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Results: 1-25 | 26-50 | 51-70
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A MUTATION IN PDS CAUSES NON-SYNDROMIC RECESSIVE DEAFNESS
Authors: LI XC EVERETT LA LALWANI AK DESMUKH D FRIEDMAN TB GREEN ED WILCOX ER
Citation: Xc. Li et al., A MUTATION IN PDS CAUSES NON-SYNDROMIC RECESSIVE DEAFNESS, Nature genetics, 18(3), 1998, pp. 215-217
CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF RANDOM CHROMOSOMAL REARRANGEMENTS ACTIVATING THE DRUG-RESISTANCE GENE, MDR1 P-GLYCOPROTEIN, IN DRUG-SELECTED CELL-LINES AND PATIENTS WITH DRUG-REFRACTORY ALL/
Authors: KNUTSEN T MICKLEY LA RIED T GREEN ED DUMANOIR S SCHROCK E MACVILLE M NING Y ROBEY R POLYMEROPOULOS M TORRES R FOJO T
Citation: T. Knutsen et al., CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF RANDOM CHROMOSOMAL REARRANGEMENTS ACTIVATING THE DRUG-RESISTANCE GENE, MDR1 P-GLYCOPROTEIN, IN DRUG-SELECTED CELL-LINES AND PATIENTS WITH DRUG-REFRACTORY ALL/, Genes, chromosomes & cancer, 23(1), 1998, pp. 44-54
IDENTIFICATION OF 10 NOVEL MUTATIONS IN THE PDS GENE RESPONSIBLE FOR PENDRED-SYNDROME
Authors: VANHAUWE P EVERETT L COUCKE P CHEN A RIS C BOLDER C OTTEN B DEVIJLDER J SMITH RJH WILLEMS PJ CREMERS CWRJ GREEN ED VANCAMP G
Citation: P. Vanhauwe et al., IDENTIFICATION OF 10 NOVEL MUTATIONS IN THE PDS GENE RESPONSIBLE FOR PENDRED-SYNDROME, European journal of human genetics, 6, 1998, pp. 205-205
2 FREQUENT MISSENSE MUTATIONS IN PENDRED-SYNDROME
Authors: VANHAUWE P EVERETT LA COUCKE P SCOTT DA KRAFT ML RISSTALPERS C BOLDER C OTTEN B DEVIJLDER JJM DIETRICH NL RAMESH A SRISAILAPATHY SCR PARVING A CREMERS CWRJ WILLEMS PJ SMITH RJH GREEN ED VANCAMP G
Citation: P. Vanhauwe et al., 2 FREQUENT MISSENSE MUTATIONS IN PENDRED-SYNDROME, Human molecular genetics (Print), 7(7), 1998, pp. 1099-1104
LOCALIZATION OF 67 EXONS ON A YAC CONTIG SPANNING 1.5 MB AROUND THE MULTIDRUG-RESISTANCE GENE REGION OF HUMAN-CHROMOSOME 7Q21.1
Authors: TORIGOE K HARADA T KUSABA H UCHIUMI T KOHNO K GREEN ED SCHERER SW TSUI LC SCHLESSINGER D KUWANO M WADA M
Citation: K. Torigoe et al., LOCALIZATION OF 67 EXONS ON A YAC CONTIG SPANNING 1.5 MB AROUND THE MULTIDRUG-RESISTANCE GENE REGION OF HUMAN-CHROMOSOME 7Q21.1, Genomics, 49(1), 1998, pp. 14-22
PROGRESSIVE SENSORINEURAL HEARING-LOSS AND A WIDENED VESTIBULAR AQUEDUCT IN PENDRED-SYNDROME
Authors: CREMERS CWRJ BOLDER C ADMIRAAL RJC EVERETT LA JOOSTEN FBM VANHAUWE P GREEN ED OTTEN BJ
Citation: Cwrj. Cremers et al., PROGRESSIVE SENSORINEURAL HEARING-LOSS AND A WIDENED VESTIBULAR AQUEDUCT IN PENDRED-SYNDROME, Archives of otolaryngology, head & neck surgery, 124(5), 1998, pp. 501-505
