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aldrich syndrome การใช้

ประโยคมือถือ
  • WIPF1 has been shown to interact with Wiskott-Aldrich syndrome protein, Cortactin and NCK1.
  • This mutation causes the decreased, absent, or altered Wiskoff-Aldrich syndrome protein ( WASp ).
  • Wiskott-Aldrich Syndrome claimed Mark in 1989 and Matthew in 1992.
  • Nolan's 8-year-old son, Anthony, died 23 years ago of Wiscott-Aldrich syndrome, a rare immune system disease.
  • The other children had Wiskott-Aldrich syndrome, which leaves them to open to infection, autoimmune diseases and cancer.
  • Wiskott-Aldrich syndrome is a disease of the immune system, likely due to defects in regulation of actin cytoskeleton.
  • Follow up trials with gene therapy on another six children with Wiskott-Aldrich syndrome were also reported as promising.
  • Nolan's 8-year-old son, Anthony Nolan, died 23 years ago of Wiscott-Aldrich syndrome, a rare disease that affects the immune system.
  • Her 8-year-old son, Anthony Nolan, died 23 years ago of Wiscott-Aldrich syndrome, a rare disease that affects the immune system.
  • The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder.
  • The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder.
  • In the first generation of retro viral gene therapy some patients treated with viral vectors for Wiskott-Aldrich syndrome developed acute T-cell leukaemia.
  • Netherton syndrome has recently been characterised as a primary immunodeficiency, which straddles the innate and acquired immune system, much as does Wiskott-Aldrich syndrome.
  • Wilson's comment triggers an epiphany, and after ignoring Bresson's hallucinations, House concludes that Bresson has Wiskott-Aldrich syndrome, a genetic condition with symptoms that mimic AIDS.
  • Nine-month-old Ng Fan ( nicknamed Fan Tsai ) needs a bone-marrow transplant to be cured of Wiskcott Aldrich Syndrome, which has damaged his immune system.
  • This domain was first recognized as an essential element for the regulation of the cytoskeleton by the mammalian Wiskott-Aldrich syndrome protein ( WASP ) family.
  • The disease X-linked thrombocytopenia was later discovered to be also due to " WASp " mutations, but different ones from those that cause full-blown Wiskott Aldrich syndrome.
  • Additional studies have also shown that netrin-induced signaling between DCC downstream targets NcK, and Wiskott Aldrich syndrome protein WASP trigger Rac1 and Cdc42 and subsequently axonal growth.
  • Some disorders that predispose a person to lymphoproliferative disorders are severe combined immuno deficiency ( SCID ), Ch閐iak-Higashi syndrome, Wiskott-Aldrich syndrome ( an X-linked recessive disorder ), and ataxia telangiectasia.
  • The Wiskott Aldrich syndrome ( WAS ) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton.
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