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Results: 1-25 | 26-37
Results: 1-25/37
AMPLIFICATION OF CFTR EXON-9 SEQUENCES TO MULTIPLE LOCATIONS IN THE HUMAN GENOME
Authors: ROZMAHEL R HENG HHQ DUNCAN AMV SHI XM ROMMENS JM TSUI LC
Citation: R. Rozmahel et al., AMPLIFICATION OF CFTR EXON-9 SEQUENCES TO MULTIPLE LOCATIONS IN THE HUMAN GENOME, Genomics, 45(3), 1997, pp. 554-561
PHYSICAL AND TRANSCRIPTION MAP IN THE REGION 14Q24.3 - IDENTIFICATIONOF 6 NOVEL TRANSCRIPTS
Authors: ROUX AF ROMMENS JM READ L DUNCAN AMV COX DW
Citation: Af. Roux et al., PHYSICAL AND TRANSCRIPTION MAP IN THE REGION 14Q24.3 - IDENTIFICATIONOF 6 NOVEL TRANSCRIPTS, Genomics, 43(2), 1997, pp. 130-140
CHROMOSOMAL LOCALIZATION OF THE HUMAN LIVER FORM CYTOCHROME-C-OXIDASESUBUNIT VIIA GENE
Authors: MERANTE F DUNCAN AMV MITCHELL G DUFF C ROMMENS J ROBINSON BH
Citation: F. Merante et al., CHROMOSOMAL LOCALIZATION OF THE HUMAN LIVER FORM CYTOCHROME-C-OXIDASESUBUNIT VIIA GENE, Genome, 40(3), 1997, pp. 318-324
CLONING, CHARACTERIZATION, AND CHROMOSOMAL LOCALIZATION OF HUMAN LIVER FORM CYTOCHROME-C-OXIDASE SUBUNIT VIA RELATED GENES
Authors: MERANTE F LING MF DUNCAN AMV DUFF C ROBINSON BH
Citation: F. Merante et al., CLONING, CHARACTERIZATION, AND CHROMOSOMAL LOCALIZATION OF HUMAN LIVER FORM CYTOCHROME-C-OXIDASE SUBUNIT VIA RELATED GENES, Genome, 40(3), 1997, pp. 325-331
THE HUMAN MITOCHONDRIAL ELONGATION-FACTOR TU (EF-TU) GENE - CDNA SEQUENCE, GENOMIC LOCALIZATION, GENOMIC STRUCTURE, AND IDENTIFICATION OF APSEUDOGENE
Authors: LING MF MERANTE F CHEN HS DUFF C DUNCAN AMV ROBINSON BH
Citation: Mf. Ling et al., THE HUMAN MITOCHONDRIAL ELONGATION-FACTOR TU (EF-TU) GENE - CDNA SEQUENCE, GENOMIC LOCALIZATION, GENOMIC STRUCTURE, AND IDENTIFICATION OF APSEUDOGENE, Gene, 197(1-2), 1997, pp. 325-336
EVIDENCE THAT SKEWED X-INACTIVATION IS NOT NEEDED FOR THE PHENOTYPIC-EXPRESSION OF AICARDI-SYNDROME
Authors: HOAG HM TAYLOR SAM DUNCAN AMV KHALIFA MM
Citation: Hm. Hoag et al., EVIDENCE THAT SKEWED X-INACTIVATION IS NOT NEEDED FOR THE PHENOTYPIC-EXPRESSION OF AICARDI-SYNDROME, Human genetics, 100(3-4), 1997, pp. 459-464
A REPORT OF RECURRENT ANENCEPHALY WITH TRISOMY 2P23-2PTER - ADDITIONAL EVIDENCE FOR THE INVOLVEMENT OF 2P24 IN NEURAL-TUBE DEVELOPMENT AND EVALUATION OF THE ROLE FOR CYTOGENETIC ANALYSIS
Authors: WINSOR SHM MCGRATH MJ KHALIFA M DUNCAN AMV
