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The nucleolin binding activity of hepatitis delta antigen is associated with ...

Lee(C H),Chang(S C),Chen(C J),Chang(M F) J Biol Chem 1998-04-23

...XK. HDV replication was modulated by exogenous human nucleolin. In addition, a small HDAg mutant S-d65/75, which possess...

XK aprosencephaly.

al-Gazali(L I),Bakalinova(D),Bakir(M),Nath... Clin Dysmorphol 1998-07-10

...XK aprosencephaly syndrome.

VACTERL-hydrocephaly, DK-phocomelia, and cerebro-cardio-radio-reno-rectal com...

Lurie(I W),Ferencz(C) Am J Med Genet 1997-06-19

...XK-aprosencephaly, and DK-phocomelia (von Voss-Cherstvoy) syndrome as well as Mendelian forms of VACTERL-hydrocephaly sy...

Ring chromosome 13 with loss of the region D13S317-D13S285: phenotypic overla...

Guala(A),Dellavecchia(C),Mannarino(S),Rogn... Am J Med Genet 1997-11-25

...XK syndrome. The patient has a ring chromosome (13) with deletion 13q32-qter. Molecular analysis demonstrated loss of th...

Analysis of the McLeod syndrome gene in three patients with neuroacanthocytosis.

Shizuka(M),Watanabe(M),Aoki(M),Ikeda(Y),Mi... J Neurol Sci 1997-10-06

McLeod syndrome is a rare X-linked disorder involving neurological defects and acanthocytosis. We examined the XK gene i...

The production and characterization of artificial heterodimers of the restric...

Wende(W),Stahl(F),Pingoud(A) Biol Chem 1997-02-19

...XK motif, characteristic for the active sites of many restriction endonucleases, were produced. While the homodimeric Ec...

The mouse X-linked developmental mutant, tattered, lies between DXMit55 and X...

Uwechue(I C),Cooper(B F),Goble(C),Hacker(T... Genomics 1997-02-06

...XK and proximal to the evolutionary breakpoint that lies between XK and DMD. Histological analysis of dorsal skin taken ...

[A molecular approach to the structure, polymorphism and function of blood gr...

Cartron(J P) Transfus Clin Biol 1996-11-22

...XK loci. Other antigens have been located on proteins already identified, for instance the Cromer antigens on DAF, Knops...

High-resolution comparative mapping of the proximal region of the mouse X chr...

Blair(H J),Ho(M),Monaco(A P),Fisher(S),Cra... Genomics 1996-02-01

The murine homologues of the loci for McLeod syndrome (XK), Dent's disease (CICN5), and synaptophysin (SYP) have been ma...

A combination of the effects of rare genotypes at the XK and KEL blood group ...

Daniels(G L),Weinauer(F),Stone(C),Ho(M),Gr... Blood 1996-12-17

...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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