Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Dana Barberio"'
Publikováno v:
Frontiers in Microbiomes, Vol 3 (2024)
The recent FDA approvals of Rebyota™ and Vowst™ represent landmark milestones within the burgeoning field of live microbiota-based products. Future microbiota-based treatment approaches also hold significant promise for treating patients with a m
Externí odkaz:
https://doaj.org/article/218c2837c9674db7af6e92283bb20be2
Autor:
Dana Barberio, Ari Leifer
Publikováno v:
Medical Hypotheses. 88:1-5
Phytoalexins such as resveratrol and pterostilbene, produced de novo by many plant species, including grapevine (Vitis vinifera), play a role in plant defense against injury and pathogens. In human cell lines and in animal studies, phytoalexins have
Autor:
Katherine W. Klinger, Viatcheslav R. Akmaev, Brian P. Cook, Dongyu Liu, Oxana Ibraghimov-Beskrovnaya, Xiaohong Cao, Clarence J. Wang, Gregory M. Landes, Douglas M. Jefferson, Brenda Richards, Hervé Husson, Bruce L. Roberts, Dana Barberio, Partha Manavalan, Ryan J. Russo, Shelley A. Grubman
Publikováno v:
Genomics. 84:497-510
Autosomal dominant polycystic kidney disease (ADPKD) is caused by mutations in the PKD1 or PKD2 gene, but cellular mechanisms of cystogenesis remain unclear. In an attempt to display the array of cyst-specific molecules and to elucidate the disease p
Tumors Associated With Oncogenic Osteomalacia Express Genes Important in Bone and Mineral Metabolism
Autor:
Stephen L. Madden, Brian P. Cook, Justin Cho, Susan C. Schiavi, Joseph M. Petroziello, John Vassiliadis, Suzanne M. Jan de Beur, Partha Manavalan, Scott Estes, Michael A. Levine, Dana Barberio, Rajiv Kumar, Richard Finnegan
Publikováno v:
Journal of Bone and Mineral Research. 17:1102-1110
Oncogenic osteomalacia (OOM) is associated with primitive mesenchymal tumors that secrete phosphaturic factors resulting in low serum concentrations of phosphate and calcitriol, phosphaturia, and defective bone mineralization. To identify overexpress
Autor:
Michael F. Phipps, Steve K. Kotsopoulos, G. Scott Nass, Anthony P. Shuber, Lesley A. Michalowsky, Lisa M. Hire, Dana Barberio, Joel Skoletsky, Katherine W. Klinger
Publikováno v:
Human Molecular Genetics. 6:337-347
As more mutations are identified in genes of known sequence, there is a crucial need in the areas of medical genetics and genome analysis for rapid, accurate and cost-effective methods of mutation detection. We have developed a multiplex allele-speci
Publikováno v:
Molecular and Cellular Probes. 8:241-244
The largest of the commonly used probes for Southern blot diagnosis of fragile X mental retardation syndrome spans the CGG repeat cluster in the FMR-1 gene. This probe causes appearance of 'common' or 'constant' background bands which occasionally co
Publikováno v:
Molecular and Cellular Probes. 8:177-180
A deazaguanine-substituted DNA PCR product from FMR-1 (the fragile X mental retardation syndrome gene) can be efficiently visualized with ethidium bromide on standard agarose gels. Normal-sized alleles (less than 54 CGG repeats) generated strong, eas