Citation: Shm. Winsor et al., A REPORT OF RECURRENT ANENCEPHALY WITH TRISOMY 2P23-2PTER - ADDITIONAL EVIDENCE FOR THE INVOLVEMENT OF 2P24 IN NEURAL-TUBE DEVELOPMENT AND EVALUATION OF THE ROLE FOR CYTOGENETIC ANALYSIS, Prenatal diagnosis, 17(7), 1997, pp. 665-669
ASSIGNMENT OF THE PSST SUBUNIT GENE OF HUMAN MITOCHONDRIAL COMPLEX-I TO CHROMOSOME 19P13
Authors: HYSLOP SJ DUNCAN AMV PITKANEN S ROBINSON BH
Citation: Sj. Hyslop et al., ASSIGNMENT OF THE PSST SUBUNIT GENE OF HUMAN MITOCHONDRIAL COMPLEX-I TO CHROMOSOME 19P13, Genomics, 37(3), 1996, pp. 375-380
THE GENE ENCODING PROTEIN-TYROSINE-PHOSPHATASE RPTP-EPSILON (PTPRE) IS ASSIGNED TO HUMAN-CHROMOSOME 10Q26
Authors: MELHADO IG ANDERSON LL DUNCAN AMV JIRIK FR
Citation: Ig. Melhado et al., THE GENE ENCODING PROTEIN-TYROSINE-PHOSPHATASE RPTP-EPSILON (PTPRE) IS ASSIGNED TO HUMAN-CHROMOSOME 10Q26, Cytogenetics and cell genetics, 73(3), 1996, pp. 168-170
CHROMOSOME CONTENT AND ULTRASTRUCTURE OF RADIATION-INDUCED MICRONUCLEI
Authors: WALKER JA BOREHAM DR UNRAU P DUNCAN AMV
Citation: Ja. Walker et al., CHROMOSOME CONTENT AND ULTRASTRUCTURE OF RADIATION-INDUCED MICRONUCLEI, Mutagenesis, 11(5), 1996, pp. 419-424
BRIEF CLINICAL REPORT - PALLISTER-KILLIAN-SYNDROME - A MILD CASE DIAGNOSED BY FLUORESCENCE IN-SITU HYBRIDIZATION - REVIEW OF THE LITERATUREAND EXPANSION OF THE PHENOTYPE
Authors: BIELANSKA MM KHALIFA MM DUNCAN AMV
Citation: Mm. Bielanska et al., BRIEF CLINICAL REPORT - PALLISTER-KILLIAN-SYNDROME - A MILD CASE DIAGNOSED BY FLUORESCENCE IN-SITU HYBRIDIZATION - REVIEW OF THE LITERATUREAND EXPANSION OF THE PHENOTYPE, American journal of medical genetics, 65(2), 1996, pp. 104-108
A FEMALE WITH MONOSOMY-18 MOSAICISM - A PREVIOUSLY UNDESCRIBED CHROMOSOME ABNORMALITY
Authors: KHALIFA MM YAMASHIRO H DUNCAN AMV HEFFERON M MARTIN AE
Citation: Mm. Khalifa et al., A FEMALE WITH MONOSOMY-18 MOSAICISM - A PREVIOUSLY UNDESCRIBED CHROMOSOME ABNORMALITY, Clinical genetics, 49(6), 1996, pp. 318-320
SUCCINYL-COA - 3-OXOACID COA TRANSFERASE (SCOT) - HUMAN CDNA CLONING,HUMAN CHROMOSOMAL MAPPING TO 5P13, AND MUTATION DETECTION IN A SCOT-DEFICIENT PATIENT
Authors: KASSOVSKABRATINOVA S FUKAO T SONG XQ DUNCAN AMV CHEN HS ROBERT MF PEREZCERDA C UGARTE M CHARTRAND C VOBECKY S KONDO N MITCHELL GA
