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Results: 76-100/155
METABOLIC-ACTIVATION AND DNA-BINDING OF FOOD MUTAGENS AND OTHER ENVIRONMENTAL CARCINOGENS IN HUMAN MAMMARY EPITHELIAL-CELLS
Authors: CARMICHAEL PL STONE EM GROVER PL GUSTERSON BA PHILLIPS DH
Citation: Pl. Carmichael et al., METABOLIC-ACTIVATION AND DNA-BINDING OF FOOD MUTAGENS AND OTHER ENVIRONMENTAL CARCINOGENS IN HUMAN MAMMARY EPITHELIAL-CELLS, Carcinogenesis, 17(8), 1996, pp. 1769-1772
BAROCLINIC WAVE VARIATIONS OBSERVED IN MLS UPPER-TROPOSPHERIC WATER-VAPOR
Authors: STONE EM RANDEL WJ STANFORD JL READ WG WATERS JW
Citation: Em. Stone et al., BAROCLINIC WAVE VARIATIONS OBSERVED IN MLS UPPER-TROPOSPHERIC WATER-VAPOR, Geophysical research letters, 23(21), 1996, pp. 2967-2970
PREFERENTIAL ROD AND CONE PHOTORECEPTOR ABNORMALITIES IN HETEROZYGOTES WITH POINT MUTATIONS IN THE RDS GENE
Authors: JACOBSON SG CIDECIYAN AV MAGUIRE AM BENNETT J SHEFFIELD VC STONE EM
Citation: Sg. Jacobson et al., PREFERENTIAL ROD AND CONE PHOTORECEPTOR ABNORMALITIES IN HETEROZYGOTES WITH POINT MUTATIONS IN THE RDS GENE, Experimental Eye Research, 63(5), 1996, pp. 603-608
LINKAGE OF AUTOSOMAL-DOMINANT RADIAL DRUSEN (MALATTIA LEVENTINESE) TOCHROMOSOME 2P16-21
Authors: HEON E PIGUET B MUNIER F SNEED SR MORGAN CM FORNI S PESCIA G SCHORDERET D TAYLOR CM STREB LM WILES CD NISHIMURA DY SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF AUTOSOMAL-DOMINANT RADIAL DRUSEN (MALATTIA LEVENTINESE) TOCHROMOSOME 2P16-21, Archives of ophthalmology, 114(2), 1996, pp. 193-198
AN AUTOSOMAL RECESSIVE NONSYNDROMIC-HEARING-LOSS LOCUS IDENTIFIED BY DNA POOLING USING 2 INBRED BEDOUIN KINDREDS
Authors: SCOTT DA CARMI R ELBEDOUR K YOSEFSBERG S STONE EM SHEFFIELD VC
Citation: Da. Scott et al., AN AUTOSOMAL RECESSIVE NONSYNDROMIC-HEARING-LOSS LOCUS IDENTIFIED BY DNA POOLING USING 2 INBRED BEDOUIN KINDREDS, American journal of human genetics, 59(2), 1996, pp. 385-391
A MUTATION CAUSING ALPORT SYNDROME WITH TARDIVE HEARING-LOSS IS COMMON IN THE WESTERN UNITED-STATES
Authors: BARKER DF PRUCHNO CJ JIANG X ATKIN CL STONE EM DENISON LC FAIN PR GREGORY MC
Citation: Df. Barker et al., A MUTATION CAUSING ALPORT SYNDROME WITH TARDIVE HEARING-LOSS IS COMMON IN THE WESTERN UNITED-STATES, American journal of human genetics, 58(6), 1996, pp. 1157-1165
SPACE-TIME INTEGRITY OF IMPROVED STRATOSPHERIC AND MESOSPHERIC SOUNDER AND MICROWAVE LIMB SOUNDER TEMPERATURE-FIELDS AT KELVIN WAVE SCALES
Authors: STONE EM STANFORD JL ZIEMKE JR ALLEN DR TAYLOR FW RODGERS CD LAWRENCE BN FISHBEIN EF ELSON LS WATERS JW
Citation: Em. Stone et al., SPACE-TIME INTEGRITY OF IMPROVED STRATOSPHERIC AND MESOSPHERIC SOUNDER AND MICROWAVE LIMB SOUNDER TEMPERATURE-FIELDS AT KELVIN WAVE SCALES, JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 100(D7), 1995, pp. 14089-14096
NIGHT BLINDNESS IN SORSBYS-FUNDUS-DYSTROPHY REVERSED BY VITAMIN-A
Authors: JACOBSON SG CIDECIYAN AV REGUNATH G RODRIGUEZ FJ VANDENBURGH K SHEFFIELD VC STONE EM
Citation: Sg. Jacobson et al., NIGHT BLINDNESS IN SORSBYS-FUNDUS-DYSTROPHY REVERSED BY VITAMIN-A, Nature genetics, 11(1), 1995, pp. 27-32
LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE REGION OF THE RIEGER SYNDROME LOCUS (4Q25)
