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Results: 1-16 |
Results: 16
STRUCTURE OF THE HUMAN BIOTINIDASE GENE
Authors: KNIGHT HC REYNOLDS TR MEYERS GA POMPONIO RJ BUCK GA WOLF B
Citation: Hc. Knight et al., STRUCTURE OF THE HUMAN BIOTINIDASE GENE, Mammalian genome, 9(4), 1998, pp. 327-330
CERAMIC COMMODITIES AND COMMON CONTAINERS - PRODUCTION AND DISTRIBUTION OF WHITE MOUNTAIN RED WARE IN THE GRASSHOPPER REGION, ARIZONA - TRIADAN,D
Authors: REYNOLDS TR
Citation: Tr. Reynolds, CERAMIC COMMODITIES AND COMMON CONTAINERS - PRODUCTION AND DISTRIBUTION OF WHITE MOUNTAIN RED WARE IN THE GRASSHOPPER REGION, ARIZONA - TRIADAN,D, Technology and culture, 39(3), 1998, pp. 552-553
RISK AND OPPORTUNITY - THE MUSEUM AS CAREER CHOICE - OPPORTUNITIES FOR ADVANCEMENT AND PROFESSIONAL-TRAINING
Authors: REYNOLDS TR
Citation: Tr. Reynolds, RISK AND OPPORTUNITY - THE MUSEUM AS CAREER CHOICE - OPPORTUNITIES FOR ADVANCEMENT AND PROFESSIONAL-TRAINING, Museum news, 77(4), 1998, pp. 38
MUTATION (Q456H) IS THE MOST COMMON-CAUSE OF PROFOUND BIOTINIDASE DEFICIENCY IN CHILDREN ASCERTAINED BY NEWBORN SCREENING IN THE UNITED-STATES
Authors: NORRGARD KJ POMPONIO RJ SWANGO KL HYMES J REYNOLDS TR BUCK GA WOLF B
Citation: Kj. Norrgard et al., MUTATION (Q456H) IS THE MOST COMMON-CAUSE OF PROFOUND BIOTINIDASE DEFICIENCY IN CHILDREN ASCERTAINED BY NEWBORN SCREENING IN THE UNITED-STATES, Biochemical and molecular medicine, 61(1), 1997, pp. 22-27
PROFOUND BIOTINIDASE DEFICIENCY CAUSED BY A POINT MUTATION THAT CREATES A DOWNSTREAM CRYPTIC 3'-SPLICE ACCEPTOR SITE WITHIN AN EXON OF THE HUMAN BIOTINIDASE GENE
Authors: POMPONIO RJ REYNOLDS TR MANDEL H ADMONI O MELONE PD BUCK GA WOLF B
Citation: Rj. Pomponio et al., PROFOUND BIOTINIDASE DEFICIENCY CAUSED BY A POINT MUTATION THAT CREATES A DOWNSTREAM CRYPTIC 3'-SPLICE ACCEPTOR SITE WITHIN AN EXON OF THE HUMAN BIOTINIDASE GENE, Human molecular genetics, 6(5), 1997, pp. 739-745
ARG538 TO CYS MUTATION IN A CPG DINUCLEOTIDE OF THE HUMAN BIOTINIDASEGENE IS THE 2ND MOST COMMON-CAUSE OF PROFOUND BIOTINIDASE DEFICIENCY IN SYMPTOMATIC CHILDREN
Authors: POMPONIO RJ NORRGARD KJ HYMES J REYNOLDS TR BUCK GA BAUMGARTNER R SUORMALA T WOLF B
Citation: Rj. Pomponio et al., ARG538 TO CYS MUTATION IN A CPG DINUCLEOTIDE OF THE HUMAN BIOTINIDASEGENE IS THE 2ND MOST COMMON-CAUSE OF PROFOUND BIOTINIDASE DEFICIENCY IN SYMPTOMATIC CHILDREN, Human genetics, 99(4), 1997, pp. 506-512
MUTATIONS IN THE HUMAN BIOTINIDASE GENE THAT CAUSE PROFOUND BIOTINIDASE DEFICIENCY IN SYMPTOMATIC CHILDREN - MOLECULAR, BIOCHEMICAL, AND CLINICAL ANALYSIS
Authors: POMPONIO RJ HYMES J REYNOLDS TR MEYERS GA FLEISCHHAUER K BUCK GA WOLF B
Citation: Rj. Pomponio et al., MUTATIONS IN THE HUMAN BIOTINIDASE GENE THAT CAUSE PROFOUND BIOTINIDASE DEFICIENCY IN SYMPTOMATIC CHILDREN - MOLECULAR, BIOCHEMICAL, AND CLINICAL ANALYSIS, Pediatric research, 42(6), 1997, pp. 840-848
