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Results: 1-25 | 26-26
Results: 1-25/26
TRANSLOCATIONS OF 11Q13 IN MANTLE CELL LYMPHOMA FAIL TO DISRUPT THE S-MU-BP-2 GENE
Authors: GULLEY ML ZHANG Q GASCOYNE RD DUPONT BR BANKS PM CHO CG HUANG JM MONTALVO EA
Citation: Ml. Gulley et al., TRANSLOCATIONS OF 11Q13 IN MANTLE CELL LYMPHOMA FAIL TO DISRUPT THE S-MU-BP-2 GENE, Hematopathology and molecular hematology, 11(1), 1998, pp. 1-11
A NOVEL POTASSIUM CHANNEL GENE, KCNQ2, IS MUTATED IN AN INHERITED EPILEPSY OF NEWBORNS
Authors: SINGH NA CHARLIER C STAUFFER D DUPONT BR LEACH RJ MELIS R RONEN GM BJERRE I QUATTLEBAUM T MURPHY JV MCHARG ML GAGNON D ROSALES TO PEIFFER A ANDERSON VE LEPPERT M
Citation: Na. Singh et al., A NOVEL POTASSIUM CHANNEL GENE, KCNQ2, IS MUTATED IN AN INHERITED EPILEPSY OF NEWBORNS, Nature genetics, 18(1), 1998, pp. 25-29
CLONING, CHROMOSOMAL LOCALIZATION AND PROMOTER ANALYSIS OF THE HUMAN TRANSCRIPTION FACTOR YY1
Authors: YAO YL DUPONT BR GHOSH S FANG Y LEACH RJ SETO E
Citation: Yl. Yao et al., CLONING, CHROMOSOMAL LOCALIZATION AND PROMOTER ANALYSIS OF THE HUMAN TRANSCRIPTION FACTOR YY1, Nucleic acids research, 26(16), 1998, pp. 3776-3783
CHROMOSOME 18Q PARACENTRIC INVERSION IN A FAMILY WITH MENTAL-RETARDATION AND HEARING-LOSS
Authors: KEPPLERNOREUIL KM CARROLL AJ FINLEY SC DESCARTES M CODY JD DUPONT BR GAY CT LEACH RJ
Citation: Km. Kepplernoreuil et al., CHROMOSOME 18Q PARACENTRIC INVERSION IN A FAMILY WITH MENTAL-RETARDATION AND HEARING-LOSS, American journal of medical genetics, 76(5), 1998, pp. 372-378
IDENTIFICATION OF CRYPTIC REARRANGEMENTS IN PATIENTS WITH 18Q- DELETION SYNDROME
Authors: BRKANAC Z CODY JD LEACH RJ DUPONT BR
Citation: Z. Brkanac et al., IDENTIFICATION OF CRYPTIC REARRANGEMENTS IN PATIENTS WITH 18Q- DELETION SYNDROME, American journal of human genetics, 62(6), 1998, pp. 1500-1506
AMELOBLASTIN GENE (AMBN) MAPS WITHIN THE CRITICAL REGION FOR AUTOSOMAL-DOMINANT AMELOGENESIS IMPERFECTA AT CHROMOSOME 4Q21
Authors: MACDOUGALL M DUPONT BR SIMMONS D REUS B KREBSBACH P KARRMAN C HOLMGREN G LEACH RJ FORSMAN K
Citation: M. Macdougall et al., AMELOBLASTIN GENE (AMBN) MAPS WITHIN THE CRITICAL REGION FOR AUTOSOMAL-DOMINANT AMELOGENESIS IMPERFECTA AT CHROMOSOME 4Q21, Genomics, 41(1), 1997, pp. 115-118
ASSIGNMENT OF SAFB ENCODING HSP27 ERE-TATA BINDING-PROTEIN (HET) SCAFFOLD ATTACHMENT FACTOR-B (SAF-B) TO HUMAN-CHROMOSOME-19 BAND P13
Authors: DUPONT BR GARCIA DK SULLIVAN TM NAYLOR SL OESTERREICH S
Citation: Br. Dupont et al., ASSIGNMENT OF SAFB ENCODING HSP27 ERE-TATA BINDING-PROTEIN (HET) SCAFFOLD ATTACHMENT FACTOR-B (SAF-B) TO HUMAN-CHROMOSOME-19 BAND P13, Cytogenetics and cell genetics, 79(3-4), 1997, pp. 284-285
ASSIGNMENT OF DENTIN SIALOPHOSPHOPROTEIN (DSPP) TO THE CRITICAL DGI2 LOCUS ON HUMAN-CHROMOSOME-4 BAND Q21.3 BY IN-SITU HYBRIDIZATION
Authors: MACDOUGALL M SIMMONS D LUAN X GU TT DUPONT BR