Citation: S. Kassovskabratinova et al., SUCCINYL-COA - 3-OXOACID COA TRANSFERASE (SCOT) - HUMAN CDNA CLONING,HUMAN CHROMOSOMAL MAPPING TO 5P13, AND MUTATION DETECTION IN A SCOT-DEFICIENT PATIENT, American journal of human genetics, 59(3), 1996, pp. 519-528
A WIDELY DISTRIBUTED PUTATIVE MAMMALIAN TRANSCRIPTIONAL REGULATOR CONTAINING MULTIPLE PAIRED AMPHIPATHIC HELICES, WITH SIMILARITY TO YEAST SIN3
Authors: HALLECK MS POWNALL S HARDER KW DUNCAN AMV JIRIK FR SCHLEGEL RA
Citation: Ms. Halleck et al., A WIDELY DISTRIBUTED PUTATIVE MAMMALIAN TRANSCRIPTIONAL REGULATOR CONTAINING MULTIPLE PAIRED AMPHIPATHIC HELICES, WITH SIMILARITY TO YEAST SIN3, Genomics, 26(2), 1995, pp. 403-406
CHROMOSOMAL LOCALIZATION OF THE HUMAN PROSTANOID RECEPTOR GENE FAMILY
Authors: DUNCAN AMV ANDERSON LL FUNK CD ABRAMOVITZ M ADAM M
Citation: Amv. Duncan et al., CHROMOSOMAL LOCALIZATION OF THE HUMAN PROSTANOID RECEPTOR GENE FAMILY, Genomics, 25(3), 1995, pp. 740-742
PROTEIN-TYROSINE-PHOSPHATASE SH-PTP2 (PTPN11) IS LOCALIZED TO 12Q24.1-24.3
Authors: DECHERT U DUNCAN AMV BASTIEN L DUFF C ADAM M JIRIK FR
Citation: U. Dechert et al., PROTEIN-TYROSINE-PHOSPHATASE SH-PTP2 (PTPN11) IS LOCALIZED TO 12Q24.1-24.3, Human genetics, 96(5), 1995, pp. 609-615
HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE - ISOLATION OF CDNA, MAPPING AND MUTATION IDENTIFICATION (VOL 7, PG 195, 1994)
Authors: GOYETTE P SUMNER JS MILOS R DUNCAN AMV ROSENBLATT DS MATTHEWS RG ROZEN R
Citation: P. Goyette et al., HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE - ISOLATION OF CDNA, MAPPING AND MUTATION IDENTIFICATION (VOL 7, PG 195, 1994), Nature genetics, 7(4), 1994, pp. 551-551
HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE - ISOLATION OF CDNA, MAPPING AND MUTATION IDENTIFICATION
Authors: GOYETTE P SUMNER JS MILOS R DUNCAN AMV ROSENBLATT DS MATTHEWS RG ROZEN R
Citation: P. Goyette et al., HUMAN METHYLENETETRAHYDROFOLATE REDUCTASE - ISOLATION OF CDNA, MAPPING AND MUTATION IDENTIFICATION, Nature genetics, 7(2), 1994, pp. 195-200
THE E-SUBUNIT OF VACUOLAR H-ATPASE LOCALIZES CLOSE TO THE CENTROMERE ON HUMAN-CHROMOSOME 22()
Authors: BAUD V MEARS AJ LAMOUR V SCAMPS C DUNCAN AMV MCDERMID HE LIPINSKI M
Citation: V. Baud et al., THE E-SUBUNIT OF VACUOLAR H-ATPASE LOCALIZES CLOSE TO THE CENTROMERE ON HUMAN-CHROMOSOME 22(), Human molecular genetics, 3(2), 1994, pp. 335-339
ASSIGNMENT OF THE ENDOTHELIAL-SPECIFIC PROTEIN-RECEPTOR TYROSINE KINASE GENE (TEK) TO HUMAN-CHROMOSOME 9P21
