AAAAAA

   
Results: 1-16 |
Results: 16
MUTATIONS IN YEAST PROLIFERATING CELL NUCLEAR ANTIGEN DEFINE DISTINCTSITES FOR INTERACTION WITH DNA-POLYMERASE-DELTA AND DNA-POLYMERASE-EPSILON
Authors: EISSENBERG JC AYYAGARI R GOMES XV BURGERS PMJ
Citation: Jc. Eissenberg et al., MUTATIONS IN YEAST PROLIFERATING CELL NUCLEAR ANTIGEN DEFINE DISTINCTSITES FOR INTERACTION WITH DNA-POLYMERASE-DELTA AND DNA-POLYMERASE-EPSILON, Molecular and cellular biology, 17(11), 1997, pp. 6367-6378
BLUE CONE MONOCHROMACY - MOLECULAR-REARRANGEMENTS AND GENOTYPE-PHENOTYPE CORRELATIONS
Authors: AYYAGARI R BINGHAM EL TODA Y SIEVING PA
Citation: R. Ayyagari et al., BLUE CONE MONOCHROMACY - MOLECULAR-REARRANGEMENTS AND GENOTYPE-PHENOTYPE CORRELATIONS, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3179-3179
AUTOSOMAL-DOMINANT CONGENITAL CATARACT WITH INTEROCULAR PHENOTYPIC VARIABILITY - LOCALIZATION TO CHROMOSOME 2Q AND CANDIDATE GENE ANALYSIS OF THE GAMMA-E-CRYSTALLIN PSEUDOGENE
Authors: LI A MADUPU R PADMA T AYYAGARI R SCOTT MH KAISERKUPFER MI HEJTMANCIK JF
Citation: A. Li et al., AUTOSOMAL-DOMINANT CONGENITAL CATARACT WITH INTEROCULAR PHENOTYPIC VARIABILITY - LOCALIZATION TO CHROMOSOME 2Q AND CANDIDATE GENE ANALYSIS OF THE GAMMA-E-CRYSTALLIN PSEUDOGENE, Investigative ophthalmology & visual science, 38(4), 1997, pp. 2720-2720
DIVERSITY IN THE STRUCTURAL REARRANGEMENTS OF RED AND GREEN COLOR GENES IN INDIVIDUALS AFFECTED WITH BLUE CONE MONOCHROMACY
Authors: AYYAGARI R TODA Y KAKUK L SZCZSNY J BINGHAM E SIEVING PA
Citation: R. Ayyagari et al., DIVERSITY IN THE STRUCTURAL REARRANGEMENTS OF RED AND GREEN COLOR GENES IN INDIVIDUALS AFFECTED WITH BLUE CONE MONOCHROMACY, American journal of human genetics, 61(4), 1997, pp. 2390-2390
CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THE USHER SYNDROME TYPE 1C AND FAMILIAL HYPERINSULINISM LOCI ON CHROMOSOME 11P14-15.1
Authors: AYYAGARI R NESTOROWICZ A LI Y CHANDRASEKHARAPPA S CHINAULT C VANTUINEN P SMITH RJH HEJTMANCIK JF PERMUTT MA
Citation: R. Ayyagari et al., CONSTRUCTION OF A YAC CONTIG ENCOMPASSING THE USHER SYNDROME TYPE 1C AND FAMILIAL HYPERINSULINISM LOCI ON CHROMOSOME 11P14-15.1, PCR methods and applications, 6(6), 1996, pp. 504-514
A YAC CONTIG ENCOMPASING THE USHER SYNDROME TYPE 1C LOCUS ON CHROMOSOME
Authors: HEJTMANCIK JF NESTOROWICZ A LI Y VANTUINEN P SMITH RJH KAISERKUPFER M PERMUTT MA AYYAGARI R
Citation: Jf. Hejtmancik et al., A YAC CONTIG ENCOMPASING THE USHER SYNDROME TYPE 1C LOCUS ON CHROMOSOME, Investigative ophthalmology & visual science, 37(3), 1996, pp. 3028-3028
AUTOSOMAL-DOMINANT ZONULAR CATARACT WITH SUTURAL OPACITIES IN A 4-GENERATION FAMILY
Authors: BASTI S HEJTMANCIK JF PADMA T AYYAGARI R KAISERKUPFER MI MURTY JS RAO GN
Citation: S. Basti et al., AUTOSOMAL-DOMINANT ZONULAR CATARACT WITH SUTURAL OPACITIES IN A 4-GENERATION FAMILY, American journal of ophthalmology, 121(2), 1996, pp. 162-168
A MUTATIONAL ANALYSIS OF THE YEAST PROLIFERATING CELL NUCLEAR ANTIGENINDICATES DISTINCT ROLES IN DNA-REPLICATION AND DNA-REPAIR
Authors: AYYAGARI R IMPELLIZZERI KJ YODER BL GARY SL BURGERS PMJ
