Connection

PAUL OVERBEEK to Mutation

This is a "connection" page, showing publications PAUL OVERBEEK has written about Mutation.
Connection Strength

0.833
  1. Primary Ovarian Insufficiency Induced by Fanconi Anemia E Mutation in a Mouse Model. PLoS One. 2016; 11(3):e0144285.
    View in: PubMed
    Score: 0.199
  2. A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis. PLoS One. 2012; 7(11):e50634.
    View in: PubMed
    Score: 0.159
  3. Inhibition of lens fiber cell morphogenesis by expression of a mutant SV40 large T antigen that binds CREB-binding protein/p300 but not pRb. J Biol Chem. 2004 Apr 23; 279(17):17667-73.
    View in: PubMed
    Score: 0.086
  4. Mutant cohesin in premature ovarian failure. N Engl J Med. 2014 Mar 06; 370(10):943-949.
    View in: PubMed
    Score: 0.043
  5. Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice. Nucleic Acids Res. 1990 Dec 25; 18(24):7293-8.
    View in: PubMed
    Score: 0.035
  6. Symplastic spermatids (sys): a recessive insertional mutation in mice causing a defect in spermatogenesis. Proc Natl Acad Sci U S A. 1990 Jul; 87(13):5016-20.
    View in: PubMed
    Score: 0.034
  7. Insertional inactivation of the downless gene in a family of transgenic mice. Mol Biol Med. 1989 Aug; 6(4):299-307.
    View in: PubMed
    Score: 0.032
  8. Long-range activation of Sox9 in Odd Sex (Ods) mice. Hum Mol Genet. 2004 Jun 15; 13(12):1213-8.
    View in: PubMed
    Score: 0.022
  9. Activated Ras induces lens epithelial cell hyperplasia but not premature differentiation. Int J Dev Biol. 2004; 48(8-9):879-88.
    View in: PubMed
    Score: 0.021
  10. exma: an X-linked insertional mutation that disrupts forebrain and eye development. Mamm Genome. 2002 Apr; 13(4):179-85.
    View in: PubMed
    Score: 0.019
  11. Inhibition of crystallin expression and induction of apoptosis by lens-specific E1A expression in transgenic mice. Oncogene. 2002 Feb 07; 21(7):1028-37.
    View in: PubMed
    Score: 0.019
  12. Gene defect in ectodermal dysplasia implicates a death domain adapter in development. Nature. 2001 Dec 20-27; 414(6866):913-6.
    View in: PubMed
    Score: 0.019
  13. A transgenic insertion causing cryptorchidism in mice. Genesis. 2001 May; 30(1):26-35.
    View in: PubMed
    Score: 0.018
  14. A constitutive mutation of ALK5 disrupts cardiac looping and morphogenesis in mice. Dev Biol. 1998 Jul 01; 199(1):72-9.
    View in: PubMed
    Score: 0.015
  15. Sclt1 deficiency causes cystic kidney by activating ERK and STAT3 signaling. Hum Mol Genet. 2017 08 01; 26(15):2949-2960.
    View in: PubMed
    Score: 0.014
  16. Conserved left-right asymmetry of nodal expression and alterations in murine situs inversus. Nature. 1996 May 09; 381(6578):158-61.
    View in: PubMed
    Score: 0.013
  17. Meiosis-specific cohesin component, Stag3 is essential for maintaining centromere chromatid cohesion, and required for DNA repair and synapsis between homologous chromosomes. PLoS Genet. 2014 Jul; 10(7):e1004413.
    View in: PubMed
    Score: 0.011
  18. The candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organs. PLoS Genet. 2014 Jan; 10(1):e1004055.
    View in: PubMed
    Score: 0.011
  19. Histone posttranslational modifications and cell fate determination: lens induction requires the lysine acetyltransferases CBP and p300. Nucleic Acids Res. 2013 Dec; 41(22):10199-214.
    View in: PubMed
    Score: 0.010
  20. Insertional mutagenesis by a hybrid piggyBac and sleeping beauty transposon in the rat. Genetics. 2012 Dec; 192(4):1235-48.
    View in: PubMed
    Score: 0.010
  21. Hair follicles are required for optimal growth during lateral skin expansion. J Invest Dermatol. 2009 Oct; 129(10):2358-64.
    View in: PubMed
    Score: 0.008
  22. Bone morphogenetic proteins, eye patterning, and retinocollicular map formation in the mouse. J Neurosci. 2008 Jul 09; 28(28):7057-67.
    View in: PubMed
    Score: 0.007
  23. Renal cysts of inv/inv mice resemble early infantile nephronophthisis. J Am Soc Nephrol. 2004 Jul; 15(7):1744-55.
    View in: PubMed
    Score: 0.006
  24. X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling. Nat Genet. 2001 Mar; 27(3):277-85.
    View in: PubMed
    Score: 0.004
  25. Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis. Development. 2000 Nov; 127(21):4691-700.
    View in: PubMed
    Score: 0.004
  26. Regulation of mouse lens fiber cell development and differentiation by the Maf gene. Development. 2000 Jan; 127(2):307-17.
    View in: PubMed
    Score: 0.004
  27. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia. Nat Genet. 1999 Aug; 22(4):366-9.
    View in: PubMed
    Score: 0.004
  28. Functional dissection of the promoter of the interphotoreceptor retinoid-binding protein gene: the cone-rod-homeobox element is essential for photoreceptor-specific expression in vivo. J Biochem. 1999 Jun; 125(6):1189-99.
    View in: PubMed
    Score: 0.004
  29. Targeting of the rasT24 oncogene to the proximal convoluted tubules in transgenic mice results in hyperplasia and polycystic kidneys. Am J Pathol. 1993 Apr; 142(4):1051-60.
    View in: PubMed
    Score: 0.003
Connection Strength

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