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Results: 51-75/185
RISK PERCEPTION AFTER CF CARRIER TESTING AND IMPACT OF THE TEST RESULT ON REPRODUCTIVE DECISION-MAKING
Authors: DENAYER L WELKENHUYSEN M EVERSKIEBOOMS G CASSIMAN JJ VANDENBERGHE H
Citation: L. Denayer et al., RISK PERCEPTION AFTER CF CARRIER TESTING AND IMPACT OF THE TEST RESULT ON REPRODUCTIVE DECISION-MAKING, American journal of medical genetics, 69(4), 1997, pp. 422-428
SEMIQUANTITATIVE PCR OF ALPHA-2 AND ALPHA-4 INTEGRIN MESSENGER-RNA SHOWS DIFFERENTIAL RESPONSE TO THE TRANSCRIPTIONAL MODULATORS TGF-BETA-1AND TPA
Authors: ZHU YH VEKEMANS S CASSIMAN JJ
Citation: Yh. Zhu et al., SEMIQUANTITATIVE PCR OF ALPHA-2 AND ALPHA-4 INTEGRIN MESSENGER-RNA SHOWS DIFFERENTIAL RESPONSE TO THE TRANSCRIPTIONAL MODULATORS TGF-BETA-1AND TPA, Cellular and molecular biology, 43(8), 1997, pp. 1221-1226
TRISOMY-15 RESCUE WITH JUMPING TRANSLOCATION OF DISTAL 15Q IN PRADER-WILLI-SYNDROME
Authors: DEVRIENDT K PETIT P MATTHIJS G VERMEESCH JR HOLVOET M DEMUELENAERE A MARYNEN P CASSIMAN JJ FRYNS JP
Citation: K. Devriendt et al., TRISOMY-15 RESCUE WITH JUMPING TRANSLOCATION OF DISTAL 15Q IN PRADER-WILLI-SYNDROME, Journal of Medical Genetics, 34(5), 1997, pp. 395-399
PRADER-WILLI-SYNDROME IN A CHILD WITH MOSAIC TRISOMY-15 AND MOSAIC TRIPLO-X - A MOLECULAR ANALYSIS
Authors: DEVRIENDT K MATTHIJS G CLAES S LEGIUS E PROESMANS W CASSIMAN JJ FRYNS JP
Citation: K. Devriendt et al., PRADER-WILLI-SYNDROME IN A CHILD WITH MOSAIC TRISOMY-15 AND MOSAIC TRIPLO-X - A MOLECULAR ANALYSIS, Journal of Medical Genetics, 34(4), 1997, pp. 318-322
A NOVEL MODEL FOR THE FIRST NUCLEOTIDE-BINDING DOMAIN OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR
Authors: ANNEREAU JP WULBRAND U VANKEERBERGHEN A CUPPENS H BONTEMS F TUMMLER B CASSIMAN JJ STOVEN V
Citation: Jp. Annereau et al., A NOVEL MODEL FOR THE FIRST NUCLEOTIDE-BINDING DOMAIN OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR, FEBS letters, 407(3), 1997, pp. 303-308
X-LINKED SEVERE MENTAL-RETARDATION AND A PROGRESSIVE NEUROLOGICAL DISORDER IN A BELGIAN FAMILY - CLINICAL AND GENETIC-STUDIES
Authors: CLAES S DEVRIENDT K DADAMO P MEIRELEIRE J RAEYMAEKERS P TONIOLO D CASSIMAN JJ FRYNS JP
Citation: S. Claes et al., X-LINKED SEVERE MENTAL-RETARDATION AND A PROGRESSIVE NEUROLOGICAL DISORDER IN A BELGIAN FAMILY - CLINICAL AND GENETIC-STUDIES, Clinical genetics, 52(3), 1997, pp. 155-161
DEVELOPMENT OF REVERSE DOT-BLOT SYSTEM FOR SCREENING OF MITOCHONDRIAL-DNA MUTATIONS ASSOCIATED WITH LEBER HEREDITARY OPTIC ATROPHY