Authors: HEON E SHETH BP KALENAK JW SUNDEN SLF STREB LM TAYLOR CM ALWARD WLM SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF AUTOSOMAL-DOMINANT IRIS HYPOPLASIA TO THE REGION OF THE RIEGER SYNDROME LOCUS (4Q25), Human molecular genetics, 4(8), 1995, pp. 1435-1439
LINKAGE OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY TO 20Q11
Authors: HEON E MATHERS WD ALWARD WLM WEISENTHAL RW SUNDEN SLF FISHBAUGH JA TAYLOR CM KRACHMER JH SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY TO 20Q11, Human molecular genetics, 4(3), 1995, pp. 485-488
MUTATION ANALYSIS OF THE ROM1 GENE IN RETINITIS-PIGMENTOSA (VOL 4, PG1895, 1995)
Authors: BASCOM RA LIU L HECKENLIVELY JR STONE EM MCINNES RR
Citation: Ra. Bascom et al., MUTATION ANALYSIS OF THE ROM1 GENE IN RETINITIS-PIGMENTOSA (VOL 4, PG1895, 1995), Human molecular genetics, 4(12), 1995, pp. 2424-2424
MUTATION ANALYSIS OF THE ROM1 GENE IN RETINITIS-PIGMENTOSA
Authors: BASCOM RA LIU L HECKENLIVELY JR STONE EM MCINNES RR
Citation: Ra. Bascom et al., MUTATION ANALYSIS OF THE ROM1 GENE IN RETINITIS-PIGMENTOSA, Human molecular genetics, 4(10), 1995, pp. 1895-1902
USE OF A DNA POOLING STRATEGY TO IDENTIFY A HUMAN OBESITY SYNDROME LOCUS ON CHROMOSOME-15
Authors: CARMI R ROKHLINA T KWITEKBLACK AE ELBEDOUR K NISHIMURA D STONE EM SHEFFIELD VC
Citation: R. Carmi et al., USE OF A DNA POOLING STRATEGY TO IDENTIFY A HUMAN OBESITY SYNDROME LOCUS ON CHROMOSOME-15, Human molecular genetics, 4(1), 1995, pp. 9-13
NOVEL FRAMESHIFT MUTATIONS IN THE PROCOLLAGEN-2 GENE (COL2A1) ASSOCIATED WITH STICKLER SYNDROME (HEREDITARY ARTHROOPHTHALMOPATHY)
Authors: BROWN DM VANDENBURGH K KIMURA AE WEINGEIST TA SHEFFIELD VC STONE EM
Citation: Dm. Brown et al., NOVEL FRAMESHIFT MUTATIONS IN THE PROCOLLAGEN-2 GENE (COL2A1) ASSOCIATED WITH STICKLER SYNDROME (HEREDITARY ARTHROOPHTHALMOPATHY), Human molecular genetics, 4(1), 1995, pp. 141-142
A PERIPHERIN RETINAL DEGENERATION SLOW MUTATION (PRO-210-ARG) ASSOCIATED WITH MACULAR AND PERIPHERAL RETINAL DEGENERATION
Authors: GORIN MB JACKSON KE FERRELL RE SHEFFIELD VC JACOBSON SG GASS JDM MITCHELL E STONE EM
Citation: Mb. Gorin et al., A PERIPHERIN RETINAL DEGENERATION SLOW MUTATION (PRO-210-ARG) ASSOCIATED WITH MACULAR AND PERIPHERAL RETINAL DEGENERATION, Ophthalmology, 102(2), 1995, pp. 246-255
PHENOTYPIC DIFFERENCES AMONG PATIENTS WITH BARDET-BIEDL-SYNDROME LINKED TO 3 DIFFERENT CHROMOSOME LOCI
Authors: CARMI R ELBEDOUR K STONE EM SHEFFIELD VC
Citation: R. Carmi et al., PHENOTYPIC DIFFERENCES AMONG PATIENTS WITH BARDET-BIEDL-SYNDROME LINKED TO 3 DIFFERENT CHROMOSOME LOCI, American journal of medical genetics, 59(2), 1995, pp. 199-203
CLINICAL AND MOLECULAR EVALUATION OF A LARGE FAMILY WITH IRIS HYPOPLASIA AND GLAUCOMA
Authors: SHETH B HEON E KALENAK J TAYLOR CM STREB LM ALWARD WLM STONE EM SHEFFIELD VC
Citation: B. Sheth et al., CLINICAL AND MOLECULAR EVALUATION OF A LARGE FAMILY WITH IRIS HYPOPLASIA AND GLAUCOMA, Investigative ophthalmology & visual science, 36(4), 1995, pp. 554-554
FINE MAPPING OF THE CHROMOSOMAL BREAKPOINTS IN AN INDIVIDUAL WITH CONGENITAL GLAUCOMA AND A 6-13 TRANSLOCATION
Authors: NISHIMURA DYS PATIL S ALWARD WLM STONE EM SHEFFIELD VC
