Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Olga Villamizar"'
Publikováno v:
Journal of Extracellular Vesicles, Vol 10, Iss 3, Pp n/a-n/a (2021)
Abstract Cystic fibrosis is a genetic disorder that results in a multi‐organ disease with progressive respiratory decline which leads to premature death. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene disrupts the
Externí odkaz:
https://doaj.org/article/db82d567ea5a49beb8403663650e59e2
Autor:
Olga Villamizar, Christopher B. Chambers, Yin-Yuan Mo, Donald S. Torry, Reese Hofstrand, Janice M. Riberdy, Derek A. Persons, Andrew Wilber
Publikováno v:
Data in Brief, Vol 7, Iss , Pp 1288-1295 (2016)
This paper describes data related to a research article titled, “Fas-antisense long noncoding RNA is differentially expressed during maturation of human erythrocytes and confers resistance to Fas-mediated cell death” [1]. Long noncoding RNAs (lnc
Externí odkaz:
https://doaj.org/article/0c6613d8f1c54bce97d3b1df52423b59
Autor:
Christopher B Chambers, William P Halford, Joshua Geltz, Olga Villamizar, Jeffrey Gross, Alison Embalabala, Edward Gershburg, Andrew Wilber
Publikováno v:
PLoS ONE, Vol 10, Iss 3, p e0122253 (2015)
Expression systems used to study the biological function of a gene of interest can have limited utility due to three major factors: i) weak or heterogeneous gene expression; ii) poorly controlled gene expression; and iii) low efficiencies of stable i
Externí odkaz:
https://doaj.org/article/74538f029ea44fd2b4686758960c029e
Autor:
Adam Jaffe, Ryan Urak, Alicia Davis, Tristan A. Scott, Kevin V. Morris, Shafagh A. Waters, Olga Villamizar, Sheena Saayman, Nicole Grepo
Publikováno v:
Molecular Therapy
Cystic fibrosis (CF) is caused by mutations in the CF transmembrane conductance regulator (CFTR) gene. The majority of CFTR mutations result in impaired chloride channel function as only a fraction of the mutated CFTR reaches the plasma membrane. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7056f7fc925b5f393eb622d2e6a1617d
https://doi.org/10.1016/j.ymthe.2019.07.002
https://doi.org/10.1016/j.ymthe.2019.07.002
Autor:
Adam Jaffe, Olga Villamizar, Nicole Grepo, Kevin V. Morris, Shafagh A. Waters, Tristan A. Scott
Publikováno v:
Journal of Extracellular Vesicles
Journal of Extracellular Vesicles, Vol 10, Iss 3, Pp n/a-n/a (2021)
Journal of Extracellular Vesicles, Vol 10, Iss 3, Pp n/a-n/a (2021)
Cystic fibrosis is a genetic disorder that results in a multi‐organ disease with progressive respiratory decline which leads to premature death. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene disrupts the capacity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83aa85b94628f9120ba661d577d2cd13
https://pubmed.ncbi.nlm.nih.gov/33532041
https://pubmed.ncbi.nlm.nih.gov/33532041
Publikováno v:
Oncotarget
In multicellular organisms, cell growth and differentiation is controlled in part by programmed cell death or apoptosis. One major apoptotic pathway is triggered by Fas receptor (Fas)-Fas ligand (FasL) interaction. Neoplastic cells are frequently res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04091473beab231da5ecda5ef08c92e8
http://europepmc.org/articles/PMC4924680
http://europepmc.org/articles/PMC4924680
Autor:
Yin-Yuan Mo, Olga Villamizar, Andrew Wilber, Janice M. Riberdy, Donald S. Torry, Reese Hofstrand, Christopher B. Chambers, Derek A. Persons
Publikováno v:
Blood cells, moleculesdiseases. 58
Long noncoding RNAs (lncRNAs) interact with other RNAs, DNA and/or proteins to regulate gene expression during development. Erythropoiesis is one developmental process that is tightly controlled throughout life to ensure accurate red blood cell produ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5a75e54efe2f6c6121255d1115bc4c4
https://pubmed.ncbi.nlm.nih.gov/27067490
https://pubmed.ncbi.nlm.nih.gov/27067490
Autor:
Olga Villamizar, Andrew Wilber, Jeffrey Gross, Alison Embalabala, Edward Gershburg, William P. Halford, Joshua Geltz, Christopher B. Chambers
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 3, p e0122253 (2015)
PLoS ONE, Vol 10, Iss 3, p e0122253 (2015)
Expression systems used to study the biological function of a gene of interest can have limited utility due to three major factors: i) weak or heterogeneous gene expression; ii) poorly controlled gene expression; and iii) low efficiencies of stable i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1566977a25c20e757ac05954198ecf3
https://pubmed.ncbi.nlm.nih.gov/25823013
https://pubmed.ncbi.nlm.nih.gov/25823013
Publikováno v:
eLS
Sickle cell disease (SCD) and β-thalassaemia result from inherited mutations that cause structural abnormality or deficient synthesis of adult haemoglobin. Palliative therapies improve the quality/duration of life for many, but side effects result f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21523fb992a7dfc42218290d72ba53f8
https://doi.org/10.1002/9780470015902.a0025829
https://doi.org/10.1002/9780470015902.a0025829