Authors: SCHOLLEN E VANDENBERK P CASSIMAN JJ MATTHIJS G
Citation: E. Schollen et al., DEVELOPMENT OF REVERSE DOT-BLOT SYSTEM FOR SCREENING OF MITOCHONDRIAL-DNA MUTATIONS ASSOCIATED WITH LEBER HEREDITARY OPTIC ATROPHY, Clinical chemistry, 43(1), 1997, pp. 18-23
BCL6 GENE REARRANGEMENTS ALSO OCCUR IN MARGINAL ZONE B-CELL LYMPHOMA
Authors: DIERLAMM J PITTALUGA S STUL M WLODARSKA I MICHAUX L THOMAS J VERHOEF G VERHEST A DEPARDIEU C CASSIMAN JJ HAGEMEIJER A DEWOLFPEETERS C VANDENBERGHE H
Citation: J. Dierlamm et al., BCL6 GENE REARRANGEMENTS ALSO OCCUR IN MARGINAL ZONE B-CELL LYMPHOMA, British Journal of Haematology, 98(3), 1997, pp. 719-725
NEW SUBTYPE OF PRE-B ACUTE LYMPHOBLASTIC-LEUKEMIA WITH T(5-12)(Q31Q33-P12), MOLECULARLY AND CYTOGENETICALLY DISTINCT FROM T(5-12) IN CHRONIC MYELOMONOCYTIC LEUKEMIA
Authors: WLODARSKA I AVENTIN A INGLESESTEVE J FALZETTI D CRIEL A CASSIMAN JJ MECUCCI C VANDENBERGHE H MARYNEN P
Citation: I. Wlodarska et al., NEW SUBTYPE OF PRE-B ACUTE LYMPHOBLASTIC-LEUKEMIA WITH T(5-12)(Q31Q33-P12), MOLECULARLY AND CYTOGENETICALLY DISTINCT FROM T(5-12) IN CHRONIC MYELOMONOCYTIC LEUKEMIA, Blood, 89(5), 1997, pp. 1716-1722
FAMILIAL JUVENILE FOCAL AMYOTROPHY OF THE UPPER EXTREMITY (HIRAYAMA DISEASE) - SUPEROXIDE-DISMUTASE-1 GENOTYPE AND ACTIVITY
Authors: ROBBERECHT W AGUIRRE T VANDENBOSCH L THEYS P NEES H CASSIMAN JJ MATTHIJS G
Citation: W. Robberecht et al., FAMILIAL JUVENILE FOCAL AMYOTROPHY OF THE UPPER EXTREMITY (HIRAYAMA DISEASE) - SUPEROXIDE-DISMUTASE-1 GENOTYPE AND ACTIVITY, Archives of neurology, 54(1), 1997, pp. 46-50
EXHAUSTIVE MUTATION ANALYSIS OF THE PMM2 GENE IN PATIENTS WITH THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I (CDG1 OR JAEKEN-SYNDROME) AND CLONING OF THE MOUSE PMM1 AND PMM2 GENES
Authors: MATTHIJS G SCHOLLEN E JAEKEN J VANSCHAFTINGEN E CASSIMAN JJ
Citation: G. Matthijs et al., EXHAUSTIVE MUTATION ANALYSIS OF THE PMM2 GENE IN PATIENTS WITH THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I (CDG1 OR JAEKEN-SYNDROME) AND CLONING OF THE MOUSE PMM1 AND PMM2 GENES, American journal of human genetics, 61(4), 1997, pp. 52-52
LINKAGE BETWEEN A CD4 GENE POLYMORPHISM AND IDDM IN DANISH IDDM PATIENTS
Authors: KRISTIANSEN OP ZAMANI M JOHANNESEN J MANDRUPPOULSEN T CASSIMAN JJ NERUP J POCIOT F
Citation: Op. Kristiansen et al., LINKAGE BETWEEN A CD4 GENE POLYMORPHISM AND IDDM IN DANISH IDDM PATIENTS, American journal of human genetics, 61(4), 1997, pp. 1640-1640
