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Results: 1-18 |
Results: 18
EXPRESSION OF GENES (CAPN3, SGCA, SGCB, AND TTN) INVOLVED IN PROGRESSIVE MUSCULAR-DYSTROPHIES DURING EARLY HUMAN-DEVELOPMENT
Authors: FOUGEROUSSE F DURAND M SUEL L POURQUIE O DELEZOIDE AL ROMERO NB ABITBOL M BECKMANN JS
Citation: F. Fougerousse et al., EXPRESSION OF GENES (CAPN3, SGCA, SGCB, AND TTN) INVOLVED IN PROGRESSIVE MUSCULAR-DYSTROPHIES DURING EARLY HUMAN-DEVELOPMENT, Genomics, 48(2), 1998, pp. 145-156
CARDIAC MYOSIN BINDING-PROTEIN-C GENE IS SPECIFICALLY EXPRESSED IN HEART DURING MURINE AND HUMAN-DEVELOPMENT
Authors: FOUGEROUSSE F DELEOZIDE AL FISZMAN MY SCHWARTZ K BECKMANN JS CARRIER L
Citation: F. Fougerousse et al., CARDIAC MYOSIN BINDING-PROTEIN-C GENE IS SPECIFICALLY EXPRESSED IN HEART DURING MURINE AND HUMAN-DEVELOPMENT, Circulation research, 82(1), 1998, pp. 130-133
MOLECULAR COMBING - A SELF-SUFFICIENT TOOL FOR HIGH-RESOLUTION PHYSICAL MAPPING AND MOLECULAR DIAGNOSTICS
Authors: BENSIMON A MICHALET X EKONG R FOUGEROUSSE F SCHURRA C
Citation: A. Bensimon et al., MOLECULAR COMBING - A SELF-SUFFICIENT TOOL FOR HIGH-RESOLUTION PHYSICAL MAPPING AND MOLECULAR DIAGNOSTICS, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 10-10
DYNAMIC MOLECULAR COMBING - STRETCHING THE WHOLE HUMAN GENOME FOR HIGH-RESOLUTION STUDIES
Authors: MICHALET X EKONG R FOUGEROUSSE F ROUSSEAUX S SCHURRA C HORNIGOLD N VANSLEGTENHORST M WOLFE J POVEY S BECKMANN JS BENSIMON A
Citation: X. Michalet et al., DYNAMIC MOLECULAR COMBING - STRETCHING THE WHOLE HUMAN GENOME FOR HIGH-RESOLUTION STUDIES, Science, 277(5331), 1997, pp. 1518-1523
ORIENTATION OF THE CAPN3 GENE BY FLUORESCENT HYBRIDIZATION ON COMBED GENOMIC DNA OF YEAST (YAC), HUMAN AND MOUSE
Authors: MICHALET X FOUGEROUSSE F SCHURRA C BECKMANN JS BENSIMON A
Citation: X. Michalet et al., ORIENTATION OF THE CAPN3 GENE BY FLUORESCENT HYBRIDIZATION ON COMBED GENOMIC DNA OF YEAST (YAC), HUMAN AND MOUSE, American journal of human genetics, 61(4), 1997, pp. 292-292
IDENTIFICATION OF MUSCLE-SPECIFIC CALPAIN AND BETA-SARCOGLYCAN GENES IN PROGRESSIVE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHIES
Authors: BECKMANN JS RICHARD I BROUX O FOUGEROUSSE F ALLAMAND V CHIANNILKULCHAI N LIM LE DUCLOS F BOURG N BRENGUIER L PASTURAUD P QUETIER F ROUDAUT C SUNADA Y MEYER J DINCER P LEFRANC G MERLINI L TOPALOGLU H TOME FMS COHEN D JACKSON CE CAMPBELL KP FARDEAU M
Citation: Js. Beckmann et al., IDENTIFICATION OF MUSCLE-SPECIFIC CALPAIN AND BETA-SARCOGLYCAN GENES IN PROGRESSIVE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHIES, Neuromuscular disorders, 6(6), 1996, pp. 455-462
AN STS MAP OF THE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A REGION
Authors: RICHARD I ROUDAUT C FOUGEROUSSE F CHIANNILKULCHAI N BECKMANN JS
Citation: I. Richard et al., AN STS MAP OF THE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A REGION, Mammalian genome, 6(10), 1995, pp. 754-756
A GENE FOR LIMB-GIRDLE MUSCULAR-DYSTROPHY CODES FOR A PROTEASE, CALPAIN-3
Authors: RICHARD I BROUX O ALLAMAND V FOUGEROUSSE F CHIANNILKULCHAI N BOURG N BRENGUIER L DEVAUD C PASTURAUD P ROUDAUT C HILLAIRE D PASSOSBUENO MR ZATZ M TISCHFIELD JA FARDEAU M JACKSON CE COHEN D BECKMANN JS
Citation: I. Richard et al., A GENE FOR LIMB-GIRDLE MUSCULAR-DYSTROPHY CODES FOR A PROTEASE, CALPAIN-3, MS. Medecine sciences, 11(4), 1995, pp. 637-640
MUTATIONS IN THE PROTEOLYTIC-ENZYME CALPAIN-3 CAUSE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE-2A
Authors: RICHARD I BROUX O ALLAMAND V FOUGEROUSSE F CHIANNILKULCHAI N BOURG N BRENGUIER L DEVAUD C PASTURAUD P ROUDAUT C HILLAIRE D PASSOSBUENO MR ZATZ M TISCHFIELD JA FARDEAU M JACKSON CE COHEN D BECKMANN JS
