|
1
|
Mouse major histocompatibility class I gene expression begins at midsomite stage and is inducible in earlier-stage embryos by interferon.
|
Proc Natl Acad Sci U S A
|
1985
|
2.56
|
|
2
|
Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element.
|
Genome Res
|
2001
|
1.65
|
|
3
|
Physical mapping and genomic structure of the Lowe syndrome gene OCRL1.
|
Hum Genet
|
1997
|
1.15
|
|
4
|
Spectrum of mutations in the OCRL1 gene in the Lowe oculocerebrorenal syndrome.
|
Am J Hum Genet
|
1997
|
1.14
|
|
5
|
Two additional cases of osteogenesis imperfecta with substitutions for glycine in the alpha 2(I) collagen chain. A regional model relating mutation location with phenotype.
|
J Biol Chem
|
1993
|
1.04
|
|
6
|
Induction of major histocompatibility class I antigens by interferons in undifferentiated F9 cells.
|
J Cell Physiol
|
1987
|
1.01
|
|
7
|
Mutations are not uniformly distributed throughout the OCRL1 gene in Lowe syndrome patients.
|
Mol Genet Metab
|
1998
|
0.96
|
|
8
|
Serine for glycine substitutions in type I collagen in two cases of type IV osteogenesis imperfecta (OI). Additional evidence for a regional model of OI pathophysiology.
|
J Biol Chem
|
1993
|
0.87
|
|
9
|
Primary cultures of rat pancreatic acinar cells in serum-free medium.
|
In Vitro Cell Dev Biol
|
1985
|
0.83
|
|
10
|
A de novo G+1-->A mutation at the alpha 2(I) exon 16 splice donor site causes skipping of exon 16 in the cDNA of one allele of an OI type IV proband.
|
Hum Mutat
|
1993
|
0.78
|
|
11
|
New autosomal recessive syndrome of sparse hair, osteopenia, and mental retardation in Mennonite sisters.
|
Am J Med Genet
|
1992
|
0.75
|