Citation: M. Macdougall et al., ASSIGNMENT OF DENTIN SIALOPHOSPHOPROTEIN (DSPP) TO THE CRITICAL DGI2 LOCUS ON HUMAN-CHROMOSOME-4 BAND Q21.3 BY IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 79(1-2), 1997, pp. 121-122
MAGNETIC-RESONANCE-IMAGING DEMONSTRATES INCOMPLETE MYELINATION IN 18Q- SYNDROME - EVIDENCE FOR MYELIN BASIC-PROTEIN HAPLOINSUFFICIENCY
Authors: GAY CT HARDIES LJ RAUCH RA LANCASTER JL PLAETKE R DUPONT BR CODY JD CORNELL JE HERNDON RC GHIDONI PD SCHIFF JM KAYE CI LEACH RJ FOX PT
Citation: Ct. Gay et al., MAGNETIC-RESONANCE-IMAGING DEMONSTRATES INCOMPLETE MYELINATION IN 18Q- SYNDROME - EVIDENCE FOR MYELIN BASIC-PROTEIN HAPLOINSUFFICIENCY, American journal of medical genetics, 74(4), 1997, pp. 422-431
ASSIGNMENT OF THE HUMAN NUCLEAR HORMONE-RECEPTOR, NUC1 (PPARD), TO CHROMOSOME 6P21.1-P21.2
Authors: YOSHIKAWA T BRKANAC Z DUPONT BR XING GQ LEACH RJ DETERAWADLEIGH SD
Citation: T. Yoshikawa et al., ASSIGNMENT OF THE HUMAN NUCLEAR HORMONE-RECEPTOR, NUC1 (PPARD), TO CHROMOSOME 6P21.1-P21.2, Genomics, 35(3), 1996, pp. 637-638
NEW VARIANTS OF THE HUMAN AND RAT NUCLEAR HORMONE-RECEPTOR, TR4 - EXPRESSION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN GENE
Authors: YOSHIKAWA T DUPONT BR LEACH RJ DETERAWADLEIGH SD
Citation: T. Yoshikawa et al., NEW VARIANTS OF THE HUMAN AND RAT NUCLEAR HORMONE-RECEPTOR, TR4 - EXPRESSION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN GENE, Genomics, 35(2), 1996, pp. 361-366
LOCALIZATION OF A GENE FOR A GLUTAMATE BINDING SUBUNIT OF A NMDA RECEPTOR (GRINA) TO 8Q24
Authors: LEWIS TB WOOD S MICHAELIS EK DUPONT BR LEACH RJ
Citation: Tb. Lewis et al., LOCALIZATION OF A GENE FOR A GLUTAMATE BINDING SUBUNIT OF A NMDA RECEPTOR (GRINA) TO 8Q24, Genomics, 32(1), 1996, pp. 131-133
ASSIGNMENT OF DMP1 TO HUMAN-CHROMOSOME-4 BAND Q21 BY IN-SITU HYBRIDIZATION
Authors: MACDOUGALL M DUPONT BR SIMMONS D LEACH RJ
Citation: M. Macdougall et al., ASSIGNMENT OF DMP1 TO HUMAN-CHROMOSOME-4 BAND Q21 BY IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 74(3), 1996, pp. 189-189
ASSIGNMENT OF MATRIX METALLOPROTEINASE-9 (MMP9) TO MOUSE CHROMOSOME-2BANDS H1-H2
Authors: DUPONT BR LINN R KNIGHT CB ROODMAN GD SAKAGUCHI AY LALLEY PA FOURNIER REK LEACH RJ
Citation: Br. Dupont et al., ASSIGNMENT OF MATRIX METALLOPROTEINASE-9 (MMP9) TO MOUSE CHROMOSOME-2BANDS H1-H2, Cytogenetics and cell genetics, 74(1-2), 1996, pp. 118-119
REASSIGNMENT OF THE 92-KDA TYPE-IV COLLAGENASE GENE (CLG4B) TO HUMAN-CHROMOSOME-20
Authors: LINN R DUPONT BR KNIGHT CB PLAETKE R LEACH RJ
Citation: R. Linn et al., REASSIGNMENT OF THE 92-KDA TYPE-IV COLLAGENASE GENE (CLG4B) TO HUMAN-CHROMOSOME-20, Cytogenetics and cell genetics, 72(2-3), 1996, pp. 159-161
MAGNETIC-RESONANCE-IMAGING RELAXOMETRY OF DELAYED MYELINATION IN THE 18Q- SYNDROME - CORRELATION WITH MYELIN BASIC-PROTEIN GENOTYPE
Authors: GAY CT RAUCH RA LANCASTER JL PLAETKE R DUPONT BR CODY JD HARDIES LJ HERNDON RC GHIDONI PD SCHIFF JM KAYE CI LEACH RJ FOX PT
