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Items: 11


Complement Dysregulation and Disease: Insights from Contemporary Genetics.

Liszewski MK, Java A, Schramm EC, Atkinson JP.

Annu Rev Pathol. 2017 Jan 24;12:25-52. doi: 10.1146/annurev-pathol-012615-044145. Epub 2016 Dec 5. Review.


Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration.

Triebwasser MP, Roberson ED, Yu Y, Schramm EC, Wagner EK, Raychaudhuri S, Seddon JM, Atkinson JP.

Invest Ophthalmol Vis Sci. 2015 Oct;56(11):6873-8. doi: 10.1167/iovs.15-17432.


A Familial C3GN Secondary to Defective C3 Regulation by Complement Receptor 1 and Complement Factor H.

Chauvet S, Roumenina LT, Bruneau S, Marinozzi MC, Rybkine T, Schramm EC, Java A, Atkinson JP, Aldigier JC, Bridoux F, Touchard G, Fremeaux-Bacchi V.

J Am Soc Nephrol. 2016 Jun;27(6):1665-77. doi: 10.1681/ASN.2015040348. Epub 2015 Oct 15.


Rare genetic variants in the CFI gene are associated with advanced age-related macular degeneration and commonly result in reduced serum factor I levels.

Kavanagh D, Yu Y, Schramm EC, Triebwasser M, Wagner EK, Raychaudhuri S, Daly MJ, Atkinson JP, Seddon JM.

Hum Mol Genet. 2015 Jul 1;24(13):3861-70. doi: 10.1093/hmg/ddv091. Epub 2015 Mar 18.


A quantitative lateral flow assay to detect complement activation in blood.

Schramm EC, Staten NR, Zhang Z, Bruce SS, Kellner C, Atkinson JP, Kyttaris VC, Tsokos GC, Petri M, Sander Connolly E, Olson PK.

Anal Biochem. 2015 May 15;477:78-85. doi: 10.1016/j.ab.2015.01.024. Epub 2015 Feb 4.


Mapping interactions between complement C3 and regulators using mutations in atypical hemolytic uremic syndrome.

Schramm EC, Roumenina LT, Rybkine T, Chauvet S, Vieira-Martins P, Hue C, Maga T, Valoti E, Wilson V, Jokiranta S, Smith RJ, Noris M, Goodship T, Atkinson JP, Fremeaux-Bacchi V.

Blood. 2015 Apr 9;125(15):2359-69. doi: 10.1182/blood-2014-10-609073. Epub 2015 Jan 21.


Registration of Zak ERA8 Soft White Spring Wheat Germplasm with Enhanced Response to ABA and Increased Seed Dormancy.

Martinez SA, Schramm EC, Harris TJ, Kidwell KK, Garland-Campbell K, Steber CM.

J Plant Regist. 2014 May 1;8(2):217-220.


Genetic variants in the complement system predisposing to age-related macular degeneration: a review.

Schramm EC, Clark SJ, Triebwasser MP, Raychaudhuri S, Seddon J, Atkinson JP.

Mol Immunol. 2014 Oct;61(2):118-125. doi: 10.1016/j.molimm.2014.06.032. Epub 2014 Jul 15. Review.


Whole-exome sequencing identifies rare, functional CFH variants in families with macular degeneration.

Yu Y, Triebwasser MP, Wong EK, Schramm EC, Thomas B, Reynolds R, Mardis ER, Atkinson JP, Daly M, Raychaudhuri S, Kavanagh D, Seddon JM.

Hum Mol Genet. 2014 Oct 1;23(19):5283-93. doi: 10.1093/hmg/ddu226. Epub 2014 May 20.


Increased ABA sensitivity results in higher seed dormancy in soft white spring wheat cultivar 'Zak'.

Schramm EC, Nelson SK, Kidwell KK, Steber CM.

Theor Appl Genet. 2013 Mar;126(3):791-803. doi: 10.1007/s00122-012-2018-0. Epub 2012 Dec 5.


Wheat ABA-insensitive mutants result in reduced grain dormancy.

Schramm EC, Nelson SK, Steber CM.

Euphytica. 2012 Mar 31;188(1):35-49.

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