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Results: 1-16 |
Results: 16
A NOVEL C2H2 ZINC-FINGER GENE MEMBER OF THE SCAN BOX DOMAIN GENE SUBFAMILY
Authors: MAVROGIANNIS LA ARGYROKASTRITIS A DERMITZAKIS E VRONTOU S MOSCHONAS NK
Citation: La. Mavrogiannis et al., A NOVEL C2H2 ZINC-FINGER GENE MEMBER OF THE SCAN BOX DOMAIN GENE SUBFAMILY, European journal of human genetics, 6, 1998, pp. 4247-4247
DETECTION AND INCIDENCE OF CRYPTIC Y-CHROMOSOME SEQUENCES IN TURNER-SYNDROME PATIENTS
Authors: PATSALIS PC SISMANI C HADJIMARCOU MI KITSIOUTZELI S TZEZOU A HADJIATHANASIOU CG VELISSARIOU V LYMBERATOU E MOSCHONAS NK SKORDIS N
Citation: Pc. Patsalis et al., DETECTION AND INCIDENCE OF CRYPTIC Y-CHROMOSOME SEQUENCES IN TURNER-SYNDROME PATIENTS, Clinical genetics, 53(4), 1998, pp. 249-257
HUMAN HEPATOCYTE NUCLEAR FACTOR-IV (HHNF4) GENE MAPS TO 20Q12-Q13.1 BETWEEN PLCGI AND D20S17
Authors: ARGYROKASTRITIS A KAMAKARI S KAPSETAKI M KRITIS A TALIANIDIS I MOSCHONAS NK
Citation: A. Argyrokastritis et al., HUMAN HEPATOCYTE NUCLEAR FACTOR-IV (HHNF4) GENE MAPS TO 20Q12-Q13.1 BETWEEN PLCGI AND D20S17, Human genetics, 99(2), 1997, pp. 233-236
MAP INTEGRATION AT HUMAN-CHROMOSOME-10 - MOLECULAR AND CYTOGENETIC ANALYSIS OF A CHROMOSOME-SPECIFIC SOMATIC-CELL HYBRID PANEL AND GENOMIC CLONES, BASED ON A WELL-SUPPORTED GENETIC-MAP
Authors: MARZELLA R KOKKINAKI MA KAPSETAKI M RICCO A ARGYROKASTRITIS A KAMAKARI S SARAFIDOU T ARCHIDIACONO N ROUSSOU A PASPARAKI A ROCCHI M MOSCHONAS NK
Citation: R. Marzella et al., MAP INTEGRATION AT HUMAN-CHROMOSOME-10 - MOLECULAR AND CYTOGENETIC ANALYSIS OF A CHROMOSOME-SPECIFIC SOMATIC-CELL HYBRID PANEL AND GENOMIC CLONES, BASED ON A WELL-SUPPORTED GENETIC-MAP, Cytogenetics and cell genetics, 79(3-4), 1997, pp. 257-265
ISOLATION AND CHARACTERIZATION OF A 3RD ISOFORM OF HUMAN HEPATOCYTE NUCLEAR FACTOR-4
Authors: KRITIS AA ARGYROKASTRITIS A MOSCHONAS NK POWER S KATRAKILI N ZANNIS VI CEREGHINI S TALIANIDIS I
Citation: Aa. Kritis et al., ISOLATION AND CHARACTERIZATION OF A 3RD ISOFORM OF HUMAN HEPATOCYTE NUCLEAR FACTOR-4, Gene, 173(2), 1996, pp. 275-280
REPORT OF THE FIRST INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-10 MAPPING 1995
Authors: MOSCHONAS NK SPURR NK MAO J
Citation: Nk. Moschonas et al., REPORT OF THE FIRST INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-10 MAPPING 1995, Cytogenetics and cell genetics, 72(2-3), 1996, pp. 100-110
EUROPEAN GENE-MAPPING PROJECT (EUROGEM) - BREAKPOINT PANELS FOR HUMAN-CHROMOSOMES BASED ON THE CEPH REFERENCE FAMILIES
Authors: COX SA ATTWOOD J BRYANT SP BAINS R POVEY R POVEY S REBELLO M KAPSETAKI M MOSCHONAS NK GRZESCHIK KH OTTO M DIXON M SUDWORTH HE KOOY RF WRIGHT A TEAGUE P TERRENATO L VERGNAUD G MONFOUILLOUX S WEISSENBACH J ALIBERT O DIB C FAURE S BAKKER E PEARSON NM VOSSEN RHAM GAL A MUELLERMYHSOK B CANN HM SPURR NK
Citation: Sa. Cox et al., EUROPEAN GENE-MAPPING PROJECT (EUROGEM) - BREAKPOINT PANELS FOR HUMAN-CHROMOSOMES BASED ON THE CEPH REFERENCE FAMILIES, Annals of Human Genetics, 60, 1996, pp. 447-486
TETRA- DI-NUCLEOTIDE REPEAT POLYMORPHISM UPSTREAM OF THE HUMAN ALPHA-2-GLOBIN GENE LOCUS AT 16P13.3/
Authors: ARGYROKASTRITIS A MOSCHONAS NK
