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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 1 to 2 of 2

Publication Record


A Pkd1-Fbn1 genetic interaction implicates TGF-β signaling in the pathogenesis of vascular complications in autosomal dominant polycystic kidney disease.
Liu D, Wang CJ, Judge DP, Halushka MK, Ni J, Habashi JP, Moslehi J, Bedja D, Gabrielson KL, Xu H, Qian F, Huso D, Dietz HC, Germino GG, Watnick T
(2014) J Am Soc Nephrol 25: 81-91
MeSH Terms: Animals, Disease Models, Animal, Epistasis, Genetic, Female, Fibrillin-1, Fibrillins, Genetic Association Studies, Haploinsufficiency, Heterozygote, Humans, Male, Marfan Syndrome, Mice, Mice, 129 Strain, Mice, Inbred C57BL, Mice, Knockout, Mice, Mutant Strains, Microfilament Proteins, Mutation, Polycystic Kidney, Autosomal Dominant, Signal Transduction, TRPP Cation Channels, Transforming Growth Factor beta, Vascular Diseases
Added March 4, 2015
0 Communities
1 Members
0 Resources
24 MeSH Terms
Marfan syndrome caused by a novel FBN1 mutation with associated pigmentary glaucoma.
Kuchtey J, Chang TC, Panagis L, Kuchtey RW
(2013) Am J Med Genet A 161A: 880-3
MeSH Terms: Adult, Base Sequence, Fibrillin-1, Fibrillins, Glaucoma, Open-Angle, Humans, Iris, Male, Marfan Syndrome, Microfilament Proteins, Mutation, Pedigree, Pigment Epithelium of Eye
Added February 19, 2015
0 Communities
1 Members
0 Resources
13 MeSH Terms