PROGRESSIVE HEARING-LOSS, HYPOPLASIA OF THE COCHLEA AND WIDENED VESTIBULAR AQUEDUCTS ARE VERY COMMON FEATURES IN PENDREDS-SYNDROME
Authors: CREMERS CWRJ ADMIRAAL RJC HUYGEN PLM BOLDER C EVERETT LA JOOSTEN FBM GREEN ED VANCAMP G OTTEN BJ
Citation: Cwrj. Cremers et al., PROGRESSIVE HEARING-LOSS, HYPOPLASIA OF THE COCHLEA AND WIDENED VESTIBULAR AQUEDUCTS ARE VERY COMMON FEATURES IN PENDREDS-SYNDROME, International journal of pediatric otorhinolaryngology, 45(2), 1998, pp. 113-123
MOLECULAR ANATOMY OF CHROMOSOME 7Q DELETIONS IN MYELOID NEOPLASMS - EVIDENCE FOR MULTIPLE CRITICAL LOCI
Authors: LIANG H FAIRMAN J CLAXTON DF NOWELL PC GREEN ED NAGARAJAN L
Citation: H. Liang et al., MOLECULAR ANATOMY OF CHROMOSOME 7Q DELETIONS IN MYELOID NEOPLASMS - EVIDENCE FOR MULTIPLE CRITICAL LOCI, Proceedings of the National Academy of Sciences of the United Statesof America, 95(7), 1998, pp. 3781-3785
PENDRED SYNDROME IS CAUSED BY MUTATIONS IN A PUTATIVE SULFATE TRANSPORTER GENE (PDS)
Authors: EVERETT LA GLASER B BECK JC IDOL JR BUCHS A HEYMAN M ADAWI F HAZANI E NASSIR E BAXEVANIS AD SHEFFIELD VC GREEN ED
Citation: La. Everett et al., PENDRED SYNDROME IS CAUSED BY MUTATIONS IN A PUTATIVE SULFATE TRANSPORTER GENE (PDS), Nature genetics, 17(4), 1997, pp. 411-422
MUTATIONS IN TWIST, A BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTOR, INSAETHRE-CHOTZEN SYNDROME
Authors: HOWARD TD PAZNEKAS WA GREEN ED CHIANG LC MA N DELUNA RIO DELGADO CG GONZALEZRAMOS M KLINE AD JABS EW
Citation: Td. Howard et al., MUTATIONS IN TWIST, A BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTOR, INSAETHRE-CHOTZEN SYNDROME, Nature genetics, 15(1), 1997, pp. 36-41
A PHYSICAL MAP OF HUMAN-CHROMOSOME 7 - AN INTEGRATED YAC CONTIG MAP WITH AVERAGE STS SPACING OF 79 KB
Authors: BOUFFARD GG IDOL JR BRADEN VV IYER LM CUNNINGHAM AF WEINTRAUB LA TOUCHMAN JW MOHRTIDWELL RM PELUSO DC FULTON RS UELTZEN MS WEISSENBACH J MAGNESS CL GREEN ED
Citation: Gg. Bouffard et al., A PHYSICAL MAP OF HUMAN-CHROMOSOME 7 - AN INTEGRATED YAC CONTIG MAP WITH AVERAGE STS SPACING OF 79 KB, PCR methods and applications, 7(7), 1997, pp. 673-692
THE HUMAN REELIN GENE - ISOLATION, SEQUENCING, AND MAPPING ON CHROMOSOME-7
Authors: DESILVA U DARCANGELO G BRADEN VV MIAO GG CURRAN T GREEN ED
Citation: U. Desilva et al., THE HUMAN REELIN GENE - ISOLATION, SEQUENCING, AND MAPPING ON CHROMOSOME-7, PCR methods and applications, 7(2), 1997, pp. 157-164
HIGH-THROUGHPUT FINGERPRINT ANALYSIS OF LARGE-INSERT CLONES
