EWS/FLI1-induced manic fringe renders NIH 3T3 cells tumorigenic. Read more about EWS/FLI1-induced manic fringe renders NIH 3T3 cells tumorigenic.
Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation. Read more about Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation.
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients. Read more about BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients.
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Read more about The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21. Read more about Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.
Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice. Read more about Mapping of a major genetic modifier of embryonic lethality in TGF beta 1 knockout mice.
P1148A in fibrillin-1 is not a mutation anymore. Read more about P1148A in fibrillin-1 is not a mutation anymore.
Leptin activation of Stat3 in the hypothalamus of wild-type and ob/ob mice but not db/db mice. Read more about Leptin activation of Stat3 in the hypothalamus of wild-type and ob/ob mice but not db/db mice.
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Read more about A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.
A full genome search in multiple sclerosis. Read more about A full genome search in multiple sclerosis.
