Connection

RADEK SKODA to Molecular Sequence Data

This is a "connection" page, showing publications RADEK SKODA has written about Molecular Sequence Data.
Connection Strength

0.271
  1. A gain-of-function mutation of JAK2 in myeloproliferative disorders. N Engl J Med. 2005 Apr 28; 352(17):1779-90.
    View in: PubMed
    Score: 0.041
  2. Gene silencing by lentivirus-mediated delivery of siRNA in human CD34+ cells. Blood. 2004 Jun 15; 103(12):4511-3.
    View in: PubMed
    Score: 0.038
  3. Translational pathophysiology: a novel molecular mechanism of human disease. Blood. 2000 Jun 01; 95(11):3280-8.
    View in: PubMed
    Score: 0.029
  4. A single-base deletion in the thrombopoietin (TPO) gene causes familial essential thrombocythemia through a mechanism of more efficient translation of TPO mRNA. Blood. 1999 Aug 15; 94(4):1480-2.
    View in: PubMed
    Score: 0.028
  5. Thrombopoietin production is inhibited by a translational mechanism. Blood. 1998 Dec 01; 92(11):4023-30.
    View in: PubMed
    Score: 0.026
  6. The leptin receptor activates janus kinase 2 and signals for proliferation in a factor-dependent cell line. Mol Endocrinol. 1997 Apr; 11(4):393-9.
    View in: PubMed
    Score: 0.024
  7. Defective STAT signaling by the leptin receptor in diabetic mice. Proc Natl Acad Sci U S A. 1996 Jun 25; 93(13):6231-5.
    View in: PubMed
    Score: 0.022
  8. Thrombopoietin in thrombocytopenic mice: evidence against regulation at the mRNA level and for a direct regulatory role of platelets. Blood. 1996 Jan 15; 87(2):567-73.
    View in: PubMed
    Score: 0.022
  9. Murine c-mpl: a member of the hematopoietic growth factor receptor superfamily that transduces a proliferative signal. EMBO J. 1993 Jul; 12(7):2645-53.
    View in: PubMed
    Score: 0.018
  10. Somatic mutations of JAK2 exon 12 in patients with JAK2 (V617F)-negative myeloproliferative disorders. Blood. 2008 Feb 01; 111(3):1686-9.
    View in: PubMed
    Score: 0.012
  11. Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes. Hum Genet. 1999 Jul-Aug; 105(1-2):104-11.
    View in: PubMed
    Score: 0.007
  12. Characterization of the common genetic defect in humans deficient in debrisoquine metabolism. Nature. 1988 Feb 04; 331(6155):442-6.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.