Citation: I. Richard et al., MUTATIONS IN THE PROTEOLYTIC-ENZYME CALPAIN-3 CAUSE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE-2A, Cell, 81(1), 1995, pp. 27-40
PREFERENTIAL LOCALIZATION OF THE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A GENE IN THE PROXIMAL PART OF A 1-CM 15Q15.1-Q15.3 INTERVAL
Authors: ALLAMAND V BROUX O RICHARD I FOUGEROUSSE F CHIANNILKULCHAI N BOURG N BRENGUIER L DEVAUD C PASTURAUD P DESOUZA AP ROUDAUT C TISCHFIELD JA CONNEALLY PM FARDEAU M COHEN D JACKSON CE BECKMANN JS
Citation: V. Allamand et al., PREFERENTIAL LOCALIZATION OF THE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A GENE IN THE PROXIMAL PART OF A 1-CM 15Q15.1-Q15.3 INTERVAL, American journal of human genetics, 56(6), 1995, pp. 1417-1430
MAPPING OF A CHROMOSOME-15 REGION INVOLVED IN LIMB-GIRDLE MUSCULAR-DYSTROPHY
Authors: FOUGEROUSSE F BROUX O RICHARD I ALLAMAND V DESOUZA AP BOURG N BRENGUIER L DEVAUD C PASTURAUD P ROUDAUT C CHIANNILKULCHAI N HILLAIRE D BUI H CHUMAKOV I WEISSENBACH J CHERIF D COHEN D BECKMANN JS
Citation: F. Fougerousse et al., MAPPING OF A CHROMOSOME-15 REGION INVOLVED IN LIMB-GIRDLE MUSCULAR-DYSTROPHY, Human molecular genetics, 3(2), 1994, pp. 285-293
REGIONAL LOCALIZATION OF HUMAN-CHROMOSOME-15 LOCI
Authors: RICHARD I BROUX O CHIANNILKULCHAI N FOUGEROUSSE F ALLAMAND V BOURG N BRENGUIER L DEVAUD C PASTURAUD P ROUDAUT C LORENZO F SEBASTIANIKABATCHIS C SCHULTZ RA POLYMEROPOULOS MH GYAPAY G AUFFRAY C BECKMANN JS
Citation: I. Richard et al., REGIONAL LOCALIZATION OF HUMAN-CHROMOSOME-15 LOCI, Genomics, 23(3), 1994, pp. 619-627
LOCALIZATION OF THE HUMAN COPROPORPHYRINOGEN OXIDASE GENE TO CHROMOSOME BAND 3Q12
Authors: CACHEUX V MARTASEK P FOUGEROUSSE F DELFAU MH DRUART L TACHDJIAN G GRANDCHAMP B
Citation: V. Cacheux et al., LOCALIZATION OF THE HUMAN COPROPORPHYRINOGEN OXIDASE GENE TO CHROMOSOME BAND 3Q12, Human genetics, 94(5), 1994, pp. 557-559
TOWARDS THE IDENTIFICATION OF A GENE FOR LGMD2
Authors: FOUGEROUSSE F BROUX O RICHARD I ALLAMAND V DESOUZA AP BOURG N BRENGUIER L DEVAUD C PASTURAUD P ROUDAUT C CHIANNIKULCHAI N HILLAIRE D BUI H CHUMAKOVV I WEISSENBACH J CHERIF D COHEN D BECKMANN JS
Citation: F. Fougerousse et al., TOWARDS THE IDENTIFICATION OF A GENE FOR LGMD2, Cytogenetics and cell genetics, 67(1), 1994, pp. 20-20
REGIONAL LOCALIZATION OF HUMAN-CHROMOSOME-15 LOCI
Authors: RICHARD I BROUX O CHIANNIKULCHAI N FOUGEROUSSE F ALLAMAND V BOURG N BRENGUIER L DEVAUD C PASTURAUD P ROUDAUT C POLYMEROPOULOS M SCHULTZ R COHEN D BECKMANN JS
Citation: I. Richard et al., REGIONAL LOCALIZATION OF HUMAN-CHROMOSOME-15 LOCI, Cytogenetics and cell genetics, 67(1), 1994, pp. 22-22
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE LOCUS D15S222
Authors: FOUGEROUSSE F PASTURAUD P BECKMANN JS
Citation: F. Fougerousse et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE LOCUS D15S222, Human molecular genetics, 2(12), 1993, pp. 2200-2200
EVIDENCE OF GENETIC-HETEROGENEITY IN THE AUTOSOMAL RECESSIVE ADULT FORMS OF LIMB-GIRDLE MUSCULAR-DYSTROPHY FOLLOWING LINKAGE ANALYSIS WITH 15Q PROBES IN BRAZILIAN FAMILIES
Authors: PASSOSBUENO MR RICHARD I VAINZOF M FOUGEROUSSE F WEISSENBACH J BROUX O COHEN D AKIYAMA J MARIE SKN CARVALHO AA GUILHERME L KALIL J TSANACLIS AM ZATZ M BECKMANN JS
Citation: Mr. Passosbueno et al., EVIDENCE OF GENETIC-HETEROGENEITY IN THE AUTOSOMAL RECESSIVE ADULT FORMS OF LIMB-GIRDLE MUSCULAR-DYSTROPHY FOLLOWING LINKAGE ANALYSIS WITH 15Q PROBES IN BRAZILIAN FAMILIES, Journal of Medical Genetics, 30(5), 1993, pp. 385-387
TOWARDS THE IDENTIFICATION OF A GENE FOR LGMD
Authors: FOUGEROUSSE F RICHARD I BROUX O ALLAMAND V DESOUZA AP CHIANNILKULCHAI N CHERIF D WEISSENBACH J COHEN D BECKMANN JS
Citation: F. Fougerousse et al., TOWARDS THE IDENTIFICATION OF A GENE FOR LGMD, American journal of human genetics, 53(3), 1993, pp. 1289-1289
Risultati: 1-18 |