Authors: MARRA MA KUCABA TA DIETRICH NL GREEN ED BROWNSTEIN B WILSON RK MCDONALD KM HILLIER LW MCPHERSON JD WATERSTON RH
Citation: Ma. Marra et al., HIGH-THROUGHPUT FINGERPRINT ANALYSIS OF LARGE-INSERT CLONES, PCR methods and applications, 7(11), 1997, pp. 1072-1084
A COLLECTION OF 1814 HUMAN-CHROMOSOME 7-SPECIFIC STS
Authors: BOUFFARD GG IYER LM IDOL JR BRADEN VV CUNNINGHAM AF WEINTRAUB LA MOHRTIDWELL RM PELUSO DC FULTON RS LECKIE MP GREEN ED
Citation: Gg. Bouffard et al., A COLLECTION OF 1814 HUMAN-CHROMOSOME 7-SPECIFIC STS, PCR methods and applications, 7(1), 1997, pp. 59-64
REFINED MAPPING OF A GENE FOR AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS (DFNA5) TO A 2-CM REGION, AND EXCLUSION OF A CANDIDATE GENE THAT IS EXPRESSED IN THE COCHLEA
Authors: VANLAER L VANCAMP G VANZUIJLEN D GREEN ED VERSTREKEN M SCHATTEMAN I VANDEHEYNING P BALEMANS W COUCKE P GREINWALD JH SMITH RJH HUIZING E WILLEMS P
Citation: L. Vanlaer et al., REFINED MAPPING OF A GENE FOR AUTOSOMAL-DOMINANT PROGRESSIVE SENSORINEURAL HEARING-LOSS (DFNA5) TO A 2-CM REGION, AND EXCLUSION OF A CANDIDATE GENE THAT IS EXPRESSED IN THE COCHLEA, European journal of human genetics, 5(6), 1997, pp. 397-405
ISOLATION OF DNA FROM THE CENTROMERE OF HUMAN-CHROMOSOME-7 BY MICRODISSECTION
Authors: BEHRENS F CLAUSSEN U IYER LM GREEN ED HORSTHEMKE B WILIAMSON R HUXLEY G COUTELLE C
Citation: F. Behrens et al., ISOLATION OF DNA FROM THE CENTROMERE OF HUMAN-CHROMOSOME-7 BY MICRODISSECTION, Chromosome research, 5(4), 1997, pp. 215-220
LOCALIZATION AND CHARACTERIZATION OF THE HUMAN ADP-RIBOSYLATION FACTOR-5 (ARF5) GENE
Authors: MCGUIRE RE DAIGER SP GREEN ED
Citation: Re. Mcguire et al., LOCALIZATION AND CHARACTERIZATION OF THE HUMAN ADP-RIBOSYLATION FACTOR-5 (ARF5) GENE, Genomics, 41(3), 1997, pp. 481-484
MAINTENANCE OF HYPOMETHYLATION STATUS AND PREFERENTIAL EXPRESSION OF EXOGENOUS HUMAN MDR1 PGY1 GENE IN MOUSE L-CELL BY YAC MEDIATED TRANSFER/
Authors: KUSABA H NAKAYAMA M HARADA T TORIGOE K GREEN ED SCHERER SW KOHNO K KUWANO M WADA M
Citation: H. Kusaba et al., MAINTENANCE OF HYPOMETHYLATION STATUS AND PREFERENTIAL EXPRESSION OF EXOGENOUS HUMAN MDR1 PGY1 GENE IN MOUSE L-CELL BY YAC MEDIATED TRANSFER/, Somatic cell and molecular genetics, 23(4), 1997, pp. 259-274
PHYSICAL MAPPING OF THE HOXA1 GENE AND THE HNRPA2B1 GENE IN A YAC CONTIG FROM HUMAN-CHROMOSOME 7P14-P15
Authors: VANLAER L VANCAMP G GREEN ED HUIZING EH WILLEMS PJ
Citation: L. Vanlaer et al., PHYSICAL MAPPING OF THE HOXA1 GENE AND THE HNRPA2B1 GENE IN A YAC CONTIG FROM HUMAN-CHROMOSOME 7P14-P15, Human genetics, 99(6), 1997, pp. 831-833