Citation: Ct. Gay et al., MAGNETIC-RESONANCE-IMAGING RELAXOMETRY OF DELAYED MYELINATION IN THE 18Q- SYNDROME - CORRELATION WITH MYELIN BASIC-PROTEIN GENOTYPE, Annals of neurology, 38(3), 1995, pp. 520-520
PRENATAL-DIAGNOSIS OF A COMPLEX CHROMOSOME REARRANGEMENT INVOLVING 4 CHROMOSOMES
Authors: MOORE CM DUPONT BR MATTERN VL HIGBY K
Citation: Cm. Moore et al., PRENATAL-DIAGNOSIS OF A COMPLEX CHROMOSOME REARRANGEMENT INVOLVING 4 CHROMOSOMES, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 119-119
INTERSTITIAL DUPLICATION 19P
Authors: STRATTON RF DUPONT BR OLSEN AS FERTITTA A HOYER M MOORE CM
Citation: Rf. Stratton et al., INTERSTITIAL DUPLICATION 19P, American journal of medical genetics, 57(4), 1995, pp. 562-564
MOLECULAR CHARACTERIZATION OF GLYCOPHORIN-A TRANSCRIPTS IN HUMAN ERYTHROID-CELLS USING RT-PCR, ALLELE-SPECIFIC RESTRICTION, AND SEQUENCING
Authors: DUPONT BR GRANT SG OTO SH BIGBEE WL JENSEN RH LANGLOIS RG
Citation: Br. Dupont et al., MOLECULAR CHARACTERIZATION OF GLYCOPHORIN-A TRANSCRIPTS IN HUMAN ERYTHROID-CELLS USING RT-PCR, ALLELE-SPECIFIC RESTRICTION, AND SEQUENCING, Vox sanguinis, 68(2), 1995, pp. 121-129
GENOTYPE AT THE MYELIN BASIC-PROTEIN LOCUS WITH CORRELATION TO MRI INTHE 18Q- SYNDROME
Authors: DUPONT BR GAY CT CODY JD PLAETKE R HARDIES LJ RAUCH RA GHIDONI PD FOX PT KAYE CI LEACH RJ
Citation: Br. Dupont et al., GENOTYPE AT THE MYELIN BASIC-PROTEIN LOCUS WITH CORRELATION TO MRI INTHE 18Q- SYNDROME, American journal of human genetics, 57(4), 1995, pp. 1378-1378
CHARACTERIZATION OF CLINICAL CASES USING LABELED COSMID PROBES
Authors: DUPONT BR STRATTON RF FERTITTA A OLSEN AS RYAN SG MOORE CM
Citation: Br. Dupont et al., CHARACTERIZATION OF CLINICAL CASES USING LABELED COSMID PROBES, Journal of cellular biochemistry, 1994, pp. 202-202
PALLISTER-KILLIAN AND FRYNS SYNDROMES
Authors: STRATTON RF MOORE CM POPHAM CS DUPONT BR MATTERN VL
Citation: Rf. Stratton et al., PALLISTER-KILLIAN AND FRYNS SYNDROMES, American journal of medical genetics, 51(1), 1994, pp. 90-90
PRENATAL-DIAGNOSIS OF PARTIAL TRISOMY 1Q USING FLUORESCENT IN-SITU HYBRIDIZATION
Authors: DUPONT BR HUFF RW RIDGWAY LE STRATTON RF MOORE CM
Citation: Br. Dupont et al., PRENATAL-DIAGNOSIS OF PARTIAL TRISOMY 1Q USING FLUORESCENT IN-SITU HYBRIDIZATION, American journal of medical genetics, 50(1), 1994, pp. 21-27
INTERSTITIAL DUPLICATION OF 7(Q22-]Q34)
Authors: STRATTON RF DUPONT BR MATTERN VL SCHELONKA RL MOORE CM
Citation: Rf. Stratton et al., INTERSTITIAL DUPLICATION OF 7(Q22-]Q34), American journal of medical genetics, 47(3), 1993, pp. 380-382
ANALYSIS OF SOMATIC-CELL MUTATIONS AT THE GLYCOPHORIN-A LOCUS IN ATOMIC-BOMB SURVIVORS - A COMPARATIVE-STUDY OF ASSAY-METHODS
Authors: LANGLOIS RG AKIYAMA M KUSUNOKI Y DUPONT BR MOORE DH BIGBEE WL GRANT SG JENSEN RH
Citation: Rg. Langlois et al., ANALYSIS OF SOMATIC-CELL MUTATIONS AT THE GLYCOPHORIN-A LOCUS IN ATOMIC-BOMB SURVIVORS - A COMPARATIVE-STUDY OF ASSAY-METHODS, Radiation research, 136(1), 1993, pp. 111-117
Risultati: 1-25 | 26-26