Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Amanda C. Brodeur"'
Autor:
Arin K. Oestreich, Mekka R. Garcia, Xiaomei Yao, Ferris M. Pfeiffer, Sabah Nobakhti, Sandra J. Shefelbine, Yong Wang, Amanda C. Brodeur, Charlotte L. Phillips
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 5, Iss C, Pp 3-11 (2015)
Mucopolysaccharidosis type I (MPS I), is an autosomal recessive lysosomal storage disorder caused by a deficiency in the α-L-iduronidase enzyme, resulting in decreased enzymatic activity and accumulation of glycosaminoglycans. The disorder phenotypi
Externí odkaz:
https://doaj.org/article/6ad02d00d4274b6b919708fdf62ba78d
Autor:
Amy Hulme, Amanda C. Brodeur
Publikováno v:
Molecular Genetics and Metabolism. 132:S297-S298
Autor:
Amanda C. Brodeur, Matthew H. Myles, Elena Makareeva, Sergey Leikin, Charlotte L. Phillips, Craig L. Franklin, Anna M. Roberts-Pilgrim, Andrew L. Walker, Cynthia Besch-Williford
Publikováno v:
Molecular Genetics and Metabolism. 104:373-382
Col1a2-deficient (oim) mice synthesize homotrimeric type I collagen due to nonfunctional proα2(I) collagen chains. Our previous studies revealed a postnatal, progressive type I collagen glomerulopathy in this mouse model, but the mechanism of the sc
Autor:
Xiaotong Wu, Halena Hadi, Robert K. Delong, Adam K. Wanekaya, Amanda C. Brodeur, Garry Glaspell, Ravindra Thakkar, Amanda Hoffman, Molly Duszynski, Rintu Thomas, Jianjie Wang
Publikováno v:
Materials
Materials, Vol 10, Iss 12, p 1430 (2017)
Materials, Vol 10, Iss 12, p 1430 (2017)
Two-dimensional fluorescence difference spectroscopy (2-D FDS) was used to determine the unique spectral signatures of zinc oxide (ZnO), magnesium oxide (MgO), and 5% magnesium zinc oxide nanocomposite (5% Mg/ZnO) and was then used to demonstrate the
Autor:
D. A. Wirth, J. Miner, L. W. Reneker, Amanda C. Brodeur, Charlotte L. Phillips, Craig L. Franklin
Publikováno v:
Kidney international. 71(10)
In chronic renal disease, the progressive accumulation of collagen and other extracellular matrix proteins in the mesangium results in fibrosis, glomerulosclerosis, and eventual renal failure. Mice deficient in proalpha2(I) collagen are not only a mo
Autor:
Amanda C. Brodeur, Andrew L. Walker, Anna M. Roberts-Pilgrim, J. Miner, Charlotte L. Phillips, Craig L. Franklin
Publikováno v:
Matrix Biology. 25:S66-S66