Citation: Dys. Nishimura et al., FINE MAPPING OF THE CHROMOSOMAL BREAKPOINTS IN AN INDIVIDUAL WITH CONGENITAL GLAUCOMA AND A 6-13 TRANSLOCATION, Investigative ophthalmology & visual science, 36(4), 1995, pp. 554-554
POOLING STRATEGIES AND HAPLOTYPE ANALYSIS OF AUTOSOMAL-DOMINANT CORNEAL DYSTROPHIES - STUDIES IN LATTICE, GRANULAR AND AVELLINO DYSTROPHIES
Authors: KANIS AB MATHERS WD HOLLAND EJ ROSENWASSER GOD ROSA N KIM W PROUD V LAM B SHEFFIELD VC STONE EM
Citation: Ab. Kanis et al., POOLING STRATEGIES AND HAPLOTYPE ANALYSIS OF AUTOSOMAL-DOMINANT CORNEAL DYSTROPHIES - STUDIES IN LATTICE, GRANULAR AND AVELLINO DYSTROPHIES, Investigative ophthalmology & visual science, 36(4), 1995, pp. 771-771
LINKAGE ANALYSIS OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY AND ASSESSMENT OF GENETIC-HETEROGENEITY
Authors: HEON E MATHERS WD ALWARD WLM WEISENTHAL RW SUNDEN SLF FISHBAUGH J TAYLOR CM KRACHMER JH SHEFFIELD VC STONE EM
Citation: E. Heon et al., LINKAGE ANALYSIS OF POSTERIOR POLYMORPHOUS CORNEAL-DYSTROPHY AND ASSESSMENT OF GENETIC-HETEROGENEITY, Investigative ophthalmology & visual science, 36(4), 1995, pp. 771-771
GENETIC-HETEROGENEITY IN 23 CANADIAN BARDET-BIEDL FAMILIES AND EVIDENCE FOR A 5TH BBS LOCUS
Authors: SUNDEN SLF HEON E KWITEKBLACK AE GREEN J PARFREY P MUSARELLA MA NISHIMURA D HARNETT J HEFFERTON D STONE EM SHEFFIELD VC
Citation: Slf. Sunden et al., GENETIC-HETEROGENEITY IN 23 CANADIAN BARDET-BIEDL FAMILIES AND EVIDENCE FOR A 5TH BBS LOCUS, Investigative ophthalmology & visual science, 36(4), 1995, pp. 774-774
EVALUATION OF AN EFFICIENT APPROACH TO DISEASE GENE-MAPPING - APPLICATION TO BARDET-BIEDL SYNDROME
Authors: SHEFFIELD VC BLACK AEK NISHIMURA DY CARMI R SUNDEN SL STONE EM
Citation: Vc. Sheffield et al., EVALUATION OF AN EFFICIENT APPROACH TO DISEASE GENE-MAPPING - APPLICATION TO BARDET-BIEDL SYNDROME, Investigative ophthalmology & visual science, 36(4), 1995, pp. 774-774
3 FAMILIES AFFECTED WITH A RAPIDLY PROGRESSIVE SEVERE FORM OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA ASSOCIATED WITH MUTATIONS IN CODON-347 OF THE RHODOPSIN GENE (PRO-347-ALA AND PRO-347-GLN)
Authors: BROWN J WELEBER RG KIMURA AE VANDENBURGH K SHEFFIELD VC STONE EM
Citation: J. Brown et al., 3 FAMILIES AFFECTED WITH A RAPIDLY PROGRESSIVE SEVERE FORM OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA ASSOCIATED WITH MUTATIONS IN CODON-347 OF THE RHODOPSIN GENE (PRO-347-ALA AND PRO-347-GLN), Investigative ophthalmology & visual science, 36(4), 1995, pp. 825-825
HUMAN AND MOUSE GCAP GENES AND INVOLVEMENT OF GCAP GENE-MUTATIONS IN HUMAN-DISEASE
Authors: BAEHR W SUBBARAYA I DANG YL RUIZ C HELEKAR B BANERJEE P KNOWLES JA GILLIAM TC VANDENBURGH K STONE EM
Citation: W. Baehr et al., HUMAN AND MOUSE GCAP GENES AND INVOLVEMENT OF GCAP GENE-MUTATIONS IN HUMAN-DISEASE, Investigative ophthalmology & visual science, 36(4), 1995, pp. 826-826
PHOTORECEPTOR FUNCTION IN PATIENTS WITH HETEROZYGOUS PERIPHERIN RDS GENE-MUTATIONS/
Authors: CIDECIYAN AV JACOBSON SG KEMP CM AZEVEDO DFG REGUNATH G SHEFFIELD VC STONE EM
Citation: Av. Cideciyan et al., PHOTORECEPTOR FUNCTION IN PATIENTS WITH HETEROZYGOUS PERIPHERIN RDS GENE-MUTATIONS/, Investigative ophthalmology & visual science, 36(4), 1995, pp. 913-913
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