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Results:
1-8
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Results: 8
Authors:
SCHEDL A
HASTIE N
Citation: A. Schedl et N. Hastie, MULTIPLE ROLES FOR THE WILMS-TUMOR SUPPRESSOR GENE, WT1 GENITOURINARYDEVELOPMENT, Molecular and cellular endocrinology, 140(1-2), 1998, pp. 65-69
Authors:
MILES C
ELGAR G
COLES E
KLEINJAN DJ
VANHEYNINGEN V
HASTIE N
Citation: C. Miles et al., COMPLETE SEQUENCING OF THE FUGU WAGR REGION FROM WT1 TO PAX6 - DRAMATIC COMPACTION AND CONSERVATION OF SYNTENY WITH HUMAN-CHROMOSOME 11P13, Proceedings of the National Academy of Sciences of the United Statesof America, 95(22), 1998, pp. 13068-13072
Authors:
WUNDERLE VM
CRITCHER R
HASTIE N
GOODFELLOW PN
SCHEDL A
Citation: Vm. Wunderle et al., DELETION OF LONG-RANGE REGULATORY ELEMENTS UPSTREAM OF SOX9 CAUSES CAMPOMELIC DYSPLASIA, Proceedings of the National Academy of Sciences of the United Statesof America, 95(18), 1998, pp. 10649-10654
Authors:
STEWART CL
PEDERSEN R
ROTWEIN P
BESTOR T
RASTAN S
HASTIE N
NICHOLS R
MUTTER G
Citation: Cl. Stewart et al., GENOMIC IMPRINTING, Reproductive toxicology, 11(2-3), 1997, pp. 309-316
Authors:
HASTIE N
Citation: N. Hastie, INVITED LECTURE-3 - NEW TRANSGENIC APPROACHES TO THE FUNCTION OF GENES AND TO MODEL HUMAN PATHOLOGY, Kidney international, 50(5), 1996, pp. 1795-1795
Authors:
LITTLE M
HOLMES G
BICKMORE W
VANHEYNINGEN V
HASTIE N
WAINWRIGHT B
Citation: M. Little et al., DNA-BINDING CAPACITY OF THE WT1 PROTEIN IS ABOLISHED BY DENYS-DRASH SYNDROME WT1 POINT MUTATIONS, Human molecular genetics, 4(3), 1995, pp. 351-358
Authors:
GLOVER D
HALL A
HASTIE N
Citation: D. Glover et al., CELL BIOLOGY OF CANCER - PREFACE, Journal of Cell Science, 1994, pp. 5-5
Authors:
LOTHE RA
HASTIE N
HEIMDAL K
FOSSA SD
STENWIG AE
BORRESEN AL
Citation: Ra. Lothe et al., FREQUENT LOSS OF 11P13 AND 11P15 LOCI IN MALE GERM-CELL TUMORS, Genes, chromosomes & cancer, 7(2), 1993, pp. 96-101
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