… This analysis identified a frameshift mutation in BAP1 (c.1305delG, p.Gln436Asnfs*135) that
… cycles of 95 C (45 s), 57 C (45 s) and 72 C (45 s) after initial denaturation at 95 C for 5 min. …

Charcot-Marie-Tooth disease (CMT) is the most common inherited neuromuscular disease
and is characterized by considerable clinical and genetic heterogeneity 1 . We previously …

… We incubated the cells for 30 min at 4 C on a shaker and scraped them into 1.5-ml
microcentrifuge tubes. We centrifuged them at 14,000g for 30 min at 4 C. We resuspended pellets in …

In this paper, Tomlinson-Harashima Precoding for multiple-input/multiple-output systems
including multiple-antenna and multiuser systems is studied. It is shown that nonlinear …

… Gly131Glu and the splice site mutation c.240-1G>C, previously reported in patients with
arthrogryposis renal dysfunction and cholestasis syndrome. We demonstrated the pathogenicity …

Vici syndrome is a recessively inherited multisystem disorder characterized by callosal
agenesis, cataracts, cardiomyopathy, combined immunodeficiency and hypopigmentation. To …

We consider the lattice-reduction-aided detection scheme for 2/spl times/2 channels recently
proposed by H. Yao and GW Wornell (see Proc. IEEE Globecom, 2002). By using an …

… Stierstorfer, and C. Windpassinger, “Precoding and signal shaping for transmission over
MIMO channels,” in Proc. Canadian Workshop Information Theory, Waterloo, ON, Canada, May …

… by B = C I (I: identity matrix), where, by construction, C is a lower left triangular matrix with
1’s on the main diagonal. (For the zero-forcing approach, C is equal to the cascade C = VFH.) It …

… p15.31; we identified the missense change c.2035G>A (p.Gly679Arg) at a conserved residue
within … Myc vector, we performed site-directed mutagenesis to generate the c.2035G>A (p.…