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Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal-recessive disease that affects young children. It presents as a severe hyperinflammatory syndrome with activated macrophages and T lymphocytes. Mutations in the perforin 1 gene (PRF1) were found in FHL-2 in 15-50% of all cases. Defective granule exocytosis caused by mutations in the hMunc13-4(More)
Androgenetic alopecia (AGA, male pattern baldness) is the most common form of hair loss. The origin of AGA is genetic, with the X chromosome located androgen receptor gene (AR) being the only risk gene identified to date. We present the results of a genome-wide linkage study of 95 families and linkage fine mapping of the 3q21-q29, 11q14-q25, 18p11-q23, and(More)
We present a new technique for 2D compact modeling of short-channel, nanoscale DG MOSFETs. In low-doped devices working in the subthreshold regime, the potential distribution is dominated by the capacitive coupling between the body contacts. This 2D potential is determined by a solution of the Laplace equation for the body using the technique of conformal(More)
Papers published in Hydrology and Earth System Sciences Discussions are under open-access review for the journal Hydrology and Earth System Sciences Abstract A spatial probability distribution of the variables in a parametric snow depletion curve (SDC) is tailored to the assimilation of satellite snow cover data into a gridded hydrological model. The(More)
Papers published in Hydrology and Earth System Sciences Discussions are under open-access review for the journal Hydrology and Earth System Sciences Abstract A spatial probability distribution of the variables in a parametric snow depletion curve (SDC) is tailored to the assimilation of satellite snow cover data into a gridded hydrological model. The(More)
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