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Results: 1-21 |
Results: 21
IDENTIFICATION OF A 3RD EXT-LIKE GENE (EXTL3) BELONGING TO THE EXT GENE FAMILY
Authors: VANHUL W WUYTS W HENDRICKX J SPELEMAN F WAUTERS J DEBOULLE K VANROY N BOSSUYT P WILLEMS PJ
Citation: W. Vanhul et al., IDENTIFICATION OF A 3RD EXT-LIKE GENE (EXTL3) BELONGING TO THE EXT GENE FAMILY, Genomics, 47(2), 1998, pp. 230-237
ORAL TREATMENT SCHEDULES FOR ONYCHOMYCOSIS - A STUDY OF PATIENT PREFERENCE
Authors: NOLTING SK CARAZO JS DEBOULLE K LAMBERT JR
Citation: Sk. Nolting et al., ORAL TREATMENT SCHEDULES FOR ONYCHOMYCOSIS - A STUDY OF PATIENT PREFERENCE, International journal of dermatology, 37(6), 1998, pp. 454-456
MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W DEBOULLE K HENDRICKX J BAKKER E VANHOENACKER F MOLLICA F LUDECKE HJ SAYLI BS PAZZAGLIA UE MORTIER G HAMEL B CONRAD EU MATSUSHITA M RASKIND WH WILLEMS PJ
Citation: W. Wuyts et al., MUTATIONS IN THE EXT1 AND EXT2 GENES IN HEREDITARY MULTIPLE EXOSTOSES, American journal of human genetics, 62(2), 1998, pp. 346-354
IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE EXT GENEFAMILY, EXTL2
Authors: WUYTS W VANHUL W HENDRICKX J SPELEMAN F WAUTERS J DEBOULLE K VANROY N VANAGTMAEL T BOSSUYT P WILLEMS PJ
Citation: W. Wuyts et al., IDENTIFICATION AND CHARACTERIZATION OF A NOVEL MEMBER OF THE EXT GENEFAMILY, EXTL2, European journal of human genetics, 5(6), 1997, pp. 382-389
IDENTIFICATION OF THE EXT2 GENE ASSOCIATED WITH HEREDITARY MULTIPLE EXOSTOSES, AND 3 OTHER MEMBERS FROM THIS NOVEL GENE FAMILY
Authors: VANHUL W WUYTS W HENDRICKX J WAUTERS J DEBOULLE K WILLEMS PJ
Citation: W. Vanhul et al., IDENTIFICATION OF THE EXT2 GENE ASSOCIATED WITH HEREDITARY MULTIPLE EXOSTOSES, AND 3 OTHER MEMBERS FROM THIS NOVEL GENE FAMILY, Journal of bone and mineral research, 12, 1997, pp. 661-661
IDENTIFICATION OF A NEW FAMILY OF EXT-RELATED GENES
Authors: WUYTS W VANHUL W HENDRICKX J DEBOULLE K WILLEMS PW
Citation: W. Wuyts et al., IDENTIFICATION OF A NEW FAMILY OF EXT-RELATED GENES, American journal of human genetics, 61(4), 1997, pp. 2059-2059
POSITIONAL CLONING OF A GENE INVOLVED IN HEREDITARY MULTIPLE EXOSTOSES
Authors: WUYTS W VANHUL W WAUTERS J NEMTSOVA M REYNIERS E VANHUL E DEBOULLE K DEVRIES BBA HENDRICKX J HERRYGERS I BOSSUYT P BALEMANS W FRANSEN E VITS L COUCKE P NOWAK NJ SHOWS TB MALLET L VANDENOUWELAND AMW MCGAUGHRAN J HALLEY DJJ WILLEMS PJ
Citation: W. Wuyts et al., POSITIONAL CLONING OF A GENE INVOLVED IN HEREDITARY MULTIPLE EXOSTOSES, Human molecular genetics, 5(10), 1996, pp. 1547-1557
MEAN CORPUSCULAR HEMOGLOBIN IS NOT INCREASED IN FMR1 KNOCKOUT MICE
Authors: REYNIERS E VANBOCKSTAELE DR DEBOULLE K KOOY RF BAKKER CE OOSTRA BA WILLEMS PJ
Citation: E. Reyniers et al., MEAN CORPUSCULAR HEMOGLOBIN IS NOT INCREASED IN FMR1 KNOCKOUT MICE, Human genetics, 97(1), 1996, pp. 49-50
TRANSGENIC MOUSE MODEL FOR THE FRAGILE-X SYNDROME
Authors: KOOY RF DHOOGE R REYNIERS E BAKKER CE NAGELS G DEBOULLE K STORM K CLINCKE G DEDEYN PP OOSTRA BA WILLEMS PJ
Citation: Rf. Kooy et al., TRANSGENIC MOUSE MODEL FOR THE FRAGILE-X SYNDROME, American journal of medical genetics, 64(2), 1996, pp. 241-245
LONG-TERM POTENTIATION IN THE HIPPOCAMPUS OF FRAGILE-X KNOCKOUT MICE
Authors: GODFRAIND JM REYNIERS E DEBOULLE K DHOOGE R DEDEYN PP BAKKER CE OOSTRA BA KOOY RF WILLEMS PJ
Citation: Jm. Godfraind et al., LONG-TERM POTENTIATION IN THE HIPPOCAMPUS OF FRAGILE-X KNOCKOUT MICE, American journal of medical genetics, 64(2), 1996, pp. 246-251
SEVERE MENTAL-RETARDATION AND MACROORCHIDISM WITHOUT MUTATION IN THE FMR1 GENE
Authors: REYNIERS E WOLFF G TARIVERDIAN G DEBOULLE K STORM K KOOY RF WILLEMS PJ