MUTATIONS IN THE HUMAN BIOTINIDASE GENE THAT CAUSE PROFOUND BIOTINIDASE DEFICIENCY IN SYMPTOMATIC CHILDREN - MOLECULAR, BIOCHEMICAL, AND CLINICAL ANALYSIS
Authors: POMPONIO RJ HYMES J REYNOLDS TR MEYERS GA FLEISCHHAUER K BUCK GA WOLF B
Citation: Rj. Pomponio et al., MUTATIONS IN THE HUMAN BIOTINIDASE GENE THAT CAUSE PROFOUND BIOTINIDASE DEFICIENCY IN SYMPTOMATIC CHILDREN - MOLECULAR, BIOCHEMICAL, AND CLINICAL ANALYSIS, American journal of human genetics, 61(4), 1997, pp. 1508-1508
DELETION INSERTION MUTATION THAT CAUSES BIOTINIDASE DEFICIENCY MAY RESULT FROM THE FORMATION OF A QUASI-PALINDROMIC STRUCTURE/
Authors: POMPONIO RJ NARASIMHAN V REYNOLDS TR BUCK GA POVIRK LF WOLF B
Citation: Rj. Pomponio et al., DELETION INSERTION MUTATION THAT CAUSES BIOTINIDASE DEFICIENCY MAY RESULT FROM THE FORMATION OF A QUASI-PALINDROMIC STRUCTURE/, Human molecular genetics, 5(10), 1996, pp. 1657-1661
MUTATIONAL HOTSPOT IN THE HUMAN BIOTINIDASE GENE CAUSES PROFOUND BIOTINIDASE DEFICIENCY
Authors: POMPONIO RJ REYNOLDS TR COLE H BUCK GA WOLF B
Citation: Rj. Pomponio et al., MUTATIONAL HOTSPOT IN THE HUMAN BIOTINIDASE GENE CAUSES PROFOUND BIOTINIDASE DEFICIENCY, Nature genetics, 11(1), 1995, pp. 96-98
MUTATIONAL HOTSPOT IN THE HUMAN SERUM BIOTINIDASE GENE AS A CAUSE OF BIOTINIDASE DEFICIENCY
Authors: POMPONIO RJ REYNOLDS TR COLE H BUCK GA WOLF B
Citation: Rj. Pomponio et al., MUTATIONAL HOTSPOT IN THE HUMAN SERUM BIOTINIDASE GENE AS A CAUSE OF BIOTINIDASE DEFICIENCY, American journal of human genetics, 57(4), 1995, pp. 28-28
REVERSAL OF VENTRICULAR CONTRACTURE DURING HYPOTHERMIC CARDIOPLEGIC ARREST
Authors: HEDBERG PS TORCHIANA DF REYNOLDS TR GEFFIN GA TITUS JS DAGGETT WM
Citation: Ps. Hedberg et al., REVERSAL OF VENTRICULAR CONTRACTURE DURING HYPOTHERMIC CARDIOPLEGIC ARREST, The Journal of surgical research, 56(5), 1994, pp. 439-445
HUMAN SERUM BIOTINIDASE - CDNA CLONING, SEQUENCE, AND CHARACTERIZATION
Authors: COLE H REYNOLDS TR LOCKYER JM BUCK GA DENSON T SPENCE JE HYMES J WOLF B
Citation: H. Cole et al., HUMAN SERUM BIOTINIDASE - CDNA CLONING, SEQUENCE, AND CHARACTERIZATION, The Journal of biological chemistry, 269(9), 1994, pp. 6566-6570
OPTIMIZATION OF COUPLED PCR AMPLIFICATION AND CYCLE SEQUENCING OF CLONED AND GENOMIC DNA
Authors: REYNOLDS TR ULIANA SRB FLOETERWINTER LM BUCK GA
Citation: Tr. Reynolds et al., OPTIMIZATION OF COUPLED PCR AMPLIFICATION AND CYCLE SEQUENCING OF CLONED AND GENOMIC DNA, BioTechniques, 15(3), 1993, pp. 462
MOLECULAR CHARACTERIZATION OF HUMAN BIOTINIDASE
Authors: COLE H REYNOLDS TR BUCK GA LOCKYER J DENSON T SPENCE EJ HYMES J WOLF B
Citation: H. Cole et al., MOLECULAR CHARACTERIZATION OF HUMAN BIOTINIDASE, American journal of human genetics, 53(3), 1993, pp. 895-895
NAVAJOLAND - FAMILY SETTLEMENT AND LAND-USE - KELLEY,KB, WHITELEY,PM
Authors: REYNOLDS TR
Citation: Tr. Reynolds, NAVAJOLAND - FAMILY SETTLEMENT AND LAND-USE - KELLEY,KB, WHITELEY,PM, American anthropologist, 95(2), 1993, pp. 505-506
Risultati: 1-16 |