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Results: 1-25/53
Authors:
OSBORN M
SMITH JA
Citation: M. Osborn et Ja. Smith, THE PERSONAL-EXPERIENCE OF CHRONIC BENIGN LOWER BACK PAIN - AN INTERPRETATIVE PHENOMENOLOGICAL ANALYSIS, British journal of health psychology, 3, 1998, pp. 65-83
Authors:
HARBORTH J
WEBER K
OSBORN M
Citation: J. Harborth et al., A NOVEL BINDING PARTNER OF NUMA IN THE INTERPHASE NUCLEUS, Molecular biology of the cell, 9, 1998, pp. 2582-2582
Authors:
SCHERFELD D
SCHNEIDER G
GUTTMANN P
OSBORN M
Citation: D. Scherfeld et al., VISUALIZATION OF CYTOSKELETAL ELEMENTS IN THE TRANSMISSION-X-RAY MICROSCOPE, Journal of structural biology (Print), 123(1), 1998, pp. 72-82
Authors:
UPADHYAYA M
RUGGIERI M
MAYNARD J
OSBORN M
HARTOG C
MUDD S
PENTTINEN M
CORDEIRO I
PONDER M
PONDER BAJ
KRAWCZAK M
COOPER DN
Citation: M. Upadhyaya et al., GROSS DELETIONS OF THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE ARE PREDOMINANTLY OF MATERNAL ORIGIN AND COMMONLY ASSOCIATED WITH A LEARNING-DISABILITY, DYSMORPHIC FEATURES AND DEVELOPMENTAL DELAY, Human genetics, 102(5), 1998, pp. 591-597
Authors:
DRASS J
KELL S
OSBORN M
BAUSELL B
CORCORAN J
MOSKOWITZ A
FLEMING B
Citation: J. Drass et al., DIABETES CARE FOR MEDICARE BENEFICIARIES - ATTITUDES AND BEHAVIORS OFPRIMARY-CARE PHYSICIANS, Diabetes care, 21(8), 1998, pp. 1282-1287
Authors:
UPADHYAYA M
MAYNARD J
OSBORN M
HARPER PS
Citation: M. Upadhyaya et al., 6 NOVEL MUTATIONS IN THE NEUROFIBROMATOSIS TYPE-1 (NF1) GENE, Human mutation, 10(3), 1997, pp. 248-250
Authors:
WILLIAMSON CF
YATES TC
SCHMITT WM
OSBORN M
DEADY M
ZIMMERMAN PD
BLATCHLEY CC
SETH KK
SARMIENTO M
PARKER B
JIN YH
WRIGHT LE
ONLEY DS
Citation: Cf. Williamson et al., QUASI-ELASTIC ELECTRON-SCATTERING FROM CA-40, Physical review. C. Nuclear physics, 56(6), 1997, pp. 3152-3172
Authors:
OSBORN M
BROADFOOT P
PLANEL C
POLLARD A
Citation: M. Osborn et al., SOCIAL-CLASS, EDUCATIONAL-OPPORTUNITY AND EQUAL ENTITLEMENT - DILEMMAS OF SCHOOLING IN ENGLAND AND FRANCE, Comparative education, 33(3), 1997, pp. 375-393
Authors:
OSBORN M
Citation: M. Osborn, THE UNIVERSITY AND THE TEACHERS - FRANCE, THE UNITED-STATES, ENGLAND - JUDGE,H, LEMOSSE,M, PAINE,L, SEDLAK,M, Comparative education, 33(3), 1997, pp. 472-474
Authors:
OSBORN M
Citation: M. Osborn, INTERNATIONAL ENCYCLOPEDIA OF TEACHING AND TEACHER-EDUCATION - ANDERSON,LW, Comparative education, 33(1), 1997, pp. 137-138
Authors:
OSBORN M
GUPTA L
WARD J
Citation: M. Osborn et al., VALIDATION OF THE RARA CLASSIFICATION USING GENERAL-PRACTITIONER SELF-CLASSIFICATION, Medical journal of Australia, 166(6), 1997, pp. 335-336
Authors:
HILTON C
OSBORN M
SERJEANT G
Citation: C. Hilton et al., PSYCHIATRIC-DISORDER IN YOUNG-ADULTS IN JAMAICA, International Journal of Social Psychiatry, 43(4), 1997, pp. 257-268
Authors:
GUETHHALLONET C
WEBER K
OSBORN M
Citation: C. Guethhallonet et al., CLEAVAGE OF THE NUCLEAR MATRIX PROTEIN NUMA DURING APOPTOSIS, Experimental cell research, 233(1), 1997, pp. 21-24
Authors:
FRIEDMAN P
MUNGER T
STANTON MS
SHEN WK
HAMMILL S
REA R
OSBORN M
PACKER D
Citation: P. Friedman et al., GLOBAL RIGHT ATRIAL ACTIVATION IN HUMAN ATRIAL-FLUTTER - THE PRESENCEOF A RIGHT ATRIAL POSTEROMEDIAL LINE OF BLOCK, Circulation, 96(8), 1997, pp. 1458-1458