TRANSIENT GENE-EXPRESSION FROM YEAST ARTIFICIAL CHROMOSOME DNA IN MAMMALIAN-CELLS IS ENHANCED BY ADENOVIRUS
Authors: CHEN M COMPTON ST COVIELLO VF GREEN ED ASHLOCK MA
Citation: M. Chen et al., TRANSIENT GENE-EXPRESSION FROM YEAST ARTIFICIAL CHROMOSOME DNA IN MAMMALIAN-CELLS IS ENHANCED BY ADENOVIRUS, Nucleic acids research, 25(21), 1997, pp. 4416-4418
WHAT WILL WE DO WHEN ADJUDICATION ENDS - WELL SETTLE IN BUNCHES - BRINGING RULE-23 INTO THE 21ST-CENTURY
Authors: GREEN ED
Citation: Ed. Green, WHAT WILL WE DO WHEN ADJUDICATION ENDS - WELL SETTLE IN BUNCHES - BRINGING RULE-23 INTO THE 21ST-CENTURY, UCLA law review, 44(6), 1997, pp. 1773-1801
A P47-PHOX PSEUDOGENE CARRIES THE MOST COMMON MUTATION CAUSING P47-PHOX-DEFICIENT CHRONIC GRANULOMATOUS-DISEASE
Authors: GORLACH A LEE PL ROESLER J HOPKINS PJ CHRISTENSEN B GREEN ED CHANOCK SJ CURNUTTE JT
Citation: A. Gorlach et al., A P47-PHOX PSEUDOGENE CARRIES THE MOST COMMON MUTATION CAUSING P47-PHOX-DEFICIENT CHRONIC GRANULOMATOUS-DISEASE, The Journal of clinical investigation, 100(8), 1997, pp. 1907-1918
THE CMT2D LOCUS ON CHROMOSOME 7P - REFINED GENETIC LOCALIZATION AND HIGH-RESOLUTION PHYSICAL MAPPING
Authors: MCGUIRE RE SEARBY C BRADEN VV JEGATHESAN A MARRA M MCPHERSON JD IONASESCU V GREEN ED
Citation: Re. Mcguire et al., THE CMT2D LOCUS ON CHROMOSOME 7P - REFINED GENETIC LOCALIZATION AND HIGH-RESOLUTION PHYSICAL MAPPING, American journal of human genetics, 61(4), 1997, pp. 1389-1389
REFINEMENT OF THE DFNA5 CANDIDATE REGION, CONSTRUCTION OF A YAC CONTIG, AND EXCLUSION OF A FETAL-COCHLEAR EXPRESSED CANDIDATE GENE
Authors: VANLAER L VANCAMP G VANZUIJLEN D GREEN ED VERSTREKEN M SCHATTEMAN I VANDEHEYNING P BALEMANS W COUCKE P GREINWALD JH SMITH RJH HUIZING E WILLEMS P
Citation: L. Vanlaer et al., REFINEMENT OF THE DFNA5 CANDIDATE REGION, CONSTRUCTION OF A YAC CONTIG, AND EXCLUSION OF A FETAL-COCHLEAR EXPRESSED CANDIDATE GENE, American journal of human genetics, 61(4), 1997, pp. 1743-1743
MAPPING THE RP10 LOCUS FOR AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA ON7Q - REFINED GENETIC POSITIONING AND LOCALIZATION WITHIN A WELL-DEFINED YAC CONTIG
Authors: MCGUIRE RE JORDAN SA BRADEN VV BOUFFARD GG HUMPHRIES P GREEN ED DAIGER SP
Citation: Re. Mcguire et al., MAPPING THE RP10 LOCUS FOR AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA ON7Q - REFINED GENETIC POSITIONING AND LOCALIZATION WITHIN A WELL-DEFINED YAC CONTIG, PCR methods and applications, 6(4), 1996, pp. 255-266
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