Type 1 diabetes risk assessment: improvement by follow-up measurements in young islet autoantibody-positive relatives.
Diabetologia
2006
49
12
2969-76
Verification of predicted alternatively spliced Wnt genes reveals two new splice variants (CTNNB1 and LRP5) and altered Axin-1 expression during tumour progression.
BMC Genomics
2006
7
148
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
Brain
2006
129
Pt 7
1674-84
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible.
Nat Genet
2006
38
12
1397-405
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders.
Kidney Int
2006
70
6
1008-12
GPI-anchored TIMP-1 treatment renders renal cell carcinoma sensitive to FAS-meditated killing.
Oncogene
2006
25
10
1496-508
Hepatocerebral mitochondrial DNA depletion syndrome caused by deoxyguanosine kinase (DGUOK) mutations.
Arch Neurol
2006
63
8
1129-34
Epstein-Barr virus vector-mediated gene transfer into human B cells: potential for antitumor vaccination.
Gene Ther
2006
13
2
150-62