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population, AM J HU GEN, 66(2), 2000, pp. 480-493
Late infantile neuronal ceroid lipofuscinosis is due to splicing mutationsin the CLN2 gene
Authors: Hartikainen, JM Ju, WN Wisniewski, KE Moroziewicz, DN Kaczmarski, AL McLendon, L Zhong, D Suarez, CT Brown, WT Zhong, N
Citation: Jm. Hartikainen et al., Late infantile neuronal ceroid lipofuscinosis is due to splicing mutationsin the CLN2 gene, MOL GEN MET, 67(2), 1999, pp. 162-168
Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2
Authors: Carpenter, NJ Brown, WT Qu, Y Keenan, KL
Citation: Nj. Carpenter et al., Regional localization of a nonspecific X-linked mental retardation gene (MRX59) to Xp21.2-p22.2, AM J MED G, 85(3), 1999, pp. 266-270
Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients
Authors: Pang, CP Poon, PMK Chen, QL Lai, KYC Yin, CH Zhao, Z Zhong, N Lau, CH Lam, STS Wong, CK Brown, WT
Citation: Cp. Pang et al., Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients, AM J MED G, 84(3), 1999, pp. 179-183
Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians
Authors: Zhong, N Ju, WN Xu, WM Ye, LL Shen, Y Wu, GY Chen, SH Jin, RM Hu, XF Yang, AD Liu, XX Poon, P Pang, C Zheng, Y Song, L Zhao, P Fu, BJ Gu, HJ Brown, WT
Citation: N. Zhong et al., Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians, AM J MED G, 84(3), 1999, pp. 191-194
FRAXAC1 and DXS548 polymorphisms in the Chinese population
Authors: Poon, PMK Pang, CP Chen, QL Zhong, N Lai, KYC Lau, CH Wong, CK Brown, WT
Citation: Pmk. Poon et al., FRAXAC1 and DXS548 polymorphisms in the Chinese population, AM J MED G, 84(3), 1999, pp. 208-213
Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation
Authors: Zhong, N Ju, W Nelson, D Dobkin, C Brown, WT
Citation: N. Zhong et al., Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation, AM J MED G, 84(3), 1999, pp. 268-271
KH domain-containing proteins of yeast: Absence of a fragile X gene homologue
Authors: Currie, JR Brown, WT
Citation: Jr. Currie et Wt. Brown, KH domain-containing proteins of yeast: Absence of a fragile X gene homologue, AM J MED G, 84(3), 1999, pp. 272-276
Possible founder effects for FRAXE alleles
Authors: Limprasert, P Zhong, N Currie, JR Brown, WT
Citation: P. Limprasert et al., Possible founder effects for FRAXE alleles, AM J MED G, 84(3), 1999, pp. 286-290
Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease
Authors: Zhong, N Ju, WN Brown, WT Ye, LL Jenkins, EC Schupf, N
Citation: N. Zhong et al., Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease, AM J MED G, 84(3), 1999, pp. 309-310
Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997
Authors: Holden, JJA Percy, M Allingham-Hawkins, D Brown, WT Chiurazzi, P Fisch, G Gane, L Gunter, C Hagerman, R Jenkins, EC Kooy, RF Lubs, HA Murray, A Neri, G Schwartz, C Tranebjaerg, L Villard, L Willems, PJ
Citation: Jja. Holden et al., Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997, AM J MED G, 83(4), 1999, pp. 221-236
Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data
Authors: Allingham-Hawkins, SJ Babul-Hirji, R Chitayat, D Holden, JJA Yang, KT Lee, C Hudson, R Gorwill, H Nolin, SL Glicksman, A Jenkins, EC Brown, WT Howard-Peebles, PN Becchi, C Cummings, E Fallon, L Seitz, S Black, SH Vianna-Morgante, AM Costa, SS Otto, PA Mingroni-Netto, RC Murray, A Webb, J MacSwinney, F Dennis, N Jacobs, PA Syrrou, M Georgiou, I Patsalis, PC Uzielli, MLG Guarducci, S Lapi, E Cecconi, A Ricci, U
Citation: Sj. Allingham-hawkins et al., Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data, AM J MED G, 83(4), 1999, pp. 322-325
Ultrastructure of the fragile X chromosome: New observations on the fragile site
Authors: Wen, GY Jenkins, EC Goldberg, EM Genovese, M Brown, WT Wisniewski, HM
Citation: Gy. Wen et al., Ultrastructure of the fragile X chromosome: New observations on the fragile site, AM J MED G, 83(4), 1999, pp. 331-333
First transmission electron micrograph of continuous mitotic spindle fibers between polar area and chromosome ends
Authors: Wen, GY Jenkins, EC Goldberg, EM Genovese, M Brown, WT Wisniewski, HM
Citation: Gy. Wen et al., First transmission electron micrograph of continuous mitotic spindle fibers between polar area and chromosome ends, AM J MED G, 83(4), 1999, pp. 334-337
Risultati: 1-25 | 26-28