Katalin Csiszar to Phenotype
This is a "connection" page, showing publications Katalin Csiszar has written about Phenotype.
Connection Strength
0.598
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Szalontai A, Csiszar K. Genetic insights into the functional elements of language. Hum Genet. 2013 Sep; 132(9):959-86.
Score: 0.384
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Cao T, Racz P, Szauter KM, Groma G, Nakamatsu GY, Fogelgren B, Pankotai E, He QP, Csiszar K. Mutation in Mpzl3, a novel [corrected] gene encoding a predicted [corrected] adhesion protein, in the rough coat (rc) mice with severe skin and hair abnormalities. J Invest Dermatol. 2007 Jun; 127(6):1375-86.
Score: 0.062
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Hayashi K, Cao T, Passmore H, Jourdan-Le Saux C, Fogelgren B, Khan S, Hornstra I, Kim Y, Hayashi M, Csiszar K. Progressive hair loss and myocardial degeneration in rough coat mice: reduced lysyl oxidase-like (LOXL) in the skin and heart. J Invest Dermatol. 2004 Nov; 123(5):864-71.
Score: 0.053
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Urb?n Z, Peyrol S, Plauchu H, Zabot MT, Lebwohl M, Schilling K, Green M, Boyd CD, Csisz?r K. Elastin gene deletions in Williams syndrome patients result in altered deposition of elastic fibers in skin and a subclinical dermal phenotype. Pediatr Dermatol. 2000 Jan-Feb; 17(1):12-20.
Score: 0.038
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Kelemen-Valkony I, Kiss M, Csiha J, Kiss A, Bircher U, Szidonya J, Mar?y P, Juh?sz G, Komonyi O, Csisz?r K, Mink M. Drosophila basement membrane collagen col4a1 mutations cause severe myopathy. Matrix Biol. 2012 Jan; 31(1):29-37.
Score: 0.021
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Rajkumar VS, Howell K, Csiszar K, Denton CP, Black CM, Abraham DJ. Shared expression of phenotypic markers in systemic sclerosis indicates a convergence of pericytes and fibroblasts to a myofibroblast lineage in fibrosis. Arthritis Res Ther. 2005; 7(5):R1113-23.
Score: 0.014
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Le Saux O, Urban Z, Tschuch C, Csiszar K, Bacchelli B, Quaglino D, Pasquali-Ronchetti I, Pope FM, Richards A, Terry S, Bercovitch L, de Paepe A, Boyd CD. Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum. Nat Genet. 2000 Jun; 25(2):223-7.
Score: 0.010
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Lemack GE, Szabo Z, Urban Z, Boyd CD, Csiszar K, Vaughan ED, Felsen D. Altered bladder function in transgenic mice expressing rat elastin. Neurourol Urodyn. 1999; 18(1):55-68.
Score: 0.009
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Olson TM, Michels VV, Urban Z, Csiszar K, Christiano AM, Driscoll DJ, Feldt RH, Boyd CD, Thibodeau SN. A 30 kb deletion within the elastin gene results in familial supravalvular aortic stenosis. Hum Mol Genet. 1995 Sep; 4(9):1677-9.
Score: 0.007