AAAAAA

   
Results: 1-9 |
Results: 9
MAPPING OF CHROMOSOMAL IMBALANCES IN GASTRIC ADENOCARCINOMA REVEALED AMPLIFIED PROTOONCOGENES MYCN, MET, WNT2, AND ERBB2
Authors: NESSLING M SOLINASTOLDO S WILGENBUS KK BORCHARD F LICHTER P
Citation: M. Nessling et al., MAPPING OF CHROMOSOMAL IMBALANCES IN GASTRIC ADENOCARCINOMA REVEALED AMPLIFIED PROTOONCOGENES MYCN, MET, WNT2, AND ERBB2, Genes chromosomes & cancer (Print), 23(4), 1998, pp. 307-316
DMBT1, A NEW MEMBER OF THE SRCR SUPERFAMILY, ON CHROMOSOME 10Q25.3-26.1 IS DELETED IN MALIGNANT BRAIN-TUMORS
Authors: MOLLENHAUER J WIEMANN S SCHEURLEN W KORN B HAYASHI Y WILGENBUS KK VONDEIMLING A POUSTKA A
Citation: J. Mollenhauer et al., DMBT1, A NEW MEMBER OF THE SRCR SUPERFAMILY, ON CHROMOSOME 10Q25.3-26.1 IS DELETED IN MALIGNANT BRAIN-TUMORS, Nature genetics, 17(1), 1997, pp. 32-39
HIGH-RESOLUTION DELETION MAPPING OF CHROMOSOME ARM 17P IN CHILDHOOD PRIMITIVE NEUROECTODERMAL TUMORS REVEALS A COMMON CHROMOSOMAL DISRUPTION WITHIN THE SMITH-MAGENIS REGION, AN UNSTABLE REGION IN CHROMOSOME BAND 17P11.2
Authors: SCHEURLEN WG SERANSKI P MINCHEVA A KUHL J SORENSEN N KRAUSS J LICHTER P POUSTKA A WILGENBUS KK
Citation: Wg. Scheurlen et al., HIGH-RESOLUTION DELETION MAPPING OF CHROMOSOME ARM 17P IN CHILDHOOD PRIMITIVE NEUROECTODERMAL TUMORS REVEALS A COMMON CHROMOSOMAL DISRUPTION WITHIN THE SMITH-MAGENIS REGION, AN UNSTABLE REGION IN CHROMOSOME BAND 17P11.2, Genes, chromosomes & cancer, 18(1), 1997, pp. 50-58
MOLECULAR CHARACTERIZATION OF A GENETICALLY UNSTABLE REGION CONTAINING THE SMS CRITICAL AREA AND A BREAKPOINT CLUSTER FOR HUMAN PNETS
Authors: WILGENBUS KK SERANSKI P BROWN A LEUCHS B MINCHEVA A LICHTER P POUSTKA A
Citation: Kk. Wilgenbus et al., MOLECULAR CHARACTERIZATION OF A GENETICALLY UNSTABLE REGION CONTAINING THE SMS CRITICAL AREA AND A BREAKPOINT CLUSTER FOR HUMAN PNETS, Genomics, 42(1), 1997, pp. 1-10
ORDERING OF 66 STSS ALONG THE ENTIRE SHORT ARM OF HUMAN-CHROMOSOME-17AND CHROMOSOME ASSIGNMENT OF A TRANSCRIBED SEQUENCE (FMR1L2) HOMOLOGOUS TO FMR1
Authors: WILGENBUS KK COY JF MINCHEVA A NICOLAI H SOLOMON E LICHTER P POUSTKA A
Citation: Kk. Wilgenbus et al., ORDERING OF 66 STSS ALONG THE ENTIRE SHORT ARM OF HUMAN-CHROMOSOME-17AND CHROMOSOME ASSIGNMENT OF A TRANSCRIBED SEQUENCE (FMR1L2) HOMOLOGOUS TO FMR1, Cytogenetics and cell genetics, 73(3), 1996, pp. 240-243
ACUTE LETHAL NECROTIZING PANCREATITIS IN CHILDHOOD SYSTEMIC LUPUS-ERYTHEMATOSUS - POSSIBLE TOXICITY OF IMMUNOSUPPRESSIVE THERAPY
Authors: KOLK A HORNEFF G WILGENBUS KK WAHN V GERHARZ CD
Citation: A. Kolk et al., ACUTE LETHAL NECROTIZING PANCREATITIS IN CHILDHOOD SYSTEMIC LUPUS-ERYTHEMATOSUS - POSSIBLE TOXICITY OF IMMUNOSUPPRESSIVE THERAPY, Clinical and experimental rheumatology, 13(3), 1995, pp. 399-403
STRUCTURE AND LOCALIZATION ON THE X-CHROMOSOME OF THE GENE CODING FORTHE HUMAN FILOPODIAL PROTEIN MOESIN (MSN)
Authors: WILGENBUS KK HSIEH CL LANKES WT MILATOVICH A FRANCKE U FURTHMAYR H
Citation: Kk. Wilgenbus et al., STRUCTURE AND LOCALIZATION ON THE X-CHROMOSOME OF THE GENE CODING FORTHE HUMAN FILOPODIAL PROTEIN MOESIN (MSN), Genomics, 19(2), 1994, pp. 326-333
2 FETUSES WITH FRYNS-SYNDROME WITHOUT DIAPHRAGMATIC DEFECTS
Authors: WILGENBUS KK ENGERS R CROMBACH G MAJEWSKI F
Citation: Kk. Wilgenbus et al., 2 FETUSES WITH FRYNS-SYNDROME WITHOUT DIAPHRAGMATIC DEFECTS, Journal of Medical Genetics, 31(12), 1994, pp. 962-964
RADIXIN IS A COMPONENT OF HEPATOCYTE MICROVILLI IN-SITU
Authors: AMIEVA MR WILGENBUS KK FURTHMAYR H
Citation: Mr. Amieva et al., RADIXIN IS A COMPONENT OF HEPATOCYTE MICROVILLI IN-SITU, Experimental cell research, 210(1), 1994, pp. 140-144
Risultati: 1-9 |