Citation: E. Reyniers et al., SEVERE MENTAL-RETARDATION AND MACROORCHIDISM WITHOUT MUTATION IN THE FMR1 GENE, American journal of medical genetics, 64(2), 1996, pp. 408-412
N-DOCOSANOL 10-PERCENT CREAM IN THE TREATMENT OF RECURRENT HERPES LABIALIS - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY
Authors: HABBEMA L DEBOULLE K RODERS GA KATZ DH
Citation: L. Habbema et al., N-DOCOSANOL 10-PERCENT CREAM IN THE TREATMENT OF RECURRENT HERPES LABIALIS - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY, Acta dermato-venereologica, 76(6), 1996, pp. 479-481
A TRANSGENIC MOUSE MODEL FOR FRAGILE-X SYNDROME
Authors: WILLEMS PJ BAKKER CE REYNIERS E VERHEIJ C DEBOULLE K OOSTRA BA
Citation: Pj. Willems et al., A TRANSGENIC MOUSE MODEL FOR FRAGILE-X SYNDROME, Journal of cellular biochemistry, 1995, pp. 373-373
MASA SYNDROME IS DUE TO MUTATIONS IN THE NEURAL CELL-ADHESION GENE L1CAM
Authors: VITS L VANCAMP G COUCKE P FRANSEN E DEBOULLE K REYNIERS E KORN B POUSTKA A WILSON G SCHRANDERSTUMPEL C WINTER RM SCHWARTZ C WILLEMS PJ
Citation: L. Vits et al., MASA SYNDROME IS DUE TO MUTATIONS IN THE NEURAL CELL-ADHESION GENE L1CAM, Nature genetics, 7(3), 1994, pp. 408-413
APPARENT REGRESSION OF THE CGG REPEAT IN FMR1 TO AN ALLELE OF NORMAL SIZE
Authors: VITS L DEBOULLE K REYNIERS E HANDIG I DARBY JK OOSTRA B WILLEMS PJ
Citation: L. Vits et al., APPARENT REGRESSION OF THE CGG REPEAT IN FMR1 TO AN ALLELE OF NORMAL SIZE, Human genetics, 94(5), 1994, pp. 523-526
FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION
Authors: BAKKER CE VERHEIJ C WILLEMSEN R VANDERHELM R OERLEMANS F VERMEY M BYGRAVE A HOOGEVEEN AT OOSTRA BA REYNIERS E DEBOULLE K DHOOGE R CRAS P VANVELZEN D NAGELS G MARTIN JJ DEDEYN PP DARBY JK WILLEMS PJ
Citation: Ce. Bakker et al., FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION, Cell, 78(1), 1994, pp. 23-33
VARIABLE REGIONS OF CHROMOSOME-11 LOSS IN DIFFERENT PATHOLOGICAL TISSUES OF A PATIENT WITH THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-I SYNDROME
Authors: BECKERS A ABS R REYNIERS E DEBOULLE K STEVENAERT A HELLER FR KLOPPEL G MEURISSE M WILLEMS PJ
Citation: A. Beckers et al., VARIABLE REGIONS OF CHROMOSOME-11 LOSS IN DIFFERENT PATHOLOGICAL TISSUES OF A PATIENT WITH THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-I SYNDROME, The Journal of clinical endocrinology and metabolism, 79(5), 1994, pp. 1498-1502
THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM
Authors: REYNIERS E VITS L DEBOULLE K VANROY B VANVELZEN D DEGRAAFF E VERKERK AJMH JORENS HZJ DARBY JK OOSTRA B WILLEMS PJ
Citation: E. Reyniers et al., THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM, Nature genetics, 4(2), 1993, pp. 143-146
ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993)
Authors: VERKERK AJMH DEGRAAFF E DEBOULLE K EICHLER EE KONECKI DS REYNIERS E MANCA A POUSTKA A WILLEMS PJ NELSON DL OOSTRA BA
Citation: Ajmh. Verkerk et al., ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993), Human molecular genetics, 2(8), 1993, pp. 1348-1348
AN ECORI RFLP IN THE 5' REGION OF THE HUMAN NF1 GENE
Authors: REYNIERS E DEBOULLE K MARCHUK DA ANDERSEN LB COLLINS FS WILLEMS PJ
Citation: E. Reyniers et al., AN ECORI RFLP IN THE 5' REGION OF THE HUMAN NF1 GENE, Human genetics, 92(6), 1993, pp. 631-631
FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION
Authors: BUYLE S REYNIERS E VITS L DEBOULLE K HANDIG I WUYTS FLE DEELEN W HALLEY DJJ OOSTRA BA WILLEMS PJ
Citation: S. Buyle et al., FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION, Human genetics, 92(3), 1993, pp. 269-272
Risultati: 1-21 |