Connection

RADEK SKODA to Phenotype

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

0.394
  1. Iron is a modifier of the phenotypes of JAK2-mutant myeloproliferative neoplasms. Blood. 2023 04 27; 141(17):2127-2140.
    View in: PubMed
    Score: 0.103
  2. Myeloproliferative neoplasms can be initiated from a single hematopoietic stem cell expressing JAK2-V617F. J Exp Med. 2014 Oct 20; 211(11):2213-30.
    View in: PubMed
    Score: 0.057
  3. Somatic mutations in calreticulin can be found in pedigrees with familial predisposition to myeloproliferative neoplasms. Blood. 2014 Apr 24; 123(17):2744-5.
    View in: PubMed
    Score: 0.055
  4. Differential effects of hydroxyurea and INC424 on mutant allele burden and myeloproliferative phenotype in a JAK2-V617F polycythemia vera mouse model. Blood. 2013 Feb 14; 121(7):1188-99.
    View in: PubMed
    Score: 0.050
  5. Ratio of mutant JAK2-V617F to wild-type Jak2 determines the MPD phenotypes in transgenic mice. Blood. 2008 Apr 15; 111(8):3931-40.
    View in: PubMed
    Score: 0.035
  6. Lessons from familial myeloproliferative disorders. Semin Hematol. 2005 Oct; 42(4):266-73.
    View in: PubMed
    Score: 0.030
  7. Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans. Nat Commun. 2019 03 19; 10(1):1252.
    View in: PubMed
    Score: 0.019
  8. Specificity of signaling by hematopoietic cytokine receptors: instructive versus permissive effects. J Recept Signal Transduct Res. 1999 Jan-Jul; 19(1-4):741-72.
    View in: PubMed
    Score: 0.019
  9. Two mutant alleles of the human cytochrome P-450db1 gene (P450C2D1) associated with genetically deficient metabolism of debrisoquine and other drugs. Proc Natl Acad Sci U S A. 1988 Jul; 85(14):5240-3.
    View in: PubMed
    Score: 0.009
  10. The JAK2-V617F mutation is frequently present at diagnosis in patients with essential thrombocythemia and polycythemia vera. Blood. 2006 Sep 15; 108(6):1865-7.
    View in: PubMed
    Score: 0.008
  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: 0.005
  12. Expression of LIF in transgenic mice results in altered thymic epithelium and apparent interconversion of thymic and lymph node morphologies. EMBO J. 1994 Mar 15; 13(6):1375-85.
    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.