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Results: 1-25/82
Authors:
HEGELE RA
BRECKENRIDGE WC
COX DW
MAGUIRE GF
LITTLE JA
CONNELLY PW
Citation: Ra. Hegele et al., ELEVATED LDL TRIGLYCERIDE CONCENTRATIONS IN SUBJECTS HETEROZYGOUS FORTHE HEPATIC LIPASE S267F VARIANT, Arteriosclerosis, thrombosis, and vascular biology, 18(8), 1998, pp. 1212-1216
Authors:
ROBERTS EA
COX DW
Citation: Ea. Roberts et Dw. Cox, WILSON-DISEASE, Bailliere's clinical gastroenterology, 12(2), 1998, pp. 237-256
Authors:
COX DW
WALSHE JW
WALKER C
ROBERTS EA
BILODEAU M
Citation: Dw. Cox et al., EFFECT OF DIFFERENT MUTATIONS AND PRESENCE OF THE HEMOCHROMATOSIS MUTATION IN PATIENTS WITH WILSON-DISEASE, Hepatology, 28(4), 1998, pp. 1816-1816
Authors:
MAIERDOBERSBERGER T
NAZER H
FERENCI P
COX DW
Citation: T. Maierdobersberger et al., MUTATION ANALYSIS IN EXON-8 OF THE WILSON-DISEASE GENE, Hepatology, 28(4), 1998, pp. 1817-1817
Authors:
WALSHE JM
COX DW
Citation: Jm. Walshe et Dw. Cox, EFFECT OF TREATMENT OF WILSONS-DISEASE ON NATURAL-HISTORY OF HEMOCHROMATOSIS, Lancet, 352(9122), 1998, pp. 112-113
Authors:
STISKAL JA
DUNN MS
SHENNAN AT
OBRIEN KKE
KELLY EN
KOPPEL RI
COX DW
ITO S
CHAPPEL SL
RABINOVITCH M
Citation: Ja. Stiskal et al., ALPHA(1)-PROTEINASE INHIBITOR THERAPY FOR THE PREVENTION OF CHRONIC LUNG-DISEASE OF PREMATURITY - A RANDOMIZED, CONTROLLED TRIAL, Pediatrics, 101(1), 1998, pp. 89-94
Authors:
NANJI MS
COX DW
Citation: Ms. Nanji et Dw. Cox, THE -75A-]C SUBSTITUTION IN THE 5'-UTR OF THE WILSON DISEASE GENE IS A SEQUENCE POLYMORPHISM IN THE MEDITERRANEAN POPULATION - REPLY, American journal of human genetics, 62(2), 1998, pp. 484-485
Authors:
ORRU S
THOMAS G
LOIZEDDA A
COX DW
CONTU L
Citation: S. Orru et al., 24 BP DELETION AND ALA(1278) TO VAL MUTATION OF THE ATP7B GENE IN A SARDINIAN FAMILY WITH WILSON-DISEASE, Human mutation, 10(1), 1997, pp. 84-85
Authors:
NAGANO K
NAKAMURA K
UMEYAMA K
URAKAMI K
COX DW
MATSUDA I
ENDO F
Citation: K. Nagano et al., GENE-MEDIATED EXPRESSION AND PARTIAL CHARACTERIZATION OF ATPASE 7B INCULTURED-CELLS, The Journal of trace elements in experimental medicine, 10(2), 1997, pp. 111-117
Authors:
WU JS
FORBES JR
COX DW
Citation: Js. Wu et al., FURTHER CHARACTERIZATION OF THE ATP7B GENE DELETION IN LEC RATS, The Journal of trace elements in experimental medicine, 10(2), 1997, pp. 147-152
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
Authors:
WINTLE RF
NYGAARD TG
HERBRICK JAS
KVALOY K
COX DW
Citation: Rf. Wintle et al., GENETIC-POLYMORPHISM AND RECOMBINATION IN THE SUBTELOMERIC REGION OF CHROMOSOME 14Q, Genomics, 40(3), 1997, pp. 409-414
Authors:
COX DW
Citation: Dw. Cox, MOLECULAR APPROACHES TO INHERITED LIVER-DISEASE - FOCUS ON WILSON-DISEASE, Journal of gastroenterology and hepatology, 12(9-10), 1997, pp. 251-255