Citation: R. Ayyagari et al., A MUTATIONAL ANALYSIS OF THE YEAST PROLIFERATING CELL NUCLEAR ANTIGENINDICATES DISTINCT ROLES IN DNA-REPLICATION AND DNA-REPAIR, Molecular and cellular biology, 15(8), 1995, pp. 4420-4429
A YAC CONTIG ENCOMPASSING THE USHIC LOCUS ON THE SHORT ARM OF CHROMOSOME-11
Authors: AYYAGARI R SMITH RJH POLYJMEROPOLOUS M DAIGER S PELIAS MZ WOZENCRAFT L KAISERKUPFER M NESTOROWICZ A PERMUTT A LEE Y HEJTMANCIK JF
Citation: R. Ayyagari et al., A YAC CONTIG ENCOMPASSING THE USHIC LOCUS ON THE SHORT ARM OF CHROMOSOME-11, Investigative ophthalmology & visual science, 36(4), 1995, pp. 1045-1045
A CHROMOSOME 11P14-15.1 YAC CONTIG THAT ENCOMPASSES THE USHER SYNDROME TYPE 1C LOCUS
Authors: AYYAGARI R NESTOROWICZ A LI Y SMITH RJH KAISERKUPFER M PERMUTT MA HEJTMANCIK JF
Citation: R. Ayyagari et al., A CHROMOSOME 11P14-15.1 YAC CONTIG THAT ENCOMPASSES THE USHER SYNDROME TYPE 1C LOCUS, American journal of human genetics, 57(4), 1995, pp. 1484-1484
AUTOSOMAL-DOMINANT ZONULAR CATARACT WITH SUTURAL OPACITIES LOCALIZED TO CHROMOSOME 17Q11-12
Authors: PADMA T AYYAGARI R MURTY JS BASTI S FLETCHER T RAO GN KAISERKUPFER M HEJTMANCIK JF
Citation: T. Padma et al., AUTOSOMAL-DOMINANT ZONULAR CATARACT WITH SUTURAL OPACITIES LOCALIZED TO CHROMOSOME 17Q11-12, American journal of human genetics, 57(4), 1995, pp. 840-845
LINKAGE ANALYSIS OF CANDIDATE GENE REGIONS FOR AUTOSOMAL-DOMINANT ANDRECESSIVE HEREDITARY CATARACTS
Authors: PADMA T AYYAGARI R MURTY JS BASTI S RAO GN SCOTT M WOZENCRAFT L KAISERKUPFER M HEJTMANCIK JF
Citation: T. Padma et al., LINKAGE ANALYSIS OF CANDIDATE GENE REGIONS FOR AUTOSOMAL-DOMINANT ANDRECESSIVE HEREDITARY CATARACTS, Investigative ophthalmology & visual science, 35(4), 1994, pp. 2114-2114
LINKAGE AND HAPLOTYPE ANALYSIS AND PHYSICAL MAPPING OF THE USH1C GENE
Authors: AYYAGARI R SMITH RJH POLYMEROPOULOS M CHINAULT AC DAIGER S PELIAS MZ WOZENCRAFT L KAISERKUPFER M HEJTMANCIK JF
Citation: R. Ayyagari et al., LINKAGE AND HAPLOTYPE ANALYSIS AND PHYSICAL MAPPING OF THE USH1C GENE, Investigative ophthalmology & visual science, 35(4), 1994, pp. 2143-2143
EVIDENCE OF GENETIC-HETEROGENEITY IN ROMANO-WARD LONG-QT-SYNDROME - ANALYSIS OF 23 FAMILIES
Authors: TOWBIN JA LI H TAGGART RT LEHMANN MH SCHWARTZ PJ SATLER CA AYYAGARI R ROBINSON JL MOSS A HEJTMANCIK JF
Citation: Ja. Towbin et al., EVIDENCE OF GENETIC-HETEROGENEITY IN ROMANO-WARD LONG-QT-SYNDROME - ANALYSIS OF 23 FAMILIES, Circulation, 90(6), 1994, pp. 2635-2644
USHER SYNDROME TYPE-I IN THE FRENCH ACADIAN POPULATION - FINE MAPPINGAND HAPLOTYPE ANALYSIS
Authors: AYYAGARI R SMITH RJH LEE EC KIMBERLING WJ DAIGER SP PELIAS MZ KEATS BJB JAY M BIRD A REARDON W GUEST M HEJTMANCIK JF
Citation: R. Ayyagari et al., USHER SYNDROME TYPE-I IN THE FRENCH ACADIAN POPULATION - FINE MAPPINGAND HAPLOTYPE ANALYSIS, American journal of human genetics, 53(3), 1993, pp. 970-970
GENETIC-HETEROGENEITY IN 22 FAMILIES WITH LONG QT SYNDROME
Authors: TOWBIN JA SIU B ROBINSON J MOSS A AYYAGARI R HEJTMANCIK JF
Citation: Ja. Towbin et al., GENETIC-HETEROGENEITY IN 22 FAMILIES WITH LONG QT SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1092-1092
Risultati: 1-16 |