SENSITIVITY TO OXIDATIVE STRESS OF FIBROBLASTS FROM PATIENTS FROM FAMILIAL AND SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS
Authors: AGUIRRE T VANDENBOSCH L MATTHIJS G CASSIMAN JJ ROBBERECHT W
Citation: T. Aguirre et al., SENSITIVITY TO OXIDATIVE STRESS OF FIBROBLASTS FROM PATIENTS FROM FAMILIAL AND SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS, American journal of human genetics, 61(4), 1997, pp. 2387-2387
SKEWED X-CHROMOSOME INACTIVATION IN FEMALE CARRIERS OF DYSKERATOSIS-CONGENITA
Authors: DEVRIENDT K MATTHIJS G LEGIUS E SCHOLLEN E BLOCKMANS D VANGEET C DEGREEF H CASSIMAN JJ FRYNS JP
Citation: K. Devriendt et al., SKEWED X-CHROMOSOME INACTIVATION IN FEMALE CARRIERS OF DYSKERATOSIS-CONGENITA, American journal of human genetics, 60(3), 1997, pp. 581-587
NEUROFIBROMATOSIS TYPE-I GENE MUTATION IN A PATIENT WITH FEATURES OF LEOPARD-SYNDROME
Authors: WU R LEGIUS E ROBBERECHT W DUMOULIN M CASSIMAN JJ FRYNS JP
Citation: R. Wu et al., NEUROFIBROMATOSIS TYPE-I GENE MUTATION IN A PATIENT WITH FEATURES OF LEOPARD-SYNDROME, Human mutation, 8(1), 1996, pp. 51-56
BCL3 REARRANGEMENT AND T(14-19)(Q32-Q13) IN LYMPHOPROLIFERATIVE DISORDERS
Authors: MICHAUX L MECUCCI C STUL M WLODARSKA I HERNANDEZ JM MEEUS P MICHAUX JL SCHEIFF JM NOEL H LOUWAGIE A CRIEL A BOOGAERTS M VANORSHOVEN A CASSIMAN JJ VANDENBERGHE H
Citation: L. Michaux et al., BCL3 REARRANGEMENT AND T(14-19)(Q32-Q13) IN LYMPHOPROLIFERATIVE DISORDERS, Genes, chromosomes & cancer, 15(1), 1996, pp. 38-47
THE GENOMIC STRUCTURE OF THE MURINE ALPHA(4) INTEGRIN GENE
Authors: DEMEIRSMAN C JASPERS M SCHOLLEN E CASSIMAN JJ
Citation: C. Demeirsman et al., THE GENOMIC STRUCTURE OF THE MURINE ALPHA(4) INTEGRIN GENE, DNA and cell biology, 15(7), 1996, pp. 595-603
TRANSLOCATION T(8-16)(P11-P13) IN ACUTE NONLYMPHOCYTIC LEUKEMIA - REPORT ON 2 NEW CASES AND REVIEW OF THE LITERATURE
Authors: VELLOSO ERP MECUCCI C MICHAUX L VANORSHOVEN A STUL M BOOGAERTS M BOSLY A CASSIMAN JJ VANDENBERGHE H
Citation: Erp. Velloso et al., TRANSLOCATION T(8-16)(P11-P13) IN ACUTE NONLYMPHOCYTIC LEUKEMIA - REPORT ON 2 NEW CASES AND REVIEW OF THE LITERATURE, Leukemia & lymphoma, 21(1-2), 1996, pp. 137-142
A 68-KD ANTIGEN, WHICH IS PROBABLY AN N-TERMINAL FRAGMENT OF THE VLA-5 ALPHA(5)-SUBUNIT, IS SPECIFIC FOR DIFFERENTIATING KERATINOCYTES
Authors: DESTROOPER B WU RR JASPERS M VANDERSCHUEREN B VEKEMANS S CARMELIET G VANLEUVEN F VANDENOORD J CASSIMAN JJ