Authors:
DIDONATO M
NARINDRASORASAK S
FORBES JR
COX DW
SARKAR B
Citation: M. Didonato et al., EXPRESSION, PURIFICATION, AND METAL-BINDING PROPERTIES OF THE N-TERMINAL DOMAIN FROM THE WILSON DISEASE PUTATIVE COPPER-TRANSPORTING ATPASE(ATP7B), The Journal of biological chemistry, 272(52), 1997, pp. 33279-33282
Authors:
FORBES JR
COX DW
Citation: Jr. Forbes et Dw. Cox, FUNCTIONAL-CHARACTERIZATION OF ATP7B, THE P-TYPE ATPASE DEFECTIVE IN WILSON-DISEASE, American journal of human genetics, 61(4), 1997, pp. 980-980
Authors:
NANJI MS
COX DW
Citation: Ms. Nanji et Dw. Cox, IDENTIFICATION OF THE PUTATIVE PROMOTER REGION OF WILSON-DISEASE GENE, American journal of human genetics, 61(4), 1997, pp. 1028-1028
Authors:
KRAUS B
MCFADYEN D
BILLINGSLEY GD
ROMMENS JM
COX DW
Citation: B. Kraus et al., IDENTIFICATION, MAPPING AND CHARACTERIZATION OF NEW GENES IN THE DISTAL REGION OF CHROMOSOME-14 (14Q32-TER), American journal of human genetics, 61(4), 1997, pp. 1381-1381
Authors:
NANJI MS
NGUYEN VTT
KAWASOE JH
INUI K
ENDO F
NAKAJIMA T
ANEZAKI T
COX DW
Citation: Ms. Nanji et al., HAPLOTYPE AND MUTATION ANALYSIS IN JAPANESE PATIENTS WITH WILSON-DISEASE, American journal of human genetics, 60(6), 1997, pp. 1423-1429
Authors:
TOMKINS DJ
ROUX AF
WAYE J
FREEMAN VCP
COX DW
WHELAN DT
Citation: Dj. Tomkins et al., MATERNAL UNIPARENTAL ISODISOMY OF HUMAN-CHROMOSOME-14 ASSOCIATED WITHA PATERNAL T(13Q14Q) AND PRECOCIOUS PUBERTY, European journal of human genetics, 4(3), 1996, pp. 153-159
Authors:
ROFE BH
KNIGHT DJ
DUNSTER JA
COATS DJ
SIMS GP
ROCKE G
COX DW
Citation: Bh. Rofe et al., CARSINGTON RESERVOIR - RECONSTRUCTION OF THE DAM - DISCUSSION, PROCEEDINGS OF THE INSTITUTION OF CIVIL ENGINEERS-CIVIL ENGINEERING, 114(2), 1996, pp. 92-96
Authors:
THEOPHILOS MB
COX DW
MERCER JFB
Citation: Mb. Theophilos et al., THE TOXIC MILK MOUSE IS A MURINE MODEL OF WILSON DISEASE, Human molecular genetics, 5(10), 1996, pp. 1619-1624
Authors:
KANG HY
COX DW
Citation: Hy. Kang et Dw. Cox, TANDEM REPEATS 3' OF THE IGHA GENES IN THE HUMAN-IMMUNOGLOBULIN HEAVY-CHAIN GENE-CLUSTER, Genomics, 35(1), 1996, pp. 189-195
Authors:
STISKAL J
ITO S
COX DW
DUNN M
OBRIEN K
SHENNAN A
KELLY E
RABINOVITCH M
Citation: J. Stiskal et al., ALPHA(1)-PROTEINASE INHIBITOR (A(1)PI) FUNCTIONAL AND ANTIGENIC LEVELS - EFFECT OF SUPPLEMENTATION, Pediatric research, 39(4), 1996, pp. 462-462
Authors:
COX DW
THOMAS GR
WALSHE JM
ROBERTS EA
Citation: Dw. Cox et al., WILSON DISEASE IN CHILDREN - MUTATIONS AND THEIR CONSEQUENCES, Pediatric research, 39(4), 1996, pp. 845-845
Authors:
DEMIRKIRAN M
JANKOVIC J
LEWIS RA
COX DW
Citation: M. Demirkiran et al., NEUROLOGIC PRESENTATION OF WILSON DISEASE WITHOUT KAYSER-FLEISCHER RINGS, Neurology, 46(4), 1996, pp. 1040-1043