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Results:
1-14
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Results: 14
Authors:
PINGAULT V
BONDURAND N
KUHLBRODT K
GOERICH DE
PREHU MO
PULITI A
HERBARTH B
HERMANSBORGMEYER I
LEGIUS E
MATTHIJS G
AMIEL J
LYONNET S
CECCHERINI I
ROMEO G
SMITH JC
READ AP
WEGNER M
GOOSSENS M
Citation: V. Pingault et al., SOX10 MUTATIONS IN PATIENTS WITH WAARDENBURG-HIRSCHSPRUNG-DISEASE, Nature genetics, 18(2), 1998, pp. 171-173
Authors:
PINGAULT V
BONDURAND N
KUHLBRODT K
GOERICH DE
PREHU MO
PULITI A
LEMORT N
LEGIUS E
MATTHIJS G
AMIEL J
LYONNET S
CECCHERINI I
ROMEO G
CLAYTONSMITH J
READ AP
WEGNER M
GOOSSENS M
Citation: V. Pingault et al., MUTATIONS OF THE SOX10 GENE IN WAARDENBURG-HIRSCHSPRUNG-DISEASE, European journal of human genetics, 6, 1998, pp. 402-402
Authors:
PINGAULT V
HERBARTH B
BONDURAND N
KUHLBRODT K
HERMANSBORGMEYER I
PULITI A
LEMORT N
PREHU MO
GOOSSENS M
WEGNER M
Citation: V. Pingault et al., MUTATION OF THE SRY-RELATED SOX10 GENE IN DOMINANT MEGACOLON, A MOUSEMODEL FOR HUMAN HIRSCHSPRUNG DISEASE, European journal of human genetics, 6, 1998, pp. 4153-4153
Authors:
HERBARTH B
PINGAULT V
BONDURAND N
KUHLBRODT K
HERMANSBORGMEYER I
PULITI A
LEMORT N
GOOSSENS M
WEGNER M
Citation: B. Herbarth et al., MUTATION OF THE SRY-RELATED SOX10 GENE IN DOMINANT MEGACOLON, A MOUSEMODEL FOR HUMAN HIRSCHSPRUNG DISEASE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(9), 1998, pp. 5161-5165
Authors:
PRINGAULT V
PULITI A
PREHU MO
SAMADI A
BONDURAND N
GOOSSENS M
Citation: V. Pringault et al., HUMAN HOMOLOGY AND CANDIDATE GENES FOR THE DOMINANT MEGACOLON LOCUS, A MOUSE MODEL OF HIRSCHSPRUNG DISEASE, Genomics, 39(1), 1997, pp. 86-89
Authors:
TURCHI G
GLATT HR
SEIDEL A
PULITI A
SBRANA I
Citation: G. Turchi et al., STRUCTURE-ACTIVITY RELATIONSHIP IN THE INDUCTION OF CHROMOSOMAL-ABERRATIONS AND SPINDLE DISTURBANCES IN CHINESE-HAMSTER EPITHELIAL LIVER-CELLS BY REGIOISOMERIC PHENANTHRENE QUINONES, Cell biology and toxicology, 13(3), 1997, pp. 155-165
Authors:
PULITI A
CINTI R
SERI M
CECCHERINI I
ROMEO G
Citation: A. Puliti et al., ASSIGNMENT OF MOUSE GFRA1, THE HOMOLOG OF A NEW HUMAN HSCR CANDIDATE GENE, TO THE TELOMERIC REGION OF MOUSE-CHROMOSOME-19, Cytogenetics and cell genetics, 78(3-4), 1997, pp. 291-294
Authors:
PATRONE G
PULITI A
BOCCIARDI R
RAVAZZOLO R
ROMEO G
Citation: G. Patrone et al., SEQUENCE AND CHARACTERIZATION OF THE RET PROTOONCOGENE 5'-FLANKING REGION - ANALYSIS OF RETINOIC ACID RESPONSIVENESS AT THE TRANSCRIPTIONALLEVEL, FEBS letters, 419(1), 1997, pp. 76-82
Authors:
PULITI A
POIRIER V
GOOSSENS M
SIMONNEAU M
Citation: A. Puliti et al., NEURONAL DEFECTS IN GENOTYPED DOMINANT MEGACOLON (DOM) MOUSE EMBRYOS,A MODEL FOR HIRSCHSPRUNG DISEASE, NeuroReport, 7(2), 1996, pp. 489-492
Authors:
PULITI A
PREHU MO
SIMONCHAZOTTES D
FERKDADJI L
PEUCHMAUR M
GOOSSENS M
GUENET JL
Citation: A. Puliti et al., A HIGH-RESOLUTION GENETIC-MAP OF MOUSE CHROMOSOME-15 ENCOMPASSING THEDOMINANT MEGACOLON (DOM) LOCUS, Mammalian genome, 6(11), 1995, pp. 763-768
Authors:
SBRANA I
PULITI A
SEIDEL A
GLATT H
TURCHI G
Citation: I. Sbrana et al., INDUCTION OF CHROMOSOMAL-ABERRATIONS AND SPINDLE DISTURBANCES IN CHINESE-HAMSTER EPITHELIAL LIVER-CELLS IN CULTURE BY PYRENE AND BENZO[ALPHA]PYRENE QUINONES, Mutagenesis, 10(6), 1995, pp. 505-512
Authors:
PULITI A
PREHU MO
PINGAULT V
SIMONCHAZOTTES D
FERKDADJI L
PEUCHMAUR M
GUENET JL
GOOSSENS M
Citation: A. Puliti et al., MOLECULAR-GENETIC MAPPING OF THE DOMINANT MEGACOLON (DOM) MUTATION INTHE MOUSE, American journal of human genetics, 57(4), 1995, pp. 1154-1154
Authors:
LYONNET S
BOLINO A
PELET A
ABEL L
NIHOULFEKETE C
BRIARD ML
MOKSIU V
KAARIAINEN H
MARTUCCIELLO G
LERONE M
PULITI A
LUO Y
WEISSENBACH J
DEVOTO M
MUNNICH A
ROMEO G
Citation: S. Lyonnet et al., A GENE FOR HIRSCHSPRUNG DISEASE MAPS TO THE PROXIMAL LONG ARM OF CHROMOSOME-10, Nature genetics, 4(4), 1993, pp. 346-350
Authors:
PULITI A
COVONE AE
BICOCCHI MP
BOLINO A
LERONE M
MARTUCCIELLO G
JASONNI V
ROMEO G
Citation: A. Puliti et al., DELETED AND NORMAL CHROMOSOME 10 HOMOLOGS FROM A PATIENT WITH HIRSCHSPRUNG DISEASE ISOLATED IN 2 CELL HYBRIDS THROUGH ENRICHMENT BY IMMUNOMAGNETIC SELECTION, Cytogenetics and cell genetics, 63(2), 1993, pp. 102-106
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