Authors:
PENG JC
GARVEY GT
AWES TC
BEDDO ME
BROOKS ML
BROWN CN
BUSH JD
CAREY TA
CHANG TH
COOPER WE
GAGLIARDI CA
GEESAMAN DF
HAWKER EA
HE XC
ISENHOWER LD
KAUFMAN SB
KAPLAN DM
KIRK PN
KOETKE DD
KYLE G
LEE DM
LEE WM
LEITCH MJ
MAKINS N
MCGAUGHEY PL
MOSS JM
MUELLER BA
NORD PM
PARK BK
PAPAVASSILIOU V
PETITT G
REIMER PE
SADLER ME
STANKUS PW
SONDHEIM WE
THOMPSON TN
TOWELL RS
TRIBBLE RE
VASILIEV MA
WANG YC
WANG ZF
WEBB JC
WILLIS JL
WISE DK
YOUNG GR
Citation: Jc. Peng et al., (D)OVER-BAR (U)OVER-BAR ASYMMETRY AND THE ORIGIN OF THE NUCLEON SEA -ART. NO. 092004/, Physical review. D. Particles and fields, 5809(9), 1998, pp. 2004
Authors:
HAWKER EA
AWES TC
BEDDO ME
BROWN CN
BUSH JD
CAREY TA
CHANG TH
COOPER WE
GAGLIARDI CA
GARVEY GT
GEESAMAN DF
HE XC
ISENHOWER LD
KAUFMAN SB
KAPLAN DM
KIRK PN
KOETKE DD
KYLE G
LEE DM
LEE WM
LEITCH MJ
MAKINS N
MCGAUGHEY PL
MOSS JM
MUELLER BA
NORD PM
PARK BK
PAPAVASSILIOU V
PENG JC
PETITT G
REIMER PE
SADLER ME
SELDEN J
STANKUS PW
SONDHEIM WE
THOMPSON TN
TOWELL RS
TRIBBLE RE
VASILIEV MA
WANG YC
WANG ZF
WEBB JC
WILLIS JL
WISE DK
YOUNG GR
Citation: Ea. Hawker et al., MEASUREMENT OF THE LIGHT ANTIQUARK FLAVOR ASYMMETRY IN THE NUCLEON SEA, Physical review letters, 80(17), 1998, pp. 3715-3718
Authors:
WEBB JC
GOLOVLEVA I
SIMPKINS AH
KEMPSKI H
STURT N
CHESSELLS JM
BRICKELL PM
Citation: Jc. Webb et al., LOSS OF HETEROZYGOSITY, MICROSATELLITE INSTABILITY, AND GENETIC-VARIATION AT THE MLL LOCUS IN CHILDHOOD AND INFANT LEUKEMIA, British Journal of Haematology, 101, 1998, pp. 175-175
Citation: Jc. Webb et al., HEMATOSALPINX WITH PELVIC PAIN AFTER ENDOMETRIAL ABLATION CONFIRMS THE POSTABLATION-TUBAL STERILIZATION SYNDROME, The Journal of the American Association of Gynecologic Laparoscopists, 3(3), 1997, pp. 419-421
Authors:
WEBB JC
PATEL DD
SHOULDERS CC
KNIGHT BL
SOUTAR AK
Citation: Jc. Webb et al., GENETIC-VARIATION AT A SPLICING BRANCH POINT IN INTRON-9 OF THE LOW-DENSITY-LIPOPROTEIN (LDL)-RECEPTOR GENE - A RARE MUTATION THAT DISRUPTSMESSENGER-RNA SPLICING IN A PATIENT WITH FAMILIAL HYPERCHOLESTEROLEMIA AND A COMMON POLYMORPHISM, Human molecular genetics, 5(9), 1996, pp. 1325-1331
Authors:
WEBB JC
SUN XM
MCCARTHY SN
NEUWIRTH C
THOMPSON GR
KNIGHT BL
SOUTAR AK
Citation: Jc. Webb et al., CHARACTERIZATION OF MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN (LDL)-RECEPTOR GENE IN PATIENTS WITH HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA,AND FREQUENCY OF THESE MUTATIONS IN FH PATIENTS IN THE UNITED-KINGDOM, Journal of lipid research, 37(2), 1996, pp. 368-381
Authors:
SUN XM
PATEL DD
WEBB JC
KNIGHT BL
FAN LM
CAI HJ
SOUTAR AK
Citation: Xm. Sun et al., FAMILIAL HYPERCHOLESTEROLEMIA IN CHINA - IDENTIFICATION OF MUTATIONS IN THE LDL-RECEPTOR GENE THAT RESULT IN A RECEPTOR-NEGATIVE PHENOTYPE, Arteriosclerosis and thrombosis, 14(1), 1994, pp. 85-94
Authors:
WEBB JC
PATEL DD
JONES MD
KNIGHT BL
SOUTAR AK
Citation: Jc. Webb et al., CHARACTERIZATION AND TISSUE-SPECIFIC EXPRESSION OF THE HUMAN VERY-LOW-DENSITY LIPOPROTEIN (VLDL) RECEPTOR MESSENGER-RNA, Human molecular genetics, 3(4), 1994, pp. 531-537
Authors:
MORGAN K
WHARTON J
WEBB JC
KEOGH BE
SMITH PLC
TAYLOR KM
OAKLEY CM
POLAK JM
CLELAND JGF
Citation: K. Morgan et al., COEXPRESSION OF RENIN-ANGIOTENSIN SYSTEM COMPONENT GENES IN HUMAN ATRIAL TISSUE, Journal of hypertension, 12, 1994, pp. 190000011-190000019
Authors:
SHOVLIN CL
SIMMONDS HA
FAIRBANKS LD
DEACOCK SJ
HUGHES JMB
LECHLER RI
WEBSTER ADB
SUN XM
WEBB JC
SOUTAR AK
Citation: Cl. Shovlin et al., ADULT-ONSET IMMUNODEFICIENCY CAUSED BY INHERITED ADENOSINE-DEAMINASE DEFICIENCY, The Journal of immunology, 153(5), 1994, pp. 2331-2339
Citation: Ckw. Tam et Jc. Webb, RADIATION BOUNDARY-CONDITION AND ANISOTROPY CORRECTION FOR FINITE-DIFFERENCE SOLUTIONS OF THE HELMHOLTZ-EQUATION, Journal of computational physics, 113(1), 1994, pp. 122-133
Citation: Ckw. Tam et Jc. Webb, DISPERSION-RELATION-PRESERVING FINITE-DIFFERENCE SCHEMES FOR COMPUTATIONAL ACOUSTICS, Journal of computational physics, 107(2), 1993, pp. 262-281
Authors:
FEHER MD
WEBB JC
PATEL DD
LANT AF
MAYNE PD
KNIGHT BL
SOUTAR AK
Citation: Md. Feher et al., CHOLESTEROL-LOWERING DRUG-THERAPY IN A PATIENT WITH RECEPTOR-NEGATIVEHOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA, Atherosclerosis, 103(2), 1993, pp. 171-180