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Connection

Katherine Fantauzzo to Humans

This is a "connection" page, showing publications Katherine Fantauzzo has written about Humans.

 
Connection Strength
 
 
 
0.151
 
  1. Brooks EC, Griffin CW, Fantauzzo KA. Roles of the RNA-binding protein SRSF3 in development and cellular differentiation. Differentiation. 2026 May-Jun; 149:100958.
    View in: PubMed
    Score: 0.023
  2. Campaña MB, Perkins MR, McCabe MC, Neumann A, Larson ED, Fantauzzo KA. PDGFRa/ß heterodimer activation negatively affects downstream ERK1/2 signaling and cellular proliferation. Nat Commun. 2025 May 22; 16(1):4754.
    View in: PubMed
    Score: 0.022
  3. Rogers MA, Campaña MB, Long R, Fantauzzo KA. PDGFR dimer-specific activation, trafficking and downstream signaling dynamics. J Cell Sci. 2022 09 01; 135(17).
    View in: PubMed
    Score: 0.018
  4. Rogers MA, Fantauzzo KA. The emerging complexity of PDGFRs: activation, internalization and signal attenuation. Biochem Soc Trans. 2020 06 30; 48(3):1167-1176.
    View in: PubMed
    Score: 0.016
  5. Fantauzzo KA, Soriano P. Generation of an immortalized mouse embryonic palatal mesenchyme cell line. PLoS One. 2017; 12(6):e0179078.
    View in: PubMed
    Score: 0.013
  6. Fantauzzo KA, Soriano P. Receptor tyrosine kinase signaling: regulating neural crest development one phosphate at a time. Curr Top Dev Biol. 2015; 111:135-82.
    View in: PubMed
    Score: 0.011
  7. Fantauzzo KA, Kurban M, Levy B, Christiano AM. Trps1 and its target gene Sox9 regulate epithelial proliferation in the developing hair follicle and are associated with hypertrichosis. PLoS Genet. 2012; 8(11):e1003002.
    View in: PubMed
    Score: 0.009
  8. Fantauzzo KA, Tadin-Strapps M, You Y, Mentzer SE, Baumeister FA, Cianfarani S, Van Maldergem L, Warburton D, Sundberg JP, Christiano AM. A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice. Hum Mol Genet. 2008 Nov 15; 17(22):3539-51.
    View in: PubMed
    Score: 0.007
  9. Artinger KB, Fantauzzo KA, Merrill AE, Stottmann RW, Taneyhill LA, Van Otterloo E, Harris MP. The Society for Craniofacial Genetics and Developmental Biology 48th Annual Meeting. Am J Med Genet A. 2026 09; 200(9):2162-2170.
    View in: PubMed
    Score: 0.006
  10. Trainor PA, Cox TC, Clouthier DE, Fantauzzo KA, Harris MP, Jeong J, Stottmann RW, Merrill AE. The Society for Craniofacial Genetics and Developmental Biology 47th Annual Meeting. Am J Med Genet A. 2025 07; 197(7):e64059.
    View in: PubMed
    Score: 0.005
  11. Brugmann SA, Clouthier DE, Fantauzzo KA, Harris MP, Jeong J, Saint-Jeannet JP, Stottmann RW, Merrill AE. The society for craniofacial genetics and developmental biology 46th annual meeting. Am J Med Genet A. 2024 08; 194(8):e63615.
    View in: PubMed
    Score: 0.005
  12. Micke KC, Elfman HM, Fantauzzo KA, McGrath PS, Clouthier DE, McCandless SE, Larson A, Putra M, Cuneo BF, Reynolds RM, Zaretsky MV. Piloting a multidisciplinary approach to improve outcomes of fetal whole exome sequencing: An overview of workflow and case example. Prenat Diagn. 2023 04; 43(4):544-552.
    View in: PubMed
    Score: 0.005
  13. DeStefano GM, Kurban M, Anyane-Yeboa K, Dall'Armi C, Di Paolo G, Feenstra H, Silverberg N, Rohena L, López-Cepeda LD, Jobanputra V, Fantauzzo KA, Kiuru M, Tadin-Strapps M, Sobrino A, Vitebsky A, Warburton D, Levy B, Salas-Alanis JC, Christiano AM. Mutations in the cholesterol transporter gene ABCA5 are associated with excessive hair overgrowth. PLoS Genet. 2014; 10(5):e1004333.
    View in: PubMed
    Score: 0.003
  14. DeStefano GM, Fantauzzo KA, Petukhova L, Kurban M, Tadin-Strapps M, Levy B, Warburton D, Cirulli ET, Han Y, Sun X, Shen Y, Shirazi M, Jobanputra V, Cepeda-Valdes R, Cesar Salas-Alanis J, Christiano AM. Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis. Proc Natl Acad Sci U S A. 2013 May 07; 110(19):7790-5.
    View in: PubMed
    Score: 0.002
  15. Kurban M, Kim CA, Kiuru M, Fantauzzo K, Cabral R, Abbas O, Levy B, Christiano AM. Copy number variations on chromosome 4q26-27 are associated with Cantu syndrome. Dermatology. 2011; 223(4):316-20.
    View in: PubMed
    Score: 0.002
  16. Ishii Y, Wajid M, Bazzi H, Fantauzzo KA, Barber AG, Blaydon DC, Nam JS, Yoon JK, Kelsell DP, Christiano AM. Mutations in R-spondin 4 (RSPO4) underlie inherited anonychia. J Invest Dermatol. 2008 Apr; 128(4):867-70.
    View in: PubMed
    Score: 0.002
  17. Bazzi H, Fantauzzo KA, Richardson GD, Jahoda CA, Christiano AM. The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis. Dev Biol. 2007 May 15; 305(2):498-507.
    View in: PubMed
    Score: 0.002
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.

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