 Connection
Katherine Fantauzzo to Mutation
This is a "connection" page, showing publications Katherine Fantauzzo has written about Mutation.
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Connection Strength |
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0.187 |
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Fantauzzo KA, Soriano P. PDGFRß regulates craniofacial development through homodimers and functional heterodimers with PDGFRa. Genes Dev. 2016 11 01; 30(21):2443-2458.
Score: 0.056
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Fantauzzo KA, Soriano P. PI3K-mediated PDGFRa signaling regulates survival and proliferation in skeletal development through p53-dependent intracellular pathways. Genes Dev. 2014 May 01; 28(9):1005-17.
Score: 0.047
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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.
Score: 0.042
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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.
Score: 0.030
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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.
Score: 0.012
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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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