...XK. HDV replication was modulated by exogenous human nucleolin. In addition, a small HDAg mutant S-d65/75, which possess...
...XK aprosencephaly syndrome.
...XK-aprosencephaly, and DK-phocomelia (von Voss-Cherstvoy) syndrome as well as Mendelian forms of VACTERL-hydrocephaly sy...
...XK syndrome. The patient has a ring chromosome (13) with deletion 13q32-qter. Molecular analysis demonstrated loss of th...
McLeod syndrome is a rare X-linked disorder involving neurological defects and acanthocytosis. We examined the XK gene i...
...XK motif, characteristic for the active sites of many restriction endonucleases, were produced. While the homodimeric Ec...
...XK and proximal to the evolutionary breakpoint that lies between XK and DMD. Histological analysis of dorsal skin taken ...
...XK loci. Other antigens have been located on proteins already identified, for instance the Cromer antigens on DAF, Knops...
The murine homologues of the loci for McLeod syndrome (XK), Dent's disease (CICN5), and synaptophysin (SYP) have been ma...
...XK, an X-linked gene that encodes the Kx protein; absence of Kx results in reduced Kell antigen expression. Almost total...
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