Citation: A. Argyrokastritis et Nk. Moschonas, TETRA- DI-NUCLEOTIDE REPEAT POLYMORPHISM UPSTREAM OF THE HUMAN ALPHA-2-GLOBIN GENE LOCUS AT 16P13.3/, Human genetics, 95(5), 1995, pp. 593-593
PKU IN SLOVAKIA - MUTATION SCREENING AND HAPLOTYPE ANALYSIS
Authors: KADASI L POLAKOVA H FERAKOVA E HUDECOVA S BOHUSOVA T SZOMOLAYOVA I STRNOVA J HRUSKOVIC I MOSCHONAS NK FERAK V
Citation: L. Kadasi et al., PKU IN SLOVAKIA - MUTATION SCREENING AND HAPLOTYPE ANALYSIS, Human genetics, 95(1), 1995, pp. 112-114
NORMALIZED CDNA LIBRARY FROM HUMAN ERYTHROLEUKEMIA-CELLS
Authors: PUZYREV AT CHRONIARY K MOSCHONAS NK
Citation: At. Puzyrev et al., NORMALIZED CDNA LIBRARY FROM HUMAN ERYTHROLEUKEMIA-CELLS, Molecular biology, 29(1), 1995, pp. 58-61
SEQUENCES LOCATED 3' TO THE BREAKPOINT OF THE HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN-3 DELETION EXHIBIT ENHANCER ACTIVITY AND CAN MODIFY THE DEVELOPMENTAL EXPRESSION OF THE HUMAN FETAL A-GAMMA-GLOBIN GENE IN TRANSGENIC MICE
Authors: ANAGNOU NP PEREZSTABLE C GELINAS R COSTANTINI F LIAPAKI K CONSTANTOPOULOU M KOSTEAS T MOSCHONAS NK STAMATOYANNOPOULOS G
Citation: Np. Anagnou et al., SEQUENCES LOCATED 3' TO THE BREAKPOINT OF THE HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN-3 DELETION EXHIBIT ENHANCER ACTIVITY AND CAN MODIFY THE DEVELOPMENTAL EXPRESSION OF THE HUMAN FETAL A-GAMMA-GLOBIN GENE IN TRANSGENIC MICE, The Journal of biological chemistry, 270(17), 1995, pp. 10256-10263
A CHROMOSOME 10P11.2 GT-DINUCLEOTIDE REPEAT POLYMORPHISM AT THE GLUDP5 GENE LOCUS
Authors: GOULIELMOS G ANGELICHEVA D KAPSETAKI M MANIFAVA M MOSCHONAS NK
Citation: G. Goulielmos et al., A CHROMOSOME 10P11.2 GT-DINUCLEOTIDE REPEAT POLYMORPHISM AT THE GLUDP5 GENE LOCUS, Human molecular genetics, 2(8), 1993, pp. 1328-1328
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE GLUDP2 LOCUS
Authors: GOULIELMOS G MANIFAVA M MOSCHONAS NK
Citation: G. Goulielmos et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE GLUDP2 LOCUS, Human molecular genetics, 2(12), 1993, pp. 2202-2202
DINUCLEOTIDE REPEAT POLYMORPHISM (D10S608) ADJACENT TO THE GLUD1 LOCUS
Authors: MOSCHONAS NK GOULIELMOS G LUBYOVA B MANIFAVA M DELOUKAS P LOON APGM KAPSETAKI M
Citation: Nk. Moschonas et al., DINUCLEOTIDE REPEAT POLYMORPHISM (D10S608) ADJACENT TO THE GLUD1 LOCUS, Human molecular genetics, 2(11), 1993, pp. 1981-1981
3 HUMAN GLUTAMATE-DEHYDROGENASE GENES (GLUD1, GLUDP2, AND GLUDP3) ARELOCATED ON CHROMOSOME-10Q, BUT ARE NOT CLOSELY PHYSICALLY LINKED
Authors: DELOUKAS P DAUWERSE JG MOSCHONAS NK VANOMMEN GJB VANLOON APGM
Citation: P. Deloukas et al., 3 HUMAN GLUTAMATE-DEHYDROGENASE GENES (GLUD1, GLUDP2, AND GLUDP3) ARELOCATED ON CHROMOSOME-10Q, BUT ARE NOT CLOSELY PHYSICALLY LINKED, Genomics, 17(3), 1993, pp. 676-681
CHROMOSOMAL MAPPING OF 2 MEMBERS OF THE HUMAN GLUTAMATE-DEHYDROGENASE(GLUD) GENE FAMILY TO CHROMOSOMES 10Q22.3-Q23 AND XQ22-Q23
Authors: ANAGNOU NP SEUANEZ H MODI W OBRIEN SJ PAPAMATHEAKIS J MOSCHONAS NK
Citation: Np. Anagnou et al., CHROMOSOMAL MAPPING OF 2 MEMBERS OF THE HUMAN GLUTAMATE-DEHYDROGENASE(GLUD) GENE FAMILY TO CHROMOSOMES 10Q22.3-Q23 AND XQ22-Q23, Human heredity, 43(6), 1993, pp. 351-356
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