Citation: B. Destrooper et al., A 68-KD ANTIGEN, WHICH IS PROBABLY AN N-TERMINAL FRAGMENT OF THE VLA-5 ALPHA(5)-SUBUNIT, IS SPECIFIC FOR DIFFERENTIATING KERATINOCYTES, Dermatology, 193(3), 1996, pp. 212-220
NON-SYNDROMIC DEAFNESS ASSOCIATED WITH A MUTATION AND A POLYMORPHISM IN THE MITOCHONDRIAL 12S RIBOSOMAL-RNA GENE IN A LARGE ZAIREAN PEDIGREE
Authors: MATTHIJS G CLAES S LONGOMBENZA B CASSIMAN JJ
Citation: G. Matthijs et al., NON-SYNDROMIC DEAFNESS ASSOCIATED WITH A MUTATION AND A POLYMORPHISM IN THE MITOCHONDRIAL 12S RIBOSOMAL-RNA GENE IN A LARGE ZAIREAN PEDIGREE, European journal of human genetics, 4(1), 1996, pp. 46-51
EVIDENCE FOR GENETIC-HETEROGENEITY IN THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I (CDG1)
Authors: MATTHIJS G LEGIUS E SCHOLLEN E VANDENBERK P JAEKEN J BARONE R FIUMARA A VISSER G LAMBERT M CASSIMAN JJ
Citation: G. Matthijs et al., EVIDENCE FOR GENETIC-HETEROGENEITY IN THE CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-I (CDG1), Genomics, 35(3), 1996, pp. 597-599
PHILADELPHIA-CHROMOSOME-POSITIVE ACUTE MYELOID-LEUKEMIA - CYTOIMMUNOLOGIC AND CYTOGENETIC FEATURES
Authors: CUNEO A FERRANT A MICHAUX JL DEMUYNCK H BOOGAERTS M LOUWAGIE A DOYEN C STUL M CASSIMAN JJ DALCIN P CASTOLDI G VANDENBERGHE H
Citation: A. Cuneo et al., PHILADELPHIA-CHROMOSOME-POSITIVE ACUTE MYELOID-LEUKEMIA - CYTOIMMUNOLOGIC AND CYTOGENETIC FEATURES, Haematologica, 81(5), 1996, pp. 423-427
CLINICAL AND MOLECULAR-GENETIC FEATURES OF CONGENITAL SPINAL MUSCULAR-ATROPHY
Authors: DEVRIENDT K LAMMENS M SCHOLLEN E VANHOLE C DOM R DEVLIEGER H CASSIMAN JJ FRYNS JP MATTHIJS G
Citation: K. Devriendt et al., CLINICAL AND MOLECULAR-GENETIC FEATURES OF CONGENITAL SPINAL MUSCULAR-ATROPHY, Annals of neurology, 40(5), 1996, pp. 731-738
LINKAGE OF TYPE-I DIABETES TO 15Q26 (IDDM3) IN THE DANISH POPULATION
Authors: ZAMANI M POCIOT F RAEYMAEKERS P NERUP J CASSIMAN JJ
Citation: M. Zamani et al., LINKAGE OF TYPE-I DIABETES TO 15Q26 (IDDM3) IN THE DANISH POPULATION, Human genetics, 98(4), 1996, pp. 491-496
CONFIRMATION OF LINKAGE OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-1 (CDG1) TO CHROMOSOME 16P13.13-P13.11 AND LINKAGE DISEQUILIBRIUM TO D16S414, D16S497 AND D16S519
Authors: MATTHIJS G VANDENBERK P LEGIUS E JAEKEN J CASSIMAN JJ
Citation: G. Matthijs et al., CONFIRMATION OF LINKAGE OF CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE-1 (CDG1) TO CHROMOSOME 16P13.13-P13.11 AND LINKAGE DISEQUILIBRIUM TO D16S414, D16S497 AND D16S519, Cytogenetics and cell genetics, 72(4), 1996, pp. 16-16
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