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Results: 1-9 |
Results: 9
THE HUMAN CHITOTRIOSIDASE GENE - NATURE OF INHERITED ENZYME DEFICIENCY
Authors: BOOT RG RENKEMA GH VERHOEK M STRIJLAND A BLIEK J DEMEULEMEESTER TMAMO MANNENS MMAM AERTS JMFG
Citation: Rg. Boot et al., THE HUMAN CHITOTRIOSIDASE GENE - NATURE OF INHERITED ENZYME DEFICIENCY, The Journal of biological chemistry, 273(40), 1998, pp. 25680-25685
A DOMINANT-NEGATIVE ISOFORM OF THE LONG QT SYNDROME-1 GENE-PRODUCT
Authors: DEMOLOMBE S BARO I PEREON Y BLIEK J MOHAMMADPANAH R POLLARD H MORID S MANNENS M WILDE A BARHANIN J CHARPENTIER F ESCANDE D
Citation: S. Demolombe et al., A DOMINANT-NEGATIVE ISOFORM OF THE LONG QT SYNDROME-1 GENE-PRODUCT, The Journal of biological chemistry, 273(12), 1998, pp. 6837-6843
A DOMINANT-NEGATIVE ISOFORM OF KVLQT1 K-CHANNELS
Authors: DEMOLOMBE S BARO L PEREON Y BLIEK J MANNENS M BARHANIN J CHARPENTIER F ESCANDE D
Citation: S. Demolombe et al., A DOMINANT-NEGATIVE ISOFORM OF KVLQT1 K-CHANNELS, Biophysical journal, 74(2), 1998, pp. 26-26
THE HUMAN ACHAETE-SCUTE-HOMOLOG-2 (ASCL2,HASH2) MAPS TO CHROMOSOME-11P15.5, CLOSE TO IGF2 AND IS EXPRESSED IN EXTRAVILLUS TROPHOBLASTS
Authors: ALDERS M HODGES M HADJANTONAKIS AK POSTMUS J VANWIJK I BLIEK J DEMEULEMEESTER M WESTERVELD A GUILLEMOT F OUDEJANS C LITTLE P MANNENS M
Citation: M. Alders et al., THE HUMAN ACHAETE-SCUTE-HOMOLOG-2 (ASCL2,HASH2) MAPS TO CHROMOSOME-11P15.5, CLOSE TO IGF2 AND IS EXPRESSED IN EXTRAVILLUS TROPHOBLASTS, Human molecular genetics, 6(6), 1997, pp. 859-867
THE K-1 IS A COMPLEX MADE OF 3 DIFFERENT PROTEINS( CHANNEL INVOLVED IN THE LONG QT SYNDROME)
Authors: DEMOLOMBE S BARE I BLIEK J MOHAMMADPANAH R LOUSSOUARN G MANNENS M WILDE AA BARHANIN J CHARPENTIER F PEREON Y ESCANDE D
Citation: S. Demolombe et al., THE K-1 IS A COMPLEX MADE OF 3 DIFFERENT PROTEINS( CHANNEL INVOLVED IN THE LONG QT SYNDROME), Circulation, 96(8), 1997, pp. 302-302
POSITIONAL CLONING OF GENES INVOLVED IN THE BECKWITH-WIEDEMANN SYNDROME, HEMIHYPERTROPHY, AND ASSOCIATED CHILDHOOD TUMORS
Authors: MANNENS M ALDERS M REDEKER B BLIEK J STEENMAN M WIESMEYER C DEMEULEMEESTER M RYAN A KALIKIN L VOUTE T DEKRAKER J HOOVERS J SLATER R FEINBERG A LITTLE P WESTERVELD A
Citation: M. Mannens et al., POSITIONAL CLONING OF GENES INVOLVED IN THE BECKWITH-WIEDEMANN SYNDROME, HEMIHYPERTROPHY, AND ASSOCIATED CHILDHOOD TUMORS, Medical and pediatric oncology, 27(5), 1996, pp. 490-494
CLONING OF CANDIDATE GENES INVOLVED IN THE BECKWITH-WIEDEMANN SYNDROME AND CHILDHOOD TUMORS
Authors: ALDERS M BLIEK J REDEKER B RYAN A FEINBERG A WESTERVELD A LITTLE P MANNENS M
Citation: M. Alders et al., CLONING OF CANDIDATE GENES INVOLVED IN THE BECKWITH-WIEDEMANN SYNDROME AND CHILDHOOD TUMORS, Medical and pediatric oncology, 27(5), 1996, pp. 495-497
MULTIPLE GENETIC-LOCI WITHIN 11P15 DEFINED BY BECKWITH-WIEDEMANN SYNDROME REARRANGEMENT BREAKPOINTS AND SUBCHROMOSOMAL TRANSFERABLE FRAGMENTS
Authors: HOOVERS JMN KALIKIN LM JOHNSON LA ALDERS M REDEKER B LAW DJ BLIEK J STEENMAN M BENEDICT M WIEGANT J LENGAUER C TAILLONMILLER P SCHLESSINGER D EDWARDS MC ELLEDGE SJ IVENS A WESTERVELD A LITTLE P MANNENS M FEINBERG AP
Citation: Jmn. Hoovers et al., MULTIPLE GENETIC-LOCI WITHIN 11P15 DEFINED BY BECKWITH-WIEDEMANN SYNDROME REARRANGEMENT BREAKPOINTS AND SUBCHROMOSOMAL TRANSFERABLE FRAGMENTS, Proceedings of the National Academy of Sciences of the United Statesof America, 92(26), 1995, pp. 12456-12460
AN INTEGRATED PHYSICAL MAP OF 210 MARKERS ASSIGNED TO THE SHORT ARM OF HUMAN-CHROMOSOME-11
Authors: REDEKER E HOOVERS JMN ALDERS M VANMOORSEL CJA IVENS AC GREGORY S KALIKIN L BLIEK J DEGALAN L VANDENBOGAARD R VISSER J VANDERVOORT R FEINBERG AP LITTLE PFR WESTERVELD A MANNENS M
Citation: E. Redeker et al., AN INTEGRATED PHYSICAL MAP OF 210 MARKERS ASSIGNED TO THE SHORT ARM OF HUMAN-CHROMOSOME-11, Genomics, 21(3), 1994, pp. 538-550
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