Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Serina M. Mazzoni"'
Publikováno v:
Frontiers in Plant Science, Vol 9 (2018)
Across a broad range of species and biological questions, more and more studies are incorporating translation data to better assess how gene regulation occurs at the level of protein synthesis. The inclusion of translation data improves upon, and has
Externí odkaz:
https://doaj.org/article/1086c06f11b046c78b7a1f6305393377
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 17, Iss 5, Pp 463-472 (2015)
Heterozygous, germline nonsense mutations in AXIN2 have been reported in two families with oligodontia and colorectal cancer (CRC) predisposition, including an AXIN2 1989G>A mutation. Somatic AXIN2 mutations predicted to generate truncated AXIN2 (trA
Externí odkaz:
https://doaj.org/article/4a67d9ecaf584862aa8fe88ac94b13fd
Publikováno v:
Cold Spring Harbor perspectives in biology. 13(10)
Auxin is a crucial growth regulator that governs plant development and responses to environmental perturbations. It functions at the heart of many developmental processes, from embryogenesis to organ senescence, and is key to plant interactions with
Publikováno v:
BMC Genomics, Vol 20, Iss S5, Pp 1-9 (2019)
BMC Genomics
BMC Genomics
Background Ribo-seq is a popular technique for studying translation and its regulation. A Ribo-seq experiment produces a snap-shot of the location and abundance of actively translating ribosomes within a cell’s transcriptome. In practice, Ribo-seq
Autor:
Sean P. Edwards, Monica L. Marvin, Elizabeth M. Petty, Stephen B. Gruber, Serina M. Mazzoni, Casey M. Herron
Publikováno v:
American Journal of Medical Genetics Part A. 155:898-902
We describe a family with a novel, inherited AXIN2 mutation (c.1989G>A) segregating in an autosomal dominant pattern with oligodontia and variable other findings including colonic polyposis, gastric polyps, a mild ectodermal dysplasia phenotype with
Autor:
Linda J. Stuckey, N.M. Walker, Diane C. Fingar, Elizabeth A. Belloli, Andrew C. Chang, Serina M. Mazzoni, Kevin M. Chan, William R. Lynch, Vibha N. Lama, Jules Lin
Publikováno v:
The Journal of biological chemistry. 291(12)
Fibrotic diseases display mesenchymal cell (MC) activation with pathologic deposition of matrix proteins such as collagen. Here we investigate the role of mTOR complex 1 (mTORC1) and mTORC2 in regulating MC collagen expression, a hallmark of fibrotic
Autor:
Eric R. Fearon, Serina M. Mazzoni
Mutations in the APC (adenomatous polyposis coli) gene, which encodes a multi-functional protein with a well-defined role in the canonical Wnt pathway, underlie familial adenomatous polypsosis, a rare, inherited form of colorectal cancer (CRC) and co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25edde1ecef7f0fb7fe3d20065244c3b
https://europepmc.org/articles/PMC4298141/
https://europepmc.org/articles/PMC4298141/
Publikováno v:
Neoplasia: An International Journal for Oncology Research, Vol 17, Iss 5, Pp 463-472 (2015)
Neoplasia (New York, N.Y.)
Neoplasia (New York, N.Y.)
Heterozygous, germline nonsense mutations in AXIN2 have been reported in two families with oligodontia and colorectal cancer (CRC) predisposition, including an AXIN2 1989G>A mutation. Somatic AXIN2 mutations predicted to generate truncated AXIN2 (trA