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Results: 1-25 | 26-38 |
Results: 26-38/38
THE HUMAN COL11A2 GENE STRUCTURE INDICATES THAT THE GENE HAS NOT EVOLVED WITH THE GENES FOR THE MAJOR FIBRILLAR COLLAGENS
Authors: VUORISTO MM PIHLAJAMAA T VANDENBERG P PROCKOP DJ ALAKOKKO L
Citation: Mm. Vuoristo et al., THE HUMAN COL11A2 GENE STRUCTURE INDICATES THAT THE GENE HAS NOT EVOLVED WITH THE GENES FOR THE MAJOR FIBRILLAR COLLAGENS, The Journal of biological chemistry, 270(39), 1995, pp. 22873-22881
TISSUE-SPECIFIC EXPRESSION OF THE GENE FOR TYPE-I PROCOLLAGEN (COL1A1) IN TRANSGENIC MICE - ONLY 476 BASE-PAIRS OF THE PROMOTER ARE REQUIRED IF COLLAGEN GENES ARE USED AS REPORTERS
Authors: SOKOLOV BP ALAKOKKO L DHULIPALA R ARITA M KHILLAN JS PROCKOP DJ
Citation: Bp. Sokolov et al., TISSUE-SPECIFIC EXPRESSION OF THE GENE FOR TYPE-I PROCOLLAGEN (COL1A1) IN TRANSGENIC MICE - ONLY 476 BASE-PAIRS OF THE PROMOTER ARE REQUIRED IF COLLAGEN GENES ARE USED AS REPORTERS, The Journal of biological chemistry, 270(16), 1995, pp. 9622-9629
IDENTIFICATION OF COL2A1 GENE-MUTATIONS IN PATIENTS WITH CHONDRODYSPLASIAS AND FAMILIAL OSTEOARTHRITIS
Authors: RITVANIEMI P KORKKO J BONAVENTURE J VIKKULA M HYLAND J PAASSILTA P KAITILA I KAARIAINEN H SOKOLOV BP HAKALA M MANNISMAKI P MEERSON EM KLEMOLA T WILLIAMS C PELTONEN L KIVIRIKKO KI PROCKOP DJ ALAKOKKO L
Citation: P. Ritvaniemi et al., IDENTIFICATION OF COL2A1 GENE-MUTATIONS IN PATIENTS WITH CHONDRODYSPLASIAS AND FAMILIAL OSTEOARTHRITIS, Arthritis and rheumatism, 38(7), 1995, pp. 999-1004
A SINGLE-BASE MUTATION IN THE TYPE-II PROCOLLAGEN GENE (COL2A1) THAT CONVERTS GLYCINE ALPHA-1-247 TO SERINE IN A FAMILY WITH LATE-ONSET SPONDYLOEPIPHYSEAL DYSPLASIA
Authors: RITVANIEMI P SOKOLOV BP WILLIAMS CJ CONSIDINE E YURGENEV L MEERSON EM ALAKOKKO L PROCKOP DJ
Citation: P. Ritvaniemi et al., A SINGLE-BASE MUTATION IN THE TYPE-II PROCOLLAGEN GENE (COL2A1) THAT CONVERTS GLYCINE ALPHA-1-247 TO SERINE IN A FAMILY WITH LATE-ONSET SPONDYLOEPIPHYSEAL DYSPLASIA, Human mutation, 3(3), 1994, pp. 261-267
TYPE-II COLLAGEN MUTATIONS IN RARE AND COMMON CARTILAGE DISEASES
Authors: VIKKULA M METSARANTA M ALAKOKKO L
Citation: M. Vikkula et al., TYPE-II COLLAGEN MUTATIONS IN RARE AND COMMON CARTILAGE DISEASES, Annals of medicine, 26(2), 1994, pp. 107-114
SYNTHESIS OF RECOMBINANT HUMAN PROCOLLAGEN-II IN A STABLY TRANSFECTEDTUMOR-CELL LINE (HT1080)
Authors: FERTALA A SIERON AL GANGULY A LI SW ALAKOKKO L ANUMULA KR PROCKOP DJ
Citation: A. Fertala et al., SYNTHESIS OF RECOMBINANT HUMAN PROCOLLAGEN-II IN A STABLY TRANSFECTEDTUMOR-CELL LINE (HT1080), Biochemical journal, 298, 1994, pp. 31-37
MUTATION IN THE COL2A1 GENE IN A PATIENT WITH HYPOCHONDROGENESIS - EXPRESSION OF MUTATED COL2A1 GENE IS ACCOMPANIED BY EXPRESSION OF GENES FOR TYPE-I PROCOLLAGEN IN CHONDROCYTES
Authors: FREISINGER P ALAKOKKO L LEGUELLEC D FRANC S BOUVIER R RITVANIEMI P PROCKOP DJ BONAVENTURE J
Citation: P. Freisinger et al., MUTATION IN THE COL2A1 GENE IN A PATIENT WITH HYPOCHONDROGENESIS - EXPRESSION OF MUTATED COL2A1 GENE IS ACCOMPANIED BY EXPRESSION OF GENES FOR TYPE-I PROCOLLAGEN IN CHONDROCYTES, The Journal of biological chemistry, 269(18), 1994, pp. 13663-13669