Authors: DUMONT DJ ANDERSON L BREITMAN ML DUNCAN AMV
Citation: Dj. Dumont et al., ASSIGNMENT OF THE ENDOTHELIAL-SPECIFIC PROTEIN-RECEPTOR TYROSINE KINASE GENE (TEK) TO HUMAN-CHROMOSOME 9P21, Genomics, 23(2), 1994, pp. 512-513
ASSIGNMENT OF THE GENE (UQCRFS1) FOR THE RIESKE IRON-SULFUR PROTEIN SUBUNIT OF THE MITOCHONDRIAL CYTOCHROME BC(1) COMPLEX TO THE 22Q13 AND 19Q12-Q13.1 REGIONS OF THE HUMAN GENOME
Authors: DUNCAN AMV ANDERSON L DUFF C OZAWA T SUZUKI H WORTON R ROZEN R
Citation: Amv. Duncan et al., ASSIGNMENT OF THE GENE (UQCRFS1) FOR THE RIESKE IRON-SULFUR PROTEIN SUBUNIT OF THE MITOCHONDRIAL CYTOCHROME BC(1) COMPLEX TO THE 22Q13 AND 19Q12-Q13.1 REGIONS OF THE HUMAN GENOME, Genomics, 21(1), 1994, pp. 281-283
ASSIGNMENT OF HUMAN GLUTARYL-COA DEHYDROGENASE GENE (GCDH) TO THE SHORT ARM OF CHROMOSOME-19 (19P13.2) BY IN-SITU HYBRIDIZATION AND SOMATIC-CELL HYBRID ANALYSIS
Authors: GREENBERG CR DUNCAN AMV GREGORY CA SINGAL R GOODMAN SI
Citation: Cr. Greenberg et al., ASSIGNMENT OF HUMAN GLUTARYL-COA DEHYDROGENASE GENE (GCDH) TO THE SHORT ARM OF CHROMOSOME-19 (19P13.2) BY IN-SITU HYBRIDIZATION AND SOMATIC-CELL HYBRID ANALYSIS, Genomics, 21(1), 1994, pp. 289-290
ASSIGNMENT OF THE GENE FOR THE CYTOCHROME C(1) SUBUNIT OF THE MITOCHONDRIAL CYTOCHROME BC(1) COMPLEX (CYC1) TO HUMAN-CHROMOSOME 8Q24.3
Authors: DUNCAN AMV OZAWA T SUZUKI H ROZEN R
Citation: Amv. Duncan et al., ASSIGNMENT OF THE GENE FOR THE CYTOCHROME C(1) SUBUNIT OF THE MITOCHONDRIAL CYTOCHROME BC(1) COMPLEX (CYC1) TO HUMAN-CHROMOSOME 8Q24.3, Genomics, 19(2), 1994, pp. 400-401
A SUBUNIT OF VACUOLAR H-ATPASE IS ENCODED WITHIN THE CAT EYE SYNDROMECRITICAL REGION ON HUMAN-CHROMOSOME-22()
Authors: BAUD V MEARS AJ LAMOUR V SCAMPS C DUNCAN AMV MCDERMID HE LIPINSKI M
Citation: V. Baud et al., A SUBUNIT OF VACUOLAR H-ATPASE IS ENCODED WITHIN THE CAT EYE SYNDROMECRITICAL REGION ON HUMAN-CHROMOSOME-22(), Cytogenetics and cell genetics, 67(4), 1994, pp. 294-294
ICA1 ENCODING P69, A PROTEIN LINKED TO THE DEVELOPMENT OF TYPE-1 DIABETES, MAPS TO HUMAN-CHROMOSOME 7P22
Authors: GAEDIGK R DUNCAN AMV MIYAZAKI I ROBINSON BH DOSCH HM
Citation: R. Gaedigk et al., ICA1 ENCODING P69, A PROTEIN LINKED TO THE DEVELOPMENT OF TYPE-1 DIABETES, MAPS TO HUMAN-CHROMOSOME 7P22, Cytogenetics and cell genetics, 66(4), 1994, pp. 274-276
Risultati: 1-25 | 26-37