Authors:
HILTON C
OSBORN M
KNIGHT S
SINGHAL A
SERJEANT G
Citation: C. Hilton et al., PSYCHIATRIC COMPLICATIONS OF HOMOZYGOUS SICKLE-CELL DISEASE AMONG YOUNG-ADULTS IN THE JAMAICAN COHORT STUDY, British Journal of Psychiatry, 170, 1997, pp. 69-76
Authors:
OSBORN M
Citation: M. Osborn, ENCOURAGING LEARNING - TOWARDS A THEORY OF THE LEARNING SCHOOL - NIXON,J, MARTIN,J, MCKEOWN,P, RANSON,S, British journal of educational studies, 45(1), 1997, pp. 112-114
Authors:
DOMAGALA W
MARKIEWSKI M
HAREZGA B
DUKOWICZ A
OSBORN M
Citation: W. Domagala et al., PROGNOSTIC-SIGNIFICANCE OF TUMOR-CELL PROLIFERATION RATE AS DETERMINED BY THE MIB-1 ANTIBODY IN BREAST-CARCINOMA - ITS RELATIONSHIP WITH VIMENTIN AND P53 PROTEIN, Clinical cancer research, 2(1), 1996, pp. 147-154
Authors:
SEEMANN J
WEBER K
OSBORN M
PARTON RG
GERKE V
Citation: J. Seemann et al., THE ASSOCIATION OF ANNEXIN-I WITH EARLY ENDOSOMES IS REGULATED BY CA2-TERMINAL DOMAIN( AND REQUIRES AN INTACT N), Molecular biology of the cell, 7(9), 1996, pp. 1359-1374
Authors:
UPADHYAYA M
OSBORN M
MAYNARD J
HARPER P
Citation: M. Upadhyaya et al., CHARACTERIZATION OF 6 MUTATIONS IN EXON-37 OF NEUROFIBROMATOSIS TYPE-1 GENE, American journal of medical genetics, 67(4), 1996, pp. 421-423
Authors:
HUGHES RAC
CHOUDHARY PP
OSBORN M
REES JH
SANDERS EACM
Citation: Rac. Hughes et al., IMMUNIZATION AND RISK OF RELAPSE OF GUILLAIN-BARRE-SYNDROME OR CHRONIC INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY, Muscle & nerve, 19(9), 1996, pp. 1230-1231
Authors:
GUETHHALLONET C
WEBER K
OSBORN M
Citation: C. Guethhallonet et al., NUMA - A BIPARTITE NUCLEAR LOCATION SIGNAL AND OTHER FUNCTIONAL-PROPERTIES OF THE TAIL DOMAIN, Experimental cell research, 225(1), 1996, pp. 207-218
Authors:
LUNT PW
JARDINE PE
KOCH MC
MAYNARD J
OSBORN M
WILLIAMS M
HARPER PS
UPADHYAYA M
Citation: Pw. Lunt et al., CORRELATION BETWEEN FRAGMENT SIZE AT D4F104S1 AND AGE AT ONSET OR AT WHEELCHAIR USE, WITH A POSSIBLE GENERATIONAL-EFFECT, ACCOUNTS FOR MUCHPHENOTYPIC VARIATION IN 4Q35-FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD) (VOL 4, PG 951, 1995), Human molecular genetics, 4(7), 1995, pp. 1243-1244
Authors:
LUNT PW
JARDINE PE
KOCH MC
MAYNARD J
OSBORN M
WILLIAMS M
HARPER PS
UPADHYAYA M
Citation: Pw. Lunt et al., CORRELATION BETWEEN FRAGMENT SIZE AT D4F104S1 AND AGE AT ONSET OR AT WHEELCHAIR USE, WITH A POSSIBLE GENERATIONAL-EFFECT, ACCOUNTS FOR MUCHPHENOTYPIC VARIATION IN 4Q35-FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY (FSHD), Human molecular genetics, 4(5), 1995, pp. 951-958
Authors:
HARBORTH J
WEBER K
OSBORN M
Citation: J. Harborth et al., EPITOPE MAPPING AND DIRECT VISUALIZATION OF THE PARALLEL, IN-REGISTERARRANGEMENT OF THE DOUBLE-STRANDED COILED-COIL IN THE NUMA PROTEIN, EMBO journal, 14(11), 1995, pp. 2447-2460
Authors:
UPADHYAYA M
OSBORN M
MAYNARD J
ALTHERR M
IKEDA J
HARPER PS
Citation: M. Upadhyaya et al., TOWARDS THE FINER MAPPING OF FACIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY AT 4Q35 - CONSTRUCTION OF A LASER MICRODISSECTION LIBRARY, American journal of medical genetics, 60(3), 1995, pp. 244-251