A 4TH EXAMPLE SUGGESTS THAT PREMATURE TERMINATION CODONS IN THE COL2A1 GENE ARE A COMMON-CAUSE OF THE STICKLER SYNDROME - ANALYSIS OF THE COL2A1 GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS
Authors: RITVANIEMI P HYLAND J IGNATIUS J KIVIRIKKO KI PROCKOP DJ ALAKOKKO L
Citation: P. Ritvaniemi et al., A 4TH EXAMPLE SUGGESTS THAT PREMATURE TERMINATION CODONS IN THE COL2A1 GENE ARE A COMMON-CAUSE OF THE STICKLER SYNDROME - ANALYSIS OF THE COL2A1 GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS, Genomics, 17(1), 1993, pp. 218-221
AN INBRED LINE OF TRANSGENIC MICE EXPRESSING AN INTERNALLY DELETED GENE FOR TYPE-II PROCOLLAGEN (COL2A1) - YOUNG MICE HAVE A VARIABLE PHENOTYPE OF A CHONDRODYSPLASIA AND OLDER MICE HAVE OSTEOARTHRITIC CHANGES IN JOINTS
Authors: HELMINEN HJ KIRALY K PELTTARI A TAMMI MI VANDENBERG P PEREIRA R DHULIPALA R KHILLAN JS ALAKOKKO L HUME EL SOKOLOV BP PROCKOP DJ
Citation: Hj. Helminen et al., AN INBRED LINE OF TRANSGENIC MICE EXPRESSING AN INTERNALLY DELETED GENE FOR TYPE-II PROCOLLAGEN (COL2A1) - YOUNG MICE HAVE A VARIABLE PHENOTYPE OF A CHONDRODYSPLASIA AND OLDER MICE HAVE OSTEOARTHRITIC CHANGES IN JOINTS, The Journal of clinical investigation, 92(2), 1993, pp. 582-595
DELETION OF A LARGE DOMAIN IN RECOMBINANT HUMAN PROCOLLAGEN-II DOES NOT ALTER THE THERMAL-STABILITY OF THE TRIPLE-HELIX
Authors: SIERON AL FERTALA A ALAKOKKO L PROCKOP DJ
Citation: Al. Sieron et al., DELETION OF A LARGE DOMAIN IN RECOMBINANT HUMAN PROCOLLAGEN-II DOES NOT ALTER THE THERMAL-STABILITY OF THE TRIPLE-HELIX, The Journal of biological chemistry, 268(28), 1993, pp. 21232-21237
A 4TH EXAMPLE SUGGESTS PREMATURE TERMINATION CONDONS IN THE COL2A1 GENE ARE A COMMON-CAUSE OF THE STICKLER SYNDROME - ANALYSIS OF THE COL2A1 GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS
Authors: RITVANIEMI P HYLAND J IGNATIUS J KIVIRIKKO KI PROCKOP DJ ALAKOKKO L
Citation: P. Ritvaniemi et al., A 4TH EXAMPLE SUGGESTS PREMATURE TERMINATION CONDONS IN THE COL2A1 GENE ARE A COMMON-CAUSE OF THE STICKLER SYNDROME - ANALYSIS OF THE COL2A1 GENE BY DENATURING GRADIENT GEL-ELECTROPHORESIS, American journal of human genetics, 53(3), 1993, pp. 1115-1115
G-MUTATION TO A-MUTATION IN THE TYPE-II PROCOLLAGEN GENE THAT CONVERTS GLYCINE-247 TO SERINE IN A FAMILY WITH SPONDYLOEPIPHYSEAL DYSPLASIA
Authors: SOKOLOV BP RITVANIEMI P WILLIAMS CJ CONSIDINE E YURGENEV L MEERSON EM ALAKOKKO L PROCKOP DJ
Citation: Bp. Sokolov et al., G-MUTATION TO A-MUTATION IN THE TYPE-II PROCOLLAGEN GENE THAT CONVERTS GLYCINE-247 TO SERINE IN A FAMILY WITH SPONDYLOEPIPHYSEAL DYSPLASIA, American journal of human genetics, 53(3), 1993, pp. 1232-1232
MUTATION IN TYPE-II PROCOLLAGEN (COL2A1) THAT SUBSTITUTES ASPARTATE FOR GLYCINE ALPHA-1-67 AND THAT CAUSES CATARACTS AND RETINAL-DETACHMENT- EVIDENCE FOR MOLECULAR HETEROGENEITY IN THE WAGNER SYNDROME AND THESTICKLER SYNDROME (ARTHROOPHTHALMOPATHY)
Authors: KORKKO J RITVANIEMI P HAATAJA L KAARIAINEN H KIVIRIKKO KI PROCKOP DJ ALAKOKKO L
Citation: J. Korkko et al., MUTATION IN TYPE-II PROCOLLAGEN (COL2A1) THAT SUBSTITUTES ASPARTATE FOR GLYCINE ALPHA-1-67 AND THAT CAUSES CATARACTS AND RETINAL-DETACHMENT- EVIDENCE FOR MOLECULAR HETEROGENEITY IN THE WAGNER SYNDROME AND THESTICKLER SYNDROME (ARTHROOPHTHALMOPATHY), American journal of human genetics, 53(1), 1993, pp. 55-61
Risultati: 1-25 | 26-38 |